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Original research article
Randomised comparison of zofenopril and ramipril plus acetylsalicylic acid in postmyocardial infarction patients with left ventricular systolic dysfunction: a post hoc analysis of the SMILE-4 Study in patients according to levels of left ventricular ejection fraction at entry
  1. Claudio Borghi1,
  2. Stefano Omboni2,
  3. Arrigo FG Cicero1,
  4. Stefano Bacchelli1,
  5. Daniela Degli Esposti1,
  6. Salvatore Novo3,
  7. Dragos Vinereanu4,
  8. Giuseppe Ambrosio5 and
  9. Ettore Ambrosioni1
  10. on behalf of the SMILE-4 Working Party
  1. 1Unit of Internal Medicine, Policlinico S. Orsola, University of Bologna, Bologna, Italy
  2. 2Italian Institute of Telemedicine, Varese, Italy
  3. 3Division of Cardiology, University of Palermo, Palermo, Italy
  4. 4University and Emergency Hospital, Bucharest, Romania
  5. 5Division of Cardiology, University of Perugia, Perugia, Italy
  1. Correspondence to Professor Claudio Borghi; claudio.borghi{at}unibo.it

Abstract

Objective Conflicting evidence exists on the benefits of treating patients with coronary artery disease and preserved left ventricular ejection fraction (LVEF) with an ACE inhibitor. This retrospective analysis of the SMILE-4 Study sought to compare the efficacy of zofenopril 60 mg plus acetylsalicylic acid (ASA) versus ramipril 10 mg plus ASA 100 mg in patients with acute myocardial infarction (AMI) and heart failure, according to an impaired or preserved LVEF.

Methods The primary study end point was 1-year combined occurrence of death or hospitalisation for cardiovascular causes. A preserved LVEF was defined by a baseline LVEF >40% and an impaired one by an LVEF ≤40%.

Results 448 patients (63%) had preserved and 262 (37%) had impaired LVEF. The primary end point occurred in 125 patients with preserved (28%) and 106 patients with impaired LVEF (41%, p=0.001). In the first group, the rate of major cardiovascular events was significantly lower under zofenopril than under ramipril (23% vs 33%; OR and 95% CI 0.60, 0.39 to 0.91; p=0.016). This was also the case for patients with impaired LVEF, though between-group difference was not statistically significant (38% zofenopril vs 44% ramipril; OR 0.77, 0.47 to 1.26; p=0.297). LVEF values significantly (p<0.0001) increased during the follow-up in both subsets with no between-treatment differences. However, improvement rates in LVEF (increase ≥5%) were higher in patients with impaired LVEF (72% vs 61%, p=0.006).

Conclusions In the SMILE-4 Study, the cardiovascular outcome of patients with post-AMI with preserved LVEF was more favourable in the zofenopril than in the ramipril treatment group.

Trial registration number EudraCT Number: 2004-001150-88 (http://www.clinicaltrialsregister.eu); Italian Ministry of Health Code: GUIDOTT_III_2004_001 (https://oss-sper-clin.agenziafarmaco.it).

  • acute myocardial infarction
  • left ventricular dysfunction
  • left ventricular ejection fraction
  • angiotensin-converting enzyme inhibitors

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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