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Long-term analysis of left ventricular ejection fraction in patients with stable multivessel coronary disease undergoing medicine, angioplasty or surgery: 10-year follow-up of the MASS II trial.
Garzillo, Cibele Larrosa; Hueb, Whady; Gersh, Bernard J; Lima, Eduardo Gomes; Rezende, Paulo Cury; Hueb, Alexandre Ciappina; Vieira, Ricardo D'Oliveira; Favarato, Desiderio; Pereira, Alexandre Costa; Soares, Paulo Rogério; Serrano, Carlos Vicente; Ramires, José Antônio Franchini; Kalil Filho, Roberto.
Afiliação
  • Garzillo CL; Department of Atherosclerosis, Heart Institute of the University of São Paulo, Av. Dr. Eneas de Carvalho Aguiar 44, AB, Sala 114, Cerqueira César, São Paulo/SP 05403-000, Brazil.
Eur Heart J ; 34(43): 3370-7, 2013 Nov.
Article em En | MEDLINE | ID: mdl-23828828
ABSTRACT

BACKGROUND:

Assuming that coronary interventions, both coronary bypass surgery (CABG) and percutaneous coronary intervention (PCI), are directed to preserve left ventricular function, it is not known whether medical therapy alone (MT) can achieve this protection. Thus, we evaluated the evolution of LV ejection fraction (LVEF) in patients with stable coronary artery disease (CAD) treated by CABG, PCI, or MT as a post hoc analysis of a randomized controlled trial with a follow-up of 10 years.

METHODS:

Left ventricle ejection fraction was assessed with transthoracic echocardiography in patients with multivessel CAD, participants of the MASS II trial before randomization to CABG, PCI, or MT, and re-evaluated after 10 years of follow-up.

RESULTS:

Of the 611 patients, 422 were alive after 10.32 ± 1.43 years. Three hundred and fifty had LVEF reassessed 108 patients from MT, 111 from CABG, and 131 from PCI. There was no difference in LVEF at the beginning (0.61 ± 0.07, 0.61 ± 0.08, 0.61 ± 0.09, respectively, for PCI, CABG, and MT, P = 0.675) or at the end of follow-up (0.56 ± 0.11, 0.55 ± 0.11, 0.55 ± 0.12, P = 0.675), or in the decline of LVEF (reduction delta of -7.2 ± 17.13, -9.08 ± 18.77, and -7.54 ± 22.74). Acute myocardial infarction (AMI) during the follow-up was associated with greater reduction in LVEF. The presence of previous AMI (OR 2.50, 95% CI 1.40-4.45; P = 0.0007) and during the follow-up (OR 2.73, 95% CI 1.25-5.92; P = 0.005) was associated with development of LVEF <45%.

CONCLUSION:

Regardless of the therapeutic option applied, LVEF remains preserved in the absence of a major adverse cardiac event after 10 years of follow-up. CLINICAL TRIAL REGISTRATION URL http//www.controlled-trials.com. Registration number ISRCTN66068876.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Fármacos Cardiovasculares / Ponte de Artéria Coronária / Estenose Coronária / Intervenção Coronária Percutânea Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Fármacos Cardiovasculares / Ponte de Artéria Coronária / Estenose Coronária / Intervenção Coronária Percutânea Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2013 Tipo de documento: Article