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COPD 患者使用吸入性皮质类固醇的骨折风险:随机对照试验和观察性研究的系统评价和荟萃分析。

Risk of fractures with inhaled corticosteroids in COPD: systematic review and meta-analysis of randomised controlled trials and observational studies.

机构信息

School of Medicine, University of East Anglia, Norwich NR4 7TJ, UK.

出版信息

Thorax. 2011 Aug;66(8):699-708. doi: 10.1136/thx.2011.160028. Epub 2011 May 20.

Abstract

BACKGROUND

The effect of inhaled corticosteroids (ICS) on fracture risk in patients with chronic obstructive pulmonary disease (COPD) remains uncertain. The aim of this study was to evaluate the association between ICS and fractures in COPD.

METHODS

MEDLINE, EMBASE, regulatory documents and company registries were searched up to August 2010. Randomised controlled trials (RCTs) of budesonide or fluticasone versus control treatment for COPD (≥24 weeks duration) and controlled observational studies reporting on fracture risk with ICS exposure vs no exposure in COPD were included. Peto OR meta-analysis was used for fracture risk from RCTs while ORs from observational studies were pooled using the fixed effect inverse variance method. Dose-response analysis was conducted using variance-weighted least squares regression in the observational studies. Heterogeneity was assessed using the I(2) statistic.

RESULTS

Sixteen RCTs (14 fluticasone, 2 budesonide) with 17,513 participants, and seven observational studies (n=69,000 participants) were included in the meta-analysis. ICSs were associated with a significantly increased risk of fractures (Peto OR 1.27; 95% CI 1.01 to 1.58; p=0.04; I(2)=0%) in the RCTs. In the observational studies, ICS exposure was associated with a significantly increased risk of fractures (OR 1.21; 95% CI 1.12 to 1.32; p<0.001; I(2)=37%), with each 500 μg increase in beclomethasone dose equivalents associated with a 9% increased risk of fractures, OR 1.09 (95% CI 1.06 to 1.12; p<0.001).

CONCLUSION

Among patients with COPD, long-term exposure to fluticasone and budesonide is consistently associated with a modest but statistically significant increased likelihood of fractures.

摘要

背景

吸入性皮质类固醇(ICS)对慢性阻塞性肺疾病(COPD)患者骨折风险的影响尚不确定。本研究旨在评估 ICS 与 COPD 患者骨折之间的关系。

方法

检索 MEDLINE、EMBASE、监管文件和公司登记处,检索时间截至 2010 年 8 月。纳入布地奈德或氟替卡松与 COPD(≥24 周)对照治疗的随机对照试验(RCT),以及报告 ICS 暴露与 COPD 无暴露骨折风险的对照观察研究。使用 Peto OR 荟萃分析评估 RCT 中的骨折风险,使用固定效应逆方差法汇总观察研究中的 OR。在观察性研究中,使用方差加权最小二乘法回归进行剂量-反应分析。使用 I(2)统计量评估异质性。

结果

纳入 16 项 RCT(14 项氟替卡松,2 项布地奈德),共 17513 名患者,7 项观察性研究(n=69000 名患者)纳入荟萃分析。ICS 与骨折风险显著增加相关(Peto OR 1.27;95% CI 1.01 至 1.58;p=0.04;I(2)=0%)。在观察性研究中,ICS 暴露与骨折风险显著增加相关(OR 1.21;95% CI 1.12 至 1.32;p<0.001;I(2)=37%),与每次增加 500μg 倍氯米松剂量等效物,骨折风险增加 9%,OR 1.09(95% CI 1.06 至 1.12;p<0.001)。

结论

在 COPD 患者中,长期暴露于氟替卡松和布地奈德与骨折风险适度但具有统计学意义的增加相关。

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