4.5 Article

Fragility fractures and the osteoporosis care gap in women: the Canadian Multicentre Osteoporosis Study

Journal

OSTEOPOROSIS INTERNATIONAL
Volume 22, Issue 3, Pages 789-796

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s00198-010-1359-2

Keywords

Bisphosphonates; Care gap; Fragility fracture; Osteoporosis; Postmenopausal women

Funding

  1. Abbott
  2. Amgen
  3. Eli Lilly
  4. Novartis
  5. Merck
  6. Warner Chilcott
  7. Bristol-Myers-Squibb
  8. Pfizer
  9. Roche
  10. Merck Frosst
  11. Procter Gamble
  12. Sanofi-Aventis
  13. Canadian Institutes of Health Research (CIHR)
  14. Merck Frosst Canada Ltd.
  15. Eli Lilly Canada Inc.
  16. Novartis Pharmaceuticals Inc.
  17. sanofi-aventis Procter
  18. Gamble Pharmaceuticals Canada Inc.
  19. Servier Canada Inc.
  20. Amgen Canada Inc.
  21. Dairy Farmers of Canada
  22. Arthritis Society

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Canadian women over 50 years old were studied over a 10-year period to see if those who sustained a fracture (caused by minimal trauma) were receiving the recommended osteoporosis therapy. We found that approximately half of these women were not being treated, indicating a significant care gap in osteoporosis treatment. Prevalent fragility fracture strongly predicts future fracture. Previous studies have indicated that women with fragility fractures are not receiving the indicated treatment. We aimed to describe post fracture care in Canadian women using a large, population-based prospective cohort that began in 1995-1997. We followed 5,566 women over 50 years of age from across Canada over a period of 10 years in the Canadian Multicentre Osteoporosis Study. Information on medication use and incident clinical fragility fractures was obtained during a yearly questionnaire or interview and fractures were confirmed by radiographic/medical reports. Over the 10-year study period, 42-56% of women with yearly incident clinical fragility fractures were not treated with an osteoporosis medication. During year 1 of the study, 22% of the women who had experienced a fragility fracture were on treatment with a bisphosphonate and 26% were on hormone therapy (HT). We were not able to differentiate HT use for menopause symptoms vs osteoporosis. Use of bisphosphonate therapy increased over time; odds ratio (OR) for use at year 10 compared to use at year 1 was 3.65 (95% confidence interval (CI) 1.83-7.26). In contrast, HT use declined, with an OR of 0.07 (95%CI 0.02-0.24) at year 10 compared to year 1 of the study. In a large population-based cohort study, we found a therapeutic care gap in women with osteoporosis and fragility fractures. Although bisphosphonate therapy usage improved over time, a substantial gap remains.

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