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Aliskiren, Enalapril, or Aliskiren and Enalapril in Heart Failure.

McMurray, JJV; Krum, H; Abraham, WT; Dickstein, K; Køber, LV; Desai, AS; Solomon, SD; Greenlaw, N; Ali, MA; Chiang, Y; et al. McMurray, JJV; Krum, H; Abraham, WT; Dickstein, K; Køber, LV; Desai, AS; Solomon, SD; Greenlaw, N; Ali, MA; Chiang, Y; Shao, Q; Tarnesby, G; Massie, BM; ATMOSPHERE Committees Investigators (2016) Aliskiren, Enalapril, or Aliskiren and Enalapril in Heart Failure. N Engl J Med, 374 (16). pp. 1521-1532. ISSN 1533-4406 https://doi.org/10.1056/NEJMoa1514859
SGUL Authors: Anderson, Lisa

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Abstract

BACKGROUND: Among patients with chronic heart failure, angiotensin-converting-enzyme (ACE) inhibitors reduce mortality and hospitalization, but the role of a renin inhibitor in such patients is unknown. We compared the ACE inhibitor enalapril with the renin inhibitor aliskiren (to test superiority or at least noninferiority) and with the combination of the two treatments (to test superiority) in patients with heart failure and a reduced ejection fraction. METHODS: After a single-blind run-in period, we assigned patients, in a double-blind fashion, to one of three groups: 2336 patients were assigned to receive enalapril at a dose of 5 or 10 mg twice daily, 2340 to receive aliskiren at a dose of 300 mg once daily, and 2340 to receive both treatments (combination therapy). The primary composite outcome was death from cardiovascular causes or hospitalization for heart failure. RESULTS: After a median follow-up of 36.6 months, the primary outcome occurred in 770 patients (32.9%) in the combination-therapy group and in 808 (34.6%) in the enalapril group (hazard ratio, 0.93; 95% confidence interval [CI], 0.85 to 1.03). The primary outcome occurred in 791 patients (33.8%) in the aliskiren group (hazard ratio vs. enalapril, 0.99; 95% CI, 0.90 to 1.10); the prespecified test for noninferiority was not met. There was a higher risk of hypotensive symptoms in the combination-therapy group than in the enalapril group (13.8% vs. 11.0%, P=0.005), as well as higher risks of an elevated serum creatinine level (4.1% vs. 2.7%, P=0.009) and an elevated potassium level (17.1% vs. 12.5%, P<0.001). CONCLUSIONS: In patients with chronic heart failure, the addition of aliskiren to enalapril led to more adverse events without an increase in benefit. Noninferiority was not shown for aliskiren as compared with enalapril. (Funded by Novartis; ATMOSPHERE ClinicalTrials.gov number, NCT00853658.).

Item Type: Article
Additional Information: From New England Journal of Medicine, McMurray, JJV; Krum, H; Abraham, WT; Dickstein, K; Køber, LV; Desai, AS; Solomon, SD; Greenlaw, N; Ali, MA; Chiang, Y; et al., TAliskiren, Enalapril, or Aliskiren and Enalapril in Heart Failure, 374, 1521-1532. Copyright © 2016 Massachusetts Medical Society. Reprinted with permission.
Keywords: Aged, Amides, Angiotensin-Converting Enzyme Inhibitors, Chronic Disease, Diabetes Mellitus, Type 2, Double-Blind Method, Drug Therapy, Combination, Enalapril, Female, Follow-Up Studies, Fumarates, Heart Failure, Humans, Kaplan-Meier Estimate, Male, Middle Aged, Renin, Stroke Volume, Treatment Failure, ATMOSPHERE Committees Investigators, Humans, Diabetes Mellitus, Type 2, Chronic Disease, Amides, Fumarates, Renin, Enalapril, Angiotensin-Converting Enzyme Inhibitors, Stroke Volume, Treatment Failure, Drug Therapy, Combination, Follow-Up Studies, Double-Blind Method, Aged, Middle Aged, Female, Male, Heart Failure, Kaplan-Meier Estimate, 11 Medical and Health Sciences, General & Internal Medicine
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: N Engl J Med
ISSN: 1533-4406
Language: eng
Dates:
DateEvent
21 April 2016Published
4 April 2016Published Online
Publisher License: Publisher's own licence
PubMed ID: 27043774
Web of Science ID: WOS:000374383900005
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116200
Publisher's version: https://doi.org/10.1056/NEJMoa1514859

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