Suppr超能文献

新型钙拮抗剂替帕米(RO 11 - 1781)对轻、中度原发性高血压患者的降压作用

Antihypertensive properties of tiapamil (RO 11-1781)--a new calcium antagonist--in patients with mild and moderate essential hypertension.

作者信息

Velasco M, Morillo J, Urbina A, Kögler P, Leishman B, Pasquier M, Hernändez-Pieretti O

机构信息

Clinical Pharmacology Unit, Vargas Hospital, Caracas, Venezuela.

出版信息

Int J Clin Pharmacol Res. 1987;7(6):443-54.

PMID:3440635
Abstract

An open, non-comparative study, with a new calcium antagonist-tiapamil, was undertaken in 22 patients with mild and moderate essential hypertension (stage I-II WHO). After a two-week placebo period, patients were treated with tiapamil, 300-600 mg twice daily during a period of six weeks (Dose-finding period). Thereafter patients were continued on tiapamil during a 54 week period (Long-term follow-up). In some patients it was necessary to add the diuretic hydrochlorothiazide to obtain adequate control of the arterial hypertension. Monotherapy with tiapamil normalized supine diastolic blood pressure after the first six weeks in 17 of the 21 evaluable patients, and reduced it by greater than or equal to 10 mmHg (1.3 kPa) from baseline without normalization in two patients. In the two remaining cases the decrease was less than 10 mmHg. The optimal dose administered at six weeks in those patients who responded to treatment (normalization or decrease by greater than or equal to 10 mmHg.) was 600 mg/day in 32% of the cases, 750-900 mg/day in 47% and more than 900 mg/day in 21%. After completion of the dose-finding part, 19 patients continued treatment for a further 54 weeks. In 16 out of 19 patients hydrochlorothiazide was added to enhance the antihypertensive effect. All three patients who received tiapamil monotherapy throughout the trial, had normalized supine diastolic blood pressure on completing the study. In the 16 patients with the combination therapy, the addition of hydrochlorothiazide led in two patients to no further decrease in supine diastolic blood pressure, to an additional decrease by less than 10 mmHg in ten patients and by greater than or equal to 10 mmHg in four in comparison with the values obtained before starting combination therapy. At the end of the study 11 of these 16 patients had normalized supine diastolic blood pressure. The mean daily dose was 900 +/- 45 mg of tiapamil and 39 +/- 4 mg of hydrochlorothiazide. Both monotherapy and the combination regimen were well tolerated, and no effects attributable to drug interactions were observed. It may be concluded that tiapamil in oral doses of 300-600 mg twice daily is an effective antihypertensive agent with an excellent tolerance when administered for a period of 54 weeks.

摘要

一项针对新型钙拮抗剂替帕米的开放性、非对照研究纳入了22例轻度和中度原发性高血压患者(WHO分期I-II期)。经过两周的安慰剂期后,患者接受替帕米治疗,在为期六周的时间里(剂量探索期),每日两次,每次300 - 600mg。此后,患者在54周的时间里继续服用替帕米(长期随访)。在一些患者中,有必要加用利尿剂氢氯噻嗪以充分控制动脉高血压。在21例可评估患者中,17例在最初六周单用替帕米后仰卧位舒张压恢复正常,2例未恢复正常但较基线水平降低了大于或等于10mmHg(1.3kPa)。在其余2例中,血压下降小于10mmHg。在对治疗有反应的患者(血压恢复正常或降低大于或等于10mmHg)中,六周时给予的最佳剂量,32%的病例为600mg/天,47%为750 - 900mg/天,21%大于900mg/天。剂量探索部分完成后,19例患者继续治疗54周。19例患者中有16例加用氢氯噻嗪以增强降压效果。在整个试验中接受替帕米单药治疗的3例患者,在研究结束时仰卧位舒张压均恢复正常。在16例联合治疗的患者中,加用氢氯噻嗪后,2例患者仰卧位舒张压未进一步降低,10例患者额外降低小于10mmHg,4例患者较联合治疗开始前降低大于或等于10mmHg。研究结束时,这16例患者中有11例仰卧位舒张压恢复正常。替帕米的平均日剂量为900±45mg,氢氯噻嗪为39±4mg。单药治疗和联合治疗方案耐受性均良好,未观察到药物相互作用的影响。可以得出结论,替帕米每日两次口服剂量为300 - 600mg,在服用54周时是一种有效的抗高血压药物,耐受性良好。

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