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缓释尼卡地平的降压及血流动力学效应

Antihypertensive and hemodynamic effects of slow-release nicardipine.

作者信息

Mazzola C, Borgnino C, Colombo D, Lissoni F, Serra G, Turri D R, Valsecchi M A

机构信息

I.N.R.C.A., Department of Cardiology, Casatenovo, Italy.

出版信息

Int J Clin Pharmacol Ther Toxicol. 1988 Oct;26(10):503-8.

PMID:3069752
Abstract

The antihypertensive efficacy, the hemodynamic effects and the tolerability of a new slow-release nicardipine (SR-Nic) formulation, capsules containing 40 mg of active drug, have been tested in a randomized, double-blind placebo (P)-controlled study. Thirty mild-to-moderate essential hypertensives were enrolled and after a one-week single-blind placebo run-in period randomly allocated to SR-Nic or P twice-day for six weeks. Blood pressure (BP) was measured after 1, 2, 4 and 6 weeks of treatment. Hemodynamic parameters were evaluated non-invasively by the impedance cardiography technique, using the Noninvasive Continuous Cardiac Output Monitor (NNCOM 3, BoMed Medical Manufacturing Ltd), after 2 and 4 weeks of treatment. All the determinations were made before the morning administration, i.e., 12-14 h after evening intake of SR-Nic or P. The blood pressure (p less than .01) and hemodynamic response (p less than .01 for the systemic vascular resistances) in the SR-Nic group significantly differed from those in the P group. At the end of the study, there were decreases in mean systolic/diastolic BP values of 17/12 in the sitting and of 18/12 mmHg in the standing position in the SR-Nic group; in the P group, the changes were +2/-2 in the sitting and +2/-1 mmHg in the standing position. Systemic vascular resistances were reduced by 17.3% in the SR-Nic and by 1.9% in the P group after 4 weeks of treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一种新的缓释尼卡地平(SR - 尼卡地平)制剂(含40毫克活性药物的胶囊)的降压疗效、血流动力学效应和耐受性,已在一项随机、双盲、安慰剂(P)对照研究中进行了测试。招募了30名轻度至中度原发性高血压患者,在为期一周的单盲安慰剂导入期后,随机分为两组,分别接受SR - 尼卡地平或安慰剂,每日两次,持续六周。治疗1、2、4和6周后测量血压(BP)。治疗2周和4周后,使用无创连续心输出量监测仪(NNCOM 3,BoMed Medical Manufacturing Ltd),通过阻抗心动图技术无创评估血流动力学参数。所有测定均在早晨给药前进行,即晚上服用SR - 尼卡地平或安慰剂后12 - 14小时。SR - 尼卡地平组的血压(p <.01)和血流动力学反应(全身血管阻力p <.01)与P组有显著差异。研究结束时,SR - 尼卡地平组坐位平均收缩压/舒张压值下降17/12,立位下降18/12 mmHg;P组坐位变化为 +2/-2,立位为 +2/-1 mmHg。治疗4周后,SR - 尼卡地平组全身血管阻力降低17.3%,P组降低1.9%。(摘要截选至250字)

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