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充血性心力衰竭患者对首剂血管紧张素转换酶抑制剂的血压反应。

Blood pressure response to the first dose of angiotensin-converting enzyme inhibitors in congestive heart failure.

作者信息

Reid J L, MacFadyen R J, Squire I B, Lees K R

机构信息

Department of Medicine and Therapeutics, Gardiner Institute, University of Glasgow, Scotland.

出版信息

Am J Cardiol. 1993 Jun 24;71(17):57E-60E. doi: 10.1016/0002-9149(93)90954-b.

DOI:10.1016/0002-9149(93)90954-b
PMID:8392282
Abstract

Angiotensin-converting enzyme (ACE) inhibitors improve survival in heart failure and delay progression to clinical heart failure in patients with left ventricular dysfunction after myocardial infarction. Increasing numbers of older patients are being considered for such treatment. However, there are reports of excessive and prolonged decreases in blood pressure (BP) after the first dose of some ACE inhibitors. We have studied the hemodynamics, pharmacokinetics, and neurohumoral responses to the first dose of oral captopril 6.25 mg, enalapril 2.5 mg, perindopril 2.0 mg, intravenous enalaprilat 1.5 mg, and perindoprilat 1.0 mg, compared with oral or intravenous placebo in 6 parallel groups of 12 elderly patients each with moderate-to-severe (New York Heart Association classes II-IV) heart failure. Oral dosing with active drugs led to different temporal responses. After captopril, there was an early short-lived decrease in BP. Enalapril led to a later long-lasting decrease, but perindopril was not different from placebo. Intravenous enalaprilat and intravenous perindoprilat each lowered BP to a similar extent. The doses of drugs used appeared to be comparable because plasma ACE inhibition was similar following perindopril or enalapril and also comparing perindoprilat and enalaprilat. These studies indicate that oral ACE inhibitors have different profiles of acute BP changes after the first dose. The explanation is not clear, but could include physicochemical differences in the interaction between prodrug ester and diacid metabolites leading to differences in tissue distribution and local enzyme inhibition.

摘要

血管紧张素转换酶(ACE)抑制剂可提高心力衰竭患者的生存率,并延缓心肌梗死后左心室功能不全患者进展为临床心力衰竭。越来越多的老年患者正在考虑接受此类治疗。然而,有报道称,某些ACE抑制剂首剂用药后会出现血压过度且持续下降的情况。我们研究了6组、每组12例患有中重度(纽约心脏病协会II-IV级)心力衰竭的老年患者,分别口服6.25mg卡托普利、2.5mg依那普利、2.0mg培哚普利,静脉注射1.5mg依那普利拉和1.0mg培哚普利拉后,与口服或静脉注射安慰剂相比的血流动力学、药代动力学及神经体液反应。口服活性药物产生了不同的时间反应。服用卡托普利后,血压早期短暂下降。依那普利导致后期血压持续下降,但培哚普利与安慰剂无差异。静脉注射依那普利拉和静脉注射培哚普利拉降低血压的程度相似。所用药物剂量似乎具有可比性,因为培哚普利或依那普利后的血浆ACE抑制作用相似,培哚普利拉和依那普利拉之间比较也是如此。这些研究表明,口服ACE抑制剂首剂用药后急性血压变化情况各异。原因尚不清楚,但可能包括前体药物酯与二酸代谢物相互作用的物理化学差异,导致组织分布和局部酶抑制的差异。

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