This PAH agent prior authorization request form is used to collect the required information to adjudicate coverage for PAH medications. It asks the requester to indicate whether the request is for a new therapy or continuation of therapy and, for continuation, to provide start date and documentation of disease stability.
The form collects a specific diagnosis and ICD-10 code and asks the requester to select the appropriate indication (including PAH WHO Group 1, WHO Functional classes II, III, or IV, CTEPH, or other).
Prior medication trials must be documented by medication name, strength, directions, dates of therapy, and reason for failure or discontinuation. The form specifically asks about a calcium channel blocker (CCB) trial or rationale (including contraindication or AVT results) and requires documentation if the patient did not receive AVT or if AVT was contraindicated.
Combination-therapy plans must be indicated (options include combination of a phosphodiesterase inhibitor and a soluble guanylate cyclase stimulator, or combination of selexipag and a parenteral prostanoid), and for selexipag requests the form asks whether there is a history of failure, contraindication, or intolerance to an endothelin receptor antagonist.
The form requires that the request be prescribed by or in consultation with a specialist (Cardiology or Pulmonology) when applicable and mandates that chart notes and the prescriber signature, specialty, and date be attached for adjudication.