Suppr超能文献

老年患者每日一次服用缓释地尔硫䓬的降压疗效及安全性:与卡托普利的比较。地尔硫䓬对比研究组

Antihypertensive efficacy and safe use of once-daily sustained-release diltiazem in the elderly: a comparison with captopril. The Dilcacomp Study Group.

作者信息

Nicaise J, Neveux E, Blondin P

机构信息

Institut Pacheco, Brussels, Belgium.

出版信息

J Int Med Res. 1995 Jul-Aug;23(4):244-53. doi: 10.1177/030006059502300404.

Abstract

The efficacy and safety of sustained-release diltiazem, 200-300 mg once daily was compared with that of captopril, 12.5-25 mg twice-daily, in 100 elderly patients (65-85 years old) with mild to moderate essential hypertension (supine diastolic blood pressure 95-115 mmHg). All patients received placebo for 2 weeks, followed by an 8-week double-blind period, and were randomized to either diltiazem (n = 50) or captopril (n = 50). Their blood pressure was measured at trough level at week 4 immediately before dosing, i.e. 24 h post diltiazem dose or 12 h post captopril dose. Also at week 4, in non-responders, diltiazem was increased from 200 to 300 mg once daily and captopril from 12.5 to 25 mg twice daily to achieve a target supine diastolic blood pressure reduction of at least 10 mmHg or a diastolic blood pressure below 90 mmHg. Supine diastolic blood pressure, at week 8, was significantly (P < 0.001) reduced from 102 +/- 1 to 90 +/- 1 mmHg with diltiazem and from 103 +/- 1 to 89 +/- 1 mmHg with captopril, bringing this parameter within normal limits for both groups. Supine systolic blood pressure was also significantly (P < 0.001) reduced. Target blood pressure was achieved in 68% of patients taking diltiazem and in 70% taking captopril. Distribution of adverse events was comparable in both groups; no significant changes in laboratory or electrocardiographic parameters occurred. Two serious events were reported with captopril: one sudden death and one cerebrovascular stroke. Sustained-release diltiazem once a day is a convenient, well tolerated, first line treatment for hypertension in the elderly, for whom the possibility of using two dose levels allows a close regimen adjustment, 200 mg being recommended as a starting dose.

摘要

将200 - 300毫克一日一次的缓释地尔硫䓬与12.5 - 25毫克一日两次的卡托普利的疗效和安全性,在100例65 - 85岁患有轻至中度原发性高血压(仰卧位舒张压95 - 115毫米汞柱)的老年患者中进行了比较。所有患者先接受2周安慰剂治疗,随后进入8周双盲期,并随机分为地尔硫䓬组(n = 50)或卡托普利组(n = 50)。在第4周给药前(即地尔硫䓬给药后24小时或卡托普利给药后12小时)的谷值水平测量他们的血压。同样在第4周,对于无反应者,将地尔硫䓬从200毫克增至300毫克一日一次,将卡托普利从12.5毫克增至25毫克一日两次,以实现仰卧位舒张压至少降低10毫米汞柱或舒张压低于90毫米汞柱的目标。在第8周时,地尔硫䓬组仰卧位舒张压从102±1毫米汞柱显著(P < 0.001)降至90±1毫米汞柱,卡托普利组从103±1毫米汞柱降至89±1毫米汞柱,使两组该参数均处于正常范围内。仰卧位收缩压也显著(P < 0.001)降低。服用地尔硫䓬的患者中有68%达到目标血压,服用卡托普利的患者中有70%达到目标血压。两组不良事件分布相当;实验室或心电图参数无显著变化。卡托普利报告了两例严重事件:一例猝死和一例脑血管意外。一日一次的缓释地尔硫䓬是老年高血压患者方便、耐受性良好的一线治疗药物,对于这类患者,使用两种剂量水平的可能性允许进行密切的治疗方案调整,推荐200毫克作为起始剂量。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验