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Anti-Osteoporosis medication prescriptions and incidence of subsequent fracture among primary hip fracture patients in England and Wales: an interrupted time-series analysis

机译:英格兰和威尔士原发性髋部骨折患者的抗骨质疏松症药物处方和随后骨折的发生率:中断的时间序列分析

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摘要

In January 2005, the National Institute for Health and Care Excellence (NICE) in England and Wales provided new guidance on the use of antiosteoporosis therapies for the secondary prevention of osteoporotic fractures. This was shortly followed in the same year by market authorization of a generic form of alendronic acid within the UK. We here set out to estimate the actual practice impact of these events among hip fracture patients in terms of antiosteoporosis medication prescribing and subsequent fracture incidence using primary care data (Clinical Practice Research Datalink) from 1999 to 2013. Changes in level and trend of prescribing and subsequent fracture following publication of NICE guidance and availability of generic alendronic acid were estimated using an interrupted time series analysis. Both events were considered in combination within a 1-year “intervention period.” We identified 10,873 primary hip fracture patients between April 1999 and Sept 2012. Taking into account prior trend, the intervention period was associated with an immediate absolute increase of 14.9% (95% CI, 10.9 to 18.9) for incident antiosteoporosis prescriptions and a significant and clinically important reduction in subsequent major and subsequent hip fracture: –0.19% (95% CI, –0.28 to –0.09) and –0.17% (95% CI, –0.26 to –0.09) per 6 months, respectively. This equated to an approximate 14% (major) and 22% (hip) reduction at 3 years postintervention relative to expected values based solely on preintervention level and trend. We conclude that among hip fracture patients, publication of NICE guidance and availability of generic alendronic acid was temporally associated with increased prescribing and a significant decline in subsequent fractures
机译:2005年1月,位于英格兰和威尔士的国家卫生与医疗保健卓越学院(NICE)就抗骨质疏松疗法用于骨质疏松性骨折的二级预防提供了新的指导。随后在同年不久,英国也批准了通用形式的阿仑膦酸的市场许可。我们根据1999年至2013年的初级保健数据(Clinical Practice Research Datalink),根据抗骨质疏松药物处方和随后的骨折发生率,估算这些事件对髋部骨折患者的实际影响。 NICE指南发布后的后续骨折,以及使用中断的时间序列分析评估了通用阿仑膦酸的可用性。在1年的“干预期”内将这两个事件组合考虑。我们确定了1999年4月至2012年9月之间的10,873例原发性髋部骨折患者。考虑到先前的趋势,干预期间因发生抗骨质疏松症的处方立即绝对增加14.9%(95%CI,10.9至18.9),且显着且显着每6个月分别减少–0.19%(95%CI,–0.28至–0.09)和–0.17%(95%CI,–0.26至–0.09),对随后发生的重大髋关节和后继髋部骨折具有重要的临床意义。相对于仅基于干预前水平和趋势的预期值,干预后3年相当于减少了14%(主要)和22%(臀部)。我们得出的结论是,在髋部骨折患者中,NICE指南的发布和通用阿仑膦酸的可用性在时间上与处方增加和随后骨折的明显减少有关

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