Population-based study of the effectiveness of bone-specific drugs in reducing the risk of osteoporotic fracture

Sylvie Perreault, Alice Dragomir, Lucie Blais, Yola Moride, Michel Rossignol, Louis Georges Ste-Marie, Julio Cesar Fernandès

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Aim: Evidence supports bone-specific drugs (BSDs) efficacy in the fracture risk reduction. But treatment rates for osteoporosis among high-risk patients are far below the recommended guidelines. A major concern about BSDs is the lack of adherence with treatment. Objective: To determine if BSDs decrease fracture risk in high-risk elderly women in real clinical setting. Methods: A nested case-control design was used in a cohort of elderly women from the Quebec health databases. Women enter into the cohort if they are 70 years or older between 1995 and 2003. Nested case-controls were designed for women with a diagnosis of osteoporosis (OP) and for those with a prior fracture. All cases of fractures occurring during follow-up were matched with 10 randomly selected controls based on age, time period, bone mass density testing, and having a diagnosis of OP or a prior fracture. Use of BSDs before the index date was categorized as follows: short-term (≤1 year), intermediate-term (>1 and ≤3 years), and long-term (>3 years). We used an adjusted conditional logistic regression model to assess BSD effect on fracture. Results: Among 3170 women who had a fracture, of these women, 1824 had OP and 1346 had a prior fracture. Only long-term exposure to BSDs among women with OP reduced the fracture risk by 16% (odds ratio: 0.84; 0.73-0.97). Among women with OP, a high number of medical services or use of anticonvulsants or narcotics increased the fracture risk by 12-73%. Among women with a prior fracture, a high number of medical services or risk of fall or use of benzodiazepines, antidepressants, or narcotics increased the fracture risk by 23-77%. Conclusion: The incidence of fractures decreased by 16% among women with OP whenmore than 80% of BSDs was used for at least 3 years. Among women with a prior fracture, fracture risk reduction was not significant. Exposure to BSDs among women with a prior fracture is troubling, given that only approximately 12% of these individuals were being treated, and only 2% was using BSDs for the long term.

Original languageEnglish (US)
Pages (from-to)248-259
Number of pages12
JournalPharmacoepidemiology and drug safety
Volume17
Issue number3
DOIs
StatePublished - Mar 2008
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Epidemiology
  • Pharmacology (medical)

Keywords

  • Bone-specific drug
  • Effectiveness
  • Osteoporosis

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