Angiotensin Receptor Neprilysin Inhibition Compared With Enalapril on the Risk of Clinical Progression in Surviving Patients With Heart Failure

Milton Packer(British Heart Foundation), John J.V. McMurray(British Heart Foundation), Akshay S. Desai(British Heart Foundation), Jianjian Gong(British Heart Foundation), Martin Lefkowitz(British Heart Foundation), Adel R. Rizkala(British Heart Foundation), Jean L. Rouleau(British Heart Foundation), Victor Shi(British Heart Foundation), Scott D. Solomon(British Heart Foundation), Karl Swedberg(British Heart Foundation), Michael R. Zile(British Heart Foundation), Karl Andersen(British Heart Foundation), Juan Luis Arango(British Heart Foundation), J. Malcolm O. Arnold(British Heart Foundation), Jan Bělohlávek(British Heart Foundation), Michael Böhm(British Heart Foundation), S. А. Boytsov(British Heart Foundation), Lesley Burgess(British Heart Foundation), Walter Cabrera(British Heart Foundation), Carlos Calvo(Universidade de Santiago de Compostela), Chen‐Huan Chen(British Heart Foundation), Andrej Dukát(British Heart Foundation), Yan Duarte(British Heart Foundation), Andrejs Ērglis(British Heart Foundation), Michael Fu(British Heart Foundation), Efraín Gómez(British Heart Foundation), Angel Gonzàlez-Medina(British Heart Foundation), Albert Hagège(British Heart Foundation), Jun Huang(British Heart Foundation), Tzvetana Katova(British Heart Foundation), Songsak Kiatchoosakun(British Heart Foundation), Kee‐Sik Kim(British Heart Foundation), Ömer Kozan(British Heart Foundation), Edmundo Bayram Llamas(British Heart Foundation), Felipe Martínez(British Heart Foundation), Béla Merkely(British Heart Foundation), Iván Mendoza(British Heart Foundation), Arend Mosterd(British Heart Foundation), Marta Negrusz‐Kawecka(British Heart Foundation), Keijo Peuhkurinen(British Heart Foundation), Félix José Alvarez Ramires(British Heart Foundation), Jens Refsgaard(British Heart Foundation), Arvo Rosenthal(British Heart Foundation), Michele Senni(British Heart Foundation), Antonio S. Sibulo(British Heart Foundation), José Silva‐Cardoso(Universidade do Porto), Iain Squire(British Heart Foundation), Randall C. Starling(Cleveland Clinic), John R. Teerlink(British Heart Foundation), Johan Vanhaecke(British Heart Foundation), Dragoş Vinereanu(British Heart Foundation), Raymond Wong(British Heart Foundation)
Circulation
November 17, 2014
Cited by 665Open Access
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Abstract

BACKGROUND: Clinical trials in heart failure have focused on the improvement in symptoms or decreases in the risk of death and other cardiovascular events. Little is known about the effect of drugs on the risk of clinical deterioration in surviving patients. METHODS AND RESULTS: We compared the angiotensin-neprilysin inhibitor LCZ696 (400 mg daily) with the angiotensin-converting enzyme inhibitor enalapril (20 mg daily) in 8399 patients with heart failure and reduced ejection fraction in a double-blind trial. The analyses focused on prespecified measures of nonfatal clinical deterioration. In comparison with the enalapril group, fewer LCZ696-treated patients required intensification of medical treatment for heart failure (520 versus 604; hazard ratio, 0.84; 95% confidence interval, 0.74-0.94; P=0.003) or an emergency department visit for worsening heart failure (hazard ratio, 0.66; 95% confidence interval, 0.52-0.85; P=0.001). The patients in the LCZ696 group had 23% fewer hospitalizations for worsening heart failure (851 versus 1079; P<0.001) and were less likely to require intensive care (768 versus 879; 18% rate reduction, P=0.005), to receive intravenous positive inotropic agents (31% risk reduction, P<0.001), and to have implantation of a heart failure device or cardiac transplantation (22% risk reduction, P=0.07). The reduction in heart failure hospitalization with LCZ696 was evident within the first 30 days after randomization. Worsening of symptom scores in surviving patients was consistently more common in the enalapril group. LCZ696 led to an early and sustained reduction in biomarkers of myocardial wall stress and injury (N-terminal pro-B-type natriuretic peptide and troponin) versus enalapril. CONCLUSIONS: Angiotensin-neprilysin inhibition prevents the clinical progression of surviving patients with heart failure more effectively than angiotensin-converting enzyme inhibition. CLINICAL TRIAL REGISTRATION URL: http://www.clinicaltrials.gov. Unique identifier: NCT01035255.


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