Afrezza (insulin human) — United Healthcare
Type 1 diabetes mellitus
Initial criteria
- Diagnosis of type 1 diabetes mellitus AND used in combination with a basal insulin or continuous insulin pump OR diagnosis of type 2 diabetes mellitus
- Patient is unable to self-inject medications (e.g. Humalog, Lantus, Toujeo) due to one of the following: physical impairment OR visual impairment OR lipohypertrophy OR documented needle-phobia to the degree that the patient has previously refused any injectable therapy or medical procedure (refer to DSM-5 for specific phobia diagnostic criteria)
- FEV1 within the last 60 days is ≥70% of expected normal as determined by the physician
- Patient does NOT smoke cigarettes
- Patient has NOT recently quit smoking (within the past 6 months)
- Patient does NOT have chronic lung disease (e.g. asthma, COPD)
Reauthorization criteria
- Repeat pulmonary function test confirms that patient has NOT experienced a decline of 20% or more in FEV1
- Patient continues to be unable to self-inject short-acting insulin due to one of the following: physical impairment OR visual impairment OR lipohypertrophy OR documented needle-phobia to the degree that the patient has previously refused any injectable therapy or medical procedure (refer to DSM-5 for specific phobia diagnostic criteria)
- Patient continues to not smoke cigarettes
Approval duration
12 months