Duration of Bisphosphonate Drug Holidays and Associated Fracture Risk

Med Care. 2020 May;58(5):419-426. doi: 10.1097/MLR.0000000000001294.

Abstract

Background: Discontinuation of bisphosphonates (BP) or a "drug holiday" after several years of treatment is increasingly common. However, the association of drug holiday duration with future fracture risk is unclear.

Objectives: We evaluated the rate of fracture in relation to various lengths of drug holidays among women receiving long-term BP therapy.

Research design: Observational cohort study using US Medicare data 2006-2016. Incidence rates (IRs) and Cox proportional hazards models were used to evaluate the rate and adjusted hazard ratios (aHRs) controlling for potential confounders.

Subjects: Women aged 65 years and above enrolled in fee-for-service Medicare who had been adherent (≥80%) to alendronate, risedronate, or zoledronate for ≥3 years.

Measures: Hip, humerus, distal forearm, and clinical vertebral fracture.

Results: Among 81,427 eligible women observed for a median (interquartile range) of 4.0 (2.5, 5.3) years, 28% of women underwent a drug holiday. In the alendronate cohort (73% overall), the IR of hip fracture among women who discontinued BP for >2 years was 13.2 per 1000 person-years. Risk was increased (aHR=1.3, 1.1-1.4) versus continuing therapy (IR=8.8, referent). Rates were elevated for humerus fracture with discontinuation >2 years (aHR=1.3, 1.1-1.66) and for clinical vertebral fracture with discontinuation >2 years (aHR=1.2, 1.1-1.4). Results were similar for risedronate, zoledronate, and ibandronate for hip and clinical vertebral fracture.

Conclusion: Discontinuing alendronate beyond 2 years was associated with increased risk of hip, humerus, and clinical vertebral fractures.

Publication types

  • Observational Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Bisphosphonate-Associated Osteonecrosis of the Jaw / etiology
  • Bisphosphonate-Associated Osteonecrosis of the Jaw / prevention & control
  • Bone Density Conservation Agents / administration & dosage*
  • Bone Density Conservation Agents / adverse effects
  • Cohort Studies
  • Diphosphonates / administration & dosage*
  • Diphosphonates / adverse effects
  • Drug Administration Schedule
  • Female
  • Femoral Fractures / chemically induced
  • Femoral Fractures / prevention & control
  • Hip Fractures / epidemiology*
  • Humans
  • Humeral Fractures / epidemiology*
  • Medicare
  • Osteoporosis, Postmenopausal / drug therapy
  • Osteoporotic Fractures / epidemiology
  • Osteoporotic Fractures / prevention & control
  • Spinal Fractures / epidemiology*
  • Time Factors
  • United States / epidemiology
  • Withholding Treatment

Substances

  • Bone Density Conservation Agents
  • Diphosphonates