• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[室性快速性心律失常作为药物治疗的副作用]

[Ventricular tachyarrhythmia as a side effect of pharmacotherapy].

作者信息

Demming Thomas, Bonnemeier Hendrik

机构信息

Klinik für Innere Medizin III für Kardiologie, Angiologie, Intensivmedizin, Abteilung für Elektrophysiologie und Rhythmologie, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Arnold Heller Straße 3, 24105, Kiel, Deutschland.

出版信息

Herzschrittmacherther Elektrophysiol. 2017 Jun;28(2):162-168. doi: 10.1007/s00399-017-0500-8. Epub 2017 May 9.

DOI:10.1007/s00399-017-0500-8
PMID:28488108
Abstract

Ventricular tachyarrhythmia is a severe and life-threatening potential side effect of pharmacotherapy. Substances with proarrhythmic potential belong to various groups of medication. Apart from antiarrhythmic agents, especially antibiotics and psychiatric drugs are worth mentioning owing to their broad application. Interaction with cardiac potassium channels is the most important reason for drug-induced ventricular tachyarrhythmia. Over 20 years of research in animal models and clinical studies have uncovered the underlying mechanisms. Findings in this field of research have also made a contribution to the understanding of genetic long QT syndromes. Clinical concerns that take drug interactions into account have been neglected due to the mechanistic research approach. For daily clinical practice, combination therapy of several potentially arrhythmogenic drugs is of predominant concern especially in situations when the therapeutic regime is changing such as admission to the hospital, admission to an intensive care unit or consultation of a new specialist. Especially in these situations, considerations about the arrhythmogenic potential of additionally administered drugs should be paid explicit attention. Additional concern should be paid to the fact that several proarrhythmogenic agents are metabolized over single pathways and are therefore prone to drug interactions that can severely raise the drug concentration and as a result arrhythmogenic potential.

摘要

室性快速心律失常是药物治疗的一种严重且危及生命的潜在副作用。具有促心律失常潜力的物质属于不同的药物类别。除抗心律失常药物外,尤其值得一提的是抗生素和精神药物,因为它们应用广泛。与心脏钾通道的相互作用是药物诱发室性快速心律失常的最重要原因。在动物模型和临床研究方面超过20年的研究已经揭示了其潜在机制。该研究领域的发现也为理解遗传性长QT综合征做出了贡献。由于采用机制研究方法,考虑药物相互作用的临床问题被忽视了。对于日常临床实践而言,几种潜在致心律失常药物的联合治疗是主要关注点,尤其是在治疗方案发生变化的情况下,如入院、入住重症监护病房或咨询新专科医生时。特别是在这些情况下,应特别关注额外使用药物的致心律失常潜力。还应额外关注的是,几种促心律失常药物通过单一途径代谢,因此容易发生药物相互作用,这可能会严重提高药物浓度,进而增加致心律失常潜力。

相似文献

1
[Ventricular tachyarrhythmia as a side effect of pharmacotherapy].[室性快速性心律失常作为药物治疗的副作用]
Herzschrittmacherther Elektrophysiol. 2017 Jun;28(2):162-168. doi: 10.1007/s00399-017-0500-8. Epub 2017 May 9.
2
Drug-induced proarrhythmia: risk factors and electrophysiological mechanisms.药物致心律失常:危险因素和电生理学机制。
Nat Rev Cardiol. 2016 Jan;13(1):36-47. doi: 10.1038/nrcardio.2015.110. Epub 2015 Jul 21.
3
Nonclinical proarrhythmia models: predicting Torsades de Pointes.非临床致心律失常模型:预测尖端扭转型室速
J Pharmacol Toxicol Methods. 2005 Jul-Aug;52(1):46-59. doi: 10.1016/j.vascn.2005.04.011.
4
Use of arterially perfused rabbit ventricular wedge in predicting arrhythmogenic potentials of drugs.动脉灌注兔心室楔形组织在预测药物致心律失常潜力中的应用。
J Pharmacol Toxicol Methods. 2006 Nov-Dec;54(3):261-72. doi: 10.1016/j.vascn.2006.02.005. Epub 2006 Mar 6.
5
[QT prolongation and torsade de pointes tachycardia during therapy with maprotiline. Differential diagnostic and therapeutic aspects].[米安色林治疗期间的QT间期延长和尖端扭转型室性心动过速。鉴别诊断和治疗方面]
Dtsch Med Wochenschr. 2001 Dec 7;126(49):1396-400. doi: 10.1055/s-2001-18880.
6
[Risks and side effects in treatment of supraventricular tachycardia].[室上性心动过速治疗中的风险与副作用]
Z Gesamte Inn Med. 1993 Sep;48(9):459-65.
7
[Proarrhythmic (torsadogenic) effects of QT-prolonging non-antiarrhythmic drugs].[延长QT间期的非抗心律失常药物的促心律失常(扭转型室性心动过速)作用]
Orv Hetil. 2005 Mar 6;146(10):451-60.
8
Intracardiac QT variability in patients with structural heart disease on class III antiarrhythmic drugs.使用Ⅲ类抗心律失常药物的结构性心脏病患者的心内QT变异性
J Electrocardiol. 2009 Nov-Dec;42(6):505-10. doi: 10.1016/j.jelectrocard.2009.07.011. Epub 2009 Aug 22.
9
[Sudden cardiac death : Epidemiology, pathophysiology and risk stratification].[心脏性猝死:流行病学、病理生理学及危险分层]
Herz. 2017 Apr;42(2):123-131. doi: 10.1007/s00059-017-4545-6.
10
Identification of drug targets related to the induction of ventricular tachyarrhythmia through a systems chemical biology approach.通过系统化化学生物学方法鉴定与室性快速性心律失常诱导相关的药物靶点。
Toxicol Sci. 2015 Jun;145(2):321-36. doi: 10.1093/toxsci/kfv054. Epub 2015 Mar 12.

引用本文的文献

1
Use of Patient Health Records to Quantify Drug-Related Pro-arrhythmic Risk.利用患者健康记录来量化与药物相关的致心律失常风险。
Cell Rep Med. 2020 Aug 25;1(5):100076. doi: 10.1016/j.xcrm.2020.100076.

本文引用的文献

1
Drug-induced proarrhythmia: risk factors and electrophysiological mechanisms.药物致心律失常:危险因素和电生理学机制。
Nat Rev Cardiol. 2016 Jan;13(1):36-47. doi: 10.1038/nrcardio.2015.110. Epub 2015 Jul 21.
2
Interaction between digoxin and dronedarone in the PALLAS trial.在PALLAS试验中地高辛与决奈达隆的相互作用。
Circ Arrhythm Electrophysiol. 2014 Dec;7(6):1019-25. doi: 10.1161/CIRCEP.114.002046. Epub 2014 Nov 6.
3
Voriconazole associated torsades de pointes in two adult patients with haematological malignancies.
伏立康唑与两名血液系统恶性肿瘤成年患者的尖端扭转型室速相关。
Med Mycol Case Rep. 2014 Mar 13;4:23-5. doi: 10.1016/j.mmcr.2014.03.001. eCollection 2014 Apr.
4
Prolonged QTc interval and torsades de pointes induced by citalopram.西酞普兰引起的QTc间期延长和尖端扭转型室性心动过速。
Tex Heart Inst J. 2012;39(1):68-70.
5
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.钾通道突变与心律失常——诊断与治疗。
Nat Rev Cardiol. 2012 Jan 31;9(6):319-32. doi: 10.1038/nrcardio.2012.3.
6
Dronedarone in high-risk permanent atrial fibrillation.盐酸决奈达隆治疗高危持续性心房颤动
N Engl J Med. 2011 Dec 15;365(24):2268-76. doi: 10.1056/NEJMoa1109867. Epub 2011 Nov 14.
7
A new mechanism preventing proarrhythmia in chronic heart failure: rapid phase-III repolarization explains the low proarrhythmic potential of amiodarone in contrast to sotalol in a model of pacing-induced heart failure.一种预防慢性心力衰竭中致心律失常的新机制:快速Ⅲ相复极解释了与索他洛尔相比,胺碘酮在起搏诱导心力衰竭模型中致心律失常潜在风险低的原因。
Eur J Heart Fail. 2011 Oct;13(10):1060-9. doi: 10.1093/eurjhf/hfr107. Epub 2011 Aug 25.
8
Fluconazole inhibits hERG K(+) channel by direct block and disruption of protein trafficking.氟康唑通过直接阻断和蛋白转运破坏抑制 hERG K(+) 通道。
Eur J Pharmacol. 2011 Jan 10;650(1):138-44. doi: 10.1016/j.ejphar.2010.10.010. Epub 2010 Oct 15.
9
Inhibition of the Na+/Ca2+ exchanger suppresses torsades de pointes in an intact heart model of long QT syndrome-2 and long QT syndrome-3.抑制钠/钙交换体可抑制长QT综合征2型和长QT综合征3型完整心脏模型中的尖端扭转型室速。
Heart Rhythm. 2008 Oct;5(10):1444-52. doi: 10.1016/j.hrthm.2008.06.017. Epub 2008 Jun 28.
10
Augmentation of late sodium current unmasks the proarrhythmic effects of amiodarone.晚钠电流增强揭示了胺碘酮的促心律失常作用。
Cardiovasc Res. 2008 Feb 1;77(3):481-8. doi: 10.1093/cvr/cvm069. Epub 2007 Nov 13.