Physician

31.1Enrollment

Physicians, podiatrists, physician groups, and podiatry groups may enroll as Children with Special Healthcare Needs (CSHCN) Services Program providers by completing the provider enrollment application available through the Provider Enrollment and Management System (PEMS). Providers may also enroll or reenroll in the CSHCN Services Program online through PEMS. For assistance with the application process, call the TMHP-CSHCN Services Program Contact Center at 1-800-568-2413, Option 2.

In this section the term “physician” means a doctor of medicine (MD), doctor of osteopathy (DO), or doctor of podiatric medicine (DPM).

Physicians must be actively enrolled as a Medicaid provider before enrolling in the CSHCN Services Program. “Actively enrolled” physicians are those that have filed claims for clients of the CSHCN Services Program or Texas Medicaid within the past 24 months, and that do not have any type of payment holds on their enrollment status. Physicians must be licensed by the Texas licensing board. Out-of-state physicians must meet all these conditions and be located in the United States, within 50 miles of the Texas state border.

Requests for medical services provided by an out-of-state provider more than 50 miles from the Texas state border must be submitted for consideration to TMHP at the address in Section 2.1, “Provider Enrollment” in Chapter 2, “Provider Enrollment and Responsibilities.”

Refer to: Section 2.1.9, “Out-of-State Providers” in Chapter 2, “Provider Enrollment and Responsibilities” for more information about out-of-state services.

Important:CSHCN Services Program providers are responsible for knowing, understanding, and complying with the laws, administrative rules, and policies of the CSHCN Services Program and Texas Medicaid.

By enrolling in the CSHCN Services Program, providers are charged not only with knowledge of the adopted CSHCN Services Program agency rules published in Title 26 Texas Administrative Code (TAC) Chapter 38, but also with knowledge of the adopted Medicaid agency rules published in 1 TAC, Part 15, and specifically including the fraud and abuse provisions contained in Chapter 371.

CSHCN Services Program providers also are required to comply with all applicable laws, administrative rules, and policies that apply to their professions or to their facilities. Specifically, it is a violation of program rules when a provider fails to provide health-care services or items to recipients in accordance with accepted medical community standards and standards that govern occupations, as explained in 1 TAC §371.1659 for Medicaid providers, which also applies to CSHCN Services Program providers as set forth in 26 TAC §351.6(b)(1). Accordingly, CSHCN Services Program providers can be subject to sanctions for failure to deliver, at all times, health-care items and services to recipients in full accordance with all applicable licensure and certification requirements. These include, without limitation, requirements related to documentation and record maintenance, such that a CSHCN Services Program provider can be subject to sanctions for failure to create and maintain all records required by his or her profession, as well as those required by the CSHCN Services Program and Texas Medicaid.

Refer to: Section 2.1, “Provider Enrollment” in Chapter 2, “Provider Enrollment and Responsibilities” for more detailed information about CSHCN Services Program provider enrollment procedures.

Section 2.1.5.1, “Types of Providers” in Chapter 2, “Provider Enrollment and Responsibilities” for additional information.

Section 3.1.4, “Services Provided Outside of Texas” in Chapter 3, “Client Benefits and Eligibility” for more detailed information about services provided outside of Texas.

31.1.1Group Practices

Provider groups that are enrolled in Texas Medicaid can enroll in the CSHCN Services Program by completing an enrollment application. The CSHCN Services Program application must include the Medicaid group provider identifier and performing provider identifiers for all physicians in the group.

31.1.2Changes in Provider Enrollment

If additions or changes occur in the provider’s enrollment information after the enrollment process is completed, the provider must notify TMHP of the changes through PEMS.

Refer to: Section 2.1.2, “Changes in Enrollment” in Chapter 2, “Provider Enrollment and Responsibilities” for additional information.

31.1.3Substitute Physician

Physicians may bill for the services of a substitute physician who sees clients in the billing physician’s practice under either a reciprocal or locum tenens arrangement.

A reciprocal arrangement is one in which a substitute physician covers for the billing physician on an occasional basis when the billing physician is unavailable to provide services. Reciprocal arrangements are limited to a continuous period no longer than 14 days and do not have to be in writing.

A locum tenens arrangement is one in which a substitute physician assumes the practice of a billing physician for a temporary period no longer than 90 days when the billing physician is absent for reasons such as illness, pregnancy, vacation, continuing medical education, or active duty in the Armed Forces. The locum tenens arrangement may be extended for a continuous period longer than 90 days if the billing physician’s absence is due to being called or ordered to active duty as a member of a reserve component of the Armed Forces. Locum tenens arrangements must be in writing.

Substitute physicians are required to enroll with the CSHCN Services Program. Substitute physicians are also required to enroll with Texas Medicaid before enrolling in the CSHCN Services Program and cannot be on the Texas Medicaid provider exclusion list.

The billing provider’s name, address, and national provider identifier must appear in Block 33 of the claim form. The name and mailing address of the substitute physician must be documented on the claim in Block 19, not Block 33. When a physician bills for a substitute physician, the modifier Q5 or Q6 must follow the procedure code in Block 24D for services provided by the substitute physician. The Q5 modifier is used to indicate a reciprocal arrangement and the Q6 modifier is used to indicate a locum tenens arrangement.

31.2Benefits, Limitations, and Authorization Requirements

Physician and podiatrist services include reasonable and medically necessary services that are ordered and performed by a physician or under the personal supervision of a physician and that are within the scope of practice of his or her profession, as defined by state law. The physician must examine the client, make a diagnosis, establish a plan of care, and document these tasks on the appropriate client medical records before submitting claims. Payment may be recouped if the documentation is not in the client’s medical record.

To be payable by the CSHCN Services Program, services must be personally performed by the physician or by a qualified person working under the personal supervision of the physician. Personal supervision means that the physician must be in the building of the office or facility when and where the service is provided. Direct supervision means the physician must be physically present in the room at the time the service is provided.

If an attending physician provides personal and identifiable direction to interns or residents who are participating in the care of a CSHCN Services Program client in a teaching setting through an approved and accredited training program by the appropriate accreditation agencies, the attending physician’s services are a benefit. For major surgical procedures and other complex and dangerous procedures or situations, the attending physician must be physically present during the procedure or situation to provide personal and identifiable direction. Payment for services may be recouped if personal and identifiable direction is not provided or is not appropriately documented.

To demonstrate that personal and identifiable direction was provided, the attending physician must have:

Reviewed the client’s history and physical examination and personally examined the client within a reasonable period after the client’s admission and before the client’s discharge.

Confirmed or revised the client’s diagnosis.

Determined the course of treatment to be followed.

Provided appropriate supervision of the interns or residents.

Entered the appropriate daily documentation of the tasks identified above in the client’s medical record before the claim is submitted.

31.2.1Authorization and Prior Authorization Requirements

Some services, as specified throughout this chapter, require authorization or prior authorization as a condition for reimbursement. Authorization and prior authorization is not a guarantee of payment.

Authorization must occur no later than 95 days after the date of service.

Prior authorization must be obtained before the service is provided.

Authorization requests received after the authorization deadline are denied.

The 95-day filing deadline is for all services that require authorization (not prior authorization), including extensions and emergency situations.

Before submitting an authorization or prior authorization request, the provider must verify the client’s eligibility. Any service provided while the client is not eligible cannot be reimbursed. Providers are responsible for knowing which services require authorization or prior authorization.

All requests for prior authorizations or authorizations must be submitted in writing on the CSHCN Services Program-approved authorization and prior authorization forms. Forms are located on the Forms page of the TMHP website. Providers may fax their authorization or prior authorization requests to the TMHP-CSHCN Services Program Authorization Department at 1-512-514-4222. This fax number is only for authorization or prior authorization requests.

Fax transmittal confirmations are not accepted as proof of timely authorization or prior authorization submission.

Requests to extend the authorization deadline are not considered except in cases involving retroactive eligibility.

Exception:For clients that receive retroactive eligibility, the authorization and prior authorization requirement may be waived if the client’s eligibility had not been determined by the time TMHP received the request. Claims for these services must be received within 95 days of the eligibility add date and must include a completed request for authorization/prior authorization, along with all other applicable documentation.

Refer to: Chapter 4, “Prior Authorizations and Authorizations” for additional information.

Section 4.3.1, “Services that Require Authorization” in Chapter 4, “Prior Authorizations and Authorizations” for a list of some of the services requiring authorization.

Section 4.4.1, “Services that Require Prior Authorization” in Chapter 4, “Prior Authorizations and Authorizations” for a list of some of the services requiring prior authorization.

31.2.2Aerosol Treatments/Inhalation Therapy

Aerosol therapy is a benefit of the CSHCN Services Program. Continuous inhalation treatment with aerosol medication for acute airway obstruction (procedure codes 94644 and 94645) is a benefit of the CSHCN Services Program.

On physician claims, nebulizers and metered-dose inhaler treatments must be billed with procedure code 94640.

Pentamidine aerosol treatment (procedure codes 94642 and J2545) is a benefit of the CSHCN Services Program for diagnosis codes B20, D8481, D84821, D84822, and D8489 for the treatment of pneumocystis carinii.

Procedure code J7605 may be reimbursed when billed with the following diagnosis codes:

Diagnosis Codes

A150

E840

J09X1

J09X2

J09X9

J1000

J1001

J1008

J101

J1100

J1108

J111

J121

J15212

J188

J189

J210

J211

J218

J398

J410

J411

J418

J42

J430

J431

J432

J438

J439

J440

J441

J449

J4520

J4521

J4522

J4530

J4531

J4532

J4540

J4541

J4542

J4550

J4551

J4552

J45901

J45902

J45909

J45990

J45991

J45998

J470

J471

J479

J60

J61

J620

J628

J630

J631

J632

J633

J634

J635

J64

J660

J661

J662

J668

J670

J671

J672

J673

J674

J675

J676

J677

J678

J679

J680

J681

J682

J683

J684

J689

J690

J691

J698

J700

J701

J705

J708

J709

J9801

J9809

Q334

R051

R052

R053

R054

R058

R059

Z7182

Procedure code J7608 may be reimbursed when billed with the following diagnosis codes:

Diagnosis Codes

A150

E840

J09X1

J09X2

J09X9

J1000

J1001

J1008

J101

J1100

J1108

J111

J121

J15212

J188

J189

J210

J211

J218

J398

J410

J411

J418

J42

J430

J431

J432

J438

J439

J440

J441

J449

J4520

J4521

J4522

J4530

J4531

J4532

J4540

J4541

J4542

J4550

J4551

J4552

J45901

J45902

J45909

J45990

J45991

J45998

J470

J471

J479

J60

J61

J620

J628

J630

J631

J632

J633

J634

J635

J64

J660

J661

J662

J668

J670

J671

J672

J673

J674

J675

J676

J677

J678

J679

J680

J681

J682

J683

J684

J689

J690

J691

J698

J700

J701

J708

J709

J8281

J8282

J9801

J9809

Q334

R051

R052

R053

R058

R059

Z7182


Procedure codes J7622, J7631, J7639, J7644, and J7682 may be reimbursed when billed with the following diagnosis codes:

Diagnosis Codes

A150

E840

J09X1

J09X2

J09X9

J1000

J1001

J1008

J101

J1100

J1108

J111

J121

J15212

J188

J189

J210

J211

J218

J398

J410

J411

J418

J42

J430

J431

J432

J438

J439

J440

J441

J449

J4520

J4521

J4522

J4530

J4531

J4532

J4540

J4541

J4542

J4550

J4551

J4552

J45901

J45902

J45909

J45990

J45991

J45998

J470

J471

J479

J60

J61

J620

J628

J630

J631

J632

J633

J634

J635

J64

J660

J661

J662

J668

J670

J671

J672

J673

J674

J675

J676

J677

J678

J679

J680

J681

J682

J683

J684

J689

J690

J691

J698

J700

J701

J708

J709

J9801

J9809

Q334

R051

R052

R053

R054

R058

R059

Z7182

Procedure code J7626 may be reimbursed when billed with the following diagnosis codes:

Diagnosis Codes

A150

E840

J09X1

J09X2

J09X9

J1000

J1001

J1008

J101

J1100

J1108

J111

J121

J15212

J188

J189

J210

J211

J218

J398

J410

J411

J418

J42

J430

J431

J432

J438

J439

J440

J441

J449

J4520

J4521

J4522

J4530

J4531

J4532

J4540

J4541

J4542

J4550

J4551

J4552

J45901

J45902

J45909

J45990

J45991

J45998

J470

J471

J479

J60

J61

J620

J628

J630

J631

J632

J633

J634

J635

J64

J660

J661

J662

J668

J670

J671

J672

J673

J674

J675

J676

J677

J678

J679

J680

J681

J682

J683

J684

J689

J690

J691

J698

J700

J701

J708

J709

J9801

J9809

Q334

R051

R052

R053

R054

R058

R059

Z7182





Procedure code J7633 may be reimbursed when billed with the following diagnosis codes:

D

Diagnosis Codes

A150

E840

J09X1

J09X2

J09X9

J1000

J1001

J1008

J101

J1100

J1108

J111

J121

J15212

J188

J189

J210

J211

J218

J398

J410

J411

J418

J42

J430

J431

J432

J438

J439

J440

J441

J449

J4520

J4521

J4522

J4530

J4531

J4532

J4540

J4541

J4542

J4550

J4551

J4552

J45901

J45902

J45909

J45990

J45991

J45998

J470

J471

J479

J60

J61

J620

J628

J630

J631

J632

J633

J634

J635

J64

J660

J661

J662

J668

J670

J671

J672

J673

J674

J675

J676

J677

J678

J679

J680

J681

J682

J683

J684

J689

J690

J691

J698

J700

J701

J708

J709

J9801

J9809

Q334

Z7182


31.2.3Allergy Services

Allergy testing and desensitization are benefits of the CSHCN Services Program.

Providers must use the following procedure codes to bill for allergy testing:

Procedure Codes

86001

86003

86005

86008

86486

95004

95017

95018

95024

95027

95028

95076

95180

95199

Allergy blood testing (procedure codes 86001, 86003, 86005, and 86008) are a benefit of the CSHCN Services Program under the following circumstances:

The client is unable to discontinue medications

An allergy skin test is inappropriate for the client because of the following reasons:

The client is pediatric

The client is disabled

The client suffers from a skin condition such as dermatitis

Procedure code 86001 is limited to 20 allergens per rolling year, any provider. Procedure codes 86003 and 86008 are limited to 30 allergens per rolling year, any provider. Procedure code 86005 is limited to 4 screenings per rolling year, same provider.

Providers must indicate the number of allergens tested in the Units field in Block 24G of the CMS-1500 paper claim form. If the number of tests is not indicated in this field, payment is made for only one test.

31.2.3.1Collagen Skin Tests

Collagen skin tests are a benefit of the CSHCN Services Program and may be reimbursed using procedure code Q3031.

Collagen skin tests are administered to detect a hypersensitivity to bovine collagen. This skin test is given four weeks prior to any type of surgical procedure which utilizes collagen.

31.2.3.2Prior Authorization Requirements

Allergy services generally do not require prior authorization; however, prior authorization is required for unlisted procedure code 95199 and when benefit limitations are exceeded for procedure codes 86001, 86003, 86005, and 86008.

Every effort should be made to use the appropriate Healthcare Common Procedure Coding System (HCPCS) or Current Procedural terminology (CPT) procedure code which describes the procedure being performed. If a procedure code does not exist to describe the service performed, procedure code 95199 should be submitted with appropriate documentation to assist in determining coverage. The documentation submitted must include all of the following:

The client’s diagnosis

Medical records indicating prior treatment for this diagnosis and the medical necessity of the requested procedure

A clear, concise description of the procedure to be performed

Reason for recommending the procedure

A CPT or HCPCS procedure code that is comparable to the procedure being requested

Documentation that the procedure is not investigational or experimental

Place of service the procedure is to be performed

The physician’s intended fee for this procedure

Requests for prior authorization of procedure codes 86001, 86003, 86005, and 86008 must be submitted with documentation of medical necessity and include all of the following:

Results of any previous treatment

Documentation indicating that the client’s treatment could not be completed within the policy limits for the requested procedures

Client diagnosis and conditions that support the medical necessity for the additional procedures requested

Explanation of client outcomes that the requested procedures will achieve

Prior authorization requests must be submitted using the CSHCN Services Program Authorization and Prior Authorization Request Form.

31.2.4Ambulatory Blood Pressure Monitoring

Blood pressure monitoring by either self-measured blood pressure monitoring or ambulatory blood pressure monitoring are benefits of the CSHCN Services Program when used as a diagnostic tool to assist a physician in diagnosing hypertension in individuals whose blood pressure is either elevated, or inconclusive when evaluated in the office alone.

Self-measured blood pressure monitoring and ambulatory blood pressure monitoring are a benefit for the initial diagnosis of hypertension and should not be used for maintenance monitoring. Self-measured blood pressure monitoring and ambulatory blood pressure monitoring are indicated for the evaluation of one of the following conditions:

White coat hypertension, which includes all of the following:

A clinic or office blood pressure measurement greater than 140/90 mm Hg on at least three separate clinic or office visits with two separate measurements made at each visit

At least two documented separate blood pressure measurements taken outside the clinic or office, which are less than 140/90 mm Hg

No evidence of end-organ damage

Resistant hypertension

Evaluation of hypotensive symptoms as a response to hypertension medications

Nocturnal angina

Episodic hypertension

Evaluation of syncope

Providers must document that the self-measured blood pressure monitoring and ambulatory blood pressure monitoring was performed for at least 24 hours.

Providers must use procedure codes 93784, 93786, 93788, and 93790 when billing for ambulatory blood pressure monitoring.

Ambulatory blood pressure monitoring is limited to two services per lifetime, any provider. Claims that exceed the limitation of two services per lifetime may be considered for reimbursement when documentation of medical necessity is submitted with the claim.

Self-measured blood pressure monitoring procedure code 99473 is limited to one service per year, any provider. Procedure code 99473 may be considered for reimbursement more than once per year when the following documentation of medical necessity is submitted with the claim:

Documentation of erroneous blood pressure readings - excessively high or low blood pressure, blood pressure readings excessively inconsistent with those measured professionally

Documentation of erroneous blood pressure logs - day of the week, time of day, setting or location, or timing of medication administration inconsistent with prior professional instruction

Documentation of poor health literacy, developmental, or intellectual challenges that may require repeated client education

Client purchase or receipt of new blood pressure device

Self-measured blood pressure monitoring procedure code 99474 is limited to four services per year, any provider, and may be reimbursed only if a claim for procedure code 99473 has been submitted within 12 rolling months.

Only one method of blood pressure monitoring (self-measured or ambulatory) may be reimbursed within a rolling 12-month period. Self-measured blood pressure monitoring submitted within the same rolling 12-month period as ambulatory blood pressure monitoring will be denied.

31.2.5Anesthesia Services

Anesthesia services are a benefit of the CSHCN Services Program and may be reimbursed to anesthesiologists, certified registered nurse anesthetists (CRNAs), anesthesiologist assistants (AA), and other qualified professionals.

Anesthesia must be administered by an anesthesia practitioner. An anesthesia practitioner is defined as the following:

An anesthesiologist performing the anesthesia service alone or medically directs a CRNA, AA, or other qualified professional

A CRNA who is not medically directed

An AA performing delegated services

A qualified professional as identified by the Texas Medical Board performing delegated services

Authorization is not required for anesthesia services. Specific surgical procedures, however, may require prior authorization. Anesthesia may be reimbursed if prior authorization for the surgical procedure was not obtained, but services provided by the facility, surgeon, and assistant surgeon are denied.

For time-based anesthesiology procedure codes, anesthesia practitioners must document interruptions in anesthesia time in the client’s medical record. Anesthesia time begins when the anesthesia practitioner begins to prepare the client for the induction of anesthesia in the operating room or the equivalent area and ends when the anesthesia practitioner is no longer in personal attendance (e.g., when the client may be safely placed under postoperative supervision).

The anesthesiologist who medically directs the CRNA, AA, or other qualified professional must document the same time that the CRNA, AA, or other qualified professional documents.

Time units are determined on the basis of one time unit for each 15 minutes of anesthesia. Providers must submit the total anesthesia time in minutes on the claim. The claims administrator will convert total minutes to time units.

Anesthesia services for obstetrical or family planning procedures are not a benefit of the CSHCN Services Program.

Local, regional, or general anesthesia provided by a surgeon is not a separately payable benefit of the CSHCN Services Program when performed by the operating surgeon. If anesthesia services are provided and modifier 47 is used, the services are included in the global fee for the surgical procedure.

31.2.5.1Medical Direction

Personal medical direction of an anesthesia practitioner (CRNA, AA, or other qualified professional) by an anesthesiologist is a benefit of the CSHCN Services Program if the following criteria are met:

No more than four anesthesia procedures are being performed concurrently.

Exception:Anesthesiologists may simultaneously supervise more than a combination of four CRNAs, AAs, or other qualified professionals, as defined by the Texas Medical Board under emergency circumstances.

The anesthesiologist is physically present in the operating suite.

Medical direction is a covered service only if all of the following criteria are met:

The anesthesiologist performs a preanesthetic examination and evaluation.

The anesthesiologist prescribes the anesthesia plan.

The anesthesiologist personally participates in the critical and key portions of the anesthesia plan, including induction and emergence, if applicable.

The anesthesiologist must ensure that a qualified professional, including anesthesiologist assistants, can perform any procedures in the anesthesia plan that the anesthesiologist does not perform personally.

The anesthesiologist monitors the course of anesthesia administration at frequent intervals.

The anesthesiologist must provide direct supervision when medically directing an anesthesia procedure. Direct supervision means the anesthesiologist must be immediately available to furnish assistance and direction.

The anesthesiologist provides indicated postanesthesia care.

The anesthesiologist does not perform any other services (except as noted below) during the same time period. The anesthesiologist directing the administration of no more than four anesthesia procedures may provide the following without affecting the eligibility of the medical direction services:

Address an emergency of short duration in the immediate area.

Administer an epidural or caudal anesthetic to ease labor pain for a client who is not enrolled in the CSHCN Services Program.

Provide periodic, rather than continuous, monitoring of an obstetrical client who is not enrolled in the CSHCN Services Program.

Receive clients entering the operating suite for the next surgery.

Check or discharge clients in the recovery room.

Handle scheduling matters.

An anesthesiologist may medically direct up to four concurrent anesthesia procedures. Concurrent medical direction refers to involvement of the anesthesiologist in directing two, three, or four current anesthesia procedures.

Concurrency is defined as the maximum number of procedures that the anesthesiologist is medically directing within the context of a single procedure and whether those other procedures overlap each other. Concurrency is not dependent on each of the cases involving a CSHCN Services Program client. For example, if three procedures are medically directed but only two involve CSHCN Services Program clients, the CSHCN Services Program claims should be billed as concurrent medical direction of three procedures.

The following information must be available to the state upon request and is subject to retrospective review:

The name of each CRNA, AA, and other qualified professional concurrently being medically directed or supervised and a description of the procedure that was performed must be documented and maintained on file.

Signatures of the anesthesiologist, CRNAs, AAs, or other qualified professionals involved in administering anesthesia services must be documented in the client’s medical record.

For medical direction, the anesthesiologist must document in the client’s medical record that he or she:

Performed the pre-anesthetic exam and evaluation.

Provided the indicated post-anesthesia care.

Was present during the critical and key portions of the anesthesia procedure including, if applicable, induction and emergence.

Was present during the anesthesia procedure to monitor the client’s status.

31.2.5.2Monitored Anesthesia Care

Monitored anesthesia care may include any of the following:

Intraoperative monitoring by an anesthesiologist or qualified professional under the medical direction of an anesthesiologist.

Monitoring the client’s vital physiological signs in anticipation of the need for general anesthesia.

Monitoring the client to detect development of an adverse physiological reaction to a surgical procedure.

31.2.5.3Anesthesia Modifiers

Each anesthesia procedure code must be submitted with the appropriate anesthesia modifier(s) whether billing as the sole provider or for the medical direction of CRNAs, AAs, or other qualified professionals.

When an anesthesia procedure is billed without the appropriate reimbursement modifiers, or is billed with modifier combinations other than those listed in this section, the claim is denied.

A claim billed with a modifier indicating that the anesthesia was not medically directed or medically supervised (modifier AD, QK, QX, or QY) is denied if a previous claim has been billed with a modifier indicating the service was personally performed (modifier AA or QZ) and is reimbursed for the same client, date of service, and procedure code.

A claim billed with a modifier indicating that the anesthesia was personally performed by an anesthesiologist (modifier AA) is denied if another claim has been paid indicating the service was personally performed by, and reimbursed to, a CRNA (modifier QZ) for the same client, date of service, and procedure code. The opposite is also true—a CRNA-administered procedure is denied if a previous claim was paid to an anesthesiologist for the same client, date of service, and procedure code. Denied claims may be appealed with supporting documentation of any unusual circumstances.

31.2.5.3.1State-Defined Modifiers

Modifiers U1 (indicating one anesthesia claim is expected) and U2 (indicating two anesthesia claims are expected) are state-defined modifiers that may be billed by an anesthesiologist, CRNA, AA, or other qualified professional.

Modifier U3 indicates that the anesthesia was performed with dental services.

Modifier U1 indicating that only one claim will be submitted, cannot be billed by two providers for the same procedure, client, and date of service. Modifier U2, indicating that two claims will be submitted, can only be billed by two providers for the same procedure, client, and date of service if one of the providers was medically directed by the other. Denied claims may be appealed with supporting documentation of any unusual circumstances.

Anesthesia providers must submit the modifier U1 or U2 in combination with an appropriate pricing modifier when billing for any payable anesthesia procedure codes.

31.2.5.3.2Anesthesiologist Services and Modifier Combinations

When a single claim per client is billed by the anesthesiologist for personally performing the anesthesia service, the AA and U1 modifier combination must be billed together.

Anesthesiologists may be reimbursed for medical direction of anesthesia practitioners by using one of the following modifier combinations:

Modifier Combination Submitted by Anesthesiologist

When is it used?

Who will submit claims?

Anesthesiologist Providing Medical Direction or Medical Supervision to Other Qualified Professionals

QY and U1

When a single claim per client is billed by the anesthesiologist for medically directing anesthesia services of an anesthesia procedure provided by one CRNA, AA, or other qualified professional, the QY + U1 modifier combination must be billed together if the CRNA, AA, or qualified professional are a part of a clinic/group.

Only the anesthesiologist

QK and U1

When a single claim per client is billed by the anesthesiologist for medically directing anesthesia services of two, three, or four concurrent anesthesia procedures provided by CRNAs, AAs, or other qualified professionals.

Only the anesthesiologist

AA, U1, and GC

When a single claim per client is billed by the anesthesiologist for medically directing anesthesia services of an anesthesia procedure provided by one resident physician.

Only the anesthesiologist

AD and U1 (emergency circumstances only)

When a single claim per client is billed by the anesthesiologist for medically supervising anesthesia services provided by more than four concurrent procedures that are provided by a CRNA, AA, or other qualified professional. The AD modifier must be used in emergency circumstances only and limited to 6 units (90 minutes maximum) per case for each occurrence requiring supervision of five or more concurrent procedures.

Only the anesthesiologist

Anesthesiologist Providing Medical Direction or Medical Supervision of CRNAs or AAs

QY and U2

When two claims per client are billed, one by the medically directing anesthesiologist and one by the CRNA, AA, or other qualified professional.

Both the anesthesiologist and CRNA, AA, or other qualified professional

QK and U2

When two claims per client are billed for medically directing anesthesia services of two, three, or four concurrent anesthesia procedures provided by CRNA(s), AA(s), or other qualified professionals.

Both the anesthesiologist and CRNA(s), AA(s), or other qualified professional

AD and U2 (emergency circumstances only)

When two claims per client are billed for medically supervising

more than four concurrent anesthesia procedures provided by CRNA(s), AA(s), or other qualified professionals. The AD modifier must be used in emergency circumstances only and limited to 6 units (90 minutes maximum) per case for each occurrence requireing supervision of five or more concurrent procedures.

Both the anesthesiologist and CRNA(s), AA(s), or other qualified professional

31.2.5.3.3CRNA, AA, or Other Qualified Professional Services

Modifiers QZ and U1 must be submitted when a CRNA has personally performed the anesthesia services, is not medically directed by the anesthesiologist, and is directed by the physician.

Modifiers QX and U2 must be submitted by a CRNA, AA, or other qualified professional who provided services under the medical direction of an anesthesiologist.

31.2.5.3.4Monitored Anesthesia Care

Anesthesiologists, CRNAs, AAs, or other qualified professionals may use modifier QS to report monitored anesthesia care.

The QS modifier is an informational modifier, and must be billed with any combination of pricing modifiers for reimbursement.

31.2.5.4Dental General Anesthesia

Procedure code 00170 with modifier U3 should be used when billing for the appropriate reimbursement of dental general anesthesia.

Refer to: Chapter 14, “Dental” for more information about dental services.

31.2.5.5Epidural and Subarachnoid Infusion (Not including Labor and Delivery)

Epidural and subarachnoid infusion for pain management may be reimbursed for acute, chronic, and postoperative pain management.

Procedure code 01996 is limited to once per day and is denied when billed on the same day as a surgical/anesthesia procedure. If procedure code 01996 is billed longer than 30 days medical necessity documentation is required. Cancer diagnoses are excluded from the 30-day limitation.

31.2.5.6Reimbursement

To be reimbursed, providers of anesthesia services must include the following on submitted claims:

Appropriate national anesthesia procedure codes

Correct modifier(s)

Name of the anesthesiologist, CRNA, or medically directed AA administering the anesthesia

Exact amount of face-to-face time with the client

If procedure code 01996 is used, it must be reported as a medical service rather than an anesthesia service.

The anesthesiologist’s reimbursement for medical direction of CRNAs, AAs, and other qualified professionals is 50 percent of the maximum allowable fee.

The CRNA’s or AA’s reimbursement for performing an anesthesia service when supervised by a physician other than an anesthesiologist is 92 percent of the maximum allowable fee.

A CRNA or AA under the supervision of an anesthesiologist may be reimbursed the lesser of the billed charges or 50 percent of the calculated payment for a supervised anesthesia service.

Refer to: Chapter 12, “Certified Registered Nurse Anesthetist (CRNA)” for more information on CRNA services.

If multiple CRNAs, anesthesiologists, or anesthesiologist assistants under anesthesiologist supervision are providing anesthesia services for a client, only one CRNA or AA and one anesthesiologist may be reimbursed.

Procedure codes 99100, 99116, 99135, and 99140 are qualifying circumstances that impact the character of the anesthesia services provided. These procedures are not payable alone, but are payable in addition to the anesthesia service. Documentation supporting the medical necessity for use of these procedure codes may be subject to retrospective review.

31.2.5.7Conversion Factor

A conversion factor is the multiplier that transforms relative value into payment amounts. There is a standard conversion factor for anesthesia services that can be obtained from the online fee lookup on the TMHP website at www.tmhp.com.

31.2.5.8Time-Based Fees

Reimbursement of time-based anesthesia services is defined as [(Minutes/15) + Relative Value Units (RVUs)] x Conversion Factor = Anesthesia Reimbursement. It is derived from the following steps:

1)Divide the total anesthesia time in minutes (the time of all procedures performed, directed or supervised) by 15.

Add the RVUs for the procedure performed (use the procedure with the highest RVUs when multiple procedures are performed at the same time).

Multiply this sum by the appropriate conversion factor.

Reimbursement of time-based fees requires documentation of exact time in minutes of face-to-face time with the client.

If anesthesia services are performed for two surgical procedures at separate times during the same date of service, both may be reimbursed based on the documentation submitted with the claim.

31.2.6Audiometry/Hearing Services

The CSHCN Services Program may reimburse appropriately-enrolled providers for audiometry and other hearing services.

Authorization is not required for hearing services provided by physicians.

Refer to: Chapter 20, “Hearing Services” for more information about hearing services.

CSHCN Services Program clients who are 17 years of age or older, legal residents of the state of Texas, and are employable, may be eligible for assistance from the Health and Human Services Commission (HHSC). The CSHCN Services Program is the payer of last resort and may request that clients meeting these requirements apply to HHSC.

31.2.7Augmentative Communication Devices (ACDs)

The purchase, rental, replacement, modification, and repair of ACDs that function independently of any other technology (i.e., may not rely on a computer in any way) are benefits of the CSHCN Services Program when medically necessary.

Refer to: Chapter 10, “Augmentative Communication Devices (ACDs).”

31.2.8Biofeedback Services

Biofeedback is a form of therapy in which a physiologic activity is monitored, amplified, and conveyed by visual or acoustic signals. Procedure codes 90901, 90912 and 90913 may be benefits of the CSHCN Services Program for biofeedback services.

The CSHCN Services Program will cover biofeedback services with prior authorization for clients who are 4 years of age and older with the following conditions:

Urinary incontinence (i.e., stress, urge, overflow, mixed)

Fecal incontinence

Procedure codes 90901, 90912 and 90913 are limited to one procedure code for each date of service by any provider to include all modalities of the services performed during a specific session regardless of the number of modalities performed.

Any device used during a biofeedback session is considered part of the procedure and will not be reimbursed separately.

31.2.8.1Medical Record Documentation

The physician must provide correct and complete information including documentation establishing medical necessity of the service requested, which must remain in the client’s medical record and maintain the record of the performing staff member(s’) certification. Claims may be subject to retrospective review.

31.2.8.2Provider Certification

Biofeedback services must be performed by a staff member who is certified by Biofeedback Certification International Alliance (BCIA). The accepted certification types are:

Certification Type

Description

General biofeedback certification (BCB)

Professionals certified in general biofeedback covering all modalities such as SEMG, Thermal, GSR, HRV, and an overview of neurofeedback.

Pelvic muscle dysfunction biofeedback certification (BCB-PMD)

Professionals certified to use SEMG biofeedback to treat elimination disorders including incontinence and pelvic pain.

 

31.2.8.3Authorization Requirements

Prior authorization is required for biofeedback services. Requests for prior authorization must be submitted by the ordering provider using the CSHCN Services Program Authorization and Prior Authorization Request Form.

The number of sessions prior authorized will not exceed a total of 12 sessions and will not exceed a total duration of 12 weeks. The following documentation must be submitted for consideration of prior authorization:

Failure of pharmacotherapy and behavioral training

Evidence of dyssynergic or non-relaxing detrusor/voluntary sphincter activity based on urodynamic evaluation to include urinary flow testing and complex cystometry

The client has agreed to actively participate in the biofeedback sessions

Diagnosis of fecal, stress, urge, overflow, or a mix of stress and urge incontinence

Medical records indicate that the physician has excluded any underlying medical conditions that could be causing the problem

For clients who are 21 years of age or older with a diagnosis of stress, urge, overflow, or a mix of stress and urge incontinence, the medical records must indicate failed pelvic muscle exercise (PME) service

Note:A failed trial of PME training is defined as no clinically significant improvement in urinary incontinence after completing 4 weeks of PME exercises.

After completion of the initial biofeedback treatment course, prior authorization may be considered for a total of 6 follow-up sessions not to exceed 3 sessions per week and total duration not to exceed 8 weeks. Prior authorization documentation submitted must be for the same condition as the original request, must include each original symptom, and how the symptom has objectively improved. The documentation may include, but is not limited to:

For urinary incontinence, the biofeedback therapy should result in improvement of continence scores. There should be a decrease in high-grade stress incontinence, nocturnal enuresis, and loss of urine during activity. For clients who are 21 years of age and older, the pelvic floor muscle contraction strength should improve with the ability to hold the contractions longer and to increase repetitions.

For fecal incontinence, the biofeedback therapy should result in improvement of continence scores. Squeeze and anal pressures, squeeze duration, and for clients who are 21 years of age and older, pelvic floor muscle contraction strength should show improvement.

Total authorized sessions for any combination of procedure codes 90901, 90912 and 90913, including the 12 initial sessions and 6 follow-up sessions, will not exceed 18 sessions for urinary or fecal incontinence conditions.

31.2.8.4Noncovered Services

Neurofeedback (i.e., EEG biofeedback) is not a benefit of the CSHCN Services Program.

31.2.9Bone Growth Stimulators

Internal (implanted) or external (not implanted) bone growth (osteogenic) stimulators are a benefit of the CSHCN Services Program.

Electromagnetic bone growth stimulators promote healthy bone growth and repair by low intensity electrical stimulation. Electrical stimulation is provided by implanting low-voltage electrodes within the tissue surrounding the bone (internal) or by external placement of a device which transmits low-voltage currents through the soft tissue to the bone (external).

Ultrasonic bone growth stimulators promote healthy bone growth and repair through low-intensity pulsed ultrasound waves.

Bone growth stimulators are a benefit for skeletally mature individuals only.

Bone growth stimulation (procedure codes 20974, 20975, and 20979) is limited to one service every six months. Bone growth stimulation for a second fracture that occurs during the six-month limitation period may be considered on appeal with documentation of medical necessity that supports that the criteria have been met for the second fracture.

Refer to: Section 31.2.9.1, “Prior Authorization Requirements for Bone Growth Stimulators” in this chapter for information about prior authorization requirements for procedure codes 20974, 20975, and 20979.

Due to the short life of the equipment, osteogenic stimulators are purchased.

An ultrasonic bone growth stimulator may not be reimbursed concurrently with other noninvasive bone growth stimulation devices.

Monitoring the effectiveness of bone growth stimulation treatment should be billed as the appropriate evaluation and management (E/M) code.

Physician services may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

Durable medical equipment (DME) may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.9.1Prior Authorization Requirements for Bone Growth Stimulators

Prior authorization is required for bone growth stimulator devices. Inpatient admissions require prior authorization. Ambulatory or day surgery requires authorization.

Prior authorization requests for bone stimulator devices must be submitted on the CSHCN Services Program Prior Authorization and Authorization Request for Durable Medical Equipment (DME) Form.

A completed CSHCN Services Program Prior Authorization and Authorization Request for Durable Medical Equipment (DME) Form prescribing the DME or medical supplies must be signed and dated by the prescribing physician familiar with the client prior to requesting authorization. All signatures must be current, stamped signatures will not be accepted. The completed CSHCN Services Program Prior Authorization and Authorization Request for Durable Medical Equipment (DME) Form must be maintained by the requesting provider and the prescribing physician.

To avoid unnecessary authorization denials, the physician must provide correct and complete information, including documentation for medical necessity of the DME or supplies requested. The physician must maintain documentation of medical necessity in the client’s medical record. The requesting provider may be asked for additional information to clarify or complete a request for the bone growth stimulator.

Documentation that supports medical necessity for a bone growth stimulator device must be maintained by the ordering physician and requesting provider in the client’s medical record and is subject to retrospective review.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

The manufacturer will replace the bone growth stimulator device during the course of treatment should the device become nonfunctional. Repairs to purchased equipment will not be prior authorized. All repairs are considered part of the purchase price.

A new bone growth stimulator may be considered for prior authorization with documentation that supports treatment of a different fracture site when the criteria listed in the following sections are met.

31.2.9.1.1Low-Intensity Ultrasound Bone Growth Stimulators

Documentation of the following is required for prior authorization of the external, low-intensity ultrasound bone growth stimulator device (procedure code E0760):

Nonunion of a fracture other than the skull or vertebrae in a skeletally mature person, documented by a minimum of two sets of radiographs obtained prior to starting treatment with the osteogenesis stimulator, separated by a minimum of 90 days each, including multiple views of the fracture site, and with a written interpretation by a physician stating that there has been no clinically significant evidence of fracture healing between the two sets of radiographs

The fracture is not tumor-related

The fracture is not fresh (less than 7 days), closed or grade I open, tibial diaphyseal fractures, or closed fractures of the distal radius (Colles fracture)

31.2.9.1.2Non-Invasive Bone Growth Stimulators

Documentation of the following is required for prior authorization of the external, electromagnetic bone stimulator device (procedure code E0747):

At least one of the following conditions:

Nonunions, failed fusions, and congenital pseudarthrosis where there is no evidence of progression of healing for 3 months or longer despite appropriate fracture care.

Delayed unions of fractures of failed arthrodesis at high-risk sites (i.e., open or segmental tibial fractures, carpal navicular fractures).

Serial radiographs have confirmed that no progressive signs of healing have occurred.

The fractured gap is 1 cm or less.

The individual can be adequately immobilized and is likely to comply with nonweight bearing restrictions.

Documentation of one of the following is required for prior authorization of the external, electromagnetic bone stimulator device for spinal application (procedure code E0748):

One or more failed fusions

Grade II or worse spondylolisthesis

A multiple level fusion with extensive bone grafting is required

Other risk factors for fusion failure are present, including gross obesity, degenerative osteoarthritis, severe spondylolisthesis, current smoking, previous fusion surgery, previous disc surgery, or gross instability

31.2.9.1.3Invasive Bone Growth Stimulators

Documentation of one of the following is required for prior authorization of the surgically implanted osteogenesis stimulator device (procedure code E0749):

Nonunion of long bone fractures (i.e., clavicle, humerus, radius, ulna, femur, tibia, fibula, and metacarpal, metatarsal, carpal, and tarsal bones). Nonunion of long bone fractures is considered to exist only when serial radiographs have confirmed that fracture healing has ceased for three or more months prior to starting treatment with the bone growth stimulator. Serial radiographs must include a minimum of 2 sets of radiographs separated by a minimum of 90 days. Each set of radiographs must include multiple views of the fracture site.

Failed fusion of a joint other than the spine when a minimum of three months has elapsed since the joint fusion was performed.

Congenital pseudoarthrosis.

An adjunct to spinal fusion surgery for patients at high risk for pseudoarthrosis due to previously failed spinal fusion at the same site.

An adjunct to multiple-level fusion. A multiple level fusion involves three or more vertebrae (e.g., L3-L5, L4-S1, etc.).

31.2.9.2Authorization Requirements for Bone Growth Stimulation

Authorization is required for bone growth stimulation professional services (procedure codes 20974, 20975, and 20979). Providers must submit documentation of medical necessity, which includes the appropriate clinical indications for a low-intensity ultrasound, non-invasive, or invasive device, as defined in section Section 31.2.9.1, “Prior Authorization Requirements for Bone Growth Stimulators” in this chapter.

Authorization requests for bone growth stimulation must be submitted on the CSHCN Services Program Authorization and Prior Authorization Request Form.

Refer to: Section 4.3, “Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about authorization requirements.

31.2.10Casting

The CSHCN Services Program may reimburse the application of casts, splinting, and strapping in addition to an E/M procedure code when no surgery is performed. Casting, splinting and strapping are subject to global surgery fee guidelines.

Supplies used for casting, splinting, and strapping are not reimbursed separately.

Procedure codes 29450 and 29750 are benefits for the following diagnosis codes:

Diagnosis Codes

M21541

M21542

M21549

Q662

Q6651

Q6652

Q666

Q6681

Q6682

Q6689

The following procedure codes may be reimbursed for surgery when billing for casting, splinting, or strapping services:

 

Procedure Codes

Body and upper extremity casts

29000

29010

29015

29035

29040

29044

29046

29049

29055

29058

29065

29075

29085

29086

Body and upper extremity splints

29105

29125

29126

29130

29131

Body and upper extremity strapping

29200

29240

29260

29280

29799

Lower extremity casts

29305

29325

29345

29355

29358

29365

29405

29425

29435

29440

29445

29580

Lower extremity splints

29505

29515

Lower extremity strapping

29520

29530

29540

29550

Cast removal or repair

29700

29705

29710

29720

29730

29740

31.2.11Chemotherapy

Chemotherapy services are a benefit of the CSHCN Services Program when they are provided by a physician or under the supervision of a physician.

Note:Authorization is not required for administration of chemotherapy.

Providers billing for chemotherapy administration may be reimbursed by using the appropriate procedure codes shown in the following table:

Procedure Codes

95991

96401

96402

96405

96406

96409

96411

96413

96415

96416

96417

96420

96422

96423

96425

96440

96446

96450

96521

96522

96523

96542

96549

G0498

For the first 15 minutes through the first hour of chemotherapy infusion, procedure code 96409 or 96413 must be used for a single or initial chemotherapeutic medication. Procedure code 96411 must be used for each additional chemotherapeutic medication given and must be billed with procedure code 96401, 96402, 96409, 96413, or 96416.

Procedure code 96415 must be used for each additional hour beyond the initial hour and must be used in conjunction with procedure code 96409, 96413, or 96416.

Procedure code 96416 will be denied if billed with procedure code G0498 on the same date of service, any provider.

Procedure code 96417 must be used for each subsequent infusion up to 1 hour and must be used in conjunction with procedure code 96409, 96413, or 96416 on the same day, by the same provider. Procedure code 96415 must be used for each additional hour.

Procedure codes 96416 and 96425 must be used when initiating an infusion that will take more than 8 hours and requires using an implanted pump or a portable pump.

Procedure code 96422 must be used for the first hour of intra-arterial push administration. Procedure code 96423 must be used for each additional hour in conjunction with procedure code 96422.

The chemotherapy administration procedure codes listed above include charges for intravenous (IV) solutions (such as saline, dextrose and water, Ringer’s solution, etc.) and IV equipment (administration sets, needles, extension tubing, etc.).

The chemotherapy administration procedure codes 96440 and 96450 include payment for the surgical procedure. Separate reimbursement for the surgical codes will not be allowed.

The appropriate E/M procedure code may be billed by a physician for a face-to-face visit with the client to review chemotherapy options.

Chemotherapeutic drugs and other injections given in the course of chemotherapy may be reimbursed using the appropriate procedure code. The chemotherapeutic agents should be billed separately, including the name of the drug and actual amount administered for correct reimbursement.

Physicians providing a chemotherapy administration service as an inpatient service on the same day as an E/M service must bill using modifier 25 except for procedure code 99211. A different diagnosis is not required.

When a significant, separately identifiable E/M service is performed, the appropriate E/M code must be submitted with modifier 25 and the chemotherapy procedure code. A different diagnosis is not required for an E/M service provided on the same day. Documentation that supports a significant, separately identifiable E/M service must be maintained in the client’s medical record and made available to the CSHCN Services Program upon request.

Modifier 25 must be used to describe circumstances in which an office visit was provided at the same time as other separately identifiable services. This modifier may be appended to the E/M code when the services are rendered. Both services must be documented as distinct and documentation must be maintained in the client’s medical record and made available upon request by the CSHCN Services Program.

Chemotherapy planning program (procedure code 99213, 99214, or 99215) may be reimbursed.

Inpatient and outpatient hospitals must use revenue code 636 for reimbursement of the technical component. The appropriate chemotherapy procedure code must be listed on the claim.

Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.12Clinician-Directed Care Coordination Services

Clinician (physician or APRN)-directed care coordination services are a benefit of the CSHCN Services Program.

Clinician-directed care coordination services are a benefit only when provided by a primary care clinician, specialist, or subspecialist who attests that he or she is providing the medical home for the client.

The medical home is defined as:

A partnership between the child, the child’s family, and the primary care provider (or place where the child receives care).

A care delivery model that is accessible, family-centered, continuous, comprehensive, coordinated, compassionate, and culturally competent.

In providing a medical home for the client, the primary care clinician directs care coordination together with the child or youth and family. Care coordination is a family-centered process that links children or youths with special health needs and their families to services and resources in a coordinated effort to maximize the potential of the children and provide them with optimal health care.

Clinician-directed care coordination services (face-to-face and non-face-to-face) must include the following activities, with permission of the client or family:

Supervising the development and revision of a client’s written care plan (a formal document or contained in the client’s progress notes) in partnership with the client, family, and other agreed-upon contributors and sharing of this care plan with other providers, agencies, and organizations involved in the care of the client

Coordinating care among multiple providers

Maintaining a central record or database that contains all pertinent client medical information, including hospitalizations and specialty care

Assisting the client and family in communicating clinical issues when a client is referred for a consultation or additional care

Evaluating, interpreting, and managing consultant recommendations for the client and family in partnership and collaboration with consultants, other providers, the client, and the family

Clinician-directed care coordination services should also include supervision of development and revision of the client’s emergency medical plan in partnership with the client, the family, and other providers to be used by emergency medical services (EMS) personnel, utility service companies, schools, other community agencies, and caregivers.

31.2.12.1Face-to-Face Clinician-Directed Care Coordination Services

Face-to-face care coordination services are encompassed within the various levels of E/M services and prolonged services.

Providers should use the most appropriate face-to-face E/M procedure codes to bill for care coordination services.

When counseling or care coordination requires more than 50 percent of the client or family encounter (face-to-face time in the office or other outpatient setting, or floor or unit time in the hospital), then time may be considered the key or controlling factor to qualify for a particular level of E/M service.

Counseling is discussion with the client or family, concerning diagnostic studies or results, prognosis, risks and benefits, management options, importance of adhering to the treatment regimen, and client and family education.

An E/M procedure code for a face-to-face problem-focused care coordination visit may be billed on the same day as a preventive medicine visit. Modifiers must be used as appropriate for billing.

Any face-to-face inpatient or outpatient E/M procedure code that is a benefit of the CSHCN Services Program may be billed on the same day as any non-face-to-face clinician-directed care coordination (procedure codes 99367, 99374, 99375, 99377, and 99378), when the client requires significant, separately identifiable E/M service by the same physician on the same day. Modifiers must be used for appropriate billing.

31.2.12.2Non-Face-to-Face Clinician-Directed Care Coordination Services

Non-face-to-face care coordination services include:

Prolonged services (procedure codes 99358 and 99359)

Medical team conferences (procedure code 99367)

Care plan oversight/supervision (procedure codes 99374, 99375, 99377, and 99378)

Non-face-to-face specialist or subspecialist telephone consultations (procedure code 99499 with modifier U9) are a benefit for a specialist or subspecialist when the clinician providing the medical home contacts the specialist for advice or a referral and the consultation is at least 15 minutes in duration.

Telephone consultations are defined by the CSHCN Services Program as the process where the specialist or subspecialist receives a telephone call from the clinician providing the medical home. During the telephone call, the specialist or subspecialist assesses and manages the client’s condition by providing advice or referral to a more appropriate provider.

Specifically, non-face-to-face clinician supervision of the development or revision of a client’s care plan (care plan oversight services) may include the following activities. These services do not have to be contiguous:

Review of charts, reports, treatment plans, or lab or study results, except for the initial interpretation or review of lab or study results ordered during or associated with a face-to-face encounter

Telephone calls with other clinicians (not employed in the same practice), including specialists or subspecialists involved in the care of the client

Telephone or face-to-face discussions with a pharmacist about pharmacological therapies (not just ordering a prescription)

Medical decision making

Activities to coordinate services (if the coordination activities require the skill of a clinician)

Documentation of the services provided, including writing a note in the client chart describing services provided, decision making performed, and amount of time spent performing the countable services, including time spent by the physician working on the care plan after the nurse has conveyed pertinent information from agencies or facilities to the physician, including the start and stop times

The following activities are not covered as non-face-to-face clinician oversight/supervision of the development or revision of the client’s care plan (care plan oversight services):

Time that staff spends getting or filing charts, calling the home health agencies, clients, etc.

Clinician telephone calls to a client or family, except when necessary to discuss changes in client’s care plan

Clinician time spent telephoning prescriptions to the pharmacist (not a physician service; does not require a physician to perform)

Clinician time getting or filing the chart, dialing the telephone, or time on hold (these activities do not require clinician work or meaningfully contribute to the treatment of the illness or injury)

Travel time

Time spent preparing claims and for claims processing

Initial interpretation or review of lab or study results that were ordered during, or associated with, a face-to-face encounter

Services included as part of other E/M service

Consults with health professionals not involved in the client’s case

These services may be reimbursed for the clinician time involved in this coordination. The clinician billing the services must personally perform the services. Care coordination services delegated to or performed by others do not count towards care coordination reimbursement.

Clinician-directed care coordination services must be documented in the client’s medical record. Documentation must support the services being billed and must include a record of the clinician’s time spent performing specific care coordination activities, including start and stop times. The documentation should include a formal care plan and emergency services plan.

The supporting documentation maintained in the client’s medical records must be dated and include the following components and requirements:

A current medical summary containing key information about the client’s health (e.g., conditions, complexity, medications, allergies, past surgical procedures, etc.)

A current list of the main concerns, key strengths and assets, and the related current clinical information

Planned actions or interventions to address the concerns and to sustain or build strength, with the expected outcomes

Persons responsible

Timeframes and due dates

The supporting documentation must be reviewed and updated every 6 months, or more frequently, as needed.

Client medical records are subject to retrospective review.

Payment is made for care coordination to a clinician providing postsurgical care during the postoperative period only if the care coordination is documented to be unrelated to the surgery.

31.2.12.2.1Care Plan Oversight

Clinician-directed care plan oversight services may be billed with one of the procedure codes listed in the following table.

Clinician supervision of a client in the home or domiciliary or under the care of a home health agency or hospice (care plan oversight) may be billed with the following procedure codes:

Procedure Codes

99374

99375

99377

99378


The clinician who bills for the care plan oversight must be the same clinician who signed the plan of care for the home health agency (procedure codes 99374 and 99375) or hospice (procedure codes 99377 and 99378).

Care plan oversight may be reimbursed for the clinician time involved in the coordination. The clinician billing the services must personally perform the services. Care coordination services delegated to or performed by others do not count towards care coordination reimbursement.

The following end-stage renal disease procedure codes apply to a full or partial month of services and are inclusive of all the clinicians supervision services described in care plan oversight (procedure codes 99374, 99375, 99377, and 99378):

Procedure Codes

90951

90952

90953

90954

90955

90956

90957

90958

90959

90960

90961

90962

90963

90964

90965

90966

90967

90968

90969

90970


Care plan oversight may not be reimbursed to the same clinician during the same month as end-stage renal disease services.

The clinician may not have a significant financial or contractual relationship with the home health agency as defined in 42 Code of Federal Regulations (CFR) 424.

The clinician may not be the medical director or employee of the hospice and may not furnish services under arrangements with the hospice (including volunteering).

31.2.12.2.2Medical Team Conference

Medical conferences may be billed with procedure code 99367.

One medical team conference (procedure code 99367) may be reimbursed every 6 months when the coordinating clinician attests that he or she is providing the medical home for the client. The coordinating clinician may be the client’s primary care physician or a specialist.

The medical team conference time must be documented in the client’s record.

31.2.12.2.3Non-Face-to-Face Specialist or Subspecialist Telephone Consultations

Non-face-to-face specialist or subspecialist telephone consultations may be billed with procedure code 99499 and modifier U9.

A specialist or subspecialist telephone consultation is limited to two every 6 months by the same provider.

The clinician providing the medical home must maintain the following documentation in the client’s medical record:

The start and stop times indicating the consultation lasted at least 15 minutes

The reason for the call

The specialist’s or subspecialist’s medical opinion

The recommended treatment or laboratory services

The name of the consulted specialist or subspecialist

The specialist or subspecialist must maintain documentation of the telephone consultation using the CSHCN Services Program Authorization Request for Non-Face-to-Face Clinician-Directed Care Coordination Services Form or similar clinical record documentation. These records are subject to retrospective review. The supporting documentation must include, but is not limited to, the following:

The client’s name, date of birth, and CSHCN Services Program identification number

The start and stop times indicating the consultation lasted at least 15 minutes

The reason for the call

The specialist’s or subspecialist’s medical opinion

The recommended treatment or laboratory services

The name and telephone number of the referring clinician providing the medical home

The specialist’s or subspecialist’s and referring clinician’s National Provider Identifier (NPI) information

31.2.12.2.4Non-Face-to-Face Prolonged Services

Non-face-to-face prolonged services may be billed with procedure codes 99358 and 99359.

The client must be an established client and must have had a face-to-face encounter at least once during the 6 months immediately preceding provision of the first non-face-to-face prolonged service.

Non-face-to-face prolonged services (procedure code 99358 or 99359) are limited to a maximum of 90 minutes, once per client, for the same provider.

Procedure code 99358 must be used to report the first hour of prolonged services. Prolonged services of less than 30 minutes duration are considered part of the physician E/M service being provided.

Prolonged service of less than 30 minutes total duration on a given date is not separately reported.

Procedure code 99359 is used to report each additional 30 minutes beyond the first hour. It may also be used to report the final 15 to 30 minutes.

Prolonged service of less than 15 minutes beyond the first hour or less than 15 minutes beyond the final 30 minutes is not reported separately.

Procedure code 99359 must be billed for the same date of service by the same provider as procedure code 99358 or it will be denied.

Procedure codes 99358 and 99359 will be denied if billed on the same date of service as any of the following procedure codes:

Procedure Codes

99202

99203

99204

99205

99212

99213

99214

99215

99221

99222

99223

99231

99232

99233

99234

99235

99236

99242

99243

99244

99245

99252

99253

99254

99255

99281

99282

99283

99284

99285

99304

99305

99306

99307

99308

99309

99310

99341

99342

99344

99345

99347

99348

99349

99350

99417

99418

31.2.12.2.5Authorization for Non-Face-to-Face Clinician-Directed Care Coordination Services

Authorization is required for non-face-to-face clinician-directed care coordination services. A CSHCN Services Program Authorization Request for Non-Face-to-Face Clinician-Directed Care Coordination Services form, and the required documentation must be submitted.

Authorization of initial non-face-to-face clinician-directed care coordination services requires at least 1 covered face-to-face inpatient or outpatient E/M visit by the clinician directing the care coordination during the 6 months preceding the provision of the first non-face-to-face care coordination service.

Authorization for subsequent non-face-to-face clinician-directed care coordination services requires at least 1 covered face-to-face inpatient or outpatient E/M visit by the clinician directing the care coordination during the previous 12 months, or more frequently as indicated by the client’s condition.

Authorization of medical team conferences (procedure code 99367) is limited to once every 6 months. Additional medical team conferences may be considered with documentation of a change in the client’s medical home.

Authorization of non-face-to-face prolonged services (procedure codes 99358 and 99359) is limited to a maximum of 90 minutes once per client, per provider. Additional prolonged non-face-to-face services may be authorized (with documentation) if there is one of the following significant changes in the client’s clinical condition:

The client will soon be, or has recently been, discharged from a prolonged and complicated hospitalization requiring coordination of complex care with multiple providers in order for the client to be adequately cared for in the home.

Documentation of recent trauma resulting in new medical complications that require complex interdisciplinary care.

The client has a new diagnosis of a medically complex condition requiring additional interdisciplinary care with additional specialists.

Authorization of care plan oversight or supervision (procedure codes 99374, 99375, 99377, and 99378) is limited to one service a month in a 6-month authorization period.

In order for authorization to be considered, the client must require complex and multidisciplinary care modalities involving regular clinician development or revision of care plans, review of subsequent reports of client status, and review of related laboratory and other studies, such as:

Medically complex health care: Health care provided by a clinician that requires coordination of various treatment modalities or a multidisciplinary approach due to the client’s moderate or severe health condition, physical or functional limitations, or health risk factors.

Multidisciplinary health care: The coordination of clinician-ordered medically necessary health care that requires the collaboration of two or more medical, educational, social, developmental, or other professionals in order to properly devise and implement the clinician-developed plan of medical care. For CSHCN Services Program coverage, multidisciplinary health care must include medically necessary services provided by program-enrolled clinical providers. Development and implementation of the plan of medical care may, in addition, need to take into account other related care provided by nonclinical providers as required to address the overall health needs of a client.

Documentation of the following components must be submitted with the authorization form to obtain an initial authorization or renewal:

A current medical summary, containing key information about the client’s health (e.g., conditions, complexity, medications, allergies, past surgical procedures)

A current list of the main concerns as well as key strengths and assets, and the related current clinical information

Planned action steps or interventions to address the concerns and to sustain or build strengths, with the expected outcomes

Persons responsible

Timeframes or due dates

The supporting documentation can be in the form of the following:

Formal written care plan

Progress note detailing the care coordination planning

Letter of medical necessity detailing the care plan oversight and care coordination

Authorization is limited to a maximum of 6 months. Subsequent periods of authorization require submission of a new request with documentation supporting medical necessity for ongoing services.

Non-face-to-face specialist or subspecialist telephone consultations do not require authorization.

31.2.13Cochlear Implants

Cochlear implants and auditory rehabilitation are benefits for CSHCN Services Program clients.

Refer to: Section 20.3.2, “Cochlear Implants” in Chapter 20, “Hearing Services” for more information about cochlear implants.

31.2.14Colon Capsule Endoscopy

Colon capsule endoscopy (procedure code 91113) is a benefit of the CSHCN Services Program and limited to the following diagnosis codes:

Diagnosis Codes

K635

K921

K922

R195

Z5309

Z538

31.2.15Colorectal Cancer Screening

Procedure codes 74263, 81528, 82270 (CLIA waived test), G0104, G0105, G0121, and G0328 (with modifier QW) are benefits of the CSHCN Services Program. An additional screening may be considered on appeal with documentation that indicates the provider was unable to obtain the previous screening results from a different provider or the provider was new to treating the client and was not aware the client had already received colorectal cancer screening.

Procedure code 81528 may be reimbursed once every 3 years for clients who are 45 years of age or older. Procedure code G0104 may be reimbursed once every 5 years, or as recognized by the ACS or the U.S. Preventive Services Task Force (USPSTF). Procedure code G0121 may be reimbursed once every 10 rolling years.

Refer to: Chapter 25, “Enrollment” for additional information about laboratory cancer screening or pathology procedures.

High-risk individuals include clients with one or more of the following factors:

A close relative who has had colorectal cancer or an adenomatous polyp

Note:“Relative” means close blood relatives, including first-degree male or female relatives (parents, siblings, or children), second-degree relatives (aunts, uncles, grandparents, nieces, nephews), and third-degree relatives (first cousins, great grandparents) who are on the same side of the family as the client.

Family history of familial adenomatous polyposis

Family history of hereditary nonpolyposis colorectal cancer

Personal history of colorectal cancer

Personal history of adenomatous polyps

Personal history of inflammatory bowel disease, including Crohn’s disease and ulcerative colitis

During the course of a screening flexible sigmoidoscopy, if a lesion or growth is detected that results in a biopsy or removal of the growth, an appropriate diagnostic procedure classified as a flexible sigmoidoscopy with biopsy or removal should be reported.

During the course of a screening colonoscopy, if a lesion or growth is detected that results in a biopsy or removal of the growth, the procedure code for a colonoscopy with biopsy or removal of lesion should be reported.

31.2.16Critical Care Services

Critical care is a benefit of the CSHCN Services Program. Authorization is not required for these services.

Critical care is the care of a critically ill client who requires constant physician attention. Critical care involves high-complexity decision making to access, manipulate, and support vital system functions. If the physician is not at bedside, he or she must be immediately available to the client. The physician must devote his or her full attention to the client and therefore, cannot render E/M services to any other client during the same period of time. Critical care is usually given in a critical care area, such as a coronary care unit, respiratory care unit, intensive care unit, pediatric intensive care unit, neonatal intensive care unit, or emergency department care facility.

Noncritical intensive care is a benefit for infants who are very low birth weight, low birth weight, or normal weight and do not meet the definition of critically ill but continue to require intensive observation, frequent interventions, and other intensive services only available in the intensive care setting.

Neonatal critical care is the comprehensive care of the critically ill neonate. The neonatal period is defined as the period from birth through the 28th day of life. Neonatal critical care codes are comprehensive per diem (daily) care codes for providers personally delivering or supervising the delivery of care of the critically ill neonate as an inpatient.

Newborn resuscitation is a benefit for high-risk newborns who require resuscitation.

Physician standby service requiring prolonged physician attendance, each 30 minutes (procedure code 99360), is not a benefit of the CSHCN Services Program.

In accordance with CPT, critical care may be provided on multiple days, even if no changes are made in the treatment rendered to the client, provided that the client’s condition continues to require the level of physician attention as described above.

31.2.16.1General Limitations

Services for a client who is not, or is no longer, critically ill but happens to be in a critical care unit are reported using other appropriate E/M codes, such as continuing intensive care (procedure codes 99478, 99479, and 99480) or subsequent hospital care (procedure codes 99231, 99232, and 99233).

Neonatal critical care (procedure codes 99468 and 99469), pediatric critical care (procedure codes 99471, 99472, 99475, and 99476), and the initial critical care (procedure code 99291) are limited to once per day for the same provider. Subsequent critical care (procedure code 99292) is each additional 30 minutes beyond the first 74 minutes of critical care, and is limited to a quantity of 6 units (3 hours) per day.

Neonatal and pediatric critical care (procedure codes 99468, 99469, 99471, 99472, 99475, and 99476) and continuing intensive care services (procedure codes 99478, 99479, and 99480) are inpatient, per-day charges and only billable once per day by any provider. No other inpatient E/M services may be reimbursed on the same day when billed by the same provider.

When the present body weight of a neonate exceeds 5,000 grams, a subsequent hospital care service (procedure code 99231, 99232, or 99233) should be used.

If the same physician provides critical care for a neonatal or pediatric client in both the outpatient and inpatient settings on the same day, the provider should report only the appropriate inpatient neonatal or pediatric critical care service (procedure codes 99468, 99469, 99471, 99472, 99475, and 99476).

E/M services provided on the same day by the same provider as surgical procedures that meet the definition of separately identifiable and above and beyond usual preoperative and postoperative care may be billed with modifier 25. Documentation that supports the provision of a significant, separately-identifiable E/M service must be maintained in the client’s medical record and made available to the CSHCN Services Program upon request.

Critical care (procedure codes 99291, 99292, 99468, 99469, 99471, 99472, 99475, and 99476) is only billable by the provider rendering the critical care service while the client is critically ill. While providers from various specialties (e.g., cardiology or neurology) may be consulted to render an opinion or assist in the management of a particular portion of the care, only the provider managing the care of the critically ill client during a life threatening crisis may bill the critical care.

If a second physician provides critical care services on the same day at a separate and distinct time, the physician should report the appropriate time-based critical care service (procedure code 99291 or 99292).

Critical care totaling less than 30 minutes in duration on a given date should be reported with the appropriate E/M procedure code.

Actual time spent with the individual client should be recorded in the client’s record and reflect the time billed on the claim. The time that can be reported as critical care is the time spent engaged in work directly related to the individual client’s care whether that time was spent at the immediate bedside or elsewhere on the floor or unit.

The time spent in the following activities may not be included in the time reported as critical care:

Activities that occur outside of the unit or off the floor because the physician is not immediately available to the client

Activities that do not directly contribute to the treatment of the client even if they are performed in the critical care unit

Performing separately reportable procedures or services

Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

APRNs, physician assistants, and CRNAs may be reimbursed the lower of the billed amount or 92 percent of the amount allowed by Texas Medicaid for physicians for the same service.

31.2.16.2Critical Care Services

Procedure codes 99291 and 99292 are used to identify critical care services provided to clients who are 6 years of age or older.

Procedure code 99291 should be used per day for the first 30 to 74 minutes of critical care even if the time spent by the physician is not continuous on that day.

Critical care procedure codes 99291 and 99292 are used to report the total duration of time spent by a physician providing critical care services to a critically ill or critically injured client, even if the time spent by the physician on that date is not continuous.

Critical care provided to a neonatal, pediatric, or adult client in an outpatient setting (e.g., emergency room) which does not result in admission, must be billed using procedure codes 99291 and 99292.

If outpatient critical care (procedure codes 99291 and 99292) is provided to a client at a distinctly separate time than another outpatient E/M service by the same provider, both services may be reimbursed with supporting medical record documentation.

If critical care (procedure code 99291) is provided by different physicians that meet the initial 30-minute time requirement, and the care is provided at separate distinct times, the initial provider’s claim may be reimbursed. The second provider’s claim will be denied but may be considered on appeal. The time spent by each physician cannot overlap (i.e., two physicians cannot bill critical care for care delivered at the same time). Supporting medical record documentation must be provided by the second physician that includes the time in which the critical care was rendered. In addition, a statement must be submitted indicating the physician was the only provider managing the care of the critically ill client during the life-threatening crisis.

If the provider’s time exceeds the 74-minute time threshold for procedure code 99291, procedure code 99292 may be billed in addition to procedure code 99291 for each additional 30 minutes.

Procedure code 99292 must be billed by the same performing provider or by a member of the same performing provider’s group practice.

Procedure code 99292 is limited to six units per day (3 hours), any provider. If the number of units is not stated on the claim, only a quantity of one will be allowed.

Retrospective review may be performed to ensure the documentation supports the medical necessity of the service and any modifier used when billing the claim.

31.2.16.3Pediatric Critical Care

Procedure codes 99471, 99472, 99475, and 99476 are used to identify pediatric critical care services provided to clients who are 29 days through 24 months of age.

Pediatric critical care services are comprehensive per diem (daily) care procedure codes for providers personally delivering or supervising the delivery of care of the critically ill infant or child.

Inpatient pediatric critical care (procedure codes 99471, 99472, 99475, and 99476) is a per-day charge.

31.2.16.4Neonatal Critical Care

Procedure codes 99468 and 99469 are used to identify neonatal critical care services provided to clients who are 28 days of age or younger.

Procedure code 99468 is used for the first day of admission for a critically ill neonate, 28 days of age or younger, and may be reimbursed once per day, any provider.

Procedure code 99468 must be billed for the initial day of neonatal critical care irrespective of the time that the provider spends with the client.

Procedure code 99469 must be billed for subsequent neonatal critical care per day, irrespective of the time that the provider spends directing the care of the critically ill neonate or infant that is 28 days of age or younger.

Procedure code 99469 may be reimbursed once per day, any provider.

After the neonate is no longer considered critically ill, the E/M procedure codes for subsequent hospital care (procedure codes 99231, 99232, and 99233) or subsequent intensive care (procedure codes 99478, 99479, and 99480) must be used.

If the infant remains in critical care after the 28th day of age, on the 29th day of age, the provider must bill pediatric critical care codes (procedure codes 99471 and 99472).

Neonatal intensive or critical care procedure codes 99468, 99469, 99477, 99478, 99479, and 99480 are inpatient, per day charges and only billable once per day by any provider.

31.2.16.5Intensive Care (Noncritical) Services

Initial hospital care provided to neonates who require intensive observation, frequent interventions, and other intensive services may be billed using procedure code 99477. Subsequent intensive care provided to very low birth weight, low birth weight, and normal weight infants who do not meet the definition of critically ill but continue to require intensive observation, frequent interventions, and other intensive services only available in the intensive care setting, may be billed using procedure codes 99478, 99479, and 99480.

31.2.16.6Newborn Resuscitation

Newborn resuscitation may be billed using procedure code 99465.

Procedure code 99465 may be reimbursed for clients birth through 28 days of age. For cardiopulmonary resuscitation performed on clients 29 days of age or older, providers must bill procedure code 92950. Procedure code 92950 may be billed on the same day as critical care (procedure codes 99291, 99292, 99468, 99469, 99471, 99472, 99475, and 99476) when reported as a separately identifiable procedure.

Procedure code 99465 must be used by the provider who performs the resuscitation.

31.2.17Echoencephalography

Procedure code 76506 is a benefit of the CSHCN Services Program with the following diagnosis codes:

Diagnosis Codes

A066

A170

A171

A1781

A1782

A1789

C410

C6961

C6962

C700

C710

C711

C712

C713

C714

C715

C716

C717

C718

C719

C7221

C7222

C7231

C7232

C7241

C7242

C7259

C729

C751

C752

C768

C7931

C7932

C7940

C7949

C7951

C7952

C7989

D075

D098

D164

D3161

D3162

D320

D329

D330

D331

D332

D333

D3500

D3501

D3502

D420

D421

D429

D432

D433

D434

D438

D439

D47Z1

D47Z2

D480

D487

D492

D496

D497

F0390

F03911

F03918

F0392

F0393

F0394

G060

G062

G07

G08

G132

G138

G232

G233

G300

G301

G308

G309

G3101

G3109

G311

G312

G3180

G3183

G3184

G3185

G3186

G3189

G319

G910

G911

G912

G930

G932

G9340

G9341

G9342

G9343

G9344

G9345

G9349

G935

G936

G937

G9381

G9389

G939

G94

G988

G998

H35361

H4600

H4601

H4602

H4603

H4610

H4611

H4612

H4613

H462

H463

H468

H469

H47011

H47012

H47013

H47019

H47021

H47022

H47023

H47029

H47031

H47032

H47033

H47039

H47091

H47092

H47093

H47099

H4710

H4711

H4712

H4713

H47141

H47142

H47143

H47149

H4720

H47211

H47212

H47213

H47219

H4722

H47231

H47232

H47233

H47239

H47291

H47292

H47293

H47299

H47311

H47312

H47313

H47319

H47321

H47322

H47323

H47329

H47331

H47332

H47333

H47339

H47391

H47392

H47393

H47399

H4741

H4742

H4743

H4749

H47511

H47512

H47519

H47521

H47522

H47529

H47531

H47532

H47539

H47611

H47612

H47619

H47621

H47622

H47629

H47631

H47632

H47639

H47641

H47642

H47649

I6000

I6001

I6002

I6010

I6011

I6012

I602

I6030

I6031

I6032

I604

I6050

I6051

I6052

I606

I607

I608

I609

I610

I611

I612

I613

I614

I615

I616

I618

I619

I6200

I6201

I6202

I6203

I621

I629

I6330

I63311

I63312

I63319

I63321

I63322

I63323

I63329

I63331

I63332

I63333

I63339

I6339

I6340

I63411

I63412

I63419

I63421

I63422

I63429

I63431

I63432

I63439

I6349

I6350

I63511

I63512

I63513

I63519

I63521

I63522

I63523

I63529

I63531

I63532

I63533

I63539

I63543

I6381

I6389

I6601

I6602

I6603

I6609

I6611

I6612

I6613

I6619

I6621

I6622

I6623

I6629

I668

I669

I671

I6781

I6782

I6783

I67850

I67858

I6789

I680

I69098

I6921

I69210

I69211

I69212

I69213

I69214

I69215

I69218

I69219

I69220

I69221

I69222

I69223

I69269

I69290

I69291

I69292

I69293

I69298

O99411

O99412

O99413

O99419

O9942

O9943

P0082

P0700

P0701

P0702

P0703

P0710

P0714

P0715

P0716

P0717

P100

P101

P102

P103

P104

P108

P109

P112

P119

P120

P121

P122

P123

P124

P1281

P1289

P129

P150

P151

P152

P153

P154

P155

P156

P158

P352

P370

P371

P372

P373

P374

P378

P520

P521

P5221

P5222

P523

P524

P525

P526

P528

P529

P90

P912

P91811

P91819

P91821

P91822

P91823

P91829

P9188

Q010

Q011

Q012

Q018

Q02

Q030

Q031

Q038

Q040

Q041

Q042

Q045

Q046

Q048

Q050

Q051

Q052

Q054

Q0701

Q0702

Q0703

Q282

Q283

R220

R221

R5600

R569

S0190XA

S0190XD

S0190XS

S060X0A

S060X0D

S060X0S

S060X1A

S060X1D

S060X1S

S060X9A

S060X9D

S060X9S

S060XAA

S060XAD

S060XAS

S061X0A

S061X0D

S061X0S

S061X1A

S061X1D

S061X1S

S061X2A

S061X2D

S061X2S

S061X3A

S061X3D

S061X3S

S061X4A

S061X4D

S061X4S

S061X5A

S061X5D

S061X5S

S061X6A

S061X6D

S061X6S

S061X7A

S061X8A

S061X9A

S061X9D

S061X9S

S061XAA

S061XAD

S061XAS

S06305A

S06305D

S06305S

S06306A

S06306D

S06306S

S06307A

S06308A

S0630AA

S0630AD

S0630AS

S06310A

S06310D

S06310S

S06311A

S06311D

S06311S

S06312A

S06312D

S06312S

S06313A

S06313D

S06313S

S06314A

S06314D

S06314S

S06315A

S06315D

S06315S

S06316A

S06316D

S06316S

S06317A

S06318A

S06319A

S06319D

S06319S

S0631AA

S0631AD

S0631AS

S06320A

S06320D

S06320S

S06321A

S06321D

S06321S

S06322A

S06322D

S06322S

S06323A

S06323D

S06323S

S06324A

S06324D

S06324S

S06325A

S06325D

S06325S

S06326A

S06326D

S06326S

S06327A

S06328A

S06329A

S06329D

S06329S

S0632AA

S0632AD

S0632AS

S06330A

S06330D

S06330S

S06331A

S06331D

S06331S

S06332A

S06332D

S06332S

S06333A

S06333D

S06333S

S06334A

S06334D

S06334S

S06335A

S06335D

S06335S

S06336A

S06336D

S06336S

S06337A

S06338A

S06339A

S06339D

S06339S

S0633AA

S0633AD

S0633AS

S06340A

S06340D

S06340S

S06341A

S06341D

S06341S

S06342A

S06342D

S06342S

S06343A

S06343D

S06343S

S06344A

S06344D

S06344S

S06349A

S06349D

S06349S

S06350A

S06346D

S06346S

S06347A

S06348A

S06349A

S06349D

S06349S

S0634AA

S0634AD

S0634AS

S06350A

S06350D

S06350S

S06351A

S06351D

S06351S

S06352A

S06352D

S06352S

S06353A

S06353D

S06353S

S06354A

S06354D

S06354S

S06355A

S06355D

S06355S

S06356A

S06356D

S06356S

S06357A

S06358A

S06359A

S06359D

S06359S

S0635AA

S0635AD

S0635AS

S06360A

S06360D

S06360S

S06361A

S06361D

S06361S

S06362A

S06362D

S06362S

S06363A

S06363D

S06363S

S06364A

S06364D

S06364S

S06365A

S06365D

S06365S

S06366A

S06366D

S06366S

S06367A

S06368A

S06369A

S06369D

S06369S

S06370A

S06370D

S06370S

S06371A

S06371D

S06371S

S06372A

S06372D

S06372S

S06373A

S06373D

S06373S

S06374A

S06374D

S06374S

S06375A

S06375D

S06375S

S06376A

S06376D

S06376S

S06377A

S06378A

S06379A

S06379D

S06379S

S0637AA

S0637AD

S0637AS

S06380A

S06380D

S06380S

S06381A

S06381D

S06381S

S06382A

S06382D

S06382S

S06383A

S06383D

S06383S

S06384A

S06384D

S06384S

S06385A

S06385D

S06385S

S06386A

S06386D

S06386S

S06387A

S06388A

S06389A

S06389D

S06389S

S0638AA

S0638AD

S0638AS

S064X0A

S064X0D

S064X0S

S064X1A

S064X1D

S064X1S

S064X2A

S064X2D

S064X2S

S064X3A

S064X3D

S064X3S

S064X4A

S064X4D

S064X4S

S064X5A

S064X5D

S064X5S

S064X6A

S064X6D

S064X6S

S064X7A

S064X8A

S064X9A

S064X9D

S064X9S

S064XAA

S064XAD

S064XAS

S065X0A

S065X0D

S065X0S

S065X1A

S065X1D

S065X1S

S065X2A

S065X2D

S065X2S

S065X3A

S065X3D

S065X3S

S065X4A

S065X4D

S065X4S

S065X5A

S065X5D

S065X5S

S065X6A

S065X6D

S065X6S

S065X7A

S065X8A

S065X9A

S065X9D

S065X9S

S065XAA

S065XAD

S065XAS

S066X0A

S066X0D

S066X0S

S066X1A

S066X1D

S066X1S

S066X2A

S066X2D

S066X2S

S066X3A

S066X3D

S066X3S

S066X4A

S066X4D

S066X4S

S066X5A

S066X5D

S066X5S

S066X6A

S066X6D

S066X6S

S066X7A

S066X8A

S066X9A

S066X9D

S066X9S

S066XAA

S066XAD

S066XAS

S06890A

S06890D

S06890S

S06891A

S06891D

S06891S

S06892A

S06892D

S06892S

S06893A

S06893D

S06893S

S06894A

S06894D

S06894S

S06895A

S06895D

S06895S

S06896A

S06896D

S06896S

S06897A

S06898A

S06899A

S06899D

S06899S

S0689AA

S0689AD

S0689AS

S069X0A

S069X0D

S069X0S

S069X1A

S069X1D

S069X1S

S069X2A

S069X2D

S069X2S

S069X3A

S069X3D

S069X3S

S069X4A

S069X4D

S069X4S

S069X5A

S069X5D

S069X5S

S069X6A

S069X6D

S069X6S

S069X7A

S069X8A

S069X9A

S069X9D

S069X9S

S069XAA

S069XAD

S069XAS

S06A0XA

S06A0XD

S06A0XS

S06A1XA

S06A1XD

S06A1XS

S0990xA

S0990xD

S0990xS

31.2.17.1Ambulatory Electroencephalogram

Ambulatory electroencephalographic monitoring is a benefit of the CSHCN Services Program with the following diagnosis codes:

Diagnosis Codes

F05

F060

F0670

F0671

F068

G253

G40001

G40009

G40011

G40019

G40101

G40109

G40111

G40119

G40201

G40209

G40211

G40219

G40301

G40309

G40311

G40319

G40401

G40409

G40411

G40419

G40501

G40509

G40801

G40802

G40803

G40804

G40811

G40812

G40813

G40814

G40841

G40842

G40843

G40844

G4089

G40901

G40909

G40911

G40919

G40A11

G40A19

G40B01

G40B09

G40B11

G40B19

G40C01

G40C09

G40C11

G40C19

G912

G9381

G9389

P912

R561

R569

Z85020

Z85030

Z85040

Z85060

Z85110

Z85230

Z85520

Z85821

Z85841

Z85848

Z86011

Z8669

Z87728

Z87798

Procedure codes must be used when billing for ambulatory electroencephalograms:

Procedure Codes

95700

95705

95706

95707

95708

95709

95710

95711

95712

95713

95714

95715

95716

95717

95718

95719

95720

95721

95722

95723

95724

95725

95726

95957

Authorization is not required for the diagnoses listed above. All other diagnoses require authorization and documentation of medical necessity. Documentation should include the diagnosis and the specific rationale for the request. Claims for ambulatory electroencephalographic monitoring are considered for payment on appeal for diagnoses other than those listed above or if the frequency of testing exceeds the limitation.

Ambulatory electroencephalograms are limited to three every 6 months, per client, same provider. Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid for the procedure.

31.2.18Evaluation and Management (E/M) Services

E/M services are benefits of the CSHCN Services Program. When selecting the level of service provided, providers must follow either the 1995 or 1997 Documentation Guidelines for Evaluation and Management Services published by CMS.

Covered professional services provided by physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid. This manual may not list all E/M procedure codes that may be reimbursed by the CSHCN Services Program.

31.2.18.1New or Established Patient Visits

Home/residence services are those services that are provided in a private residence, temporary lodging, or short-term accommodation (e.g., hotel, campground, hostel, or cruise ship), assisted living facility, group home (that is not licensed as an intermediate care facility for individuals with intellectual disabilities), custodial care facility, or residential substance abuse treatment facility.

New patient visits will be allowed every 3 years for physician E/M services, per client, per provider.

A new patient is defined by the American Medical Association (AMA) as one who has not received any professional services from a physician or physician within the same group practice, of the same specialty, within the past 3 years. An established patient is one who has received professional services from a physician or physician within the same group practice, of the same specialty, within the last 3 years.

Providers may use procedure codes 99202, 99203, 99204, and 99205 when billing for new patient services provided in the office, or in an outpatient or other ambulatory facility.

Providers may use procedure codes 99211, 99212, 99213, 99214, and 99215 when billing for established patient services provided in the office, outpatient, or other ambulatory facility during regularly scheduled evening, weekend, holiday, or standard office hours.

Providers may use procedure codes 99341, 99342, 99344, and 99345 when billing for new patient services provided in the home/residence setting.

Providers may use procedure codes 99347, 99348, 99349, and 99350 when billing for established patient services provided in the home/residence setting.

A subsequent home/residence visit (procedure codes 99347, 99348, 99349, and 99350) billed on the same day as a new patient home/residence visit (procedure codes 99344 and 99345) by the same provider will be denied as part of another procedure billed on the same day, regardless of the diagnosis.

Subsequent home/residence evaluation and management procedure codes are limited to one per day regardless of diagnosis.

Office visits (procedure codes 99202, 99203, 99204, 99205, 99211, 99212, 99213, 99214, and 99215) provided on the same day as a planned procedure (minor or extensive), are included in the cost of the procedure and are not separately reimbursed.

Modifier 25 may be used to identify a significant, separately identifiable E/M service by the same physician on the same day of the procedure or other service. Documentation that supports the provision of a significant, separately identifiable E/M service must be maintained in the client’s medical record and made available to the CSHCN Services Program upon request. The documentation must clearly indicate what the significant problem/abnormality was, including the important, distinct correlation with signs and symptoms to demonstrate a distinctly different problem that required additional work and must support that the requirements for the level of service billed were met or exceeded. The date and time of both services performed must be outlined in the medical record and the time of the second service must be different than the time of the first service, although a different diagnosis is not required.

31.2.18.2Inpatient Professional Services

31.2.18.2.1Initial and Subsequent Hospital Care (Nonintensive Care)

Initial or subsequent hospital visits (procedure codes 99221, 99222, 99223, 99231, 99232, and 99233), observation (procedure codes 99234, 99235, and 99236), and discharge (procedure codes 99238 and 99239) are limited to one per day for the same provider.

If a subsequent inpatient/observation hospital visit (procedure codes 99231, 99232, and 99233) following admission is billed on the same day by the same provider as an emergency department visit (procedure codes 99281, 99282, 99283, 99284, and 99285), an office visit (procedure codes 99202, 99203, 99204, 99205, 99211, 99212, 99213, 99214, and 99215), or an outpatient consultation (procedure codes 99242, 99243, 99244, and 99245), the subsequent hospital visit will be paid and the other visits will be denied.

One initial inpatient/observation consultation (procedure code 99252, 99253, 99254, or 99255) is allowed for each hospitalization within a 30-day period. Any subsequent consultation that is billed as an initial consultation during this time period will be denied.

A subsequent inpatient/observation hospital visit (procedure codes 99231, 99232, and 99233) may be reimbursed on the same day to the same provider when critical care services (procedure codes 99291 and 99292) are billed.

E/M services provided in a hospital setting following a major procedure, provided by the same provider or in direct follow-up for postsurgical care, are included in the surgeon’s global surgical fee and are denied as included in another procedure.

A physician who did not perform the surgery and provides postoperative surgical care in the time frame that is included in the global surgical fee must bill with modifier 55. This may only be done when the surgeon submits a charge for surgical care only and there is an agreement between the physicians and the surgeon to split the care of the client.

31.2.18.2.2Hospital Discharge Day Management

Discharge management (procedure codes 99238 and 99239) billed on the same date of service as the admission by the same provider will be denied.

Discharge management (procedure codes 99238 and 99239) billed on the same date of service as an emergency room visit by the same provider is denied, but may be considered for reimbursement upon appeal, if provided at a separate time.

Only one discharge management service will be considered for reimbursement per day. Subsequent hospital visits billed on the same day as discharge management, by the same provider, will be denied.

Initial/observation or subsequent hospital visit (procedure codes 99221, 99222, and 99223) billed on the same day as hospital discharge day management (procedure code 99238) is denied as part of another procedure billed on the same day.

31.2.18.2.3Concurrent Inpatient Care

Concurrent care exists when services are provided to a client by more than one physician on the same day during a period of hospitalization in the inpatient hospital setting. Concurrent care is appropriate when the level of care and the documented clinical circumstances require the skills of different specialties to successfully manage the client in accordance with accepted standards of good medical practice.

Concurrent care will not be paid to providers of the same specialty for the same or related diagnoses. Diagnoses are considered to be related when up to six digits of the primary diagnosis codes match. Denied concurrent care may be considered on an appeal basis when accompanied by documentation of medical necessity.

Concurrent care may be considered for reimbursement to providers of different specialties when providing services for unrelated diagnoses involving different organ systems.

31.2.18.3Emergency Services

An emergency medical condition is defined as a medical condition that manifests itself by acute symptoms of sufficient severity (including severe pain) that if not immediately treated must reasonably be expected to result in one of the following outcomes:

Placing the client’s health in serious jeopardy

Serious impairment to bodily functions

Serious dysfunction of any bodily organ or part

An emergency department is defined as an organized hospital-based facility for the provision of unscheduled episodic services to clients who require immediate medical attention. The facility must be available to provide services 24 hours a day, 7 days a week.

31.2.18.3.1Hospital-Based Emergency Department Professional Services

Physicians may use procedure codes 99281, 99282, 99283, 99284, and 99285 to bill for services provided in the hospital-based emergency department. Office-based physicians may also use procedure codes 99202, 99203, 99204, and 99205 for new patients or procedure codes 99211, 99212, 99213, 99214, and 99215 for established patients, to bill for services provided in the office or in a hospital-based emergency department. These procedure codes are also appropriate for a physician who is attending a client in an outpatient observation room setting for less than 6 hours. Document the time for multiple visits in Block 24K of the CMS-1500 paper claim form.

Emergency department visits include the components of a diagnostic examination such as a pelvic or rectal examination. These components should not be billed with an unlisted procedure code in addition to the procedure code for the visit. These components are considered part of the examination and no separate reimbursement may be provided.

Multiple emergency department visits on the same day and billed by the same provider must have the times for each visit documented on the claim form. More than one visit on the same day can also be indicated by adding the appropriate modifier to the claim form. Medical documentation is required to support this charge.

Emergency department visits may be paid to different providers on the same day, when medically necessary, regardless of specialty and diagnosis.

Separate charges are allowed for emergency department treatment room and minor surgery or diagnostic procedures billed on the same day. Use the appropriate procedure code from the CPT manual.

Payment for an additional emergency department visit by an anesthesiologist following a surgical procedure is denied as part of the global anesthesia payment (base plus time). A distinct and separate diagnosis beyond the diagnosis for which the global anesthesia services were provided should be documented in order for payment to be considered on an appeal basis.

If an emergency department visit (procedure codes 99281, 99282, 99283, 99284, and 99285) is billed on the same day, by the same provider, as an office visit (procedure codes 99202, 99203, 99204, 99205, 99211, 99212, 99213, 99214, and 99215), or outpatient consultation (procedure codes 99242, 99243, 99244, and 99245), the emergency department visit may be considered for reimbursement and the office or consultation visit is denied.

Emergency department visits (procedure codes 99281, 99282, 99283, 99284, and 99285) are denied when billed on the same day as an inpatient/observation service (procedure codes 99238 and 99239) by the same provider.

Binocular microscopy (procedure code 92504) and noninvasive ear or pulse oximetry for oxygen (procedure code 94760) will be denied when billed on the same day, by the same provider, as emergency department visit (procedure code 99281, 99282, 99283, 99284, or 99285).

31.2.18.4Consultations

A consultation is an E/M service provided at the request of another provider for the evaluation of a specific condition or illness. To be billed as such, a consultation must consist of the following:

There must be a request from the referring provider for the evaluation of a particular condition or illness.

There must be correspondence from the consulting provider back to the referring provider indicating the medical findings.

During a consultation, the consulting provider may initiate diagnostic and therapeutic services if necessary. If treatment is initiated and the client returns for follow up care, an established patient visit should be billed. If the purpose of the referral is to transfer care, a consultation may not be billed.

The medical records maintained by both the referring and consulting providers must identify their counterpart and reason for consultation.

Consultations may be billed using the following procedure codes:

Procedure Codes

99242

99243

99244

99245

99252

99253

99254

99255

Office or outpatient consultations will be limited to one consultation every six-month period by the same provider for the same diagnosis. Subsequent office or outpatient consultation visits during this time period will be denied.

31.2.18.5Services Outside of Business Hours

The CSHCN Services Program limits reimbursement for after hours charges (procedure codes 99050, 99056, and 99060) to office-based providers rendering services after routine office hours or on an emergency basis.

An office-based provider may bill an after hours charge in addition to a visit for providing services after routine office hours. After hours charges may be billed when the provider’s clinical judgment deems it medically necessary to interrupt the routine schedule to care for a client with an emergent condition. A provider’s routine office hours are those hours posted at the physician’s office as the usual office hours. The CSHCN Services Program may reimburse office-based physicians when any of the following exists:

The physician leaves the office or home to see a client in the emergency room.

The physician leaves the home and returns to the office to see a client after the physician’s routine office hours.

The physician is interrupted from routine office hours to attend to another client’s emergency outside of the office.

After-hours procedure codes are limited to one per day, same provider.

Procedure codes 99050, 99056, and 99060 are not reimbursed separately to emergency department-based physicians or emergency department-based groups.

31.2.18.6Prolonged Physician Services

Prolonged services may be provided in an office, outpatient, or inpatient setting and involves direct (face-to-face) client contact that is beyond the usual service and exceeds the time threshold of the E/M procedure code (listed in the table below) being billed on that day:

Procedure Codes

99205

99215

99223

99233

99236

99245

99255

99345

99350

Prolonged services of less than 30 minutes duration should not be reported separately.

Procedure code 99417 should only be used when an outpatient evaluation and management service has been selected using time alone as the basis, and only after the minimum time required to report the addition to the code of the outpatient evaluation and management service has been exceeded by 15 minutes.

Procedure codes 99417 and 99418 are limited to 4 units (1 hour) per day and should not be used to report an additional time increment of less than 15 minutes.

Procedure code 99418 is only used when inpatient or observation evaluation and management service has been selected using time alone as the basis and only after the minimum time required to report the addition to the code of the inpatient and observation evaluation and management service has been exceeded by 15 minutes.

Physician standby service without face-to-face contact (procedure code 99360) is not a benefit of the CSHCN Services Program.

31.2.18.7Observation Room Services

When a client’s status changes from observation to inpatient, the date of inpatient admission is the date the client was admitted to the hospital as an inpatient. Charges are to be billed as specified in Section 24.4, “Outpatient Services” in Chapter 24, “Hospital.”

Inpatient/observation care discharge day management (procedure codes 99238 and 99239) may be used to report services provided to a client upon discharge from “observation status” if the discharge date differs from the initial date of admission.

The following limitations apply to these procedure codes:

Procedure codes 99211, 99212, 99213, 99214, 99215, 99221, 99222, and 99223 are denied if billed on the same day as procedure codes 99238 and 99239 by the same provider.

If a physician inpatient/observation visit (procedure codes 99221, 99222, 99234, 99235, 99238, and 99239) is billed on the same day as prolonged services (procedure codes 99417 and 99418) by the same provider, the prolonged services are denied as part of another procedure on the same day.

If procedure codes 99234, 99235, and 99236 are billed on the same day as a subsequent hospital visit (procedure codes 99231, 99232, and 99233) by the same provider, the subsequent visit is denied.

If procedure codes 99234, 99235, and 99236 are billed on the same day as a consultation by the same provider, the consultation is paid and the physician inpatient hospital observation is denied.

If a chemotherapy planning program (procedure codes 99213, 99214, or 99215) and physician outpatient hospital observation are billed on the same day by the same provider, the chemotherapy planning is paid and the physician outpatient hospital observation will be denied.

Procedure codes 99234, 99235, and 99236 are not payable on the same day as procedure codes 99238 and 99239.

Procedure codes 99234, 99235, and 99236 are subject to the global surgical fee pre-/postcare days assigned to certain surgical procedures.

E/M services provided at any place of service (POS) other than an inpatient hospital and billed on the same day as a physician observation visit by the same provider are denied.

If dialysis treatment and physician observation visits are billed the same day by the same provider, same specialty (other than nephrology and internal medicine specialists), the dialysis treatment may be paid and the physician observation visit is denied.

31.2.18.8Preventive Care Services

The CSHCN Services Program may reimburse for preventive health-care services. Providers should submit claims with the following E/M procedure codes and include the appropriate diagnosis code. Diagnosis code Z00121 or Z00129 should be used for children’s preventive care medical checkups. Diagnosis code Z0000 or Z0001 should be used for an adult preventive care medical checkup.

Procedure Codes

99381

99382

99383

99384

99385

99386

99387

99391

99392

99393

99394

99395

99396

99397


Providers may be reimbursed for an acute care visit on the same day as a preventive care visit. The acute care visit should be billed as an established patient visit. Modifier 25 must be used to describe circumstances in which a visit was provided at the same time as other separately identifiable services (e.g., preventive visits, minor procedure). Both services must be documented as distinct, and documentation that supports the provision of a significant, separately identifiable E/M service must be maintained in the client’s medical record and made available to the CSHCN Services Program upon request. This modifier must be appended to the evaluation procedure code when the services rendered are distinct, provided for different diagnosis, or are performed for different reasons.

When the client visit is only for immunization, a preventive care visit will not be reimbursed. The administration fee and any vaccine or toxoid not obtained through Texas Vaccines for Children (TVFC) may be reimbursed when diagnosis code Z23 and the appropriate procedure code referencing an immunization is submitted with the claim.

Vaccinations, vaccine administration procedure codes, and laboratory services may be billed in addition to the preventive care E/M procedure code. Providers must append modifier 25 to one of the preventive care E/M procedure codes listed in the table above to identify a significant, separately identifiable E/M service that was rendered by the same provider on the same day as the vaccine administration.

The CSHCN Services Program reimburses for only one preventive health visit per day per client for any provider. The program does not cover family planning services and inpatient newborn examinations.

Preventive care medical checkups are not a benefit of a telemedicine or telehealth service.

31.2.18.9Preventive Care Medical Checkups and Developmental Testing

When a new patient acute care E/M visit is billed for the same date of service as a new patient preventive care medical checkup, both new patient services may be reimbursed when billed by the same provider if that provider has not billed other acute care E/M visits or preventive care medical checkups for the client in the preceding 3 years.

Modifier 25 must be used to describe circumstances in which an acute care E/M visit was provided at the same time as a preventive care medical checkup. This modifier must be appended to the E/M procedure code when the services are distinct and provided for a different diagnosis. An appropriate level E/M procedure code must be billed with the diagnosis supporting the acute care claim.

If the provider or provider group has billed for a new patient preventive care medical checkup within the past 3 years, subsequent preventive care medical checkups and acute care visits billed as new patient services will be denied when billed by the same provider. Another new checkup will only be allowed when the client has not received any professional services from the same provider or another provider who belongs to the same group practice in the past 3 years, because subsequent acute care visits after the initial new patient preventive care medical checkup continue the established relationship with the provider. Subsequent preventive care medical checkups and acute care visits after the initial new patient preventive care medical checkup continue the established relationship with the provider.

31.2.18.9.1Laboratory Tests

Documented laboratory results obtained prior to the current medical checkup may be used as follows to complete the laboratory testing requirement:

Results obtained within 30 days before the current medical checkup for clients who are 2 years of age and younger

Results obtained within 90 days before the current medical checkup for clients who are 3 years of age and older

Documentation must include the date of service and one of the following:

A clear reference to the previous visit by the same provider

Results obtained from a different provider

31.2.18.9.2Medical Checkup Follow-up Visit

A follow-up checkup is a visit that is scheduled to complete checkup components that could not be completed at the original medical checkup due to circumstances beyond the provider’s control. If the parent or guardian did not give consent for a missing component, a follow-up visit is not necessary. The most appropriate procedure code for the follow-up visit will be determined by the components that could not be completed during the original medical checkup.

Procedure code 99211 may be submitted for a follow-up visit that includes a separately identifiable evaluation and management (E/M) component. When the follow-up visit does not include a separately identifiable E/M component, the following procedure codes must be used instead of procedure code 99211:

Developmental testing (procedure code 96110) and autism screening (procedure code 96110 with modifier U6)

Hearing screening (procedure code 92551)

Immunization administration (procedure codes 90460 and 90461)

If a separately identifiable E/M component is required before completing one of the above checkup components, claims for the follow-up visit (procedure code 99211) and the checkup component may be submitted.

31.2.18.9.3Denied Medical Checkups

Providers may be reimbursed for denied medical checkups through the appeal process when all of the following criteria are met for clients who are birth through 3 years of age:

The client changed to a new provider in a new practice.

The previous provider billed the maximum number of checkups in the procedure code age range for that client.

The new provider’s claim was denied for exceeding periodicity.

Note:In addition to the criteria listed above, at least 1 year must have elapsed since the last checkup for clients who are 3 years of age or older.

31.2.18.9.4Developmental Screening and Testing

Developmental screening and testing may be a benefit when the services are provided during a preventive care medical checkup in accordance with accepted guidelines or when a parent expresses concern with a client’s developmental progress. If the developmental screening was not completed during a previous checkup, or if the provider is seeing the client for the first time at a checkup for birth through 6 years of age, a standardized developmental screening must be completed.

Standardized developmental screening and testing may also be a benefit when they are performed outside of a preventive care medical checkup.

Clients with abnormal screening results must be referred to an appropriate provider for further testing. Clients who are birth through 35 months of age with suspected developmental delay must be referred to Texas Early Childhood Intervention (ECI) as soon as possible, but no longer than 7 days after identification, even if the client is referred to an appropriate provider for further testing.

31.2.18.9.5Developmental Screening

Developmental screening (procedure code 96110) is a required component of each checkup for clients who are birth through 6 years of age. Procedure code 96110 is a benefit when performed by an APRN or physician in the office, home, or outpatient hospital setting.

Providers must submit modifier U6 with procedure code 96110 to bill for autism screening. Autism screening is required at 18 and 24 months of age.

If the provider administers a standardized developmental screening at an additional checkup, the provider must document the rationale for the additional screen(s), which may be due to provider or parental concern. Retrospective review may be performed to ensure documentation supports medical necessity.

Additional parental or guardian consent may be required if online or web-based screening tools are used, which could result in client data being stored electronically in an outside database other than the provider’s electronic medical record system, or if the data is used for purposes other than CSHCN Services Program screening. The provider should seek legal advice regarding the need for this consent.

Procedure code 96110, with or without modifier U6, must be billed with the appropriate E/M procedure code. Providers must use a standardized tool to complete the developmental screening. The CSHCN Services Program recognizes the following standardized tools:

The Ages and Stages Questionnaire (ASQ), Ages and Stages Questionnaire: Social - Emotional (ASQ:SE)

Parents’ Evaluation of Developmental Status (PEDS)

The Modified Checklist for Autism in Toddlers (M-CHAT)

The Modified Checklist for Autism in Toddlers, Revised with Follow-up (M-CHAT - R/F)

The Survey of Well-being of Young Children (SWYC)

A provider who chooses a standardized developmental screening tool different from those listed above must provide medical documentation that supports the use of the tool.

Developmental screening procedure code 96110 and autism screening procedure code 96110 with modifier U6 may be reported separately when provided as part of a medical checkup or follow up visit. Developmental screening and testing may also be billed with other office visits when medically necessary.

Procedure codes 96110 and 96110 with modifier U6 are each limited to once per day, same provider and will be denied unless a checkup, follow up visit or office visit is paid for the same date of service by the same provider. Providers may be reimbursed for both procedures on the same day.

Developmental screening, which is not expected to last longer than 30 minutes, is included in the limitation of 12 hours of behavioral health services per day, per provider. Physicians are not limited to the 12-hour limitation since they can delegate services and may submit claims in excess of 12 hours per day. The individuals delegated by a physician to perform these services are subject to the 12-hour limitation.

A Mini Mental State Examination is considered part of any E/M service and is not separately reimbursed.

31.2.18.9.6Developmental Testing

Procedure codes 96112 and 96113, which consists of an extended evaluation, require the use of a standardized tool and are limited to clients who are birth through 20 years of age. Procedure codes 96112 and 96113 are a benefit when performed by an APRN, physician, or psychologist in the office, home, or outpatient hospital setting. Developmental testing is medically necessary when there is suspected developmental delay that is supported by the following clinical evidence:

Suspected developmental delay or atypical development when the diagnosis cannot be clearly identified through clinical interview or standardized screening tools alone

Retesting of a client to evaluate a change in developmental status that results in a change of treatment plan

The following procedure codes will be denied when billed on the same day as procedure codes 96112 and 96113:

Procedure Codes

99202

99203

99204

99205

99211

99212

99213

99214

99215

Developmental testing procedure codes 96112 and 96113 are included in the system limitation of 12 hours of behavioral health services per day, per provider. Each additional 30 minutes may be reimbursed using add-on procedure code 96113. Retrospective review may be performed on billed hours and total hours worked per day since providers who perform developmental testing may possibly bill in excess of 12 hours per day. Providers must maintain clinical documentation in the client’s medical record to support medical necessity.

Developmental testing that is performed when a development delay or change in the client’s developmental status is not suspected would constitute developmental screening and is not covered. Providers may not bill clients for developmental testing that is considered developmental screening.

31.2.18.10Preventive Care Medical Checkup Components

Referral to Establish a Dental Home

The American Academy of Pediatric Dentistry’s (AAPD) definition of a dental home, the CSHCN Services Program defines a dental home as the dental provider who supports an ongoing relationship with the client that is inclusive of all aspects of oral health care delivered in a comprehensive, continuously accessible, coordinated, and family-centered way. In Texas, establishment of a client’s dental home begins at 6 months of age but no later than 12 months of age and includes referral to dental specialists when appropriate.

The provider must refer clients to establish a dental home beginning at 6 months of age or earlier if trauma or early childhood caries are identified. For established clients after the six-month medical checkup visit, the provider must confirm whether a dental home has been established and is on-going. If a dental home has not been established, the provider must make additional referrals at subsequent medical checkup visits until the parent or guardian confirms that a dental home has been established for the client. A parent or guardian of the client may self-refer for dental care at any age, including 12 months of age or younger.

31.2.18.10.1Oral Evaluation and Fluoride Varnish in the Medical Home (OEFV)

An intermediate oral evaluation with fluoride varnish application (procedure code 99429) is a benefit for clients 6 months of age through 35 months of age. Procedure code 99429 must be submitted with modifier U5, and diagnosis code Z00121 or Z00129.

The intermediate oral evaluation with fluoride varnish application must be billed on the same date of service as a medical checkup or an exception to the periodicity visit (procedure codes 99381, 99382, 99391, or 99392) and is limited to six services per lifetime by any provider.

An intermediate oral evaluation with fluoride varnish application is limited to preventive care medical checkup providers who have completed the required benefit education and who are certified by the DSHS Oral Health Program to perform an intermediate oral evaluation with fluoride varnish application.

The intermediate oral evaluation with fluoride varnish application add-on includes the following component:

Intermediate oral evaluation

Fluoride varnish application

Dental anticipatory dental guidance to include:

The need for thorough daily oral hygiene practices

Education in potential gingival manifestations for clients with diabetes and clients under long-term medication therapy

Diet, nutrition, and food choices

Fluoride needs

Injury prevention

Antimicrobials, medications, and oral health

Referral to a dentist to establish a dental home

Additional dental anticipatory guidance if the client has no erupted teeth

Note:The provider must complete the intermediate oral evaluation but can delegate all other components.

31.2.18.10.2Mental Health Screening

Mental health screening is a benefit at each preventive care medical checkup when it is provided in accordance with accepted guidelines or when a parent expresses concern about the client’s mental health.

Mental health screening using one of the following validated, standardized mental health screening tools recognized by the CSHCN Services Program is required once per calendar year, any provider for clients who are 12 through 18 years of age:

Pediatric Symptom Checklist (PSC-35)

Pediatric Symptom Checklist for Youth (Y-PSC)

Patient Health Questionnaire (PHQ-9)

Patient Health Questionnaire (PHQ-9) Modified for Adolescents (PHQ-A [depression screen])

Pediatric Symptom Checklist-17 (PSC-17)

Car, Relax, Alone, Forget, Family, and Trouble Checklist (CRAFFT)

Patient Health Questionnaire (PHQ-A [anxiety, eating problems, mood problems and substance use])

Rapid Assessment for Adolescent Preventive Services (RAAPS)

Providers may be reimbursed separately when using one of the required screening tools during a preventive care medical checkup.

Procedure code 96160 or 96161 must be submitted for the required mental health screening. Procedure codes 96160 and 96161 are a benefit for clients who are 12 through 18 years of age.

Mental health screening at other medical checkups does not require the use of a validated, standardized mental health screening tool.

Procedure code 96160 or 96161 must be submitted on the same date of service and by the same provider as procedure code 99384, 99385, 99394, or 99395. Procedure codes 96160 and 96161 are limited to once per calendar year, any provider.

Procedure codes 96160 and 96161 will not be reimbursed for the same client for any date of service.

The client’s medical record must include documentation identifying the tool that was used, the screening results, and any referrals.

31.2.18.10.3Postpartum Depression Screening

Postpartum depression screening is a benefit of the CSHCN Services Program. Procedure codes G8431 and G8540 may be reimbursed when billing for postpartum depression screening.

Postpartum depression screening must be submitted under the infant’s Medicaid client number.

Procedure codes G8431 and G8510 must be submitted on the same claim, for the same date of service, by the same provider as the checkup or follow-up visit procedure codes below:

 

Procedure Codes

99211

99381

99382

99391

99392


Providers may receive separate reimbursement for postpartum depression screening in addition to the infant’s preventive care medical checkup or follow-up visit. The reimbursement amount for procedure codes G8431 and G8510 covers all postpartum depression screenings provided during the checkup or follow-up visit.

Only one procedure code, either G8431 or G8510, may be reimbursed per provider in the 12 months following the infant’s birth.

Postpartum Depression Screening and Referral Services

The American Academy of Pediatrics (AAP) recommends the infant’s provider screen mothers for postpartum depression. Postpartum depression is the most common form of postpartum mood disturbance. Screening mothers for postpartum depression is appropriate for the general postpartum population.

Note:Screening for postpartum depression during the infant’s preventive care medical checkup is recommended, not required.

Postpartum depression meets the same clinical criteria as major depressive disorder, with the main difference being onset during pregnancy or after delivery.

While postpartum depression is the most common form of postpartum mood disturbance, providers should be aware that other mood disorders that may arise during the postpartum period include anxiety and panic disorders, obsessive-compulsive disorder, and postpartum psychosis.

Postpartum psychosis is a much more severe form of postpartum depression accompanied by psychotic features. Postpartum psychosis is rare, typically develops in the first few days to weeks after delivery, and is a psychiatric emergency requiring immediate medical attention.

In addition to postpartum psychosis, immediate or emergent medical attention may be necessary when the risk of imminent harm or danger is present.

Screening Guidelines

Screening using a validated tool is required. At a minimum, screening should occur at least once during the postpartum period. Validated tools may include the following:

Edinburgh Postnatal Depression Scale

Postpartum Depression Screening Scale

Patient Health Questionnaire 9

Screening alone is inadequate for improving clinical outcomes. A positive screening for postpartum depression requires the THSteps provider to develop a referral plan with the mother.

Positive Screenings: Referrals and Follow-Up

Providers must discuss the screening results with the mother, discuss the possibility of depression, and the impact depression may have on the mother, family, and health of the infant.

The provider and mother should discuss the mother’s options so the provider can refer her to an appropriate provider. Screening and referral is not contingent upon the mother’s Medicaid eligibility. When needed, referrals should be made regardless of the funding source, including referral to local mental health authorities and local behavioral health authorities.

Providers should refer the mother to a provider who can perform further evaluation and determine an appropriate course of treatment. Appropriate providers include, but are not limited to:

Mental health clinicians

The mother’s primary care provider

Obstetricians and gynecologists

Family physicians

Community resources such as Local Mental Health Authorities (LMHAs)

Resources should be provided for support in the interim until the mother is able to access care.

Scheduling a return visit for the infant sooner than the next scheduled visit may be appropriate in some cases.

Prior Authorization Requirements

Screening for postpartum mood disorders at the checkup or follow up visit does not require prior authorization.

While recommended, screening for postpartum depression is not a compulsory requirement of the infant visit.

Documentation Requirements

Documentation in the infant’s record must include the name of the screening tool used and date the screening was completed.

If the mother screens positive for depression, at a minimum, the provider must note that a referral plan was discussed with the mother and a referral to a provider was made. Providers may give the mother a copy of the completed screening tool to take with her to referral appointments.

Documentation should also include any health education or anticipatory guidance provided, along with the time period recommended for the infant’s next appointment.

31.2.18.10.4Sensory Screening

Providers may use test results from a different provider or a school vision and hearing screening program to replace the required visual acuity or hearing screening that requires the use of calibrated electronic equipment as long as the previous screening was performed within 12 months preceding the current medical checkup.

Procedure code 92551 may be reimbursed separately for a hearing screening (for hearing loss) with pure tone audiometric testing that is performed with the use of calibrated electronic equipment.

31.2.18.11Teaching Physicians

Teaching physicians who provide E/M services may bill the CSHCN Services Program for lower- and mid-level E/M services (procedure codes 99202, 99203, 99211, 99212, and 99213) that are provided by residents if they meet the primary care exception under Medicare.

31.2.19Evoked Response Tests and Neuromuscular Procedures

The following services are a benefit of the CSHCN Services Program:

Autonomic function test (AFT)

Electromyography (EMG)

Nerve conduction studies (NCS)

Evoked potential (EP) procedures

Motion analysis (MAS) studies

All procedures must be medically indicated and testing must be performed using appropriate equipment that provides assessment of all parameters of the recorded signals. Studies performed with devices designed only for screening, rather than diagnosis, are not benefits of the CSHCN Services Program.

Client medical records must clearly document the medical necessity for all procedures and must reflect the actual results of specific procedures. All client medical records are subject to retrospective review.

31.2.19.1Autonomic Function Tests (AFTs)

AFTs are a benefit of the CSHCN Services Program when submitted with procedure codes 95921, 95922, 95923, and 95924. Prior authorization is not required for AFTs.

Procedure codes 95921, 95922, 95923, and 95924 are limited to once per date of service, by the same provider.

Autonomic disorders may be congenital or acquired (primary or secondary). Some of the conditions under which autonomic function testing may be appropriate include, but are not limited to, the following:

Amyloid neuropathy

Diabetic autonomic neuropathy

Distal small fiber neuropathy

Excessive sweating

Gastrointestinal dysfunction

Idiopathic neuropathy

Irregular heart rate

Multiple system atrophy

Orthostatic symptoms

Pure autonomic failure

Reflex sympathetic dystrophy or causalgia (sympathetically maintained pain)

Sjogren’s syndrome

31.2.19.2Electromyography and Nerve Conduction Studies

EMG and NCS are a benefit of the CSHCN Services Program when billed with the following procedure codes:

EMG Procedure Codes

51784

51785

95860

95861

95863

95864

95865

95866

95867

95868

95869

95870

95872

95875

NCS Procedure Codes

95885

95886

95887

95905

95907

95908

95909

95910

95911

95912

95913

95933

95937

Prior authorization is not required for EMGs.

EMG and NCS are restricted to the following diagnosis codes:

Diagnosis Codes

C701

C720

C721

D510

D511

D513

D518

D519

D538

E0842

E0942

E1041

E1042

E10610

E1141

E1142

E1144

E11610

E1342

E5111

E5112

E512

E518

E519

E52

E530

E531

E538

E550

E559

E560

E568

E610

E7281

E7289

E7841

E7849

E786

E851

E852

E853

E8581

E8582

E8589

E859

G120

G121

G1221

G1222

G1223

G1224

G1225

G1229

G128

G129

G130

G243

G2589

G260

G320

G360

G370

G375

G501

G510

G511

G512

G5131

G5132

G5133

G5139

G514

G518

G519

G522

G523

G527

G528

G540

G541

G542

G543

G544

G545

G548

G549

G5601

G5602

G5603

G5611

G5612

G5613

G5621

G5622

G5623

G5631

G5632

G5633

G5641

G5642

G5643

G5681

G5682

G5683

G5691

G5692

G5693

G5701

G5702

G5703

G5711

G5712

G5713

G5721

G5722

G5723

G5731

G5732

G5733

G5741

G5742

G5743

G5751

G5752

G5753

G5761

G5762

G5763

G5771

G5772

G5773

G5781

G5782

G5783

G5791

G5792

G5793

G587

G588

G589

G590

G600

G601

G602

G603

G608

G609

G610

G6181

G6182

G6189

G619

G620

G621

G622

G6281

G6282

G629

G630

G650

G651

G652

G7000

G7001

G701

G702

G7081

G7089

G709

G7100

G7101

G7102

G7109

G7111

G7112

G7113

G7114

G7119

G7120

G7121

G71220

G71228

G7129

G713

G718

G719

G721

G722

G723

G7241

G7249

G7281

G7289

G729

G731

G733

G737

G800

G801

G802

G803

G804

G808

G809

G8311

G8312

G8313

G8314

G8321

G8322

G8323

G8324

G834

G8381

G8382

G8383

G8384

G8389

G839

G9009

G902

G904

G9050

G90511

G90512

G90513

G90519

G90521

G90522

G90523

G90529

G9059

G909

G950

G9511

G9519

G9520

G9529

G9581

G9589

G959

G990

G992

I776

I951

J3800

J3801

J3802

K5902

K5903

K5904

K5909

K592

K594

K624

K6289

M05411

M05412

M05421

M05422

M05431

M05432

M05441

M05442

M05451

M05452

M05461

M05462

M05471

M05472

M0549

M05511

M05512

M05521

M05522

M05531

M05532

M05541

M05542

M05551

M05552

M05561

M05562

M05571

M05572

M0559

M05711

M05712

M05721

M05722

M05731

M05732

M05741

M05742

M05751

M05752

M05761

M05762

M05769

M05771

M05772

M05779

M0579

M057A

M05811

M05812

M05821

M05822

M05831

M05832

M05841

M05842

M05851

M05852

M05861

M05862

M05871

M05872

M0589

M058A

M06011

M06012

M06021

M06022

M06031

M06032

M06041

M06042

M06051

M06052

M06061

M06062

M06071

M06072

M0608

M0609

M060A

M06811

M06812

M06821

M06822

M06831

M06832

M06841

M06842

M06852

M06861

M06862

M06871

M06872

M0688

M0689

M068A

M069

M21271

M21272

M21331

M21332

M21511

M21512

M216X1

M216X2

M21831

M21832

M21931

M21932

M320

M3210

M3211

M3212

M3213

M3214

M3215

M3219

M328

M329

M3300

M3301

M3302

M3309

M3310

M3311

M3312

M3319

M3320

M3321

M3322

M3329

M3390

M3391

M3392

M3399

M340

M341

M342

M3481

M3482

M3483

M3489

M3500

M3501

M3502

M3503

M3504

M3505

M3506

M3507

M3508

M3509

M350A

M350B

M350C

M3581

M3589

M360

M4321

M4322

M4323

M4324

M4325

M4326

M4327

M4328

M436

M438X9

M4644

M4645

M4646

M4647

M4711

M4712

M4713

M4714

M4715

M4716

M4721

M4722

M4723

M4724

M4725

M4726

M4727

M4728

M47811

M47812

M47813

M47814

M47815

M47816

M47817

M47818

M47891

M47892

M47893

M47894

M47895

M47896

M47897

M47898

M4801

M4802

M4803

M4804

M4805

M48062

M4807

M4808

M5000

M5001

M50020

M50021

M50022

M50023

M5003

M5011

M50120

M50121

M50122

M50123

M5013

M5020

M5021

M50220

M50221

M50222

M50223

M5023

M5030

M5031

M50320

M50321

M50322

M50323

M5033

M5080

M5081

M50820

M50821

M50822

M50823

M5083

M5091

M50920

M50921

M50922

M50923

M5093

M5104

M5105

M5106

M5124

M5125

M5126

M5127

M5134

M5135

M51360

M51361

M51362

M51369

M51370

M51371

M51372

M51379

M5184

M5185

M5186

M5187

M5410

M5411

M5412

M5413

M5414

M5415

M5416

M5417

M5431

M5432

M5450

M5451

M5459

M546

M5489

M60011

M60012

M60021

M60022

M60031

M60032

M60041

M60042

M60044

M60045

M60046

M60051

M60052

M60061

M60062

M60070

M60071

M60073

M60074

M60076

M60077

M6008

M6009

M60111

M60112

M60121

M60122

M60131

M60132

M60141

M60142

M60151

M60152

M60161

M60162

M60171

M60172

M6018

M6019

M6090

M6250

M62511

M62512

M62519

M62521

M62522

M62529

M62531

M62532

M62539

M62541

M62542

M62549

M62551

M62552

M62559

M62561

M62562

M62569

M62571

M62572

M62579

M6258

M6259

M625A0

M625A1

M625A2

M625A9

M6281

M6284

M6285

M629

M7910

M7911

M7912

M7918

M792

M79601

M79602

M79604

M79605

M79621

M79622

M79631

M79632

M79641

M79642

M79651

M79652

M79661

M79662

M79671

M79672

M797

M961

N393

N3941

N3942

N3943

N3944

N3945

N3946

N39490

N39491

N39492

N39498

N94819

R150

R151

R152

R159

R200

R201

R202

R203

R208

R209

R260

R261

R2681

R2689

R269

R290

R295

R29701

R29702

R29703

R29704

R29705

R29706

R29707

R29708

R29709

R29710

R29711

R29712

R29713

R29714

R29715

R29716

R29717

R29718

R29719

R29720

R29721

R29722

R29723

R29724

R29725

R29726

R29727

R29728

R29729

R29730

R29731

R29732

R29733

R29734

R29735

R29736

R29737

R29738

R29739

R29740

R29741

R29742

R320

R3914

R39191

R39192

R39198

R4702

R471

R4781

R4789

R498

R6884

S14101A

S14101D

S14101S

S14102A

S14102D

S14102S

S14103A

S14103D

S14103S

S14104A

S14104D

S14104S

S14105A

S14105D

S14105S

S14106A

S14106D

S14106S

S14107A

S14107D

S14107S

S14108A

S14108D

S14108S

S14109A

S14109D

S14109S

S14111A

S14111D

S14111S

S14112A

S14112D

S14112S

S14113A

S14113D

S14113S

S14114A

S14114D

S14114S

S14115A

S14115D

S14115S

S14116A

S14116D

S14116S

S14117A

S14117D

S14117S

S14118A

S14118D

S14118S

S14121A

S14121D

S14121S

S14122A

S14122D

S14122S

S14123A

S14123D

S14123S

S14124A

S14124D

S14124S

S14125A

S14125D

S14125S

S14126A

S14126D

S14126S

S14127A

S14127D

S14127S

S14128A

S14128D

S14128S

S14131A

S14131D

S14131S

S14132A

S14132D

S14132S

S14133A

S14133D

S14133S

S14134A

S14134D

S14134S

S14135A

S14135D

S14135S

S14136A

S14136D

S14136S

S14137A

S14137D

S14137S

S14138A

S14138D

S14138S

S14141A

S14141D

S14141S

S14142A

S14142D

S14142S

S14143A

S14143D

S14143S

S14144A

S14144D

S14144S

S14145A

S14145D

S14145S

S14146A

S14146D

S14146S

S14147A

S14147D

S14147S

S14148A

S14148D

S14148S

S14151A

S14151D

S14151S

S14152A

S14152D

S14152S

S14153A

S14153D

S14153S

S14154A

S14154D

S14154S

S14155A

S14155D

S14155S

S14156A

S14156D

S14156S

S14157A

S14157D

S14157S

S14158A

S14158D

S14158S

S142XXA

S142XXD

S142XXS

S143XXA

S143XXD

S143XXS

S144XXA

S144XXD

S144XXS

S145XXA

S145XXD

S145XXS

S148XXA

S148XXD

S148XXS

S149XXA

S149XXD

S149XXS

S24101A

S24101D

S24101S

S24102A

S24102D

S24102S

S24103A

S24103D

S24103S

S24104A

S24104D

S24104S

S24109A

S24109D

S24109S

S24111A

S24111D

S24111S

S24112A

S24112D

S24112S

S24113A

S24113D

S24113S

S24114A

S24114D

S24114S

S24131A

S24131D

S24131S

S24132A

S24132D

S24132S

S24133A

S24133D

S24133S

S24134A

S24134D

S24134S

S24141A

S24141D

S24141S

S24142A

S24142D

S24142S

S24143A

S24143D

S24143S

S24144A

S24144D

S24144S

S24151A

S24151D

S24151S

S24152A

S24152D

S24152S

S24153A

S24153D

S24153S

S24154A

S24154D

S24154S

S242XXA

S242XXD

S242XXS

S243XXA

S243XXD

S243XXS

S244XXA

S244XXD

S244XXS

S248XXA

S248XXD

S248XXS

S249XXA

S249XXD

S249XXS

S34109A

S34109D

S34109S

S34111A

S34111D

S34111S

S34112A

S34112D

S34112S

S34113A

S34113D

S34113S

S34114A

S34114D

S34114S

S34115A

S34115D

S34115S

S34121A

S34121D

S34121S

S34122A

S34122D

S34122S

S34123A

S34123D

S34123S

S34124A

S34124D

S34124S

S34125A

S34125D

S34125S

S34131A

S34131D

S34131S

S34132A

S34132D

S34132S

S34139A

S34139D

S34139S

S3421XA

S3421XD

S3421XS

S3422XA

S3422XD

S3422XS

S343XXA

S343XXD

S343XXS

S344XXA

S344XXD

S344XXS

S345XXA

S345XXD

S345XXS

S4400XA

S4400XD

S4400XS

S4400XX

S4401XA

S4401XD

S4401XS

S4402XA

S4402XD

S4402XS

S4410XA

S4410XD

S4410XS

S4411XA

S4411XD

S4411XS

S4412XA

S4412XD

S4412XS

S4420XA

S4420XD

S4420XS

S4421XA

S4421XD

S4421XS

S4422XA

S4422XD

S4422XS

S4430XA

S4430XD

S4430XS

S4431XA

S4431XD

S4431XS

S4432XA

S4432XD

S4432XS

S4440XA

S4440XD

S4440XS

S4441XA

S4441XD

S4441XS

S4442XA

S4442XD

S4442XS

S4450XA

S4450XD

S4450XS

S4451XA

S4451XD

S4451XS

S4452XA

S4452XD

S4452XS

S448X1A

S448X1D

S448X1S

S448X2A

S448X2D

S448X2S

S448X9A

S448X9D

S448X9S

S4490XA

S4490XD

S4490XS

S4491XA

S4491XD

S4491XS

S4492XA

S4492XD

S4492XS

S5400XA

S5400XD

S5400XS

S5401XA

S5401XD

S5401XS

S5402XA

S5402XD

S5402XS

S5410XA

S5410XD

S5410XS

S5411XA

S5411XD

S5411XS

S5412XA

S5412XD

S5412XS

S5420XA

S5420XD

S5420XS

S5421XA

S5421XD

S5421XS

S5422XA

S5422XD

S5422XS

S5430XA

S5430XD

S5430XS

S5431XA

S5431XD

S5431XS

S5432XA

S5432XD

S5432XS

S5490XA

S5490XD

S5490XS

S5491XA

S5491XD

S5491XS

S5492XA

S5492XD

S5492XS

S6400XA

S6400XD

S6400XS

S6401XA

S6401XD

S6401XS

S6402XA

S6402XD

S6402XS

S6410XA

S6410XD

S6410XS

S6411XA

S6411XD

S6411XS

S6412XA

S6412XD

S6412XS

S6420XA

S6420XD

S6420XS

S6421XA

S6421XD

S6421XS

S6422XA

S6422XD

S6422XS

S6430XA

S6430XD

S6430XS

S6431XA

S6431XD

S6431XS

S6432XA

S6432XD

S6432XS

S64490A

S64490D

S64490S

S64491A

S64491D

S64491S

S64492A

S64492D

S64492S

S64493A

S64493D

S64493S

S64494A

S64494D

S64494S

S64495A

S64495D

S64495S

S64496A

S64496D

S64496S

S64497A

S64497D

S64497S

S64498A

S64498D

S64498S

S648X1A

S648X1D

S648X1S

S648X2A

S648X2D

S648X2S

S648X9A

S648X9D

S648X9S

S6490XA

S6490XD

S6490XS

S6491XA

S6491XD

S6491XS

S6492XA

S6492XD

S6492XS

S7401XA

S7401XD

S7401XS

S7402XA

S7402XD

S7402XS

S7411XA

S7411XD

S7411XS

S7412XA

S7412XD

S7412XS

S7421XA

S7421XD

S7421XS

S7422XA

S7422XD

S7422XS

S748X1A

S748X1D

S748X1S

S748X2A

S748X2D

S748X2S

S7491XA

S7491XD

S7491XS

S7492XA

S7492XD

S7492XS

S8401XA

S8401XD

S8401XS

S8402XA

S8402XD

S8402XS

S8410XS

S8411XA

S8411XD

S8411XS

S8412XA

S8412XD

S8412XS

S8421XA

S8421XD

S8421XS

S8422XA

S8422XD

S8422XS

S84801A

S84801D

S84801S

S84802A

S84802D

S84802S

S8491XA

S8491XD

S8491XS

S8492XA

S8492XD

S8492XS

S9421XA

S9421XD

S9421XS

S9422XA

S9422XD

S9422XS

S9431XA

S9431XD

S9431XS

S9432XA

S9432XD

S9432XS

S948X1A

S948X1D

S948X1S

S948X2A

S948X2D

S948X2S

S948X9A

S948X9D

S948X9S

S9490XA

S9490XD

S9490XS

S9491XA

S9491XD

S9491XS

S9492XA

S9492XD

S9492XS

T85840A

T85840D

T85840S


The electrodiagnostic testing must be guided by accepted practice parameters and physician guidelines. The number of studies performed is expected to be tailored to the clinical findings of the individual client.

Any electrodiagnostic testing procedures may be reimbursed up to four distinct dates of service per calendar year by the same provider.

Any evaluation and management service will be denied as part of another service when billed for the same date of service as EMG or NCS service by the same provider.

31.2.19.2.1EMG

The needle EMG examination must be performed by a physician specially trained in electrodiagnostic medicine.

The following procedure codes may be reimbursed for one service per day for each procedure by the same provider:

Procedure Codes

51784

51785

95860

95861

95863

95864

95865

95867

95868

95869

95872

95875

Procedure code 95866 may be reimbursed up to one service per day, same provider.

Procedure code 95870 may be reimbursed in multiple quantities of up to four services per day, if specific muscles are documented.

Procedure codes 95872 and 95875 may be reimbursed up to two services per day, same provider.

31.2.19.2.2NCS

NCS must be performed by a physician or a trained individual under the direct supervision of a physician. Direct supervision means that the physician is in close physical proximity to the electrodiagnostic laboratory while testing is underway, immediately available to provide the trained individual with assistance and direction, and responsible for selecting the appropriate NCS to be performed.

When the same studies are performed on unique sites by the same provider for the same date of service, studies for the first site must be billed without a modifier and studies for each additional site must be billed with modifier XE, XP, XS, XU, or 59. Modifier 59 should be used only when modifier XE, XP, XS, or XU is not appropriate.

Procedure codes 95907, 95908, 95909, 95910, 95911, 95912, and 95913 may be reimbursed only once when multiple sites on the same nerve are stimulated or recorded.

Procedure codes 95885 and 95886 may be reimbursed once per extremity up to 2 units, any combination of procedure codes, per day, by any provider.

Procedure codes 95885, 95886, and 95887 must be billed with one of the primary procedure codes 95907, 95908, 95909, 95910, 95911, 95912, or 95913 on the same day, by the same provider.

Prior authorization is required for NCS for any diagnosis other than those listed above or when the anticipated number of studies planned for an evaluation exceeds the maximum number of studies, per date of service, by the same provider:

NCS Procedure Code

Studies Allowed per Date of Service

95937

3

Claims for nerve conduction studies that are denied for exceeding the maximum number of studies allowed per day may be appealed with documentation of medical necessity.

Prior authorization is required for more than three studies per day. Documentation must be submitted to establish medical necessity for the additional studies, including one or more of the following:

Additional diagnoses to be considered

Clinical signs, symptoms, or electrodiagnostic findings that necessitate the consideration of the additional diagnosis

Requests must include documentation supporting medical necessity for the number of studies requested, and they must be received on or before the requested DOS.

Medical record documentation must establish medical necessity for any additional studies, including one or more of the following:

Other diagnoses in the differential requires consideration. The provider must identify both of the additional diagnoses considered and the clinical signs, symptoms, or electrodiagnostic findings that necessitated the inclusion.

Multiple diagnoses are established by NCS, and the limitations listed above for a single diagnostic category do not apply. Providers must document all diagnoses established as a result of electrodiagnostic testing.

Testing of an asymptomatic contralateral limb to establish normative values for an individual client (particularly the elderly, diabetic, and clients with a history of ethyl alcohol usage) has been conducted.

Comorbid clinical conditions are identified. The clinical condition must be one that may cause sensory or motor symptoms. Some examples include underlying metabolic disease (e.g., thyroid condition or diabetes mellitus), nutritional deficiency (alcoholism), malignant disease, or inflammatory disorder (including, but not limited to, lupus, sarcoidosis, or Sjögren’s syndrome).

NCS prior authorization requests must be submitted by the ordering provider on the CSHCN Services Program Authorization and Prior Authorization Request Form. The form must be signed and dated by the ordering provider.

Note:An APRN or a physician assistant (PA) may sign all documentation related to the provision of evoked response tests and neuromuscular procedures on behalf of the client’s physician when the physician delegates this authority to the APRN or PA. The APRN or PA provider’s signature and license number must appear on the forms where the physician signature and license number blocks are required.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

31.2.19.3Evoked Potential Procedures

Evoked potential (EP) procedures are a benefit of the CSHCN Services Program. The most common EP procedures are:

Brainstem auditory evoked potentials (BAEPs)

Motor evoked potentials (MEPs)

Somatosensory evoked potentials (SEPs)

Visual evoked potentials (VEPs)

Prior authorization is not required for EP procedures.

Each EP test (procedure codes 92650, 92651, 92652, 92653, 95925, 95926, 95927, 95928, 95929, 95930, 95938, or 95939) is considered a bilateral procedure and is limited to once per date of service any provider regardless of modifiers that indicate multiple sites were tested.

EP tests may be reimbursed up to four services per rolling year, any combination of services by any provider. Claims that exceed the limitation of four services per rolling year may be considered for reimbursement on appeal with documentation that supports the medical necessity.

31.2.19.3.1Vestibular Evoked Myogenic Potentials (VEMP)

VEMP testing procedure codes 92517, 92518, and 92519 are benefits of the CSHCN Services Program.

Some conditions under which VEMP testing (procedure codes 92517, 92518, and 92519) may be appropriate include:

Evaluation of chronic symptoms of pressure, tinnitus, disorientation, or chronic vertigo after all other recommended vestibular tests are completed and is lacking a definitive diagnosis.

Evaluation after a positive CT scan for Superior Semicircular Canal Dehiscence Syndrome (SCDS).

Documentation must include the following:

The other differential diagnoses under consideration

The additional diagnoses considered

The clinical signs, symptoms or electrodiagnostic findings that necessitated the inclusion

VEMP testing must be medically indicated, and reimbursement requires one of the diagnosis codes listed:

Diagnosis Codes

H81311

H81312

H81313

H81319

H81391

H81392

H81393

H81399

H814

H818X1

H818X2

H818X3

H818X9

H8190

H8191

H8192

H8193

H821

H822

H823

H829

H8301

H8302

H8303

H8309

H8311

H8312

H8313

H8319

H832X1

H832X2

H832X3

H832X9

H833X1

H833X2

H833X3

H833X9

H838X1

H838X2

H838X3

H838X9

H8390

H8391

H8392

H8393

H9311

H9312

H9313

H9319

R110

R111

R112

R42

VEMP testing is not medically necessary for any other indications and will not be covered.

All of the following criteria are documentation requirements for VEMP testing:

For each VEMP test performed, the referral reason must include a clear diagnostic impression documented in the client’s medical record.

Medical necessity for the VEMP test must be clearly documented in the client’s medical record and reflect the actual results of specific tests (which could include latency and amplitude).

Medical necessity for client reevaluation after the initial consultation and testing must be clearly documented in the client’s medical record. Supporting documentation must include the following:

New symptoms unrelated to previously evaluated symptoms that may result in a new diagnosis

Rapidly changing client condition documentation supported by the following:

Diagnosis

Current clinical signs and symptoms

Prior clinical condition

Expected clinical disease course

Clinical benefit of additional studies

The client’s medical records are subject to retrospective review.

31.2.19.3.2Intraoperative Neurophysiology Monitoring (IONM)

Intraoperative neurophysiology monitoring (procedure codes 95940 and 95941) are a benefit when performed in addition to each evoked potential test on the same day. Prior authorization is not required for intraoperative neurophysiology monitoring.

The documentation for the intraoperative neurophysiology testing must include the time for which each test is performed.

Procedure code 95940 and 95941 are limited to a maximum of two hours per date of service, per client, per same procedure, by any provider.

Procedure code 95940 and 95941 must be billed in conjunction with one of the following procedure codes on the same day, by the same provider, or the service will be denied:

Procedure Codes

95822

95860

95861

95863

95864

95865

95866

95867

95868

95869

95870

95907

95908

95909

95910

95911

95912

95913

95925

95926

95927

95928

95929

95930

95933

95937

95938

95939


Procedure codes 95940 and 95941 cannot be reported by the surgeon or anesthesiologist.

31.2.19.4Motion Analysis Studies (MAS)

MA studies (procedure codes 96000, 96001, and 96002) will be considered for reimbursement through the CSHCN Services Program for clients who are 3 through 20 years of age and have a diagnosis of, but not limited to, cerebral palsy, traumatic brain injury, myelomeningocele, or stroke. Motion analysis is most often used as a diagnostic tool for clients with neuromuscular conditions, primarily as part of the surgical decision-making process when all conservative measures have been exhausted and surgical intervention is being considered.

Procedure codes 96000, 96001, and 96002 are limited to one per date of service by the same provider and two per year, any provider.

Procedure code 96000 will be denied if billed with 96001 by the same provider for the same date of service.

Procedure codes 95860, 95861, 95863, 95864, 95865, 95866, 95869, 95870, and 95872 will be denied if billed with 96002 by the same provider for the same date of service.

Prior authorization requests for a diagnosis other than cerebral palsy, traumatic brain injury, myelomeningocele, or stroke, or for more than two services per year, will be considered with medical necessity on a case-by-case basis upon review by the CSHCN Services Program medical director or designee.

Prior authorization requests for MA studies must include documentation with the following information that indicates the client meets all the requirements for MA studies:

Ambulatory for a minimum of ten consecutive steps, with or without assistive devices

Client is 3 through 20 years of age

Physically able to tolerate up to three hours of testing

Clear documentation that indicates the study is performed as part of a preoperative or postoperative assessment based on the surgical plan of the client

Providers must complete the CSHCN Services Program Authorization and Prior Authorization Request Form for MA studies prior authorization requests.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

31.2.19.5Prior Authorization for Unlisted Procedure Code 95999

Prior authorization is required for unlisted neurological or neuromuscular diagnostic procedure code 95999; the following information is required to determine coverage:

The client’s diagnosis

A clear description of the neurological procedure that will be performed

Documentation that indicates medical necessity of the neurological procedure

Place of service where the neurological procedure is to be performed

The physician’s intended fee for the neurological procedure being requested or a CPT or HCPCS procedure code that is comparable to the procedure.

Providers must complete the CSHCN Services Program Authorization and Prior Authorization Request Form for prior authorization requests.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

31.2.20Extracapsular Cataract Removal

Extracapsular cataract removal (procedure codes 66989 and 66991) is a benefit of the CSHCN Services Program for clients who are 21 years of age or older.

Procedure codes 66989 and 66991 are limited to the following diagnosis codes:

Diagnosis Codes

H401111

H401112

H401121

H401122

H401131

H401132

Procedure codes 66989 and 66991 are limited to two services per lifetime, and must be billed with modifier LT or RT to identify the eye on which the service was performed.

Procedure code 66989 is denied if billed on the same date of service by the same provider as procedure code 67015, 67025, 67027, 67030, or 67031.

31.2.21Extracorporeal Shock Wave Lithotripsy (ESWL)

Procedure code 50590 is a benefit for the following diagnosis codes:

Di

Diagnosis Codes

N130

N131

N132

N1330

N1339

N200

N201

N202

N209

N219

N22

All claims received for ESWL must include one of these diagnoses.

31.2.22Gastrostomy Devices

Low-profile gastrostomy devices are a benefit of the CSHCN Services Program when prescribed by a physician. Authorization is required.

Physicians may be reimbursed for nonobturated and obturated gastrostomy devices.

Refer to: Section 18.2.4.1, “Gastrostomy Devices” in Chapter 18, “Expendable Medical Supplies” for more information about documentation requirements, limitations, and additional devices.

Chapter 18, “Expendable Medical Supplies” for more information about related supplies and equipment.

Section 4.3, “Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about authorization requirements.

31.2.23Genetics

Genetic services are a benefit of the CSHCN Services Program.

Genetic services may be used to diagnose a condition, optimize disease treatment, predict future disease risk, and prevent adverse drug response.

Genetic services may be provided by a physician and typically include one or more of the following:

Comprehensive physical exams

Diagnosis, management, and treatment for clients with genetically-related health problems

Evaluation of family histories for the client and the client’s family members

Genetic risk assessment

Interpretation and evaluation of laboratory test results

Education and counseling of clients, their families, and other medical professionals on the causes of genetic disorders

Consultation with other medical professionals to provide treatment

The following procedure codes may be reimbursed for geneticists when provided in the office, inpatient hospital, or outpatient hospital setting:

Procedure Codes

96041

99213

99214

99215

99244

99245

99254

99255

99402

99404

Office or other outpatient consultations (procedure codes 99244, 99245, or 99404) are limited to once every 3 years. One office or other outpatient consultation (procedure codes 99244 or 99245) may be reimbursed if an office/outpatient/inpatient consultation has not been reimbursed in the previous 3 years.

Inpatient or observation consultations (procedure code 99254 or 99255) may be reimbursed once every 3 years regardless of whether an office consultation was reimbursed in the previous 3 years.

A comprehensive follow up visit (procedure code 99215) is limited to once per year.

No authorization is required for genetic services that are a benefit of the CSHCN Services Program.

31.2.23.1Family History

It is important for primary care providers to recognize potential genetic risk factors in a client so that they can make appropriate referrals to a genetic specialist.

Obtaining an accurate family history is an important part of clinical evaluations, even when genetic abnormalities are not suspected. Knowing the family history may help health-care providers identify single-gene disorders or chromosomal abnormalities that occur in multiple family members or through multiple generations. Some genetic disorders that can be traced through an accurate family history include diabetes, hypertension, certain forms of cancer, and cystic fibrosis. Early identification of the client’s risk for one of these diseases can lead to early intervention and preventive measures that can delay onset or improve health conditions.

Using a genetics-specific questionnaire helps to obtain the information needed to identify possible genetic patterns or disorders. The most commonly used questionnaires are provided by the American Medical Association and include the “Prenatal Screening Questionnaire,” the “Pediatric Clinical Genetics Questionnaire,” and the “Adult History Form.”

31.2.23.2Genetic Tests

Diagnostic tests to check for genetic abnormalities must be performed only if the test results will affect treatment decisions or provide prognostic information. Tests for conditions that are treated symptomatically are not appropriate since the treatment would not change. Providers who are uncertain whether a test is appropriate are encouraged to contact a geneticist or other specialist to discuss the client’s needs.

Any genetic testing and screening procedure must be accompanied by appropriate nondirective counseling, both before and after the procedure. Information must be provided to the client and family (if appropriate) about the possible risks and purpose and nature of the tests being performed.

Providers who are uncertain whether a test is appropriate are encouraged to contact a geneticist or other specialist to confer about the client and his or her needs.

The interpretation of certain tests, such as nuchal translucency, requires additional education and experience. The CSHCN Services Program supports national certification standards when available.

31.2.23.3Laboratory Practices

For many heritable diseases and conditions, test performance and interpretation of test results require information about client race and ethnicity, family history, and other pertinent clinical and laboratory information. To facilitate test requests and ensure prompt initiation of appropriate testing procedures and accurate interpretation of test results, the requesting provider must be aware of the specific client information needed by the laboratory before tests are ordered.

To help providers make appropriate test selections and requests, handle and submit specimens, and provide clinical care, laboratories that perform molecular genetic testing for heritable diseases and conditions must educate providers that request services about the molecular genetic tests that the laboratory performs. For each molecular genetic test, the laboratory must provide the following information:

Indications for testing

Relevant clinical and laboratory information

Client race and ethnicity

Family history

Pedigree

Testing performed on a client to provide genetic information for a family member, and testing performed on a non-CSHCN Services Program client to provide genetic information for a CSHCN Services Program client are not benefits of the CSHCN Services Program.

31.2.23.4Genetic Counselors

Genetic counselor services may be billed by a physician when the genetic counselor is an employee of the physician. Services provided by independent genetic counselors are not a benefit of the CSHCN Services Program.

Refer to: Section 25.2.5.2, “Cytogenetics Testing” in Chapter 25, “Laboratory Services” for more information on cytogenetic testing.

31.2.24Hyperbaric Oxygen Therapy (HBOT)

Hyperbaric oxygen therapy is a type of treatment that increases the environmental oxygen pressure to promote the movement of oxygen from the environment into the client’s body tissues. HBOT is a benefit when it is performed in specially constructed hyperbaric chambers, pressurized to 1.4 atmospheric absolute (atm.abs) or higher, that may hold one or several clients.

The CSHCN Services Program recognizes the following indications for HBOT, as approved by the Undersea & Hyperbaric Medical Society (UHMS):

Air or gas embolism

Carbon monoxide poisoning

Central retinal artery occlusion

Compromised skin grafts and flaps

Crush injuries, compartment syndrome, and other acute traumatic ischemias

Decompression sickness

Diabetic foot ulcer

Severe anemia

Clostridial myositis and myonecrosis (gas gangrene)

Necrotizing soft tissue infections

Delayed radiation injury (soft tissue and bony necrosis)

Refractory osteomyelitis

Acute thermal burn injury

Intracranial abscess

CSHCN Services Program considers HBOT experimental and investigational for any indications other than the ones approved by UHMS and outlined in this section. Non-covered indications, include, but are not limited to, autism and traumatic brain injury.

Oxygen administered outside of a hyperbaric chamber, by any means, is not considered hyperbaric treatment.

HBOT services must be provided in facilities that have experience in HBOT treatment of pediatric clients. The physician must be in constant attendance of hyperbaric oxygen therapy during compression and decompression of the chamber, and may not delegate this service.

Both the facility’s medical record and the client’s medical record must contain documentation to support that there was a physician in attendance who provided supervision of the compression and decompression phases of the HBOT treatment. All documentation pertaining to HBOT is subject to retrospective review.

Physicians who bill for the professional component of HBOT must use procedure code 99183.

Hospital providers who bill for the chamber time must use procedure code G0277 with revenue code 413.

31.2.24.1Prior Authorization Requirements

HBOT procedure codes 99183 and G0277 require prior authorization. When requesting prior authorization, providers should use the CSHCN Services Program Authorization and Prior Authorization Request Form.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

The prior authorization request must include documentation that supports medical necessity and is specific to each appropriate covered indication as listed in the following table:

Covered
Indication

Total Number of 30 Minute Intervals Allowed for Procedure Code G0277

Total Number of Professional Sessions Allowed for Procedure Code 99183

Medical Necessity Documentation of the Following is Required

Air or gas embolism

6

2

Evidence that gas bubbles are detectable by ultrasound, Doppler or other diagnostics

Carbon monoxide poisoning - initial authorization

15

5

Persistent neurological dysfunction secondary to carbon monoxide inhalation

Carbon monoxide poisoning - one subsequent authorization

9

3

Evidence of continuing improvement in cognitive functioning

Central retinal artery occlusion

36

6

Evidence of central retinal artery occlusion with treatment initiated within 24 hours of the occlusion

Compromised skin grafts and flaps - initial authorization

80

10

Evidence the flap or graft is failing because tissue is/has been compromised by irradiation or there is decreased perfusion or hypoxia

Compromised skin grafts and flaps - one
subsequent authorization

40

5

Evidence of stabilization of graft or flap

Crush injury, compartment syndrome and other acute traumatic ischemias

36

12

Adjunct to standard medical and surgical interventions

Decompression sickness

28

1

Diagnosis based on signs and/or symptoms of decompression sickness after a dive or altitude exposure

Diabetic foot
ulcer -initial authorization

60

30

After at least 30 days of standard medical wound therapy, with a wound pO2 less than 40 mmHg AND wound classified as Wagner grade 3 or higher. *

Diabetic foot ulcer - two subsequent authorizations

60

20

Evidence of continuing healing and wound pO2 less than 40 mmHg

Severe anemia

50

10

Hgb less than 6.0 sustained secondary to hemorrhage, hemolysis, or aplasia, when the client is unable to be cross matched or refuses transfusion because of religious beliefs

Clostridial myositis and myonecrosis (gas gangrene)

39

13

Evidence of unsuccessful medical and/or surgical wound treatment and positive Gram-stained smear of the wound fluid

Necrotizing soft tissue infections – initial authorization

36

12

Evidence of unsatisfactory response to standard medical and surgical treatment and advancement of dying tissue

Necrotizing soft tissue infections - two subsequent authorizations

15

5

Evidence that advancement of dying tissue has slowed

Delayed radiation injury (soft tissue and bony necrosis) - initial authorization

40

10

Evidence of unsatisfactory response to conventional treatment

Delayed radiation injury - one
subsequent authorization

40

10

Evidence of improvement demonstrated by clinical response

Refractory osteomyelitis - initial authorization

40

10

Evidence of unsatisfactory clinical response to conventional multidisciplinary treatment

Refractory osteomyelitis - one subsequent authorization

15

5

Evidence of improvement demonstrated by clinical response

Acute thermal burn injury - initial authorization

45

15

Partial or full thickness burns covering greater than 20% of total body surface area OR with involvement of the hands, face, feet or perineum

Acute thermal burn injury – three subsequent authorizations

30

10

Evidence of continuing improvement demonstrated by clinical response

Intracranial abscess - initial authorization

15

5

Adjunct to standard medical and surgical interventions when one or more of the following conditions exist:

Multiple abscesses

Abscesses in a deep or dominant location

Compromised host

Surgery contraindicated or client is a poor surgical risk

Intracranial abscess - one subsequent authorization

15

5

Evidence of improvement demonstrated by clinical response and radiological findings

*Note: The following Wagner wound classification grades apply only to the diabetic foot ulcer indications:

• Grade 1: Superficial diabetic ulcer

• Grade 2: Ulcer extension - involves ligament, tendon, joint capsule or fascia (No abscess or osteomyelitis)

• Grade 3: Deep ulcer with abscess or osteomyelitis

• Grade 4: Gangrene to portion of forefoot

• Grade 5: Extensive gangrene of foot

Procedure code 99183 is authorized according to the number of professional sessions (total HBOT treatments), and procedure code G0277 is authorized according to the number of 30-minute intervals of chamber time. The units in the columns for procedure codes 99183 and G0277 represent the maximum number of sessions and intervals that are allowed for that procedure code per authorization

Example:In accordance with recommended protocols, a client with an air/gas embolus may receive up to 6 units (180 minutes) of HBOT over two treatments.

One prior authorization number may be issued for a quantity of 6 units for procedure code G0277 for the facility and 2 professional sessions for procedure code 99183.

The 6 units of chamber time for procedure code G0277 may be divided in any manner across the two professional sessions. For procedure code 99183, the usual protocol is two 90-minute treatments.

The facility bills 90 consecutive minutes (3 units) per HBOT treatment for procedure code G0277. The physician bills per treatment, which in this case would be 2 professional sessions for procedure code 99183.

Limitations beyond those listed in the table above are considered experimental and investigational.

31.2.25Immunizations (Vaccines and Toxoids)

Vaccines and vaccine administration, as recommended by the Advisory Committee on Immunization Practices (ACIP), is a benefit of the Children with Special Health Care Needs (CSHCN) Services Program.

A vaccine stimulates a person’s immune system to produce immunity to a disease, thereby providing protection from that disease.

Vaccines may be administered orally, nasally, or by subcutaneous or intramuscular injection.

Providers must follow current ACIP recommendations; however, in the event of conflict, providers are required to more closely follow the Texas Vaccines for Children (TVFC) guidelines.

31.2.25.1Texas Vaccines for Children (TVFC) Program

The CSHCN Services Program encourages providers administering vaccines to enroll in TVFC. Providers interested in enrollment information for TVFC may call the Department of State Health Services (DSHS), Immunizations Branch at 1-800-252-9152 or access the TVFC website at www.dshs.texas.gov/immunize/tvfc/.

If the provider is enrolled in TVFC, the provider must screen the client and, if indicated, immunize the client using TVFC-obtained vaccine.

Providers must provide the appropriate vaccine information statements (VISs) produced by the Centers for Disease Control and Prevention (CDC) to each client. VISs explain the benefits and risks of the vaccine.

31.2.25.2Documentation Recommendations

Providers must document the following information in the client’s medical record for each vaccine administered:

   The vaccine given

   The date of the vaccine administration (day, month, year)

   The name of the vaccine manufacturer

   The vaccine lot number

   The signature and title of the person who administered the vaccine

   The location of where the vaccine was administered

   The publication date of the VIS issued to the client, parent, or guardian

If a vaccine was administered outside of ACIP’s recommended routine immunization schedules, the reason must be included in the client’s medical record. Reasons for administering a vaccine outside the routine schedule may include but are not limited to:

   An impaired immune system.

   Suspected exposure to a disease.

The client’s medical records are subject to retrospective review to determine whether the utilization and reimbursement of this service was appropriate.

Procedure codes 90460 and 90461 include counseling by a qualified healthcare professional. Documentation of the counseling must be noted in the client’s medical record.

31.2.25.3Vaccine Reporting to the DSHS

All administered vaccines and toxoids must be reported to DSHS. DSHS submits all reported vaccinations with consent to a centralized repository of immunization histories. This repository is known in Texas as ImmTrac2.

Note:Documentation of the injection site is recommended, but not required.

31.2.25.3.1Vaccine Adverse Event Reporting System (VAERS)

VAERS encourages providers to report any adverse event that occurs after a vaccine has been administered. Even if the provider is unclear whether the adverse event was caused by the vaccine, it should still be reported. The National Childhood Vaccine Injury Act (NCVIA) requires health care providers to report:

   “Any adverse event listed by the vaccine manufacturer as a contraindication to subsequent doses of the vaccine.

   “Any reaction that is listed in the VAERS Reportable Events Table that occurs within the specified time period post vaccination.

A copy of the Reportable Events Table can be obtained by calling VAERS at 1-800-822-7967 or by downloading it from https://vaers.hhs.gov/resources/materials.html.

31.2.25.4Authorization Requirements

Authorization is not required for any vaccine or its associated administration fee. Providers enrolled in TVFC are responsible for determining the eligibility of clients to receive TVFC reimbursement.

31.2.25.5Vaccine Reimbursement

The diagnosis code Z23 should be reported regardless of the type of encounter when a vaccine was given. It must be reported and linked to both the vaccine product and the vaccine administration code.

When the client visit is only for vaccine administration, diagnosis code Z23 should be used as the appropriate vaccine diagnosis code.

When vaccines are given during a preventive health visit (e.g., well child exam), diagnosis code Z23 will follow the age appropriate diagnosis code for the preventive health visit.

When the client visit is only for vaccine administration, the office visit will not be reimbursed.

If a vaccine is administered as part of a preventive health visit (e.g., well child exam), or a visit due to a medical condition, the office visit will be reimbursed in addition to the vaccine given.

Reimbursement may be considered for any vaccine if it is not obtained through TVFC but has been recommended by ACIP and approved by the Health and Human Services Commission (HHSC).

Each vaccine and its administration must be submitted on the same claim in the following sequence: the vaccine procedure code immediately followed by the applicable vaccine administration procedure code(s). All of the vaccine administration procedure codes that correspond to a single vaccine procedure code must be submitted on the same claim as the vaccine procedure code.

Vaccines that are purchased by a provider may be reimbursed if the state-defined modifier U4 is billed with the vaccine and one of the following conditions is met:

   The provider is not enrolled in TVFC.

   The client does not meet the TVFC criteria.

   TVFC resolutions do not match the ACIP’s general usage recommendations.

   The provider purchases an ACIP-recommended vaccine that is not distributed by TVFC.

Providers purchasing the vaccine are reimbursed the lower of the billed amount for the vaccine or the amount allowed by Texas Medicaid or the maximum fee established by the CSHCN Services Program. The maximum fee will be determined from the least average wholesale price (AWP) per vaccine dose according to the current information reflected in the Texas Vendor Drug Program system.

Providers must submit claims for procedure codes 90460 (administration of first/only component of vaccine, with counseling) and 90461 (administration of each additional vaccine component, with counseling) based on the number of components per vaccine.

31.2.25.6Vaccine Administration

Procedure code 90460 must be submitted for the administration of the first component.

Procedure code 90461 must be submitted for the administration of each additional component identified in the vaccine.

Procedure code 90461 will be denied if procedure code 90460 has not been submitted on the same claim for the same vaccine.

Procedure codes 90471, 90472, 90473, and 90474 do not require counseling and can be reimbursed at any age.

RSV monoclonal antibodies (nirsevimab, procedure codes 90380 and 90381) may be administered to clients who are birth through 19 months of age.

Administration of nirsevimab (procedure codes 96380 and 96381) are limited to two per lifetime.

The age ranges for vaccine administration are listed in the following table:

Procedure Codes

Age Range

90460

Birth through 18 years of age

90461

Birth through 18 years of age

90471

All ages

90472

All ages

90473

All ages

90474

All ages

90653

65 years of age or older

96372

All ages

96372

All ages

96374

All ages

96380

Birth through 19 months of age

96381

Birth through 19 months of age

31.2.25.6.1Administration With Counseling

Providers must submit claims for immunization administration procedure codes 90460 or 90461 based on the number of components per vaccine. Providers must specify the number of components per vaccine by billing 90460 and 90461 as defined by the procedure code descriptions:

Procedure code 90460 is submitted for the administration of the 1st component.

Procedure code 90461 is submitted for the administration of each additional component identified in the vaccine.

Procedure code 90461 will be denied if procedure code 90460 has not been submitted on the same claim for the same vaccine or toxoid.

The following is an example of how to submit claims for immunization administration procedure codes when counseling is provided:

Procedure Code

Quantity Billed

Vaccine or toxoid procedure code with 1 component

1

90460 (1st component)

1

Vaccine or toxoid procedure code with 3 components

1

90460 (1st component)

1

90461 (2nd and 3rd components)

2

Vaccine or toxoid procedure code with 2 components

1

90460 (1st component)

1

90461 (2nd component)

1

Vaccine or toxoid procedure code with 4 components

1

90460 (1st component)

1

90461 (2nd, 3rd, and 4th components)

3

Vaccine or toxoid procedure code with 5 components

1

90460 (1st component)

1

90461 (2nd, 3rd, 4th, and 5th components)

4

Note:The term “components” refers to the number of antigens that prevent disease(s) caused by one organism. Combination vaccines are those that contain multiple vaccine components.

31.2.25.6.2Administration Without Counseling

Procedure codes 90471, 90472, 90473, and 90474 may be reimbursed per vaccine based on the route of administration.

The following is an example of how to submit claims for injection administration procedure codes when counseling is not provided:

Procedure Code

Quantity Billed

Vaccine or toxoid procedure code

1

90471 (Injection administration)

1

Vaccine or toxoid procedure code

1

90472 (Injection administration)

1

Vaccine or toxoid procedure code

1

90472 (Injection administration)

1

The following is an example of how to submit claims for oral or nasal administration procedure codes when counseling is not provided:

Procedure Code

Quantity Billed

Vaccine or toxoid procedure code

1

90473 (Oral/nasal administration)

1

Vaccine or toxoid procedure code

1

90474 (Oral/nasal administration)

1

31.2.25.7Vaccine and Toxoid Procedure Codes

The vaccine procedure codes listed in the following table are benefits of the CSHCN Services Program.

Note:A component refers to all antigens in a vaccine that prevent disease(s) caused by one organism. Combination vaccines are those vaccines that contain multiple components. All procedure codes with an asterisk (*) can be distributed through TVFC.

Procedure Code

Age Range

Number of Recognized Components

90287

All ages

1

90585

All ages

1

90611

18 years of age and older

1

90619

19 years of age and older

1

90620*

All ages

1

90621*

All ages

1

90623

10 years of age through 23 years of age

1

90632*

Birth through 20 years of age

1

90633*

Birth through 20 years of age

2

90636*

All ages

2

90647*

All ages

1

90648*

All ages

1

90651*

All ages

1

90670*

All ages

1

90678

10 years of age and older

1

90680*

Birth through 11 months of age

1

90681*

All ages

1

90684

19 years of age or older

1

90696*

4 years of age through 6 years of age

4

90698*

All ages

5

90700*

Birth through 6 years of age

3

90702*

Birth through 6 years of age

2

90707*

All ages

3

90710*

All ages

4

90713*

All ages

1

90714*

7 years of age and older

2

90715*

7 years of age and older

3

90716*

All ages

1

90723*

All ages

5

90732*

2 years of age and older

1

90733*

All ages

1

90734*

All ages

1

90736

60 years of age and older

1

90739

18 years of age and older

1

90740

All ages

1

90743*

All ages

1

90744*

All ages

1

90746*

All ages

1

90747

All ages

1

90748

All ages

2

90749

All ages

1

90750

50 years of age and older

1


Procedure code 90670 is limited to one per day for clients who are birth through five years of age, same procedure, any provider, and to one per lifetime for clients who are age six and older.

The following immunizations are not a benefit of the CSHCN Services Program:

Cholera vaccine, injectable

Plague vaccine, intramuscular (IM)

Typhoid vaccines

Yellow fever vaccine, subcutaneous (SC)

31.2.25.8Influenza Vaccines

The Advisory Committee on Immunization Practices (ACIP) reviews the composition of influenza vaccines annually and frequently makes updates to their recommendations. Providers should refer to the Centers for Disease Control and Prevention (CDC) website for current recommendations.

Providers should refer to the TVFC website for the most up-to-date list of the influenza vaccines that TVFC is distributing for clients and their age group for the current flu season.

Reimbursement for influenza vaccines is limited to three occurrences per one rolling year. Claims submitted for any influenza vaccine beyond three occurrences in a rolling year will be denied.

The age ranges for influenza vaccines are listed in the following table:

Procedure Code

Age Range

90655

6 months of age through 35 months of age

90656

3 years of age and older

90657

6 months of age through 35 months of age

90658

3 years of age and older

90660

All ages

90661

All ages

90662

All ages

90672

All ages

90673

All ages

90674

All ages

90682

18 years of age and older

90685

6 months of age through 35 months of age

90686

All ages

90687

6 months of age through 35 months of age

90688

All ages

90756

4 years of age and older

31.2.25.9Bacille Calmette-Guerin (BCG) Vaccine

BCG vaccine (procedure code 90585) is a benefit of the CSHCN Services Program for diagnosis code Z23.

31.2.25.10Botulinum Antitoxin

Procedure code 90287 is a benefit of the CSHCN Services Program for diagnosis code A051, A4851, A4852, or one of the following diagnosis codes for botulinum overdose or misinjection:

 

Diagnosis Codes

T50901A

T50901D

T50901S

T50902A

T50902D

T50902S

T50903A

T50903D

T50903S

T50904A

T50904D

T50904S

T50991A

T50991D

T50991S

T50992A

T50992D

T50992S

T50993A

T50993D

T50993S

T50994A

T50994D

T50994S

T50Z91A

T50Z91D

T50Z91S

T50Z92A

T50Z92D

T50Z92S

T50Z93A

T50Z93D

T50Z93S

T50Z94A

T50Z94D

T50Z94S

31.2.25.11Hepatitis B Vaccine

Procedure codes 90740 and 90747 are not considered routine vaccines and must be billed using administration procedure code 96372 or 96374.

31.2.25.12Rabies Postexposure Prophylaxis

Postexposure prophylaxis for rabies (procedure codes 90375, 90376, 90377, and 90675) is a benefit of the CSHCN Services Program.

An exposed person who has never received a complete pre- or postexposure rabies vaccine series will first receive a dose of rabies immune globulin (HRIG). This is a blood product that contains antibodies against rabies and gives immediate, short-term protection. The recommended dose of HRIG is 20 IU/kg body weight. This formula is applicable to all age groups, including children. The injection should be given in or near the wound area.

The postexposure treatment will also include 5 doses of rabies vaccine (1.0 ml. intramuscular). The first dose should be given as soon as possible after the exposure (day 0). Additional doses should be given on days 3, 7, 14, and 28 after the first shot. For an exposed person wh

21o has previously been vaccinated with a complete pre- or postexposure vaccine series, 2 doses of rabies vaccine should be given, one on day 0 and one on day 3.

HRIG that is not administered when vaccination begins can be administered up to 7 days after the administration of the first dose of vaccine. Beyond the seventh day, HRIG is not recommended since an antibody response to the vaccine is presumed to have occurred, and HRIG may inhibit the immune response to the vaccine.

Reimbursement for postexposure rabies vaccine is limited to 1 per client, per day, by any provider, not to exceed a total of 5 per 90 rolling days.

Animal bites to people must be reported as soon as possible to the local rabies control authority. Postexposure prophylaxis for rabies is not necessary following exposure to an animal that tests negative for the rabies virus. Health-care providers who determine that their client requires the preventive rabies vaccination series after valid rabies exposure may obtain the biologicals directly from the manufacturer or through one of the DSHS depots around the state. The physician must maintain documentation of the exposure in the client’s medical record.

Postexposure rabies treatment is limited to clients with diagnosis code Z203.

Injection administration is a benefit for administration of postexposure rabies vaccine.

31.2.25.13Respiratory Syncytial Virus (RSV) Prophylaxis

The RSV prophylaxis drug palivizumab (Synagis) must be obtained through the Texas Vendor Drug Program (VDP). Providers must obtain prior authorization through the CSHCN Services Program using the CSHCN Services Program Synagis Prior Authorization form.

Providers may refer to the Texas Vendor Drug Program website at www.txvendordrug.com/formulary/respiratory-syncytial-virus-treatment for more information about obtaining palivizumab for CSHCN Services Program clients.

Prior authorization request forms are reviewed annually. Providers must use the most current version of the CSHCN Synagis Prior Authorization Request (HHS Form 1055) to submit prior authorization requests. Forms received outside the RSV season schedule will not be processed.

31.2.26Injections and Oral Medications

Oral medication must be used in preference to injectable medication in the office and outpatient hospital unless one of the following circumstances applies:

No acceptable oral equivalent is available.

Injectable medication is the standard treatment of choice.

The oral route is contraindicated.

The client has a temperature over 102°F (documented on the claim and in the medical record) and a high blood level of antibiotic is needed quickly.

The client has demonstrated noncompliance with orally prescribed medication (documented on the claim and in the medical record).

Previously attempted oral medication regimens have proven ineffective and are supported by the medical record.

An emergency situation occurs.

Claims submitted for antibiotic or steroid injections billed in a physician’s office or in the outpatient hospital setting must include modifiers AT, ET, or KX.

Providers dispensing physician-administered drugs in an outpatient setting may utilize an optional delivery method referred to as “white bagging,” in which the treating provider submits prescriptions to pharmacies and the prescription is shipped or mailed to the provider’s office. Providers must use the following steps for this delivery method:

1) The treating provider identifies a CSHCN Services Program-enrolled client.

2) The treating provider or treating provider’s agent sends a single prescription with no additional refills to a CSHCN Services Program-enrolled pharmacy and obtains any necessary prior authorizations. (The provider must write a new prescription for any additional refills.)

3) Once approved, the dispensing pharmacy fills the prescription and overnight ships an individual dose of the medication, in the name of the CSHCN Services Program client, directly to the treating provider. These medications must not be used on any other patient and cannot be returned to the pharmacy for credit.

4) The treating provider administers the medication to the CSHCN Services Program client in the office setting. The treating provider bills for an administration fee and any medically necessary service provided at time of administration. The treating provider must not bill the CSHCN Services Program for the drug.

Note:Providers may perform other services in addition to any evaluation and management during the client’s white bagging medication administration visit, such as: administering other medications or immunizations maintained in the office, administering treatments, X-rays, or labs.

31.2.26.1Reimbursement for the Unused Portion of the Single-Dose Vial

Providers may bill and receive reimbursement for the unused portion of weight-based or variable dosing clinician-administered drugs (CADs) manufactured only in single-dose vials.

Providers must also include modifier JW on their claims for consideration of reimbursement. The JW modifier on the claim will identify the unused portion and discarded portion of the vial contents.

This only applies to medical claims for weight-based or variable dosing CADs billed with HCPCS procedure codes, manufactured only in single-dose vials, and provided in a professional or outpatient setting.

31.2.26.2Injection Administration Billed by a Physician

Injection administration billed by a physician may be reimbursed separately from the medication. Injection administration must be billed using procedure code 96372. Procedure code 96372 may be reimbursed in addition to an E/M or consultation visit. This ensures that each injection receives one administration fee regardless of the dosage.

Most injectable medications may be reimbursed the average wholesale price (AWP) minus 10.5 percent. However, the CSHCN Services Program reserves the option to use other data services when the AWP results have been determined as unreasonable or inefficient.

31.2.26.3Unit Calculations for Billing Drugs

Providers must calculate the number of units to be billed on the claim based on the number of units indicated in the procedure code description and the amount of the drug actually administered. Providers should refer to the procedure code description for the unit amount to calculate the number of units to be billed.

The formula to calculate the appropriate quantity of units to bill is the amount administered divided by the units indicated in the procedure code description. For example:

Units Indicated in the Description

Amount Administered by the Provider

Calculation

Quantity to Bill on the Claim

50 mg

100 mg

100/50 = 2

2 units

per unit

20 units

20/1 = 20

20 units

per 100 units

2500 units

2500/100 = 25

25 units

per 50 mg

250 mg

250/50 = 5

5 units

Claims submitted with incorrect unit calculations may cause delayed or incorrect payment.

The specific National Drug Code (NDC) of the drug actually dispensed should be entered on the claim form.

Refer to:Section 5.6.2.4, “National Drug Codes (NDC)” in Chapter 5, “Claims Filing, Third-Party Resources, and Reimbursement” for more information.

Section 5.6.2.5, “Drug Rebate Program” in Chapter 5, “Claims Filing, Third-Party Resources, and Reimbursement” for information about the reimbursement of clinician-administered drugs and biologicals

Additional information about NDC code requirements is also available on the NDC page of the TMHP website at www.tmhp.com.

31.2.26.4JW Modifier Claims Filing Instructions

Providers must not use the JW modifier for medications manufactured in a multi-dose vial format.

Providers must choose the most appropriate vial size(s) required to prepare a dose to minimize the discarded portion of the vial payable.

Claims considered for reimbursement must not exceed the package size of the vial used for preparation of the dose. Providers must not bill for vial contents overfill.

Providers must not use the JW modifier when the actual dose of the drug or biological administered is less than the billing unit.

Example: One billing unit for a drug is equal to 10mg of the drug in a single use vial. A 7mg dose is administered to a client while 3mg of the remaining drug is discarded. The 7mg dose is billed using one billing unit that represents 10mg on a single line item. The single line item of 1 unit would process for payment of the total 10mg of drug administered and discarded. Billing another unit on a separate line item with the JW modifier for the discarded 3mg of drug is not permitted because it would result in overpayment. Therefore, when the billing unit is equal to or greater than the total actual dose and the amount discarded, the use of the JW modifier is not permitted.

Reimbursement for JW modifier claims is only available for drugs covered in an outpatient setting.

Inpatient and diagnostic radiopharmaceuticals claims are not eligible for reimbursement, and may not include the JW modifier.

Coverage is for “buy and bill” providers only. Specialty pharmacies billing through the medical benefit must not submit claims with a JW modifier because they are unaware of how much the provider administered or discarded.

Federally Qualified Health Center (FQHC) and Rural Healthcare Clinic RHC) are not eligible to bill with the JW modifier because these providers do not bill for the coverage of drugs or biologicals separately.

Critical Access Hospitals (CAH) are eligible to bill with the JW modifier because these providers bill for the coverage of drugs or biologicals separately.

The JW modifier is not allowed for medications prepared in an institutional setting via “batch processing or bulk productions” methods. An example of a batch processing method is when a hospital or repackaging facility produces multiple non-patient specific doses of medications in advance of anticipated use. These preparations are labeled and distributed with client specific information only when orders are received. Because these doses may be recycled for other client use, they are not eligible.

Providers may utilize automatic systems to calculate dose and discard amounts. However, providers must continue to document the exact usage/discard accurately.

Providers must enter the dose administered (used portion) line item detail of the CAD and also enter the dose discarded (unused portion) line item detail of the CAD on the same claim. The dose discarded (unused portion) line item detail must include the JW modifier to be considered for reimbursement. When billing for reimbursement of wastage on an outpatient claim, the HCPCS and Current Procedural Terminology (CPT) code should always be provided along with the revenue code.

31.2.26.5Injection Procedure Codes

The following injections are benefits of the CSHCN Services Program and are subject to the indicated limitations:

Name of Injection

Procedure Code(s)

Limitation(s)

Alglucosidase alfa

J0220

Diagnosis limitations: E7400, E7401, E7402, E7403, E7404, E7409

Andexxa

J7169

Restricted to clients who are 18 years of age or older

Anifrolumab-fnia

J0491

Restricted to clients who are 18 years of age or older

Antithrombin

J7197

Diagnosis limitations: D6800, D6801, D68020, D68021, D68022, D68023, D68029, D6803, D6804, D6809, D6851, D6852, D6859, D6861, D6862, D6869, D75821, D75822, D75828, D75829, D75838, D7584

Avalglucosidase Alfa-ngpt

J0219

Restricted to clients who are 1 year of age or older

Azacitidine (Vidaza)

J9025

Benefit for clients 13 years of age or older

Diagnosis limitations: C9200, C9202, C9210, C9212, C9220, C9222, C9232, C9242, C9252, C9262, C9290, C9292, C92A2, C92Z0, C92Z2, C9310, C9312, C9330, C9332, C9502, C9510, C9512, C9592, D460, D461, D4621, D4622, D469, D46A, D46B, D46C, D640, D641, D642, D643

Must be submitted with an 11-digit NDC

Bevacizumab-maly (Alymsys)

Q5126

Restricted to clients who are 18 years of age or older

Blood Factor Product VIII (Jivi)

J7208

N/A

Bupivacaine

J0665

Restricted to clients who are 18 years of age or older

Cabotegravir (Apretude)

J0739

Restricted to clients who are 10 years of age or older

Cantharidin

J7354

Restricted to clients who are 2 years of age or older

Diagnosis limitation: B081

Cidofovir

J0740

N/A

Ciltacabtagene autoleucel

Q2056

Restricted to clients who are 18 years of age or older

Clofarabine (Clorar)

J9027

Prior authorization is required. Requests for prior authorization must be submitted by the ordering provider using the CSHCN Services Program Authorization and Prior Authorization Request Form.

Documentation of the following must be submitted with the prior authorization request form:

Diagnosis code C9100 or C9102

At least 2 prior failed regimens

Coagulation Factor IX (Ixinity)

J7213

Restricted to clients who are 12 years of age or older

C1 Esterase Inhibitor (Human) (Cinryze)

J0598

Restricted to clients who are 6 years of age or older

C1 Esterase Inhibitor (Human) (Haegarda)

J0599

Restricted to clients who are 6 years of age or older

Diagnosis limitation: D841

C1 Esterase Inhibitor (Recombinant) (Ruconest)

J0596

Restricted to clients who are 13 years of age or older

Diagnosis limitation: D841

Dalteparin sodium

J1645

N/A

Eculizumab

J1300

Diagnosis limitations: D588, D5910, D5911, D5912, D5913, D5919, D5930, D5932, D5939, D594, D595, D596, D598

Efgartigimod Alfa-fcab (Vyvgart)

J9332

Restricted to clients who are 18 years of age or older

Diagnosis limitations: G700, G7001

Eflapegrastim-xnst

J1449

Restricted to clients who are 18 years of age or older

Emapalumab-lzsg (Gamifant)

J9210

N/A

Enoxaparin sodium

J1650

N/A

Epcoritamab-bysp (Epkinly)

C9155

Restricted to clients who are 18 years of age or older

Epoprostenol

J1325

Diagnosis limitations: I270, I2720, I2721, I2722, I2723, I2724, I2729, I2783, P2930

Esmolol hydrochloride

J1805

Restricted to clients who are 18 years of age or older

Faricimab-svoa

J2777

Restricted to clients who are 18 years of age or older

Fecal microbiota

J1440

Restricted to clients who are 18 years of age or older

Diagnosis limitations: A0471, A0472

Fondaparinux sodium

J1652

N/A

Furosemide (Furoscix)

J1941

Restricted to clients who are 18 years of age or older

Galsulfase

J1458

Diagnosis limitations: E7601, E7602, E7603, E761, E76210, E76211, E76219, E7622, E7629, E763, E768, E769

Granisetron hydrochloride

J1626

Diagnosis limitations: Z510, Z5111, Z5112

The quantity used must appear on the claim.

Idursulfase

J1743

Diagnosis limitations: E7601, E7602, E7603, E761, E76210, E76211, E76219, E7622, E7629, E763, E768, E769

Inclisiran

J1306

Restricted to clients who are 18 years of age or older

Invega hafyera

J2427

Restricted to clients who are 18 years of age or older

Ixabepilone

J9207

Diagnosis limitations: C50011, C50012, C50019, C50111, C50112, C50119, C50211, C50212, C50219, C50311, C50312, C50319, C50411, C50412, C50419, C50511, C50512, C50519, C50611, C50612, C50619, C50811, C50812, C50819, C50911, C50912, C50919, C563, C7963, C847A, D0500, D0501, D0502, D0510, D0511, D0512, D0580, D0581, D0582, D0590, D0591, D0592

Lanoxin (Digoxin)

J1920

Restricted to clients who are 1 year of age or older

Lanreotide (Cipla)

J1932

Restricted to clients who are 18 years of age or older

Lefamulin

J0691

Restricted to clients who are 18 years of age and older

Linezolid

J2020

N/A

Lioresal

J0475

J0476

Separate payment for the device is not a benefit for the physician or the hospital.

Loncastuximab Tesirine-lpyl

J9359

Restricted to clients who are 18 years of age or older

Diagnosis limitations: C8330, C8331, C8332, C8333, C8334, C8335, C8336, C8337, C8338, C8339

Melphalan

J9245

Diagnosis limitations: C9000, C9001, C9002

Melphalan (Evomela)

J9246

Diagnosis limitations: C9000, C9001, C9002

Methotrexate (Jylamvo)

J8611

Restricted to clients who are 18 years of age or older

Midazolam hydrochloride

J2250

N/A

Moxetumomab Pasudotox-tdfk (Lumoxiti)

J9313

Restricted to clients who are 18 years of age and older

Natalizumab injection

J2323

Diagnosis limitations: G35, K5000, K50011, K50012, K50013, K50014, K50018, K5010, K50111, K50112, K50113, K50114, K50118, K5080, K50811, K50812, K50813, K50814, K50818, K5090, K50911, K50912, K50913, K50914, K50918, K50919, K5650, K5651, K5652, K56600, K56601, K56609, K56690, K56691, K56699, K9130, K9131, K9132

Naxitamab-gqgk (Danyelza)

J9348

Restricted to clients who are 1 year of age or older.

Nivolumab and Relatlimab-rmbw

J9298

Restricted to clients who are 12 years of age or older

Nitroglycerin

J2305

Restricted to clients who are 18 years of age or older

Nogapendekin Alfa Inbakicept-pmln (Anktiva)

J9028

Restricted to clients who are 18 years of age or older

Oliceridine

C9101

Restricted to clients who are 18 years of age or older

Omadacycline

J0121

Restricted to clients who are 8 years of age and older

Pegcetacoplan

J2781

Restricted to clients who are 18 years of age or older

Phenylephrine hydrochloride (Immphentiv)

J2373

Restricted to clients who are 18 years of age or older

Plazomicin

J0291

Restricted to clients who are 18 years of age and older

Porfimer sodium

J9600

Diagnosis limitations: C153, C154, C155, C158, C159, C787, C7880, C7889

Ranibizumab-eqrn (Cimerli)

Q5128

Restricted to clients who are 18 years of age or older

Ravulizumab-cwvz (Ultomiris)

J1303

Diagnosis limitations: D5930, D5931, D5932, D5939, G360

Releuko

Q5125

N/A

Remimazolam

J2249

Restricted to clients who are 18 years of age or older

Retifanlimab-dlwr (Zynyz)

J9345

Restricted to clients who are 18 years of age or older

Rituximab

J9310

N/A

Sirolimus Protein-bound Particles (Fyarro)

J9331

Restricted to clients who are 18 years of age or older

Sumatriptan succinate

J3030

Limited to treatment of classical migraines

Diagnosis limitations: G43001, G43011, G43101, G43109, G43111, G43119, G43401, G43409, G43411, G43419, G43501, G43509, G43511, G43519, G43601, G43609, G43611, G43619, G43701, G43709, G43711, G43719, G43801, G43809, G43811, G43819, G43821, G43829, G43831, G43839, G43901, G43909, G43911, G43919, G43A0, G43A1, G43B0, G43B1, G43C0, G43C1, G43D0, G43D1

Sutimlimab-jome (Enjaymo)

J1302

Restricted to clients who are 18 years of age or older

Tebentafusp-tebn

J9274

Restricted to clients who are 18 years of age or older

Tezepelumab-ekko (Tezspire)

J2356

Restricted to clients who are 12 years of age or older

Tildrakizumab (Ilumya)

J3245

Restricted to clients who are 18 years of age and older

Tisotumab Vedotin-tftv

J9273

Restricted to female clients who are 18 years of age or older

Triamcinolone Acetonide (Xipere)

J3299

Restricted to clients who are 18 years of age or older

Ublituximab-xiiy (Briumvi)

J2329

Restricted to clients who are 18 years of age or older

Valrubicin

J9357

Diagnosis limitation: D090

Vasopressin

J2598

J2599

J2601

Restricted to clients who are 18 years of age or older

Verteporfin

J3396

Diagnosis limitations: H35021, H35022, H35023, H353110, H353111, H353112, H353113, H353114, H353120, H353121, H353122, H353123, H353124, H353130, H353131, H353132, H353133, H353134, H353190, H353191, H353192, H353193, H353194, H353210, H353211, H353212, H353213, H353220, H353221, H353222, H353223, H353230, H353231, H353232, H353233, H353290, H353291, H353292, H353293

(Diagnosis limitations) The procedure code must be billed with one of the codes listed.

In addition to the injections listed in the above table, the following sections indicate additional injections that may be reimbursed by the CSHCN Services Program and the applicable limitations.

31.2.26.6Adalimumab

Adalimumab (procedure codes J0139 and Q5140) is a benefit of the CSHCN Services Program with the following diagnosis limitations:

Diagnosis Codes

K5000

K50011

K50012

K50013

K50014

K50018

K5010

K50111

K50112

K50113

K50114

K50118

K5080

K50811

K50812

K50813

K50814

K50818

K5090

K50911

K50912

K50913

K50914

K50918

K50919

K5100

K51011

K51012

K51013

K51014

K51018

K51019

K5120

K51211

K51212

K51213

K51214

K51218

K5130

K51311

K51312

K51313

K51314

K51318

K5140

K51411

K51412

K51413

K51414

K51418

K51419

K5150

K51511

K51512

K51513

K51514

K51518

K51519

K5180

K51811

K51812

K51813

K51814

K51818

K51819

K5190

K51911

K51912

K51913

K51914

K51918

K5650

K5651

K5652

K56600

K56601

K56609

K56690

K56691

K56699

K9130

K9131

K9132

L400

L401

L402

L403

L404

L4050

L4051

L4052

L4053

L4054

L4059

L408

M00039

M00071

M00072

M00079

M00171

M00172

M00179

M00271

M00272

M00279

M00871

M00872

M00879

M0500

M05011

M05012

M05019

M05021

M05022

M05029

M05031

M05032

M05039

M05041

M05042

M05049

M05051

M05052

M05059

M05061

M05062

M05069

M05071

M05072

M05079

M0509

M05271

M0530

M0540

M05411

M05412

M05419

M05421

M05422

M05429

M05431

M05432

M05439

M05441

M05442

M05449

M05451

M05452

M05459

M05461

M05462

M05469

M05471

M05472

M05479

M0549

M0550

M05511

M05512

M05519

M05521

M05522

M05529

M05531

M05532

M05539

M05541

M05542

M05549

M05551

M05552

M05559

M05561

M05562

M05569

M05571

M05572

M05579

M0559

M0560

M05611

M05612

M05619

M05621

M05622

M05629

M05631

M05632

M05639

M05641

M05642

M05649

M05651

M05652

M05659

M05661

M05662

M05669

M05671

M05672

M05679

M0569

M0570

M05711

M05712

M05719

M05721

M05722

M05729

M05731

M05732

M05739

M05741

M05742

M05749

M05751

M05752

M05759

M05761

M05762

M05769

M05771

M05772

M05779

M0579

M057A

M0580

M05811

M05812

M05819

M05821

M05822

M05829

M05831

M05832

M05839

M05841

M05842

M05849

M05851

M05852

M05859

M05861

M05862

M05869

M05871

M05872

M05879

M0589

M058A

M059

M0600

M06011

M06012

M06019

M06021

M06022

M06029

M06031

M06032

M06039

M06041

M06042

M06049

M06051

M06052

M06059

M06061

M06062

M06069

M06071

M06072

M06079

M0608

M0609

M060A

M061

M0620

M06211

M06212

M06219

M06221

M06222

M06229

M06231

M06232

M06239

M06241

M06242

M06249

M06251

M06252

M06259

M06261

M06262

M06269

M06271

M06272

M06279

M0628

M0629

M0630

M06311

M06312

M06319

M06321

M06322

M06329

M06331

M06332

M06339

M06341

M06342

M06349

M06351

M06352

M06359

M06361

M06362

M06369

M06371

M06372

M06379

M0638

M0639

M0680

M06811

M06812

M06819

M06821

M06822

M06829

M06831

M06832

M06839

M06841

M06842

M06849

M06851

M06852

M06859

M06861

M06862

M06869

M06871

M06872

M06879

M0688

M0689

M068A

M069

M0800

M08011

M08012

M08019

M08021

M08022

M08029

M08031

M08032

M08039

M08041

M08042

M08049

M08051

M08052

M08059

M08061

M08062

M08069

M08071

M08072

M08079

M0808

M0809

M081

M08811

M08812

M08821

M08822

M08831

M08832

M08839

M08841

M08842

M08849

M08851

M08852

M08859

M08861

M08862

M08871

M08872

M0888

M0889

M08911

M08912

M08919

M08921

M08922

M08929

M08931

M08932

M08939

M08941

M08942

M08949

M08951

M08952

M08959

M08961

M08962

M08969

M08971

M08972

M0898

M13871

M13872

M13879

M450

M451

M452

M453

M454

M455

M456

M457

M458

M459

M45A0

M45A1

M45A2

M45A3

M45A4

M45A5

M45A6

M45A7

M45A8

M45AB

M48061

M48062

M488X1

M488X2

M488X3

M488X4

M488X5

M488X6

M488X7

M488X8

M488X9

31.2.26.7Ado-Trastuzumab Emtansine

Ado-trastuzumab emtansine (procedure code J9354) is a benefit of the CSHCN Services Program with the following diagnosis limitations:

Diagnosis Codes

C50011

C50012

C50019

C50021

C50022

C50029

C50111

C50112

C50119

C50121

C50122

C50129

C50211

C50212

C50219

C50221

C50222

C50229

C50311

C50312

C50319

C50321

C50322

C50329

C50411

C50412

C50419

C50421

C50422

C50429

C50511

C50512

C50519

C50521

C50522

C50529

C50611

C50612

C50619

C50621

C50622

C50629

C50811

C50812

C50819

C50821

C50822

C50829

C50911

C50912

C50919

C50921

C50922

C50929

Documentation must support the administration of Ado-trastuzumab emtansine and include all of the following:

Evidence of HER2 positive breast cancer as evidenced by an immunochemistry (IHC) test or fluorescent in situ hybridization (FISH) test

Evidence of metastatic breast cancer

Evidence of prior treatment for HER2 positive metastatic breast cancer with trastuzumab and a taxane oncology agent given separately or in combination

Evidence demonstrating receipt of prior therapy for HER2 positive metastatic breast cancer or recurrent disease, including previous treatment protocol, within six months of completing adjuvant therapy.

All documentation must be maintained in the client’s medical record and is subject to retrospective review.

31.2.26.8Bevacizumab

Bevacizumab (procedure code J9035) is a benefit of the CSHCN Services Program with the following diagnosis limitations:

Diagnosis Codes

C180

C181

C182

C183

C184

C185

C186

C187

C188

C189

C19

C20

C210

C211

C218

C3400

C3401

C3402

C3410

C3411

C3412

C342

C3430

C3431

C3432

C3480

C3481

C3482

C3490

C3491

C3492

C538

C539

C563

C641

C642

C649

C711

C712

C713

C714

C715

C716

C717

C718

C719

C7800

C7801

C7802

C7931

C7963

Z85038

Z85048

Z85118

Z853

31.2.26.9Botulinum Toxin (Type A and Type B)

The CSHCN Services Program may reimburse botulinum toxin, types A and B, for clients with specific diagnoses. Botulinum toxin, type A procedure code J0585 is payable when billed with the following diagnosis codes:

 

Diagnosis Codes

G114

G2401

G2402

G241

G243

G244

G245

G248

G250

G251

G252

G253

G35

G360

G370

G371

G372

G373

G374

G375

G3781

G3789

G379

G43701

G43709

G43711

G43719

G5131

G5132

G5133

G5139

G800

G801

G802

G803

G804

G808

G809

G8110

G8111

G8112

G8113

G8114

G8191

G8192

G8193

G8194

G8220

G8221

G8222

G8250

G8251

G8252

G8253

G8254

G830

G8310

G8311

G8312

G8313

G8314

G8320

G8321

G8322

G8323

G8324

G8330

G8331

G8332

G8333

G8334

G834

G8921

H4901

H4902

H4903

H4911

H4912

H4913

H4921

H4922

H4923

H4931

H4932

H4933

H4941

H4942

H4943

H499

H5000

H50011

H50012

H50021

H50022

H50031

H50032

H50041

H50042

H5005

H5006

H5007

H5008

H5010

H50111

H50112

H50121

H50122

H50131

H50132

H50141

H50142

H5015

H5016

H5017

H5018

H5021

H5022

H5030

H50311

H50312

H5032

H50331

H50332

H5034

H5040

H50411

H50412

H5042

H5043

H5050

H5051

H5052

H5053

H5054

H5055

H5060

H50611

H50612

H50621

H50622

H50629

H50631

H50632

H50639

H50641

H50642

H50649

H50651

H50652

H50659

H50661

H50662

H50669

H50671

H50672

H50679

H50681

H50682

H50689

H5069

H50811

H50812

H5089

H510

H5111

H5112

H5121

H5122

H5123

H518

H519

I69031

I69032

I69033

I69034

I69041

I69042

I69043

I69044

I69051

I69052

I69053

I69054

I69061

I69062

I69063

I69064

I69065

I69098

I69131

I69132

I69133

I69134

I69141

I69142

I69143

I69144

I69151

I69152

I69153

I69154

I69161

I69162

I69163

I69164

I69165

I69198

I69231

I69232

I69233

I69234

I69241

I69242

I69243

I69244

I69251

I69252

I69253

I69254

I69261

I69262

I69263

I69264

I69265

I69298

I69331

I69332

I69333

I69334

I69341

I69342

I69343

I69344

I69351

I69352

I69353

I69354

I69361

I69362

I69363

I69364

I69365

I69398

I69831

I69832

I69833

I69834

I69841

I69842

I69843

I69844

I69851

I69852

I69853

I69854

I69861

I69862

I69863

I69864

I69865

I69898

J385

K117

K220

K594

K600

K601

K602

M436

M62838

M722

N310

N311

N312

N318

N319

N3281

N3644

R490

R498

R532

Procedure code J0586 is payable when billed with the following diagnosis codes:

Diagnosis Codes

G114

G2401

G2402

G241

G243

G244

G245

G248

G35

G360

G370

G371

G372

G373

G374

G375

G3781

G3789

G379

G800

G801

G802

G803

G804

G808

G809

G8110

G8111

G8112

G8113

G8114

G8191

G8192

G8193

G8194

G8253

G8254

G830

G8320

G8321

G8322

G8323

G8324

I69031

I69032

I69033

I69034

I69039

I69051

I69052

I69053

I69054

I69059

I69131

I69132

I69133

I69134

I69139

I69151

I69152

I69153

I69154

I69231

I69232

I69233

I69234

I69239

I69251

I69252

I69253

I69254

I69259

I69331

I69332

I69333

I69334

I69339

I69351

I69352

I69353

I69354

I69359

I69831

I69832

I69833

I69834

I69839

I69851

I69852

I69853

I69854

I69859

I69931

I69932

I69933

I69934

I69939

I69951

I69952

I69953

I69954

I69959

J385

M436

M62838

M722

R532


The chemodenervation procedure codes in the following table are a benefit in addition to botulinum toxin type A:

Procedure Codes

64600

64605

64610

64611

64612

64615

64616

64617

64620

64624

64625

64630

64632

64633

64634

64635

64636

64640

64642

64643

64644

64645

64646

64647

64680

64681

67345


Procedure code 64612 requires prior authorization. All other chemodenervation and nerve destruction by neurolytic agent procedure codes do not require prior authorization. Add-on procedure codes 95873 and 95874 will be reimbursed only when billed with the appropriate primary procedure code on the same day, by the same provider.

Procedure code J0588 is a benefit and is limited to the following diagnosis codes:

Diagnosis Codes

G243

G245

G800

G801

G802

G8110

G8111

G8112

G8113

G8114

G8253

G8254

G830

G8320

G8321

G8322

G8323

G8324

I69031

I69032

I69033

I69034

I69039

I69051

I69052

I69053

I69054

I69059

I69131

I69132

I69133

I69134

I69139

I69151

I69152

I69153

I69154

I69231

I69232

I69233

I69234

I69239

I69251

I69252

I69253

I69254

I69259

I69331

I69332

I69333

I69334

I69339

I69351

I69352

I69353

I69354

I69359

I69831

I69832

I69833

I69834

I69839

I69851

I69852

I69853

I69854

I69859

I69931

I69932

I69933

I69934

I69939

I69951

I69952

I69953

I69954

I69959

Procedure code J0587 must be submitted for reimbursement of the type B botulinum toxin (per 100 units) and is limited to the following diagnosis codes:

Diagnosis Codes

G243

G8921

K117

Procedure code J0587 is limited to a billed quantity of 100 units. Any claim billed in excess of 100 billing units will be denied.

The CSHCN Services Program requires a trial of type A botulinum toxin prior to the use of type B botulinum toxin.

Injections of either toxin are limited to no more than once every three months. Supplies used to administer the toxins will not be reimbursed separately.

Medications other than botulinum toxins may be used for chemodenervation procedures.

Claims for Botulinum Toxin Type A and B must indicate the number of units used. Providers should bill the amount of injections per units used for Botulinum Toxin. If the units are not specified, the claim may be reimbursed as a quantity of one.

 

Procedure Codes

Quantity Limitations of Medication

Billing Units

J0585

400 units

One billing unit is equal to 1 unit of medication.

Example:A provider that administers 400 units of medication would submit a claim for a quantity of 400.

J0586

1,500 units

One billing unit is equal to 5 units of medication.

Example:A provider that administers 1,500 units of medication would submit a claim for a quantity of 300.

J0587

10,000 units

One billing unit is equal to 100 units of medication.

Example:A provider that administers 10,000 units of medication would submit a claim for a quantity of 100.

J0588

400 units

One billing unit is equal to 1 unit of medication.

Example:A provider that administers 400 units of medication would submit a claim for a quantity of 400.

Procedure codes J0586, J0587, and J0588 will be denied when billed on the same date of service, by any provider with procedure code J0585.

Procedure codes J0587 and J0588 will be denied when billed on the same date of service, by any provider with procedure code J0586.

Procedure code J0587 will be denied when billed on the same date of service, by any provider with procedure code J0588.

Providers may not bill for an office visit if botulinum injections are the only reason for the visit.

31.2.26.9.1Prior Authorization Requirements

Prior authorization is required for quantities of medication greater than the defined limitations for botulinum toxins. Documentation of medical need for exceeding the limit must be submitted with the request for prior authorization.

Prior authorization and medical review is required for diagnoses other than those listed above. Documentation for consideration of other diagnoses must include the diagnosis, clinical course, clinical history, and other treatments with an explanation of ineffective results. This documentation to support medical necessity must be submitted to the TMHP-CSHCN Services Program Authorization Department with the CSHCN Services Program Authorization and Prior Authorization Request Form. Prior authorization requests may be approved for a 12-month period. All extension requests must include diagnosis, clinical course, and result of previous botulinum toxin therapy and expected length of treatment.

Refer to: Chapter 4, “Prior Authorizations and Authorizations” for more information about authorization and prior authorization requirements.

Procedures incidental to the administration of botulinum toxin, such as EMGs, do not require authorization and may be reimbursed in the quantity billed.

APRNs and physician assistants administering botulinum toxin therapy must be supervised by a physician who is board eligible or board certified in the physician’s specialty. Documentation of the APRN’s and physician assistant’s training must be kept in the supervising physician’s records and be available for review on request by the CSHCN Services Program or its designee.

31.2.26.9.2Reimbursement

Botulinum toxin may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.26.10Epirubicin Hydrochloride

Epirubicin hydrochloride (procedure code J9178) is a benefit of the CSHCN Services Program with the following diagnosis limitations:

Diagnosis Codes

C50011

C50012

C50019

C50021

C50022

C50029

C50111

C50112

C50119

C50121

C50122

C50129

C50211

C50212

C50219

C50221

C50222

C50229

C50311

C50312

C50319

C50321

C50322

C50329

C50411

C50412

C50419

C50421

C50422

C50429

C50511

C50512

C50519

C50521

C50522

C50529

C50611

C50612

C50619

C50621

C50622

C50629

C50811

C50812

C50819

C50821

C50822

C50829

C50911

C50912

C50919

C50921

C50922

C50929

C847A

31.2.26.11Erythropoietin Alfa (EPO) and Darbepoetin

EPO and darbepoietin (procedure codes J0881 and J0885) are benefits of the CSHCN Services Program for the following diagnosis codes:

Diagnosis Codes

B20

C880

C9000

C9001

C9002

D500

D501

D508

D509

D510

D511

D512

D513

D518

D519

D520

D521

D528

D529

D530

D531

D532

D538

D539

D550

D551

D553

D558

D560

D561

D562

D563

D564

D565

D568

D569

D5701

D5702

D571

D5720

D57211

D57212

D573

D5740

D57411

D57412

D5780

D57811

D57812

D580

D581

D582

D588

D590

D592

D594

D595

D596

D598

D600

D601

D608

D6101

D6109

D611

D612

D613

D61810

D61811

D61818

D6182

D6189

D619

D62

D630

D631

D638

D640

D641

D642

D643

D644

D6481

D6489

D649

D7801

D7802

D7821

D7822

E3601

E3602

G9731

G9732

G9751

G9752

H59111

H59112

H59113

H59119

H59121

H59122

H59123

H59129

H59311

H59312

H59313

H59319

H59321

H59322

H59323

H59329

H9521

H9522

H9541

H9542

I120

I129

I130

I1310

I1311

I132

I97410

I97411

I97418

I9742

I97610

I97611

I97618

I9762

J9561

J9562

J95830

J95831

K9161

K9162

K91840

K91841

L7601

L7602

L7621

L7622

M0540

M05411

M05412

M05419

M05421

M05422

M05429

M05431

M05432

M05439

M05441

M05442

M05449

M05451

M05452

M05459

M05461

M05462

M05469

M05471

M05472

M05479

M0549

M0550

M05511

M05512

M05519

M05521

M05522

M05529

M05531

M05532

M05539

M05541

M05542

M05549

M05551

M05552

M05559

M05561

M05562

M05569

M05571

M05572

M05579

M0559

M0570

M05711

M05712

M05719

M05721

M05722

M05729

M05731

M05732

M05739

M05741

M05742

M05749

M05751

M05752

M05759

M05761

M05762

M05769

M05771

M05772

M05779

M0579

M0580

M05811

M05812

M05819

M05821

M05822

M05829

M05831

M05832

M05839

M05841

M05842

M05849

M05851

M05852

M05859

M05861

M05862

M05869

M05871

M05872

M05879

M0589

M059

M0600

M06011

M06012

M06019

M06021

M06022

M06029

M06031

M06032

M06039

M06041

M06042

M06049

M06051

M06052

M06059

M06061

M06062

M06069

M06071

M06072

M06079

M0608

M0609

M0620

M06211

M06212

M06219

M06221

M06222

M06229

M06231

M06232

M06239

M06241

M06242

M06249

M06251

M06252

M06259

M06261

M06262

M06269

M06271

M06272

M06279

M0628

M0629

M0630

M06311

M06312

M06319

M06321

M06322

M06329

M06331

M06332

M06339

M06341

M06342

M06349

M06351

M06352

M06359

M06361

M06362

M06369

M06371

M06372

M06379

M0638

M0639

M0680

M06811

M06812

M06819

M06821

M06822

M06829

M06831

M06832

M06839

M06841

M06842

M06849

M06851

M06852

M06859

M06861

M06862

M06869

M06871

M06872

M06879

M0688

M0689

M069

M96810

M96811

M96830

M96831

N19

N2589

N9961

N9962

N99820

N99821

Z48298

Z5111

Z5112

Z7682

In addition to the diagnosis codes listed above, procedure code J0885 may also be considered for reimbursement with the following diagnosis codes:

Diagnosis Codes

N181

N182

N184

N185

N186

N189


Procedure code J0882 is a benefit of the CSHCN Services Program for the following diagnosis codes:

Diagnosis Codes

B20

C880

C9000

C9001

C9002

D500

D501

D508

D509

D510

D511

D512

D513

D518

D519

D520

D521

D528

D529

D530

D531

D532

D538

D539

D550

D551

D553

D558

D560

D561

D562

D563

D564

D565

D568

D569

D5701

D5702

D571

D5720

D57211

D57212

D573

D5740

D57411

D57412

D5780

D57811

D57812

D580

D581

D582

D588

D590

D592

D594

D595

D596

D598

D600

D601

D608

D6101

D6109

D611

D612

D613

D61810

D61811

D61818

D6182

D6189

D619

D62

D630

D631

D638

D640

D641

D642

D643

D644

D6481

D6489

D649

D7801

D7802

D7821

D7822

E3601

E3602

G9731

G9732

G9751

G9752

H59111

H59112

H59113

H59119

H59121

H59122

H59123

H59129

H59311

H59312

H59313

H59319

H59321

H59322

H59323

H59329

H9521

H9522

H9541

H9542

I120

I129

I130

I1310

I1311

I132

I97410

I97411

I97418

I9742

I97610

I97611

I97618

I9762

J9561

J9562

J95830

J95831

K9161

K9162

K91840

K91841

L7601

L7602

L7621

L7622

M0540

M05411

M05412

M05419

M05421

M05422

M05429

M05431

M05432

M05439

M05441

M05442

M05449

M05451

M05452

M05459

M05461

M05462

M05469

M05471

M05472

M05479

M0549

M0550

M05511

M05512

M05519

M05521

M05522

M05529

M05531

M05532

M05539

M05541

M05542

M05549

M05551

M05552

M05559

M05561

M05562

M05569

M05571

M05572

M05579

M0559

M0570

M05711

M05712

M05719

M05721

M05722

M05729

M05731

M05732

M05739

M05741

M05742

M05749

M05751

M05752

M05759

M05761

M05762

M05769

M05771

M05772

M05779

M0579

M0580

M05811

M05812

M05819

M05821

M05822

M05829

M05831

M05832

M05839

M05841

M05842

M05849

M05851

M05852

M05859

M05861

M05862

M05869

M05871

M05872

M05879

M0589

M059

M0600

M06011

M06012

M06019

M06021

M06022

M06029

M06031

M06032

M06039

M06041

M06042

M06049

M06051

M06052

M06059

M06061

M06062

M06069

M06071

M06072

M06079

M0608

M0609

M0620

M06211

M06212

M06219

M06221

M06222

M06229

M06231

M06232

M06239

M06241

M06242

M06249

M06251

M06252

M06259

M06261

M06262

M06269

M06271

M06272

M06279

M0628

M0629

M0630

M06311

M06312

M06319

M06321

M06322

M06329

M06331

M06332

M06339

M06341

M06342

M06349

M06351

M06352

M06359

M06361

M06362

M06369

M06371

M06372

M06379

M0638

M0639

M0680

M06811

M06812

M06819

M06821

M06822

M06829

M06831

M06832

M06839

M06841

M06842

M06849

M06851

M06852

M06859

M06861

M06862

M06869

M06871

M06872

M06879

M0688

M0689

M069

M96810

M96811

M96830

M96831

N19

N2589

N9961

N9962

N99820

N99821

Z48298

Z5111

Z5112

Z7682

EPO is limited to three injections per calendar week (Sunday through Saturday). Procedure code J0885 must be submitted with an 11-digit NDC.

31.2.26.12Growth Hormone

The Vendor Drug Program (VDP) reimburses growth hormone (hGH) injections for CSHCN Services Program clients for any of the following conditions:

Chronic kidney disease

Pituitary gland insufficiency

Prader-Willi syndrome

Turner syndrome

Noonan syndrome

SHOX deficiency

Other specified disorders resulting from impaired renal function

Pharmacies must submit claims to the VDP. Pharmacies are reimbursed the same drug costs and dispensing fees allowed by the Texas Medicaid VDP.

Providers may refer to Form 1327 - Children with Special Health Care Needs (CSHCN) Services Program Biosynthetic Growth Hormone Agents Prior Authorization Request.

31.2.26.12.1Prior Authorization Requirements

Requests for prior approval of the medical criteria for growth hormone therapy must be submitted on the CSHCN Biosynthetic Growth Hormone Agents Prior Authorization Request (Form 1327) by a program-approved endocrinologist. In addition to the conditions listed in the section above, the following criteria must also be met for an initial request:

Normal thyroid function or may be corrected with medication

Normal pituitary function studies or may be corrected with medication

Documentation of open epiphyses (done in last 12 months)

Evidence of deficient growth hormone (GH) production on two pharmacological provocative tests (GH peak less than 10 ng/ml)

Physical stature less than the 3rd percentile

Growth velocity 4cm or less per year

Below normal somatomedin C level or insulin-like growth factor binding protein 3 (IGF/BP3)

Nutropin® is the only product approved for the treatment of chronic renal failure, and Genotropin® is the only product approved for the treatment of Prader-Willi syndrome.

Clients with Turner’s syndrome or Prader-Willi syndrome, Noonan Syndrome, or SHOX deficiency may be approved without evidence of deficient growth hormone production on provocative testing if other criteria are met.

Clients with a diagnosis of panhypopituitarism whose epiphyses have closed will be considered for approval with documentation of deficient growth hormone levels.

Initial approval is for a 6-month period. Requests for extensions may be granted for an additional 12 months at a time. Approval for continued growth hormone therapy may be granted if the following criteria are met:

Growth chart documents growth equal to a minimum of 4cm per year and documents a significant increase from pretreatment levels

Epiphyses must be open

Bone age must be documented annually after a boy has reached a chronological age of 16 years and a girl has reached a chronological age of 14 years.

If an initial or extension request cannot be approved based on the above criteria, the approval request may be sent for medical review and reconsideration to the CSHCN Services Program.

Refer to: Section 3.1.1, “Prescription Drug Benefits” in Chapter 3, “Client Benefits and Eligibility” for more information about the VDP.

31.2.26.13Immune Globulins

Immune globulins may be indicated for treatment of certain immune disorders and states of immunodeficiency.

Immune and gamma globulins and the administration of immune and gamma globulins are benefits of the CSHCN Services Program.

Providers are responsible for administering immune globulins based on the Food and Drug Administration (FDA)-approved guidelines. In the absence of FDA indications, a drug must meet the following criteria for consideration of coverage:

The drug is recognized by the American Hospital Formulary Service Drug Information, the U.S. Pharmacopoeia Dispensing Information, Vol. I., or two articles from major peer-reviewed journals that have validated data supporting the proposed use for the specific medical condition is safe and effective.

It is medically necessary to treat the specific medical condition, including life-threatening conditions or chronic debilitating conditions.

The drug is not experimental or investigational.

The following procedure codes may be used to submit claims for immune and gamma globulin injections:

Procedure Codes

90281

90283

90284

90291

90371

90389

90396

90399

J0850

J1459

J1460

J1551

J1555

J1556

J1557

J1559

J1561

J1566

J1568

J1569

J1571

J1572

J1573

J1575

J1576

J1670

J2788

J2791

J2792

The following conditions apply when billing immune globulin procedure codes:

If procedure codes 90389 and J1670 are billed with the same date of service by any provider, only one is considered for reimbursement.

If procedure codes J1571 and 90371 are billed with the same date of service by any provider, only one may be reimbursed.

Administration procedure codes 96369, 96370, 96372, and 96374 may be billed with the immune globulins listed in this section.

Procedure code 96370 is an add-on code and must be billed with the appropriate primary procedure code on the same date of service, by the same provider, or the service will be denied.

Reimbursement for the following procedure codes will be based on the lowest AWP, minus 10.5 percent, according to the prices in the current edition of the Red Book, published by Thomson Healthcare, on file with the CSHCN Services Program.

 

Procedure Codes

90281

90283

90291

90371

90389

90396

All other procedure codes for immune and gamma globulins may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

Retrospective review may be performed to ensure that the documentation supports the medical necessity of the service submitted on the claim.

31.2.26.13.1Authorization Requirements

Unlisted procedure code 90399 may be considered for reimbursement with prior authorization. Requests for prior authorization must be submitted using the CSHCN Services Program Authorization and Prior Authorization Request Form. The requesting provider must submit the following documentation with the authorization request:

The client’s diagnosis

Medical records that indicate any prior treatments for this diagnosis

A clear, concise description of the medical necessity of the immune globulin and the rationale for the recommendation of this particular immune globulin

A procedure code that is comparable to the immune globulin being requested

Documentation that this immune globulin is not investigational or experimental

The place of service at which the immune globulin is to be administered

The provider’s intended fee for this immune globulin

31.2.26.14Infliximab, Inflectra, Renflexis, and Zymfentra

Infliximab (procedure code J1745), inflectra (procedure code Q5103), and renflexis (procedure code Q5104) are benefits of the CSHCN Services Program with the following diagnosis limitations:

Dia

Diagnosis Codes

H2013

K5000

K50011

K50012

K50013

K50014

K50018

K50019

K5010

K50111

K50112

K50113

K50114

K50118

K50119

K5080

K50811

K50812

K50813

K50814

K50818

K50819

K5090

K50911

K50912

K50913

K50914

K50918

K50919

K5100

K51011

K51012

K51013

K51014

K51018

K51019

K5120

K51211

K51212

K51213

K51214

K51218

K51219

K5130

K51311

K51312

K51313

K51314

K51318

K51319

K5140

K51411

K51412

K51413

K51414

K51418

K51419

K5150

K51511

K51512

K51513

K51514

K51518

K51519

K5180

K51811

K51812

K51813

K51814

K51818

K51819

K5190

K51911

K51912

K51913

K51914

K51918

K51919

K603

K632

L400

L401

L402

L403

L4050

L4051

L4052

L4053

L4054

L4059

L408

L409

M0500

M05011

M05012

M05019

M05021

M05022

M05029

M05031

M05032

M05039

M05041

M05042

M05049

M05051

M05052

M05059

M05061

M05062

M05069

M05071

M05072

M05079

M0509

M0510

M05111

M05112

M05119

M05121

M05122

M05129

M05131

M05132

M05139

M05141

M05142

M05149

M05151

M05152

M05159

M05161

M05162

M05169

M05171

M05172

M05179

M0519

M0520

M05211

M05212

M05219

M05221

M05222

M05229

M05231

M05232

M05239

M05241

M05242

M05249

M05251

M05252

M05259

M05261

M05262

M05269

M05271

M05272

M05279

M0529

M0530

M05311

M05312

M05319

M05321

M05322

M05329

M05331

M05332

M05339

M05341

M05342

M05349

M05351

M05352

M05359

M05361

M05362

M05369

M05371

M05372

M05379

M0539

M0540

M05411

M05412

M05419

M05421

M05422

M05429

M05431

M05432

M05439

M05441

M05442

M05449

M05451

M05452

M05459

M05461

M05462

M05469

M05471

M05472

M05479

M0549

M0550

M05511

M05512

M05519

M05521

M05522

M05529

M05531

M05532

M05539

M05541

M05542

M05549

M05551

M05552

M05559

M05561

M05562

M05569

M05571

M05572

M05579

M0559

M0560

M05611

M05612

M05619

M05621

M05622

M05629

M05631

M05632

M05639

M05641

M05642

M05649

M05651

M05652

M05659

M05661

M05662

M05669

M05671

M05672

M05679

M0569

M0570

M05711

M05712

M05719

M05721

M05722

M05729

M05731

M05732

M05739

M05741

M05742

M05749

M05751

M05752

M05759

M05761

M05762

M05769

M05771

M05772

M05779

M0579

M0580

M05811

M05812

M05819

M05821

M05822

M05829

M05831

M05832

M05839

M05841

M05842

M05849

M05851

M05852

M05859

M05861

M05862

M05869

M05871

M05872

M05879

M0589

M059

M060A

M068A

M069

M08011

M08012

M08021

M08022

M08031

M08032

M08041

M08042

M08051

M08052

M08061

M08062

M08071

M08072

M0809

M08832

M08841

M08842

M08851

M08852

M08861

M08931

M08932

M08941

M08942

M08951

M08952

M08961

M08962

M1389

M450

M451

M452

M453

M454

M455

M456

M457

M458

M459

M45A0

M45A1

M45A2

M45A3

M45A4

M45A5

M45A6

M45A7

M45A8

M45AB

Procedure codes J1745, Q5103, and Q5104 will not be reimbursed for the same date of service by any provider.

Procedure code J1748 is a benefit for clients who are 18 years of age or older with the following diagnosis limitations:

Diagnosis Codes

K5000

K50011

K50012

K50013

K50014

K50018

K50019

K5010

K50111

K50112

K50113

K50114

K50118

K5080

K50811

K50812

K50813

K50814

K50818

K50819

K5090

K50911

K50912

K50913

K50914

K50918

K5100

K51011

K51012

K51013

K51014

K51018

K51019

K5120

K51211

K51212

K51213

K51214

K51218

K5130

K51311

K51312

K51313

K51314

K51318

K5180

K51811

K51812

K51813

K51814

K51818

K5190

K51911

K51912

K51913

K51914

K51918

K51919

31.2.26.15Inotuzumab ozogamicin (Besponsa)

Inotuzumab ozogamicin (Besponsa) (procedure code J9229) is a benefit of the CSHCN Services Program for pediatric and adult clients who are 1 year of age or older.

Inotuzumab ozogamicin is indicated for the treatment of relapsed or refractory precursor B-cell acute lymphoblastic leukemia (ALL) and must be prescribed by an oncologist or in consultation with an oncologist.

Procedure code J9229 requires prior authorization and may be approved when all of the following criteria is met:

The client has a confirmed diagnosis of precursor B-cell ALL.

The client must have relapsed or refractory disease.

The client is 1 year of age or older.

The provider must agree to monitor the client for signs and symptoms of hepatic veno-occlusive disease (VOD) during the duration of Besponsa therapy.

Requests for prior authorization of procedure code J9229 must be submitted using the CSHCN Services Program Authorization and Prior Authorization Request form.

31.2.26.16Leuprolide Acetate Injection

Procedure code J1950 is limited to reimbursement once every 28 days. Procedure code J9217 is allowed for use in monthly, 3-month, 4-month, and 6-month doses. Providers must bill the following dosage increments:

Dose Period

Dose Quantity

Quantity Billed

Limitation

Monthly

7.5 mg

1

Once per 28 days

3-month

22.5 mg

3

Once every 84 days

4-month

30 mg

4

Once every 112 days

6-month

45 mg

6

Once every 168 days

31.2.26.17Monoclonal Antibodies - Asthma and Chronic Idiopathic Urticaria

31.2.26.17.1Omalizumab

Omalizumab (procedure code J2357) is a benefit of the CSHCN Services Program when medically necessary and must be prior authorized.

Omalizumab is FDA approved for the treatment of clients who are 6 years of age and older with moderate to severe asthma. Omalizumab is also approved for the treatment of clients who are 12 years of age and older with chronic idiopathic urticaria, who remain symptomatic despite H1 antihistamine treatment. Clients who are younger than the FDA-approved age will be considered on a case-by-case basis by the CSHCN Services Program Medical Director or designee.

31.2.26.17.2 Benralizumab

Benralizumab (procedure code J0517) is a benefit of the CSHCN Services Program with prior authorization.

Benralizumab is an injectable drug that is FDA-approved and indicated for the treatment of clients who are 12 years of age and older that have severe asthma with an eosinophilic phenotype. Clients who are younger than the FDA-approved age will be considered on a case-by-case basis by the CSHCN Services Program medical director or designee.

31.2.26.17.3Mepolizumab

Mepolizumab (procedure code J2182) is a benefit of the CSHCN Services Program when prior authorized.

Mepolizumab is an injectable drug that is approved by the U.S. Food and Drug Administration (FDA) for the treatment of clients who are 12 years of age and older and have severe asthma with an eosinophilic phenotype. Clients who are younger than the FDA-approved age will be considered on a case-by-case basis by the CSHCN Services Program medical director or designee.

Providers may not bill for an office visit if the only reason for the visit is an omalizumab, benralizumab, mepolizumab, or reslizumab injection.

31.2.26.17.4Reslizumab

Reslizumab (procedure code J2786) is a benefit of the CSHCN Services Program when prior authorized.

Reslizumab is an injectable drug that is FDA-approved and indicated for the treatment of clients who are 18 years of age and older and have severe asthma with an eosinophilic phenotype. Clients who are younger than the FDA-approved age will be considered on a case-by-case basis by the CSHCN Services Program medical director or designee.

Procedure codes J0517, J2182, J2786, and J2357 may not be billed in any combination for the same date of services by any provider.

31.2.26.17.5Prior Authorization Requirements

Omalizumab (procedure code J2357), benralizumab (procedure code J0517), mepolizumab (procedure code J2182), or reslizumab (procedure code J2786) must be used to request prior authorization and the exact dosage must be indicated on the CSHCN Services Program Authorization and Prior Authorization Request Form.

Prior authorization of omalizumab may be approved for clients who are 6 years of age or older with moderate to severe asthma (as defined by the National Heart, Lung, and Blood Institute’s Guidelines for the Diagnosis and Management of Asthma).

Prior authorization of benralizumab and mepolizumab may be approved for clients who are 12 years of age or older that have severe asthma with an eosinophilic phenotype (as defined by the National Heart, Lung, and Blood Institute’s Guidelines for the Diagnosis and Management of Asthma).

Prior authorization of reslizumab may be approved for clients who are 18 years of age or older with severe asthma (as defined by the National Heart, Lung, and Blood Institute’s Guidelines for the Diagnosis and Management of Asthma).

Prior authorizations for omalizumab, benralizumab, mepolizumab, or reslizumab are for intervals of six months at a time. Clients must be compliant with their omalizumab, benralizumab, mepolizumab, or reslizumab regimen in order to qualify for additional authorizations. The provider must submit a statement documenting compliance with the requests for each renewal.

Benralizumab, mepolizumab or reslizumab may only be initiated after a six-month trial of omalizumab therapy that has resulted in inadequate response. Criteria is detailed below in the benralizumab, mepolizumab, and reslizumab sections.

Treatment of benralizumab, mepolizumab or reslizumab may not be used concurrently with omalizumab or any other interleukin-5 antagonist.

31.2.26.17.6Chronic Idiopathic Urticaria

Prior authorization for omalizumab will be considered for clients who are 12 years of age or older with chronic idiopathic urticaria (CIU).

Documentation supporting medical necessity for treatment of CIU with omalizumab must be submitted with the request and include all of the following:

Documented failure of, or contraindication to, antihistamine and leukotriene inhibitor therapies.

Evidence of an evaluation that excludes other medical diagnoses associated with chronic urticaria.

31.2.26.17.7Asthma Moderate to Severe (Omalizumab) and Severe (Benralizumab, Mepolizumab, and Reslizumab)

Documentation supporting medical necessity for treatment of asthma with omalizumab, benralizumab, mepolizumab, or reslizumab must be submitted with the request and must indicate the following:

Symptoms are inadequately controlled with use of one of the following combination therapies:

12 months of high-dose inhaled corticosteroid (ICS) given in combination with a minimum of 3 months of controller medication (either a long-acting beta2-agonist [LABA], leukotriene receptor antagonist [LTRA], or theophylline), unless the individual is intolerant of, or has a medical contraindication to these agents

6 months of ICS with daily oral glucocorticoids given in combination with a minimum of 3 months of controller medication (a LABA, LTRA, or theophylline), unless the individual is intolerant of, or has a medical contraindication to these agents

Note:Exceptions to the criteria above will be considered on a case-by-case basis, which will require a letter from the prescribing provider stating the medical necessity for omalizumab, benralizumab, mepolizumab, or reslizumab, the client’s asthma severity level, and the duration of current and past therapies and lack of asthma control. Consideration for these exceptions will be reviewed by the CSHCN Services Program Medical Director or designee.

Pulmonary function tests must have been performed within a three-month period and be documented for all clients.

Note:Exceptions may be considered with documentation of medical reasons explaining why pulmonary function tests cannot be performed.

Client is not currently smoking.

When requesting prior authorization, the exact dosage must be included with the request.

31.2.26.17.8Omalizumab

Additional documentation of the following must also be submitted for treatment with omalizumab:

A positive skin test or RAST to a perennial (not seasonal) aeroallergen within the past 36 months

Total IgE level greater than 30 IU/ml but less than 1300 IU/ml within the past 12 months

31.2.26.17.9Benralizumab

The following additional documentation for treatment with benralizumab must be submitted with the initial prior authorization request:

Documented diagnosis of severe eosinophilic asthma

Blood eosinophil count greater than or equal to 150 cells/microliter before the initiation of therapy, in the absence of other potential causes of eosinophilia, including hypereosinophilic syndromes, neoplastic disease, and known or suspected parasitic infection

Note:1microliter (ul) is equal to 1 cubic millimeter (mm3).

Prior authorization for an initial request for benralizumab will be considered when the client meets the criteria for benralizumab and has had an inadequate response after being compliant with 6 months of omalizumab treatment. Failure to respond to omalizumab must be documented in a letter that is signed and dated by the prescribing provider and submitted with the prior authorization request.

Note:Exceptions may be considered for clients who meet the requirements for treatment with benralizumab but who do not meet the criteria for omalizumab. Supporting documentation (IgE level falls outside of required range, negative skin test, or RAST to a perennial aeroallergen) must be submitted along with the other required documentation for treatment with benralizumab.

31.2.26.17.10Mepolizumab

Additional documentation of the following must also be submitted for treatment with mepolizumab:

One of the following blood eosinophil counts in the absence of other potential causes of eosinophilia, including hypereosinophilic syndromes, neoplastic disease, and known or suspected parasitic infection:

Greater than or equal to 150 cells/microliter at initiation of therapy

Greater than or equal to 300 cells/microliter within 12 months prior to initiation of therapy

Note:1 microliter (ul) is equal to 1 cubic millimeter (mm3)

Prior authorization for an initial request for mepolizumab will be considered when the client has had an inadequate response after being compliant for 6 months of treatment with omalizumab. Failure to respond to omalizumab must be documented in a letter, signed and dated by the prescribing provider and submitted with the request.

Note:Exceptions may be considered for clients who meet the criteria for treatment with mepolizumab but do not meet the criteria for omalizumab. Supporting documentation, such as an IgE level fall outside of the required range or a negative skin test/RAST to a perennial aeroallergen, must be submitted along with the documentation for treatment with mepolizumab, as described above.

31.2.26.17.11Reslizumab

Additional documentation of the following must also be submitted for treatment with reslizumab:

Has an eosinophilic phenotype as determined by blood eosinophils of 400 cells/microliter or higher to initiation of therapy (within 3-4 weeks of dosing).

Note:1 microliter (9ul) is equal to 1 cubic millimeter (mm3).

Prior authorization for an initial request for reslizumab will be considered when the client has had an inadequate response after being compliant for 6 months of treatment with omalizumab and meets the criteria for reslizumab. Failure to respond to omalizumab must be documented in a letter, signed and dated by the prescribing provider and submitted with the request.

Note:Exceptions may be considered for clients who meet the requirements for treatment with reslizumab, but who do not meet the criteria for omalizumab. Supporting documentation (IgE level falls outside of required range and/or negative skin test/RAST to a perennial aeroallergen) must be submitted along with the documentation for treatment with reslizumab as described above.

When requesting prior authorization, the exact dosage must be included with the request.

31.2.26.17.12Requirements for Continuation of Therapy

For continuation of therapy with omalizumab, benralizumab, mepolizumab, or reslizumab after 6 continuous months, the requesting provider must submit the following documentation of the client’s compliance and satisfactory clinical response to omalizumab, benralizumab, mepolizumab, or reslizumab:

Documentation of clinical improvement must include one or more of the following:

Decreased utilization of rescue medications

Increase in predicted FEV1 (forced expiratory volume) from pretreatment baseline

Reduction in reported asthma-related symptoms, as evidenced by decreases in frequency or magnitude of one or more of the following symptoms:

Asthma attacks

Chest tightness or heaviness

Coughing or clearing throat

Difficulty taking deep breath or difficulty breathing out

Shortness of breath

Sleep disturbance, night wakening, or symptoms upon awakening

Tiredness

Wheezing/heavy breathing/fighting for air

Client has not exhibited symptoms of hypersensitivity or anaphylaxis (bronchospasm, hypotension, syncope, urticaria, and/or angioedema) after administration of omalizumab, benralizumab, mepolizumab, or reslizumab.

After lapses in treatment of 3 months or greater, prior authorization requests submitted with documentation will be reviewed by the CSHCN Services Program Medical Director or designee.

Requests for clients who do not meet the above criteria will be reviewed for medical necessity by the CSHCN Services Program Medical Director or designee.

31.2.26.18Secukinumab

Procedure code J3247 is a benefit for clients who are 18 years of age or older and limited to the following diagnosis codes:

Diagnosis Codes

L400

L401

L402

L403

L404

L4050

L4051

L4052

L4053

L4054

L4059

L408

L409

M0880

M450

M451

M452

M453

M454

M455

M456

M457

M458

M459

M4680

M4681

M4682

M4683

M4684

M4685

M4686

M4687

M4688

M4689

31.2.26.19Tocilizumab-aazg (Tyenne)

Tocilizumab-aazg (Tyenne) (procedure code Q5135) is a benefit of the CSHCN Services Program for clients who are 2 years of age or older and is limited to the following diagnosis codes:

Diagnosis Codes

M0500

M05011

M05012

M05019

M05021

M05022

M05029

M05031

M05032

M05039

M05041

M05042

M05049

M05050

M05052

M05059

M05061

M05062

M05069

M05071

M05072

M05079

M0509

M0510

M05111

M05112

M05119

M05121

M05122

M05129

M05131

M05132

M05139

M05141

M05142

M05149

M05151

M05152

M05159

M05161

M05162

M05169

M05171

M05172

M05179

M0519

M0520

M05211

M05212

M05219

M05221

M05222

M05229

M05231

M05232

M05239

M05241

M05242

M05249

M05251

M05252

M05259

M05261

M05262

M05269

M05271

M05272

M05279

M0259

M0530

M05311

M05312

M05319

M05321

M05322

M05329

M05331

M05332

M05339

M05341

M05342

M05349

M05351

M05352

M05359

M05361

M05362

M05369

M05371

M05372

M05379

M0539

M0540

M05411

M05412

M05419

M05421

M05422

M05429

M05431

M05432

M05439

M05441

M05442

M05449

M05451

M05452

M05459

M05461

M05462

M05469

M05471

M05472

M05479

M0549

M0550

M05511

M05512

M05519

M05521

M05522

M05529

M05531

M05532

M05539

M05541

M05542

M05549

M05551

M05552

M05559

M05561

M05562

M05569

M05571

M05572

M05579

M0559

M0560

M05611

M05612

M05619

M05621

M05622

M05629

M05631

M05632

M05639

M05641

M05642

M05649

M05651

M05652

M05659

M05661

M05662

M05669

M05671

M05672

M05679

M0569

M0570

M05711

M05712

M05719

M05721

M05722

M05729

M05731

M05732

M05739

M05741

M05742

M05749

M05751

M05752

M05759

M05761

M05762

M05769

M05771

M05772

M05779

M0579

M057A

M0580

M05811

M05812

M05819

M05821

M05822

M05829

M05831

M05832

M05839

M05841

M05842

M05849

M05851

M05852

M05859

M05861

M05862

M05869

M05871

M05872

M05879

M0589

M058A

M059

M0600

M06011

M06012

M06019

M06021

M06022

M06029

M06031

M06032

M06039

M06041

M06042

M06049

M06051

M06052

M06059

M06061

M06062

M06069

M06071

M06072

M06079

M0609

M060A

M0680

M06811

M06812

M06819

M06821

M06822

M06829

M06831

M06832

M06839

M06841

M06842

M06849

M06851

M06852

M06859

M06861

M06862

M06869

M06871

M06872

M06879

M0689

M068A

M069

M0820

M08211

M08212

M08219

M08221

M08222

M08229

M08231

M08232

M08239

M08241

M08242

M08249

M08251

M08252

M08259

M08261

M08262

M08269

M08271

M08272

M08279

M0829

M082A

M083

M315

M316

31.2.26.20Trastuzumab

Trastuzumab (procedure code J9355) is a benefit of the CSHCN Services Program as part of a treatment regimen containing doxorubicin, cyclophosphamide, and paclitaxel for the adjuvant treatment of clients with HER2 overexpressing, node positive breast cancer. Procedure code J9355 is payable when billed with the following diagnosis codes:

Diagnosis Codes

C50011

C50012

C50019

C50021

C50022

C50029

C50111

C50112

C50119

C50121

C50122

C50129

C50211

C50212

C50219

C50221

C50222

C50229

C50311

C50312

C50319

C50321

C50322

C50329

C50411

C50412

C50419

C50421

C50422

C50429

C50511

C50512

C50519

C50521

C50522

C50529

C50611

C50612

C50619

C50621

C50622

C50629

C50811

C50812

C50819

C50821

C50822

C50829

C50911

C50912

C50919

C50921

C50922

C50929

C563

C7963

C847A


31.2.26.21 Triamcinolone Acetonide

Triamcinolone acetonide (procedure code J3304) is a benefit of the CSHCN Services Program and is restricted to the following diagnosis codes:

Diagnosis Codes

M170

M1711

M1712

M172

M1731

M1732

M174

M175

M1909

M1919

M1929

Procedure code J3304 is limited to one per 12 weeks, any provider.

31.2.27Intracranial Pressure Monitoring

Intracranial pressure monitoring is a benefit of the CSHCN Services Program.

Authorization is not required for intracranial pressure monitoring and is not limited to specific diagnoses. Physicians should use procedure code 61210 to submit a claim for intracranial pressure monitoring. Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.28Laboratory Services

31.2.28.1Clinical Pathology Services and Pathology Consultations

Clinical pathology consultations (procedure codes 80503, 80504, 80505, or 80506) are a benefit when they are performed by a clinical pathologist or geneticist. A geneticist may submit claims for procedure codes 80503, 80504, 80505, or 80506 using their physician provider identifier.

Routine conversations between a consultant and an attending physician about test orders or results are not considered consultations.

The service does not qualify as a consultation if the information could ordinarily be furnished by a non-physician laboratory specialist.

Claims for clinical pathology consultations must be submitted with the following documentation:

The name and address, or the CSHCN Services Program provider identifier for the physician requesting the consultation, must be included on the claim. The national provider identifier (NPI) of the physician requesting the consultation should also be included, if known.

A copy of the written narrative report describing the consultation findings.

Documented interaction that clearly outlines that the consultant interpreted the test results and made specific recommendations to the ordering physician.

If the claim does not include all of this information, the clinical pathology consultation will be denied.

31.2.28.2Claims Filing for Laboratory Tests

Physicians may only be reimbursed for the total component of laboratory tests that are actually performed in their office laboratories.

Interpretation of laboratory tests is considered part of a physician’s professional services (hospital, office, or emergency room visits) and must not be billed separately.

The claim must indicate the specific type of laboratory procedure performed. Providers who perform only the technical service must bill for the technical component.

31.2.28.3Reimbursement

Clinical laboratory services performed in a physician’s office may be reimbursed 60 percent of the prevailing charge levels.

Refer to: Chapter 25, “Enrollment” for additional information concerning coding and reimbursement for laboratory procedures.

31.2.28.4Cytopathology Studies (Gynecological, Pap Smears)

Pap smears for early detection of cancer are a benefit of the CSHCN Services Program.

Procurement and handling of the Pap smears are considered part of the E/M of the client and will not be reimbursed separately. Physicians interpreting a cytopathology specimen (Pap smears) must report the place of service according to where the cytopathology specimen is interpreted (office, inpatient hospital, outpatient hospital, or independent lab).

Because of the technical nature of processing and interpreting Pap smears or specimens for cytopathology, pathologists are the only physician specialty that may be reimbursed for these services.

Refer to: Section 25.2.5.3, “Genetic Testing for Colorectal Cancer” in Chapter 25, “Laboratory Services” for additional information concerning coding and reimbursement for gynecological cytopathology studies.

31.2.28.5Cytogenetics Testing

Clinical evidence supports the significance of cytogenetics evaluation in the diagnosis, prognosis, and treatment of acute leukemias, lymphomas, and other tumors, especially in children. The detection of the well-defined, recurring, genetic abnormalities often enables a correct diagnosis along with important prognostic information affecting the treatment protocol. Cytogenetics testing may be a part of an evaluation for unusual physical features or learning difficulties.

Refer to: Section 25.2.5.2, “Cytogenetics Testing” in Chapter 25, “Laboratory Services” for additional information about reimbursement for cytogenetics testing.

31.2.28.6Helicobacter pylori (H. pylori)

The following procedure codes are benefits for physicians in the office setting:

Procedure Codes

78267

78268

83009

83013

83014

86677

87338^

87513

^ QW modifier required


Refer to: Section 25.2.9, “Helicobacter pylori (H. pylori)” in Chapter 25, “Laboratory Services” for additional information about reimbursement for H. pylori testing.

31.2.28.7CLIA Requirement

Refer to: Section 2.1.5.6, “Clinical Laboratory Improvement Amendments (CLIA) of 1988” in Chapter 2, “Provider Enrollment and Responsibilities.”

Section 25.1.1, “Clinical Laboratory Improvement Amendments (CLIA) of 1988” in Chapter 25, “Laboratory Services” for additional information regarding CLIA regulations.

31.2.29Magnetoencephalography (MEG)

MEG is a benefit of the CSHCN Services Program when used in pre-surgical planning for clients with intractable focal epilepsy, brain tumors, or vascular malformations.

Procedure codes 95965, 95966, and 95967 may be reimbursed for MEG services that are provided in the office, inpatient hospital, and outpatient hospital settings. Procedure code 95967 must be submitted along with primary procedure code 95966 on the same day, by the same provider.

Physicians may be reimbursed for the professional component of MEG services and the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.29.1Authorization Requirements

Prior authorization is required for MEG procedures and must be obtained prior to the date of service. Requests for MEG must be submitted on the CSHCN Services Program Authorization and Prior Authorization Request Form to the TMHP CSHCN Services Program Authorization Department.

The provider must complete and submit a prior authorization request, which should include all required documentation through any CSHCN approved method. A copy of the prior authorization request and all submitted documentation must be maintained in the client’s medical record.

Note:All prior authorization requests must be submitted with the ordering practitioner’s signature.

To facilitate a determination of medical necessity and avoid unnecessary denials, the physician must provide correct and complete information, including documentation of medical necessity for the service(s) requested.

Documentation must support the medical need of pre-surgical planning for clients with intractable focal epilepsy, brain tumors, or vascular malformations, and must include the following, as applicable:

Evidence of intractable focal epilepsy, neoplasm, or arterial venous malformations (AVMs), and

Evidence of prior treatment failures with antiepileptic drugs, if applicable, and

Evidence demonstrating failure of previous brain surgery or failure of more traditional testing to locate the epileptic foci, and

Evidence of current and past diagnostic studies indicating the need for MEG.

Note:Requests for repeat MEG scans must include the date of the previous MEG and documentation supporting the medical necessity for the repeat scan.

If the service is medically necessary, provided after hours or on a recognized holiday or weekend, the service may be authorized when the request is submitted on the next business day. A completed CSHCN Services Program Authorization and Prior Authorization Request Form and supporting documentation must be received within these deadlines for prior authorization to be considered. Extensions to these deadlines are not given by the CSHCN Services Program for providers to correct incomplete PA requests.

Prior authorization and medical review is required for all other indications. Documentation for consideration must include diagnosis, clinical course, clinical history, and other treatments with an explanation of ineffective results. This documentation to support medical necessity must be submitted to the CSHCN Services Program Medical Director or designee.

31.2.29.2Documentation Requirements

All services are subject to retrospective review to ensure that the documentation in the client’s medical record supports the medical necessity of the service(s) provided. Documentation in the client’s medical record must be maintained by the physician and support the medical necessity for the services provided. Services not supported by documentation are subject to recoupment.

Providers may be asked to provide additional documentation to clarify a prior authorization request or to clarify medical necessity of the client.

31.2.29.3Exclusions

MEG is not a stand-alone test, and is not the first order test after clinical and routine EEG diagnosis of epilepsy, and cannot replace, but may guide, the placement of intracranial EEG.

Services and procedures that are investigational or experimental are not benefits of the CSHCN Services Program.

31.2.30Neurostimulator Devices and Supplies

Neurostimulator devices and supplies are benefits of the CSHCN Services Program.

Refer to: Chapter 27, “Neurostimulators and Neuromuscular Stimulators” for information about benefits for neurostimulator devices and supplies.

31.2.31Ophthalmological Services

Ophthalmological services are benefits of the CSHCN Services Program.

Refer to: Chapter 40, “Vision Services” for additional information about reimbursement for ophthalmology.

31.2.31.1Intraocular Lenses (IOL)

An ophthalmologist who performs cataract extractions and IOL implants in the office may be reimbursed for the lens. The provider must submit a copy of the manufacturer’s invoice for the IOL with the claim. Reimbursement for the lens is limited to the actual acquisition cost for the lens (minus any discount) plus a handling fee not to exceed 5 percent of the actual acquisition cost.

Note:The CSHCN Services Program does not reimburse physicians who supply IOLs to ASCs or HASCs. Payment for the IOL is included in the facility fee.

31.2.31.2Vitrasert Ganciclovir Implant

Procedure code 67027 is a benefit with diagnosis code B251, B258, B259, H3090, H3091, H3092, or H3093. If a provider bills vitrectomy and implantation of intravitreal drug delivery system with the same date of service, the insertion code may be reimbursed and the vitrectomy code payment is denied as part of the other service.

31.2.32Osteopathic Manipulative Treatment (OMT)

OMT, performed by a physician, is a benefit for acute musculoskeletal conditions, acute exacerbations of a chronic condition, and acute pre or postsurgery treatments when they are directly related to surgery.

Refer to: Chapter 30, “Physical Medicine and Rehabilitation” for more information about OMT services.

31.2.33Physical Medicine and Physical Therapy (PT) Services

PT performed by a physician or physical therapist is a benefit of the CSHCN Services Program.

Refer to: Chapter 30, “Physical Medicine and Rehabilitation” for more information about PT services.

The CSHCN Services Program may reimburse physicians for therapy services performed in their offices.

The following procedure codes may be used for physical medicine and rehabilitation services:

Procedure Codes

97012

97016

97018

97022

97024

97026

97028

97032

97033

97034

97035

97036

97110

97112

97113

97116

97124

97140

97150

97161

97162

97163

97164

97165

97166

97167

97168

97530

97535

97537

97542

97750

97755

97760

97761

97762

97799

Physical therapy services must be billed with the GP modifier.

31.2.34Podiatry

Services provided by a licensed podiatrist (DPM) are a benefit of the CSHCN Services Program. Podiatry services may be reimbursed when provided by a physician (MD or DO).

Surgery procedure codes 11055, 11056, 11057, 11719, and G0127 are limited to one service every 6 months per client.

Supportive devices such as molds, inlays, shoes, or supports and all services connected with the fitting or application of these devices must meet the CSHCN Services Program requirements for foot orthotics.

Refer to: Section 28.2.2, “Orthoses and Prostheses (Not All-Inclusive)” in Chapter 28, “Orthotic and Prosthetic Devices” and Section 28.3.7.2, “Prescription Shoes” in Chapter 28, “Orthotic and Prosthetic Devices” for additional information about foot orthotics.

Podiatrists may be reimbursed for medically necessary laboratory services and radiological procedures that include the foot, ankle, toes, or heel.

Podiatrists may prescribe medications, supplies, braces, and prosthetic devices for conditions of the foot and ankle.

Authorization and prior authorization requirements applied to services provided by physicians also apply to services provided by a podiatrist. All CSHCN Services Program requirements concerning reimbursement for surgical procedures, such as the global fee concept, apply to podiatrists.

Podiatrists may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

Refer to: Chapter 4, “Prior Authorizations and Authorizations” for detailed information about authorization and prior authorization requirements.

31.2.35Psychological Testing

Psychological testing (procedure codes 96130, 96131, 96136 and 96137), neurobehavioral status exams (procedure codes 96116 and 96121), and neuropsychological testing (procedure codes 96132, 96133, 96136, and 96137) are benefits of the CSHCN Services Program and may be reimbursed up to 4 hours per day and 8 hours per calendar year, per client, for any provider. Providers must bill the units of each half hour of testing and indicate that number of units on the claim form. Claim submissions for over 4 hours per day and 8 hours per calendar year must include documentation of medical necessity. Add-on procedure codes 96121, 96131, 96133, and 96137 must be billed with their corresponding primary procedure code 96116, 96130, 96132, or 96136 on the same day, by the same provider.

Procedure codes 96121, 96130, 96131, 96132, 96133, 96136, and 96137 are included in the system limitation of 12 hours of behavioral health services per day, per provider.

Reimbursement of psychological testing, neuropsychological testing, and neurobehavioral status exams include testing scoring and interpretation of results. The number of units on the claim must reflect the time spent face-to-face testing with the client, as well as the time spent scoring and interpreting the results in one hour increments.

If the performance, interpretation, and reporting of the testing are performed on different dates of service, then the date of service on the claim must reflect the date and time spent for each service performed. Even if scoring and interpretation are completed on a different date from the testing, providers must submit only one claim for each psychological or neuropsychological test or neurobehavioral status exam performed. If necessary, providers can submit the claim with multiple details for each date of service. A claim must not be submitted until performance, interpretation, and reporting of the testing is complete.

Behavioral health testing and neurobehavioral status exams may be performed during an assessment by an APRN or physician assistant but will not be reimbursed separately.

Psychological testing (procedure codes 96130, 96131, 96136 and 96137) and neurobehavioral testing (procedure codes 96132, 96133, 96136, and 96137) may be reimbursed on the same date of service as procedure code 90791 or procedure code 90792.

Testing procedure codes 96116, 96121, 96130, 96131, 96132, 96133, 96136, and 96137 count towards the 30 per calendar year limitation.

Psychological testing (procedure codes 96130, 96131, 96136 and 96137), neurobehavioral status exams (procedure codes 96116 and 96121), and neuropsychological testing (procedure codes 96132, 96133, 96136, and 96137) will not be reimbursed on the same date of service by the same provider.

Refer to: Section 24.3.1.3, “Inpatient Behavioral Health” in Chapter 24, “Hospital” for additional information about behavioral health services.

Chapter 29, “Outpatient Behavioral Health” for additional information about behavioral health services.

31.2.36Sign Language Interpreting Services

Sign language interpreting services are available to CSHCN Services Program clients who are deaf or hard of hearing or to a parent or guardian of a person receiving CSHCN Services Program benefits, who is deaf or hard of hearing.

The sign language interpreting services must be requested by a physician and provided by a qualified interpreter. A physician’s determination of the need for sign language interpreting services must give primary consideration to the needs of the individual who is deaf or hard of hearing.

Sign language interpreting services are benefits of the CSHCN Services Program. Providers must use procedure code T1013 with modifier U1 for the first hour of service, and modifier UA for each additional 15 minutes of service. Procedure code T1013 billed with modifier U1 is limited to once per day, per provider, and procedure code T1013 billed with modifier UA is limited to a quantity of 28 per day.

Physicians in private or group practices with fewer than 15 employees may be reimbursed for this service. The physician will be responsible for arranging and paying for the sign language interpreting services to facilitate the medical services being provided. The physician will then seek reimbursement from the CSHCN Services Program for providing this service.

Sign language interpreting services must be provided by an interpreter who possesses one of the following certification levels (i.e., levels a through h) issued by either HHSC, the Office for Deaf and Hard of Hearing Services, the Board for Evaluation of Interpreters (BEI), or the National Registry of Interpreters for the Deaf (RID):

a)BEI Level I/Ii and BEI OC: B (Oral Certificate: Basic).

b)BEI Basic and RID NIC (National Interpreter Certificate) Certified.

c)BEI Level II/IIi, RID CI (Certificate of Interpretation), RID CT (Certificate of Transliteration), RID IC (Interpretation Certificate), and RID TC (Transliteration Certificate).

d)BEI Level III/IIIi, BEI OC: C (Oral Certificate: Comprehensive), BEI OC: V (Oral Certificate: Visible), RID CSC (Comprehensive Skills Certificate), RID IC/TC, RID CI/CT, RID RSC (Reverse Skills Certificate), and RID CDI (Certified Deaf Interpreter).

e)BEI Advanced and RID NIC Advanced.

f)BEI IV/IVi, RID MCSC (Master Comprehensive Skills Certificate), and RID SC: L (Specialist Certificate: Legal).

g)EI V/VI.

h)BEI Master; and RID NIC Master.

Interpreting services include the provision of voice-to-sign, sign-to-voice, gestural-to-sign, sign-to-gestural, voice-to-visual, visual-to-voice, sign-to-visual, or visual-to-sign services for communication access provided by a certified interpreter.

The physician requesting interpreting services must maintain documentation verifying the provision of interpreting services. Documentation of the service must be included in the client’s medical record and must include the name of the sign language interpreter and the interpreter’s certification level. Documentation must be made available if requested by the CSHCN Services Program or its designee.

31.2.37Skin Therapy

Procedure codes 96900, 96910, 96912, and 96913 are benefits of the CSHCN Services Program for the following diagnosis codes:

Diagnosis Codes

A672

B070

B081

B550

B551

B552

B559

C8401

C8402

C8403

C8404

C8405

C8406

C8407

C8408

C8409

H02731

H02732

H02734

H02735

L100

L101

L102

L103

L104

L105

L1081

L1089

L120

L121

L122

L128

L130

L131

L138

L139

L14

L200

L2081

L2082

L2084

L2089

L209

L210

L211

L218

L219

L22

L230

L231

L232

L233

L234

L235

L236

L237

L2381

L2389

L239

L240

L241

L242

L243

L244

L245

L246

L247

L2481

L2489

L249

L250

L252

L258

L259

L270

L271

L272

L278

L279

L300

L302

L308

L309

L401

L560

L561

L562

L563

L564

L565

L570

L571

L572

L573

L574

L575

L580

L581

L589

L598

L599

L700

L701

L702

L703

L704

L705

L708

L730

L80

L811

L812

L813

L815

L816

L818

31.2.38Sleep Studies

Polysomnography, multiple sleep latency tests, and pediatric pneumograms are benefits of the CSHCN Services Program.

Sleep facilities that perform services for CSHCN Services Program clients must be accredited with the American Academy of Sleep Medicine (AASM) or the Joint Commission on Accreditation of Healthcare Organizations (JCAHO). Documentation of accreditation must be maintained in the facility and be available for review. Sleep facilities must also follow current AASM practice parameters and clinical guidelines. Providers may refer to the AASM website at https://aasm.org/ for AASM facility certification requirements or to the JCAHO website at www.jointcommission.org for JCAHO facility accreditation information.

Sleep facility technicians and technologists must demonstrate that they have the skills, competencies, education, and experience that are set forth by their certifying agencies and AASM as necessary for advancement in the profession.

The sleep facility must have one or more supervision physicians who are responsible for the direct and ongoing oversight of the quality of the testing performed, the proper operation and calibration of the equipment used to perform the tests, and the qualifications of the non-physician staff who use the equipment.

31.2.38.1Polysomnography

Polysomnography is the recording, analysis, and interpretation of the multiple simultaneous physiological measurements of sleep for 6 or more hours. The studies are performed to diagnose a variety of sleep disorders, such as sleep apnea, and are considered part of the clinical workup performed before the surgical procedure uvulopalatopharyngoplasty.

Polysomnography is distinguished from sleep studies by the inclusion of sleep staging which includes a 1-4 lead electroencephalogram (EEG), electro-oculogram (EOG), and a submental electromyogram (EMG).

Additional parameters of sleep include, but are not limited to:

Airflow.

Body positions.

Continuous blood pressure monitoring.

Electrocardiogram (ECG).

Extended EEG monitoring.

Extremity/motor activity movement.

Gas exchange by oximetry.

Gastroesophageal reflux.

Penile tumescence.

Snoring.

Ventilation and respiratory effort.

For a study to be reported as polysomnography, sleep must be recorded and staged.

Polysomnographic technologists, technicians, and trainees must meet the following supervision requirements:

A polysomnographic trainee provides basic polysomnographic testing and associated interventions under the direct supervision of a polysomnographic technician, polysomnographic technologist or physician.

Note:Direct supervision means that the supervising licensed/certified professional must be present in the office suite or building and immediately available to furnish assistance and direction throughout the performance of the service. It does not mean that the supervising professional must be present in the room while the service is being provided.

A polysomnographic technologist provides comprehensive evaluation and treatment of sleep disorders under the general supervision of the clinical director (M.D. or D.O.).

A polysomnographic technician provides comprehensive polysomnographic testing and analysis, and associated interventions under the general supervision of a polysomnographic technologist or clinical director (M.D. or D.O.).

Note:The supervising physician must be readily available to the performing technologist throughout the duration of the study but is not required to be in the building.

Services provided without the required level of supervision are not considered medically appropriate and will be recouped upon retrospective record review.

Polysomnography (procedure codes 95782, 95783, 95808, 95810, and 95811) is restricted to the following diagnosis codes:

Diagnosis Codes

E662

F5101

F5102

F5103

F5104

F5109

F5111

F5112

F5113

F5119

F513

F514

F515

F518

F519

F984

G253

G2589

G259

G26

G4700

G4701

G4710

G4711

G4712

G4713

G4714

G4719

G4720

G4721

G4722

G4723

G4724

G4725

G4726

G4727

G4729

G4730

G4731

G4733

G4734

G4735

G4736

G4737

G4739

G47411

G47419

G47421

G47429

G4750

G4751

G4752

G4753

G4754

G4759

G4761

G4769

G478

G479

J9610

J9611

J9612

R0600

R0609

R063

R0683

R0689

R069

R0901

Polysomnography is payable to physicians in outpatient hospital and office settings. Procedure codes 95782, 95783, 95808, 95810, and 95811 are limited to one per day by any provider. When multiple procedure codes are billed on the same day, the most inclusive code is paid and all other codes are denied.

31.2.38.2Multiple Sleep Latency Test

Multiple sleep latency tests involve the client being given a chance to sleep every 2 hours during normal wake time. Observations are made of the time taken to reach stages of sleep. This test measures the degree of daytime sleepiness and how soon rapid eye movement (REM) sleep begins. This test is a benefit for diagnosing narcolepsy.

Multiple sleep latency tests (procedure code 95805) are restricted to the following diagnosis codes:

Diagnosis Codes

E662

G4700

G4710

G4711

G4712

G4720

G4733

G47411

G47419

G47421

G47429

G478

G479

Multiple sleep latency tests are payable to physicians in outpatient hospital and office settings. Procedure code 95805 is limited to one per day by any provider. Sleep study procedure codes 95806 and 95807 are not a benefit of the CSHCN Services Program.

31.2.38.3Pediatric Pneumogram

A pneumogram is a 12- to 24-hour recording of breathing effort, heart rate, oxygen level, and airflow to the lungs during sleep. The study is useful in identifying abnormal breathing patterns, with or without bradycardia, especially in premature infants.

Procedure code 94772 is a benefit for CSHCN Services Program clients from birth through 12 months of age with one of the following diagnosis codes:

Diagnosis Codes

K2080

K2081

K2090

K2091

K2100

K2101

K219

K220

P220

P228

P229

P270

P271

P278

P279

P282

P2830

P2831

P2832

P2833

P2839

P2840

P2841

P2842

P2843

P2849

P285

P2881

P2889

P84

R0600

R0609

R062

R063

R0681

R0682

R0683

R0689

R069

R6813

Pediatric pneumograms are payable to physicians in office, inpatient hospital, and outpatient hospital settings. A pediatric pneumogram is limited to two services per lifetime without authorization based on the diagnoses listed above. Authorization is required for more than two pneumograms. Requests for prior authorization must be submitted using the CSHCN Services Program Authorization and Prior Authorization Request form.

EMGs, polysomnography, EEGs, and ECGs are denied when billed on the same day as a pediatric pneumogram.

Pediatric pneumograms may be reimbursed on the same date of service as an apnea monitor (rented monthly) if documentation supports the medical necessity.

Pneumogram supplies are considered part of the technical component of the reimbursement and are denied if billed separately.

31.2.38.4Home Sleep Study Test

Home sleep study tests are unattended studies that are performed in the client’s home using a portable monitoring device. The portable monitoring device must meet AASM practice parameters and clinical guidelines.

Home sleep study testing is a benefit of the CSHCN Services Program only when performed in conjunction with a comprehensive sleep evaluation that has been performed by a physician who is board-certified or board-eligible, as outlined in the AASM guidelines. Documentation of the comprehensive sleep evaluation must be kept in the client’s medical record. The evaluation must indicate probability of moderate to severe obstructive sleep apnea to support medical necessity for home sleep study testing.

Procedure codes G0398, G0399, and G0400 are a benefit for CSHCN Services Program clients who are 18 years of age and older with suspected or proven simple, uncomplicated obstructive sleep apnea. Procedure codes G0398, G0399, and G0400 are restricted to diagnosis code G4733.

Home sleep study tests are payable to physicians in the office setting. Procedure codes G0398, G0399, and G0400 are limited to one per day and a combined total of two tests per rolling year, with any provider. If a client needs more than two tests in a rolling year, subsequent tests must be performed in a sleep facility.

31.2.39Surgery

Surgical services, including surgical procedures involving an assistant surgeon or cosurgeon, are a benefit of the CSHCN Services Program.

Authorization of cosurgeon and assistant surgeon services is not required; however, all other authorization requirements associated with the surgical procedure must be met.

Reminder:An authorization request can be submitted up to 95 days after the date of service. The completed authorization form can be attached to the paper claim.

Specific surgical procedures, as specified throughout this section, require prior authorization. If a prior authorization is not obtained for the procedure, the facility’s services, the surgeon’s services, and the assistant surgeon’s services are denied; however, anesthesia services may be paid.

Prior authorization must be obtained for procedures that are completed by a specialty team or in a specialty center. Criteria unique to specific surgical procedures must be satisfied as indicated in the appropriate sections below.

Unless otherwise stated, no additional reimbursement is provided to physicians who elect to use special instruments or advanced technology to accomplish a surgical procedure.

Surgical procedures may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.39.1Anesthesia Administered by Surgeon

If the physician submits a surgical procedure and anesthesia for the same surgery for reimbursement, the anesthesia procedure code is denied as part of the surgical procedure.

31.2.39.2Primary Surgeons

The primary surgeon is the lead surgeon who participates and directs the technical aspects of a surgical case.

Physicians cannot provide services as a surgeon and assistant surgeon, or as a surgeon and anesthesiologist during the same surgical procedure. A physician may bill as a surgeon and assistant surgeon on the same client, if two separate procedures are performed. Full payment is allowed for surgery, and the assistant surgical procedure may be reimbursed half of the reimbursement amount for an assistant surgery.

If the physician is an anesthesiologist who is billing for general anesthesia and a surgical procedure which is considered part of the anesthesia, the surgical procedure is not reimbursed.

31.2.39.3Assistant Surgeons

An assistant surgeon assists the primary surgeon during a complex surgical procedure that warrants an assistant to safely and effectively accomplish the procedure.

Assistant surgeons may be reimbursed 16 percent of the prevailing fee for the surgical procedure performed.

The CSHCN Services Program follows the Tax Equity and Fiscal Responsibility Act (TEFRA) of 1982 regulation for assistant surgeons in teaching hospitals.

An assistant surgeon is not paid in a hospital classified by Medicare as a teaching facility with an approved graduate training program in the performing physician’s specialty. These claims are paid only if modifiers 82 or 80 (assistant surgeon) and KX (documentation on file) are present on the claim. These modifiers should be used in the following situations:

There are exceptional medical circumstances, such as emergency or life-threatening situations that require immediate attention.

The primary surgeon has a policy of never, without exception, involving a resident in the preoperative, operative, or postoperative care of their clients.

The surgical procedure is complex and qualifies for more than one physician.

Use modifier 82 when no qualified resident was available to assist with the surgery.

If the physician seeks an exception to the TEFRA regulation based on unavailability of a qualified resident, the following certification statement must appear on or be attached to the claim form:

“I understand that Section 1842(b)(6)(D) of the Social Security Act generally prohibits reasonable charge payment for the services of assistants at surgery in teaching hospitals when qualified residents are available to furnish such services. I certify that the services for which payment is claimed were medically necessary, and that no qualified residents were available to perform the services. I further understand that these services are subject to postpayment review by TMHP-CSHCN.”

Payment to an assistant surgeon for multiple surgical procedures follows the same guidelines as payment to the primary surgeon.

If an assistant surgeon bills separate charges for local or regional anesthesia and assistant surgery on the same day, the anesthesia is included as part of the surgical procedure and not reimbursed separately.

31.2.39.4Cosurgery

Cosurgery is a benefit of the CSHCN Services Program if the CMS fee schedule indicates that the procedure allows for cosurgeons.

When billing for cosurgery, each surgeon must bill the same procedure codes and modifier 62 (cosurgeon).

Cosurgery occurs when two surgeons, usually with different specialties or skills, work together as primary surgeons performing distinct parts of a single reportable procedure. Neither surgeon is acting as an assistant surgeon; both have comparable roles in the procedure. When two surgeons work together as primary surgeons performing distinct parts of the procedure, each surgeon should report their distinct operative work by adding modifier 62 to the procedure code and any associated add-on codes for that procedure, as long as both surgeons continue to work together as primary surgeons. Each surgeon should report the cosurgery once using the same procedure codes. If additional procedures (including add-on procedures) are performed during the same surgical session, separate codes may be reported without modifier 62 added.

Authorization is not specifically required for procedures using cosurgeons, although all other authorization requirements must be met. Prior authorization must be obtained for those procedures completed by a specialty team or in a specialty center. Criteria unique to specific surgical procedures must be satisfied as indicated in Section 31.2.39.11, “Cleft/Craniofacial Procedures” in this chapter and Section 31.2.42.2, “Transplants - Nonsolid Organ” in this chapter.

If a cosurgeon acts as an assistant in the performance of additional procedures during the same surgical session, those services can be reported using separate procedure codes with the modifier 80 or 81 (minimum assistant surgeon) added, as appropriate.

Each surgeon receives 62.5 percent of the amount allowed for the intraoperative portion of the surgical procedure’s fee. Additional payment is not made for an assistant surgeon on the same procedure being reimbursed as cosurgery.

Claims submitted without the cosurgery modifier 62 are not considered cosurgery. Reimbursement for these claims is determined by other surgery reimbursement methodology.

Note:Each surgeon that performs cosurgery must bill only the appropriate procedure code for the specific surgery performed.

The CSHCN Services Program does not reimburse for team surgery. Surgeons and assistant surgeons participating in a team surgery should bill for procedures they personally completed, and may be reimbursed based on the multiple surgery guidelines.

31.2.39.5Bilateral Procedures

When a bilateral procedure is performed and an appropriate bilateral procedure code is not available, a unilateral procedure code must be used. The unilateral procedure code must be billed twice with a quantity of one for each procedure code. For all procedures, modifiers LT (left side), and RT (right side) must be used as appropriate.

Bilateral procedures performed on separate limbs are paid the full allowance for the major procedure and half the allowance for subsequent procedures performed on the same day, when medically justified.

31.2.39.6Global Fees

The CSHCN Services Program uses global surgical periods to determine reimbursement for surgical procedures. The following services are included in the global surgical period:

Preoperative care, including history and physical

Hospital admission work-up

Anesthesia (when administered and monitored by the primary surgeon)

Surgical procedure (intraoperative)

Postoperative follow-up and related services

Complications following the surgical procedure that do not require return trips to the operating room

The CSHCN Services Program will adhere to a global fee concept for minor and major surgeries and invasive diagnostic procedures. Global surgical periods are defined as follows:

0-day Global Period—Reimbursement includes the surgical procedure and all associated services that are provided on the same day.

10-day Global Period—Reimbursement includes the surgical procedure and all associated services provided on the day of the surgery through 10 days after the surgical procedure.

90-day Global Period—Reimbursement includes the surgical procedure, preoperative services that are provided on the day before the surgical procedure, and all associated services that are provided on the day of the surgery through 90 days after the surgical procedure.

Procedure codes that are designated as “Carrier Discretion” will have their global periods determined by the CSHCN Services Program.

Note:Note: All unlisted surgical procedure codes have a 42-day global period assigned by the CSHCN Services Program.

The global surgical fee period applies to both emergency and nonemergency surgical procedures. Physicians who are in the same group practice and specialty must bill, and are reimbursed, as if they were a single provider.

Radiology and laboratory services related to the surgical procedure are not subject to the global period and are reimbursed separately.

31.2.39.6.1Modifiers

To align with CMS, the CSHCN Services Program will add certain modifiers that are related to surgical services. For services that are rendered in the preoperative, intraoperative, or postoperative period to be correctly reimbursed, providers must use the appropriate modifiers from the following table. Failure to use the appropriate modifier may result in recoupment.

Modifiers Related to Surgical Fees

24

25

54

55

56

57

58

62

76

77

78

79

For services that are billed with modifier 54, 55, or 56, medical record documentation must be maintained by both the surgeon and the provider performing preoperative or postoperative care. Reimbursement for claims associated with modifiers 54, 55, and 56 is limited to the same total amount as would have been paid if only one physician provided all of the care, regardless of the number of physicians who actually provide the care.

If a physician provided all of the preoperative, intraoperative, and postoperative care, claims may be considered for reimbursement when they are submitted without a modifier.

31.2.39.6.2Documentation Requirements

For services that are billed with any of the listed modifiers to be considered for reimbursement, providers must maintain documentation in the client’s medical record that supports the medical necessity of the services. Acceptable documentation includes, but is not limited to:

Progress notes.

Operative reports.

Laboratory reports.

Hospital records.

On a case-by-case basis, providers may be required to submit additional documentation that supports the medical necessity of services before the claim will be reimbursed.

Note:Retrospective review may be performed to ensure documentation supports the medical necessity of the surgical procedure and any modifier used to bill the claim.

31.2.39.6.3Preoperative Services

Preoperative physician E/M services (such as office or hospital visits) that are directly related to the planned surgical procedure and provided during the preoperative limitation period will be denied if they are billed by the surgeon or anesthesiologist who was involved in the surgical procedure.

Reimbursement will be considered when the E/M services are performed for distinct reasons that are unrelated to the procedure. E/M services that meet the definition of a separately identifiable service and are above and beyond the usual preoperative and postoperative care, may be billed with modifier 25 if they are provided on the same day by the same provider as the surgical procedure.

Modifier 25 is not used to report an E/M service that results in a decision to perform a surgical procedure. Documentation that supports the provision of a significant, separately identifiable E/M service must be maintained in the client’s medical record and made available to the CSHCN Services Program upon request. If the decision to perform a minor procedure is made during an E/M visit immediately before the surgical procedure, the E/M visit is considered a routine preoperative service and is not separately billable.

Physicians who provide only preoperative services for surgical procedures with a 10- or 90-day global period may submit claims using the surgical procedure code with identifying modifier 56. Reimbursement will be limited to a percentage of the fee for the surgical procedure.

E/M services that are provided during the preoperative period (one day before or the same day) of a major surgical procedure (90-day global period) and result in the initial decision to perform the surgical procedure may be considered for reimbursement when they are billed with modifier 57. The client’s medical record should clearly indicate when the initial decision to perform the procedure was made.

31.2.39.6.4Intraoperative Services

Physicians who perform a surgical procedure with a 10- or 90-day global period but do not render postoperative services must bill the surgical procedure code with modifier 54. Documentation in the medical record must support the transfer of care and must indicate that an agreement has been made with another physician to provide the postoperative management.

31.2.39.6.5Postoperative Services

Postoperative services that are directly related to the surgical procedure are included in the global surgical fee and are not reimbursed separately. Postoperative services include, but are not limited to, all of the following:

Follow-up visits (any place of service)

Pain management

Miscellaneous services, including:

Dressing changes

Local incision care

Platelet gel

Removal of operative packs

Removal of cutaneous sutures, staples, lines, wires, drains, casts, or splints

Replacement of vascular access lines

Insertion, irrigation, and removal of urinary catheters, routine peripheral intravenous lines, nasogastric tubes, and rectal tubes

Changes or removal of tracheostomy tubes

Note:Removal of postoperative dressings or anesthetic devices is not eligible for separate reimbursement as the removal is considered part of the allowance for the primary surgical procedure.

If the surgeon provides the surgery and only the postoperative care for a procedure that has a 10- or 90-day global period, the surgeon must include the following details on the claim form:

The surgical procedure, date of surgery, and modifier 54, which indicates that he or she was the surgeon

The surgical procedure, date of service, and modifier 55 to denote the postoperative care

Note:Providers must not submit a claim for a procedure until after the client has been seen during a face-to-face follow-up visit.

When transfer of care occurs for postoperative care for procedures that have a 10- or 90-day global period, the following conditions apply:

When transfer of care occurs immediately after surgery, the surgeon or other provider who assumes in-hospital postoperative care must bill subsequent care procedure code 99231, 99232, or 99233.

The surgeon or other provider who provides postdischarge care must bill the appropriate surgical code with modifier 55. Reimbursement will be limited to a percentage of the allowable fee for the surgical procedure.

Documentation in the medical record must include all of the following:

A copy of the written transfer agreement

The dates the care was assumed and relinquished

The claim must indicate in the comments field of the claim form the dates on which care was assumed and relinquished, and the units field must reflect the total number of postoperative care days provided. Claims that are submitted on the CMS-1500 paper claim form must include the date of surgery in Block 14 and the dates on which care was assumed and relinquished in Block 19.

When a transfer of postoperative care occurs, the receiving physician cannot bill for any part of the global services until at least one service has been provided.

Staged or related surgical procedures or services that are performed during the postoperative period may be reimbursed when they are billed with modifier 58. A postoperative period will be assigned to the subsequent procedure. Documentation must indicate that the subsequent procedure or service was not the result of a complication and was one of the following:

It was planned at the time of the initial surgical procedure

It is more extensive than the initial surgical procedure

It is for therapy following an invasive diagnostic surgical procedure

Note:Modifier 58 does not apply to procedure codes that are already defined as staged or sessioned services in the Current Procedural Terminology (CPT) Manual (e.g., 65855 or 66821).

Hospital visits by the surgeon during the same hospitalization as the surgery are considered to be related to the surgery and, as a result, not separately billable; however, separate payment for such visits can be allowed if any of the following conditions apply:

Immunotherapy management is provided by the transplant surgeon. Immunosuppressant therapy following transplant surgery is covered separately from other postoperative services, so postoperative immunosuppressant therapy is not part of the global fee allowance for the transplant surgery. This coverage applies regardless of the setting.

Critical care is provided by the surgeon for a burn or trauma patient.

The hospital visit is for a diagnosis that is unrelated to the original surgery.

E/M services that are provided by the same provider for reasons that are unrelated to the operative surgical procedure may be considered for reimbursement if they are billed with modifier 24. Documentation must substantiate the reasons for providing E/M services.

Modifier 24 may be billed with modifier 25 if a significant, separately identifiable E/M service that was performed on the day of a procedure falls within the postoperative period of another unrelated procedure.

Modifier 24 may be billed with modifier 57 if an E/M service that was performed within the postoperative period of another unrelated procedure results in the decision to perform major surgery.

31.2.39.6.6Return Trips to the Operating Room

Return trips to the operating room for a repeat surgical procedure may be considered for reimbursement when billed with modifiers 76 and 77. Billing with modifiers 76 and 77 initiates the beginning of a new global period. Medical record documentation must support the need for a repeat procedure.

All surgical procedure codes with a predefined limitation (e.g., once per lifetime, one every 5 years) must not be submitted with modifier 76 or 77.

For modifiers 76 and 77, the repeated procedure must be the same as the initial surgical procedure. The repeat procedure should be billed with the appropriate modifier. The reason for the repeat surgical procedure should be entered in the narrative field on the claim form.

Return trips to the operating room for surgical procedures that are related to the initial surgery (i.e., complications) may be considered for reimbursement when they are billed with modifier 78 by the same provider.

When a surgical procedure has a 0-day global period, the full value of the surgical procedure will be reimbursed; when the procedure has a 10- or 90-day global period, only the intraoperative portion will be reimbursed.

When an unlisted procedure is billed because no code exists to describe the treatment for the complications, reimbursement is a maximum of 50 percent of the value of the intraoperative services that were originally performed.

Reimbursement for the postoperative period of the first surgical procedure includes follow-up services from both surgical procedures, and no additional postoperative reimbursement is allotted. The global period will be based on the first surgical procedure.

Billing with modifier 78 does not begin a new global period.

Surgical procedures that are performed by the same provider during the postoperative period may be considered for reimbursement when they are billed with modifier 79 for any of the following:

When the same procedure is performed with a different diagnosis

When the same procedure is performed on the left and right side of the body in different operative sessions and that procedure is billed with the RT or LT modifier

When a different procedure is performed with the same diagnosis

When a different procedure is performed with a different diagnosis

Billing with modifier 79 initiates a new global surgical period.

31.2.39.7Multiple Surgeries

The CSHCN Services Program payment for multiple surgeries is based on the following guidelines:

When two surgical procedures are performed on the same day, the major procedure (e.g., the highest paying procedure) is paid at the full amount allowed by Texas Medicaid. Secondary procedures performed on the same day are paid at half of the amount allowed by Texas Medicaid when medically justified.

When a surgical procedure and a biopsy on the same organ or structure are performed on the same day, the procedures are reviewed and only the service with the higher of the allowed amounts may be reimbursed.

31.2.39.8Second Opinions

CSHCN Services Program benefits include payment to physicians when a CSHCN Services Program client requests a second opinion regarding surgery. The claim must be coded with the appropriate office or hospital visit procedure code, and the notation “Client Initiated Second Opinion” must be noted in Block 24D of the CMS-1500 paper claim form.

31.2.39.9Unlisted Surgical Procedure Code Considerations

Unlisted surgical procedure codes are commonly used when a matching description of a procedure performed cannot be found within HCPCS.

Note:All unlisted surgical procedure codes have a 42-day global period assigned by the CSHCN Services Program.

Providers may use the procedure code that best matches the surgery performed. If an unlisted procedure code is used, the following must be included with the claim:

A complete description of all procedures performed

An operative report of procedures

Providers must verify whether a procedure requires authorization. Filing a claim correctly the first time helps ensure that the claim is processed in a timely manner.

Refer to: Section 31.2.1, “Authorization and Prior Authorization Requirements” in this chapter for specific information on procedures that must be performed by an approved specialty team/center.

Section 31.2.39.11, “Cleft/Craniofacial Procedures” in this chapter for specific information on procedures that must be performed by an approved specialty team/center.

Section 31.2.42.2, “Transplants - Nonsolid Organ” in this chapter for specific information on procedures that must be performed by an approved specialty team/center.

31.2.39.10Circumcision

Circumcision (procedure codes 54150, 54160, and 54161) is a benefit of the CSHCN Services Program when medically necessary.

Conditions that may require circumcision include, but are not limited to, the following:

Congenital obstructive urinary tract anomalies

Neurogenic bladder

Spina bifida

History of recurrent urinary tract infections

Vesicoureteral reflux of at least a Grade III

Paraphimosis

Phimosis causing urinary obstruction

Elective circumcision of a newborn male for cosmetic, routine, or ritual purposes is not a benefit of the CSHCN Services Program. The newborn period is defined as the first 28 days of life. Circumcision of a female of any age is not a benefit of the CSHCN Services Program.

Authorization is required for a circumcision. Documentation should include the diagnosis and the specific medical necessity for the circumcision.

Refer to: Section 4.3, “Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about authorization requirements.

Procedure codes 54162 and 54163 are also a benefit of the CSHCN Services Program when medically necessary and do not require authorization.

When anesthesia or analgesia stronger than topical analgesia is used during the procedure, providers must follow applicable modifier guidelines and bill their usual and customary charges.

If a circumcision is billed in addition to a hypospadias or epispadias repair, the circumcision is denied as part of another procedure. A circumcision billed in addition to other surgical procedures on the male genital or urinary system is paid according to multiple surgery reimbursement guidelines. Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid. Claims submitted by an assistant surgeon for a circumcision are denied.

31.2.39.11Cleft/Craniofacial Procedures

Cleft and craniofacial services provided by a cleft and craniofacial (C/C) team or through a coordinated multidisciplinary team, including surgical interventions required to treat cleft lip, cleft palate, and craniofacial anomalies, are benefits of the CSHCN Services Program.

The CSHCN Services Program recognizes the standard of care needed to appropriately address the repair of C/C anomalies, as outlined in the guidelines prepared by the American Cleft Palate-Craniofacial Association (acpacares.org).

A comprehensive, multidisciplinary approach is medically necessary to meet all of the needs of clients who have complex medical conditions that require treatment by a broad range of medical specialists. The standard of care for the comprehensive repair or reconstruction of craniofacial anomalies for CSHCN Services Program clients requires a team approach by either a C/C team or an equivalent coordinated multidisciplinary team. The following exceptions to this requirement may be considered:

A C/C or equivalent multidisciplinary team is not available in the area and the client is unable to travel. Medical record documentation must explain the reasons for which the client is unable to travel.

A C/C or equivalent multidisciplinary team is not available in the area and the team approach cannot be coordinated over multiple locations. Medical record documentation must describe the attempts that were made to coordinate a team approach.

A C/C or equivalent multidisciplinary team is available but the client or the client’s parent or guardian refuses care from the team. Medical record documentation must document the reason that the client or the client’s parent or guardian gave for refusing care from the team.

The C/C or equivalent coordinated multidisciplinary team must have surgical and medical specialists, including, but not limited to the following:

Operating surgeon

Orthodontist

Speech-language pathologist

At least one of the following specialists:

Otolaryngologist

Audiologist

Pediatrician

Geneticist

Social worker

Psychologist

General pediatric or prosthetic dentist

Each C/C or equivalent coordinated multidisciplinary team must identify the following:

An administrator who is responsible for coordinating and maintaining C/C team records and ensuring that the C/C team adheres to CSHCN Services Program rules and regulations

A team care coordinator to ensure that the focus of the service is client and family oriented, and that the client, family, and C/C team jointly develop a comprehensive treatment plan for the client

The comprehensive treatment plan must be maintained in the client’s medical record and must be provided to the client and family, the referring physician, other collaborating providers, and the Department of State Health Services (DSHS) regional social worker upon request.

The plan will include the specific services that will be provided by the members of the C/C team, action steps, persons responsible, and time-frame objectives for meeting treatment outcomes.

Documentation of medical necessity must be kept in the client’s medical record if the requested surgical procedure is being performed because of injury or other trauma that is not associated with the repair or reconstruction of cleft lip, cleft palate, or craniofacial anomalies.

The following procedure codes must be prior authorized:

Surgery and Assistant Surgery Procedure Codes

20902

21120

21121

21122

21123

21125

21127

21137

21138

21139

21141

21142

21143

21145

21146

21147

21150

21151

21154

21155

21159

21160

21172

21175

21179

21180

21181

21182

21183

21184

21188

21193

21194

21195

21196

21198

21199

21206

21209

21210

21230

21244

21247

21255

21256

21260

21261

21263

21267

21268

21275

21299

40799

42210

61550

61552

61556

61557

61558

61559

62115

62117

Surgery Only Procedure Codes

14040

14041

14060

14061

15120

15121

15135

15136

15155

15156

15157

15240

15241

15260

15261

15576

21076

21077

21079

21080

21081

21082

21083

21084

21085

21086

21087

21088

21089

21100

21110

21208

21215

21235

21245

21246

21248

21249

21270

21280

21282

21295

21296

21497

30400

30410

30420

30435

30450

30460

30462

30465

30520

30540

30545

30560

30580

30600

30620

30630

40527

40650

40652

40654

40700

40701

40702

40720

40761

42145

42200

42205

42215

42220

42225

42226

42227

42235

42260

42280

42281

67950

67961

67966

67971

67973

67974

67975

Documentation of medical necessity must be submitted with the prior authorization request form if the surgical procedure is to be performed for reasons unrelated to the repair or reconstruction of cleft lip, cleft palate, or craniofacial anomalies.

Prior authorization is also required for orthodontic services that are performed in conjunction with C/C services.

Refer to: CSHCN Services Program Prior Authorization Request for Inpatient Surgery—For Surgeons Only

CSHCN Services Program Prior Authorization and Authorization Request for Outpatient Surgery—For Outpatient Facilities and Surgeons

31.2.40Diagnostic and Surgical/Reconstructive Breast Therapies

The following services are benefits of the CSHCN Services Program:

Breast therapies

Diagnostic

Surgical

Reconstructive

Treatment of complications of breast reconstruction

External breast prostheses

Corrective procedures

Surgical, reconstructive, and corrective procedures must be medically necessary.

Only new, unused durable medical equipment will be purchased for CSHCN clients.

Diagnostic and surgical/reconstructive breast therapies and corrective procedures include:

Diagnostic procedures for the breast

Mastectomy for the treatment of breast cancer

Prophylactic mastectomy

Mastectomy for gynecomastia

Reconstructive procedures

Treatment of complications of breast reconstruction

External breast prostheses

Corrective procedures

The following provider types, services and settings apply:

Diagnostic and surgical/reconstructive breast therapies may be provided by physicians, physician assistants, and advanced practice registered nurses, in the office, outpatient and inpatient hospital settings.

Corrective procedures may be provided by physicians, dentists, podiatrists, physician assistants, and advanced practice registered nurses, in office, inpatient and outpatient hospital settings.

Breast prostheses which are considered DME and may be provided by DME providers in the home setting.

To be considered for reimbursement, a LT or RT modifier must be appropriately appended to the procedure codes submitted for diagnostic and surgical/reconstructive breast therapies, external breast prostheses, or corrective procedures.

31.2.40.1Breast Therapies

31.2.40.1.1Diagnostic Breast Procedures

Diagnostic breast procedures are a benefit of the CSHCN Services Program for a diagnosis of a condition or malignancy of the breast.

Diagnostic procedures may include:

Puncture aspiration

Mastotomy

Injection procedure for ductogram or galactogram

Percutaneous biopsy, with or without imaging guidance

Incisional biopsy

Nipple exploration

Excision of the following:

Lactiferous duct fistula

Benign or malignant breast lesion

Chest wall tumor

The following procedure codes may be reimbursed for diagnostic procedures:

Procedure Codes

19000

19001

19020

19030

19081

19082

19083

19084

19085

19086

19100

19101

19110

19112

19120

19125

19126

19281

19282

19283

19284

19285

19286

19287

19288

21601

21602

21603

*Procedure code 21603 is limited to one procedure per lifetime.

The following procedure codes are add-on codes and must be billed with the appropriate primary procedure code, on the same day, by the same provider:

Add-on Procedure Codes

19001

19082

19084

19086

19126

19282

19284

19286

19288

31.2.40.2Surgical Breast Procedures

31.2.40.2.1Mastectomy

Mastectomy and partial mastectomy (e.g., lumpectomy, tylectomy, quadrantectomy, or segmentectomy) is a benefit of the CSHCN Services Program when it is medically necessary to remove a breast or portion of a breast for conditions including, but not limited to:

Developmental abnormality

Congenital defect

Trauma or injury to chest wall

Primary or secondary malignancy of the breast

Carcinoma in situ of the breast

The following mastectomy procedure codes are benefits of the CSHCN Services Program for male and female clients of all ages:

Procedure Codes

Limitations

Partial Mastectomy

19301, 19302

One left breast per lifetime

One right breast per lifetime

Simple, Subcutaneous, Radical, and Modified Radical Mastectomy

19303 19305, 19306, 19307

One left breast per lifetime

One right breast per lifetime

31.2.40.2.2Prophylactic Mastectomy

Prophylactic mastectomy is a benefit of the CSHCN Services Program and is limited to clients who are at moderate or high-risk for the development of breast cancer and have one or more of the following conditions:

Personal history

Current or previous history of breast cancer

Lobular carcinoma in situ (LCIS)

Radiation therapy to the chest before the age of 30

Family history of breast or ovarian cancer in mother, sister, or daughter

Presence of any of the following genetic mutations:

Breast cancer gene 1 (BRCA1)

Breast cancer gene 2 (BRCA2)

Tumor protein 53 ( TP 53)

Phosphatase and tensin homolog (PTEN)

Note:The above risk factors are identified by the National Cancer Institute and the National Comprehensive Cancer Network.

Documentation that supports medical necessity for the procedure must be maintained in the client’s medical record and must indicate the following:

The client is moderate-to-high risk, as previously defined

As a candidate for prophylactic mastectomy, the client has undergone counseling from a health professional other than the operating surgeon. The counseling must include assessment of the following:

The client’s ability to understand the risks and long-term implications of the surgical procedure

The client’s informed choice to proceed with the surgical procedure

31.2.40.2.3Mastectomy for Gynecomastia

Surgery to correct gynecomastia is a benefit of the CSHCN Services Program for males who are 20 years of age or younger, when the criteria is met.

Procedure code 19300 may be reimbursed when billing for a mastectomy for pubertal gynecomastia.

31.2.40.2.4Breast Reconstruction

Breast reconstruction is a benefit of the CSHCN Services Program when performed to correct or repair abnormal structures of the breast caused by one or more of the following:

Mastectomy or a history of complications of mastectomy

Tumor or disease (e.g., following a primary mastectomy procedure in order to establish symmetry with a contralateral breast or following bilateral mastectomy)

Congenital defect

Developmental abnormality

Infection

Trauma or injury to the chest wall

Breast reconstruction may be performed using one of the following:

Implants (saline or silicone)

Tissue transfers, including, but not limited to:

Latissimus dorsi flap

Transverse rectus abdominis myocutaneous (TRAM) flap

Deep inferior epigastric perforator (DIEP) flap

Superficial inferior epigastric artery (SIEA) flap

Nipple or areola reconstruction

Reduction mammaplasty

Mastopexy

Tattooing to correct color defects of the skin

Treatment for complications of breast reconstruction

Breast reconstruction may be performed as single or multiple, staged procedures (e.g., tissue expansion followed by implants, nipple or areola reconstruction). Nipple-areola pigmentation, commonly known as medical tattooing, is the final stage of breast reconstruction surgery. All of the following criteria must be met for breast reconstruction following a medically necessary mastectomy.

The client is eligible for CSHCN Services Program at the time of the breast reconstruction.

The client has a documented history of a mastectomy.

The client meets age and gender criteria for the requested procedure.

The following procedure codes may be reimbursed for breast reconstruction:

Procedure Code

Client Gender and Ages

Limitation

11920

Male and female clients

Two procedures per lifetime

11921

Male and female clients

Two procedures per lifetime

11922

Male and female clients

Two procedures per lifetime

11970

Male and female clients

11971

Male and female clients

19316

Female clients

19318

Female clients

19325

Female clients

19340

Female clients

19342

Female clients

19350

Male and female clients

19355

Male and female clients

19357

Female clients

19361

Male and female clients

19364

Male and female clients

19367

Male and female clients

19368

Male and female clients

19369

Female clients

19396

Female clients

S2068

Male and female clients

Tattooing (procedure codes 11920, 11921, and 11922) is limited to clients with a documented history of a breast reconstruction performed while the client was eligible for the CSHCN Services Program.

Denied claims for tattooing may be appealed with supporting documentation stating the date of breast reconstruction.

Denied claims for breast reconstruction may be appealed with supporting documentation which includes the date of mastectomy.

31.2.40.2.5Excision or Destruction of Benign Lesions

The client must have a documented history of mastectomy or a history of complications of mastectomy performed while eligible for the CSHCN Services Program.

Documentation supporting medical necessity for treatment of a benign lesion, cyst, or lipoma must be maintained in the client’s medical record and identify that the lesion requiring treatment is one or more of the following:

Inflamed

Infected

Irritated

Bleeding

Increasing in size

Obstructing vision

Interfering with oral function

Located in an area that could affect motion or function

When a lesion is suspicious for malignancy, documentation supporting medical necessity for excision or destruction of the lesion must be maintained in the client’s medical record.

For blepharoplasty procedures (procedure codes 15820, 15821, 15822, and 15823) additional documentation of medical necessity must be submitted with both of the following:

Photographs of the eyelid problem

Visual field measurements

Excision or destruction of multiple lesions, cysts, or lipomas are reimbursed according to the multiple surgery payment guidelines. Initial or follow-up visits billed in addition to a lesion excision and/or destruction for the same diagnosis are subject to global surgery payment criteria.

Refer to: Section 31.2.39.6, “Global Fees” in this chapter and Section 31.2.39.7, “Multiple Surgeries” in this chapter for additional information about global surgery and multiple surgery fees.

31.2.40.2.6Treatment for Complications of Breast Reconstruction

The following procedure codes are benefits of the CSHCN Services Program for the treatment of complications of breast reconstruction:

 

Procedure Codes

19328*

19330*

19370*

19371*

19380

* A benefit for female clients only


Regardless of the client’s eligibility at the time of the original breast reconstruction, the treatment of complications is considered for reimbursement when medical criteria are met.

31.2.40.2.7Reduction Mammaplasty

Procedure code 19318 may be reimbursed with prior authorization for reduction mammaplasty. This procedure is limited to two per lifetime.

31.2.40.2.8External Breast Prostheses

External breast prostheses must be provided by a durable medical equipment (DME) provider to a female client with a history of a medically necessary mastectomy procedure.

External breast prostheses may be reimbursed if the client has a documented history of breast surgery in the past.

Refer to: Chapter 17, “Durable Medical Equipment (DME)” for breast prosthesis benefits and limitations.

31.2.40.3Prior Authorization and Authorization Requirements

All prior authorization and authorization requests must be submitted with documentation of medical necessity.

Prior authorization requests must be submitted using a CSHCN Services Program Authorization and Prior Authorization Request form. Prior authorization requests that do not contain required information are considered incomplete and will be denied. The requesting provider may be asked for additional information to clarify or support the authorization request.

Prior authorization requests for external breast prostheses must be submitted using the CSHCN Services Program Prior Authorization and Authorization Request for Durable Medical Equipment (DME) Form and Instructions.

Requests must include the physician’s original signature and the date signed. Stamped signatures and dates will not be accepted. Requests will be considered incomplete without this information.

Requests for DME quantities exceeding limitations must be prior authorized by the CSHCN medical director and must be submitted with documentation of medical necessity.

Procedure code 15828 requires prior authorization. All requests must be reviewed by the CSHCN Services Program Medical Director or designee.

31.2.40.4Prior Authorization and Authorization Requirements for Mastectomy, Breast Reconstruction, and External Prostheses

Prior authorization is not required when:

The client is 18 years of age or older, meets gender criteria and the procedure is a mastectomy or breast reconstruction, or

The client is 18 years of age or older, meets gender criteria, and the request is for one of the following external breast prosthesis procedure codes:

Procedure Codes

L8000

L8001

L8002

L8010

L8015

L8020

L8030

Partial mastectomy, procedure codes 19301 and 19302 are exceptions. Procedure codes 19301 and 19302 are eligible for reimbursement regardless of the client’s age, and therefore they do not require prior authorization.

Prior authorization is required for the following:

Mastectomy or breast reconstruction when the client does not meet criteria

Mastectomy for pubertal gynecomastia

Unlisted breast procedure code 19499

Tattooing for clients without an established history of breast reconstruction during eligibility for the CSHCN Services Program

External breast prosthesis procedure codes L8035 and L8039

31.2.40.4.1Mastectomy and Breast Reconstruction

Prior authorization for mastectomy, prophylactic mastectomy, or breast reconstruction is required for one or more of the following:

The client is 17 years of age or younger, or

The client does not meet the gender criteria for the requested procedure, as required by the CSHCN Services Program, or

The client does not have an established history of related services while eligible for the CSHCN Services Program.

Documentation for a mastectomy must be submitted for conditions, including but not limited to:

Developmental abnormality

Congenital defect

Trauma or injury to chest wall

Primary or secondary malignancy of the breast

Carcinoma in situ of the breast

31.2.40.4.2Breast Reconstruction

Documentation must be submitted which identifies one or more of the following:

Mastectomy or a history of complications of mastectomy

Tumor or disease (e.g., following a primary mastectomy procedure in order to establish symmetry with a contralateral breast or following bilateral mastectomy)

Congenital defect

Developmental abnormality

Infection

Trauma or injury to the chest wall

31.2.40.4.3Mastectomy for Gynecomastia

Prior authorization is required for procedure code 19300, which indicates mastectomy for pubertal gynecomastia. The following documentation must be submitted with all prior authorization requests:

Gynecomastia is classified as Grade II, III or IV per the American Society of Plastic Surgeons classification.

Puberty is at or near completion, as evidenced by documentation of the following:

95 percent of adult height based on bone age, and

Tanner stage V

Glandular breast tissue confirming true gynecomastia is documented on physical examination or mammography.

Hormonal causes, including hyperthyroidism, estrogen excess, prolactinomas and hypogonadism, have been excluded by appropriate laboratory testing. If present, hormonal causes must have been treated for at least one year and are resolved, as supported by appropriate laboratory test results.

Medical documentation must be submitted with a prior authorization request for a client that has used gynecomastia inducing drugs or other substances, when identified as the cause of gynecomastia. The documentation must indicate that the client has been off the drugs or other substances for a minimum of one year and must include the dates that the client has been off such substances.

Psychological and psycho-social effects which were identified in the pre-surgical history and physical.

Identification of left breast, right breast or both breasts, which require mastectomy.

31.2.40.4.4Reduction Mammaplasty

Prior authorization is required for procedure code 19318, which indicates reduction mammaplasty.

When requesting prior authorization for procedure code 19318, the following documentation must be submitted with all prior authorization requests:

Surgeons are required to include the following information documenting medical necessity when requesting prior authorization:

Client’s name and CSHCN Services Program client number,

Complete history and physical, including height, weight, and breast size

Description of functional debility caused by the condition

Preoperative photographs (both front and side views)

Description of past treatments and outcomes

Number of grams of tissue to be removed from each side

Requesting surgeon’s National Provider Identifier (NPI) number, and

Name and address of facility where services are to be performed and the provider’s NPI.

31.2.40.4.5Unlisted Procedure

Prior authorization is required for procedure code 19499, which indicates an unlisted breast procedure.

When requesting a prior authorization for procedure code 19499, the following documentation must be submitted to determine coverage:

A clear, concise description of the procedure to be performed

Reason for recommending this particular procedure

A CPT or HCPCS procedure code, which is comparable to the procedure being requested

Documentation this procedure is not investigational or experimental

Place of service the procedure is to be performed, and

The provider’s intended fee for this procedure.

Prior authorization requests must be submitted using a CSHCN Services Program Authorization and Prior Authorization Request form.

Prior authorization requests that do not contain the required information are considered incomplete and will be denied.

31.2.40.4.6Breast Prostheses

Prior authorization requests for external breast prostheses must be submitted using the CSHCN Services Program Prior Authorization and Authorization Request for Durable Medical Equipment (DME) Form and Instructions.

External breast prostheses of the same type will be considered for coverage at any time, through the prior authorization process, if it is lost, stolen, or irreparably damaged.

An external breast prosthesis that is a replacement or a different type will be considered for coverage at any time, through the prior authorization process, if the prosthesis is needed due to a change in the client’s medical condition.

Prior authorization is required for procedure codes L8035 and L8039 when the request is for new or replacement external breast prosthesis. The following documentation of medical necessity must be submitted with the prior authorization request:

The client’s diagnosis

Prior treatment for this diagnosis, and

Medical necessity of the requested prosthesis.

When requesting a prior authorization for procedure code L8039, the following additional information must also be submitted in order to determine coverage:

A clear, concise description of the prosthesis which is requested

Reason for recommending this particular prosthesis

A CPT or HCPCS procedure code, which is comparable to the prosthesis requested

Documentation that this prosthesis is not investigational or experimental

Provider’s place of service, and

The provider’s intended fee for this prosthesis.

31.2.40.5Documentation Requirements

In addition to documentation requirements outlined in the Prior Authorization and Authorization Requirements section, the following requirements apply:

All services are subject to retrospective review to ensure that the documentation in the client’s medical record supports the medical necessity of the service(s) provided, and

Services not supported by documentation are subject to recoupment.

31.2.40.6Reconstructive and Corrective Procedures (Not Related to Breast Therapies)

Reconstructive and corrective procedures are performed on structures of the body for any of the following purposes:

Improving or restoring bodily functions

Correcting significant deformity resulting from:

Disease

Trauma

Previous surgical procedure

Congenital or developmental anomalies

Excision or destruction of a benign lesion, cyst, or lipoma is a benefit only when the lesion is:

Inflamed

Infected

Irritated

Bleeding

Increasing in size

Obstructing vision

Interfering with oral function

Located in an area that could affect motion or function

Excision or destruction of a lesion may be a benefit when there is suspicion of malignancy.

The following procedure codes may be reimbursed for corrective procedures:

Procedure Codes

10040

11200

11201

11300

11301

11302

11303

11305

11306

11307

11308

11310

13111

11312

11313

11400

11401

11402

11403

11404

11406

11420

11421

11422

11423

11424

11426

11440

11441

11442

11443

11444

11446

11760

11762

11960

15781

15782

15783

15786

15787

15788

15789

15792

15793

15820

15821

15822

15823

15830

15847

17000

17003

17004

17106

17107

17108

17110

17111

17311

17312

17313

17314

17315

21555

21740

21742

21743

21930

21931

22900

22901

22902

22903

23071

23073

23075

23076

23077

23078

24071

24073

24075

24076

24077

24079

25075

26115

27043

27045

27047

27048

27049

27327

27328

27337

27339

27618

27619

27634

28039

28041

28043

28045

28313

40818

54660

The following procedure codes are add-on codes and must be billed with the appropriate primary procedure code, on the same day, by the same provider:

Add-on Procedure Codes

11201

15777

15787

15847

17003

17312

17314

17315

31.2.40.7Prior Authorization and Authorization for Corrective Procedures

31.2.40.7.1Oral Procedures

Procedures that are performed as part of cleft-craniofacial surgery require prior authorization.

Refer to: Section 31.2.39.11, “Cleft/Craniofacial Procedures” in this chapter for information about CSHCN Services Program cleft-craniofacial benefits and limitations.

31.2.40.7.2Dermatological and Blepharoplasty Procedures

Acne surgeries, dermabrasion, and chemical peel, and blepharoplasty procedures (procedure codes 10040, 15781, 15782, 15783, 15788, 15789, 15792, 15793, 15820, 15821, 15822, and 15823) require prior authorization, and must meet one of the following criteria:

Correction or repair of severe disfigurement due to disease or accidental injury (photographic documentation is required), or

Restoration of physical function resulting from disease or accidental injury (specific function must be detailed in prior authorization request).

31.2.40.7.3Panniculectomy and Abdominoplasty

Procedure codes 15830 and 15847 are benefits for panniculectomy and abdominoplasty procedures.

Panniculectomy and abdominoplasty procedures are limited to once per lifetime, by the same provider.

Panniculectomy and abdominoplasty procedure codes 15830 and 15847 require prior authorization. The following documentation supporting medical necessity must be submitted with all prior authorization requests:

Photographic documentation that the panniculus hangs below the level of the pubis,

The panniculus is the result of weight loss of at least 75 pounds that has been sustained for over one year, and

Documentation of one or more of the following conditions which directly impairs physical function:

Interference with ambulation, urination or other activities of daily living, or

Recurring persistent fungal and bacterial panniculitis that is refractory to good personal hygiene and documented optimal medical management including topical anti-infectives, and at least three systemic medication treatments.

31.2.40.7.4Noncovered Services

The following services are not a benefit of the CSHCN Services Program:

Alteration of a natural, undamaged, or unimpaired body part, except as specifically outlined in this chapter.

The following cosmetic procedures are not a benefit of the CSHCN Services Program:

Rhytidectomies (procedure codes 15824, 15825, 15826, and 15829)

Excisions of excessive skin and subcutaneous tissue (includes lipectomy) (procedure codes 15832, 15833, 15834, 15835, 15836, 15837, and 15839)

Suction assisted lipectomies (procedure codes 15877, 15878, and 15879)

Cryotherapy for acne (procedure code 17340)

Chemical exfoliation (procedure code 17360)

Electrolysis epilation (procedure code 17380)

31.2.40.8Rhizotomy

Rhizotomy for clients with spastic cerebral palsy is a benefit of the CSHCN Services Program.

Rhizotomies (procedure codes 63185 and 63190) must be prior authorized.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

CSHCN Services Program Prior Authorization Request for Inpatient Surgery—For Surgeons Only Form.

Rhizotomies are a benefit when submitted for reimbursement with one of the following diagnosis codes:

Diagnosis Codes

G800

G801

G802

G808

G809

G835

G8389

Documentation of whether or not the client has spastic cerebral palsy with no athetosis or fluctuations in muscle tone, but does have underlying muscle strength, must be included with the prior authorization request form.

Either electromyography or intraoperative neurophysiology testing is paid, but not both during the same procedure, when performed on the same day.

PT and occupational therapy (OT) are benefits up to three times a week (each) for a period of 1 year postoperatively.

31.2.40.9Septoplasty

Septoplasty (procedure code 30520) that is not related to the repair or reconstruction of a cleft lip, cleft palate, or craniofacial anomaly may be prior authorized with documentation to support medical necessity.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

CSHCN Services Program Prior Authorization Request for Inpatient Surgery—For Surgeons Only

CSHCN Services Program Prior Authorization and Authorization Request for Outpatient Surgery—For Outpatient Facilities and Surgeons

31.2.41Therapeutic Apheresis

Therapeutic apheresis does not require authorization.

Reimbursement for procedure codes 36511, 36512, 36513, 36514, and 36516 is limited to the following diagnosis codes:

Diagnosis Codes

C8800

C8801

C8820

C8821

C8830

C8831

C8880

C8881

C9000

C9002

C9010

C9012

C9020

C9022

C9030

C9032

C9100

C9102

C9110

C9112

C9130

C9132

C9140

C9142

C9150

C9152

C9160

C9162

C9190

C9192

C91A0

C91A2

C91Z0

C91Z2

C9200

C9202

C9210

C9220

C9230

C9232

C9240

C9242

C9250

C9252

C9260

C9262

C9290

C9292

C92A0

C92A2

C92Z0

C92Z2

C9300

C9302

C9310

C9312

C9330

C9332

C9390

C9392

C93Z0

C93Z2

C9400

C9402

C9420

C9422

C9430

C9432

C9440

C9442

C9480

C9482

C9500

C9502

C9510

C9512

C9590

C9592

D45

D472

D473

D474

D5700

D5701

D5702

D5703

D5704

D5709

D571

D5720

D57211

D57212

D57213

D57214

D57218

D57219

D5780

D57811

D57812

D57813

D57818

D57819

D588

D589

D590

D5910

D5911

D5912

D5913

D5919

D592

D5930

D5931

D5932

D5939

D594

D599

D6182

D65

D682

D68311

D688

D690

D691

D692

D693

D6941

D6942

D6949

D696

D698

D699

D72828

D740

D748

D749

D750

D751

D7589

D759

D761

D762

D763

D77

D890

D8940

D8941

D8942

D8943

D8949

D892

E0842

E0942

E1042

E1142

E7800

E7801

E7841

E7849

G603

G610

G6181

G6182

G6189

G620

G621

G622

G6281

G6282

G63

G64

G650

G7000

G7001

G731

I00

I010

I012

I018

I019

I773

I776

I7789

K716

K7200

K7201

K7581

K759

K760

K762

K7689

K77

L100

L101

L102

L103

L104

L105

L1081

L1089

L109

L900

L940

L941

L943

M05011

M05012

M05021

M05022

M05031

M05032

M05041

M05042

M05051

M05052

M05061

M05062

M05071

M05072

M0509

M05411

M05412

M05421

M05422

M05431

M05432

M05441

M05442

M05451

M05452

M05461

M05462

M05471

M05472

M0549

M05611

M05612

M05621

M05622

M05631

M05632

M05641

M05642

M05651

M05652

M05661

M05662

M05671

M05672

M0569

M069

M08011

M08012

M08021

M08022

M08031

M08032

M08041

M08042

M08051

M08052

M08061

M08062

M08071

M08072

M0809

M080A

M083

M08411

M08412

M08421

M08422

M08431

M08432

M08441

M08442

M08451

M08452

M08461

M08462

M08471

M08472

M0848

M084A

M08832

M08841

M08842

M08851

M08852

M08861

M08931

M08932

M08941

M08942

M08951

M08952

M08961

M08962

M089A

M310

M3110

M3111

M3119

M320

M3210

M3219

M328

M3300

M3301

M3302

M3309

M3310

M3311

M3312

M3319

M3320

M3321

M3322

M3329

M3390

M3391

M3392

M3399

M340

M341

M342

M3481

M3482

M3483

M3489

N000

N001

N002

N003

N004

N005

N006

N007

N008

N00A

N010

N011

N012

N013

N014

N015

N016

N017

N018

N01A

N02B1

N02B2

N02B3

N02B4

N02B5

N02B6

N02B9

N032

N034

N035

N037

N03A

N040

N0420

N0421

N0422

N0429

N044

N045

N046

N047

N048

N049

N04A

N052

N053

N054

N055

N056

N058

N059

N05A

N08

N171

N172

T8690

T8691

T8692

T8699

Other diagnoses may be considered upon appeal with documentation of medical necessity.

Therapeutic apheresis with extracorporeal affinity column adsorption and plasma reinfusion may be considered for reimbursement when billed for the low density lipoprotein (LDL) apheresis (such as Liposorber® LA 15) or the protein A immunoadsorption columns (such as Prosorba®).

Claims for apheresis services must be submitted with procedure codes 36511, 36512, 36513, 36514, and 36516, as appropriate.

Therapeutic apheresis requires direct supervision by a physician.

Procedure codes for therapeutic apheresis may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

31.2.42Transplants

31.2.42.1Renal (Kidney) Transplant

Renal transplants are a benefit for CSHCN Services Program clients when the projected costs of the transplant and follow-up care are less than the cost of continuing dialysis treatments. The estimated cost of the renal transplant over a 1-year period versus the cost of renal dialysis for 1 year at the requesting facility must be both documented and reviewed.

Clients who have not previously applied for Medicare and Kidney Health Care coverage and are anticipating the need for a renal transplant must apply for Medicare and Kidney Health Care coverage.

Renal transplants may only be considered for reimbursement when performed in a Medicaid-approved, CSHCN Services Program-enrolled transplant center facility, certified by the United Network of Organ Sharing (UNOS).

Refer to: Section 2.1.7, “Transplant Specialty Centers” in Chapter 2, “Provider Enrollment and Responsibilities.”

For any client who is 18 years of age or older, the transplant team must also provide a plan of care to be implemented after the client reaches 21 years of age and is no longer eligible for services through the CSHCN Services Program.

Renal transplants must be prior authorized, and approval is subject to the availability of funds. Only an initial and one subsequent renal transplant may be reimbursed for a client as a lifetime benefit.

Documentation supporting the prior authorization request must include the following:

The CSHCN Services Program Prior Authorization Request for Stem Cell or Renal Transplant form

A recent and complete history and physical

A statement of the client’s status including why a transplant is being recommended at this time

Documentation of the cost effectiveness of the transplant versus continued dialysis

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

Nationally, hospital stays for renal transplants are 5 to 10 days followed by outpatient follow-up; therefore, no additional hospital days beyond the 60 per year allowed by the CSHCN Services Program may be authorized without an appeal documenting medical necessity.

If the transplant is not prior authorized, services directly related to the transplant within 3 days preoperative and during the 6 weeks postoperative period are denied for the surgeon, assistant surgeon, or facility. The anesthesiologist may be reimbursed.

The following procedure codes must be used to bill for physician services related to the renal transplant:

Surgery and Assistant Surgery Procedure Codes

50300

50320

50323

50325

50327

50328

50329

50340

50360

50365

50370

50380

50547

Anesthesia Procedure Code

00868

Radiology Procedure Code

76776

Procedure codes 50323, 50325, 50327, 50328, and 50329 are payable under the organ recipient, and may only be reimbursed when procedure code 50360 or 50365 has been paid for the same date of service.

Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

Reimbursement for renal transplants includes the cost of the transplant services and one of the following:

The cost of procuring a cadaveric organ and services associated with procurement from an organ procurement organization (OPO) designated by the Secretary of Health and Human Services. Documentation validating the organ’s source must accompany the claim.

Donor costs for living donors. Donor costs must be included on the client’s inpatient hospital claim and may only be reimbursed if another source of payment is not available. Donor costs for CSHCN Services Program clients who also have Medicaid will not be reimbursed.

A maximum amount of $200,000 per client may be reimbursed for a transplant hospitalization. All hospital charges for patient care (inpatient hospital only) during the time of the hospital stay are applied to the $200,000 limit. Donor costs are included in this $200,000 limit.

Renal transplant recipients are eligible for follow-up care (outside the $200,000 limit) immediately following hospital discharge.

31.2.42.2Transplants - Nonsolid Organ

Stem cell transplants and post-transplantation cellular infusions must be performed in a Texas facility that is a designated children’s hospital or a facility in compliance with the criteria set forth by the Organ Procurement and Transplantation Network (OPTN), UNOS, or the National Marrow Donor Program (NMDP). TMHP maintains a current list of approved centers.

Refer to: Section 2.1.7, “Transplant Specialty Centers” in Chapter 2, “Provider Enrollment and Responsibilities.”

The following surgery procedure codes should be used to submit claims for reimbursement of transplantation and post-transplantation cellular infusion procedures:

Procedure Codes

38206

38230

38232

38240

38241

38242

38243

38999

S2142

Stem cell transplants and post-transplantation cellular infusions must be prior authorized. Prior authorization must be obtained by both the facility and the physician.

Providers may fax prior authorization requests to 1-512-514-4222.

Refer to: Section 4.4, “Prior Authorizations” in Chapter 4, “Prior Authorizations and Authorizations” for detailed information about prior authorization requirements.

CSHCN Services Program Prior Authorization Request for Stem Cell or Renal Transplant Form and Instructions.

The CSHCN Services Program does not authorize the following:

Experimental or investigational services, supplies, or procedures

Human leukocyte antigen (HLA)-typing of possible donors

The CSHCN Services Program may cover post-transplantation cellular infusions and only autologous and matched related and matched nonrelated allogenic transplants.

The CSHCN Services Program will recognize the following covered indications for allogenic stem cell transplants:

Bone marrow disorders

Hemoglobinopathies

Immunodeficiency disorders

Inherited metabolic disorders

Leukemias

Lymphomas

Multiple myeloma/plasma cell disorders

Platelet function disorder

The CSHCN Services Program will recognize the following covered indications for autologous stem cell transplants:

Brain tumors

Germ cell tumors

Leukemias

Lymphomas

Multiple myeloma/plasma cell disorders

Small round blue cell tumors of childhood

Indications for post-transplantation cellular infusions include the following:

Stem cell infusion for failure to graft (autologous)

Donor leukocyte infusion for persistent or relapsed malignant disease (allogenic)

Donor hematopoietic progenitor cell (HPC) boost infusion for relapse and post-transplantation cytopenias (allogenic)

Post-transplantation cellular infusions must be prior authorized separately with evidence of previous stem cell transplantation.

Stem cell transplants and post-transplantation cellular infusions may be considered for other conditions if documentation provides clinical evidence of the efficacy for the condition.

Coverage is limited to an initial transplant and one subsequent transplant, for a total of two transplants per lifetime regardless of payer. Indications for re-transplantation include the following:

Relapse of disease

Failure to engraft or poor graft function

Graft rejection

The subsequent transplant must be prior authorized separately from the initial transplant.

31.2.42.2.1Physician Reimbursement

Physicians may be reimbursed the lower of the billed amount or the amount allowed by Texas Medicaid.

If approved, a letter with the authorization number is sent to the physician (when applicable) and to the hospital where the procedure is to be performed. This authorization number must be placed in Block 23 of the CMS-1500 paper claim form.

Note:A benefit of up to 60 inpatient days may be granted to a client, to begin the date of an approved stem cell transplant. Any days remaining from the standard 60 inpatient day limit may be added to the 60 days for the transplant if the $200,000 limit for the transplant maximum amount has not been exceeded. Donor costs must be included on the client’s inpatient hospital claim for the transplant and are included in the $200,000 limit for the transplant maximum amount. If prior authorization is received for a second stem cell transplant after a client has already received an initial transplant, an additional benefit of up to 60 inpatient days may be reimbursed for an additional maximum amount of $200,000, beginning with the actual first day of the second transplant.

31.2.43Wound Care Management

Wound care management includes first- and second-line therapies.

The following services are not a benefit of the CSHCN Services Program:

Infrared therapy

Ultraviolet therapy

Topical hyperbaric oxygen therapy

Low-energy ultrasound wound cleanser (MIST therapy)

Services that are submitted as debridement but do not include the removal of devitalized tissue. Examples include removal of non-tissue integrated fibrin exudates, crusts, biofilms, or other materials from a wound, without the removal of tissue.

Electrical stimulation and electromagnetic therapy

More than 10 applications of skin substitute grafts per episode of wound care in a 12- week period of care per rolling year, which will begin on the first day of the first skin substitute application

Separately billed repeated use of the skin substitute product after 12 weeks for a single wound or episode

Skin substitute grafting for partial thickness loss with the retention of epithelial appendages as epithelium will repopulate the deficit from the appendages, negating the benefit of over grafting

Skin substitute products not billed concurrently with procedure codes 15271, 15272, 15273, 15274, 15275, 15276, 15277, and 15278 are not separately reimbursed.

31.2.43.1First-Line Wound Care Therapy

First-line wound care therapy includes the following:

Cleaning, antibiotics, and pressure off-loading

Compression

Debridement

Dressings may include wet and dry dressings (Dressings applied to the wound are considered part of the service for wound debridement)

Whirlpool for burns

31.2.43.1.1Compression

Compression therapy is an important component in the standard of care for treatment of venous ulcers. An Unna boot may be used as part of compression therapy to promote healing, control edema, increase blood return to the heart, and reduce infection. Compression or off-loading performed as part of wound care management may be reimbursed when billed with procedure codes 29445, 29580, or 29581.

31.2.43.1.2Debridement

Selective debridement consists of the following:

Conservative sharp debridement

High-pressure lavage to selected areas

Non-selective debridement consists of the following:

Autolytic debridement

Blunt debridement

Enzymatic debridement

Hydrotherapy and wound immersion

Mechanical debridement

The following procedure codes are a benefit for wound debridement:

Procedure Codes

11000

11001

11042

11043

11044

11045

11046

11047

16020

16025

16030

97597

97598

97602

The procedure code submitted on the claim must reflect the level of debrided tissue, e.g., partial-thickness skin, full-thickness skin, subcutaneous tissue, muscle, and/or bone, and not the extent, depth, or grade of the ulcer or wound.

Wound debridement procedure codes 11042, 11043, 11044, 11045, 11046, and 11047 are not appropriate and will not be approved for the following:

Washing bacteria or fungal debris from the feet

Paring or cutting of corns or calluses

Incision and drainage of an abscess

Trimming or debridement of nails, or avulsion of nail plates

Acne surgery

Destruction of warts

Burn debridement

31.2.43.2Second-Line Wound Care Therapy

Second-line wound care therapy is limited to chronic Stage 3 or 4 wounds and is a benefit only after first-line therapy has been tried for at least 30 days without measurable signs of improved healing. First-line wound care therapy may continue as appropriate, with the addition of second-line wound care measures as indicated by the client’s medical condition. Second-line wound care therapy includes the following:

Application of metabolically active skin equivalents/skin substitutes

Pulsatile jet irrigation

Whirpool

31.2.43.2.1Pulsatile-Jet Irrigation

Pulsatile-jet irrigation is a benefit for the treatment of Stage 3 or 4 wounds when other forms of treatment have failed. To cleanse a wound bed, pulsatile-jet irrigation uses lavage, which increases impaired circulation and removal of waste from the lymphatic system. Removal of devitalized tissue using pulsatile-jet irrigation may be reimbursed when claims are submitted for procedure code 97597 or 97598.

Professional services for selective wound debridement (procedure codes 97597 and 97598) may also be reimbursed to a licensed physical therapist or physical therapy group when the service is determined to be within the provider’s scope of practice and the service is prescribed by a supervising physician or qualified non-physician provider who is enrolled in the CSHCN Services Program.

31.2.43.2.2Application of Metabolically Active Skin Equivalents and Wound Preparation

Metabolically active skin equivalents/skin substitutes may be a benefit when provided in accordance with the material’s Food and Drug Administration (FDA) approved package label and applied according to the manufacturer’s instructions for use. Skin substitutes are used for partial- or full- thickness wounds, which do not involve tendon, muscle, joint capsule, or exposed bone or sinus tracts, and are applied to wounds that have demonstrated failed or insufficient response to conservative wound care measures.

The application of skin substitutes may be a benefit for the treatment of chronic Stage 3 or 4 wounds that have failed to respond to standard wound care treatment after 30 days. A failed response is defined as a wound that has increased in size or depth, or has not changed in baseline size or depth, and shows no measurable signs of healing improvements after 30 days of appropriate wound-care measures.

Use of the appropriate specific skin substitute product(s) for the episode of each documented wound is expected. Compliance with the Food and Drug Administration (FDA) assessments and submitted guidelines for the specific skin substitute product(s) used is expected.

Wound care services that include the use of skin substitutes must be provided in accordance with the FDA-approved package label and applied according to the manufacturer’s instructions for use. Skin substitute products not used within the scope of the FDA’s intended use and indications are considered experimental and or investigational.

Procedure codes 15271, 15272, 15273, 15274, 15275, 15276, 15277, and 15278 are a benefit for the application of skin substitute grafts.

Procedure codes 15002, 15003, 15004, 15005, 15040, and 15050 are a benefit for surgical wound preparation.

31.2.43.3Documentation Requirements

For all wound care management services, documentation that supports the medical necessity of the service must be maintained in the client’s medical records, including the following information:

Accurate diagnostic information that pertains to the underlying diagnosis and condition as well as any other medical diagnoses and conditions, which include the client’s overall health status.

Appropriate medical history related to the current wound, including the following:

Wound location

Wound measurements, which includes length, width, and depth, any tunneling and/or undermining

Wound color, drainage (type and amount), and odor, if present

The prescribed wound care regimen, which includes frequency, duration, and supplies needed

Treatment for infection, if present

All previous wound care therapy regimens, if appropriate

The client’s use of a pressure reducing support surface, mattress, and/or cushion, when appropriate

Documentation maintained in the client’s medical record must support the level of debridement service provided.

Fewer than five surgical debridements that involve removal of muscle or bone are typically required for management of most wounds. Documentation that is maintained in the client’s medical record must support the number of debridements involving muscle or bone that are performed.

All wound care management services are subject to retrospective review.

All wound treatments involving the application of skin substitutes must include, but are not limited to, documentation of the following:

Wound treatments are accompanied by the appropriate adjunctive measures, and identify the specific adjunctive therapies being provided to the client as part of the wound treatment regimen.

All wounds must be free of infection, necrotic tissue, or exudate and any underlying conditions that compromise wound healing. The documentation in the client’s record must reflect the conditions have been treated and resolved.

Clients who use tobacco will have ceased smoking or have refrained from systemic tobacco intake for at least 4 weeks prior to beginning skin substitute applications and during the conservative wound care.

Adequate circulation/oxygenation to support tissue growth/wound healing must be present as evidenced by physical examination (e.g., Ankle-Brachial Index [ABI] of no less than 0.60, toe pressure greater than 30 millimeters of mercury [mmHg]).

The wound has a skin deficit at least 1.0 square centimeter in size.

For diabetic foot ulcers, the client’s medical record reflects a diagnosis of Type 1 or Type 2 diabetes. Partial or full thickness ulcers must have a clean granular base without tendon and or muscle involvement, bone exposure, or sinus tracts.

Documentation of the wound’s response to the treatment is required at least every 30 days for each treatment episode. The documentation requirements must include measurements of the initial wound, measurements at the completion of appropriate wound care every 30 days, and measurements immediately prior to placement and with each subsequent placement of the skin substitute.

Documentation maintained in the client’s medical record must support the need for skin substitute applications and the product used.

31.3Claims Information

To avoid claim denials, providers billing as a group must use the performing provider identifier number on their claims.

Physician services must be submitted to TMHP in an approved electronic format or on the CMS-1500 paper claim form. Providers may purchase CMS-1500 paper claim forms from the vendor of their choice. TMHP does not supply the forms.

When completing a CMS-1500 paper claim form, all required information must be included on the claim, as TMHP does not key any information from claim attachments. Superbills, or itemized statements, are not accepted as claim supplements.

Physicians who submit a claim using the physician’s own provider identifier for services provided by an APRN or physician assistant must submit one of the following modifiers on each claim detail if the physician does not make a decision regarding the client’s care or treatment on the same date of service as the billable medical visit:

SA - Services were provided by an APRN

U7 - Services were provided by a physician assistant

The HCPCS/CPT codes included in policy are subject to NCCI relationships. Exceptions to NCCI code relationships that may be noted in CSHCN Services Program medical policy are no longer valid. Providers should refer to the CMS NCCI web page for correct coding guidelines and specific applicable code combinations. In instances when CSHCN Services Program medical policy quantity limitations are more restrictive than NCCI Medically Unlikely Edits (MUE) guidance, medical policy prevails.

Refer to: Chapter 41, “TMHP Electronic Data Interchange (EDI)” for information about electronic claims submissions.

Chapter 5, “Claims Filing, Third-Party Resources, and Reimbursement” for general information about claims filing.

Section 5.7.2.4, “CMS-1500 Paper Claim Form Instructions” in Chapter 5, “Claims Filing, Third-Party Resources, and Reimbursement” for instructions on completing paper claims. Blocks that are not referenced are not required for processing by TMHP and may be left blank.

31.3.1General Medical Record Documentation Requirements

The CSHCN Services Program routinely performs a retrospective review of all providers. This review may include comparing services billed to the client’s medical record. The provider must document the following information in the client’s medical record:

Service

Date the service was rendered

Any pertinent information about the client’s condition that supports the need for the service

Care provided

Note:If a provider bills for an office visit, the client’s medical record must contain documentation for that date of service about the client’s complaint, physician’s findings, and any physician orders. If the visit is a follow-up office visit, the client’s progress relating to the previous condition must be documented for the date of service billed. If billing for a hospital visit, whether it is a routine hospital visit or other type of hospital visit, documentation of that visit must be part of the client’s medical record and must be written in the physician’s orders or the client’s progress notes.

The following are general requirements for all providers. Mandatory requirements not present in the client’s medical record subject the associated services to recoupment.

Note:This list is not all-inclusive. Additional and more specific requirements may apply to special services areas.

Requirement

Mandatory/Desirable

All entries are legible to individuals other than the author, dated (month, day, and year), and signed by the performing provider.

Mandatory

Each page of the medical record documents the client’s name and CSHCN Services Program identification number.

Mandatory

Allergies and adverse reactions (including immunization reactions) are prominently noted in the record.

Mandatory

The selection of E/M codes (levels of service) is supported by the client’s clinical record documentation. The AMA’s CPT descriptors of key/contributory components with level of service descriptions are used to evaluate the selection of levels of service.

Mandatory

Necessary follow-up visits specify the time of return by at least the week or month.

Mandatory

The history and physical documents the presenting complaint with appropriate subjective and objective information, e.g., medical and surgical history, current medications and supplements, family history, social history, diet, pertinent physical examination measurements and findings, etc.

Mandatory

The services provided are clearly documented in the medical record with all pertinent information about the client’s condition to substantiate the need for the services.

Mandatory

Medically necessary diagnostic lab and X-ray results are included in the medical record and abnormal findings have an explicit notation of follow-up plans.

Mandatory

Unresolved problems are noted in the record.

Mandatory

Immunizations are noted in the record as complete or up-to-date.

Mandatory

Personal data includes address, employer, home/work telephone numbers, sex, marital status, and emergency contacts.

Desirable

31.4Reimbursement

Physicians may be reimbursed for most physician services according to the Texas Medicaid Reimbursement Methodology (TMRM).

Physicians may be reimbursed 92 percent of the established reimbursement rate for services provided by an APRN or physician assistant if the physician does not make a decision regarding the client’s care or treatment on the same date of service as the billable medical visit. The 92 percent reimbursement rate will not apply to laboratory services, radiology services, and injections provided by an APRN or physician assistant.

For fee information, providers can refer to the Online Fee Lookup (OFL) on the TMHP website at www.tmhp.com.

The CSHCN Services Program implemented rate reductions for certain services. The OFL includes a column titled “Adjusted Fee” to display the individual fees with all percentage reductions applied. Additional information about rate changes is available on the TMHP website at www.tmhp.com/resources/rate-and-code-updates/rate-changes.

Note:Certain rate reductions including, but not limited to, reductions by place of service, client type program, or provider specialty may not be reflected in the Adjusted Fee column.

Refer to: Section 31.2.5, “Anesthesia Services” in this chapter for more information about anesthesia services that may be reimbursed according to relative value units (RVUs).

31.4.1Physician Services in Outpatient Hospital Setting

31.4.1.1Reimbursement Reduction

Nonemergent and nonurgent services provided by physician providers in an outpatient setting (POS 5) may be reimbursed at 60 percent of the allowed amount. The 40 percent reduction in reimbursement will be based upon the emergency department service that is submitted on the claim.

Note:Rural hospital outpatient imaging services may be reimbursed at 65 percent of the allowed amount for nonemergent services provided by physician providers in an outpatient setting (POS 5).

31.5TMHP-CSHCN Services Program Contact Center

The TMHP-CSHCN Services Program Contact Center at 1-800-568-2413 is available Monday through Friday from 7 a.m. to 7 p.m., Central Time, and is the main point of contact for the CSHCN Services Program provider community.