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致 QT 间期延长的风险因素:证据的系统综述。

Risk factors for QTc-prolongation: systematic review of the evidence.

机构信息

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Herestraat 49, O&N2, Box 521, 3000, Leuven, Belgium.

Department of Cardiovascular Sciences, KU Leuven, 3000, Leuven, Belgium.

出版信息

Int J Clin Pharm. 2017 Feb;39(1):16-25. doi: 10.1007/s11096-016-0414-2. Epub 2016 Dec 23.

Abstract

Background QTc-interval prolongation has been associated with serious adverse events, such as Torsade de Pointes and sudden cardiac death. In the prevention of QTc-prolongation, special attention should go to high-risk patients. Aim of the review The aim of this review is to summarize and assess the evidence for different risk factors for QTc-prolongation (demographic factors, comorbidities, electrolytes, QTc-prolonging medication). Methods Potential studies were retrieved based on a systematic search of articles published until June 2015 in the databases Medline and Embase. Both terms about QTc-prolongation/Torsade de Pointes and risk factors were added in the search strategy. The following inclusion criteria were applied: randomized controlled trials and observational studies; inclusion of ≥500 patients from a general population (not limited to specific disease states); assessment of association between QTc-interval and risk factors. For the articles that met the inclusion criteria, the following data were extracted: study design, setting and study population, number of patients and cases of QTc-prolongation, method of electrocardiogram-monitoring, QTc-correction formula, definition of QTc-prolongation, statistical methods and results. Quality assessment was performed using the GRADE approach (for randomized controlled trials) and the STROBE-recommendations (for observational studies). Based on the number of significant results and the level of significance, a quotation of the evidence was allocated. Results Ten observational studies could be included, with a total of 89,532 patients [prospective cohort design: N = 6; multiple regression analyses: N = 5; median STROBE score = 17/22 (range 15-18)]. Very strong evidence was found for hypokalemia, use of diuretics, antiarrhythmic drugs and QTc-prolonging drugs of list 1 of CredibleMeds. Little or no evidence was found for hyperlipidemia, the use of digoxin or statins, neurological disorders, diabetes, renal failure, depression, alcohol abuse, heart rate, pulmonary disorders, hormone replacement therapy, hypomagnesemia, history of a prolonged QTc-interval/Torsade de Pointes, familial history of cardiovascular disease, and the use of only QTc-prolonging drugs of list 2 or 3 of CredibleMeds. Conclusion This systematic review gives a clear overview of the available evidence for a broad range of risk factors for QTc-prolongation.

摘要

背景

QTc 间期延长与严重不良事件相关,如尖端扭转型室性心动过速和心脏性猝死。在预防 QTc 延长方面,应特别注意高危患者。目的:综述的目的是总结和评估不同的 QTc 延长危险因素(人口统计学因素、合并症、电解质、QTc 延长药物)的证据。方法:基于系统搜索 2015 年 6 月前在 Medline 和 Embase 数据库中发表的文章,检索了潜在的研究。搜索策略中添加了关于 QTc 延长/尖端扭转型室性心动过速和危险因素的术语。应用的纳入标准包括:随机对照试验和观察性研究;纳入一般人群(不限于特定疾病状态)中的≥500 例患者;评估 QTc 间期与危险因素之间的关系。对于符合纳入标准的文章,提取了以下数据:研究设计、地点和研究人群、QTc 延长患者和病例数、心电图监测方法、QTc 校正公式、QTc 延长的定义、统计方法和结果。使用 GRADE 方法(随机对照试验)和 STROBE 建议(观察性研究)进行质量评估。根据显著结果的数量和显著性水平,分配证据的引文。结果:纳入了 10 项观察性研究,共 89532 例患者[前瞻性队列设计:N=6;多元回归分析:N=5;中位数 STROBE 评分=17/22(范围 15-18)]。低钾血症、利尿剂、抗心律失常药物和 CredibleMeds 清单 1 的 QTc 延长药物的使用存在非常强的证据。高脂血症、地高辛或他汀类药物的使用、神经系统疾病、糖尿病、肾衰竭、抑郁症、酗酒、心率、肺部疾病、激素替代疗法、低镁血症、QTc 间期延长/尖端扭转型室性心动过速病史、心血管疾病家族史以及仅使用 CredibleMeds 清单 2 或 3 的 QTc 延长药物的使用证据很少或没有。结论:本系统综述清楚地概述了广泛的 QTc 延长危险因素的现有证据。

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