This protocol applies to patients with osteoporosis at high risk of fracture — defined by a bone mineral density T-score of ≤−2.5 at any site, or a FRAX 10-year major osteoporotic fracture probability of ≥20% — and who do not have very-high-risk features (no multiple vertebral fractures, no fragility fracture within the previous two years).
First-line anti-resorptive therapy — oral bisphosphonates (alendronate, risedronate), intravenous zoledronate, or denosumab, combined with calcium, vitamin D, and weight-bearing exercise — did not achieve the required bone mineral density response: a ≥0.2-unit (3%) improvement in total hip T-score and a ≥0.5-unit (6%) improvement in lumbar spine T-score over three years.
When these bone density targets are not reached, a structured escalation is indicated.
The next step involves a sequential transition to an osteoanabolic agent — a bone-building therapy — followed by a return to anti-resorptive therapy to consolidate and extend the gains achieved.
Agent selection, phase duration, and the full treatment algorithm remain in the complete protocol below.
Continued increase in total hip, femoral neck, and lumbar spine bone mineral density toward the personalised T-score target over three years.
DOI: 10.1136/bmj‐2024‐081250