Abstract
Purpose:
In clinical trials, bisphosphonate therapy reduces but does not eliminate the risk of fracture. The objective of this retrospective observational study was to examine fracture rates among women who were adherent to bisphosphonate therapy for at least 1 year.
Methods:
We studied outcomes for women ≥50 years old who received their first osteoporosis therapy as an oral bisphosphonate during 2002–2008 and were enrolled in a large claims database for ≥3 consecutive years, including a baseline year before and 2 years after the index prescription (thus, the full study period was 2001–2010). Adherence during the first year of therapy was defined as a medication possession ratio (MPR) ≥80% (total number of days’ supply/365 days × 100%).
Results:
Of the 62,446 women who met the eligibility criteria, 26,852 (43%) had an MPR ≥80% for osteoporosis therapy during year 1. In year 2, the fracture rate was 52/1000 patient-years. Fragility fractures were recorded for 1292 patients (4.8%) during the baseline year (before initiating therapy); for 1051 patients (3.9%) during year 1 (adherence year); and for 871 patients (3.2%) during year 2. Significant predictors of fracture in year 2 were older age, higher comorbidity score, comorbid inflammatory joint disease, and prior fragility fracture during the baseline year or first year of treatment. The primary limitation of these results is the scope of the claims database, which did not provide information on bone mineral density, supplemental use of calcium or vitamin D, or reasons for initiating oral bisphosphonates.
Conclusions:
Despite being adherent to bisphosphonate treatment for 1 year, 3.2% of women experienced a fracture in the subsequent year. These results suggest an unmet need in patients with osteoporosis and an opportunity for newer therapies to help address this need.
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Transparency
Declaration of funding
This study was funded by Merck Sharp & Dohme Corp., Lebanon, NJ, USA.
Declaration of financial/other relationships
A.M. and S.S. have disclosed that they are employees of Merck Sharp & Dohme Corp., and hold stock in the company. J.T. has disclosed that he is an employee of Asclepius Analytics Ltd, a company supported by Merck to develop this study. A.D.-P. has disclosed that he has received unrestricted grants from Amgen, and has been a consultant to Amgen, Lilly, and Pfizer, and is on the Speakers’ Bureau of Lilly and Amgen. He has also received fees from GSK, Merck & Co. Inc., and Novartis and holds stock in Active Life Scientific.
CMRO peer reviewers on this manuscript have received an honorarium for their review work from CMRO. Peer reviewer 1 has disclosed that he is a consultant to Amgen, Lilly and Merck Sharp & Dohme. Peer reviewer 2 has no relevant financial or other relationships to disclose.
Acknowledgments
Medical writing and editorial assistance was provided by Elizabeth V. Hillyer, DVM. This assistance was funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co. Inc., Lebanon, NJ, USA.
Previous presentation: the work was presented as a poster at the American Society of Bone and Mineral Research (ASBMR) 2012 annual conference.