Exclusion Criteria. Required Medical Documentation

Transcription

1 Partnership HealthPlan of California: New and Revised, th Quarter P & T 2016 Effective //2016 Generic substitution required when there is an FDA approved generic equivalent; additional criteria apply for brand name requests per PHC Policy MPRP4033. HEADING Drug/PA Group Products Included in Group Covered Uses Restriction Restriction Duration Other Requirements DEFINITION For PHC Internal use, used for grouping drugs with like criteria. Drugs covered by the same TAR criteria. Trade names, strengths, dosage forms are for example only. apply to the active ingredient entity, unless separate criteria exist for different strengths/forms of same drug. Indications for which PHC will consider prior authorization based on the stated criteria. Other uses may require additional documentation of safety, efficacy & medical necessity. Specified reasons for denial (if any), other than not meeting criteria requirements. Documents to be submitted with the TAR for clinical review. Absence of these documents will result in delay or denial of the request. Any age limit or CCS screening associated with the drug. specialty requirement for TAR consideration, if any. The maximum duration of TAR approval before renewal is required, when all criteria are met. Less than the maximum may be authorized when additional clinical information is required. Other criteria and notations not included elsewhere. This page is for general information only, to assist with interpretation of the TAR/PA criteria. Please review the information above if you are unfamiliar with this criteria format. New & revised criteria begin on the next page. Contents: (Create table with no borders, then each item becomes a link to its page in criteria via bookmark tools first mark each entry then highlight each drug in this list and add bookmark/within document). Ustekinumab (Stelara ) Belimumab (Benlysta ) Lisdexamphetamine (Vyvanse ) Hyaluronic Acid Derivatives, Orthopedic: Gelsyn-3, Euflexxa, Genvisc, Hyalgan, Orthovisc, Supartz FX, Synvisc, Synvisc-One, Hymovis, Gel-One, Monovisc ) Colchicine (Colcrys, Mitigare ) Dextromethorphan 20mg/Quinidine Gluconate 10mg (Neudexta )

2 Ustekinumab (Stelara ) Drug Group Covered Uses Interleukin 12 and IL-23 inhibitors Treatment of adults (18 years and older) with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy. Treatment of adults with active psoriatic arthritis (as monotherapy or in combination with methotrexate). Untreated latent TB infections. Active tuberculosis infection. Stelara may not be approved for investigational diagnoses including, but not limited to the treatment of ankylosing spondylitis, relapsing-remitting multiple sclerosis, and rheumatoid arthritis. Requests for use of biologic therapy with alcohol use as a reason for avoiding methotrexate (when indicated) is not sufficient justification. Requests for greater dose or frequency than recommended by the FDA. Specialist s clinic notes documenting Disease course, Previous therapies tried and responses, Current evaluation (lab and imaging reports as appropriate). TB Screening For plaque psoriasis, documentation of % body surface area affected and area of body effected if less than 10%. 18 years and Dermatologist for older. plaque psoriasis. Rheumatologist for psoriatic arthritis. Duration Starting: initial dose at 0- and 4 weeks (2 doses total). Continued therapy: 12 months (one dose per 12 weeks). Other Plaque psoriasis: Patient has a minimum BSA involvement of plaque psoriasis of 10% or BSA<10% involving areas which significantly impact daily function (ie. palms of hands, soles of feet, head/neck, or genitalia). Patient has had trial and inadequate response (or medical contraindication) to phototherapy AND systemic therapy including methotrexate (cyclosporin or acitretin if contraindication to methotrexate exists) at adequate dose and duration (3 month minimum trial). Patient has documented trial and failure, or contraindication to 2 TNF inhibitors (PHC preferred options are Enbrel and Humira, 3 month minimum trial of each). Drug must be prescribed by a dermatologist. Psoriatic Arthritis: Patient has documented trial and failure of, or contraindication to adequate trial of systemic therapy with nonbiologic DMARD including methotrexate (3 month minimum trial) AND documented trial and failure, or contraindication to 2 TNF inhibitors (PHC preferred options are Enbrel and Humira, 3 month minimum trial of each). Drug must be prescribed by a rheumatologist. While not approved for <18 years, still appropriate to screen for eligible condition for provider to pursue CCS coverage in ages <21 if applicable. MC = PHC Medi-Cal F = Formulary QL = Quantity Limit NF = Non-formulary, TAR required (aka, PA Required) 2 of 7

3 Belimumab (Benlysta ) Drug Group Covered Uses Monoclonal For the treatment of active, Antibody autoantibody- positive, systemic lupus erythematosus (SLE) in combination with standard therapy Use is not recommended in patients with severe active lupus nephritis, severe active CNS lupus, or in combination with other biologics, including B- cell targeted therapies or IV cyclophosphamide. Required lab reports: CBC, Creatinine, Sed Rate, Anti-DS DNA, Complement (C3 and C4). In the event that lab results do not support the diagnosis of active disease, an in-office second opinion is required. Requested dose does not exceed the FDA approved dose and frequency per manufacturers labeling. 18 years and older Duration Other 6 months Approval is limited to those requests for adult members with SLE, which document: Active, Antibody positive musculo-skeletal or cutaneous systemic lupus erythematosus. Member does not have severe active lupus nephritis Member does not have severe active CNS lupus Member is currently receiving standard therapy such as NSAIDs, corticosteroids, antimalarials(eg, chloroquine, hydroxychloroquine) or immunosuppressives (eg, cyclophosphamide, azathioprine, mycophenolate or methotrexate), and requires the equivalent of at least 10mg prednisone per day in combination with either azathioprine or mycophenolate. Treatment will not be in combination with other biologics, nor in combination with IV cyclophosphamide. Approval duration is limited to 6 months, with clinical reassessment prior to renewal request. Renewals are limited to those which document improvement. MC = PHC Medi-Cal F = Formulary QL = Quantity Limit NF = Non-formulary, TAR required (aka, PA Required) 3 of 7

4 Lisdexamphetamine (Vyvanse ) Drug Group Covered Uses Stimulant, ADHD Binge Eating Weight loss or Disorders (BED) pharmacotherapy alone. Doses under 50mg (have not shown any improvement over placebo) Chart notes documenting BMI, binge eating episodes per week, and duration of binge eating issues Enrollment in psychotherapy (for example, but not limited to, CBT/interpersonal therapy) for 3 months prior to request, and plans to continue while on medication 3 month trial periods of formulary medication options or contraindications (2 SSRI s, in combination with either topiramate or zonisamide). IF BMI greater than 25 must have t/f (zonisamide or topiramate). Continuations requests: must include change from baseline to week 12 in number of binge eating days per week. If improved allowed 3 month Duration Other FDA approved for Psychiatry or 3 month trial; 3 month Psychiatry or behavioral health 18 and older. upon continuation specialist. of: 1. Chart Younger teen use recommendation approvals if notes documenting BMI, weekly BE subject to case-bycase from psychiatry or improvement seen. episodes (greater than 3/wk) and review. other behavioral Not studied past 6 duration (3 months) and is not assoc. health specialist months of use. with purging, laxatives, or excessive exercise. 2. Psychotherapy enrollment (must have been tried alone for 3 months prior to med request and continue while on meds), 3. Trial and failure of formulary meds or contraindication/intolerances to: (3 consecutive months of: either (a): 2 SSRI s AND topiramate or (b) 3 consecutive months of 2 SSRIs AND zonisamide). If patient s BMI is greater than 25: Pt must have trial and failure to topiramate or zonisamide only. Initial approval: 3 month trial with request for updated psych notes and treatment success. Renewals: 3 month intervals. Pt must show improvement in BED/wk from baseline to 12 weeks for continuation. Only approved for doses 50mg to 70mg. MC = PHC Medi-Cal F = Formulary QL = Quantity Limit NF = Non-formulary, TAR required (aka, PA Required) 4 of 7

5 Colchicine (Colcrys, Mitigare ) Drug Group Covered Uses FAMILIAL MEDITERRANEAN FEVER ACUTE GOUT Required Medical Duration Other Minimum age N/A Maximum quantity of 120 Documented diagnosis of Familial Mediterranean requirement: 4 years tablets per 30 days Fever old Minimum age N/A requirement: 18 years old Maximum approved dose is 1.8mg every 3 days. #9 per month (3 episodes). Documented or contraindication to NSAIDS & COX2 inhibitor if colchicine is not being requested concurrently with either an NSAID or COX2 (improved efficacy when used together). May be approved for acute treatment regardless of presence or absence of allopurinol in the treatment regimen. PROPHYLAXIS OF GOUT FLARES Renewal: Patient has elevated urate level ( 6) in Minimum age N/A requirement: 18 years old PERICARDITIS 18 years and older Cardiologist Quantity of 60 tablets per 30 days. Duration: See prophylaxis requirements for maintenance use, which does have an allopurinol requirement. A quantity limit of sixty Chronic (recommend capsule). (60) tablets per thirty (30) days will be applied, when criteria met. May be approved up to 6 months per authorization. Documented failure with or contraindication with probenecid or colchicine/probenecid (ColBenemid) AND allopurinol at max dosage. When drug is requested and the criteria are not met, then request will be reviewed on a case by case basis. of concurrent therapy with NSAIDs. BEHÇET S SYNDROME Prescribed or recommended by an appropriate specialist. Approve up to 3 months for acute and up to 6 months for recurrent. Dose is from 0.6-2mg/day Confirmed diagnosis of Behçet s Syndrome by an appropriate specialist such as rheumatologist, gynecologist, dermatologist or infectious disease specialist. MC = PHC Medi-Cal F = Formulary QL = Quantity Limit NF = Non-formulary, TAR required (aka, PA Required) 5 of 7

6 Hyaluronic Acid Derivatives, Orthopedic (Gelsyn-3, Euflexxa, Genvisc, Hyalgan, Orthovisc, Supartz FX, Synvisc, Synvisc-One, Hymovis, Gel-One, Monovisc ) Drug Group Viscosupplementation Covered Uses For the treatment of knee osteoarthritis pain when criteria are met. Required Medical Clinic Notes from Orthopedic or Pain Management Specialist Duration Other Ortho or Pain Management Approval limited to one treatment series per knee per year. Treatment of Osteoarthritis of the knee in which each of the following are met: (1) Members who have been evaluated by an appropriate specialist. (2) of trial and failure of, or contraindication to, at least 2 prescription strength NSAIDs at adequate doses for 3 months each of consistent usage. (3) If intolerant to NSAIDs, must have 3 month trial of topical NSAID (TAR required). (4) Trial and failure of physical therapy. (5) of at least 3 intra-articular steroid injections within the last year or documentation of complete lack of response to less than 3 injections. MC = PHC Medi-Cal F = Formulary QL = Quantity Limit NF = Non-formulary, TAR required (aka, PA Required) 6 of 7

7 Dextromethorphan 20mg/Quinidine Gluconate 10mg (Nuedexta ) Drug Group Covered Uses PBA For the treatment of nts pseudobulbar affect (PBA) Specialist s clinic notes with evaluation of PBA and having had other causes of emotional lability ruled out. 18 years and older Neurologist or psychiatrist Duration TBD Other Limited to the treatment of Pseudobulbar Affect (PBA) in members who have been evaluated by a neurologist and only have episodic outbursts of crying or laughing which are involuntary and are incongruent with the member s emotional state. Must rule out depression or other emotional events, manifested as either intermittent or prolonged crying episodes. Treatment of other emotional labilities is not FDA indicated. Notes: (A) Studies to support the effectiveness of Nuedexta were performed in patients with ALS (amyotrophic lateral sclerosis) and MS (Multiple Sclerosis). (B) Nuedexta has not been shown to have significant clinical benefit in the types of emotional lability that occur in Alzheimer s disease and other dementias. (C)PBA occasionally spontaneously improves, therefore patients should be periodically reassessed for the need for continued treatment. MC = PHC Medi-Cal F = Formulary QL = Quantity Limit NF = Non-formulary, TAR required (aka, PA Required) 7 of 7