Callaly Edward Patrick, Tan Peter Shuangyue, Schembri Emily, Borosak Marija, Dewey Helen, Choi Philip
Department of Neurosciences, Eastern Health, Box Hill, Victoria, Australia
Department of Neurosciences, Alfred Health, Melbourne, Victoria, Australia.
BMJ Open. 2025 Jun 27;15(6):e102092. doi: 10.1136/bmjopen-2025-102092.
Direct oral anticoagulants (DOACs) are preferred over vitamin K antagonists for stroke prophylaxis in non-valvular atrial fibrillation. Yet, DOAC use is regarded as a contraindication for intravenous thrombolysis in acute ischaemic stroke. The stratification of patients into 'on-therapy' and 'off-therapy' categories based on their plasma DOAC concentrations is particularly crucial in the acute phase of stroke when decisions for thrombolysis or anticoagulation reversal are time-sensitive. The novel point-of-care DOAC dipstick assay (DOASENSE) rapidly assesses urine for clinically significant DOAC levels, potentially broadening eligibility for thrombolysis or targeted reversal therapy. This multicentre prospective observational registry study aims to evaluate the accuracy and clinical utility of DOAC dipstick testing compared with plasma DOAC assays in acute stroke management across regional Australian hospitals.
This multicentre, prospective, observational study will enrol participants presenting to hospitals across Victoria and Tasmania with acute ischaemic stroke or intracerebral haemorrhage with DOAC ingestion within 48 hours of presentation. Plasma DOAC concentrations measured by chromogenic assays will be compared with rapid urine dipstick results from DOASENSE testing. There is a target sample size of 146 participants. The primary outcomes are as follows: (1) proportion of ischaemic stroke participants with off-therapy plasma DOAC levels and (2) eligibility for reperfusion therapy based on DOASENSE and plasma DOAC concentrations. Secondary outcomes are follows: (1) ischaemic stroke aetiology for participants with on-therapy vs off-therapy DOAC levels; (2) proportion of participants meeting criteria for pharmacological DOAC reversal based on DOASENSE outcomes; (3) incidence of false-negative and false positive DOASENSE results in clinically significant DOAC plasma concentrations at a threshold of ≥30 ng/mL and (4) an exploratory analysis of any false negative DOASENSE assays to identify potential contributing factors.
Ethics approval has been granted by the Eastern Health Human Research Ethics Committee (reference number: 99628). Dissemination of findings will occur through peer-reviewed publications and academic conferences.
在非瓣膜性心房颤动的卒中预防中,直接口服抗凝剂(DOACs)比维生素K拮抗剂更受青睐。然而,DOAC的使用被视为急性缺血性卒中静脉溶栓的禁忌症。在卒中急性期,当溶栓或抗凝逆转的决策对时间敏感时,根据患者血浆DOAC浓度将其分为“治疗中”和“未治疗”类别尤为关键。新型即时检验DOAC试纸检测法(DOASENSE)可快速评估尿液中具有临床意义的DOAC水平,可能会扩大溶栓或靶向逆转治疗的适用范围。这项多中心前瞻性观察性注册研究旨在评估在澳大利亚各地区医院的急性卒中管理中,与血浆DOAC检测相比,DOAC试纸检测的准确性和临床实用性。
这项多中心、前瞻性、观察性研究将纳入在维多利亚州和塔斯马尼亚州各医院就诊的急性缺血性卒中或脑出血患者,且在就诊后48小时内服用过DOAC。将通过显色测定法测量的血浆DOAC浓度与DOASENSE检测的快速尿液试纸结果进行比较。目标样本量为146名参与者。主要结局如下:(1)缺血性卒中参与者血浆DOAC水平处于未治疗状态的比例;(2)根据DOASENSE和血浆DOAC浓度确定的再灌注治疗适用性。次要结局如下:(1)治疗中与未治疗的DOAC水平的参与者的缺血性卒中病因;(2)根据DOASENSE结果符合药物性DOAC逆转标准的参与者比例;(3)在血浆DOAC浓度≥30 ng/mL阈值时,DOASENSE结果在具有临床意义的DOAC血浆浓度中的假阴性和假阳性发生率;(4)对任何DOASENSE检测假阴性进行探索性分析,以确定潜在的影响因素。
已获得东部健康人类研究伦理委员会的伦理批准(参考编号:99628)。研究结果将通过同行评审的出版物和学术会议进行传播。