Safety and Efficacy of Direct Oral Anticoagulants Versus Warfarin in Patients With Chronic Kidney Disease and Atrial Fibrillation

医学 心房颤动 内科学 华法林 肾脏疾病 心脏病学 重症监护医学
作者
Amber Makani,Samir Saba,Sandeep Jain,Aditya Bhonsale,Michael Sharbaugh,Floyd Thoma,Yisi Wang,Oscar C. Marroquin,Joon S. Lee,N.A. Mark Estes,Suresh Mulukutla
出处
期刊:American Journal of Cardiology [Elsevier]
卷期号:125 (2): 210-214 被引量:45
标识
DOI:10.1016/j.amjcard.2019.10.033
摘要

Patients with atrial fibrillation (AF) commonly have impaired renal function. The safety and efficacy of direct oral anticoagulants (DOACs) in patients with chronic kidney disease (CKD) and end-stage renal disease has not been fully elucidated. This study evaluated and compared the safety outcomes of DOACs versus warfarin in patients with nonvalvular AF and concomitant CKD. Patients in our health system with AF prescribed oral anticoagulants during 2010 to 2017 were identified. All-cause mortality, bleeding and hemorrhagic, and ischemic stroke were evaluated based on degree of renal impairment and method of anticoagulation. There were 21,733 patients with a CHA2DS2-VASc score of ≥2 included in this analysis. Compared with warfarin, DOAC use in patients with impaired renal function was associated with lower risk of mortality with a hazard ratio (HR): 0.76 (95% confidence interval [CI] 0.70 to 0.84, p value <0.001) in patients with eGFR >60, HR 0.74 (95% CI 0.68 to 0.81, p value <0.001) in patients with eGFR >30 to 60, and HR 0.76 (95% CI 0.63 to 0.92, p value <0.001) in patients with eGFR ≤30 or on dialysis. Bleeding requiring hospitalization was also less in the DOAC group with a HR 0.93 (95% CI 0.82 to 1.04, p value 0.209) in patients with eGFR >60, HR 0.83 (95% CI 0.74 to 0.94, p value 0.003) in patients with eGFR >30 to 60, and HR 0.69 (95% CI 0.50 to 0.93, p value 0.017) in patients with eGFR ≤30 or on dialysis. In conclusion, in comparison to warfarin, DOACs appear to be safe and effective with a lower risk of all-cause mortality and lower bleeding across all levels of CKD.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI6.2应助木口采纳,获得50
1秒前
1秒前
宋佳丽给宋佳丽的求助进行了留言
2秒前
2秒前
852应助liuyuxin采纳,获得10
2秒前
聪明无敌小腚宝完成签到,获得积分10
3秒前
烟花应助uouuo采纳,获得10
4秒前
4秒前
香蕉觅云应助半颗橙子采纳,获得10
4秒前
HUU完成签到,获得积分20
5秒前
yunan完成签到,获得积分10
5秒前
高高很厉害完成签到,获得积分10
7秒前
田様应助吾问无为谓采纳,获得10
7秒前
苗龙伟完成签到,获得积分10
7秒前
zxc发布了新的文献求助10
8秒前
WangC完成签到,获得积分10
8秒前
小马甲应助米娜采纳,获得10
8秒前
蓝从发布了新的文献求助10
9秒前
9秒前
文艺鞋子发布了新的文献求助10
9秒前
李爱国应助虚心的若翠采纳,获得10
10秒前
科研通AI6.1应助NinjiaQiu采纳,获得10
10秒前
Tomi完成签到,获得积分10
11秒前
11秒前
张洁完成签到,获得积分10
13秒前
SKSK完成签到,获得积分10
14秒前
尘寰完成签到,获得积分10
14秒前
阿迪发布了新的文献求助10
14秒前
山阳县藏兵洞谷二完成签到,获得积分10
15秒前
YY发布了新的文献求助10
15秒前
Frank完成签到,获得积分10
16秒前
uouuo发布了新的文献求助10
17秒前
丘比特应助真的起不来名采纳,获得10
17秒前
爆米花应助七七采纳,获得10
17秒前
汉堡包应助palmer采纳,获得10
17秒前
18秒前
精明凝丹发布了新的文献求助10
18秒前
19秒前
我是老大应助小唐采纳,获得10
20秒前
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Modern Epidemiology, Fourth Edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6023821
求助须知:如何正确求助?哪些是违规求助? 7653041
关于积分的说明 16174203
捐赠科研通 5172300
什么是DOI,文献DOI怎么找? 2767456
邀请新用户注册赠送积分活动 1750917
关于科研通互助平台的介绍 1637326