作者
Frédéric Clarençon,Isabelle Durand‐Zaleski,Kévin Premat,Amandine Baptiste,Emmanuel Chabert,Anna Ferrier,Marc‐Antoine Labeyrie,Peggy Reiner,Laurent Spelle,Christian Denier,Titien Tuilier,Hassan Hosseini,Christine Rodriguez-Régent,Guillaume Turc,Cédric Fauché,M Lamy,Bertrand Lapergue,Arturo Consoli,Charlotte Barbier,Marion Boulanger,Nicolas Bricout,Hilde Hénon,Benjamin Gory,Sébastien Richard,Aymeric Rouchaud,Francisco Macian Montoro,Omer Eker,Tae‐Hee Cho,Laurent Pierot,Solène Moulin,Jean‐Christophe Gentric,Serge Timsit,Jean Darcourt,Jean‐François Albucher,Kévin Janot,Mariam Annan,Fernando Pico,Vincent Costalat,Caroline Arquizan,Gaultier Marnat,Igor Sibon,Raoul Pop,Valérie Wolff,Eimad Shotar,Stéphanie Lenck,Nader Sourour,Anne Radenne,Sonia Alamowitch,Agnès Dechartres
摘要
Rationale: Mechanical thrombectomy (MT) associated with the best medical treatment (BMT) has recently shown efficacy for the management of acute ischemic stroke (AIS) secondary to a large vessel occlusion. However, evidence is lacking regarding the benefit of MT for more distal occlusions. Aim: To evaluate the efficacy in terms of good clinical outcome at 3 months of MT associated with the BMT over the BMT alone in AIS related to a distal occlusion. Methods: The DISCOUNT trial is a multicenter open-label randomized controlled trial involving French University hospitals. Adult patients (⩾18 years) with an AIS involving the anterior or posterior circulation secondary to a distal vessel occlusion within 6 h of symptom onset or within 24 h if no hyperintense signal on fluid attenuation inversion recovery acquisition will be randomized 1:1 to receive either MT associated with the BMT (experimental group) or BMT alone (control group). The number of patients to be included is 488. Study outcomes: The primary outcome is the rate of good clinical outcome at 3 months defined as a modified Rankin scale (mRS) ⩽2 and evaluated by an independent assessor blinded to the intervention arm. Secondary outcomes include recanalization of the occluded vessel within 48 h, angiographic reperfusion in the experimental group, 3-month excellent clinical outcome (mRS ⩽ 1), all adverse events, and death. A cost utility analysis will estimate the incremental cost per quality-adjusted life year (QALY) gained. Discussion: If positive, this study will open new insights in the management of AISs. Trial registration: ClinicalTrials.gov: NCT05030142 registered on 1 September 2021.