• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

异搏定和普萘洛尔对轻至中度高血压患者血压和心率的等张及等长反应

Isotonic and isometric responses of blood pressure and heart rate in mild to moderate hypertension with isradipine and propranolol.

作者信息

Cantor A, Cristal N

机构信息

Rehabilitation Service, Soroka Medical Center, Beer Sheva, Israel.

出版信息

J Cardiovasc Pharmacol. 1990;15 Suppl 1:S76-8.

PMID:1695309
Abstract

The objectives of this study were (a) to evaluate the dose-response effect of isradipine, a dihydropyridine calcium antagonist, on the heart rate and blood pressure of males with mild to moderate hypertension; and (b) to compare these results with those obtained with propranolol, a beta-adrenoceptor blocker, on a matched patient population. Twenty-four patients entered a single-blind study, beginning with a 2-week washout placebo period followed by a forced-titration period. Treadmill and hand-grip tests were also performed. Two weeks were allocated to each stage of the therapy. The end point of the study was normalization of blood pressure with a minimum of side effects. Results and conclusions include the following: both drugs were effective in reducing systolic blood pressure (SBP) and diastolic blood pressure (DBP), but isradipine was more effective in reducing the DBP; isometric exercise can predict accurately the results of the isotonic exercise; the maximum therapeutic effect of propranolol was achieved during the second study-dose level; increases in the isradipine dose were reflected in a proportional reduction of SBP and DBP; and the incidence of side effects is lower among isradipine-treated patients compared to propranolol-treated patients.

摘要

本研究的目的是

(a)评估二氢吡啶类钙拮抗剂伊拉地平对轻至中度高血压男性患者心率和血压的剂量反应效应;(b)在匹配的患者群体中,将这些结果与β肾上腺素能受体阻滞剂普萘洛尔所获得的结果进行比较。24名患者进入一项单盲研究,首先是为期2周的洗脱期,期间服用安慰剂,随后是强制滴定期。还进行了跑步机和握力测试。每个治疗阶段分配两周时间。研究的终点是血压正常化且副作用最小。结果与结论如下:两种药物均能有效降低收缩压(SBP)和舒张压(DBP),但伊拉地平在降低DBP方面更有效;等长运动能够准确预测等张运动的结果;普萘洛尔在第二个研究剂量水平时达到最大治疗效果;伊拉地平剂量增加会使SBP和DBP成比例降低;与普萘洛尔治疗的患者相比,伊拉地平治疗的患者副作用发生率更低。

相似文献

1
Isotonic and isometric responses of blood pressure and heart rate in mild to moderate hypertension with isradipine and propranolol.异搏定和普萘洛尔对轻至中度高血压患者血压和心率的等张及等长反应
J Cardiovasc Pharmacol. 1990;15 Suppl 1:S76-8.
2
Efficacy and tolerability of the new calcium antagonist isradipine in essential hypertension.新型钙拮抗剂伊拉地平治疗原发性高血压的疗效及耐受性
J Cardiovasc Pharmacol. 1990;15 Suppl 1:S55-9.
3
Isradipine vs propranolol in hydrochlorothiazide-treated hypertensives. A multicenter evaluation.伊拉地平与普萘洛尔治疗氢氯噻嗪控制的高血压患者的多中心评估
Arch Intern Med. 1989 Nov;149(11):2453-7.
4
Efficacy and safety of isradipine in hypertension.
J Cardiovasc Pharmacol. 1989 Apr;13(4):580-5.
5
[Antihypertensive effect and adverse effects of isradipine in patients with sever hypertension. Results of an open multicenter study].[伊拉地平对重度高血压患者的降压作用及不良反应。一项开放性多中心研究的结果]
Arzneimittelforschung. 1996 Jun;46(6):600-5.
6
Calcium antagonists as first-line antihypertensive agents: a placebo-controlled, comparative trial of isradipine and nifedipine.钙拮抗剂作为一线抗高血压药物:一项关于伊拉地平与硝苯地平的安慰剂对照比较试验。
J Cardiovasc Pharmacol. 1990;15 Suppl 1:S70-4.
7
Clinical efficacy and tolerability of isradipine in the treatment of mild-to-moderate hypertension in young and elderly patients.
J Cardiovasc Pharmacol. 1992;19 Suppl 3:S53-7.
8
Evaluation of isradipine and captopril alone or in combination for the treatment of hypertension.评估伊拉地平与卡托普利单独或联合使用治疗高血压的效果。
J Cardiovasc Pharmacol. 1991;18 Suppl 3:S12-4.
9
Isradipine in the treatment of mild-to-moderate hypertension in Portugal.伊拉地平治疗葡萄牙轻至中度高血压。
J Cardiovasc Pharmacol. 1992;19 Suppl 3:S49-52.
10
The long-term effect of isradipine in pindolol-treated patients.
J Hypertens Suppl. 1987 Dec;5(5):S567-70.