Mechanical Thrombectomy Versus Best Medical Treatment in the Late Time Window in Non-DEFUSE-Non-DAWN Patients: A Multicenter Cohort Study

Author:

Dittrich Tolga D.1ORCID,Sporns Peter B.23ORCID,Kriemler Lilian F.14,Rudin Salome1,Nguyen Anh2ORCID,Zietz Annaelle1ORCID,Polymeris Alexandros A.1ORCID,Tränka Christopher1,Thilemann Sebastian1ORCID,Wagner Benjamin1ORCID,Altersberger Valerian L.1ORCID,Piot Ines1ORCID,Barinka Filip5ORCID,Müller Susanne6ORCID,Hänsel Martin7ORCID,Gensicke Henrik18ORCID,Engelter Stefan T.18ORCID,Lyrer Philippe A.1ORCID,Sutter Raoul9ORCID,Nickel Christian H.10,Katan Mira1ORCID,Peters Nils15,Kulcsár Zsolt11ORCID,Karwacki Grzegorz M.12ORCID,Pileggi Marco2ORCID,Cereda Carlo13ORCID,Wegener Susanne7ORCID,Bonati Leo H.114ORCID,Fischer Urs1ORCID,Psychogios Marios15ORCID,De Marchis Gian Marco1ORCID

Affiliation:

1. Department of Neurology, University Hospital Basel and University of Basel, Switzerland (T.D.D., L.F.K., S.R., A.Z., A.A.P., C.T., S.T., B.W., V.L.A., I.P., H.G., S.T.E., P.A.L., M.K., N.P., L.H.B., U.F., G.M.D.M.).

2. Department of Neuroradiology, University Hospital Basel, Switzerland (P.B.S., A.N., M.P.).

3. Department of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Germany (P.B.S.).

4. Clinic for Internal Medicine, Cantonal Hospital Schaffhausen, Switzerland (L.F.K.).

5. Department of Neurology and Stroke Center, Hirslanden Hospital Zurich, Switzerland (F.B., N.P.).

6. Department of Neuroradiology, University Hospital Zurich, Switzerland (S.M.).

7. Department of Neurology, University Hospital Zurich and University of Zurich, Switzerland (M.H., S.W.).

8. Neurology and Neurorehabilitation, University Department of Geriatric Medicine Felix Platter, Basel, Switzerland (H.G., S.T.E.).

9. Department of Intensive Care Medicine, University Hospital Basel, Switzerland (R.S.).

10. Emergency Department University Hospital Basel and University of Basel, Switzerland (C.H.N.).

11. Department of Neuroradiology, University Hospital Zurich, Switzerland (Z.K.).

12. Department of Radiology and Nuclear Medicine, Cantonal Hospital of Lucerne, Switzerland (G.M.K.).

13. Department of Neurology and Stroke Center, EOC Neurocenter of Southern Switzerland, Lugano, Switzerland (C.C.).

14. Rheinfelden Rehabilitation Clinic, Switzerland (L.H.B.).

15. Department of Neuroradiology, EOC Neurocenter of Southern Switzerland, Lugano, Switzerland (M.P.).

Abstract

Background: We assessed the efficacy and safety of mechanical thrombectomy (MT) in adult stroke patients with anterior circulation large vessel occlusion presenting in the late time window not fulfilling the DEFUSE-3 (Thrombectomy for Stroke at 6 to 16 Hours With Selection by Perfusion Imaging trial) and DAWN (Thrombectomy 6 to 24 Hours After Stroke With a Mismatch Between Deficit and Infarct trial) inclusion criteria. Methods: Cohort study of adults with anterior circulation large vessel occlusion admitted between 6 and 24 hours after last-seen-well at 5 participating Swiss stroke centers between 2014 and 2021. Mismatch was assessed by computer tomography or magnetic resonance imaging perfusion with automated software (RAPID or OLEA). We excluded patients meeting DEFUSE-3 and DAWN inclusion criteria and compared those who underwent MT with those receiving best medical treatment alone by inverse probability of treatment weighting using the propensity score. The primary efficacy end point was a favorable functional outcome at 90 days, defined as a modified Rankin Scale score shift toward lower categories. The primary safety end point was symptomatic intracranial hemorrhage within 7 days of stroke onset; the secondary was all-cause mortality within 90 days. Results: Among 278 patients with anterior circulation large vessel occlusion presenting in the late time window, 190 (68%) did not meet the DEFUSE-3 and DAWN inclusion criteria and thus were included in the analyses. Of those, 102 (54%) received MT. In the inverse probability of treatment weighting analysis, patients in the MT group had higher odds of favorable outcomes compared with the best medical treatment alone group (modified Rankin Scale shift: acOR, 1.46 [1.02–2.10]; P =0.04) and lower odds of all-cause mortality within 90 days (aOR, 0.59 [0.37–0.93]; P =0.02). There were no significant differences in symptomatic intracranial hemorrhage (MT versus best medical treatment alone: 5% versus 2%, P =0.63). Conclusions: Two out of 3 patients with anterior circulation large vessel occlusion presenting in the late time window did not meet the DEFUSE-3 and DAWN inclusion criteria. In these patients, MT was associated with higher odds of favorable functional outcomes without increased rates of symptomatic intracranial hemorrhage. These findings support the enrollment of patients into ongoing randomized trials on MT in the late window with more permissive inclusion criteria.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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