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长QT间期综合征和尖端扭转型室速的电生理机制

Electrophysiologic mechanisms of the long QT interval syndromes and torsade de pointes.

作者信息

Tan H L, Hou C J, Lauer M R, Sung R J

机构信息

Stanford University School of Medicine, California, USA.

出版信息

Ann Intern Med. 1995 May 1;122(9):701-14. doi: 10.7326/0003-4819-122-9-199505010-00009.

Abstract

PURPOSE

To review the current understanding of the mechanisms and treatment of the long QT interval syndromes and torsade de pointes.

DATA SOURCES

Personal databases of the authors and a search of the MEDLINE database from 1966 to 1994.

STUDY SELECTION

Experimental and clinical studies and topical reviews on the electrophysiologic mechanisms and treatment of torsade de pointes were analyzed.

RESULTS

The long QT interval syndromes have been classified into acquired and hereditary forms, both of which are associated with a characteristic type of life-threatening polymorphic ventricular tachycardia called torsade de pointes. The acquired form is caused by various agents and conditions that reduce the magnitude of outward repolarizing K+ currents, enhance inward depolarizing Na+ or Ca2+ currents, or both, thereby triggering the development of early afterdepolarizations that initiate the tachyarrhythmia. The hereditary form appears to result from an abnormal response to adrenergic or sympathetic nervous system stimulation. At least some cases of the hereditary long QT interval syndromes may result from a single gene defect that alters the intracellular regulatory proteins responsible for the modulation of K+ channel function. Treatment of the acquired form is primarily directed at identifying and withdrawing the offending agent, although emergent therapy using maneuvers and agents that favorably modulate transmembrane ion currents can be lifesaving. In torsade de pointes associated with the hereditary long QT interval syndromes, early diagnosis leading to treatments designed to both shorten the QT interval and block the beta-adrenergic-induced instability of the QT interval is essential.

CONCLUSIONS

The long QT interval syndromes and torsade de pointes are potentially life-threatening conditions caused by various agents, conditions, and genetic defects. The mechanisms responsible for these conditions and available treatment options for them are reviewed.

摘要

目的

综述目前对长QT间期综合征及尖端扭转型室速的发病机制和治疗的认识。

资料来源

作者的个人数据库以及对1966年至1994年MEDLINE数据库的检索。

研究选择

分析了关于尖端扭转型室速电生理机制和治疗的实验及临床研究以及专题综述。

结果

长QT间期综合征已被分为获得性和遗传性两种类型,二者均与一种特征性的、危及生命的多形性室性心动过速——尖端扭转型室速相关。获得性类型由多种因素和情况引起,这些因素会降低外向复极化钾电流的幅度、增强内向去极化钠电流或钙电流,或二者兼而有之,从而引发早期后除极,进而引发快速心律失常。遗传性类型似乎是由于对肾上腺素能或交感神经系统刺激的异常反应所致。遗传性长QT间期综合征的至少一些病例可能是由单个基因缺陷引起的,该缺陷改变了负责调节钾通道功能的细胞内调节蛋白。获得性类型的治疗主要针对识别和停用致病因素,尽管使用能有利地调节跨膜离子电流的方法和药物进行紧急治疗可能挽救生命。在与遗传性长QT间期综合征相关的尖端扭转型室速中,早期诊断并采取旨在缩短QT间期以及阻断β肾上腺素能诱导的QT间期不稳定的治疗至关重要。

结论

长QT间期综合征和尖端扭转型室速是由多种因素、情况和基因缺陷引起的潜在危及生命的病症。本文综述了导致这些病症的机制以及针对它们的可用治疗选择。

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