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培哚普利对充血性心力衰竭的全身和局部血流动力学影响。

Systemic and regional hemodynamic effects of perindopril in congestive heart failure.

作者信息

Thuillez C, Richard C, Loueslati H, Auzepy P, Giudicelli J F

机构信息

Department of Clinical Pharmacology, Hôpital de Bicêtre, France.

出版信息

J Cardiovasc Pharmacol. 1990 Apr;15(4):527-35. doi: 10.1097/00005344-199004000-00002.

DOI:10.1097/00005344-199004000-00002
PMID:1691380
Abstract

The acute systemic and regional hemodynamic responses to a single oral dose (4 mg) of the angiotensin converting enzyme inhibitor perindopril were investigated in 10 patients with severe congestive heart failure. Perindopril produced significant and long-lasting decreases in systemic vascular resistance (-18%), right atrial pressure (-60%), and mean pulmonary capillary wedge pressure (-28%), whereas it significantly increased cardiac index (+ 12%). Brachial (+ 130%, pulsed Doppler technique) and renal (+ 34%) blood flows were also significantly increased whereas hepatic blood flow remained unchanged. Brachial flow/cardiac output and renal flow/cardiac output ratios increased significantly from 0.8 to 1.6 and from 13.2 to 16.5, respectively. The maximal decreases in forearm and renal (but not in systemic) vascular resistances were correlated with the basal plasma norepinephrine concentrations but not plasma epinephrine concentrations or plasma renin activity. We conclude that in severe heart failure (a) perindopril considerably improves systemic hemodynamics and exerts an inhomogeneous vasodilating effect, resulting in a redistribution of flows toward the forearm and renal territories, (b) norepinephrine is a major determinant of the arteriolar tone in these two vascular beds, and (c) the pulsed Doppler is a particularly suitable method to non-invasively detect and assess hemodynamic improvements in heart failure patients.

摘要

在10例重度充血性心力衰竭患者中,研究了口服单剂量(4毫克)血管紧张素转换酶抑制剂培哚普利后的急性全身和局部血流动力学反应。培哚普利可使全身血管阻力显著且持久降低(-18%)、右心房压力降低(-60%)、平均肺毛细血管楔压降低(-28%),而心脏指数显著升高(+12%)。肱动脉血流(+130%,脉冲多普勒技术)和肾血流(+34%)也显著增加,而肝血流保持不变。肱动脉血流/心输出量和肾血流/心输出量比值分别从0.8显著增加至1.6和从13.2增加至16.5。前臂和肾血管阻力(而非全身血管阻力)的最大降低与基础血浆去甲肾上腺素浓度相关,而与血浆肾上腺素浓度或血浆肾素活性无关。我们得出结论,在重度心力衰竭中:(a)培哚普利可显著改善全身血流动力学,并产生不均匀的血管舒张作用,导致血流向前臂和肾区域重新分布;(b)去甲肾上腺素是这两个血管床小动脉张力的主要决定因素;(c)脉冲多普勒是一种特别适合于无创检测和评估心力衰竭患者血流动力学改善情况的方法。

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Clinical pharmacokinetics of drugs in patients with heart failure: an update (part 2, drugs administered orally).心力衰竭患者药物的临床药代动力学:最新进展(第2部分,口服给药)
Clin Pharmacokinet. 2014 Dec;53(12):1083-114. doi: 10.1007/s40262-014-0189-3.
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Perindopril: in congestive heart failure.培哚普利:用于充血性心力衰竭。
Drugs. 2002;62(9):1367-77; discussion 1378-9. doi: 10.2165/00003495-200262090-00013.
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Pharmacokinetic-pharmacodynamic model for perindoprilat regional haemodynamic effects in healthy volunteers and in congestive heart failure patients.培哚普利拉对健康志愿者和充血性心力衰竭患者局部血流动力学影响的药代动力学-药效学模型
Br J Clin Pharmacol. 2001 Jul;52(1):25-33. doi: 10.1046/j.0306-5251.2001.01410.x.
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Pharmacokinetic changes in patients with oedema.水肿患者的药代动力学变化。
Clin Pharmacokinet. 1995 May;28(5):405-18. doi: 10.2165/00003088-199528050-00005.
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Perindopril. A review of its pharmacological properties and therapeutic use in cardiovascular disorders.培哚普利。对其药理特性及在心血管疾病治疗中的应用综述。
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