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硝苯地平每日一次新剂型的24小时疗效。意大利硝苯地平控释片研究组

The 24-hour efficacy of a new once-daily formulation of nifedipine. Italian Nifedipine GITS Study Group.

作者信息

Zanchetti A

机构信息

Istituto di Clinica Medica Generale e Terapia Medica, Università di Milano, Italy.

出版信息

Drugs. 1994;48 Suppl 1:23-30; discussion 30-1. doi: 10.2165/00003495-199400481-00007.

DOI:10.2165/00003495-199400481-00007
PMID:7533703
Abstract

Nifedipine GITS (Gastro-Intestinal Therapeutic System) is a recently launched long-acting formulation of nifedipine. The aim of the Italian Nifedipine GITS Study was to determine the duration of the antihypertensive effect of once-daily nifedipine GITS in outpatients with essential hypertension. After a 2-week placebo run-in period, 126 patients with mild to moderate essential hypertension (diastolic BP95 to 114mm Hg) were randomised to receive nifedipine GITS 30mg (n = 42), nifedipine GITS 60mg (n = 42) or placebo (n = 42), once daily in a double-blind fashion for 4 weeks. At the end of the run-in and treatment periods, ambulatory BP monitoring was performed (Spacelabs 90202 or 90207 device) to provide regular 15-minute BP readings for 24 to 36 hours. In the 81 patients with at least 24 hours of valid ambulatory BP data, the average systolic and diastolic BP changes after treatment with nifedipine GITS 30mg (n = 25), nifedipine GITS 60mg (n = 28) and placebo (n = 28) were -16.5/-10.8, -16.3/-10.0 and +0.4/+0.9mm Hg, respectively. BP changes with nifedipine GITS differed significantly (p < 0.01) from those with placebo. Heart rate was not significantly altered by nifedipine GITS. The effects of nifedipine GITS and placebo on ambulatory BP 24 hours and 36 hours after the last dose were evaluated in 56 patients with complete 36-hour ambulatory BP profiles. After 24 hours, both doses of nifedipine GITS caused significant (p < 0.01) reductions in systolic and diastolic BP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

硝苯地平胃肠道治疗系统(GITS)是一种最近推出的长效硝苯地平制剂。意大利硝苯地平GITS研究的目的是确定每日一次服用硝苯地平GITS对原发性高血压门诊患者的降压作用持续时间。经过2周的安慰剂导入期后,126例轻度至中度原发性高血压患者(舒张压95至114mmHg)被随机分为接受30mg硝苯地平GITS(n = 42)、60mg硝苯地平GITS(n = 42)或安慰剂(n = 42),以双盲方式每日一次服用4周。在导入期和治疗期结束时,进行动态血压监测(使用Spacelabs 90202或90207设备),以提供24至36小时内每15分钟的血压读数。在81例有至少24小时有效动态血压数据的患者中,服用30mg硝苯地平GITS(n = 25)、60mg硝苯地平GITS(n = 28)和安慰剂(n = 28)治疗后的平均收缩压和舒张压变化分别为-16.5/-10.8、-16.3/-10.0和+0.4/+0.9mmHg。硝苯地平GITS引起的血压变化与安慰剂相比有显著差异(p < 0.01)。硝苯地平GITS对心率无显著影响。在56例有完整36小时动态血压记录的患者中,评估了最后一剂后24小时和36小时硝苯地平GITS和安慰剂对动态血压的影响。24小时后,两种剂量的硝苯地平GITS均导致收缩压和舒张压显著降低(p < 0.01)。(摘要截选至250字)

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Ambulatory blood pressure normalcy: the PAMELA Study.动态血压正常:帕梅拉研究
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