Your browser doesn't support javascript.
loading
Effect of Left Ventricular Systolic Dysfunction on Response to Warfarin.
Ather, Sameer; Shendre, Aditi; Beasley, T Mark; Brown, Todd; Hill, Charles E; Prabhu, Sumanth D; Limdi, Nita A.
Afiliação
  • Ather S; Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Alabama.
  • Shendre A; Department of Epidemiology, University of Alabama at Birmingham, Alabama.
  • Beasley TM; Section on Statistical Genetics, Department of Biostatistics, University of Alabama at Birmingham, Alabama.
  • Brown T; Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Alabama.
  • Hill CE; Department of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia.
  • Prabhu SD; Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Alabama.
  • Limdi NA; Department of Neurology, University of Alabama at Birmingham, Alabama. Electronic address: nlimdi@uab.edu.
Am J Cardiol ; 118(2): 232-6, 2016 07 15.
Article em En | MEDLINE | ID: mdl-27241839
ABSTRACT
Candidates for chronic warfarin therapy often have co-morbid conditions, such as heart failure, with reduced left ventricular ejection fraction. Previous reports have demonstrated an increased risk of over-anticoagulation due to reduced warfarin dose requirement in patients with decompensated heart failure. However, the influence of left ventricular systolic dysfunction (LVSD), defined as left ventricular ejection fraction <40%, on warfarin response has not been evaluated. Here, we assess the influence of LVSD on warfarin dose, anticoagulation control (percent time in target range), and risk of over-anticoagulation (international normalized ratio >4) and major hemorrhage. Of the 1,354 patients included in this prospective cohort study, 214 patients (16%) had LVSD. Patients with LVSD required 11% lower warfarin dose compared with those without LVSD (p <0.001) using multivariate linear regression analyses. Using multivariate Cox proportional hazards model, patients with LVSD experienced similar levels of anticoagulation control (percent time in target range 51% vs 53% p = 0.15), risk of over-anticoagulation (international normalized ratio >4; hazard ratio 1.01, 95% confidence interval 0.82 to 1.25; p = 0.91), and risk of major hemorrhage (hazard ratio 1.11; 95% confidence interval 0.70 to 1.74; p = 0.66). Addition of LVSD variable in the model increased the variability explained from 35% to 36% for warfarin dose prediction. In conclusion, our results demonstrate that patients with LVSD require lower doses of warfarin. Whether warfarin dosing algorithms incorporating LVSD in determining initial doses improves outcomes needs to be evaluated.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Varfarina / Disfunção Ventricular Esquerda / Insuficiência Cardíaca / Hemorragia / Anticoagulantes Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Varfarina / Disfunção Ventricular Esquerda / Insuficiência Cardíaca / Hemorragia / Anticoagulantes Idioma: En Ano de publicação: 2016 Tipo de documento: Article