Wolzt M, Schmetterer L, Gouya G, Zanaschka G, Eichler H G
Department of Clinical Pharmacology, Vienna University, Austria.
J Cardiovasc Pharmacol. 1995 Oct;26(4):660-5. doi: 10.1097/00005344-199510000-00023.
Previous animal experiments suggest that the increase in the amplitude from the R-wave to the S-wave (RSh) may be more sensitive than other ECG measures to sodium channel blocking drug actions. We measured RSh of three orthogonal leads at baseline and during intravenous pharmacologic stimulation with adenosine, ajmaline, atropine, disopyramide, isoproterenol, lidocaine, norepinephrine (NE), propranolol, and verapamil in an observer-blinded placebo-controlled study in healthy young men. The short-term reproducibility of RSh was high. Ajmaline increased RSh in the anteroposterior lead, disopyramide in the anteroposterior and vertical lead, and lidocaine in the vertical and horizontal lead, respectively. Isoproterenol increased RSh in the anteroposterior lead; atropine decreased RSh in the vertical lead. The other drugs did not affect RSh significantly. Our data do not support the concept that RSh measure is a more sensitive technique for assessing class I antiarrhythmic drug action in humans, at least in healthy subjects. In addition, our results indicate that changes in autonomic tone may influence RSh measurements.
先前的动物实验表明,从R波到S波的振幅增加(RSh)可能比其他心电图测量指标对钠通道阻滞剂的药物作用更敏感。在一项针对健康年轻男性的观察者盲法安慰剂对照研究中,我们在基线时以及静脉注射腺苷、阿义马林、阿托品、丙吡胺、异丙肾上腺素、利多卡因、去甲肾上腺素(NE)、普萘洛尔和维拉帕米进行药理刺激期间,测量了三个正交导联的RSh。RSh的短期可重复性很高。阿义马林分别增加了前后导联的RSh,丙吡胺增加了前后导联和垂直导联的RSh,利多卡因增加了垂直导联和水平导联的RSh。异丙肾上腺素增加了前后导联的RSh;阿托品降低了垂直导联的RSh。其他药物对RSh无显著影响。我们的数据不支持RSh测量是评估人类I类抗心律失常药物作用更敏感技术的概念,至少在健康受试者中如此。此外,我们的结果表明自主神经张力的变化可能会影响RSh测量。