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Comparison of one- and three-lead ECG to measure cardiac intervals and differentiate drug-induced multi-channel block

机译:一种和三引导ECG测量心脏间隔和分化药物诱导的多通道块的比较

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Introduction: FDA has established initiatives to characterize clinical and non-clinical biomarkers to enable more precise prediction of proarrhythmia risk based upon knowledge of drug effect on multiple cardiac ion channels (Colatsky et al., 2016). The FDA has recently demonstrated superiority of early ventricular repolarization interval (JTp) in differentiating pure hERG block from multi-channel block in human subjects. Preclinical studies often acquire a single lead ECG, whereas FDA measurements of JTp were derived from a spatial vectorcardiogram computed using multiple leads. This study compares QT subintervals derived from single lead vs. spatial magnitude (SM) ECG and contrasts information obtained from multilead and single lead ECGs in the canine model.
机译:介绍:FDA建立了表征临床和非临床生物标志物的举措,以便基于对多功能离子通道的药物影响的知识来实现更精确的预测性风险(Colatsky等,2016)。 FDA最近阐述了早期心室复极间隔(JTP)的优越性,以在人类受试者中的多通道块中区分纯Herg块。 临床前研究经常获取单一引出ECG,而JTP的FDA测量源自使用多个引线计算的空间载体卡片造影。 该研究将来自单引线与空间幅度(SM)ECG的QT子宫内壁进行比较,并对比犬模型中的多地和单引线ECG获得的信息。

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