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MedicaidPrior AuthMedium impact

Visudyne® (verteporfin) (Revised)

Humana·FL, KY, SC, VA · Ophthalmology·Medicaid
Effective date
Jan 1, 2025
We identified it
Jun 25, 2026
Days to comply

Summary

Humana revised its Visudyne (verteporfin) prior authorization policy effective January 1, 2025, with the latest revision dated February 25, 2026. The policy now applies to four state Medicaid programs (Florida, Kentucky, South Carolina, Virginia) and specifies prior authorization requirements for three indications: neovascular age-related macular degeneration (with a bevacizumab prior therapy/contraindication/intolerance requirement, except in Florida), presumed ocular histoplasmosis, and pathologic myopia. All uses require plan year-based prior authorization approval.

Action Required

Action needed
By January 1, 2025, the billing team must: (1) Update the billing system and prior authorization workflow to require prior authorization for all Visudyne (verteporfin) claims submitted under Medicaid plans in Florida, Kentucky, South Carolina, and Virginia; (2) For Kentucky, South Carolina, and Virginia Medicaid: Verify that prior therapy, contraindication, or intolerance to bevacizumab intravitreal injection is documented before submitting authorization requests for age-related macular degeneration cases (this requirement does NOT apply to Florida Medicaid); (3) Configure the system to accept diagnoses of neovascular AMD, presumed ocular histoplasmosis, and pathologic myopia as eligible indications; (4) Set prior authorization approval durations to plan year duration for both initial and renewal requests; (5) Train billing staff and providers to always obtain prior authorization before dispensing Visudyne in these four states; (6) Update internal documentation requirements to capture bevacizumab history for non-Florida Medicaid claims. Failure to obtain prior authorization will result in claim denials and potential member liability.