Efficacy and safety of early anticoagulation after endovascular treatment in patients with atrial fibrillation.

IF 4.4 1区 医学 Q1 CLINICAL NEUROLOGY
Stroke and Vascular Neurology Pub Date : 2023-10-01 Epub Date: 2023-03-27 DOI:10.1136/svn-2022-002082
Yaning Xu, Chengchun Liu, Wei Li, Ximing Nie, Shuhan Huang, Xiaoshu Li, Ya Wu, Wang-Sheng Jin, Jiaojin Jiang, Jun Dong, Yi Yang, Zhiqiang Sun, Wenjun Han, Yanjiang Wang, Liping Liu, Meng Zhang
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引用次数: 0

Abstract

Background: The timing for initiating anticoagulant therapy in acute ischaemic stroke (AIS) patients with atrial fibrillation who recanalised after endovascular treatment (EVT) is unclear. The objective of this study was to evaluate the effect of early anticoagulation after successful recanalisation in AIS patients with atrial fibrillation.

Methods: Patients with anterior circulation large vessel occlusion and atrial fibrillation who were successfully recanalised by EVT within 24 hours after stroke in the Registration Study for Critical Care of Acute Ischemic Stroke after Recanalization registry were analysed. Early anticoagulation was defined as the initiation of unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH) within 72 hours after EVT. Ultra-early anticoagulation was defined if it was initiated within 24 hours. The primary efficacy outcome was the score on the modified Rankin Scale (mRS) at day 90, and the primary safety outcome was symptomatic intracranial haemorrhage within 90 days.

Results: Overall, 257 patients were enrolled, of whom 141 (54.9%) initiated anticoagulation within 72 hours after EVT, including 111 within 24 hours. A significant shift towards better mRS scores at day 90 was associated with early anticoagulation (adjusted common OR 2.08 (95% CI 1.27 to 3.41)). Symptomatic intracranial haemorrhage was comparable between patients treated with early and routine anticoagulation (adjusted OR 0.20 (95% CI 0.02 to 2.18)). Comparison of different early anticoagulation regimens showed that ultra-early anticoagulation was more significantly associated with favourable functional outcomes (adjusted common OR 2.03 (95% CI 1.20 to 3.44)) and reduced the incidence of asymptomatic intracranial haemorrhage (OR 0.37 (95% CI 0.14 to 0.94)).

Conclusions: In AIS patients with atrial fibrillation, early anticoagulation with UFH or LMWH after successful recanalisation is associated with favourable functional outcomes without increasing the risk of symptomatic intracranial haemorrhages.

Trial registration number: ChiCTR1900022154.

心房颤动患者血管内治疗后早期抗凝的有效性和安全性。
背景:血管内治疗(EVT)后再通的急性缺血性中风(AIS)心房颤动患者开始抗凝治疗的时间尚不清楚。本研究的目的是评估房颤AIS患者成功再通后早期抗凝的效果。方法:对在急性缺血性卒中危重症登记研究中,在卒中后24小时内通过EVT成功再通的前循环大血管闭塞和心房颤动患者进行分析。早期抗凝定义为EVT后72小时内开始使用普通肝素(UFH)或低分子肝素(LMWH)。如果在24小时内开始,则定义为超早期抗凝。主要疗效结果为第90天改良兰金量表(mRS)评分,主要安全性结果为90天内出现症状性颅内出血。结果:总共有257名患者入选,其中141人(54.9%)在EVT后72小时内开始抗凝,其中111人在24小时内开始。在第90天,mRS评分向更好方向的显著转变与早期抗凝有关(调整后的普通OR 2.08(95%CI 1.27至3.41))。早期和常规抗凝治疗的患者之间症状性颅内出血具有可比性(调整后OR 0.20(95%CI 0.02至2.18))。不同早期抗凝方案的比较表明与良好的功能结果更显著相关(调整后的普通OR 2.03(95%CI 1.20至3.44)),并降低无症状颅内出血的发生率(OR 0.37(95%CI 0.14至0.94)),成功再通后早期使用UFH或LMWH抗凝与良好的功能结果相关,而不会增加症状性颅内出血的风险。试验注册号:ChiCTR1900022154。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Stroke and Vascular Neurology
Stroke and Vascular Neurology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
11.20
自引率
1.70%
发文量
63
审稿时长
15 weeks
期刊介绍: Stroke and Vascular Neurology (SVN) is the official journal of the Chinese Stroke Association. Supported by a team of renowned Editors, and fully Open Access, the journal encourages debate on controversial techniques, issues on health policy and social medicine.
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