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Osteoporosis International

, Volume 29, Issue 11, pp 2409–2417 | Cite as

Medication persistence and risk of fracture among female Medicare beneficiaries diagnosed with osteoporosis

  • J. Liu
  • H. Guo
  • P. Rai
  • L. Pinto
  • R. Barron
Original Article

Abstract

Summary

We examined the relationship between persistent osteoporosis medication use and fracture risk among female Medicare beneficiaries diagnosed with osteoporosis using Medicare claims, 2009–2012. Persistent use was associated with reduced risk of fracture and significantly lower total health care costs in the follow-up period. Results were consistent using different analytical methods.

Introduction

This study aimed to examine the relationship between medication persistence and fracture risk among female Medicare beneficiaries diagnosed with osteoporosis.

Methods

Elderly female Medicare beneficiaries diagnosed with osteoporosis and initiated on osteoporosis medication January 1, 2009–June 30, 2011, were included. Persistent medication use was defined as continuous use (no gap ≥ 60 days) for 1 year or longer. The key outcome was fragility fracture. A difference-in-difference analysis was performed at the log scale of fracture rate using a Poisson regression model with months 1–6 before medication initiation as the pre-initiation period and up to 18 months after as the post-initiation period. Total health care costs were compared using a similar approach. Sensitivity analyses were conducted using different pre- and post-initiation periods.

Results

The study included 294,369 patients; 32.9% were persistent osteoporosis medication users and 67.1% non-persistent (< 12 months continuous use). Fracture incidence rates were 16.2 per 100 patient-years pre-initiation and 4.1 post-initiation for persistent users; corresponding rates for non-persistent users were 19.0 and 7.3 per 100 patient-years. The adjusted post-/pre-initiation fracture rate ratios were 0.284 for persistent and 0.411 for non-persistent users. The ratio of the two rate ratios was 0.692 (persistent vs. non-persistent, p < 0.0001), suggesting a significantly greater fracture rate reduction for persistent users. Adjusted cost ratios were significantly lower for persistent users. Sensitivity analyses results were similar.

Conclusions

Persistent use of osteoporosis medications was associated with reduced risk of fracture and significantly lower total health care costs. Payers and patients would benefit from interventions aimed at improving medication persistence.

Keywords

Fractures Medication Osteoporosis Persistence 

Notes

Acknowledgments

The authors thank Chronic Disease Research Group colleagues Anne Shaw for manuscript preparation and Nan Booth, MSW, MPH, and ELS, for manuscript editing.

Compliance with ethical standards

Conflicts of interest

This study was funded by Amgen Inc. and conducted by Chronic Disease Research Group, Minneapolis Medical Research Foundation, Minneapolis, Minnesota. Jiannong Liu and Haifeng Guo are employed by the Chronic Disease Research Group. Lionel Pinto and Rich Barron are employed by and shareholders in Amgen Inc. Pragya Rai was employed by Amgen.

Supplementary material

198_2018_4630_MOESM1_ESM.docx (169 kb)
ESM 1 (DOCX 168 kb)

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Copyright information

© International Osteoporosis Foundation and National Osteoporosis Foundation 2018

Authors and Affiliations

  1. 1.Chronic Disease Research GroupMinneapolis Medical Research FoundationMinneapolisUSA
  2. 2.Global Health Economics, Amgen Inc.Thousand OaksUSA
  3. 3.School of PharmacyWest Virginia University, Robert C. Byrd Health Sciences CenterMorgantownUSA

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