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两种相关剂量口服尼可地尔对中心血流动力学、左心室功能和心肌收缩性急性效应的双盲比较。

Double-blind comparison of the acute effects of two relevant doses of oral nicorandil on central hemodynamics, left ventricular function, and myocardial contractility.

作者信息

Baumbach A, Braun U, Döring G, Haase K K, Voelker W, Karsch K R

机构信息

Department of Internal Medicine III, University of Tübingen, Germany.

出版信息

Cardiovasc Drugs Ther. 1995 Mar;9 Suppl 2:213-20. doi: 10.1007/BF00878468.

DOI:10.1007/BF00878468
PMID:7647025
Abstract

Nicorandil is a nicotinamide derivative with potent vasodilator properties. Oral and sublingual administration of this compound in patients with coronary artery disease resulted in a predominant reduction of afterload and a small decrease in left ventricular preload. The effects of nicorandil in different doses on contractile left ventricular (LV) function, however, are not well defined. The aim of the present study was to assess the effects of nicorandil on hemodynamics, left ventricular volume and function, as well as the LV contractility index dP/dt measured by Millar-tip manometers. A total of 16 patients with coronary artery disease were included in this study. After diagnostic coronary angiography and ventriculography, the patients randomly received either 10 or 20 mg of oral nicorandil. The hemodynamic parameters, cardiac output, and LV end-diastolic and systolic pressures were determined after 15, 30, and 60 minutes, and a second angiogram was performed 60 minutes after administration. The predominant effect was a decrease in the mean aortic pressure with a concomitant decrease in the peripheral arterial resistance. Clinically relevant changes in aortic pressure, systemic vascular resistance, and rate-pressure product, however, were documented only after oral administration of 20 mg nicorandil, as opposed to minimal changes in the 10 mg group. LV volume and cardiac output were not changed significantly. LV contractility remained unchanged during the observation period. The hemodynamic profile of this compound is dose-dependent afterload reduction without a change in contractility. Because there was no concomitant increase in heart rate, calculated oxygen consumption was reduced, especially in the higher dose group.

摘要

尼可地尔是一种具有强效血管舒张特性的烟酰胺衍生物。在冠状动脉疾病患者中口服和舌下给予该化合物,主要导致后负荷降低,左心室前负荷略有下降。然而,不同剂量的尼可地尔对左心室(LV)收缩功能的影响尚不明确。本研究的目的是评估尼可地尔对血流动力学、左心室容积和功能的影响,以及通过Millar尖端压力计测量的左心室收缩指数dP/dt。本研究共纳入16例冠状动脉疾病患者。在诊断性冠状动脉造影和心室造影后,患者随机接受10或20mg口服尼可地尔。在15、30和60分钟后测定血流动力学参数、心输出量以及左心室舒张末期和收缩期压力,并在给药后60分钟进行第二次血管造影。主要作用是平均主动脉压降低,同时外周动脉阻力降低。然而,仅在口服20mg尼可地尔后记录到主动脉压、全身血管阻力和心率-压力乘积的临床相关变化,而10mg组变化极小。左心室容积和心输出量无显著变化。在观察期内左心室收缩性保持不变。该化合物的血流动力学特征是剂量依赖性降低后负荷,而收缩性无变化。由于心率没有同时增加,计算得出的氧耗降低,尤其是在高剂量组。

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Myocardial properties of the new dihydropyridine calcium antagonist isradipine compared to nifedipine with or without additional beta blockade in coronary artery disease.
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8
Effects of intravenous administration of nicorandil on cardiovascular hemodynamics and left ventricular function.
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Am J Cardiol. 1989 Jun 20;63(21):49J-55J. doi: 10.1016/0002-9149(89)90205-1.
10
Acute hemodynamic effects of single-dose nicorandil in coronary artery disease.
Am J Cardiol. 1989 Jun 20;63(21):34J-39J. doi: 10.1016/0002-9149(89)90202-6.