MedicaidOctober 2, 2024
Medical Policies and Clinical Utilization Management Guidelines update
Effective November 3, 2024
The Medical Policies, Clinical Utilization Management (UM) Guidelines, and Third-Party Criteria below were developed and/or revised during Quarter Two, 2024. Note, several policies and guidelines were revised to provide clarification only and are not included. Some may have expanded rationales, medical necessity indications, or criteria, and some may involve changes to policy position statements that might result in services that previously were covered being found to be not medically necessary.
Please share this notice with other providers in your practice and office staff.
To view a guideline, visit Provider Medical Policies.
Notes/updates
Updates marked with an asterisk (*) notate that the criteria may be perceived as more restrictive:
- MED.00148 — Gene Therapy for Metachromatic Leukodystrophy:
- Outlines the Medically Necessary and Not Medically Necessary criteria for gene therapy for metachromatic leukodystrophy
- RAD.00069 — Absolute Quantitation of Myocardial Blood Flow Measurement:
- The use of absolute quantitation of myocardial blood flow testing is considered Investigational & Not Medically Necessary for all indications
- SURG.00011 — Allogeneic, Xenographic, Synthetic, Bioengineered, and Composite Products for Wound Healing and Soft Tissue Grafting:
- Revised ocular indications, including the addition of SurSight to Medically Necessary and Not Medically Necessary section and added new Medically Necessary criterion addressing non-healing or persistent corneal epithelial defects
- Removed VersaWrap from Investigational & Not Medically Necessary statement
- Removed Phasix Mesh from Investigational & Not Medically Necessary statement
- Added Phasix Mesh and Phasix ST Mesh to Medically Necessary and Not Medically Necessary statements
- CG-DME-54 — Mechanical Insufflation-Exsufflation Devices:
- Outlines the Medically Necessary and Not Medically Necessary criteria for use of mechanical insufflation-exsufflation devices
Medical Policies
On May 9, 2024, the Medical Policy and Technology Assessment Committee (MPTAC) approved the following Medical Policies applicable to Anthem. These medical policies take November 3, 2024.
Publish Date | Medical Policy Number | Medical Policy Title | New or Revised |
6/28/2024 | ANC.00009 | Cosmetic and Reconstructive Services of the Trunk, Groin, and Extremities | Revised |
5/16/2024 | *MED.00148 | Gene Therapy for Metachromatic Leukodystrophy | Revised |
6/28/2024 | *RAD.00069 | Absolute Quantitation of Myocardial Blood Flow Measurement | New |
6/28/2024 | *SURG.00011 | Allogeneic, Xenographic, Synthetic, Bioengineered, and Composite Products for Wound Healing and Soft Tissue Grafting | Revised |
6/28/2024 | SURG.00121 | Transcatheter Heart Valve Procedures | Revised |
Clinical UM Guidelines
On May 9, 2024, the MPTAC approved the following Clinical UM Guidelines applicable to Anthem. These guidelines were adopted by the medical operations committee for Medicaid members on June 27, 2024. These guidelines take effect November 3, 2024.
Publish Date | Clinical UM Guideline Number | Clinical UM Guideline Title | New or Revised |
6/28/2024 | *CG-DME-54 | Mechanical Insufflation-Exsufflation Devices | New |
6/28/2024 | CG-DME-55 | Automated External Defibrillators for Home Use | New |
6/28/2024 | CG-MED-68 | Therapeutic Apheresis | Revised |
6/28/2024 | CG-MED-97 | Biofeedback and Neurofeedback | New |
Medicaid services provided by Anthem Blue Cross and Blue Shield HP, trade name of Anthem HP, LLC.
Independent licensees of the Blue Cross Blue Shield Association. Anthem is a registered trademark of Anthem Insurance Companies, Inc.
NYBCBS-CD-068657-24-CPN68109
PUBLICATIONS: November 2024 Provider Newsletter
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