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Improving reperfusion time within the ESCAPE Endovascular Clinical Trial

  • Noreen Kamal*
  • , Eric E. Smith
  • , Bijoy K. Menon
  • , Muneer Eesa
  • , Karla J. Ryckborst
  • , Alexandre Y. Poppe
  • , Daniel Roy
  • , John Thornton
  • , David Williams
  • , Leanne K. Casaubon
  • , Frank L. Silver
  • , Kenneth Butcher
  • , Ashfaq Shuaib
  • , Jeremy L. Rempel
  • , Tudor G. Jovin
  • , Biggya L. Sapkota
  • , Andrew M. Demchuk
  • , Mayank Goyal
  • , Michael D. Hill
  • *Autor correspondiente de este trabajo
  • University of Calgary
  • Foothills Medical Centre
  • Centre Hospitalier de L'Universite de Montreal
  • Royal College of Surgeons in Ireland
  • University Health Network and Mount Sinai Hospital
  • Toronto Western Hospital University of Toronto
  • University of Alberta
  • University of Pittsburgh
  • Providence Health & Services

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

8 Citas (Scopus)

Resumen

Introduction: Endovascular treatment of acute ischemic stroke is more effective when performed quickly. In this report, we describe quality interventions to ensure fast endovascular treatment times in the ESCAPE (Endovascular Treatment for Small Core and Anterior circulation Proximal Occlusion with Emphasis on Minimizing CT to Recanalization Times) trial. Methods: An “audit and feedback” intervention using webinar and letter was used to improve treatment time over the course of the trial. The time metrics were computed tomography-to-groin-puncture (target < 60 min) and computed tomography-to-first-reperfusion (target < 90 min). Each site was provided with their data for computed tomography-to-groin-puncture and computed tomography-to-first-reperfusion for all their patients that were randomized to the treatment arm, and their median time was compared to the overall median times of all sites in the trial. We assessed for changes in treatment time over the course of the trial. Results: There were 165 patients enrolled into the endovascular arm from 22 sites. The computed tomography-to-groin-puncture time dropped from 57 to 47 min (p = 0.14) while computed tomography-to-reperfusion time dropped from 89 to 81 min (p = 0.48). Over the course of the trial, the absolute treatment benefit increased by 7.8% (p < 0.001). Conclusions: An “audit and feedback” intervention throughout the conduct of the ESCAPE trial was a feasible way to ensure fast treatment times. Quality improvement processes should continue as standard practice beyond the trial to encourage good patient selection and the best clinical outcomes.

Idioma originalInglés
Páginas (desde-hasta)64-69
Número de páginas6
PublicaciónEuropean Stroke Journal
Volumen2
N.º1
DOI
EstadoPublicada - 1 mar 2017
Publicado de forma externa

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