School of Medicine and Public Health, College of Health, Medicine and Wellbeing, The University of Newcastle, Callaghan, New South Wales, Australia.
Hunter Medical Research Institute, New Lambton Heights, New South Wales, Australia.
BMJ Open. 2022 Feb 11;12(2):e055461. doi: 10.1136/bmjopen-2021-055461.
Stroke reperfusion therapies, comprising intravenous thrombolysis (IVT) and/or endovascular thrombectomy (EVT), are best practice treatments for eligible acute ischemic stroke patients. In Australia, EVT is provided at few, mainly metropolitan, comprehensive stroke centres (CSC). There are significant challenges for Australia's rural and remote populations in accessing EVT, but improved access can be facilitated by a 'drip and ship' approach. TACTICS (Trial of Advanced CT Imaging and Combined Education Support for Drip and Ship) aims to test whether a multicomponent, multidisciplinary implementation intervention can increase the proportion of stroke patients receiving EVT.
This is a non-randomised controlled, stepped wedge trial involving six clusters across three Australian states. Each cluster comprises one CSC hub and a minimum of three primary stroke centre (PSC) spokes. Hospitals will work in a hub and spoke model of care with access to a multislice CT scanner and CT perfusion image processing software (MIStar, Apollo Medical Imaging). The intervention, underpinned by behavioural theory and technical assistance, will be allocated sequentially, and clusters will move from the preintervention (control) period to the postintervention period.
Proportion of all stroke patients receiving EVT, accounting for clustering.
Proportion of patients receiving IVT at PSCs, proportion of treated patients (IVT and/or EVT) with good (modified Rankin Scale (mRS) score 0-2) or poor (mRS score 5-6) functional outcomes and European Quality of Life Scale scores 3 months postintervention, proportion of EVT-treated patients with symptomatic haemorrhage, and proportion of reperfusion therapy-treated patients with good versus poor outcome who presented with large vessel occlusion at spokes.
Ethical approval has been obtained from the Hunter New England Human Research Ethics Committee (18/09/19/4.13, HREC/18/HNE/241, 2019/ETH01238). Trial results will be disseminated widely through published manuscripts, conference presentations and at national and international platforms regardless of whether the trial was positive or neutral.
ACTRN12619000750189; UTNU1111-1230-4161.
急性缺血性脑卒中患者,在符合条件的情况下,采用静脉溶栓(IVT)和/或血管内取栓(EVT)的再灌注治疗,是最佳治疗方法。在澳大利亚,EVT 主要在少数大都市的综合卒中中心(CSC)提供。对于澳大利亚农村和偏远地区的患者来说,接受 EVT 治疗存在重大挑战,但通过“滴注和转运”方法可以改善这种情况。TACTICS(滴注和转运的高级 CT 成像和联合教育支持试验)旨在测试多组分、多学科实施干预措施是否可以增加接受 EVT 治疗的卒中患者比例。
这是一项非随机对照、逐步楔形试验,涉及澳大利亚三个州的六个集群。每个集群包括一个 CSC 中心和至少三个初级卒中中心(PSC)的辐条。医院将以多部位 CT 扫描仪和 CT 灌注图像处理软件(MIStar、阿波罗医疗成像)为依托,采用“中心-辐条”模式开展工作。该干预措施以行为理论和技术援助为基础,将按顺序分配,集群将从干预前(对照)期过渡到干预后期。
所有接受 EVT 治疗的卒中患者比例,考虑到聚类效应。
PSC 接受 IVT 治疗的患者比例、接受治疗(IVT 和/或 EVT)的患者中功能良好(改良 Rankin 量表(mRS)评分 0-2)或不良(mRS 评分 5-6)的比例以及欧洲生活质量量表评分 3 个月后的比例、接受 EVT 治疗的患者中症状性出血的比例以及在辐条处出现大血管闭塞的接受再灌注治疗的患者中,预后良好(mRS 评分 0-2)与不良(mRS 评分 5-6)的比例。
亨特新英格兰人类研究伦理委员会已批准该试验(18/09/19/4.13、HREC/18/HNE/241、2019/ETH01238)。无论试验结果是阳性还是中性,研究结果都将通过发表的论文、会议演讲以及国家和国际平台广泛传播。
ACTRN12619000750189;UTNU1111-1230-4161。