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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2006-1856
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The Journal of Clinical Endocrinology & Metabolism Vol. 92, No. 3 887-894
Copyright © 2007 by The Endocrine Society

Discontinuation of Antiresorptive Therapies: A Comparison between 1998–2001 and 2002–2004 among Osteoporotic Women

Julie Blouin, Alice Dragomir, Louis-Georges Ste-Marie, Julio Cesar Fernandes and Sylvie Perreault

Faculties of Pharmacy (J.B., A.D., S.P.) and Medicine (L.-G.S.-M., J.C.F.), University of Montréal, Montréal, Québec, Canada H3C 3J7

Address all correspondence and requests for reprints to: Sylvie Perreault, Ph.D., P.O. Box 6128, Centre-Ville Station, Montréal, Québec, Canada H3C 3J7. E-mail: sylvie.perreault{at}umontreal.ca.

Context: Studies having reported high rates of discontinuation of antiresorptive therapies (ART) may not reflect their actual use.

Objectives: We compared probability of discontinuation among women aged 70 yr or older with a diagnosis of osteoporosis or recent osteoporotic fracture having started ART (alendronate, risedronate, cyclical etidronate, raloxifene, nasal calcitonin) between 1998–2001 or 2002–2004.

Patients and Methods: We constructed two cohorts of women using Régie de l’Assurance Maladie du Québec databases. Discontinuation was defined as a lapse of 30 d or longer after completion of a refill. Switching from one ART to another was allowed. Probability of discontinuation was estimated using Kaplan-Meier analysis. Multivariate Cox models were used to identify potential determinants of ART discontinuation over 1 yr.

Results: After 1 yr, probability of discontinuation was slightly lower in the 2002–2004 cohort than the 1998–2001 cohort (52.2 vs. 57.5%; P < 0.001). This difference remained significant after adjusting for determinants [adjusted rate ratio (RR) 0.92, 95% confidence interval (CI) 0.87–0.98]. Significant determinants of ART discontinuation within 1 yr included bone mineral density testing (RR 0.77; CI 0.73–0.82) performed within 2 yr prior to initiation of therapy and having consulted more than two pharmacies (RR 1.15; CI 1.06–1.25) in the year before starting therapy. In the 2002–2004 cohort, when switching was allowed, women initiating a once-weekly regimen of alendronate or risedronate did not show a 1-yr risk of discontinuation different from women initiating daily regimens of the same drugs (RR 0.90; CI 0.82–1.00).

Conclusions: Even if new dosing regimens were introduced, discontinuation of ART among osteoporotic women remains high.







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Copyright © 2007 by The Endocrine Society