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评分系统在STRATHE试验中的应用,以比较高血压管理中不同治疗策略的疗效和耐受性。

Application in the STRATHE trial of a score system to compare the efficacy and the tolerability of different therapeutic strategies in the management of hypertension.

作者信息

Waeber Bernard, Mourad Jean-Jacques

机构信息

Division de Physiopathologie Clinique, Centre Hospitalier Universitaire Vaudois et Universite de Lausanne, Lausanne, Switzerland.

出版信息

Vasc Health Risk Manag. 2008;4(1):249-52. doi: 10.2147/vhrm.2008.04.01.249.

Abstract

A score system integrating the evolution of efficacy and tolerability over time was applied to a subpopulation of the STRATHE trial, a trial performed according to a parallel group design, with a double-blind, random allocation to either a fixed-dose combination strategy (perindopril/indapamide 2 mg/0.625 mg, with the possibility to increase the dose to 3 mg/0.935 mg, and 4 mg/1.250 mg if needed, n = 118), a sequential monotherapy approach (atenolol 50 mg, followed by losartan 50 mg and amlodipine 5 mg if needed, n = 108), or a stepped-care strategy (valsartan 40 mg, followed by valsartan 80 mg and valsartan 80 mg+ hydrochlorothiazide 12.5 mg if needed, n = 103). The aim was to lower blood pressure below 140/90 mmHg within a 9-month period. The treatment could be adjusted after 3 and 6 months. Only patients in whom the study protocol was strictly applied were included in this analysis. At completion of the trial the total score averaged 13.1 +/- 70.5 (mean +/- SD) using the fixed-dose combination strategy, compared with -7.2 +/- 81.0 using the sequential monotherapy approach and -17.5 +/- 76.4 using the stepped-care strategy. In conclusion, the use of a score system allows the comparison of antihypertensive therapeutic strategies, taking into account at the same time efficacy and tolerability. In the STRATHE trial the best results were observed with the fixed-dose combination containing low doses of an angiotensin enzyme converting inhibitor (perindopril) and a diuretic (indapamide).

摘要

一个整合了疗效和耐受性随时间变化情况的评分系统应用于STRATHE试验的一个亚组,该试验按照平行组设计进行,采用双盲、随机分配至固定剂量联合策略(培哚普利/吲达帕胺2毫克/0.625毫克,必要时剂量可增至3毫克/0.935毫克和4毫克/1.250毫克,n = 118)、序贯单药治疗方法(阿替洛尔50毫克,必要时随后使用氯沙坦50毫克和氨氯地平5毫克,n = 108)或阶梯式治疗策略(缬沙坦40毫克,必要时随后使用缬沙坦80毫克和缬沙坦80毫克 + 氢氯噻嗪12.5毫克,n = 103)。目标是在9个月内将血压降至140/90 mmHg以下。治疗可在3个月和6个月后进行调整。本分析仅纳入严格遵循研究方案的患者。试验结束时,使用固定剂量联合策略的总评分平均为13.1 +/- 70.5(均值 +/- 标准差),序贯单药治疗方法为 -7.2 +/- 81.0,阶梯式治疗策略为 -17.5 +/- 76.4。总之,使用评分系统能够同时考虑疗效和耐受性来比较抗高血压治疗策略。在STRATHE试验中,含低剂量血管紧张素转换酶抑制剂(培哚普利)和利尿剂(吲达帕胺)的固定剂量联合方案取得了最佳结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1442/2464763/5b8d36d7085e/vhrm0401-249-01.jpg

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