Verteporfin Photodynamic Therapy Policy
Defines medical necessity, investigational use, coding, and prior authorization guidance for verteporfin photodynamic therapy (PDT) for commercial and Medicare members, including covered ocular indications and combinations considered investigational.
Annual policy review on 5/2024 updated description, summary, and references; policy statements unchanged.
10/2017 clarified coding information.
Coverage Summary
This policy defines medical necessity and investigational uses for verteporfin photodynamic therapy (PDT) to treat choroidal neovascularization and other specified ocular conditions. Key covered indications for commercial members include pathologic myopia, CNV associated with age-related macular degeneration, presumed ocular histoplasmosis, choroidal hemangioma, and chronic central serous chorioretinopathy. Use of verteporfin PDT in combination with any anti-VEGF therapy (pegaptanib, ranibizumab, bevacizumab, aflibercept) or monotherapy for indications not listed is considered investigational. Precertification/preauthorization is required if performed inpatient; outpatient prior authorization requirements vary by product. Payer: Blue Cross Blue Shield (Policy number 599); Effective date / policy history: effective 2015-10-01 with last review Annual update on 5/2024 and policy statements unchanged.