4.7 Article

Incidence of sudden cardiac death after ventricular fibrillation complicating acute myocardial infarction: a 5-year cause-of-death analysis of the FAST-MI 2005 registry

期刊

EUROPEAN HEART JOURNAL
卷 35, 期 2, 页码 116-+

出版社

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/eht453

关键词

Sudden death; Acute coronary syndrome; Ventricular fibrillation; Implantable cardioverter defibrillator; Prognosis

资金

  1. Astra-Zeneca
  2. Daiichi-Sankyo
  3. Eli-Lilly
  4. GSK
  5. Merck
  6. Novartis
  7. Pfizer
  8. Sanofi-aventis
  9. Servier
  10. Medicines Company

向作者/读者索取更多资源

Aims Limited data are available on long-term prognosis or causes-of-death analysis among survivors of acute myocardial infarction (MI) according to whether or not they developed ventricular fibrillation (VF) during the acute stage of MI. Methods and results Among 3670 MI patients hospitalized in France in 2005 and enrolled in this prospective follow-up cohort study, we assessed in-hospital mortality and 5-year cause of death among those who survived to hospital discharge, according to whether they developed VF (116 cases) or not, during the acute stage. 94.5 of patients had complete follow-up at 5 years. In-hospital mortality was significantly higher among VF patients (adjusted OR 7.38, 95 CI 4.2712.75, P 0.001). Among 3463 survivors at hospital discharge, 1024 died during a mean follow-up of 52 2 months. The overall survival rate at 5 years was 74.4 (95 CI 72.876.0). In Cox multivariate analysis, occurrence of VF during the acute phase of MI was not associated with an increased mortality at 5 years (HR 0.78, 95 CI 0.381.58, P 0.21). The distribution of causes of death at 5 years did not statistically differ according to the presence or absence of VF, especially for sudden cardiac death (13.1 in VF group vs.12.9 in non-VF group), despite a very low rate of implantation of cardioverter defibrillator in both groups (Overall rate 1.2). Conclusion Patients developing VF in the setting of acute MI are at higher risk of in-hospital mortality. However, VF is not associated with a higher long-term all-cause or sudden cardiac death mortality.

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