Target Short-Acting Growth Hormone Agent(s) — Blue Cross Blue Shield of Illinois
chronic renal insufficiency
Initial criteria
- Patient is a child (open epiphysis)
 - Has one of the listed diagnoses
 - For each diagnosis, chart notes required
 - For chronic renal insufficiency: height >2 SD below mean AND serum creatinine >1.5 mg/dL or CrCl ≤75 mL/min/1.73 m2
 - For SGA: age ≥2 years, birth weight/length ≥2 SD below mean, failed catch-up growth at 24 months (height ≥2 SD below mean)
 - For GHD/short stature/growth failure: clinical diagnostic criteria as specified including stimulation test failure or pituitary defect or imaging evidence of open epiphyses as applicable
 - Patient does NOT have any FDA labeled contraindications
 - Prescriber is a specialist in the area of diagnosis or has consulted a specialist
 - Requested dose within FDA labeling or supported compendia
 - Request meets preferred or nonpreferred agent criteria: either preferred agent, or nonpreferred with documented reasons (current stable use, inadequate response, intolerance, contraindication, expected inefficacy, medical necessity, or better efficacy evidence as listed)
 
Reauthorization criteria
- Previously approved for GH through prior authorization
 - Patient is a child (open epiphysis)
 - Request meets preferred/nonpreferred agent criteria same as initial
 - Prader-Willi: evidence of clinical benefit OR for other listed diagnoses (Turner, Noonan, SHOX, SGA, panhypopituitarism/multiple pituitary deficiency, chronic renal insufficiency, GHD/short stature/growth failure): imaging shows epiphyses not closed if female >12 or male >14, height or velocity improved since last approval
 - Patient monitored for adverse effects of GH therapy
 - No FDA labeled contraindications
 - Prescriber is a specialist or has consulted specialist
 - Requested dose within FDA labeling or supported compendia
 
Approval duration
12 months