Mechanical thrombectomy for large vessel occlusion between 6 and 24 h: outcome comparison of DEFUSE-3/DAWN eligible versus non-eligible patients.


Journal

International journal of stroke : official journal of the International Stroke Society
ISSN: 1747-4949
Titre abrégé: Int J Stroke
Pays: United States
ID NLM: 101274068

Informations de publication

Date de publication:
07 2023
Historique:
medline: 29 6 2023
pubmed: 12 11 2022
entrez: 11 11 2022
Statut: ppublish

Résumé

The DEFUSE-3 and DAWN trials showed that mechanical thrombectomy (MT) improves the outcome of selected patients with anterior circulation large vessel occlusions (LVO) up to 24 h after stroke onset. However, it is unknown whether only those patients fulfilling the trial inclusion criteria benefit, or whether benefit is seen in a broader range of patients presenting between 6 and 24 h. We determined whether fulfilling the DEFUSE-3 and DAWN selection criteria affects outcomes in MT patients in clinical practice. We reviewed adult patients with LVO treated with MT between 6 and 24 h after stroke onset at five Swiss stroke centers between 2014 and 2021. We compared two groups: (1) patients who satisfied neither DEFUSE-3 nor DAWN criteria (NDND) and (2) those who satisfied DEFUSE-3 or DAWN criteria (DOD). We used logistic regression to examine the impact of trial eligibility on two safety outcomes (symptomatic intracranial hemorrhage [sICH] and all-cause mortality at 3 months) and two efficacy outcomes (modified Rankin Score [mRS] shift toward lower categories and mRS of 0-2 at 3 months). Of 174 patients who received MT, 102 (59%) belonged to the NDND group. Rates of sICH were similar between the NDND group and the DOD group (3% vs. 4%, p  Among adult patients with LVO treated with MT between 6 and 24 h, safety and efficacy outcomes were similar between DEFUSE-3/DAWN eligible and ineligible patients. Our data provide a compelling rationale for randomized trials with broader inclusion criteria for MT.

Sections du résumé

BACKGROUND
The DEFUSE-3 and DAWN trials showed that mechanical thrombectomy (MT) improves the outcome of selected patients with anterior circulation large vessel occlusions (LVO) up to 24 h after stroke onset. However, it is unknown whether only those patients fulfilling the trial inclusion criteria benefit, or whether benefit is seen in a broader range of patients presenting between 6 and 24 h.
AIMS
We determined whether fulfilling the DEFUSE-3 and DAWN selection criteria affects outcomes in MT patients in clinical practice.
METHODS
We reviewed adult patients with LVO treated with MT between 6 and 24 h after stroke onset at five Swiss stroke centers between 2014 and 2021. We compared two groups: (1) patients who satisfied neither DEFUSE-3 nor DAWN criteria (NDND) and (2) those who satisfied DEFUSE-3 or DAWN criteria (DOD). We used logistic regression to examine the impact of trial eligibility on two safety outcomes (symptomatic intracranial hemorrhage [sICH] and all-cause mortality at 3 months) and two efficacy outcomes (modified Rankin Score [mRS] shift toward lower categories and mRS of 0-2 at 3 months).
RESULTS
Of 174 patients who received MT, 102 (59%) belonged to the NDND group. Rates of sICH were similar between the NDND group and the DOD group (3% vs. 4%, p 
CONCLUSION
Among adult patients with LVO treated with MT between 6 and 24 h, safety and efficacy outcomes were similar between DEFUSE-3/DAWN eligible and ineligible patients. Our data provide a compelling rationale for randomized trials with broader inclusion criteria for MT.

Identifiants

pubmed: 36367319
doi: 10.1177/17474930221140793
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

697-703

Auteurs

Tolga D Dittrich (TD)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Peter B Sporns (PB)

Department of Neuroradiology, University Hospital Basel, Basel, Switzerland.
Department of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Lilian F Kriemler (LF)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.
Clinic for Internal Medicine, Cantonal Hospital Schaffhausen, Schaffhausen, Switzerland.

Salome Rudin (S)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Anh Nguyen (A)

Department of Neuroradiology, University Hospital Basel, Basel, Switzerland.

Annaelle Zietz (A)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Alexandros A Polymeris (AA)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Christopher Tränka (C)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Sebastian Thilemann (S)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Benjamin Wagner (B)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Valerian L Altersberger (VL)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Ines Piot (I)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Filip Barinka (F)

Department of Neurology and Stroke Center, Hirslanden Hospital Zurich, Zurich, Switzerland.

Martin Hänsel (M)

Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.

Henrik Gensicke (H)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.
Neurology and Neurorehabilitation, University Department of Geriatric Medicine Felix Platter, Basel, Switzerland.

Stefan T Engelter (ST)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.
Neurology and Neurorehabilitation, University Department of Geriatric Medicine Felix Platter, Basel, Switzerland.

Philippe A Lyrer (PA)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Raoul Sutter (R)

Department of Intensive Care Medicine, University Hospital Basel and University of Basel, Basel, Switzerland.

Christian H Nickel (CH)

Emergency Department, University Hospital Basel and University of Basel, Basel, Switzerland.

Mira Katan (M)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.
Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.

Nils Peters (N)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.
Department of Neurology and Stroke Center, Hirslanden Hospital Zurich, Zurich, Switzerland.

Lars Michels (L)

Department of Neuroradiology, University Hospital Zurich, Zurich, Switzerland.
Neuroscience Center Zurich, University of Zurich and Swiss Federal Institute of Technology Zurich, Zurich, Switzerland.

Zsolt Kulcsár (Z)

Department of Neuroradiology, University Hospital Zurich, Zurich, Switzerland.

Grzegorz M Karwacki (GM)

Department of Radiology and Nuclear Medicine, Cantonal Hospital of Lucerne, Lucerne, Switzerland.

Marco Pileggi (M)

Department of Neuroradiology, EOC Neurocenter of Southern Switzerland, Lugano, Switzerland.

Carlo Cereda (C)

Department of Neurology and Stroke Center, EOC Neurocenter of Southern Switzerland, Lugano, Switzerland.

Susanne Wegener (S)

Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.

Leo H Bonati (LH)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.
Rheinfelden Rehabilitation Clinic, Rheinfelden, Switzerland.

Urs Fischer (U)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

Marios Psychogios (M)

Department of Neuroradiology, University Hospital Basel, Basel, Switzerland.

Gian Marco De Marchis (GM)

Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland.

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