A Systematic Review and Network Meta-Analysis of Pharmacological Treatment of Heart Failure With Reduced Ejection Fraction

被引:167
|
作者
Tromp, Jasper [1 ,2 ,3 ,4 ,5 ]
Ouwerkerk, Wouter [2 ,3 ,4 ,6 ]
van Veldhuisen, Dirk J. [1 ]
Hillege, Hans L. [1 ]
Richards, A. Mark [7 ,8 ,9 ]
van der Meer, Peter [1 ]
Anand, Inder S. [10 ]
Lam, Carolyn S. P. [1 ,2 ,3 ,4 ,5 ]
Voors, Adriaan A. [1 ]
机构
[1] Univ Groningen, Dept Cardiol, Univ Med Ctr Groningen, Groningen, Netherlands
[2] Saw Swee Hock Sch Publ Hlth, Singapore, Singapore
[3] Natl Univ Singapore, Singapore, Singapore
[4] Natl Univ Hlth Syst, Singapore, Singapore
[5] Duke NUS Med Sch Singapore, Singapore, Singapore
[6] Univ Amsterdam, Amsterdam Infect & Immun Inst, Dept Dermatol, Amsterdam UMC, Amsterdam, Netherlands
[7] Natl Univ Singapore, Yong Loo Lin Sch Med, Cardiovasc Res Inst, Singapore, Singapore
[8] Natl Univ Heart Ctr, Singapore, Singapore
[9] Univ Otago, Christchurch Heart Inst, Christchurch, New Zealand
[10] Vet Affairs Med Ctr, Minneapolis, MN USA
基金
英国医学研究理事会;
关键词
  heart failure; network meta-analysis; pharmacotherapy; HF; HETEROGENEITY; COMBINATION; GUIDELINES; THERAPIES;
D O I
10.1016/j.jchf.2021.09.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES This study sought to estimate and compare the aggregate treatment benefit of pharmacological therapy for heart failure (HF) with reduced ejection fraction. BACKGROUND The estimated treatment effects of various combinations of contemporary HF medical therapies are not well characterized. METHODS We performed a systematic network meta-analysis, using MEDLINE/EMBASE and the Cochrane Central Register of Controlled Trials for randomized controlled trials published between January 1987 and January 2020. We included angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, beta-blockers (BB), mineralocorticoid receptor antagonists (MRAs), digoxin, hydralazine-isosorbide dinitrate, ivabradine, angiotensin receptor-neprilysin inhibitors (ARNi), sodium glucose cotransporter-2 inhibitors (SGLT2i), vericiguat, and omecamtiv-mecarbil. The primary outcome was all-cause death. We estimated the life-years gained in 2 HF populations (BIOSTAT-CHF [BIOlogy Study to TAilored Treatment in Chronic Heart Failure] and ASIAN-HF [Asian Sudden Cardiac Death in Heart Failure Registry]). RESULTS We identified 75 relevant trials representing 95,444 participants. A combination of ARNi, BB, MRA, and SGLT2i was most effective in reducing all-cause death (HR: 0.39; 95% CI: 0.31-0.49); followed by ARNi, BB, MRA, and vericiguat (HR: 0.41; 95% CI: 0.32-0.53); and ARNi, BB, and MRA (HR: 0.44; 95% CI: 0.36-0.54). Results were similar for the composite outcome of cardiovascular death or first hospitalization for HF (HR: 0.36; 95% CI: 0.29-0.46 for ARNi, BB, MRA, and SGLT2i; HR: 0.44; 95% CI: 0.35-0.56 for ARNi, BB, MRA, and omecamtiv-mecarbil; and HR: 0.43; 95% CI: 0.34-0.55 for ARNi, BB, MRA, and vericiguat). The estimated additional number of life-years gained for a 70-year-old patient on ARNi, BB, MRA, and SGLT2i was 5.0 years (2.5-7.5 years) compared with no treatment in secondary analyses. CONCLUSIONS In patients with HF with reduced ejection fraction, the estimated aggregate benefit is greatest for a combination of ARNi, BB, MRA, and SGLT2i. (J Am Coll Cardiol HF 2022;10:73-84) (c) 2022 by the American College of Cardiology Foundation.
引用
收藏
页码:73 / 84
页数:12
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