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Plasma free captopril concentrations during short and long term treatment with oral captopril for heart failure.

机译:口服卡托普利用于心力衰竭的短期和长期治疗期间血浆无卡托普利浓度。

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摘要

Plasma free captopril concentrations and haemodynamic response to captopril were studied in 20 patients with severe chronic heart failure. A 25 mg oral dose of captopril produced a 36% reduction in systemic vascular resistance, with individual responses varying from 13% to 64%. Mean systemic pressure fell by 20% and cardiac output rose 28%. The absorption of captopril was rapid. Peak plasma free captopril concentration occurred at 45 minutes after the dose and was followed by a smaller second peak. Peak plasma free captopril concentrations varied more than 20-fold but did not correlate with the maximal reduction in systemic vascular resistance. Elimination half life was seven hours. Fourteen patients were restudied after 1-2 months of captopril treatment and 12 showed symptomatic benefit. There was a sustained improvement in haemodynamic state and in non-invasive indices of myocardial function. During long term treatment the predose plasma free captopril concentration correlated well with dosage, but steady state captopril concentrations did not show a significant relation with haemodynamic response. On a dosage regimen of 25-50 mg three times daily the morning predose plasma free captopril concentration and plasma renin activity were relatively low and suggested that maximal inhibition of the renin-angiotensin system was not maintained throughout the dosage interval.
机译:在20例严重的慢性心力衰竭患者中研究了血浆游离卡托普利浓度和对卡托普利的血流动力学反应。口服卡托普利25 mg可使全身血管阻力降低36%,个体反应范围为13%至64%。平均体压下降20%,心输出量增长28%。卡托普利的吸收迅速。给药后45分钟时血浆游离卡托普利浓度达到峰值,随后出现一个较小的第二个峰值。血浆中游离卡托普利的峰值浓度变化超过20倍,但与全身血管阻力的最大降低无关。消除半衰期为七个小时。卡托普利治疗1-2个月后对14例患者进行了重新研究,其中12例表现出对症治疗。血流动力学状态和心肌功能的非侵入性指标持续改善。在长期治疗期间,给药前血浆中无血浆卡托普利的浓度与剂量具有很好的相关性,但稳态卡托普利的浓度与血流动力学反应没有显着关系。在每天三剂25-50 mg的剂量方案下,早晨服药前血浆中无血浆的卡托普利浓度和血浆肾素活性相对较低,这表明在整个剂量间隔中并未维持对肾素-血管紧张素系统的最大抑制作用。

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