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依房颤预测因子评估,利伐沙班与阿司匹林比较用于复发性卒中: NAVIGATE ESUS 随机临床试验的二次分析。

Recurrent Stroke With Rivaroxaban Compared With Aspirin According to Predictors of Atrial Fibrillation: Secondary Analysis of the NAVIGATE ESUS Randomized Clinical Trial.

机构信息

Division of Cardiology, Hamilton Health Sciences, Population Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Division of Neurology and Hurvitz Brain Sciences Program, Sunnybrook Health Sciences Centre and Sunnybrook Research Institute, Toronto, Ontario, Canada.

出版信息

JAMA Neurol. 2019 Jul 1;76(7):764-773. doi: 10.1001/jamaneurol.2019.0617.

Abstract

IMPORTANCE

The NAVIGATE ESUS randomized clinical trial found that 15 mg of rivaroxaban per day does not reduce stroke compared with aspirin in patients with embolic stroke of undetermined source (ESUS); however, it substantially reduces stroke risk in patients with atrial fibrillation (AF).

OBJECTIVE

To analyze whether rivaroxaban is associated with a reduction of recurrent stroke among patients with ESUS who have an increased risk of AF.

DESIGN, SETTING, AND PARTICIPANTS: Participants were stratified by predictors of AF, including left atrial diameter, frequency of premature atrial contractions, and HAVOC score, a validated scheme using clinical features. Treatment interactions with these predictors were assessed. Participants were enrolled between December 2014 and September 2017, and analysis began March 2018.

INTERVENTION

Rivaroxaban treatment vs aspirin.

MAIN OUTCOMES AND MEASURES

Risk of ischemic stroke.

RESULTS

Among 7112 patients with a mean (SD) age of 67 (9.8) years, the mean (SD) HAVOC score was 2.6 (1.8), the mean (SD) left atrial diameter was 3.8 (1.4) cm (n = 4022), and the median (interquartile range) daily frequency of premature atrial contractions was 48 (13-222). Detection of AF during follow-up increased for each tertile of HAVOC score: 2.3% (score, 0-2), 3.0% (score, 3), and 5.8% (score, >3); however, neither tertiles of the HAVOC score nor premature atrial contractions frequency impacted the association of rivaroxaban with recurrent ischemic stroke (P for interaction = .67 and .96, respectively). Atrial fibrillation annual incidence increased for each tertile of left atrial diameter (2.0%, 3.6%, and 5.2%) and for each tertile of premature atrial contractions frequency (1.3%, 2.9%, and 7.0%). Among the predefined subgroup of patients with a left atrial diameter of more than 4.6 cm (9% of overall population), the risk of ischemic stroke was lower among the rivaroxaban group (1.7% per year) compared with the aspirin group (6.5% per year) (hazard ratio, 0.26; 95% CI, 0.07-0.94; P for interaction = .02).

CONCLUSIONS AND RELEVANCE

The HAVOC score, left atrial diameter, and premature atrial contraction frequency predicted subsequent clinical AF. Rivaroxaban was associated with a reduced risk of recurrent stroke among patients with ESUS and moderate or severe left atrial enlargement; however, this needs to be independently confirmed before influencing clinical practice.

摘要

重要性

NAVIGATE ESUS 随机临床试验发现,与阿司匹林相比,每天服用 15 毫克利伐沙班不能降低栓塞性卒中来源不明(ESUS)患者的卒中风险;然而,它显著降低了伴有心房颤动(AF)风险的患者的卒中风险。

目的

分析利伐沙班是否与 ESUS 患者中复发性卒中风险降低相关,这些患者有 AF 的风险增加。

设计、设置和参与者:根据 AF 的预测因素对参与者进行分层,包括左心房直径、房性期前收缩的频率和 HAVOC 评分,这是一种使用临床特征的验证方案。评估了治疗与这些预测因素的相互作用。参与者于 2014 年 12 月至 2017 年 9 月入组,分析于 2018 年 3 月开始。

干预措施

利伐沙班治疗与阿司匹林。

主要结局和测量指标

缺血性卒中风险。

结果

在 7112 名平均(SD)年龄为 67(9.8)岁的患者中,平均(SD)HAVOC 评分为 2.6(1.8),平均(SD)左心房直径为 3.8(1.4)cm(n=4022),中位数(四分位距)每日房性期前收缩频率为 48(13-222)。随着 HAVOC 评分的每一个三分位数增加,在随访期间检测到 AF 的比例也随之增加:2.3%(评分 0-2)、3.0%(评分 3)和 5.8%(评分>3);然而,HAVOC 评分的三分位数或房性期前收缩频率均未影响利伐沙班与复发性缺血性卒中的相关性(交互检验 P 值分别为.67 和.96)。随着左心房直径每增加一个三分位数(2.0%、3.6%和 5.2%)和房性期前收缩频率每增加一个三分位数(1.3%、2.9%和 7.0%),AF 的年发生率也随之增加。在左心房直径大于 4.6 cm(总体人群的 9%)的预先设定亚组中,与阿司匹林组相比,利伐沙班组缺血性卒中风险较低(每年 1.7%)(风险比,0.26;95%CI,0.07-0.94;交互检验 P 值为.02)。

结论和相关性

HAVOC 评分、左心房直径和房性期前收缩频率预测了随后的临床 AF。利伐沙班与 ESUS 患者和中重度左心房扩大患者的复发性卒中风险降低相关;然而,这需要在独立确认后才能影响临床实践。

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