培哚普利和吲达帕胺固定联合治疗2型糖尿病的疗效和安全性:ADVANCE在现有证据背景下的结果

John Chalmers, Rohina Joshi, Andre Pascal Kengne, Toshiharu Ninomiya, Yufang Bi, Severine Bompoint, Laurent Billot, Anushka Patel
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引用次数: 0

摘要

目的:ADVANCE试验旨在确定使用perindopril-indapamide固定组合常规降压对2型糖尿病患者主要血管结局的影响,无论初始血压水平或使用其他降压药物,包括血管紧张素转换酶抑制剂。方法:在6周的磨合期后,11,140例2型糖尿病高危患者被随机分配到固定的培哚普利-吲达帕胺联合组或匹配的安慰剂组,除当前治疗外。两个主要结局是主要大血管和主要微血管事件的组合,根据治疗意向联合和单独分析。结果:与对照组相比,接受积极治疗的参与者血压降低5.6/2.2 mmHg。积极治疗使合并主要结局,主要大血管或微血管事件的风险降低了9% (P = 0.041),导致全因死亡率降低14% (P = 0.025),心血管死亡率降低18% (P = 0.027)。总冠状动脉事件减少14% (P = 0.02),总肾事件减少21% (P < 0.0001)。治疗耐受性良好,在平均4.3年的随访后,积极治疗组和安慰剂组中分别有73%和74%的患者仍坚持随机治疗。结论:无论初始血压水平或接受的伴随治疗如何,培哚普利和吲达帕胺固定联合常规治疗耐受性良好,可降低死亡和主要血管事件的风险。结果表明,每79名患者以这种方式治疗,5年内可避免1例死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of fixed combination of perindopril and indapamide in type 2 diabetes: results from ADVANCE in context of available evidence.

Objectives: The ADVANCE trial was designed to determine the effects of routine blood pressure lowering using a fixed combination of perindopril-indapamide on major vascular outcomes in patients with type 2 diabetes, regardless of initial blood pressure levels or the use of other blood pressure-lowering drugs, including angiotensin-converting enzyme inhibitors.

Methods: After a 6-week run-in period, 11,140 high-risk individuals with type 2 diabetes were randomized to fixed combination perindopril-indapamide or matching placebo, in addition to current therapy. The two primary outcomes were composites of major macrovascular and major microvascular events, analysed jointly and separately by intention to treat.

Results: The reduction in blood pressure in participants assigned to active treatment was 5.6/2.2 mmHg greater than that observed in the control group. Active treatment reduced the risk of the combined primary outcome, a major macrovascular or microvascular event by 9% (P = 0.041) and resulted in a 14% (P = 0.025) reduction in all-cause mortality and an 18% (P = 0.027) reduction in cardiovascular mortality. There were reductions of 14% (P = 0.02) in total coronary events and 21% (P < 0.0001) in total renal events. The treatment was well tolerated, with 73% and 74% of patients in the active treatment and placebo groups still adherent to randomized therapy after an average of 4.3 years of follow-up.

Conclusions: Routine treatment with the fixed combination of perindopril and indapamide was well tolerated and reduced the risk of death and major vascular events, regardless of the initial blood pressure level or concomitant treatments received. The results suggest that for every 79 patients treated in this manner, one death would be avoided over 5 years.

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