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质子泵抑制剂的使用剂量和类型对澳大利亚老年女性骨折风险及骨质疏松症治疗的影响:一项前瞻性队列研究。

The effect of dose and type of proton pump inhibitor use on risk of fractures and osteoporosis treatment in older Australian women: A prospective cohort study.

作者信息

van der Hoorn Mariëlle M C, Tett Susan E, de Vries Oscar J, Dobson Annette J, Peeters G M E E Geeske

机构信息

The University of Queensland, School of Public Health, Brisbane, QLD 4006, Australia; VU University Amsterdam, Faculty of Medicine, Amsterdam 1081 BT, Netherlands.

The University of Queensland, School of Pharmacy, Brisbane, QLD 4072, Australia.

出版信息

Bone. 2015 Dec;81:675-682. doi: 10.1016/j.bone.2015.08.024. Epub 2015 Aug 28.

Abstract

OBJECTIVES

Proton pump inhibitors (PPIs) are among the most prescribed medications worldwide, however, there is growing concern regarding potential negative effects on bone health. The aim was to examine the effect of dose and type of PPI use on subsequent use of osteoporosis medication and fractures in older Australian women.

METHODS

Data were included from 4432 participants (born 1921-26) in the 2002 survey of the Australian Longitudinal Study on Women's Health. Medication data were from the national pharmaceutical administrative database (2003-2012, inclusive). Fractures were sourced from linked hospital datasets available for four major States of Australia. Competing risk regression models used PPI exposure as a time-dependent covariate and either time to first osteoporosis medication prescription or fracture as the outcome, with death as a competing risk.

RESULTS

Of the 2328 PPI users and 2104 PPI non-users, 827 (36%) and 550 (26%) became users of osteoporosis medication, respectively. PPI use was associated with an increased risk of subsequent use of osteoporosis medication (adjusted sub-hazard ratio [SHR]=1.28; 95% confidence interval [CI]=1.13-1.44) and subsequent fracture (SHR=1.29, CI=1.08-1.55). Analysis with PPI categorized according to defined daily dose (DDD), showed some evidence for a dose-response effect (osteoporosis medication: <400 DDD: SHR=1.23, CI=1.06-1.42 and ≥400 DDD: SHR=1.39, CI=1.17-1.65, compared with non-users; SHRs were in the same range for fractures). Esomeprazole was the most common PPI prescribed (22.9%). Analysis by type of PPI use showed an increased subsequent risk for: (1) use of osteoporosis medication for rabeprazole (SHR=1.51, CI=1.08-2.10) and esomeprazole (SHR=1.48, CI=1.17-1.88); and (2) fractures for rabeprazole (SHR=2.06, CI=1.37-3.10). Users of multiple types of PPI also had increased risks for use of osteoporosis medication and fractures.

CONCLUSION

An appropriate benefit/risk assessment should be made when prescribing PPIs, especially for esomeprazole and rabeprazole, as osteoporosis and fracture risks were increased in this cohort of elderly females subsequent to PPI prescription.

摘要

目的

质子泵抑制剂(PPIs)是全球范围内处方量最大的药物之一,然而,人们越来越担心其对骨骼健康的潜在负面影响。本研究旨在探讨PPIs的使用剂量和类型对澳大利亚老年女性后续骨质疏松药物使用及骨折情况的影响。

方法

数据来自2002年澳大利亚女性健康纵向研究调查中的4432名参与者(出生于1921年至1926年)。用药数据来自国家药品管理数据库(涵盖2003年至2012年)。骨折数据来自澳大利亚四个主要州的相关医院数据集。竞争风险回归模型将PPI暴露作为时间依存协变量,将首次骨质疏松药物处方时间或骨折作为结局,将死亡作为竞争风险。

结果

在2328名PPI使用者和2104名非PPI使用者中,分别有827人(36%)和550人(26%)后来使用了骨质疏松药物。使用PPI与后续使用骨质疏松药物的风险增加相关(调整后亚风险比[SHR]=1.28;95%置信区间[CI]=1.13 - 1.44)以及后续骨折风险增加相关(SHR=1.29,CI=1.08 - 1.55)。根据限定日剂量(DDD)对PPI进行分类分析,显示出一定的剂量反应效应证据(骨质疏松药物:<400 DDD:SHR=1.23,CI=1.06 - 1.42;≥400 DDD:SHR=1.39,CI=1.17 - 1.65,与非使用者相比;骨折的SHR处于相同范围)。埃索美拉唑是最常用的PPI(占22.9%)。按PPI使用类型分析显示,后续风险增加的情况如下:(1)雷贝拉唑(SHR=1.51,CI=1.08 - 2.10)和埃索美拉唑(SHR=1.48,CI=1.17 - 1.88)使用者使用骨质疏松药物的风险;(2)雷贝拉唑使用者发生骨折的风险(SHR=2.06,CI=1.37 - 3.10)。多种类型PPI使用者使用骨质疏松药物和发生骨折的风险也增加。

结论

开具PPIs处方时应进行适当的效益/风险评估,尤其是对于埃索美拉唑和雷贝拉唑,因为在该老年女性队列中,PPI处方后骨质疏松和骨折风险增加。

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