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Multicenter Study
. 2015 Jul;26(7):1919-28.
doi: 10.1007/s00198-015-3098-x. Epub 2015 May 12.

Anti-osteoporosis drug prescribing after hip fracture in the UK: 2000-2010

Affiliations
Multicenter Study

Anti-osteoporosis drug prescribing after hip fracture in the UK: 2000-2010

C Klop et al. Osteoporos Int. 2015 Jul.

Abstract

The probability of initiating with anti-osteoporosis therapy increased from 7 % in 2000 to 46 % in 2010. This improvement was greater for patients over the age of 75 years. Men, those overweight, having dementia or exposed to antipsychotics, sedatives/hypnotics or opioid analgesics were significantly less likely to receive anti-osteoporosis drugs.

Introduction: The objective of this study was to examine trends and determinants of anti-osteoporosis drug prescribing after hip fracture in the UK between 2000 and 2010.

Methods: Data were extracted from the UK Clinical Practice Research Datalink for patients ≥50 years who had a first hip fracture between 2000 and 2010 and who did not currently (≤6 months prior) receive anti-osteoporosis drugs (bisphosphonates, strontium ranelate, parathyroid hormone, calcitonin and raloxifene) (n = 27,542). The cumulative incidence probability of being prescribed anti-osteoporosis drugs within 1 year after hip fracture was estimated by Kaplan-Meier life-table analyses. Determinants for treatment initiation were estimated by Cox proportional hazards models.

Results: The probability of being prescribed any anti-osteoporosis drug after hip fracture increased from 7 % in 2000 to 46 % in 2010. This trend was more marked in patients ≥75 years. The increase in prescribing of anti-osteoporosis drugs was complemented by a similar increase in vitamin D/calcium provision. Cumulative incidence of receiving anti-osteoporosis therapy was greater at any given point in time in women (8 % in 2000, 51 % in 2010) compared to men (4 % in 2000, 34 % in 2010). In addition to male gender, multivariable Cox regression identified reduced likelihood of receiving anti-osteoporosis drugs for those being overweight, having dementia and exposed to psychotropic drugs (antipsychotics, sedatives/hypnotics) or opioid analgesics.

Conclusion: Although the prescribing of anti-osteoporosis drugs after hip fracture has increased substantially since 2000, the overall rate remained inadequate, particularly in men. With the continuing increase in the absolute number of hip fractures, further research should be made into the barriers to optimise osteoporosis management.

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Figures

Fig. 1
Fig. 1
Trends in anti-osteoporosis drug prescribing after hip fracture (by Kaplan-Meier method), stratified by sex (a), age categories (b) and region (c)
Fig. 2
Fig. 2
Trends in anti-osteoporosis drug prescribing after hip fracture (by Kaplan-Meier method), stratified by drug class (a) and type of bisphosphonate (b)
Fig. 3
Fig. 3
Trends in anti-osteoporosis drug and calcium/vitamin D prescribing individually or combined (by Kaplan-Meier method)

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