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尼群地平治疗老年高血压患者的疗效及其对脑血流量的影响。

Efficacy of nitrendipine in the treatment of elderly hypertensive subjects, and its effect on cerebral blood flow.

作者信息

Pandita-Gunawardena N D, Dorrance D E, MacDonald G

机构信息

Department of Geriatric Medicine, Hither Green Hospital, London, England.

出版信息

J Cardiovasc Pharmacol. 1989;14 Suppl 10:S52-8.

PMID:2483572
Abstract

The ability of nitrendipine to control blood pressure (BP) over a 12- or 24-h period was assessed in patients greater than 65 years of age who had a systolic BP (SBP) greater than 170 mm Hg and a diastolic BP (DBP) greater than 100-130 mm Hg. Thirty patients were randomized equally into two groups: Group 1 received the drug once daily and Group 2 received it twice daily after a 2-week run-in on placebo. The study was double blind. BP was recorded 24 h (Group 1) or 12 h (Group 2) postnitrendipine. The study design permitted one dose titration if BP exceeded 170/100 mm Hg after 3 weeks of active therapy when the dose was doubled. Patients received 6 weeks of therapy at the preferred dosage. Patients underwent measurements of cerebral blood flow (CBF) initially and on three further occasions: after the final dose of placebo, and after the first and last doses of nitrendipine. With active therapy, mean SBP and DBP fell in both groups when subjects were in the sitting and standing postures, except that in Group 1 at Week 5 only, standing SBP and DBP were not significantly reduced on the 10 mg once daily regimen. At the preferred dose, eight of the 15 patients in Group 1 and 13 of the 15 patients in Group 2 responded with a reduction of standing DBP of 10 mm Hg or greater, 24 and 12 h, respectively, after the last dose.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在年龄大于65岁、收缩压(SBP)大于170 mmHg且舒张压(DBP)大于100 - 130 mmHg的患者中,评估了尼群地平在12或24小时内控制血压(BP)的能力。30名患者被平均随机分为两组:第1组每日服用一次药物,第2组在服用2周安慰剂的导入期后每日服用两次药物。该研究为双盲研究。在服用尼群地平后24小时(第1组)或12小时(第2组)记录血压。如果在积极治疗3周后血压超过170/100 mmHg,则将剂量加倍,该研究设计允许进行一次剂量滴定。患者以优选剂量接受6周治疗。患者最初以及在另外三个时间点进行脑血流量(CBF)测量:安慰剂最后一剂后,以及尼群地平第一剂和最后一剂后。在积极治疗期间,两组患者在坐位和站立位时平均SBP和DBP均下降,但仅在第5周时,第1组采用每日10 mg一次的给药方案时,站立位SBP和DBP未显著降低。在优选剂量下,第1组15名患者中有8名、第2组15名患者中有13名在最后一剂后24小时和12小时,站立位DBP分别降低了10 mmHg或更多。(摘要截断于250字)

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