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KeveyisCareFirst (Caremark)

Primary hypokalemic periodic paralysis

Preferred products

  • acetazolamide

Initial criteria

  • Diagnosis supported by at least one of the following: genetic test results OR member has a family history of primary hypokalemic periodic paralysis OR member’s attacks are associated with hypokalemia AND both Andersen-Tawil syndrome and thyrotoxic periodic paralysis have been ruled out
  • Member had a trial and suboptimal response to treatment with acetazolamide

Reauthorization criteria

  • Member has demonstrated a response to therapy as evidenced by an improvement in their condition (e.g. decrease in the number or severity of attacks)

Approval duration

initial 60 days, continuation 12 months