Amitiza (lubiprostone) — Blue Cross Blue Shield of Montana
Opioid-Induced Constipation (OIC)
Preferred products
- Symproic (naldemedine)
- Movantik (naloxegol)
Initial criteria
- The patient has a diagnosis of opioid-induced constipation (OIC) AND all of the following:
- 1. ONE of the following:
- A. BOTH of the following:
- 1. ONE of the following:
- a. Requested agent is Relistor (methylnaltrexone) tablet OR
- b. Requested agent is Amitiza (lubiprostone) AND patient is not receiving a diphenylheptane opioid (e.g., methadone)
- 2. ONE of the following:
- a. Patient has chronic non-cancer pain OR
- b. Chronic pain related to prior cancer or its treatment OR
- c. Active cancer pain OR
- B. Request is for Relistor injection AND patient receiving palliative care AND ONE of:
- 1. Advanced illness OR
- 2. Pain caused by active cancer
- 2. Chronic use of opioid agent in past 30 days AND
- 3. ONE of the following:
- 1. BOTH of the following:
- a. Stage four metastatic cancer diagnosis and appropriate use documented [chart notes required] AND
- b. Use consistent with evidence-based literature and FDA approved OR
- 2. Tried and inadequate response to ≥2 laxative therapy classes (stimulant, enema, osmotic, stool softener, not including fiber/bulking) OR
- 3. Intolerance/hypersensitivity to ≥2 laxative classes OR
- 4. FDA labeled contraindication to ALL standard laxative classes
- 4. If patient has an FDA labeled indication, ONE of:
- A. Age within FDA labeling for the indication OR
- B. Support exists for using requested agent by age for indication