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使用III类抗心律失常药物进行单药治疗与联合治疗以减轻复极跨壁离散度:尖端扭转型室速的一个潜在危险因素

Monotherapy versus combination therapy with class III antiarrhythmic agents to attenuate transmural dispersion of repolarization: a potential risk factor for torsade de pointes.

作者信息

Shah Sachin A, Kluger Jeffrey, White C Michael

机构信息

Department of Drug Information, Hartford Hospital, Hartford, Connecticut 06102-5037, USA.

出版信息

Pharmacotherapy. 2007 Sep;27(9):1297-305. doi: 10.1592/phco.27.9.1297.

Abstract

Class III antiarrhythmic agents are used for conversion to and maintenance of sinus rhythm from arrhythmias of atrial or ventricular origin. Monotherapy can be limited by adverse events or recurrent arrhythmias. Sotalol, dofetilide, and ibutilide may induce torsade de pointes in 2-8% of patients, whereas amiodarone induces torsade de pointes in less than 1%. We reviewed the literature regarding the possible combination of class III antiarrhythmics and risk for inducing torsade de pointes. Animal studies using amiodarone plus sotalol or d-sotalol suggest that these drug combinations prolong the QTc interval but do not induce torsade de pointes. Similar data extracted from human studies of ibutilide in patients also receiving amiodarone or sotalol showed greater efficacy with combination therapy than with monotherapy, without increased torsade de pointes induction. Reduced transmural dispersion of repolarization with amiodarone and sotalol combination therapy may serve as a mechanism for reducing the risk of torsade de pointes compared with sotalol monotherapy.

摘要

III类抗心律失常药物用于将房性或室性心律失常转复为窦性心律并维持窦性心律。单一疗法可能会受到不良事件或心律失常复发的限制。索他洛尔、多非利特和伊布利特可使2%至8%的患者发生尖端扭转型室性心动过速,而胺碘酮引起尖端扭转型室性心动过速的比例不到1%。我们回顾了关于III类抗心律失常药物联合使用以及诱发尖端扭转型室性心动过速风险的文献。使用胺碘酮加索他洛尔或d - 索他洛尔的动物研究表明,这些药物组合可延长QTc间期,但不会诱发尖端扭转型室性心动过速。从同时接受伊布利特和胺碘酮或索他洛尔治疗的患者的人体研究中提取的类似数据显示,联合治疗比单一疗法疗效更佳,且不会增加尖端扭转型室性心动过速的诱发率。与索他洛尔单一疗法相比,胺碘酮和索他洛尔联合治疗可减少跨壁复极离散度,这可能是降低尖端扭转型室性心动过速风险 的一种机制。

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