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Review Article
Drug Therapy
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Volume 350:1013-1022 March 4, 2004 Number 10
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Drug-Induced Prolongation of the QT Interval
Dan M. Roden, M.D.

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In the past decade, the single most common cause of the withdrawal or restriction of the use of drugs that have already been marketed has been the prolongation of the QT interval associated with polymorphic ventricular tachycardia, or torsade de pointes (Figure 1), which can be fatal.1 Nine structurally unrelated drugs that were marketed in the United States or elsewhere for a range of noncardiovascular indications have been removed from the market or had their availability severely restricted because of this rare form of toxicity. These drugs are terfenadine, astemizole, grepafloxicin, terodiline, droperidol, lidoflazine, sertindole, levomethadyl, and cisapride.

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The Clinical Background of Long-QT Syndrome

Problems Posed by Technological and Scientific Advances

Measurement and Interpretation of the QT Interval

Basic Electrophysiological Mechanisms

Identification of Drugs That Cause Torsade de Pointes

Weighing Risks and Benefits

Decision Making and Drugs with QT-Interval–Prolonging Potential

Broader Implications


Source Information

From the Division of Clinical Pharmacology, Vanderbilt University School of Medicine, Nashville.

Address reprint requests to Dr. Roden at the Division of Clinical Pharmacology, Vanderbilt University School of Medicine, 532 Medical Research Bldg. I, Nashville, TN 37232, or at dan.roden@vanderbilt.edu.


Related Letters:

Drug-Induced Prolongation of the QT Interval
Korantzopoulos P., Siogas K., Viskin S., Justo D., Zeltser D., Curigliano G., Cipolla C., de Braud F., Cruciani R. A., Portenoy R. K., Homel P., Roden D. M.
Extract | Full Text | PDF  
N Engl J Med 2004; 350:2618-2621, Jun 17, 2004. Correspondence

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