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为监测正常志愿者中药物的药效学作用,对后负荷降低的循环效应进行无创测量。

Non-invasive measuring of the circulatory effect of afterload reduction in order to monitor the pharmacodynamic effect of drugs in normal volunteers.

作者信息

Buch J, Waldorff S, Hansen P B, Rasmussen O O

出版信息

Br Heart J. 1983 Aug;50(2):170-5. doi: 10.1136/hrt.50.2.170.

Abstract

In order to measure the effect of a decrease in afterload on systolic time intervals, left ventricular end-systolic diameter, and left ventricular wall stress, eight healthy young persons underwent a randomised placebo controlled trial of terbutaline before and during atenolol treatment. Pre-ejection period index, left ventricular end-systolic diameter, and wall stress all decreased after terbutaline, the decrease being clearly dose dependent. This was identical before and during atenolol administration. Consequently the observed changes were induced by beta-2 elicited vasodilatation, possibly combined with some decrease of parasympathetic tone. A close correlation between changes in pre-ejection period index (PEPI) and changes in left ventricular end-systolic diameter (LVESD) and wall stress was shown both before and during atenolol treatment. When using non-invasive methods in the evaluation of changes in contractility, it is important to correct for changes in preload and afterload. For normal subjects it is suggested that the relation between delta PEPI and delta LVESD as a percentage of the mean values should be used for evaluation of afterload changes. A method is suggested for estimating changes in pre-ejection period index induced by changes in left ventricular end-systolic diameter or wall stress.

摘要

为了测量后负荷降低对收缩期时间间期、左心室收缩末期直径和左心室壁应力的影响,8名健康年轻人在阿替洛尔治疗前和治疗期间接受了特布他林的随机安慰剂对照试验。特布他林给药后,射血前期指数、左心室收缩末期直径和壁应力均降低,且降低明显呈剂量依赖性。在阿替洛尔给药前和给药期间情况相同。因此,观察到的变化是由β2介导的血管舒张引起的,可能还伴有副交感神经张力的某种降低。在阿替洛尔治疗前和治疗期间,射血前期指数(PEPI)的变化与左心室收缩末期直径(LVESD)和壁应力的变化之间均显示出密切相关性。在使用非侵入性方法评估收缩性变化时,校正前负荷和后负荷的变化很重要。对于正常受试者,建议使用ΔPEPI与ΔLVESD相对于平均值的百分比之间的关系来评估后负荷变化。本文提出了一种估计左心室收缩末期直径或壁应力变化引起的射血前期指数变化的方法。

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引用本文的文献

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Influence of atenolol and nifedipine on digoxin-induced inotropism in humans.
Br J Clin Pharmacol. 1984 Dec;18(6):817-22. doi: 10.1111/j.1365-2125.1984.tb02550.x.

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