Arkansas Administrative Code
Agency 016 - DEPARTMENT OF HUMAN SERVICES
Division 06 - Medical Services
Rule 016.06.16-001 - Notice of Rule Making 002-15 (CPT) and 003-15 (HCPCS) Conversion Notices

Universal Citation: AR Admin Rules 016.06.16-001

Current through Register Vol. 49, No. 9, September, 2024

I. General Information

A review of the 2015 HCPCS procedure codes has been completed and the Arkansas Medicaid Program will begin accepting updated Healthcare Common Procedural Coding System Level II (HCPCS) procedure codes on claims with dates of service on and after December 18, 2015. Drug procedure codes require National Drug Code (NDC) billing protocol. Drug procedure codes that represent radiopharmaceuticals, vaccines and allergen immunotherapy are exempt from the NDC billing protocol.

Procedure codes that are identified as deletions in 2015 HCPCS Level II will become non-payable for dates of service on and after December 18, 2015.

Please NOTE: The Arkansas Medicaid website fee schedules will be updated soon after the implementation of the 2015 CPT and HCPCS conversions.

II. 2015 HCPCS Payable Procedure Codes Tables Information

Procedure codes are in separate tables. Tables are created for each affected provider type (i.e., prosthetics, home health, etc.).

The tables of payable procedure codes for all affected programs are designed with eight columns of information. All columns may not be applicable for each covered program, but are devised for ease of reference.

Please NOTE: An asterisk indicates that the procedure code requires a paper claim.

1. The first column of the list contains the HCPCS procedure codes. The procedure code may be on multiple lines on the table, depending on the applicable modifier(s) based on the service performed.

2. The second column indicates any modifiers that must be used in conjunction with the procedure code, when billed, either electronically or on paper.

3. The third column indicates that the coverage of the procedure code is restricted based on the beneficiary's age in number of years.

4. Certain procedure codes are covered only when the primary diagnosis is covered within a specific ICD diagnosis range. This information is used, for example, by physicians and hospitals. The fourth column, for all affected programs, indicates the beginning and ending range of ICD CM diagnoses for which a procedure code may be used.

5. The fifth column contains information about the diagnosis list for which a procedure code may be used. (See Section V of this notice for more information about diagnosis range and lists.)

6. The sixth column indicates whether a procedure is subject to medical review before payment. The column is titled "Review." The word "Yes" or "No" in the column indicates whether a review is necessary or not. Providers should consult their program manual to obtain the information that is needed for a review.

7. The seventh column shows procedure codes that require prior authorization (PA) before the service may be provided. The column is titled "PA." The word "Yes" or "No" in the column indicates if a procedure code requires prior authorization. Providers should consult their program manual to ascertain what information should be provided for the prior authorization process.

8. The eighth column indicates a procedure code requires a prior approval letter from the Arkansas Medicaid Medical Director for Clinical Affairs for the Division of Medical Services. The word "Yes" or "No" in the column indicates if a procedure code requires a prior approval letter.

III. Acquisition of Prior Approval Letter

A prior approval letter, when required, must be attached to a paper claim when it is filed. Providers must obtain prior approval in accordance with the following procedures for special pharmacy, therapeutic agents and treatments:

A. Process for Acquisition: Before treatment begins, the Medical Director for Clinical Affairs in the Division of Medical Services (DMS) must approve any drug, therapeutic agent or treatment not listed as covered in a provider manual or in official DMS correspondence. This requirement also applies to any drug, therapeutic agent or treatment with a prior approval letter indicated for coverage in a provider manual or official DMS correspondence.

B. The Medical Director for Clinical Affairs' review is necessary to ensure approval for medical necessity. Additionally, all other requirements must be met for reimbursement.
1. The provider must submit a history and physical examination with the treatment plan before beginning any treatment.

2. The provider will be notified by mail of the DMS Medical Director for Clinical Affairs' decision. No prior authorization number is assigned if the request is approved, but a prior approval letter is issued and must be attached to each paper claim submission.

Any change in approved treatment requires resubmission and a new prior approval letter.

3. Requests for a prior approval letter must be addressed to the attention of the Medical Director for Clinical Affairs. Contact the Medical Director for Clinical Affairs' office for any additional coverage information and instructions.

Mailing address:

Attention:

Arkansas Medicaid Medical Director for Clinical Affairs

1020 West 4th Street, Suite 300

Little Rock, AR 72201

Fax: 501-212-8741 Phone: 501-212-8663

IV. Process for Obtaining Prior Authorization

When obtaining a prior authorization from the Arkansas Foundation for Medical Care, please send your request to the following:

In-state and out-of-state toll free for inpatient reviews, prior authorizations for surgical procedures and assistant surgeons only

1-800-426-2234

General telephone contact, local or long distance - Fort Smith

(479) 649-8501 1-877-650 -2362

Fax for CHMS only

(479) 649-0776

Fax for Molecular Pathology only

(479) 649-9413

Fax

(479) 649-0799

Web portal

http://review.afmc.org/MedicaidReview/iEXCHANGE%c2%ae.aspx

Mailing address

Arkansas Foundation for Medical Care, Inc.

P.O. Box 180001

Fort Smith, AR 72918-0001

Physical site location

5111 Rogers Avenue, Suite 476 Fort Smith, AR 72903

Office hours

8:00 a.m. until 4:30 p.m. (Central Time), Monday through Friday, except holidays

V. International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM), Diagnosis Range and Diagnosis Lists

Diagnosis is documented using the International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM). Certain procedure codes are covered only for a specific primary diagnosis or a particular diagnosis range. Diagnosis list 103 is specified here (View ICD Codes.). For any other diagnosis restrictions, reference the table for each individual program.

VI. Dental

The following 2015 ADA Dental procedure codes are not covered by Arkansas Medicaid.

D0171

D0351

D1353

D6110

D6111

D6112

D6113

D6114

D6115

D6116

D6117

D6549

D9219

D9931

D9986

D9987

VII. HCPCS Procedure Codes Payable to End-Stage Renal Disease Providers

The following information is related to procedure codes payable to End-Stage Renal Disease providers:

Procedure Code

Modifier

Age Restriction

Diagnosis Diagnosis List

Review

PA

Prior

Approval

Letter

J0887

No

21y & up

Yes; see No

No

No

No

NOTE: The primary diagnosis should be (View ICD Codes.) with a secondary diagnosis of (View ICD Codes.). For patients with CKD on dialysis:

* Initiate Mircera treatment when the hemoglobin level is less than 10 g/dL.

* If the hemoglobin level approaches or exceeds 11 g/dL, reduce or interrupt the dose of Mircera.

* The recommended starting dose of Mircera for the treatment of anemia in adult CKD patients who are not currently treated with an ESA is 0.6 mcg/kg body weight administered as a single IV or SC injection once every two weeks. The IV route is recommended for patients receiving hemodialysis because the IV route may be less immunogenic.

* Once the hemoglobin has been stabilized, Mircera may be administered once monthly using a dose that is twice that of the every-two-week dose and subsequently titrated as necessary.

J0888

No

21y & up

View ICD No Codes.

No

No

No

NOTE: For patients with CKD not on dialysis:

* Consider initiating Mircera treatment only when the hemoglobin level is less than 10 g/dL and the following considerations apply:

* The rate of hemoglobin decline indicates the likelihood of requiring an RBC transfusion, and

* Reducing the risk of alloimmunization and/or other RBC transfusion-related risks is a goal.

* If the hemoglobin level exceeds 10 g/dL, reduce or interrupt the dose of Mircera and use the lowest dose of Mircera sufficient to reduce the need for RBC transfusions.

VIII. HCPCS Procedure Codes Payable to Home Health Providers

The following information is related to procedure codes payable to Home Health providers.

Procedure Code

Modifier

Age Restriction

Diagnosis Diagnosis List

Review

PA

Prior

Approval

Letter

J0887

No

21y & up

Yes; see No below

No

No

No

NOTE: The primary diagnosis should be (View ICD Codes.) with a secondary diagnosis of (View ICD Codes.). For patients with CKD on dialysis:

* Initiate Mircera treatment when the hemoglobin level is less than 10 g/dL.

* If the hemoglobin level approaches or exceeds 11 g/dL, reduce or interrupt the dose of Mircera.

* The recommended starting dose of Mircera for the treatment of anemia in adult CKD patients who are not currently treated with an ESA is 0.6 mcg/kg body weight administered as a single IV or SC injection once every two weeks. The IV route is recommended for patients receiving hemodialysis because the IV route may be less immunogenic.

* Once the hemoglobin has been stabilized, Mircera may be administered once monthly using a dose that is twice that of the every-two-week dose and subsequently titrated as necessary.

J0888

No

21y & up

View ICDNo Codes.

No

No

No

NOTE: For patients with CKD not on dialysis:

* Consider initiating Mircera treatment only when the hemoglobin level is less than 10 g/dL and the following considerations apply:

* The rate of hemoglobin decline indicates the likelihood of requiring an RBC transfusion, and

* Reducing the risk of alloimmunization and/or other RBC transfusion-related risks is a goal.

* If the hemoglobin level exceeds 10 g/dL, reduce or interrupt the dose of Mircera and use the lowest dose of Mircera sufficient to reduce the need for RBC transfusions.

IX. HCPCS Procedure Codes Payable to Hospitals

The following information is related to procedure codes payable to Hospital providers:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

C9025 C9026

No No

18y & up 18y & up

No

View ICD Codes.

103 No

No Yes

No No

No Yes

NOTE: Entyvio is an integrin receptor antagonist for adult ulcerative colitis (UC). For adults with UC it must be moderately to severely active and have had an inadequate response with, or lost response to, or were intolerant to a tumor necrosis factor (TNF) blocker or immunomodulator, or had an inadequate response with, were intolerant to, or demonstrated dependence on corticosteroids:

1) inducing and maintaining clinical response;

2) inducing and maintaining clinical remission;

3) improving endoscopic appearance of the mucosa; or

4) achieving corticosteroid-free remission. Patient must have tried and failed Enbrel, Humiraand Cimzia. For adults with Crohn's disease, it must be moderately to severely active with an inadequate response with, lost response to, or were intolerant to a TNF blocker or immunomodulator, or had an inadequate response with, were intolerant to, or demonstrated dependence on corticosteroids:

1) achieving clinical response;

2) achieving clinical remission; or

3) achieving corticosteroid-free remission. Patient must have tried and failed Enbrel, Humiraand Cimzia. Physician must submit a history and physical exam with the Prior Approval Letter to the Medical Director for Clinical Affairs.

C9027

No

18y & up

Yes

103

Yes

No

Yes

NOTE: Keytruda is a human programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of patients with unresectable or metastatic melanoma (View ICD Codes.) and disease progression following ipilimumab and, if BRAF V600 mutation positive, a BRAF inhibitor, in adult patients. The maximum dose is 2mg/kg. There will not be approvals for over this dose. If the patient is on high dose corticosteroids, Keytruda should be discontinued. If the patient has disease progression, Keytruda should be discontinued. Medical records documenting a history and physical exam showing use of ipilimumab first or a BRAF inhibitor should be forwarded to the Medical Director for Clinical Affairs. The patient should have a prognosis of 6 months. All treatments should be included in the medical records. Prior surgeries or other chemotherapeutics should be documented. A letter of Prior Approval will be approved for the length of treatment.

C9136

No

No

View ICD Codes.

No

No

No

No

C9349

No

No

No

No

No

No

No

C9442

No

18y & up

View ICD Codes.

No

Yes

No

Yes

NOTE: Beleodaqis a histone decacetylase inhibitor indicated for the treatment of adult patients with relapsed or refractory peripheral T-cell lymphoma (PTCL). All previous treatments should be documented. A complete history and physical exam documenting previous treatments and results should be submitted to the Medical Director for Clinical Affairs for a Prior Approval letter. Length of treatment should be specified.

C9443 No 18y & up

No

No

No

No

No

C9444 No 18y & up

No

No

No

No

No

C9446 No 18y & up

No

No

No

No

No

C9739 No No

No

No

No

No

No

NOTE: Covered for males only.

C9740 No No

No

No

No

No

No

NOTE: Covered for males only.

G6015 No No

No

No

No

No

No

J0153 No No

No

No

No

No

No

J0887 No 21y & up

Yes; see

No

No

No

No

NOTE: The primary diagnosis should be (View ICD Codes.) with a secondary diagnosis of (View ICD Codes.). For patients with CKD on dialysis:

* Initiate Mircera treatment when the hemoglobin level is less than 10 g/dL.

* If the hemoglobin level approaches or exceeds 11 g/dL, reduce or interrupt the dose of Mircera.

* The recommended starting dose of Mircera for the treatment of anemia in adult CKD patients who are not currently treated with an ESA is 0.6 mcg/kg body weight administered as a single IV or SC injection once every two weeks. The IV route is recommended for patients receiving hemodialysis because the IV route may be less immunogenic.

* Once the hemoglobin has been stabilized, Mircera may be administered once monthly using a dose that is twice that of the every-two-week dose and subsequently titrated as necessary.

Procedure Code

Modifier Age

Restriction

Diagnosis

Diagnosis List

Review PA

Prior

Approval

Letter

J0888

No 21y & up

View ICD Codes.

No

No No

No

NOTE: For patients with CKD not on dialysis:

* Consider initiating Mircera treatment only when the hemoglobin level is less than 10 g/dL and the following considerations apply:

* The rate of hemoglobin decline indicates the likelihood of requiring an RBC transfusion, and

* Reducing the risk of alloimmunization and/or other RBC transfusion-related risks is a goal.

* If the hemoglobin level exceeds 10 g/dL, reduce or interrupt the dose of Mircera and use the lowest dose of Mircera sufficient to reduce the need for RBC transfusions.

J1071 No

No

No

View ICD Codes.

No

No

No

J1439 No

18y & up

View ICD Codes.

No

No

No

No

J2274 No

No

No

No

No

No

No

J2704 No

3y & up

No

No

No

No

No

J3121 No

No

No

103

No

No

No

NOTE: Covered for males only.

J3145 No

No

No

103

No

No

No

NOTE: Covered for males only.

J7181 No

No

View ICD Codes.

No

No

No

No

J7201 No

No

No

No

No

No

No

J7327 No

18y & up

No

No

No

Yes

No

NOTE: Prior authorization is required for coverage of the Hyaluronon injection in the physician's office for procedure codes J7321, J7323, J7324, J7325 and J7327. Providers must specify the brand name of Hyaluronon (sodium hyaluronate) or derivative when requesting prior authorization for this procedure code. A written request must be submitted to the Division of Medical Services Utilization Review Section. Refer to the Utilization Review prior authorization information in the provider manual. The request must include the patient's name, Medicaid ID number, physician's name, physician's Arkansas Medicaid provider identification number, patient's date of birth and medical records that document the severity of osteoarthritis, previous treatments and site of injection. Hyaluronon is limited to one injection or series of injections per knee, per beneficiary, per lifetime.

J9267

No

No

No

103

No

No

No

J9301

No

18y &up

View ICD Codes.

No

Yes

No

Yes

NOTE: Gazyvais a CD-20 directed cytolytic antibody and is indicated, in combinations witii ciilorambucil, fertile treatment of adult patients with previously untreated chronic lymphocytic leukemia. Patients should have a protocol with chlorambucil and a history and physical exam covering all treatments including failures to submit to the Medical Director for Clinical Affairs for a Prior Approval Letter. Dates of Service need to be included.

Q4150

No

No

No

No

No

No

No

Q4152

No

No

No

No

No

No

No

Q4157

No

No

No

No

No

No

No

Q4160

No

No

No

No

No

No

No

X. HCPCS Procedure Codes Payable to Independent Radiology

The following information is related to procedure codes payable to Independent Radiology providers:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

G6015

No

No

No

No

No

No

No

XI. HCPCS Procedure Codes Payable to Nurse Practitioners

The following information is related to procedure codes payable to Nurse Practitioner providers:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

G6015 J0887

No No

No

21y & up

No Yes; see

No No

No No

No No

No No

NOTE: The primary diagnosis should be (View ICD Codes.) with a secondary diagnosis of (View ICD Codes.). For patients with CKD on dialysis:

* Initiate Mircera treatment when the hemoglobin level is less than 10 g/dL.

* If the hemoglobin level approaches or exceeds 11 g/dL, reduce or interrupt the dose of Mircera.

* The recommended starting dose of Mircera for the treatment of anemia in adult CKD patients who are not currently treated with an ESA is 0.6 mcg/kg body weight administered as a single IV or SC injection once every two weeks. The IV route is recommended for patients receiving hemodialysis because the IV route may be less immunogenic.

* Once the hemoglobin has been stabilized, Mircera may be administered once monthly using a dose that is twice that of the every-two-week dose and subsequently titrated as necessary.

J0888

No

21y & up

View ICD Codes.

No

No

No

No

NOTE: For patients with CKD not on dialysis:

* Consider initiating Mircera treatment only when the hemoglobin level is less than 1 g/dL and the following considerations apply:

* The rate of hemoglobin decline indicates the likelihood of requiring an RBC transfusion, and

* Reducing the risk of alloimmunization and/or other RBC transfusion-related risks is a goal.

* If the hemoglobin level exceeds 10 g/dL, reduce or interrupt the dose of Mircera and use the lowest dose of Mircera sufficient to reduce the need for RBC transfusions.

J3121

No

No

No

103

No

No

No

NOTE: Covered for males only.

J3145

No

No

No

103

No

No

No

NOTE: Covered for males only.

J9267

No

No

No

103

No

No

No

XII. HCPCS Procedure Codes Payable to Physicians and Area Health Education Centers (AHECs)

The following information is related to procedure codes payable to Physician and AHEC providers:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

C9025 C9026

No No

18y & up 18y & up

No

View ICD Codes.

103 No

No Yes

No No

No Yes

NOTE: Entyvio is an integrin receptor antagonist for adult ulcerative colitis (UC). For adults with UC it must be moderately to severely active and have had an inadequate response with, or lost response to, or were intolerant to a tumor necrosis factor (TNF) blocker or immunomodulator, or had an inadequate response with, were intolerant to, or demonstrated dependence on corticosteroids:

1) inducing and maintaining clinical response;

2) inducing and maintaining clinical remission;

3) improving endoscopic appearance of the mucosa; or

4) achieving corticosteroid-free remission. Patient must have tried and failed Enbrel, Humira and Cimzia. For adults with Crohn's disease, it must be moderately to severely active with an inadequate response with, lost response to, or were intolerant to a TNF blocker or immunomodulator, or had an inadequate response with, were intolerant to, or demonstrated dependence on corticosteroids:

1) achieving clinical response;

2) achieving clinical remission; or

3) achieving corticosteroid-free remission. Patient must have tried and failed Enbrel, Humira and Cimzia. Physician must submit a history and physical exam with the Prior Approval Letter to the Medical Director for Clinical Affairs.

C9027

No

18y & up

Yes

103

Yes

No

Yes

NOTE: Keytruda is a human programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of patients with unresectable or metastatic melanoma (View ICD Codes.) and disease progression following ipilimumab and, if BRAF V600 mutation positive, a BRAF inhibitor, in adult patients. The maximum dose is 2mg/kg. There will not be approvals for over this dose. If the patient is on high dose corticosteroids, Keytruda should be discontinued. If the patient has disease progression, Keytruda should be discontinued. Medical records documenting a history and physical exam showing use of ipilimumab first or a BRAF inhibitor should be forwarded to the Medical Director for Clinical Affairs. The patient should have a prognosis of 6 months. All treatments should be included in the medical records. Prior surgeries or other chemotherapeutics should be documented. A letter of Prior Approval will be approved for the length of treatment.

C9136

No

No

View ICD Codes.

No

No

No

No

C9349

No

No

No

No

No

No

No

C9442

No

18y & up

View ICD Codes.

No

Yes

No

Yes

NOTE: Beleodaq is a histone decacetylase inhibitor indicated for the treatment of adult patients with relapsed or refractory peripheral T-cell lymphoma (PTCL). All previous treatments should be documented. A complete history and physical exam documenting previous treatments and results should be submitted to the Medical Director for Clinical Affairs for a Prior Approval letter. Length of treatment should be specified.

C9443

No

18y & up

No

No

No

No

No

C9444

No

18y & up

No

No

No

No

No

C9446

No

18y & up

No

No

No

No

No

C9739

No

No

No

No

No

No

No

NOTE: Covered for males only.

C9740

No

No

No

No

No

No

No

NOTE: Covered for males only.

G6015

No

No

No

No

No

No

No

J0153

No

No

No

No

No

No

No

J0887

No

21y & up

Yes; see below

No

No

No

No

NOTE: The primary diagnosis should be (View ICD Codes.) with a secondary diagnosis of (View ICD Codes.). For patients with CKD on dialysis:

* Initiate Mircera treatment when the hemoglobin level is less than 10 g/dL.

* If the hemoglobin level approaches or exceeds 11 g/dL, reduce or interrupt the dose of Mircera.

* The recommended starting dose of Mircera for the treatment of anemia in adult CKD patients who are not currently treated with an ESA is 0.6 mcg/kg body weight administered as a single IV or SC injection once every two weeks. The IV route is recommended for patients receiving hemodialysis because the IV route may be less immunogenic.

* Once the hemoglobin has been stabilized, Mircera may be administered once monthly using a dose that is twice that of the every-two-week dose and subsequently titrated as necessary.

J0888

No

21y & up

View ICD Codes.

No

No

No

No

NOTE: For patients with CKD not on dialysis:

* Consider initiating Mircera treatment only when the hemoglobin level is less than 10 g/dL and the following considerations apply:

* The rate of hemoglobin decline indicates the likelihood of requiring an RBC transfusion, and

* Reducing the risk of alloimmunization and/or other RBC transfusion-related risks is a goal.

* If the hemoglobin level exceeds 10 g/dL, reduce or interrupt the dose of Mircera and use the lowest dose of Mircera sufficient to reduce the need for RBC transfusions.

J1071

No

No

No

103

No

No

No

J1439

No

18y & up

View ICD Codes.

No

No

No

No

J2274

No

No

No

No

No

No

No

J3121

No

No

No

103

No

No

No

NOTE: Covered for males only.

J3145

No

No

No

103

No

No

No

NOTE: Covered for males only.

J7181

No

No

View ICD Codes.

No

No

No

No

J7201

No

No

No

No

No

No

No

J7327

No

18y & up

No

No

No

Yes

No

NOTE: Prior authorization is required for coverage of the Hyalurononinjection in the physician's office for procedure codes J7321, J7323, J7324, J7325 and J7327. Providers must specify the brand name of Hyaluronon (sodium hyaluronate) or derivative when requesting prior authorization for this procedure code. A written request must be submitted to the Division of Medical Services Utilization Review Section. Refer to the Utilization Review prior authorization information in the provider manual. The request must include the patient's name, Medicaid ID number, physician's name, physician's Arkansas Medicaid provider identification number, patient's date of birth and medical records that document the severity of osteoarthritis, previous treatments and site of injection. Hyaluronon is limited to one injection or series of injections per knee, per beneficiary, per lifetime.

J9267

No

No

No

103

No

No

No

J9301

No

18y &up

View ICD Codes.

No

Yes

No

Yes

NOTE: Gazyvais a CD-20 directed cytolytic antibody and is indicated, in combinations witii ciilorambucil, fertile treatment of adult patients with previously untreated chronic lymphocytic leukemia Patients should have a protocol with chlorambucil and a history and physical exam covering all treatments including failures to submit to the Medical Director for Clinical Affairs for a Prior Approval Letter. Dates of Service need to be included.

Q4150

No

No

No

No

No

No

No

Q4152

No

No

No

No

No

No

No

Q4157

No

No

No

No

No

No

No

Q4160

No

No

No

No

No

No

No

XIII. HCPCS Procedure Codes Payable to Podiatrists

The following information is related to procedure codes payable to Podiatrist providers:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

C9349

No

No

No

No

No

No

No

Q4150

No

No

No

No

No

No

No

Q4152

No

No

No

No

No

No

No

Q4157

No

No

No

No

No

No

No

Q4160

No

No

No

No

No

No

No

XIV. HCPCS Procedure Codes Payable to Prosthetics Providers

The following information is related to procedure codes payable to Prosthetics providers:

Procedure codes in the table must be billed with appropriate modifiers. For procedure codes that require a prior authorization, the written PA request must be submitted to the Utilization Review Section of the Division of Medical Services (DMS) for wheelchairs and wheelchair related equipment and services.

For other durable medical equipment (DME), a written request must be submitted to the Arkansas Foundation for Medical Care. Please refer to your Arkansas Medicaid Prosthetics Provider Manual for details on requesting a DME prior authorization.

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

K0901

EP

0-20y

No

No

No

No

No

K0901

No

21y & up

No

No

No

Yes

No

K0902

EP

0-20y

No

No

No

No

No

K0902

No

21y & up

No

No

No

Yes

No

L3981

EP

0-20y

No

No

No

No

No

L3981

No

21y & up

No

No

No

No

No

L7259

EP

0-20y

No

No

No

No

No

L7259

No

21y & up

No

No

No

Yes

No

XV. HCPCS Procedure Codes Payable to Transportation Providers

The following information is related to procedure codes payable to Transportation providers:

Procedure Code

Modifier

Age Restriction

Diagnosis Diagnosis List

Review

PA

Prior

Approval

Letter

J0153

No

No

No No

No

No

No

XVI. Miscellaneous Information

An asterisk (*) after the procedure code denotes the requirement of a paper claim.

A. Existing HCPCS procedure codes A6208, A6250, A6266 and A6457 are payable to Prosthetics and Home Health providers:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

A6208

NU

No

No

No

No

No

No

A6250

NU

No

No

No

No

No

No

A6266

NU

No

No

No

No

No

No

A6457

NU

No

No

No

No

No

No

B. Effective July 1, 2015, for beneficiaries age 21 and over, a benefit limit of $60,000 per State Fiscal Year (July 1 through June 30) has been established for reimbursement for prosthetic devices. When the Medicaid maximum allowable for a prosthetic device item is $1,000 or more, prior authorization is required.

C. ICD code (View ICD Codes.) has been added to existing HCPCS procedure code J0490. All other criteria remain unchanged:

Procedure Code

Modifier

Age Restriction

Diagnosis Diagnosis List

Review

PA

Prior

Approval

Letter

J0490

No

18y & up

View ICDNo Codes.

Yes

No

Yes

NOTE: This drug is indicated for treatment of patients age 18 years and above with active,

autoantibody-positive, systemic lupus erythematosus who are receiving standard therapy, such as non-steroidal anti-inflammatory drugs, hydroxychloroquine, corticosteroids or immunosuppressive drugs. Use of this drug is not recommended for use in combination with other biologics or intravenous cyclophosphamide, or patients with severe active lupus nephritis, or severe active central nervous system lupus. This drug administration requires a prior approval letter which must include a history and physical exam documenting all prior treatment and documented failure of treatment. The patient should continue to receive the standard therapy. This drug should be administered by healthcare providers prepared to manage anaphylaxis and must be prescribed by a rheumatologist.

D. Existing HCPCS procedure code J1446 is now payable to Hospital, Physician, and Nurse Practitioner providers:

Procedure Code

Modifier

Age Restriction

Diagnosis Diagnosis List

Review

PA

Prior

Approval

Letter

J1446

No

21y & up

No No

No

No

No

E. Existing HCPCS procedure code J9228will require ICD diagnosis as listed below in the Diagnosis table:

Procedure Code

Modifier

Age Restriction

Diagnosis Diagnosis List

Review

PA

Prior

Approval

Letter

J9228

No

18y & up

View ICDNo Codes.

Yes

No

Yes

NOTE: Iplimumabis indicated for treatment of unresectable or metastatic melanoma. It should be given every 3 weeks for a total of four doses. Liver function tests, thyroid function and clinical chemistries must be monitored before each dose. Iplimumabshould only be prescribed by physicians who are prepared to treat immune mediated complications. Participation in the risk evaluation and mitigation program is essential. Use of Iplimumabrequires a detailed history and physical exam including all previous treatments and clear documentation that the melanoma is not treatable by surgery or has metastasized. Patients considered for treatment should be at least 18 years old and have a life expectancy of at least 4 months. It should not be used if patient had previous autoimmune disease requiring systemic therapy. A Prior Approval Letter with a history and physical exam must be sent to the Medical Director of Clinical Affairs.

F. Existing HCPCS procedure code J9047 no longer requires a Prior Approval letter. All other criteria remain unchanged:

Procedure Code

Modifier

Age Restriction

Diagnosis

Diagnosis List

Review

PA

Prior

Approval

Letter

J9047*

No

18y & up

View ICD Codes.

No

No

No

No

NOTE: Kyprolisis indicated for the treatment of adult patients with multiple myeloma, who have received at least two prior therapies including Velcade and an immunomodulary agent and have demonstrated disease progression on or within 60 days of completion of the last therapy. Approval is based upon response rate. A physical exam and history documenting the above requirements must be included. All monitoring and warnings and precautions from the Federal Drug Administration must be complied with for this drug to be approved. Females should avoid becoming pregnant. Consideration will be on a case-by-case basis.

XVII. Non-Covered 2015 HCPCS with Elements of CPT or Other Procedure Codes

The following new 2015 HCPCS procedure codes are not payable because these services are covered by a CPT code, another HCPCS code or a revenue code.

A9606

C2624

C2644

C9742

XVIII. Non-Covered 2015 HCPCS Procedure Codes

The following procedure codes are not covered by Arkansas Medicaid.

A4459

A4602

A7048

G0464

G0466

G0467

G0473

G6001

G6002

G6008

G6009

G6010

G6017

G6018

G0619

G6025

G6027

G6028

G6036

G6037

G6038

G6044

G6045

G6046

G6052

G6053

G6054

G9363

G9364

G9365

G9376

G9377

G9378

G9384

G9385

G9386

G9394

G9395

G9396

G9404

G9405

G9406

G9412

G9413

G9414

G9420

G9421

G9422

G9428

G9429

G9430

G9436

G9437

G9438

G9448

G9449

G9450

G9456

G9457

G9458

G9466

G9467

G9468

J0572

J0573

J0574

L6026

L8696

Q2052

Q4158

Q4159

S1034

C9447

C9741

G0276

G0277

G0279

G0468

G0469

G0470

G0471

G0472

G6003

G6004

G6005

G6006

G6007

G6011

G6012

G6013

G6014

G6016

G0620

G0621

G6022

G6023

G6024

G6030

G6031

G6032

G6034

G6035

G6039

G6040

G6041

G6042

G6043

G6047

G6048

G6049

G6050

G6051

G6055

G6056

G6057

G6058

G9362

G9366

G9367

G9368

G9369

G9370

G9379

G9380

G9381

G9382

G9383

G9389

G9390

G9391

G9392

G9393

G9399

G9400

G9401

G9402

G9403

G9407

G9408

G9409

G9410

G9411

G9415

G9416

G9417

G9418

G9419

G9423

G9424

G9425

G9426

G9427

G9431

G9432

G9433

G9434

G9435

G9439

G9440

G9441

G9442

G9443

G9451

G9452

G9453

G9454

G9455

G9459

G9460

G9463

G9464

G9465

G9469

G9470

G9471

G9472

J0571

J0575

J1322

J7182

J7200

J7336

Q4151

Q4153

Q4154

Q4155

Q4156

S1035

S1036

S1037

S8032

S9901

If you have questions regarding this notice, please contact the Hewlett Packard Enterprise Provider Assistance Center at 1-800-457 -4454 (Toll-Free) within Arkansas or locally and Out-of-State at (501) 376-2211.

If you need this material in an alternative format, such as large print, please contact the Program Development and Quality Assurance Unit at (501) 320-6429.

Arkansas Medicaid provider manuals (including update transmittals), official notices, notices of rule making and remittance advice (RA) messages are available for download from the Arkansas Medicaid website: www.medicaid.state.ar.us.

Thank you for your participation in the Arkansas Medicaid Program.

____________________________________________________

Dawn Stehle Director

Summary for 2015 CPT and HCPCS Procedure Code Conversion

To comply with federal regulation 45 CFR Subpart J, Section 162.1002, these Notices of Rulemaking informs providers of the implementation of the annual Current Procedure Codes, (CPT), and the annual Healthcare Common Procedure Codes Systems, (HCPCS). These data sets are created and published by the American Medical Association and the Centers for Medicare and Medicaid on an annual basis. This Rule is necessary for consistency with the utilization of procedure codes used by Medicare and other third party payers of medical claims. These data sets are standardized and are used nationally for claims processing. This emergency notice will help expedite claims processing. Payable procedure codes will be added to the provider fee schedules and policy manuals will be updated as necessary. This will ensure that additional claims system testing will not be needed before implementation, resulting in subsequent delays and further lost efficiency of time. It will also help to put 2016 CPT/HCPCS planning, programming, testing, and promulgation processes back on its regular timelines.

Emergency filing is necessary to allow providers to bill on the 2015 codes. Due to the implementation of ICD-10, work could not begin on implementing these codes until August 2015. The work will not be completed until December 2015.

Disclaimer: These regulations may not be the most recent version. Arkansas may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
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