Endovascular treatment vs. best medical management for late window ischemic stroke patients with large vessel occlusion

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Charlotte Zerna - , University of Calgary , Municipal Hospital Dresden (Author)
  • Johann Ospel - , University of Calgary (Author)
  • Emma Harrison - , Princess Alexandra Hospital Brisbane (Author)
  • Timothy J Kleinig - , Royal Adelaide Hospital (Author)
  • Volker Puetz - , Department of Neurology (Author)
  • Daniel Po Kaiser - , Institute and Polyclinic of Diagnostic and Interventional Neuroradiology, University Hospital Carl Gustav Carus Dresden (Author)
  • Brett Graham - , Saskatchewan Health Authority (Author)
  • Amy Yx Yu - , Sunnybrook Health Science Centre (Author)
  • Brian van Adel - , Hamilton Health Sciences (Author)
  • Jai J Shankar - , University of Manitoba (Author)
  • Ryan A McTaggart - , Unity Health Toronto (Author)
  • Vitor Pereira - , Unity Health Toronto (Author)
  • Donald F Frei - , Colorado Neurological Institute (Author)
  • Mayank Goyal - , University of Calgary (Author)
  • Michael D Hill - , University of Calgary (Author)

Abstract

BackgroundTo compare the benefit of endovascular treatment(EVT) in acute ischemic stroke(AIS) patients with large vessel occlusion(LVO) presenting > 6 h from last known well outside a clinical trial setting to best medical management and to EVT in a randomized trial setting.MethodsData from a retrospective multicenter cohort study (ESCAPE-LATE) of AIS-LVO patients treated with EVT beyond 6 hours from last known well at former ESCAPE trial sites were pooled with historical data from ESCAPE trial late time window patients. Unadjusted and adjusted 90-day modified Rankin Scale (mRS) score was compared between ESCAPE-LATE patients, ESCAPE late time window EVT arm and control arm patients.ResultsA total of 249 patients were included in the analysis: 200 ESCAPE-LATE patients (for 141 of whom 90-day clinical outcomes were available) and 49 ESCAPE patients, for all of whom clinical outcome data were available (control arm: 20 and EVT arm: 29). Good clinical outcome (mRS 0-2 at 90 days) was nominally, albeit not significantly, lower in patients not treated with EVT (5/19[26.3%]) as compared to ESCAPE EVT arm patients (13/29[44.8%] and ESCAPE-LATE patients (66/141[46.8%]). After adjustment, a graded mRS pattern was seen, whereby patients treated with EVT did better as compared to non-treated patients, and those who underwent EVT in the ESCAPE trial had better mRS as compared to those included in ESCAPE-LATE who underwent EVT in clinical routine.ConclusionPatients presenting beyond 6 hours from last known well who are treated with EVT in a real-world setting show comparable benefit to patients treated in a clinical trial setting.

Details

Original languageEnglish
Journal Interventional neuroradiology : INR : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences
Publication statusE-pub ahead of print - 10 Nov 2025
Peer-reviewedYes

External IDs

PubMedCentral PMC12602283
ORCID /0000-0001-5258-0025/work/197321503
Scopus 105021874037

Keywords