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BCBS Michigan Medical Policy Updates – July 2019
Click here to view the Blue Cross Blue Shield Michigan Medical Policy Updates »
July 2019 BCBS Michigan Medical Policy Updates:
- Actigraphy For Obstructive Sleep Apnea and Sleep Disorders
- Allergy Testing and Immunotherapy
- Alpha –1 Proteinase Inhibitors
- Analysis of Human DNA in Stool Samples as a Technique for Colorectal Cancer Screening
- Antigen Leukocyte Antibody Test
- Automated Audiometry
- Benlysta® (belimumab)
- Botulinum Toxin Type B Injection
- Cataract Removal Surgery
- Confocal Laser Endomicroscopy
- Continuous Intraocular Pressure Monitoring
- Corneal Hysteresis Measurement for Glaucoma
- Cranial Orthosis (Helmet or Band Therapy) as a Treatment of Plagiocephaly
- Crizanlizumab ™ (SEG101)
- Denosumab (Prolia®/Xgeva®)
- Denosumab (Prolia®/Xgeva®)
- Desferal® (deferoxamine)
- Dopamine Transporter Imaging with Single Photon Emission Computed Tomography (DaTscan™)
- Drug Testing of Urine, Oral Fluids and Hair
- Dynamic Posturography
- Electroconvulsive Therapy
- Elzonris™ (tagraxofusp-erzs)
- Endovascular Repair of Iliac Artery Bifurcation
- Endovenous Ablation for the Treatment of Varicose Veins (e.g., ClariVein®, VenaSeal™ Closure System)
- Entyvio® (vedolizumab)
- Erwinaze® (asparaginase Erwinia chrysanthemi)
- EvenityTM (romosozumab-aqqg)
- Ex Vivo Lung Perfusion (EVLP)
- Exondys 51® (eteplirsen
- Exondys 51® (eteplirsen)
- Fasenra ™ (benralizumab)
- Galectin-3 Testing in the Assessment and Management of Chronic Heart Failure
- Gamifant® (emapalumab-lzsg intravenous injection)
- General Drug Utilization Management Policy
- Genetic Testing – DNA Based Testing for Adolescent Idiopathic Scoliosis
- Genetic Testing (Single Nucleotide Variants) to Predict Risk of Nonfamilial Breast Cancer
- Genetic Testing for Alpha-Thalassemia
- Genetic Testing for Alzheimer’s Disease
- Genetic Testing for Amyotrophic Lateral Sclerosis
- Genetic Testing for Familial Cutaneous Malignant Melanoma (CDKN2A)
- Genetic Testing for Hereditary Hearing Loss
- Genetic Testing for Heterozygous Familial Hypercholesterolemia
- Genetic Testing for Lynch Syndrome and Other Inherited Colon Cancer Syndromes
- Genetic Testing for Macular Degeneration
- Genetic Testing for Retinal Dystrophies
- Genetic Testing for Rett Syndrome
- Genetic Testing for Tay-Sachs Disease
- Genetic Testing-Expanded Molecular Panel Testing of Cancers to Identify Targeted Therapies
- Genetic Testing-Human Platelet Antigen Genotyping
- Genetic, Molecular and Other Tests-Experimental/Investigational Status
- GiaprezaTM (angiotension II)
- Golodirsen TM (SRP-4053)
- Hemophilia Class Policy
- Herceptin Hylecta TM (trastuzumab and hyaluronidase-oysk)
- Infliximab Policy
- Intravenous Bisphosphonates
- Intravitreal Injections for Retinal Conditions
- Khapzory™ (levoleucovorin)
- Krystexxa® (pegloticase)
- Luxturna TM (voretigene neparvovec-rzyl)
- Medical Specialty Drug Site of Care Optimization
- Medications for Hereditary Angioedema
- Medications for Hereditary Angioedema
- Noninvasive Techniques for the Evaluation and Monitoring of Patients With Chronic Liver Disease
- Trazimera TM (trastuzumab-qyyp)
- Treatment Guidelines for Pulmonary Arterial Hypertension
- Ultomiris™ (ravulizumab)
- Xolair ® (omalizumab)
- Zinplava™ (bezlotoxumab)
- Zoladex ® (goserelin acetate implant)
- Zolgensma® (onasemnogene abeparvovec)
Click here to view the Blue Cross Blue Shield Michigan Medical Policy Updates »
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