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Inhaled anticholinergics and risk of major adverse cardiovascular events in patients with chronic obstructive pulmonary disease: a systematic review and meta-analysis.

机译:慢性阻塞性肺疾病患者吸入抗胆碱能药物和重大心血管不良事件的风险:系统评价和荟萃分析。

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CONTEXT: Inhaled anticholinergics (ipratropium bromide or tiotropium bromide) are widely used in patients with chronic obstructive pulmonary disease (COPD) but their effect on the risk of cardiovascular outcomes is unknown. OBJECTIVE: To ascertain the cardiovascular risks of inhaled anticholinergics, including cardiovascular death, myocardial infarction (MI), and stroke. DATA SOURCES: Systematic searches were conducted on March 19, 2008, of relevant articles in MEDLINE, the Cochrane Database of systematic reviews, regulatory authority Web sites in the United States and the United Kingdom, and manufacturers' trial registries with no date restrictions. STUDY SELECTION: Randomized controlled trials of any inhaled anticholinergic for treatment of COPD that had at least 30 days of treatment and reported on cardiovascular events. DATA EXTRACTION: The primary outcome was a composite of cardiovascular death, MI, or stroke. The secondary outcome was all-cause mortality. Relative risks (RRs) were estimated usingfixed-effects models and statistical heterogeneity was estimated with the I(2) statistic. DATA SYNTHESIS: After a detailed screening of 103 articles, 17 trials enrolling 14 783 patients were analyzed. Follow-up duration ranged from 6 weeks to 5 years. Cardiovascular death, MI, or stroke occurred in 135 of 7472 patients (1.8%) receiving inhaled anticholinergics and 86 of 7311 patients (1.2%) receiving control therapy (RR, 1.58 [95% confidence interval {CI}, 1.21-2.06]; P < .001, I(2) = 0%). Among individual components of the primary end point, inhaled anticholinergics significantly increased the risk of MI (RR, 1.53 [95% CI 1.05-2.23]; P = .03, I(2) = 0%) and cardiovascular death (RR, 1.80 [95% CI, 1.17-2.77]; P = .008, I(2) = 0%) without a statistically significant increase in the risk of stroke (RR, 1.46 [95% CI, 0.81-2.62]; P = .20, I(2) = 0%). All-cause mortality was reported in 149 of the patients treated with inhaled anticholinergics (2.0%) and 115 of the control patients (1.6%) (RR, 1.26 [95% CI, 0.99-1.61]; P = .06, I(2) = 2%). A sensitivity analysis restricted to 5 long-term trials (>6 months) confirmed the significantly increased risk of cardiovascular death, MI, or stroke (2.9% of patients treated with anticholinergics vs 1.8% of the control patients; RR, 1.73 [95% CI, 1.27-2.36]; P < .001, I(2) = 0%). CONCLUSION: Inhaled anticholinergics are associated with a significantly increased risk of cardiovascular death, MI, or stroke among patients with COPD.
机译:背景:吸入性抗胆碱药(异丙托溴铵或噻托溴铵)被广泛用于慢性阻塞性肺疾病(COPD)患者,但它们对心血管结局风险的影响尚不清楚。目的:确定吸入抗胆碱药的心血管风险,包括心血管死亡,心肌梗塞和中风。数据来源:系统搜索于2008年3月19日对MEDLINE中的相关文章,系统评价的Cochrane数据库,美国和英国的监管机构网站以及制造商的试验注册地进行了无日期限制。研究选择:至少治疗30天并报告心血管事件的任何吸入性抗胆碱能药物治疗COPD的随机对照试验。数据提取:主要结果是心血管死亡,心梗或中风的综合结果。次要结果是全因死亡率。使用固定效应模型估算相对风险(RR),并使用I(2)统计量估算统计异质性。数据综合:在对103篇文章进行详细筛选之后,对17项纳入14783名患者的试验进行了分析。随访时间从6周到5年不等。接受抗胆碱能药物的7472例患者中有135例发生心血管死亡,MI或中风(1.8%),接受对照治疗的7311例患者中有86例(1.2%)发生心血管死亡(RR,1.58 [95%置信区间{CI},1.21-2.06]; P <0.001,I(2)= 0%)。在主要终点的各个组成部分中,吸入抗胆碱能药物显着增加发生MI的风险(RR,1.53 [95%CI 1.05-2.23]; P = .03,I(2)= 0%)和心血管死亡(RR,1.80) [95%CI,1.17-2.77]; P = .008,I(2)= 0%),但中风风险没有统计学上的显着增加(RR,1.46 [95%CI,0.81-2.62]; P =。 20,I(2)= 0%)。据报告,吸入型抗胆碱能药物治疗的患者中有149人(2.0%),对照组患者有115%(1.6%)的全因死亡率(RR,1.26 [95%CI,0.99-1.61]; P = .06,I( 2)= 2%)。限于5个长期试验(> 6个月)的敏感性分析证实,心血管死亡,心肌梗死或中风的风险显着增加(接受抗胆碱能药物治疗的患者为2.9%,对照组为1.8%; RR为1.73 [95% CI,1.27-2.36]; P <.001,I(2)= 0%)。结论:吸入抗胆碱能药与COPD患者心血管死亡,心梗或中风的风险显着增加有关。

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