Effect of incomplete reperfusion patterns on clinical outcome: insights from the ESCAPE-NA1 trial.

Angiography Stroke Thrombectomy

Journal

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

Informations de publication

Date de publication:
25 Jul 2023
Historique:
received: 08 05 2023
accepted: 13 07 2023
medline: 26 7 2023
pubmed: 26 7 2023
entrez: 25 7 2023
Statut: aheadofprint

Résumé

Incomplete reperfusion (IR) after mechanical thrombectomy (MT) can be a consequence of residual occlusion, no-reflow phenomenon, or collateral counterpressure. Data on the impact of these phenomena on clinical outcome are limited. Patients from the ESCAPE-NA1 trial with IR (expanded Thrombolysis In Cerebral Infarction (eTICI) 2b) were compared with those with complete or near-complete reperfusion (eTICI 2c-3) on the final angiography run. Final runs were assessed for (a) an MT-accessible occlusion, or (b) a non-MT-accessible occlusion pattern. The primary clinical outcome was modified Rankin Scale (mRS) 0-2 at 90 days. Our imaging outcome was infarction in IR territory on follow-up imaging. Unadjusted and adjusted incidence rate ratios (aIRR) with 95% confidence intervals (95% CI) were obtained. Of 1105 patients, 443 (40.1%) with IR and 506 (46.1%) with complete or near-complete reperfusion were included. An MT-accessible occlusion was identified in 147/443 patients (33.2%) and a non-MT-accessible occlusion in 296/443 (66.8%). As compared with patients with near-complete/complete reperfusion, patients with IR had significantly lower chances of achieving mRS 0-2 at 90 days (aIRR 0.82, 95% CI 0.74 to 0.91). Rates of mRS 0-2 were lower in the MT-accessible occlusion group as compared with the non-MT-accessible occlusion pattern group (aIRR 0.71, 95% CI 0.60 to 0.83, and aIRR 0.89, 95% CI 0.81 to 0.98, respectively). More patients with MT-accessible occlusion patterns developed infarcts in the non-reperfused territory as compared with patients with non-MT occlusion patterns (68.7% vs 46.3%). IR was associated with worse clinical outcomes than near-complete/complete reperfusion. Two-thirds of our patients with IR had non-MT-accessible occlusion patterns which were associated with better clinical and imaging outcomes compared with those with MT-accessible occlusion patterns.

Sections du résumé

BACKGROUND BACKGROUND
Incomplete reperfusion (IR) after mechanical thrombectomy (MT) can be a consequence of residual occlusion, no-reflow phenomenon, or collateral counterpressure. Data on the impact of these phenomena on clinical outcome are limited.
METHODS METHODS
Patients from the ESCAPE-NA1 trial with IR (expanded Thrombolysis In Cerebral Infarction (eTICI) 2b) were compared with those with complete or near-complete reperfusion (eTICI 2c-3) on the final angiography run. Final runs were assessed for (a) an MT-accessible occlusion, or (b) a non-MT-accessible occlusion pattern. The primary clinical outcome was modified Rankin Scale (mRS) 0-2 at 90 days. Our imaging outcome was infarction in IR territory on follow-up imaging. Unadjusted and adjusted incidence rate ratios (aIRR) with 95% confidence intervals (95% CI) were obtained.
RESULTS RESULTS
Of 1105 patients, 443 (40.1%) with IR and 506 (46.1%) with complete or near-complete reperfusion were included. An MT-accessible occlusion was identified in 147/443 patients (33.2%) and a non-MT-accessible occlusion in 296/443 (66.8%). As compared with patients with near-complete/complete reperfusion, patients with IR had significantly lower chances of achieving mRS 0-2 at 90 days (aIRR 0.82, 95% CI 0.74 to 0.91). Rates of mRS 0-2 were lower in the MT-accessible occlusion group as compared with the non-MT-accessible occlusion pattern group (aIRR 0.71, 95% CI 0.60 to 0.83, and aIRR 0.89, 95% CI 0.81 to 0.98, respectively). More patients with MT-accessible occlusion patterns developed infarcts in the non-reperfused territory as compared with patients with non-MT occlusion patterns (68.7% vs 46.3%).
CONCLUSION CONCLUSIONS
IR was associated with worse clinical outcomes than near-complete/complete reperfusion. Two-thirds of our patients with IR had non-MT-accessible occlusion patterns which were associated with better clinical and imaging outcomes compared with those with MT-accessible occlusion patterns.

Identifiants

pubmed: 37491383
pii: jnis-2023-020553
doi: 10.1136/jnis-2023-020553
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: PC reports honoraria from A-care Medical, outside the submitted work. JO reports consultancy fee from NicoLab. ADM received grants from NoNO; honoraria from Medtronic; patent Circle NVI. MT is CEO of NoNO; patents owned by NoNO. MDH received grants from Canadian Institutes for Health Research, Alberta Innovates, NoNO, Heart & Stroke Foundation of Canada, National Institutes of Neurological Disorders and Stroke, Covidien, Boehringer-Ingleheim, Stryker, and Medtronic; fees from Merck; patent for systems of acute stroke diagnosis; a patent issued and licensed to US Patent office Number: 62/086,077; stock in Calgary Scientific. MG reports consultancy for Medtronic, Stryker, Microvention, GE Healthcare, Mentice, outside the submitted work. All other authors have nothing to disclose.

Auteurs

Petra Cimflova (P)

Department of Radiology, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Department of Medical Imaging and Faculty of Medicine, Masaryk University, St. Anne's University Hospital Brno, Brno, Czechia.

Nishita Singh (N)

Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Department of Internal Medicine - Neurology division, University of Manitoba Max Rady College of Medicine, Winnipeg, Manitoba, Canada.

Manon Kappelhof (M)

Department of Radiology and Nuclear Medicine, Amsterdam UMC Location AMC, Amsterdam, The Netherlands.

Johanna M Ospel (JM)

Department of Radiology, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Clinic of Radiology and Nuclear Medicine, Universitatsspital Basel, Basel, Switzerland.

Arshia Sehgal (A)

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

Nima Kashani (N)

University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.

Mohammed A Almekhlafi (MA)

Department of Radiology, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Hotchkis Brain Institute, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.
Community Health Sciences, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.

Andrew M Demchuk (AM)

Department of Radiology, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Hotchkis Brain Institute, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.

Joerg Berrouschot (J)

Klinik für Neurologie und Neurologische Intensivmedizin, Klinikum Altenburger Land GmbH, Altenburg, Germany.

Franziska Dorn (F)

Klinik für Neuroradiologie, Universitätsklinikum Bonn, Bonn, Germany.

Michael E Kelly (ME)

Department of Neurosurgery, University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.

Brian H Buck (BH)

Division of Neurology, University of Alberta, Edmonton, Alberta, Canada.

Thalia S Field (TS)

Division of Neurology, The University of British Columbia Faculty of Medicine, Vancouver, British Columbia, Canada.

Dariush Dowlatshahi (D)

Division of Neurology, University of Ottawa Faculty of Medicine, Ottawa, Ontario, Canada.

Michael Tymianski (M)

NoNO Inc, Toronto, Ontario, Canada.

Michael D Hill (MD)

Department of Radiology, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Hotchkis Brain Institute, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.
Community Health Sciences, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.

Mayank Goyal (M)

Department of Radiology, University of Calgary, Calgary, Alberta, Canada mgoyal2412@gmail.com.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Hotchkis Brain Institute, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.

Classifications MeSH