Direct transfer to angiosuite for patients with severe acute stroke treated with thrombectomy: the multicentre randomised controlled DIRECT ANGIO trial protocol

Author:

Riou-Comte Nolwenn,Zhu François,Cherifi Aboubaker,Richard SébastienORCID,Nace Lionel,Audibert Gérard,Achit Hamza,Costalat Vincent,Arquizan Caroline,Beaufils Olivier,Consoli Arturo,Lapergue Bertrand,Loeb Thomas,Rouchaud Aymeric,Macian Francisco,Cailloce Dominique,Biondi Alessandra,Moulin Thierry,Desmettre Thibaut,Marnat Gaultier,Sibon Igor,Combes Xavier,Lebedinsky Ariel Pablo,Vuillemet Francis,Kempf Nicolas,Pierot Laurent,Moulin Solene,Lemmel Philippe,Mazighi Mikael,Blanc Raphael,Sabben Candice,Schluck Eric,Bracard Serge,Anxionnat René,Guillemin Francis,Hossu Gabriela,Gory BenjaminORCID

Abstract

IntroductionMechanical thrombectomy (MT) increases functional independence in patients with acute ischaemic stroke with anterior circulation large vessel occlusion (LVO), and the probability to achieve functional independence decreases by 20% for each 1-hour delay to reperfusion. Therefore, we aim to investigate whether direct angiosuite transfer (DAT) is superior to standard imaging/emergency department-based management in achieving 90-day functional independence in patients presenting with an acute severe neurological deficit likely due to LVO and requiring emergent treatment with MT.Methods and analysisDIRECT ANGIO (Effect of DIRECT transfer to ANGIOsuite on functional outcome in patient with severe acute stroke treated with thrombectomy: the randomised DIRECT ANGIO Trial) trial is an investigator-initiated, multicentre, prospective, randomised, open-label, blinded endpoint (PROBE) study. Eligibility requires a patient ≤75 years, pre-stroke modified Rankin Scale (mRS) 0–2, presenting an acute severe neurological deficit and admitted within 5 hours of symptoms onset in an endovascular-capable centre. A total of 208 patients are randomly allocated in a 1:1 ratio to DAT or standard management. The primary outcome is the rate of patients achieving a functional independence, assessed as mRS 0–2 at 90 days. Secondary endpoints include patients presenting confirmed LVO, patients eligible to intravenous thrombolysis alone, patients with intracerebral haemorrhage and stroke-mimics, intrahospital time metrics, early neurological improvement (reduction in National Institutes of Health Stroke Scale by ≥8 points or reaching 0–1 at 24 hours) and mRS overall distribution at 90 days and 12 months. Safety outcomes are death and intracerebral haemorrhage transformation. Medico-economics analyses include health-related quality of life and cost utility assessment.Ethics and disseminationThe DIRECT ANGIO trial was approved by the ethics committee of Ile de France 1. Study began in April 2020. Results will be published in an international peer-reviewed medical journal.Trial registration numberNCT03969511.

Funder

French Ministry of Health (Programme Hospitalier de Recherche Clinique Inter Régional

Publisher

BMJ

Subject

General Medicine

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