Effect of Left Ventricular Systolic Dysfunction on Response to Warfarin

被引:7
|
作者
Ather, Sameer [1 ]
Shendre, Aditi [2 ]
Beasley, T. Mark [3 ]
Brown, Todd [1 ]
Hill, Charles E. [5 ]
Prabhu, Sumanth D. [1 ]
Limdi, Nita A. [4 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Cardiovasc Dis, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Epidemiol, Birmingham, AL USA
[3] Univ Alabama Birmingham, Dept Biostat, Sect Stat Genet, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Dept Neurol, UAB Stn, Birmingham, AL 35294 USA
[5] Emory Univ, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2016年 / 118卷 / 02期
基金
美国国家卫生研究院;
关键词
ATRIAL-FIBRILLATION; ORAL ANTICOAGULATION; EUROPEAN-AMERICANS; AFRICAN-AMERICANS; RANDOMIZED TRIAL; MAINTENANCE; THERAPY; CYP2C9; RISK; PREVALENCE;
D O I
10.1016/j.amjcard.2016.04.047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:232 / 236
页数:5
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