Medical Policy and Coding Updates November 2017

  • Special notice: medical policies effective in February

    Effective February 2, 2018

    Autografts and Allografts in the Treatment of Focal Articular Cartilage Lesions, 7.01.78
    These services may be considered medically necessary for the knee or ankle when criteria are met. They're considered investigational when criteria aren't met. The policy also lists investigational indications. Read the full policy.

    Intraoperative Neurophysiologic Monitoring, 7.01.562
    Intraoperative monitoring may be medically necessary for spinal, brain and vascular surgeries. Intraoperative monitoring of the recurrent laryngeal nerve is considered medically necessary for high-risk thyroid and anterior cervical spine surgeries. Intraoperative neurophysiologic monitoring for peripheral nerve surgery is considered not medically necessary. Visual-evoked potentials and motor evoked potentials using transcranial magnetic stimulation are considered investigational. Read the full policy.

    New medical policies

    Effective November 1, 2017

    General Approach to Evaluating the Utility of Genetic Panels, 12.04.520
    Genetic panels that use next-generation sequencing or chromosomal microarray may be considered medically necessary when criteria are met. (Criteria on cancer and reproductive panels are addressed in separate policies.)
    Note: Effective January 4, 2019 the services originally described in this policy are reviewed by AIM Specialty Health®.

    Psychiatric Evaluation in Inpatient and Residential Behavioral Health Treatment, 3.01.521
    This utilization management guideline supports InterQual medical necessity requirements for psychiatric evaluations and provides clarification on the provider types that must conduct the evaluations. Read the full policy.

    Revised medical policies

    Effective November 1, 2017

    Bioengineered Skin and Soft Tissue Substitutes, 7.01.113
    The policy was revised to update the medical necessity criteria for products used for breast reconstructive surgery. CellerateRX® (CRXa™) was removed from the investigational policy statement. Integra® Omnigraft™ Dermal Regeneration Matrix was removed from the investigational policy statement and may be considered medically necessary if criteria are met. DermaPure™ is considered investigational. Read the full policy.

    Immune Globulin Therapy, 8.01.503
    The policy was revised to update the criteria for the use of immune globulin therapy to treat ITP in adults and children. Read the full policy.

    Rhinoplasty, 7.01.558
    The medical necessity policy statement was revised to add trauma and other congenital craniofacial deformity. The conservative care requirements for obstructive symptoms were clarified. Read the full policy.

    Total Artificial Hearts and Implantable Ventricular Assist Devices, 7.03.11
    The medical necessity policy statements were revised to add criteria regarding total artificial hearts and implantable ventricular assist devices. Percutaneous ventricular assist devices remain investigational. Read the full policy.

    Revised pharmacy policies

    Effective November 1, 2017

    Medical Necessity Criteria for Pharmacy Edits, 5.01.605
    The policy was revised to update the medical necessity criteria for oral acne antibiotics and brand testosterone products. Read the full policy.

    Pharmacotherapy of Spinal Muscular Atrophy (SMA), 5.01.574
    The policy was clarified to include medical necessity criteria for Spinraza® (nusinersen) for spinal muscular atrophy 1, 2, and 3 when confirmed by genetic testing. Using Spinraza for type 4 SMA (adult onset) is investigational. Read the full policy.

    Pharmacotherapy of Type I and Type II Diabetes Mellitus, 5.01.569
    The policy was revised to update the medical necessity criteria in those instances when metformin is contraindicated. Read the full policy.

    Archived policies

    An archived policy is no longer active and is not used for reviews.

    Archived on October 31, 2017

    Prophylactic Mastectomy, 7.01.561

    Coding updates

    Added codes

    Effective November 1, 2017

    Preimplantation Genetic Testing in Embryos, 12.04.305
    Now requires review for medical necessity, now requires prior authorization.

    89290 - Biopsy, oocyte polar body or embryo blastomere, microtechnique (for preimplantation genetic diagnosis); less than or equal to 5 embryos.

    89291 - Biopsy, oocyte polar body or embryo blastomere, microtechnique (for preimplantation genetic diagnosis); greater than 5 embryos.

    Removed codes

    Effective November 1, 2017

    Erythropoiesis-Stimulating (ESAs) Agents, 5.01.535
    No longer requires medical necessity review; no longer requires prior authorization

    J0890 - Injection, peginesatide, 0.1 mg (for ESRD on dialysis)

  •    Email this article