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硝苯地平与尼卡地平治疗心绞痛副作用的随机双盲比较。尼卡地平研究小组。

Randomized double-blind comparison of side effects of nicardipine and nifedipine in angina pectoris. The Nicardipine Investigators Group.

作者信息

DeWood M A, Wolbach R A

机构信息

Deaconess Medical Center, Spokane, Wash. 99204.

出版信息

Am Heart J. 1990 Feb;119(2 Pt 2):468-78. doi: 10.1016/s0002-8703(05)80071-7.

Abstract

Nicardipine and nifedipine are structurally similar dihydropyridine calcium channel blockers with demonstrated efficacy in the treatment of stable angina pectoris. The present study was a prospective randomized trial designed to evaluate the relative incidence of dizziness, flushing, headache, pedal edema, and palpitations during use of these drugs in patients with angina pectoris. Of 250 patients who entered into the comparative treatment part of the study, 140 patients were susceptible to developing symptoms to nifedipine as identified during a 1-month open-label treatment with nifedipine. These patients were compared with a parallel cohort of 110 patients, who were identified during the same open-label period, but remained mostly asymptomatic. After a 1-week washout of nifedipine, equal numbers of patients in each cohort began an 8-week period of randomized, double-blind treatment with nifedipine (20 mg three times daily) or nicardipine (30 mg three times daily). Patients who experienced these symptoms during the open-label nifedipine treatment had a higher incidence of the same symptoms during the blinded treatment regimen. Nicardipine-treated patients had a lower incidence of each of the symptoms than did the nifedipine-treated patients. Statistically significant differences were reported for dizziness, the most common of the side effects. Patients who were free of these symptoms in the open-label period usually remained free of them in the blinded comparison. However, even among those free of dizziness during the open-label nifedipine treatment, more patients reported experiencing dizziness in the blinded phase from nifedipine than from nicardipine (18% vs 6%; p = 0.02).

摘要

尼卡地平与硝苯地平在结构上相似,均为二氢吡啶类钙通道阻滞剂,已证实对稳定型心绞痛有治疗效果。本研究是一项前瞻性随机试验,旨在评估心绞痛患者使用这些药物期间头晕、潮红、头痛、足部水肿及心悸的相对发生率。在进入研究比较治疗部分的250例患者中,140例患者在硝苯地平1个月开放标签治疗期间被确定易出现硝苯地平相关症状。将这些患者与同期开放标签治疗期间确定的110例患者组成的平行队列进行比较,后者大多无症状。硝苯地平洗脱1周后,每个队列中数量相等的患者开始为期8周的随机双盲治疗,一组服用硝苯地平(每日3次,每次20 mg),另一组服用尼卡地平(每日3次,每次30 mg)。在开放标签硝苯地平治疗期间出现这些症状的患者,在盲法治疗方案期间出现相同症状的发生率更高。与硝苯地平治疗的患者相比,尼卡地平治疗的患者每种症状的发生率更低。报告显示,最常见的副作用头晕存在统计学显著差异。在开放标签期未出现这些症状的患者在盲法比较中通常也未出现。然而,即使在开放标签硝苯地平治疗期间未出现头晕的患者中,报告在盲法阶段出现头晕的硝苯地平治疗患者也多于尼卡地平治疗患者(18%对6%;p = 0.02)。

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