Long QT syndrome and anaesthesia.

N A Wisely, E A Shipton

Journal: European journal of anaesthesiology 2003;19(12):853-9

PMID: 12510903

Abstract

The long QT syndrome is a disorder of myocardial electrical conduction that leaves the heart vulnerable to the ventricular tachydysrhythmia torsade de pointes. Clinically, this results in syncope or sudden death. The long QT syndrome may be congenital, if caused by abnormal myocardial potassium or sodium ion channels, or acquired, if due to drugs, electrolyte abnormalities or metabolic conditions. Triggers for the development of torsade de pointes include both anaesthesia and surgery. Some anaesthetic agents prolong the QT interval. The condition is reviewed and suggestions are made for the anaesthetic management of affected patients.

Address: University of Otago, Department of Anaesthesia, Christchurch School of Medicine and Health Sciences, Christchurch, New Zealand.

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