已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Comparison of clinical outcomes of edoxaban versus apixaban, dabigatran, rivaroxaban, and vitamin K antagonists in patients with atrial fibrillation in Germany: A real-world cohort study

依杜沙班 医学 阿哌沙班 拜瑞妥 达比加群 心房颤动 内科学 维生素K拮抗剂 华法林 危险系数 心脏病学 麻醉 置信区间
作者
Xiaocong Li Marston,R. Wang,Yu‐Chen Yeh,Lisa Zimmermann,X. Ye,Xīn Gào,Bernd Brüggenjürgen,Martin Unverdorben
出处
期刊:International Journal of Cardiology [Elsevier BV]
卷期号:346: 93-99 被引量:27
标识
DOI:10.1016/j.ijcard.2021.11.008
摘要

The aim of the study was to compare the real-world effectiveness and safety in atrial fibrillation (AF) patients treated with edoxaban versus other oral anticoagulants (OACs) (apixaban, dabigatran, rivaroxaban, and vitamin K antagonists [VKA]) in Germany.Using a representative database of 3.5 million statutory health-insured lives in Germany, a retrospective cohort study was conducted to examine ischemic stroke (IS) or systemic embolism (SE) and major bleeding in AF patients initiating anticoagulant therapy from January 2014 through June 2017. Inverse probability of treatment weighting using propensity score was applied for baseline covariate adjustment. Cox proportional hazards models were used to estimate the adjusted risk (hazard ratio [HR]) of each outcome comparing edoxaban versus other OACs. Among 21,038 patients treated with OACs, 1236 edoxaban, 6053 apixaban, 1306 dabigatran, 7013 rivaroxaban, and 5430 VKA patients were included. The adjusted combined risks of IS or SE were lower (p < 0.05) for each edoxaban pairwise comparison with other OACs (HR: 0.83 vs. apixaban, 0.60 vs. dabigatran, 0.72 vs. rivaroxaban, 0.64 vs. VKA). Edoxaban favored lower risks of major bleeding compared with rivaroxaban (HR: 0.74) and VKA (HR: 0.47). No differences in the risk of major bleeding were found between edoxaban and apixaban (p = 0.33), and between edoxaban and dabigatran (p = 0.06).Edoxaban was associated with better effectiveness compared with other OACs in AF patients from Germany. Edoxaban also demonstrated a favorable safety profile.
最长约 10秒,即可获得该文献文件

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
如意安莲完成签到,获得积分10
1秒前
QQ完成签到 ,获得积分10
1秒前
zc完成签到,获得积分10
1秒前
过眼云烟发布了新的文献求助10
2秒前
2秒前
HarrisonChan发布了新的文献求助10
4秒前
FashionBoy的应助被牙牙乐采纳,获得10
7秒前
xy发布了新的文献求助10
7秒前
温暖砖头发布了新的文献求助10
8秒前
9秒前
黄老师完成签到,获得积分10
12秒前
Lycoris林曦发布了新的文献求助10
13秒前
李沅翰完成签到,获得积分10
17秒前
18秒前
CodeCraft的应助被林期采纳,获得10
20秒前
wanci的应助被sgybws采纳,获得10
22秒前
23秒前
doudou完成签到 ,获得积分10
23秒前
Akim的应助被小小采纳,获得10
24秒前
28秒前
科研通AI6.4的应助被HarrisonChan采纳,获得10
30秒前
嗯嗯完成签到 ,获得积分10
31秒前
小蘑菇的应助被清脆的南珍采纳,获得10
32秒前
秋风的应助被炙热的小海豚采纳,获得10
32秒前
32秒前
Badada完成签到,获得积分10
33秒前
充电宝的应助被成就的迎夏采纳,获得10
35秒前
析纹时光完成签到 ,获得积分10
35秒前
amengptsd完成签到,获得积分10
36秒前
林期发布了新的文献求助10
37秒前
38秒前
科研民工完成签到 ,获得积分10
38秒前
40秒前
42秒前
斯文败类的应助被秀丽的大门采纳,获得10
42秒前
砺行的应助被明朝采纳,获得10
43秒前
qinqin发布了新的文献求助20
43秒前
45秒前
46秒前
47秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
A Will for the Machine: Computerization, Automation, and the Arts in South Africa 400
Decentring Leadership 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7809301
求助须知:如何正确求助?哪些是违规求助? 9341585
关于积分的说明 20507429
捐赠科研通 7401805
什么是DOI,文献DOI怎么找? 3329074
关于科研通互助平台的介绍 2475843
邀请新用户注册赠送积分活动 2347644