首页> 美国卫生研究院文献>Current Therapeutic Research Clinical and Experimental >Antihypertensive effect of barnidipine 10 mg or amlodipine 5 to 10 mg once daily in treatment-naive patients with essential hypertension: A 24-week randomized open-label pilot study
【2h】

Antihypertensive effect of barnidipine 10 mg or amlodipine 5 to 10 mg once daily in treatment-naive patients with essential hypertension: A 24-week randomized open-label pilot study

机译:初次治疗的原发性高血压患者中巴尼地平10 mg或氨氯地平5至10 mg每天一次的抗高血压作用:一项为期24周随机开放标签的先导研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Background: Dihydropyridine calcium antagonists are largely employed for the treatment of hypertension, coronary heart disease, and heart failure.>Objective: The aim of our study was to compare the antihypertensive effect of the dihydropyridine calcium antagonists barnidipine and amlodipine.>Methods: This was a 24-week, randomized, open-label, pilot study. Consecutive treatment-naive patients with grade I or II essential hypertension (office sitting systolic blood pressure [BP] of 140–179 mm Hg and diastolic BP of 90–109 mm Hg) were enrolled. The primary end points were the effect of treatment with either barnidipine 10 mg or amlodipine 5 mg once daily on office and ambulatory BP, left ventricular mass index (LVMI), and markers of cardiac damage, serum procollagen type I C-terminal propeptide, and plasma amino-terminal pro-B-type natriuretic peptide concentrations. Patients were assessed at enrollment, and 12 and 24 weeks. During each visit, the prevalence of adverse events (AEs) was also monitored using spontaneous reporting, patient interview, and physical examination, the relationship to study drug being determined by the investigators. Compliance with treatment was assessed at each study visit by counting returned tablets.>Results: Thirty eligible patients (20 men, 10 women; mean [SD] age, 47 [12] years) were included in the study; all patients completed the 24 weeks of study treatment. Twelve weeks after randomization, 6 patients in the amlodipine group had their dose doubled to 10 mg due to inadequate BP control. Mean BP reductions at study end were not significantly different between the barnidipine and amlodipine groups (office BP, −10.3/−9.4 vs −16.6/−9.1 mm Hg; ambulatory BP, 9.4/6.4 vs 8.1/5.1 mm Hg). Reductions in LVMI and markers of cardiac damage were not significantly different between the 2 groups. Significantly more patients in the amlodipine group reported drug-related AEs compared with those in the barnidipine group (9 [60%] vs 2 [13%]; P < 0.05).>Conclusion: In this small sample of treatment-naive hypertensive patients, the antihypertensive effect of barnidipine 10 mg once daily was not significantly different from that of amlodipine 5 to 10 mg once daily.
机译:>背景:二氢吡啶类钙拮抗剂被广泛用于治疗高血压,冠心病和心力衰竭。>目的:我们的研究目的是比较氟哌啶醇的降压作用二氢吡啶类钙拮抗剂巴尼地平和氨氯地平。>方法:这是一项为期24周的随机,开放标签,先导性研究。首次接受初治的连续性I级或II级高血压患者(办公室坐位收缩压[BP]为140–179 mm Hg,舒张压为90–109 mm Hg)。主要终点为每天1次苯尼地平或5 mg氨氯地平在办公室和门诊BP的治疗效果,左心室质量指数(LVMI),心脏损伤标志物,血清I型C前胶原原肽和血浆氨基末端前B型利钠肽浓度。在入组时以及第12和24周对患者进行评估。在每次访问期间,还使用自发报告,患者访谈和体格检查监测不良事件(AE)的发生率,研究人员确定与研究药物的关系。在每次研究访视时,通过计数返回的药片来评估治疗的依从性。>结果:研究纳入了30例合格患者(20名男性,10名女性;平均[SD]年龄为47 [12]岁) ;所有患者均完成了24周的研究治疗。随机分组后十二周,由于血压控制不充分,氨氯地平组中有6名患者的剂量翻倍至10 mg。巴尼地平组和氨氯地平组在研究结束时的平均BP降低无显着差异(办公室BP,-10.3 / -9.4与-16.6 / -9.1 mm Hg;门诊BP,9.4 / 6.4与8.1 / 5.1 mm Hg)。两组之间LVMI的降低和心脏损害的指标无明显差异。与巴尼地平组相比,氨氯地平组中有更多的患者报告了药物相关的不良事件(9 [60%]对2 [13%]; P <0.05)。>结论:对于未接受过治疗的高血压患者,巴尼地平10 mg每天一次的降压作用与氨氯地平5-10 mg每天一次的降压作用没有显着差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号