Association between pharmacotherapy and secondary hip fracture in a real-world setting: a nationwide database study

J Bone Miner Metab. 2023 Mar;41(2):248-257. doi: 10.1007/s00774-023-01411-4. Epub 2023 Feb 28.

Abstract

Introduction: This study aimed to assess the association between pharmacotherapy and secondary hip fracture incidence.

Materials and methods: The correlation between secondary hip fracture incidence and the presence, type, and medication possession ratio (MPR) of pharmacotherapy was investigated using medical insurance data acquired from the National Database of Health Insurance Claims and Specific Health Checkups of Japan.

Results: Data collected from female patients (n = 1,435,347) were analyzed. The 2-year secondary hip fracture incidence was 3.48% (n = 49,921). Secondary hip fracture was significantly more common in patients without medications (3.80%) than in those with medications (3.00%). Patients receiving selective estrogen receptor modulators (SERMs) had the lowest average age. The crude incidence of secondary hip fracture was the lowest in patients receiving SERMs (n = 2088 [2.52%]), followed by those taking bisphosphonates (n = 11,355 [2.88%]), denosumab (n = 1118 [2.90%]), no medications (n = 32,747 [3.80%]), and parathyroid hormone (PTH: n = 2163 [4.55%]), whereas the age-adjusted incidence was the lowest in patients administered denosumab (2.27%), followed by those taking bisphosphonates (2.47%), SERMs (2.55%), PTH (3.67%), and no medications (3.80%). The mean MPR was the highest in patients taking denosumab (64.9%), followed by those receiving bisphosphonates (58.7%), SERMs (58.2%), and PTH (40.6%) in the no hip fracture group.

Conclusion: Secondary hip fractures were less likely to occur with medication versus no medication. Differences in the crude incidence of secondary hip fracture based on medications usage might be attributed to background characteristics.

Keywords: Health insurance claims database; Hip fracture; Nationwide study; Pharmacotherapy; Secondary fracture.

MeSH terms

  • Bone Density Conservation Agents* / adverse effects
  • Denosumab / therapeutic use
  • Diphosphonates / adverse effects
  • Female
  • Hip Fractures* / complications
  • Humans
  • Osteoporosis* / drug therapy
  • Osteoporotic Fractures* / epidemiology
  • Selective Estrogen Receptor Modulators / therapeutic use

Substances

  • Bone Density Conservation Agents
  • Denosumab
  • Selective Estrogen Receptor Modulators
  • Diphosphonates