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奎尼丁目前在心律失常治疗中临床应用的理论与实践。

Theory and practice of present clinical use of Quinidine in the management of cardiac arrhythmias.

作者信息

Belhassen Bernard, Milman Anat

机构信息

Heart Institute, Hadassah Medical Center, Jerusalem, Israel; Grey Faculty of Medical and Health Science, Tel-Aviv University, Tel Aviv, Israel.

Grey Faculty of Medical and Health Science, Tel-Aviv University, Tel Aviv, Israel; Arrhythmia Institute, Cardiovascular Division, Shamir Medical Center (Assaf Harofeh), Israel.

出版信息

Indian Pacing Electrophysiol J. 2025 Jul-Aug;25(4):264-273. doi: 10.1016/j.ipej.2025.07.017. Epub 2025 Jul 30.

DOI:10.1016/j.ipej.2025.07.017
PMID:40750064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12461717/
Abstract

At the beginning of the last century, quinidine had been shown to be highly effective in the management of atrial fibrillation and soon after, of ventricular arrhythmias. At the end of the same century, quinidine was quickly abandoned, and its manufacturing ceased, resulting in limited accessibility across numerous countries. Paradoxically, this decline in use occurred alongside accumulating evidence supporting quinidine's therapeutic benefit in managing rare, life-threatening ventricular arrhythmias occurring in patients with no organic heart disease (Idiopathic ventricular fibrillation, Brugada syndrome, Early repolarization syndrome, Short QT syndrome, Multifocal ectopic Purkinje-related premature contractions), as well as in those with organic heart disease involving the Purkinje network (acute myocardial infarction and hypertrophic cardiomyopathy). The present review will extensively deal with all these topics.

摘要

上世纪初,奎尼丁已被证明在治疗心房颤动方面非常有效,不久之后,在治疗室性心律失常方面也很有效。在同一世纪末,奎尼丁很快被弃用,其生产也停止了,导致在许多国家难以获得。矛盾的是,在使用量下降的同时,越来越多的证据支持奎尼丁在治疗无器质性心脏病患者(特发性室性心动过速、Brugada综合征、早期复极综合征、短QT综合征、多灶性与浦肯野相关的异位早搏)以及患有涉及浦肯野网络的器质性心脏病(急性心肌梗死和肥厚型心肌病)患者中发生的罕见、危及生命的室性心律失常方面具有治疗益处。本综述将广泛探讨所有这些主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/0a7b97fafdb4/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/74d1996881d9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/651394d35593/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/72e614ce9533/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/2fa51ae78969/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/22aa7afb0edc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/840fb38da0f3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/0a7b97fafdb4/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/74d1996881d9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/651394d35593/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/72e614ce9533/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/2fa51ae78969/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/22aa7afb0edc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/840fb38da0f3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb99/12461717/0a7b97fafdb4/gr7.jpg

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本文引用的文献

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Characteristics of patients with Brugada syndrome and monomorphic ventricular tachycardia.布加综合征合并单形性室性心动过速患者的特征。
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A Gain-of -Function SLC4A3 Mutation Causes Short-QT Syndrome: From Molecular Analysis to Novel Diagnostic Testing.功能获得性SLC4A3突变导致短QT综合征:从分子分析到新型诊断检测
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Short coupled Ventricular Fibrillation in a patient with TRPM4 mutation.
一名患有TRPM4突变的患者出现短联律室性心动过速。
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Interpreting the actionable clinical role of rare variants associated with short QT syndrome.解读与短 QT 综合征相关的罕见变异的可操作临床作用。
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Efficacy of quinidine for suppressing Purkinje-related ventricular fibrillation in a patient with hypertrophic cardiomyopathy associated with midventricular obstruction.奎尼丁对一名伴有心室中部梗阻的肥厚型心肌病患者抑制浦肯野相关室颤的疗效。
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Contributions of Israel to the field of clinical cardiac electrophysiology and implantable devices.以色列对临床心脏电生理学和植入式设备领域的贡献。
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Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome.遗传分析确定 SLC4A3 阴离子交换器为短 QT 综合征的主要基因。
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