Suppr超能文献

厄贝沙坦的长期安全性和降压疗效:五项开放标签研究的汇总结果。

Long-term safety and antihypertensive efficacy of irbesartan: pooled results of five open-label studies.

作者信息

Littlejohn T, Saini R, Kassler-Taub K, Chrysant S G, Marbury T

机构信息

Piedmont Medical Research Associates, Winston-Salem, NC, USA.

出版信息

Clin Exp Hypertens. 1999 Nov;21(8):1273-95. doi: 10.3109/10641969909070849.

Abstract

An analysis of 5 multicenter, open-label studies was conducted to evaluate the long-term safety and efficacy of irbesartan in 1,006 patients with seated diastolic blood pressure (SeDBP) 95-110 mm Hg. Irbesartan monotherapy was started at 75 mg and titrated to 300 mg at 2- to 4-week intervals to achieve normalized blood pressure (SeDBP <90 mm Hg). If normalized BP was not attained with irbesartan 300 mg alone, adjunctive medications could be added. At 12 months of therapy, the mean reduction in seated systolic blood pressure/SeDBP was 21.0/15.8 mm Hg, and 83% (684/821) of patients were normalized. Of those normalized, 64% were receiving irbesartan monotherapy and 86% were receiving irbesartan or irbesartan/hydrochlorothiazide only. No evidence of tachyphylaxis to the antihypertensive effect of irbesartan was noted. Thus, long-term irbesartan therapy, with or without other antihypertensives, achieved and maintained normalized BP in the majority of patients and was well tolerated.

摘要

开展了一项对5项多中心、开放标签研究的分析,以评估厄贝沙坦对1006例坐位舒张压(SeDBP)为95 - 110 mmHg患者的长期安全性和疗效。厄贝沙坦单药治疗起始剂量为75 mg,每2至4周滴定至300 mg,以实现血压正常化(SeDBP <90 mmHg)。若仅使用300 mg厄贝沙坦未实现血压正常化,则可加用辅助药物。在治疗12个月时,坐位收缩压/SeDBP的平均降低幅度为21.0/15.8 mmHg,83%(684/821)的患者血压正常化。在血压正常化的患者中,64%接受厄贝沙坦单药治疗,86%仅接受厄贝沙坦或厄贝沙坦/氢氯噻嗪治疗。未观察到对厄贝沙坦降压作用快速耐受的证据。因此,无论是否联合其他抗高血压药物,长期使用厄贝沙坦治疗均可使大多数患者实现并维持血压正常化,且耐受性良好。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验