Association between renin-angiotensin system antagonist use and mortality in heart failure with severe renal insufficiency: a prospective propensity score-matched cohort study

被引:83
作者
Edner, Magnus [1 ]
Benson, Lina [2 ]
Dahlstrom, Ulf [3 ]
Lund, Lars H. [1 ,4 ]
机构
[1] Karolinska Inst, Unit Cardiol, Dept Med, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Sci & Educ, SoS, S-11883 Stockholm, Sweden
[3] Linkoping Univ, Dept Cardiol UHL, Dept Med & Hlth Sci, Div Cardiovasc Med,Fac Hlth Sci,Cty Council Oster, S-58191 Linkoping, Sweden
[4] Karolinska Univ Hosp, Dept Cardiol, S-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Heart failure; Renin-angiotensin system antagonists; ACE-inhibitor; Angiotensin receptor blocker; Renal insufficiency; Chronic kidney disease; Creatinine clearance; CONVERTING-ENZYME-INHIBITORS; VENTRICULAR SYSTOLIC FUNCTION; OLDER PATIENTS; TASK-FORCE; OUTCOMES; CANDESARTAN; DYSFUNCTION; GUIDELINE; LOSARTAN; BLOCKERS;
D O I
10.1093/eurheartj/ehv268
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims In heart failure (HF) with reduced ejection fraction (EF), renin-angiotensin receptor (RAS) antagonists reduce mortality. However, severe renal insufficiency was an exclusion criterion in trials. We tested the hypothesis that RAS antagonists are associated with reduced mortality also in HF with severe renal insufficiency. Methods and results We studied patients with EF <= 39% registered in the prospective Swedish Heart Failure Registry. In patients with creatinine >221 mu mol/L or creatinine clearance <30 mL/min, propensity scores for RAS-antagonist use were derived from 36 variables. The association between RAS antagonist use and all-cause mortality was assessed with Cox regression in a cohort matched 1:1 based on age and propensity score. To assess consistency, we performed the same analysis as a 'positive control' in patients without severe renal insufficiency. Between 2000 and 2013, there were 24 283 patients of which 2410 [age, mean (SD), 82 (9), 45% women] had creatinine >221 mu mol/L or creatinine clearance <30 mL/min and were treated (n = 1602) or not treated (n = 808) with RAS antagonists. In the matched cohort of 602 vs. 602 patients [age 83 (8), 42% women], RAS antagonist use was associated with 55% [95% confidence interval (CI) 51-59] vs. 45% (41-49) 1-year survival, P < 0.001, with a hazard ratio (HR) for mortality of 0.76 (95% CI 0.67-0.86, P < 0.001). In positive control patients without severe renal insufficiency [n = 21 873; age 71 (12), 27% women], the matched HR was 0.79 (95% CI 0.72-0.86, P < 0.001). Conclusion In HF with severe renal insufficiency, the use of RAS antagonists was associated with lower all-cause mortality. Prospective randomized trials are needed before these findings can be applied to clinical practice.
引用
收藏
页码:2318 / 2326
页数:9
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