Efficacy of endovascular thrombectomy in patients with M2 segment middle cerebral artery occlusions: meta-analysis of data from the HERMES Collaboration.


Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 18 12 2018
revised: 06 03 2019
accepted: 11 03 2019
pubmed: 13 4 2019
medline: 1 1 2020
entrez: 13 4 2019
Statut: ppublish

Résumé

The Society of Neurointerventional Surgery revised its operational definition of emergent large vessel occlusion (ELVO) recently to include proximal M2 segment middle cerebral artery (MCA) occlusions. We sought to assess the benefit of endovascular thrombectomy (EVT) over best medical care for M2 segment MCA occlusion. Patient level data from trials in the HERMES Collaboration were included. The HERMES core laboratory identified patients with M2 segment MCA occlusions and further classified them as proximal versus distal, anterior versus posterior division, and dominant versus co-dominant versus non-dominant. Primary outcome was modified Rankin Scale (mRS) score 0-2 at 90 days. Secondary outcomes were modified Thrombolysis in Cerebral Infarction (mTICI) rates at end of procedure, 90-day mRS shift, 90-day mRS 0-1, 24 hours National Institute of Health Stroke Scale (NIHSS) score 0-2, symptomatic intracerebral hemorrhage (ICH), and death. 130 patients with M2 MCA (proximal location n=116 vs distal n=14, anterior division n=72 vs posterior n=58, dominant n=73 vs co-dominant n=50 vs non-dominant n=7) were included. Successful reperfusion (mTICI 2b or 3) among those undergoing EVT was seen in 59.2% of patients. Treatment effect favored EVT (adjusted OR 2.39, 95% CI 1.08 to 5.28, p=0.03) for 90-day mRS 0-2 (58.2% EVT vs 39.7% control). Direction of benefit favored EVT for other outcomes. Treatment effect favoring EVT was maximal in patients with proximal M2 segment MCA occlusions (n=116, adjusted OR 2.68, 95% CI 1.13 to 6.37) and in dominant M2 segment MCA occlusions (n=73, adjusted OR 4.08, 95% CI 1.08 to 15.48). No sICH (0%) was observed in patients treated with EVT compared with five (7.9%) in the control arm. Patients with proximal M2 segment MCA occlusions eligible for EVT trial protocols benefited from EVT.

Sections du résumé

BACKGROUND BACKGROUND
The Society of Neurointerventional Surgery revised its operational definition of emergent large vessel occlusion (ELVO) recently to include proximal M2 segment middle cerebral artery (MCA) occlusions. We sought to assess the benefit of endovascular thrombectomy (EVT) over best medical care for M2 segment MCA occlusion.
METHODS METHODS
Patient level data from trials in the HERMES Collaboration were included. The HERMES core laboratory identified patients with M2 segment MCA occlusions and further classified them as proximal versus distal, anterior versus posterior division, and dominant versus co-dominant versus non-dominant. Primary outcome was modified Rankin Scale (mRS) score 0-2 at 90 days. Secondary outcomes were modified Thrombolysis in Cerebral Infarction (mTICI) rates at end of procedure, 90-day mRS shift, 90-day mRS 0-1, 24 hours National Institute of Health Stroke Scale (NIHSS) score 0-2, symptomatic intracerebral hemorrhage (ICH), and death.
RESULTS RESULTS
130 patients with M2 MCA (proximal location n=116 vs distal n=14, anterior division n=72 vs posterior n=58, dominant n=73 vs co-dominant n=50 vs non-dominant n=7) were included. Successful reperfusion (mTICI 2b or 3) among those undergoing EVT was seen in 59.2% of patients. Treatment effect favored EVT (adjusted OR 2.39, 95% CI 1.08 to 5.28, p=0.03) for 90-day mRS 0-2 (58.2% EVT vs 39.7% control). Direction of benefit favored EVT for other outcomes. Treatment effect favoring EVT was maximal in patients with proximal M2 segment MCA occlusions (n=116, adjusted OR 2.68, 95% CI 1.13 to 6.37) and in dominant M2 segment MCA occlusions (n=73, adjusted OR 4.08, 95% CI 1.08 to 15.48). No sICH (0%) was observed in patients treated with EVT compared with five (7.9%) in the control arm.
CONCLUSION CONCLUSIONS
Patients with proximal M2 segment MCA occlusions eligible for EVT trial protocols benefited from EVT.

Identifiants

pubmed: 30975736
pii: neurintsurg-2018-014678
doi: 10.1136/neurintsurg-2018-014678
doi:

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

1065-1069

Subventions

Organisme : Department of Health
ID : HTA/14/08/47
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MDH owns stock in Calgary Scientific Inc, a company that focuses on medical imaging software, is a director of the Canadian Federation of Neurological Sciences, a not-for-profit group and has received grant support from Alberta Innovates Health Solutions, CIHR, Heart & Stroke Foundation of Canada, National Institutes of Neurological Disorders and Stroke. YBWEMR reports Stock ownership of Nico-Lab, outside the submitted work. BCVC reports grants from National Health and Medical Research Council, Royal Australasian College of Physicians, Royal Melbourne Hospital Foundation, National Heart Foundation, National Stroke Foundation of Australia, Covidien (Medtronic) during the conduct of the study. KM reports grants from Medtronic and from Codman outside the submitted work. AMD reports personal fees from Medtronic during the conduct of the study. TJ has consulted for Codman Neurovascular and Neuravi; holds stock in Silk Road, Anaconda, Route 92, and Blockade; received travel expenses from Stryker as primary investigator of the DAWN trial and from Fundacio Ictus related to the REVASCAT and RACECAT trials. PM reports receiving consulting fees from Medtronic and Stryker, personal fees from Stryker and Microvention outside the submitted work. PW reports grants from National Institutes for Health Research, the Stroke Association, Medtronic (Covidien), and Codman and has consulted for Microvention Terumo and Codman. AvdL reports grants from Dutch Heart Foundation, and consulting fees from AngioCare BV, from Covidien/EV3, from MEDAC Gmbh/LAMEPRO, from Stryker, from Penumbra Inc, during the conduct of the study; grants from Stryker, grants from Penumbra Inc, grants from Medtronic outside the submitted work. JLS has acted as a scientific consultant regarding trial design and conduct for Medtronic. SB reports personal fees from University of Calgary during the conduct of the study; personal fees from Medtronic outside the submitted work. MG reports grants from Medtronic and personal fees from Stryker, Medtronic, Microvention, and Cerenovus during the conduct of the study; grants from Stryker outside the submitted work. In addition, MG has a patent Systems of Acute Stroke Diagnosis issued to GE Healthcare.

Auteurs

Bijoy K Menon (BK)

Clinical Neurosciences, Radiology and Community Health Sciences, HBI, University of Calgary, Calgary, Alberta, Canada.

Michael D Hill (MD)

Clinical Neurosciences, Radiology, Medicine, Community Health Sciences, HBI, University of Calgary, Calgary, Alberta, Canada.

Antoni Davalos (A)

Department of Neurology, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.

Yvo B W E M Roos (YBWEM)

Department of Neurology, Academic Medical Centre, Amsterdam, The Netherlands.

Bruce C V Campbell (BCV)

Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.
Department of Neurology, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Diederik W J Dippel (DWJ)

Department of Neurology, Erasmus MC University Medical Center, Rotterdam, Netherlands.

Francis Guillemin (F)

INSERM CIC 1433 Clinical Epidemiology, Universite de Lorraine, Nancy, France.
University Hospital of Nancy, Nancy, France.

Jeffrey L Saver (JL)

Department of Neurology, UCLA, Los Angeles, California, USA.

Aad van der Lugt (A)

Department of Radiology, Rotterdam, The Netherlands.

Andrew M Demchuk (AM)

Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.

Keith Muir (K)

Institute of Neuroscience & Psychology, University of Glasgow, Glasgow, UK.

Scott Brown (S)

Altair Biostatistics, St Louis Park, Minnesota, USA.

Tudor Jovin (T)

Department of Neurology, UPMC, Pittsburgh, Pennsylvania, USA.

Peter Mitchell (P)

Department of Radiology, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Phil White (P)

Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.
Department of Neuroradiology, Newcastle upon Tyne Hospitals, Newcastle upon Tyne, UK.

Serge Bracard (S)

Department of Diagnostic and Interventional Neuroradiology, INSERM U 947, Université de Lorraine and University Hospital of Nancy, Nancy, France.

Mayank Goyal (M)

Department of Diagnostic Imaging, University of Calgary, Calgary, Alberta, Canada.

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