Title of article
Randomized, double-blind, placebo-controlled trial of oral enalapril in patients with neurally mediated syncope, , ,
Author/Authors
Chunyu Zeng، نويسنده , , Zhiming Zhu، نويسنده , , Guangyao Liu، نويسنده , , Wenhui Hu، نويسنده , , Xukai Wang، نويسنده , , Chengming Yang، نويسنده , , Hongyong Wang، نويسنده , , Duofen He، نويسنده , , Jiancong Tan، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1998
Pages
7
From page
852
To page
858
Abstract
Background The purpose of this study was to study the effect of enalapril on neurally mediated syncope (NMS). Several agents (except for angiotensin-converting enzyme [ACE] inhibitors) have been used to treat patients with NMS. It is unknown whether ACE inhibitors have beneficial effects on NMS. Methods and Results Thirty subjects who had reproducible NMS induced with head-up tilt table test (HUT) were randomly assigned and divided in double-blind fashion into placebo and enalapril (an ACE inhibitor) groups. Hemodynamics and plasma catecholamine concentrations were studied. Before administration of enalapril, syncope induced by HUT was associated with vigorous hypotension and bradycardia. Plasma catecholamine concentrations were significantly elevated during NMS compared with the supine position before tilt. Oral enalapril rather than placebo produced a marked reduction in diastolic blood pressure during supine positioning before tilt. Administration of enalapril prevented HUT-induced NMS and increase of plasma catecholamine concentrations in all patients examined. Conversely, placebo had no effect in the majority of patients with NMS (12 of 15 subjects). Follow-up data showed that NMS disappeared in 14 (93%) of 15 patients treated with enalapril. Conclusions This study demonstrates that ACE inhibitors may efficiently prevent NMS, presumably through inhibition of sympathetic system activation and peripheral hypotensive effect. (Am Heart J 1998;136:852-8.)
Journal title
American Heart Journal
Serial Year
1998
Journal title
American Heart Journal
Record number
531390
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