TY - JOUR
T1 - The Morphology of the QT Interval Predicts Torsade de Pointes During Acquired Bradyarrhythmias
AU - Topilski, Ian
AU - Rogowski, Ori
AU - Rosso, Rafael
AU - Justo, Dan
AU - Copperman, Yitschak
AU - Glikson, Michael
AU - Belhassen, Bernard
AU - Hochenberg, Marek
AU - Viskin, Sami
PY - 2007/1/23
Y1 - 2007/1/23
N2 - Objectives: The purpose of this study was to define the electrocardiographic (ECG) predictors of torsade de pointes (TdP) during acquired bradyarrhythmias. Background: Complete atrioventricular block (CAVB) might lead to downregulation of potassium channels, QT interval prolongation, and TdP. Because potassium-channel malfunction causes characteristic T-wave abnormalities in the congenital long QT syndrome (LQTS), we reasoned that T-wave abnormalities like those described in the congenital LQTS would identify patients at risk for TdP during acquired bradyarrhythmias. Methods: In a case-control study, we compared 30 cases of bradyarrhythmias complicated by TdP with 113 cases of uncomplicated bradyarrhythmias. On the basis of the criteria used for the congenital LQTS, T waves were defined as LQT1-like (long QT interval with broad T waves), LQT2-like (notched T waves), and LQT3-like (small and late) T waves. Results: Neither the ventricular rate nor the QRS width at the time of worst bradyarrhythmia predicted the risk of TdP. However, the QT, corrected QT (QTc), and Tpeak-Tend intervals correlated with the risk of TdP. The best single discriminator was a Tpeak-Tend of 117 ms. LQT1-like and LQT3-like morphologies were rare during bradyarrhythmias. In contrast, LQT2-like "notched T waves" were observed in 55% of patients with TdP but in only 3% of patients with uncomplicated bradyarrhythmias (p < 0.001). A 2-step model based on QT duration and the presence of LQT2-like T waves identified patients at risk for TdP with a positive predictive value of 84%. Conclusions: Prolonged QT interval, QTc interval, and Tpeak-Tend correlate with increased risk for TdP during acquired bradyarrhythmias, particularly when accompanied by LQT2-like notched T waves.
AB - Objectives: The purpose of this study was to define the electrocardiographic (ECG) predictors of torsade de pointes (TdP) during acquired bradyarrhythmias. Background: Complete atrioventricular block (CAVB) might lead to downregulation of potassium channels, QT interval prolongation, and TdP. Because potassium-channel malfunction causes characteristic T-wave abnormalities in the congenital long QT syndrome (LQTS), we reasoned that T-wave abnormalities like those described in the congenital LQTS would identify patients at risk for TdP during acquired bradyarrhythmias. Methods: In a case-control study, we compared 30 cases of bradyarrhythmias complicated by TdP with 113 cases of uncomplicated bradyarrhythmias. On the basis of the criteria used for the congenital LQTS, T waves were defined as LQT1-like (long QT interval with broad T waves), LQT2-like (notched T waves), and LQT3-like (small and late) T waves. Results: Neither the ventricular rate nor the QRS width at the time of worst bradyarrhythmia predicted the risk of TdP. However, the QT, corrected QT (QTc), and Tpeak-Tend intervals correlated with the risk of TdP. The best single discriminator was a Tpeak-Tend of 117 ms. LQT1-like and LQT3-like morphologies were rare during bradyarrhythmias. In contrast, LQT2-like "notched T waves" were observed in 55% of patients with TdP but in only 3% of patients with uncomplicated bradyarrhythmias (p < 0.001). A 2-step model based on QT duration and the presence of LQT2-like T waves identified patients at risk for TdP with a positive predictive value of 84%. Conclusions: Prolonged QT interval, QTc interval, and Tpeak-Tend correlate with increased risk for TdP during acquired bradyarrhythmias, particularly when accompanied by LQT2-like notched T waves.
UR - http://www.scopus.com/inward/record.url?scp=33846297330&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2006.08.058
DO - 10.1016/j.jacc.2006.08.058
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AN - SCOPUS:33846297330
SN - 0735-1097
VL - 49
SP - 320
EP - 328
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 3
ER -