Literature DB >> 27241839

Effect of Left Ventricular Systolic Dysfunction on Response to Warfarin.

Sameer Ather1, Aditi Shendre2, T Mark Beasley3, Todd Brown1, Charles E Hill4, Sumanth D Prabhu1, Nita A Limdi5.   

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.
Copyright © 2016 Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27241839      PMCID: PMC4962063          DOI: 10.1016/j.amjcard.2016.04.047

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  22 in total

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2.  Standardised initial warfarin treatment: evaluation of initial treatment response and maintenance dose prediction by randomised trial, and risk factors for an excessive warfarin response.

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4.  Racial differences in the prevalence of Factor V Leiden mutation among patients on chronic warfarin therapy.

Authors:  N A Limdi; T M Beasley; D B Allison; C A Rivers; R T Acton
Journal:  Blood Cells Mol Dis       Date:  2006-08-02       Impact factor: 3.039

5.  Clinical predictors of prolonged delay in return of the international normalized ratio to within the therapeutic range after excessive anticoagulation with warfarin.

Authors:  E M Hylek; S Regan; A S Go; R A Hughes; D E Singer; S J Skates
Journal:  Ann Intern Med       Date:  2001-09-18       Impact factor: 25.391

6.  A new regimen for starting warfarin therapy in out-patients.

Authors:  A Oates; P R Jackson; C A Austin; K S Channer
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Review 7.  The story of the discovery of heparin and warfarin.

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8.  A method to determine the optimal intensity of oral anticoagulant therapy.

Authors:  F R Rosendaal; S C Cannegieter; F J van der Meer; E Briët
Journal:  Thromb Haemost       Date:  1993-03-01       Impact factor: 5.249

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Authors:  William L Baker; Deborah A Cios; Stephen D Sander; Craig I Coleman
Journal:  J Manag Care Pharm       Date:  2009-04

10.  Warfarin Dosing Algorithms and the Need for Human Intervention.

Authors:  Scott E Kasner; Le Wang; Benjamin French; Steven R Messé; Jonas Ellenberg; Stephen E Kimmel
Journal:  Am J Med       Date:  2015-11-28       Impact factor: 4.965

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  1 in total

1.  Influence of Age on Warfarin Dose, Anticoagulation Control, and Risk of Hemorrhage.

Authors:  Aditi Shendre; Gaurav M Parmar; Chrisly Dillon; Timothy Mark Beasley; Nita A Limdi
Journal:  Pharmacotherapy       Date:  2018-02-27       Impact factor: 4.705

  1 in total

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