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美托洛尔与非洛地平固定复方制剂与单药治疗中各单药相比的降压疗效及耐受性。瑞典/英国研究小组。

Antihypertensive efficacy and tolerability of a fixed combination of metoprolol and felodipine in comparison with the individual substances in monotherapy. The Swedish/United Kingdom Study Group.

作者信息

Dahlöf B, Hosie J

机构信息

Department of Medicine, Ostra Hospital, Gothenburg, Sweden.

出版信息

J Cardiovasc Pharmacol. 1990 Dec;16(6):910-6. doi: 10.1097/00005344-199012000-00008.

DOI:10.1097/00005344-199012000-00008
PMID:1704983
Abstract

In this double-blind, randomized, parallel-group study, the aim was to compare the efficacy and tolerability of a new fixed combination of felodipine and metoprolol with the individual components in monotherapy. After a placebo period of 4 weeks, 159 patients with mild to moderate essential hypertension were randomized to extended-release formulations of either felodipine plus metoprolol 10 + 100 mg (FM), felodipine 10 mg (F), or metoprolol 100 mg (M) once daily if supine diastolic blood pressure greater than 95 mm Hg. After 12 weeks of active treatment, the reductions in supine blood pressure (24 h after dosing) were 20/14, 13/10, and 11/8 mm Hg for FM, F, and M, respectively. The difference in change was 7/4 mm Hg (p = 0.004/p = 0.006) and 8/5 mm Hg (p = 0.0002/p less than 0.0001) for the fixed combination and F or M, respectively. Blood pressure control (diastolic blood pressure less than 90 mm Hg after 12 weeks) was significantly better for the combination than for F and M, i.e., 71%, 49% (p = 0.008), and 34% (p = 0.004), respectively. Adverse experiences were those to be expected from previous studies with felodipine and metoprolol and did not differ in frequency between groups. It can be concluded that a fixed combination of metoprolol and felodipine has a clinically relevant and significantly better blood pressure reduction 24 h postdose than the individual substances in monotherapy, without decreased tolerability.

摘要

在这项双盲、随机、平行组研究中,目的是比较非洛地平与美托洛尔新的固定复方制剂与单一成分单药治疗的疗效和耐受性。经过4周的安慰剂期后,159例轻度至中度原发性高血压患者被随机分配至非洛地平加美托洛尔10 + 100 mg(FM)、非洛地平10 mg(F)或美托洛尔100 mg(M)的缓释制剂组,若仰卧位舒张压大于95 mmHg则每日给药1次。经过12周的积极治疗后,FM、F和M组的仰卧位血压(给药后24小时)降低分别为20/14、13/10和11/8 mmHg。固定复方制剂与F或M相比,变化差异分别为7/4 mmHg(p = 0.004/p = 0.006)和8/5 mmHg(p = 0.0002/p<0.0001)。联合用药组的血压控制情况(12周后舒张压低于90 mmHg)明显优于F组和M组,分别为71%、49%(p = 0.008)和34%(p = 0.004)。不良事件是之前非洛地平和美托洛尔研究中预期出现的,且各组之间在发生频率上没有差异。可以得出结论,美托洛尔和非洛地平的固定复方制剂在给药后24小时具有临床相关且显著更好的血压降低效果,优于单一成分单药治疗,且耐受性未降低。

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