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Short QT Syndrome in Current Clinical Practice.

作者信息

Khera Sahil, Jacobson Jason T

机构信息

From the Division of Cardiology, Department of Medicine, New York Medical College/Westchester Medical Center, Valhalla, NY.

出版信息

Cardiol Rev. 2016 Jul-Aug;24(4):190-3. doi: 10.1097/CRD.0000000000000091.

DOI:10.1097/CRD.0000000000000091
PMID:26440650
Abstract

Short QT syndrome is a rare inherited autosomal dominant cardiac channelopathy associated with malignant ventricular and atrial arrhythmias. A shortened corrected QT interval is a marker for risk of malignant arrhythmias, which are secondary to increased transmural dispersion of repolarization. The underlying gain of function mutations in the potassium channels are most common but genetic testing remains low yield. This review discusses the cellular mechanisms, genetic involvement, clinical presentation, and current recommended management of patients with short QT syndrome relevant to current clinical practice.

摘要

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