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CystaranCareFirst (Caremark)

cystinosis with corneal cystine crystal accumulation or deposits

Initial criteria

  • Diagnosis of cystinosis confirmed by increased cystine concentration in leukocytes or by genetic testing
  • Member has corneal cystine crystal accumulation
  • Medication prescribed by or in consultation with an ophthalmologist or a physician who specializes in the treatment of metabolic disease and/or lysosomal storage disorders

Reauthorization criteria

  • Member has experienced a decrease in corneal cystine crystal accumulation
  • OR Member did not experience an increase in corneal cystine crystal accumulation

Approval duration

12 months