Multicenter investigation of technical and clinical outcomes after thrombectomy for distal vessel occlusion by frontline technique.
Device
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:
Sep 2023
Sep 2023
Historique:
received:
11
04
2022
accepted:
12
07
2022
medline:
31
8
2023
pubmed:
3
8
2022
entrez:
2
8
2022
Statut:
ppublish
Résumé
Endovascular thrombectomy (EVT) is the standard-of-care for proximal large vessel occlusion (LVO) stroke. Data on technical and clinical outcomes in distal vessel occlusions (DVOs) remain limited. This was a retrospective study of patients undergoing EVT for stroke at 32 international centers. Patients were divided into LVOs (internal carotid artery/M1/vertebrobasilar), medium vessel occlusions (M2/A1/P1) and isolated DVOs (M3/M4/A2/A3/P2/P3) and categorized by thrombectomy technique. Primary outcome was a good functional outcome (modified Rankin Scale ≤2) at 90 days. Secondary outcomes included recanalization, procedure-time, thrombectomy attempts, hemorrhage, and mortality. Multivariate logistic regressions were used to evaluate the impact of technical variables. Propensity score matching was used to compare outcome in patients with DVO treated with aspiration versus stent retriever RESULTS: We included 7477 patients including 213 DVOs. Distal location did not independently predict good functional outcome at 90 days compared with proximal (p=0.467). In distal occlusions, successful recanalization was an independent predictor of good outcome (adjusted odds ratio (aOR) 5.11, p<0.05) irrespective of technique. Younger age, bridging therapy, and lower admission National Institutes of Health Stroke Scale (NIHSS) were also predictors of good outcome. Procedure time ≤1 hour or ≤3 thrombectomy attempts were independent predictors of good outcomes in DVOs irrespective of technique (aOR 4.5 and 2.3, respectively, p<0.05). There were no differences in outcomes in a DVO matched cohort of aspiration versus stent retriever. Rates of hemorrhage and good outcome showed an exponential relationship to procedural metrics, and were more dependent on time in the aspiration group and attempts in the stent retriever group. Outcomes following EVT for DVO are comparable to LVO with similar results between techniques. Techniques may exhibit different futility metrics; stent retriever thrombectomy was influenced by attempts whereas aspiration was more dependent on procedure time.
Sections du résumé
BACKGROUND
BACKGROUND
Endovascular thrombectomy (EVT) is the standard-of-care for proximal large vessel occlusion (LVO) stroke. Data on technical and clinical outcomes in distal vessel occlusions (DVOs) remain limited.
METHODS
METHODS
This was a retrospective study of patients undergoing EVT for stroke at 32 international centers. Patients were divided into LVOs (internal carotid artery/M1/vertebrobasilar), medium vessel occlusions (M2/A1/P1) and isolated DVOs (M3/M4/A2/A3/P2/P3) and categorized by thrombectomy technique. Primary outcome was a good functional outcome (modified Rankin Scale ≤2) at 90 days. Secondary outcomes included recanalization, procedure-time, thrombectomy attempts, hemorrhage, and mortality. Multivariate logistic regressions were used to evaluate the impact of technical variables. Propensity score matching was used to compare outcome in patients with DVO treated with aspiration versus stent retriever RESULTS: We included 7477 patients including 213 DVOs. Distal location did not independently predict good functional outcome at 90 days compared with proximal (p=0.467). In distal occlusions, successful recanalization was an independent predictor of good outcome (adjusted odds ratio (aOR) 5.11, p<0.05) irrespective of technique. Younger age, bridging therapy, and lower admission National Institutes of Health Stroke Scale (NIHSS) were also predictors of good outcome. Procedure time ≤1 hour or ≤3 thrombectomy attempts were independent predictors of good outcomes in DVOs irrespective of technique (aOR 4.5 and 2.3, respectively, p<0.05). There were no differences in outcomes in a DVO matched cohort of aspiration versus stent retriever. Rates of hemorrhage and good outcome showed an exponential relationship to procedural metrics, and were more dependent on time in the aspiration group and attempts in the stent retriever group.
CONCLUSIONS
CONCLUSIONS
Outcomes following EVT for DVO are comparable to LVO with similar results between techniques. Techniques may exhibit different futility metrics; stent retriever thrombectomy was influenced by attempts whereas aspiration was more dependent on procedure time.
Identifiants
pubmed: 35918129
pii: jnis-2022-019023
doi: 10.1136/jnis-2022-019023
doi:
Types de publication
Multicenter Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e93-e101Informations 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: AMA: None, RMC: None, SAK: Grant Funding-Stryker; PJ: Consultant-Balt, Cerus, Microvention, Medtronic. M-NP Honoraria - Stryker, Medtronic, Penumbra, Acandis, Phenox, Siemens Healthineers, Research Support-Swiss National Science Foundation, Bangerter-Rhyner Stiftung, Stryker, Phenox, Medtronic, Rapid, Penumbra, Siemens Healthineers; RMS: None; ASA: Consultant for Arsenal, Balt, Johnson and Johnson, Medtronic, Microvention, Penumbra, Scientia, Siemens, Stryker, Research support from Balt, Medtronic, Microvention, Penumbra and Siemens, Shareholder-Azimuth, Bendit, Cerebrotech, Endostream, Magneto, Mentice, Neurogami, Neuros, Scientia, Serenity, Synchron, Tulavi, Vastrax, VizAI; KMF: Editorial Board-JNIS; RDL: Consultant-Stryker, Imperative Care, Cerenovus, Asahi Intec, Research Funding-Hypervention, Kaneka, Siemens Healthineers, SNIS Foundation, Equity-Synchron, Endostream, Q’Apel, Spartan Micro, Editorial Board-JNIS; PK: Consultant- Stryker, Imperative Care, Microvention, Grant Support-NIH, Editorial-Board JNIS; TD: None; AR: None; RJC: None; IM: None; NG: None; SQW: Board of Directors-AANS, Associate Editor- S:VIN Journal; CMC: None; JM: PI on trials funded by- Stryker Neurovascular, Microvention, and Penumbra, Consultant-Cerebrotech, Viseon, Endostream, Vastrax, RIST, Synchron, Viz.ai, Perflow, CVAid, Stockholder-Cerebrotech, Imperative Care, Endostream, Viseon, BlinkTBI, Myra Medical, Serenity, Vastrax, NTI, RIST, Viz.ai, Synchron, Radical, and Truvic; Editorial Board-JNIS; SIT: Consultant- Microvention, Medtronic; BMH: None; LD: None; HS: None; CSO: Grant Support- Bee Foundation, Brain Aneurysm Foundation, DSMB- Medtronic; RWC: Consultant/Proctor: Medtronic, Microvention; JMa: consultant-Stryker; IF: None; MRL: Educational Grant-Stryker, Medtronic, Consultant-Medtronic, Aeaean Advisers, Travel Support-Penumbra, Editorial Board, JNIS, Stock- Hyperion Surgical, Proprio, Synchron, Cerebrotech, Fluid Biomed, Stereotaxis, Advisor-Metis Innovative; J-tK: None; MSP: DSMB-Medtronic; BG: None; AJP: Consultant-Depuy Synthes, Stryker, CM: Consultant-Silk Road, Penumbra, Microvention, Cerevasc, Stryker, Speaker-Silk Road, Penumbra; JAG: Grant Support- Georgia Research Alliance, Department of Defense, Emory Medical Care Foundation, Neurosurgery Catalyst, Stock- NTI, Cognition; AMS: Consultant- Stryker, Penumbra, Terumo, RapidAI; STAR: funded by Penumbra, Medtronic, Stryker.