The 6-months follow-up of the TREAT-CAD trial: Aspirin versus anticoagulation for stroke prevention in patients with cervical artery dissection.

IF 5.8 3区 医学 Q1 CLINICAL NEUROLOGY
Stefan T Engelter, Lukas S Enz, Flavia Ravanelli, Josefin E Kaufmann, Henrik Gensicke, Sabine Schaedelin, Andreas R Luft, Christoph Globas, Barbara Goeggel-Simonetti, Urs Fischer, Davide Strambo, Georg Kägi, Krassen Nedeltchev, Timo Kahles, Lars Kellert, Sverre Rosenbaum, Regina von Rennenberg, Alex Brehm, David Seiffge, Susanne Renaud, Tobias Brandt, Hakan Sarikaya, Annaelle Zietz, Johannes Wischmann, Alexandros A Polymeris, Sandro Fischer, Leo H Bonati, Gian Marco De Marchis, Nils Peters, Christian H Nolte, Hanne Christensen, Susanne Wegener, Marios-Nikos Psychogios, Marcel Arnold, Philippe Lyrer, Christopher Traenka
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引用次数: 0

Abstract

Introduction: Cervical artery dissection is a major cause of stroke in the young. The optimal choice and duration of antithrombotic treatment for stroke prevention are debated, particularly beyond 3 months after symptom onset.

Patients and methods: TREAT-CAD (TREATment of Cervical Artery Dissection) was a randomized controlled trial with blinded outcome assessment comparing non-inferiority of aspirin to anticoagulation (Vitamin-K-antagonists) in participants with symptomatic, Magnetic-Resonance-(MR)-imaging-verified cervical artery dissection. TREAT-CAD could not establish non-inferiority of aspirin to anticoagulation at 3 months. Thereafter participants could continue antithrombotic medication and obtained a standardized assessment of clinical and MR-Imaging outcomes between 3 and 6 months. As crossover to the other treatment arm was possible, we performed an as-treated analysis as main analysis. The main outcomes were new clinical (ischemic stroke, intracranial/major extracranial bleeding, or death) and new MR-Imaging outcomes (ischemic or hemorrhagic brain lesions).

Results: Among the 122 participants in the as-treated analysis, 3/93 (3.2%) aspirin-treated participants had new clinical (n = 1) and MRI-outcomes (n = 2) between 3 and 6 months while 1/29 (3.4%) anticoagulated participants had an MRI-outcome (n = 1). All outcome events were hemorrhagic while ischemic events were absent. No deaths occurred. This yields an absolute difference of 0.2% (95% CI -8.0% to 7.5%, p = 1.0).

Discussion and conclusion: During the extended follow-up period of a controlled randomized trial comparing aspirin to anticoagulation in cervical artery dissection, outcomes between 3 and 6 months after randomization occurred rarely, similarly often in both groups and were exclusively hemorrhagic events. Thus, studies balancing benefits versus harms of antithrombotic treatment beyond 3 months are warranted. Registration: ClinicalTrials.gov: NCT02046460. https://clinicaltrials.gov/ct2/show/NCT02046460.

治疗- cad试验的6个月随访:阿司匹林与抗凝预防颈动脉夹层患者卒中
颈动脉夹层是年轻人中风的主要原因。抗血栓治疗预防中风的最佳选择和持续时间存在争议,特别是在症状发作后3个月以上。患者和方法:TREATment - cad(治疗颈动脉夹层)是一项随机对照试验,对有症状的、磁共振(MR)成像证实的颈动脉夹层患者进行阿司匹林与抗凝剂(维生素k拮抗剂)的非劣效性评估。治疗- cad在3个月时不能确定阿司匹林对抗凝的非劣效性。此后,参与者可以继续抗血栓药物治疗,并在3至6个月内获得临床和磁共振成像结果的标准化评估。由于可能与另一个治疗组交叉,我们进行了治疗分析作为主要分析。主要结局是新的临床结果(缺血性卒中、颅内/大颅外出血或死亡)和新的磁共振成像结果(缺血性或出血性脑病变)。结果:在122名接受治疗的患者中,3/93(3.2%)阿司匹林治疗的患者在3 - 6个月内有新的临床(n = 1)和mri结果(n = 2),而1/29(3.4%)抗凝治疗的患者有mri结果(n = 1)。所有结局事件均为出血性事件,而缺血性事件无发生。没有人员死亡。这产生0.2%的绝对差异(95% CI -8.0%至7.5%,p = 1.0)。讨论和结论:在一项比较阿司匹林与抗凝治疗颈动脉夹层的随机对照试验的延长随访期间,随机分组后3至6个月的结果很少发生,两组的结果相似,并且都是出血事件。因此,平衡3个月以上抗血栓治疗的利弊的研究是有必要的。注册:ClinicalTrials.gov: NCT02046460。https://clinicaltrials.gov/ct2/show/NCT02046460。
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
CiteScore
7.50
自引率
6.60%
发文量
102
期刊介绍: Launched in 2016 the European Stroke Journal (ESJ) is the official journal of the European Stroke Organisation (ESO), a professional non-profit organization with over 1,400 individual members, and affiliations to numerous related national and international societies. ESJ covers clinical stroke research from all fields, including clinical trials, epidemiology, primary and secondary prevention, diagnosis, acute and post-acute management, guidelines, translation of experimental findings into clinical practice, rehabilitation, organisation of stroke care, and societal impact. It is open to authors from all relevant medical and health professions. Article types include review articles, original research, protocols, guidelines, editorials and letters to the Editor. Through ESJ, authors and researchers have gained a new platform for the rapid and professional publication of peer reviewed scientific material of the highest standards; publication in ESJ is highly competitive. The journal and its editorial team has developed excellent cooperation with sister organisations such as the World Stroke Organisation and the International Journal of Stroke, and the American Heart Organization/American Stroke Association and the journal Stroke. ESJ is fully peer-reviewed and is a member of the Committee on Publication Ethics (COPE). Issues are published 4 times a year (March, June, September and December) and articles are published OnlineFirst prior to issue publication.
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