Electrocardiographic implications of the prolonged QT interval

被引:11
作者
Moskovitz, Joshua B. [1 ]
Hayes, Bryan D. [2 ]
Martinez, Joseph P. [2 ]
Mattu, Amal [2 ]
Brady, William J. [3 ]
机构
[1] Hofstra North Shore Long Isl Jewish Sch Med, Dept Emergency Med, Hempstead, NY USA
[2] Univ Maryland, Sch Med, Dept Emergency Med, Baltimore, MD 21201 USA
[3] Univ Virginia, Dept Emergency Med, Charlottesville, VA USA
关键词
TORSADES-DE-POINTES; SUDDEN-DEATH; CLINICAL-FEATURES; RISK; CHANNEL; MUTATION; DISEASE; GENES;
D O I
10.1016/j.ajem.2012.12.013
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The QT interval measures the time from the start of the QRS complex to the end of the T wave. Prolongation of the QT interval may lead to malignant ventricular tachydysrhythmias, including torsades de pointes. Causes of QT prolongation include congenital abnormalities of the sodium or potassium channel, electrolyte abnormalities, and medications; idiopathic causes have also been identified. Patients can be asymptomatic or present with syncope, palpitations, seizure-like activity, or sudden cardiac death. Management involves looking for and treating reversible causes. For patients with congenital or idiopathic QT interval prolongation, the use of beta-blockers can be considered. Certain subsets of patients benefit from implantation of a cardioverter-defibrillator. Clinicians must remain vigilant for QT interval prolongation when interpreting electrocardiograms, especially in patients presenting with syncope or ventricular arrhythmias. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:866 / 871
页数:6
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