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Methods for ECG Evaluation of Indicators of Cardiac Risk, and Susceptibility to Aconitine-induced Arrhythmias in Rats Following Status Epilepticus
Published on: April 5, 2011
Drug-induced proarrhythmia: Discussion and considerations for clinical practice
Ralph J Klotzbaugh1, Alejandra Martin, J Rick Turner
1Ralph J. Klotzbaugh is an assistant professor in the University of New Mexico College of Nursing in Albuquerque, N.M. Alejandra Martin is a physician assistant and clinical educator at Goodwin Community Health Center in Somersworth, N.H. J. Rick Turner is an adjunct professor in the Department of Pharmacy Practice at Campbell University College of Pharmacy and Health Sciences in Buies Creek, N.C. The authors have disclosed no potential conflicts of interest, financial or otherwise.
Abstract:
Clinical practice includes contributions from physicians, pharmacists, NPs, and physician assistants. Drug safety considerations are of considerable importance. This article discusses drug-induced proarrhythmia, with a specific focus on torsades de pointes, a polymorphic ventricular tachycardia that typically occurs in self-limiting bursts that can lead to dizziness, palpitations, syncope, and seizures, but on rare occasions can progress to ventricular fibrillation and sudden cardiac death. A dedicated clinical pharmacology study conducted during a drug's clinical development program has assessed its propensity to induce torsades using prolongation of the QT interval as seen on the ECG as a biomarker.Identification of QT-interval prolongation does not necessarily prevent a drug from receiving marketing approval if its overall benefit-risk balance is favorable, but, if approved, a warning is placed in its prescribing information. This article explains why drugs can have a proarrhythmic propensity.
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