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Mechanical Thrombectomy For Large Vessel Occlusion Between 6 And 24 Hours: Outcome Comparison Of Defuse-3/Dawn Eligible Versus Non-Eligible Patients

Dittrich, Tolga Daniel and Sporns, Peter and Kriemler, Lilian and Rudin, Salome and Nguyen, Anh and Zietz, Annaelle and Polymeris, Alexandros A. and Tränka, Christopher and Thilemann, Sebastian and Wagner, Benjamin and Altersberger, Valerian and Piot, Ines and Barinka, Filip and Hänsel, Martin and Gensicke, Henrik and Engelter, Stefan and Lyrer, Philippe A. and Sutter, Raoul and Nickel, Christian and Katan, Mira and Peter, Nils and Michels, Lars and Kulcsar, Zsolt and Karwacki, Grzegorz and Pileggi, Marco and Cereda, Carlo W. and Wegener, Susanne and Bonati, Leo and Fischer, Urs and Psychogios, Marios and De Marchis, Gian Marco. (2022) Mechanical Thrombectomy For Large Vessel Occlusion Between 6 And 24 Hours: Outcome Comparison Of Defuse-3/Dawn Eligible Versus Non-Eligible Patients. International Journal of Stroke, 18 (6). pp. 697-703.

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Official URL: https://edoc.unibas.ch/90280/

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Abstract

The DEFUSE-3 and DAWN trials showed that mechanical thrombectomy (MT) improves the outcome of selected patients with large vessel occlusions in the anterior circulation (LVO) up to 24 hours of 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 hours.; 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 hours 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 three months) and two efficacy outcomes (modified Rankin Score [mRS] shift toward lower categories and mRS of 0-2 at three 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=1.00). Multivariable regression revealed no differences in 3-month all-cause mortality (aOR 2.07, 95%CI 0.64-6.84, p=0.23) or functional outcomes (mRS shift: acOR 0.81, 95%CI 0.37-1.79, p=0.60; mRS 0-2: aOR 0.91, 95%CI 0.31-2.57, p=0.85).; Among adult patients with LVO treated with MT between 6 and 24 hours, safety and efficacy outcomes were similar between DEFUSE-3/DAWN eligible vs. ineligible patients. Our data provide a compelling rationale for randomized trials with broader inclusion criteria for MT.
Faculties and Departments:03 Faculty of Medicine
03 Faculty of Medicine > Bereich Medizinische Fächer (Klinik)
03 Faculty of Medicine > Departement Klinische Forschung > Bereich Medizinische Fächer (Klinik)
03 Faculty of Medicine > Bereich Medizinische Fächer (Klinik) > Intensivmedizin > Intensivmedizin (Marsch)
03 Faculty of Medicine > Departement Klinische Forschung > Bereich Medizinische Fächer (Klinik) > Intensivmedizin > Intensivmedizin (Marsch)
03 Faculty of Medicine > Bereich Medizinische Fächer (Klinik) > Neurologie
03 Faculty of Medicine > Departement Klinische Forschung > Bereich Medizinische Fächer (Klinik) > Neurologie
03 Faculty of Medicine > Departement Klinische Forschung
UniBasel Contributors:Sutter, Raoul Christian
Item Type:Article, refereed
Article Subtype:Research Article
Publisher:SAGE Publications
ISSN:1747-4930
e-ISSN:1747-4949
Note:Publication type according to Uni Basel Research Database: Journal article
Identification Number:
Last Modified:24 Jul 2023 12:33
Deposited On:24 Jul 2023 12:33

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