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高血压患者漏服一剂群多普利和依那普利对血压控制的不同影响。

Differential effects of a missed dose of trandolapril and enalapril on blood pressure control in hypertensive patients.

作者信息

Vaur L, Dutrey-Dupagne C, Boussac J, Genes N, Bouvier d'Yvoire M, Elkik F, Meredith P A

机构信息

Medical Department Laboratories, Roussel, Paris.

出版信息

J Cardiovasc Pharmacol. 1995 Jul;26(1):127-31. doi: 10.1097/00005344-199507000-00020.

DOI:10.1097/00005344-199507000-00020
PMID:7564352
Abstract

A double blind randomised comparison of two angiotensin-converting enzyme (ACE) inhibitors was made in a study in which ambulatory blood pressure was monitored over a steady-state dosage interval and the subsequent 24-h period, the latter being designed to mimic a missed dose of drug. The blood pressure responses on active therapy were compared to an identical recording made at the end of a 3-week placebo run in period. Eighty-eight essential hypertensives were treated with a morning dose of either trandolapril 2 mg or enalapril 20 mg. Mean systolic (SBP) and diastolic blood pressure (DBP) were calculated on each of the following periods: daytime (8:31 a.m.-10:30 p.m.), nighttime (10:31 p.m.-6:30 a.m.), and early morning (6:31 a.m.-8:30 a.m.). Trough/peak was calculated for each group both on active treatment and after a missed dose. Twelve patients were excluded from analysis before opening the randomisation code because of inadequate ambulatory blood pressure monitoring (ABPM) recordings. Demographic data, placebo-period office blood pressure, and ABPM recordings were not significantly different between the two groups. Both trandolapril and enalapril effectively reduced blood pressure over the 24-h period. Twenty four-hour ambulatory SBP and DBP decreased from 148 +/- 14/92 +/- 10 mm Hg to 135 +/- 14/83 +/- 10 mm Hg in the trandolapril group (p < 0.001). The same parameters decreased to a quite similar extent after enalapril, from 143 +/- 13/91 +/- 5 mm Hg to 133 +/- 15/83 +/- 8 mm Hg (p < 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项研究中,对两种血管紧张素转换酶(ACE)抑制剂进行了双盲随机比较。该研究在稳态给药间隔及随后的24小时期间监测动态血压,后者旨在模拟漏服一剂药物的情况。将积极治疗时的血压反应与3周安慰剂导入期结束时进行的相同记录相比较。88名原发性高血压患者早晨服用2毫克群多普利或20毫克依那普利。在以下各时间段计算平均收缩压(SBP)和舒张压(DBP):白天(上午8:31 - 晚上10:30)、夜间(晚上10:31 - 上午6:30)和清晨(上午6:31 - 上午8:30)。计算每组在积极治疗时和漏服一剂药物后的谷值/峰值。在打开随机分组代码之前,有12名患者因动态血压监测(ABPM)记录不充分而被排除在分析之外。两组间的人口统计学数据、安慰剂期诊室血压和ABPM记录无显著差异。群多普利和依那普利在24小时期间均有效降低血压。群多普利组24小时动态SBP和DBP从148±14/92±10毫米汞柱降至135±14/83±10毫米汞柱(p<0.001)。依那普利治疗后相同参数下降程度相当,从143±13/91±5毫米汞柱降至133±15/83±8毫米汞柱(p<0.001)。(摘要截短于250字)

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