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噻托溴铵的心血管风险:是否真实存在?

The cardiovascular risk of tiotropium: is it real?

机构信息

University of Rome Tor Vergata, Department of Internal Medicine, Unit of Respiratory Clinical Pharmacology, Rome, Italy.

出版信息

Expert Opin Drug Saf. 2010 Sep;9(5):783-92. doi: 10.1517/14740338.2010.500611.

Abstract

IMPORTANCE OF THE FIELD

Anticholinergic agents are of noteworthy value in the treatment of chronic obstructive pulmonary disease (COPD), but concerns have been raised about a possible association between their use and cardiovascular (CV) morbidity and mortality. In this review, we have examined whether and why an anticholinergic agent, and in particular tiotropium, might cause CV risks.

AREAS COVERED IN THIS REVIEW

We first examine the potential pharmacological mechanisms that justify the CV risk with an anticholinergic agent, and then the main clinical trials, observational (cohort or case-control) studies, descriptive reviews and meta-analyses that have looked at the CV risks associated with long-term tiotropium, which are available in MEDLINE, EMBASE and Cochrane Controlled Trials Register databases, using the following MeSH, full text and keyword terms: tiotropium bromide OR Spiriva AND COPD OR chronic obstructive pulmonary disease.

WHAT THE READER WILL GAIN

The almost absolute confidence that there is no real increased risk for death or CV morbidity during treatment with this inhaled anticholinergic agent in patients with COPD because of the results of a large 4-year trial and a robust and extensive analysis of > 19,000 patients participating in placebo-controlled tiotropium clinical trials. Nonetheless, because high-risk patients such as those with coronary artery disease, heart failure, cardiac arrhythmia, hypoxemia requiring daytime oxygen therapy and a creatinine > 2 mg/dl were excluded from Phase III clinical trials, it is impossible to exclude these patients from an increased risk of drug-related cardiac events in a real-world setting.

TAKE HOME MESSAGE

Despite the recently raised concerns about an excess risk of CV adverse events with inhaled short-acting anticholinergic agents, the risk:benefit ratio of tiotropium bromide appears still favorable, although it is not known whether high-risk patients are at an increased risk of drug-related CV events.

摘要

重要性领域

抗胆碱能药物在慢性阻塞性肺疾病(COPD)的治疗中具有重要价值,但人们对它们的使用与心血管(CV)发病率和死亡率之间可能存在关联表示担忧。在这篇综述中,我们研究了抗胆碱能药物,特别是噻托溴铵,是否以及为什么会引起 CV 风险。

涵盖的领域

我们首先检查了潜在的药理学机制,这些机制证明了抗胆碱能药物存在 CV 风险,然后检查了主要的临床试验、观察性(队列或病例对照)研究、描述性综述和荟萃分析,这些研究都着眼于与长期噻托溴铵相关的 CV 风险,这些研究可在 MEDLINE、EMBASE 和 Cochrane 对照试验登记数据库中使用以下 MeSH、全文和关键字词进行检索:噻托溴铵溴化物 OR 思力华 AND COPD OR 慢性阻塞性肺疾病。

读者将获得

由于一项为期 4 年的大型试验和对 >19000 名参加噻托溴铵安慰剂对照临床试验的患者进行的强有力和广泛的分析,几乎可以肯定,在 COPD 患者中使用这种吸入性抗胆碱能药物治疗不会增加死亡或 CV 发病率的风险。尽管如此,由于高风险患者(如患有冠状动脉疾病、心力衰竭、心律失常、需要日间氧疗的低氧血症和肌酐 >2mg/dl 的患者)被排除在 III 期临床试验之外,因此无法在真实环境中排除这些患者因药物相关的心脏事件而面临的风险增加。

重要信息

尽管最近对吸入性短效抗胆碱能药物引起 CV 不良事件风险增加表示担忧,但噻托溴铵溴化物的风险效益比似乎仍然有利,尽管尚不清楚高风险患者是否存在药物相关 CV 事件风险增加的情况。

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