Suppr超能文献

用于识别真正低风险房颤卒中的CHADS-VASc评分:一项韩国全国性队列研究

CHADS-VASc Score for Identifying Truly Low-Risk Atrial Fibrillation for Stroke: A Korean Nationwide Cohort Study.

作者信息

Kim Tae-Hoon, Yang Pil-Sung, Kim Daehoon, Yu Hee Tae, Uhm Jae-Sun, Kim Jong-Youn, Pak Hui-Nam, Lee Moon-Hyoung, Joung Boyoung, Lip Gregory Y H

机构信息

From the Division of Cardiology, Department of Internal Medicine, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea (T.-H.K., P.-S.Y., D.K., H.T.Y., J.-S.U., J.-Y.K., H.-N.P., M.-H.L., B.J.); Institute of Cardiovascular Sciences, University of Birmingham, United Kingdom (G.Y.H.L.); and Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, Denmark (G.Y.H.L.).

出版信息

Stroke. 2017 Nov;48(11):2984-2990. doi: 10.1161/STROKEAHA.117.018551. Epub 2017 Sep 22.

Abstract

BACKGROUND AND PURPOSE

As the threshold of stroke risk for initiating oral anticoagulants is lowered after the introduction of the nonvitamin K antagonist oral anticoagulants, the focus of stroke prevention in patients with nonvalvular atrial fibrillation has shifted away from predicting high-risk patients toward initially identifying patients with a truly low risk of ischemic stroke, who do not need antithrombotic therapy. We tested the predictive ability of the congestive heart failure, hypertension, age ≥75, diabetes mellitus, prior stroke or transient ischemic attack (doubled; CHADS), congestive heart failure, hypertension, age ≥75 (doubled), diabetes mellitus, prior stroke or transient ischemic attack (doubled), vascular disease, age 65 to 74, female (CHADS-VASc), and Anticoagulation and Risk Factors in Atrial Fibrillation (ATRIA) risk stratification schemes in oral anticoagulants naive patients with atrial fibrillation in a Korean nationwide sample cohort.

METHODS

From January 2002 to December 2008, a total of 5855 oral anticoagulant naive patients with nonvalvular atrial fibrillation aged ≥20 years were enrolled from Korea National Health Insurance Service-Sample Cohort database and were followed-up until December 2013.

RESULTS

At baseline, the proportions categorized as low risk using CHADS, CHADS-VASc, and ATRIA risk stratification schemes were 1049 (17.9%), 860 (14.7%), and 3280 (56.0%), respectively. During follow-up, the low-risk category using CHADS, CHADS-VASc, and ATRIA scores was retained in 811 (13.9%), 667 (11.4%), and 2729 (46.6%) patients, respectively. Rates of ischemic stroke (100 person-years) in the low risk categories of CHADS, CHADS-VASc, and ATRIA scores were 0.42, 0.26, and 1.43, respectively. CHADS-VASc had the best sensitivity (98.8% versus 85.7% in CHADS and 74.8% in ATRIA) and negative predictive value (98.8% versus 95.3% for CHADS and 93.7% for ATRIA) for the prediction of stroke incidence and was best for the prediction of the absence of ischemic stroke during 5 years of follow-up (odds ratio, 16.4 [95% confidence interval, 8.8-30.8]).

CONCLUSIONS

The CHADS-VASc score shows good performance in defining truly low-risk Asian patients with atrial fibrillation for stroke compared with CHADS and ATRIA scores.

摘要

背景与目的

随着新型非维生素K拮抗剂口服抗凝药的应用,启动口服抗凝药的卒中风险阈值降低,非瓣膜性心房颤动患者的卒中预防重点已从预测高危患者转向最初识别真正缺血性卒中低风险、无需抗血栓治疗的患者。我们在一个韩国全国性样本队列中,测试了充血性心力衰竭、高血压、年龄≥75岁、糖尿病、既往卒中或短暂性脑缺血发作(加倍;CHADS)、充血性心力衰竭、高血压、年龄≥75岁(加倍)、糖尿病、既往卒中或短暂性脑缺血发作(加倍)、血管疾病、年龄65至74岁、女性(CHADS-VASc)以及心房颤动抗凝与危险因素(ATRIA)风险分层方案对未使用过口服抗凝药的心房颤动患者的预测能力。

方法

2002年1月至2008年12月,从韩国国民健康保险服务样本队列数据库中纳入了5855例年龄≥20岁、未使用过口服抗凝药的非瓣膜性心房颤动患者,并随访至2013年12月。

结果

基线时,使用CHADS、CHADS-VASc和ATRIA风险分层方案分类为低风险的比例分别为1049例(17.9%)、860例(14.7%)和3280例(56.0%)。随访期间,使用CHADS、CHADS-VASc和ATRIA评分的低风险类别分别在811例(13.9%)、667例(11.4%)和2729例(46.6%)患者中得以维持。CHADS、CHADS-VASc和ATRIA评分低风险类别中缺血性卒中发生率(每100人年)分别为0.42、0.26和1.43。CHADS-VASc在预测卒中发生率方面具有最佳的敏感性(CHADS为85.7%,ATRIA为74.8%,CHADS-VASc为98.8%)和阴性预测值(CHADS为95.3%,ATRIA为93.7%,CHADS-VASc为98.8%),并且在5年随访期间对预测无缺血性卒中方面表现最佳(优势比,16.4[95%置信区间,8.8 - 30.8])。

结论

与CHADS和ATRIA评分相比,CHADS-VASc评分在定义真正低风险的亚洲心房颤动卒中患者方面表现良好。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验