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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