Early versus late start of direct oral anticoagulants after acute ischaemic stroke linked to atrial fibrillation: an observational study and individual patient data pooled analysis

医学 心房颤动 内科学 冲程(发动机) 观察研究 队列研究 缺血性中风 比例危险模型 子群分析 心脏病学 危险系数 队列 儿科 倾向得分匹配 置信区间 荟萃分析 机械工程 工程类
作者
Gian Marco De Marchis,David Seiffge,Sabine Schaedelin,Duncan Wilson,Valeria Caso,Monica Acciarresi,Georgios Tsivgoulis,Masatoshi Koga,Sohei Yoshimura,Ḱazunori Toyoda,Manuel Cappellari,Bruno Bonetti,Kosmas Macha,Bernd Kallmünzer,Carlo W. Cereda,Philippe Lyrer,Leo H. Bonati,Maurizio Paciaroni,Stefan T. Engelter,David J. Werring
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:93 (2): 119-125 被引量:36
标识
DOI:10.1136/jnnp-2021-327236
摘要

Objective The optimal timing to start direct oral anticoagulants (DOACs) after an acute ischaemic stroke (AIS) related to atrial fibrillation (AF) remains unclear. We aimed to compare early (≤5 days of AIS) versus late (>5 days of AIS) DOAC-start. Methods This is an individual patient data pooled analysis of eight prospective European and Japanese cohort studies. We included patients with AIS related to non-valvular AF where a DOAC was started within 30 days. Primary endpoints were 30-day rates of recurrent AIS and ICH. Results A total of 2550 patients were included. DOACs were started early in 1362 (53%) patients, late in 1188 (47%). During 212 patient-years, 37 patients had a recurrent AIS (1.5%), 16 (43%) before a DOAC was started; 6 patients (0.2%) had an ICH, all after DOAC-start. In the early DOAC-start group, 23 patients (1.7%) suffered from a recurrent AIS, while 2 patients (0.1%) had an ICH. In the late DOAC-start group, 14 patients (1.2%) suffered from a recurrent AIS; 4 patients (0.3%) suffered from ICH. In the propensity score-adjusted comparison of late versus early DOAC-start groups, there was no statistically significant difference in the hazard of recurrent AIS (aHR=1.2, 95% CI 0.5 to 2.9, p=0.69), ICH (aHR=6.0, 95% CI 0.6 to 56.3, p=0.12) or any stroke. Conclusions Our results do not corroborate concerns that an early DOAC-start might excessively increase the risk of ICH. The sevenfold higher risk of recurrent AIS than ICH suggests that an early DOAC-start might be reasonable, supporting enrolment into randomised trials comparing an early versus late DOAC-start.
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