Covered when the relevant indication-specific branching criteria on the prior authorization form are met. Follow the branch for the selected indication and the nested questions to determine approval.
Indication selection: Select one indication: Postmenopausal osteoporosis (continue to #2), Osteoporosis in a male patient (continue to #20), Glucocorticoid-induced osteoporosis (continue to #100), Breast Cancer (continue to #30), Prostate Cancer (continue to #31), Other (No Further Questions)
Forms branch to distinct criteria sets based on indication
Postmenopausal initial therapy branch: If this is NOT a continuation request: evaluate fragility fracture, DEXA T-score, FRAX scores, and prior bisphosphonate history per the form flowIf fragility fracture present → No Further Questions; DEXA T-score ≤ -2.5 → continue to FRAX; FRAX major >20% or FRAX hip >3% → No Further Questions; or documented inadequate response/intolerance to ≥1‑year oral or injectable bisphosphonate or clinical reason to avoid bisphosphonates
Follow questions #2–#15 for detailed branching
Postmenopausal lower-risk branch: If pretreatment DEXA T-score is between -1.0 and -2.5: use FRAX to stratify. If FRAX major >20% or FRAX hip >3% may proceed; if below thresholds, approval requires documentation of inadequate response/intolerance to prior injectable therapy or clinical reason to avoid bisphosphonates per the formDEXA T-score between -1.0 and -2.5; FRAX major >20% or FRAX hip >3%
Follow questions #5 and #10–#15
Postmenopausal continuation and prior authorization history: If request is for continuation and the medication was previously authorized by HMSA/CVS, form indicates No Further Questions; otherwise continue evaluation per initial-therapy branch
Questions #2–#4 govern continuation and prior auth history
Osteoporosis in men: Follow similar flow as postmenopausal pathway: continuation and prior authorization checks; inadequate response/intolerance to ≥1‑year bisphosphonate or clinical reason to avoid qualifies; presence of vertebral or hip fracture or pretreatment T‑score ≤ -2.5 qualifies; FRAX ≥20% qualifiesT‑score ≤ -2.5 OR FRAX ≥20% OR history of vertebral/hip fracture; 1‑year bisphosphonate trial
Follow questions #20–#27 for male pathway branching
Glucocorticoid-induced osteoporosis: For new therapy vs continuation follow form flow. For new therapy, documentation must support current or planned glucocorticoid therapy ≥2.5 mg prednisone equivalent per day for ≥3 months. Prior inadequate response/intolerance to ≥1‑year bisphosphonate or clinical reason to avoid may allow approval; fragility fracture or improvement on therapy is assessed for continuationGlucocorticoid dose ≥2.5 mg/day for ≥3 months; 1‑year bisphosphonate trial
Follow questions #100–#106
Breast cancer and prostate cancer–related bone loss: For patients on aromatase inhibitors (breast cancer) or androgen deprivation therapy (prostate cancer), submit supporting documentation of therapy. For breast cancer, pretreatment DEXA T‑score ≤ -2.5, or FRAX major >20% or FRAX hip >3% allow proceeding per the form; other T‑score ranges follow FRAX branchingBreast cancer: DEXA T‑score ≤ -2.5; FRAX major >20%; FRAX hip >3%
Follow questions #30–#31 and #107–#109 for cancer-related pathways