根据亚临床心房颤动的基线频率和持续时间得出的中风或全身栓塞风险:来自 ARTESiA 试验的启示。

IF 35.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
William F McIntyre, Alexander P Benz, Jeff S Healey, Stuart J Connolly, Mu Yang, Shun Fu Lee, Thalia S Field, Marco Alings, J Benezet-Mazuecos, Giuseppe Boriani, J Cosedis Nielsen, Michael R Gold, Francesco Pergolini, Taya V Glotzer, Christopher B Granger, Renato D Lopes
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引用次数: 0

摘要

研究背景在 ARTESiA 试验(阿哌沙班用于减少器械检测到的亚临床心房颤动患者的血栓栓塞)中,与阿司匹林相比,阿哌沙班可减少器械检测到的亚临床心房颤动(SCAF)患者的中风或全身性栓塞。临床指南建议,在决定是否为这类人群开具口服抗凝药时,应考虑SCAF发作持续时间:我们在 ARTESiA 中进行了一项回顾性队列研究。通过调整 CHA2DS2-VASc 评分和治疗分配(阿哌沙班或阿司匹林)的 Cox 回归,我们评估了随机化前 6 个月内 SCAF 发作频率和最长 SCAF 发作持续时间,以此作为卒中风险和阿哌沙班治疗效果的预测因素:在3986名有完整基线SCAF数据的患者中,703人(17.6%)在入组前6个月内SCAF发作时间未≥6分钟。在入组前 6 个月中≥1 次 SCAF 发作(≥6 分钟)的 3283 名患者(82.4%)中,2542 人(77.4%)最多发作 5 次,741 人(22.6%)≥6 次。最长发作持续 6 小时的患者有 832 人(25.3%)。较高的基线 SCAF 频率与中风或全身性栓塞风险的增加无关:1 至 5 次发作为 1.1%,而≥6 次发作为 1.2%/患者年(调整后危险比为 0.89 [95% CI, 0.59-1.34])。在一项探索性分析中,在入组前 6 个月内曾发生过 SCAF 但未发作≥6 分钟的患者发生卒中或全身性栓塞的风险低于在此期间至少发作过一次的患者(0.5% 对 1.1%/患者-年;调整后危险比为 0.48 [95% CI, 0.27-0.85])。SCAF的发生频率并不影响阿哌沙班降低中风或全身性栓塞的效果(Pinteraction=0.1)。入组前 6 个月内最长 SCAF 发作持续时间与随访期间中风或全身性栓塞风险无关(6 小时:1.0%/患者-年;6 小时:1.0%/患者-年;6 小时:1.0%/患者-年):1.0%/患者-年[调整后危险比为 1.02 (95% CI, 0.63-1.66)])。SCAF持续时间不会改变阿哌沙班减少中风或全身性栓塞的效果(Ptrend=0.1):在 ARTESiA 中,基线 SCAF 频率和最长发作持续时间与中风或全身性栓塞风险无关,也不会改变阿哌沙班减少中风或全身性栓塞的效果:URL: https://www.clinicaltrials.gov; Unique identifier:NCT01938248。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Stroke or Systemic Embolism According to Baseline Frequency and Duration of Subclinical Atrial Fibrillation: Insights From the ARTESiA Trial.

Background: In the ARTESiA trial (Apixaban for the Reduction of Thromboembolism in Patients With Device-Detected Subclinical Atrial Fibrillation), apixaban, compared with aspirin, reduced stroke or systemic embolism in patients with device-detected subclinical atrial fibrillation (SCAF). Clinical guidelines recommend considering SCAF episode duration when deciding whether to prescribe oral anticoagulation for this population.

Methods: We performed a retrospective cohort study in ARTESiA. Using Cox regression adjusted for CHA2DS2-VASc score and treatment allocation (apixaban or aspirin), we assessed frequency of SCAF episodes and duration of the longest SCAF episode in the 6 months before randomization as predictors of stroke risk and of apixaban treatment effect.

Results: Among 3986 patients with complete baseline SCAF data, 703 (17.6%) had no SCAF episode ≥6 minutes in the 6 months before enrollment. Among 3283 patients (82.4%) with ≥1 episode of SCAF ≥6 minutes in the 6 months before enrollment, 2542 (77.4%) had up to 5 episodes, and 741 (22.6%) had ≥6 episodes. The longest episode lasted <1 hour in 1030 patients (31.4%), 1 to <6 hours in 1421 patients (43.3%), and >6 hours in 832 patients (25.3%). Higher baseline SCAF frequency was not associated with increased risk of stroke or systemic embolism: 1.1% for 1 to 5 episodes versus 1.2%/patient-year for ≥6 episodes (adjusted hazard ratio, 0.89 [95% CI, 0.59-1.34]). In an exploratory analysis, patients with previous SCAF but no episode ≥6 minutes in the 6 months before enrollment had a lower risk of stroke or systemic embolism than patients with at least one episode during that period (0.5% versus 1.1%/patient-year; adjusted hazard ratio, 0.48 [95% CI, 0.27-0.85]). The frequency of SCAF did not modify the reduction in stroke or systemic embolism with apixaban (Pinteraction=0.1). The duration of the longest SCAF episode in the 6 months before enrollment was not associated with the risk of stroke or systemic embolism during follow-up (<1 hour: 1.0%/patient-year [reference]; 1-6 hours: 1.2%/patient-year [adjusted hazard ratio, 1.27 (95% CI, 0.85-1.90)]; >6 hours: 1.0%/patient-year [adjusted hazard ratio, 1.02 (95% CI, 0.63-1.66)]). SCAF duration did not modify the reduction in stroke or systemic embolism with apixaban (Ptrend=0.1).

Conclusions: In ARTESiA, baseline SCAF frequency and longest episode duration were not associated with risk of stroke or systemic embolism and did not modify the effect of apixaban on reduction of stroke or systemic embolism.

Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01938248.

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来源期刊
Circulation
Circulation 医学-外周血管病
CiteScore
45.70
自引率
2.10%
发文量
1473
审稿时长
2 months
期刊介绍: Circulation is a platform that publishes a diverse range of content related to cardiovascular health and disease. This includes original research manuscripts, review articles, and other contributions spanning observational studies, clinical trials, epidemiology, health services, outcomes studies, and advancements in basic and translational research. The journal serves as a vital resource for professionals and researchers in the field of cardiovascular health, providing a comprehensive platform for disseminating knowledge and fostering advancements in the understanding and management of cardiovascular issues.
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