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Imaging criteria across pivotal randomized controlled trials for late window thrombectomy patient selection.
Menon, Bijoy K; Ospel, Johanna Maria; McTaggart, Ryan A; Nogueira, Raul G; Demchuk, Andrew M; Poppe, Alexandre; Rempel, Jeremy L; Zerna, Charlotte; Joshi, Manish; Almekhlafi, Mohammed A; Field, Thalia S; Dowlatshahi, Dariush; van Adel, Brian Anthony; Sauvageau, Eric; Tarpley, Jason; Moreira, Tiago; Bang, Oh Young; Heck, Don; Psychogios, Marios N; Tymianski, Michael; Hill, Michael D; Goyal, Mayank.
Afiliação
  • Menon BK; Calgary Stroke Program, University of Calgary, Calgary, Alberta, Canada.
  • Ospel JM; Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
  • McTaggart RA; Calgary Stroke Program, University of Calgary, Calgary, Alberta, Canada.
  • Nogueira RG; Department of Neuroradiology, Clinic of Radiology and Nuclear Medicine, University Hospital Basel, Basel, Switzerland.
  • Demchuk AM; Warren Alpert School of Medicine & Brown University, Providence, Rhode Island, USA.
  • Poppe A; Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Rempel JL; Calgary Stroke Program, University of Calgary, Calgary, Alberta, Canada.
  • Zerna C; Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
  • Joshi M; Department of Neurology/ Neurosciences, Universite de Montreal, Montreal, Quebec, Canada.
  • Almekhlafi MA; Department of Radiology, University of Alberta, Edmonton, Alberta, Canada.
  • Field TS; Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
  • Dowlatshahi D; Diagnostic Imaging, University of Calgary, Calgary, Alberta, Canada.
  • van Adel BA; Calgary Stroke Program, University of Calgary, Calgary, Alberta, Canada.
  • Sauvageau E; Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
  • Tarpley J; Neurology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Moreira T; Neurology, University of Ottawa Faculty of Medicine, Ottawa, Ontario, Canada.
  • Bang OY; Clinical Neurological Sciences, London Health Sciences Centre, London, Ontario, Canada.
  • Heck D; Lyerly Neurosurgery, Baptist Hospital, Jacksonville, Florida, USA.
  • Psychogios MN; Vascular Neurology, Providence Saint John's Health Center and The Pacific Neuroscience Institute, Torrance, California, USA.
  • Tymianski M; Neurology, Karolinska University Hospital, Stockholm, Sweden.
  • Hill MD; Department of Neurology, Samsung Medical Center, Seoul, Republic of Korea.
  • Goyal M; Radiology, Forsyth Medical Center, Winston Salem, North Carolina, USA.
J Neurointerv Surg ; 2020 Nov 25.
Article em En | MEDLINE | ID: mdl-33239306
BACKGROUND: The DAWN and DEFUSE-3 trials showed the benefit of endovascular treatment (EVT) in acute ischemic stroke patients presenting beyond 6 hours from last known well (LKW) and selected by perfusion imaging criteria. The ESCAPE NA1-trial selected patients based on non-contrast CT (NCCT) Alberta Stroke Program Early CT Score (ASPECTS) and multiphase CT angiography (CTA) collateral status. This study compares baseline characteristics, workflow, and outcomes in the EVT arms of DAWN and DEFUSE-3 with late-window patients from the EVT-only arm of ESCAPE-NA1. METHODS: Aggregate data on baseline characteristics, workflow, reperfusion quality, final infarct volume, and clinical outcomes (modified Rankin Score [mRS] at 90 days) in subjects enrolled in the DAWN and DEFUSE-3 EVT arms were compared with similar data from the ESCAPE-NA1 control arm (EVT-only arm) presenting beyond 6 hours from LKW using descriptive statistics. RESULTS: Baseline characteristics among late-window patients in the ESCAPE NA1 trial were similar to those in the DAWN and DEFUSE-3 EVT arms. Median time from LKW-to-puncture in subjects enrolled in the ESCAPE NA1 trial was 9 hrs (IQR: 7.5-11 hours) when compared with DAWN (n=107; 12.8 hours, IQR: 10.6-16.7 hours) and DEFUSE-3 (n=92; 11.5 hours, IQR: 9.2-12.8 hours). Median post-treatment infarct-volume was largest in the ESCAPE NA1-patients (47 mL [IQR: 19-146] vs median 8 mL [IQR: 0-48] in the DAWN group and 35 mL [IQR: 18-82] in DEFUSE-3), while % mRS 0-2 at 90 days were similar across the three trials (ESCAPE NA1: 50/111 [45%], DAWN: 52/107 [49%], DEFUSE-3: 41/92 [45%]). CONCLUSION: Patients enrolled beyond 6 hours from LKW in the ESCAPE-NA1 trial based on NCCT-ASPECTS and mCTA had similar clinical outcomes when compared with patients selected by perfusion imaging in the DAWN and DEFUSE-3 trials.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article