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Factors and outcomes associated with improved left ventricular systolic function in patients with cardiomyopathy.
Eiger, Dylan S; Inoue, Lurdes Y T; Li, Qijun; Bardy, Gust; Lee, Kerry; Poole, Jeanne; Mark, Daniel; Samad, Zainab; Friedman, Daniel; Fishbein, Daniel; Sanders, Gillian; Al-Khatib, Sana M.
Afiliação
  • Eiger DS; Department of Medicine, Duke University, Durham, NC, USA. dylan.eiger@duke.edu.
  • Inoue LYT; Department of Biostatistics, University of Washington, Seattle, WA, USA.
  • Li Q; Department of Biostatistics, University of Washington, Seattle, WA, USA.
  • Bardy G; The Seattle Institute for Cardiac Research, Seattle, WA, USA.
  • Lee K; Department of Medicine, Duke University, Durham, NC, USA.
  • Poole J; Department of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA.
  • Mark D; Department of Medicine, University of Washington, Seattle, WA, USA.
  • Samad Z; Department of Medicine, Duke University, Durham, NC, USA.
  • Friedman D; Duke Clinical Research Institute, Duke University, Durham, NC, USA.
  • Fishbein D; Department of Medicine, Duke University, Durham, NC, USA.
  • Sanders G; Department of Medicine, Duke University, Durham, NC, USA.
  • Al-Khatib SM; Department of Medicine, University of Washington, Seattle, WA, USA.
Cardiol J ; 29(6): 978-984, 2022.
Article em En | MEDLINE | ID: mdl-33438181
BACKGROUND: Many patients in the Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT) had a significant improvement (> 10%) in the left ventricular ejection fraction (LVEF) during the course of the study, but the factors and outcomes associated with such improvement are uncertain. METHODS: We examined factors and rates of mortality, cause-specific mortality, and implantable cardioverter-defibrillator (ICD) shocks associated with improvement in LVEF by analyzing patients in the SCD-HeFT who were randomized to placebo or an ICD and who had an LVEF checked during follow-up. RESULTS: During a median follow-up of 3.99 years, of 837 patients who had at least two follow-up LVEF measurements, 276 (33%) patients had > 10% improvement in LVEF and 561 (67%) patients had no significant change in LVEF. Factors significantly associated with LVEF improvement included female sex, white race, history of hypertension, a QRS duration < 120 ms, and beta-blocker use. Improvement in LVEF was associated with a significant improvement in survival. There was no significant association between improvement in LVEF and cause-specific death, but there was a significant association between improvement in LVEF and reduced risk of receiving appropriate ICD shocks. CONCLUSIONS: About a third of patients in this analysis, who were randomized to placebo or an ICD in SCD-HeFT, had a significant improvement in LVEF during follow-up; improvement in LVEF was associated with improved survival but not with cause-specific death, and with decreased likelihood of receiving appropriate ICD shocks.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Desfibriladores Implantáveis / Insuficiência Cardíaca / Cardiomiopatias Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Cardiol J Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Desfibriladores Implantáveis / Insuficiência Cardíaca / Cardiomiopatias Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Cardiol J Ano de publicação: 2022 Tipo de documento: Article