Topilski Ian, Rogowski Ori, Rosso Rafael, Justo Dan, Copperman Yitschak, Glikson Michael, Belhassen Bernard, Hochenberg Marek, Viskin Sami
Department of Cardiology, Tel Aviv Sourasky Medical Center and Sheba Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
J Am Coll Cardiol. 2007 Jan 23;49(3):320-8. doi: 10.1016/j.jacc.2006.08.058. Epub 2007 Jan 4.
The purpose of this study was to define the electrocardiographic (ECG) predictors of torsade de pointes (TdP) during acquired bradyarrhythmias.
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.
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.
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 T(peak)-T(end) intervals correlated with the risk of TdP. The best single discriminator was a T(peak)-T(end) 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%.
Prolonged QT interval, QTc interval, and T(peak)-T(end) correlate with increased risk for TdP during acquired bradyarrhythmias, particularly when accompanied by LQT2-like notched T waves.
本研究旨在确定获得性缓慢性心律失常期间尖端扭转型室速(TdP)的心电图(ECG)预测指标。
完全性房室传导阻滞(CAVB)可能导致钾通道下调、QT间期延长和TdP。由于钾通道功能异常在先天性长QT综合征(LQTS)中会导致特征性T波异常,我们推断,与先天性LQTS中描述的类似的T波异常可识别获得性缓慢性心律失常期间有TdP风险的患者。
在一项病例对照研究中,我们将30例并发TdP的缓慢性心律失常患者与113例未并发缓慢性心律失常的患者进行了比较。根据先天性LQTS的诊断标准,T波被定义为LQT1样(QT间期长且T波宽大)、LQT2样(T波有切迹)和LQT3样(T波小且延迟)T波。
最严重缓慢性心律失常时的心室率和QRS波宽度均不能预测TdP风险。然而,QT、校正QT(QTc)和T(峰)-T(末)间期与TdP风险相关。最佳单一判别指标是T(峰)-T(末)间期为117毫秒。缓慢性心律失常期间,LQT1样和LQT3样形态罕见。相比之下,55%的TdP患者出现LQT2样“有切迹T波”,而未并发缓慢性心律失常的患者中只有3%出现(p<0.001)。基于QT间期和LQT2样T波的两步模型可识别有TdP风险的患者,其阳性预测值为84%。
QT间期、QTc间期和T(峰)-T(末)间期延长与获得性缓慢性心律失常期间TdP风险增加相关,尤其是伴有LQT2样有切迹T波时。