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Electrocardiographic Predictors of Torsadogenic Risk During Dofetilide or Sotalol Initiation: Utility of a Novel T Wave Analysis Program

Authors :
Paul A. Friedman
Christopher V. DeSimone
Michael J. Ackerman
Samuel J. Asirvatham
Vaclav Kremen
Bryan L. Striemer
Peter A. Brady
Yehu Sapir
Seth H. Sheldon
Alan Sugrue
Bo Qiang
Peter A. Noseworthy
Source :
Cardiovascular Drugs and Therapy. 29:433-441
Publication Year :
2015
Publisher :
Springer Science and Business Media LLC, 2015.

Abstract

Initiation of class III anti-arrhythmic medications requires telemetric monitoring for ventricular arrhythmias and QT prolongation to reduce the risk of torsades de pointes (TdP). Heart rate-corrected QT interval (QTc) is an indicator of risk, however it is imperfect, and subtle abnormalities of repolarization have been linked with arrhythmogenesis.Identification of electrocardiographic predictors of torsadogenic risk through the application of a novel T wave analysis tool.Among all patients admitted to Mayo Clinic for initiation of dofetilide or sotalol, we identified 13 cases who developed drug-induced TdP and 26 age and sex matched controls that did not develop TdP. The immediate pre-TdP ECG of those with TdP was compared to the last ECG performed prior to hospital discharge in controls using a novel T wave program that quantified subtle changes in T wave morphology.The QTc and 12 T wave parameters successfully distinguished TdP cases from controls. The top performing parameters were the QTc in lead V3 (mean case vs control 480 vs 420 msec, p 0.001, r = 0.72) and T wave right slope in lead I (mean case vs control -840.29 vs -1668.71 mV/s, p = 0.002, r = 0.45). The addition of T wave right slope to QTc improved prediction accuracy from 79 to 88 %.Our data demonstrate that, in addition to QTc, the T wave right slope is correlated strongly with TdP risk. This suggests that a computer-based repolarization measurement tool that integrates additional data beyond the QTc may identify patients with the greatest torsadogenic potential.

Details

ISSN :
15737241 and 09203206
Volume :
29
Database :
OpenAIRE
Journal :
Cardiovascular Drugs and Therapy
Accession number :
edsair.doi.dedup.....c5cbe0300031fa9e15f67812d3befb95
Full Text :
https://doi.org/10.1007/s10557-015-6619-0