Endovascular therapy in the distal neurovascular territory: results of a large prospective registry.


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 2021
Historique:
received: 14 09 2020
revised: 13 11 2020
accepted: 13 11 2020
pubmed: 17 12 2020
medline: 21 10 2021
entrez: 16 12 2020
Statut: ppublish

Résumé

There is a paucity of data regarding mechanical thrombectomy (MT) in distal arterial occlusions (DAO). We aim to evaluate the safety and efficacy of MT in patients with DAO and compare their outcomes with proximal arterial occlusion (PAO) strokes. The Trevo Registry was a prospective open-label MT registry including 2008 patients from 76 sites across 12 countries. Patients were categorized into: PAO: intracranial ICA, and MCA-M1; and DAO: MCA-M2, MCA-M3, ACA, and PCA. Baseline and outcome variables were compared across the PAO vs DAO patients with pre-morbid mRS 0-2. Among 407 DAOs including 350 (86.0%) M2, 25 (6.1%) M3, 10 (2.5%) ACA, and 22 (5.4%) PCA occlusions, there were 376 DAO with pre-morbid mRS 0-2 which were compared with 1268 PAO patients. The median baseline NIHSS score was lower in DAO (13 [8-18] vs 16 [12-20], P<0.001). There were no differences in terms of age, sex, IV-tPA use, co-morbidities, or time to treatment across DAO vs PAO. The rates of post-procedure reperfusion, symptomatic intracranial hemorrhage (sICH), and 90-mortality were comparable between both groups. DAO showed significantly higher rates of 90-day mRS 0-2 (68.3% vs 56.5%, P<0.001). After adjustment for potential confounders, the level of arterial occlusion was not associated with the chances of excellent outcome (DAO for 90-day mRS 0-1: OR; 1.18, 95% CI [0.90 to 1.54], P=0.225), successful reperfusion or SICH. However, DAO patients were more likely to be functionally independent (mRS 0-2: OR; 1.45, 95% CI [1,09 to 1.92], P=0.01) or dead (OR; 1.54, 95% CI [1.06 to 2.27], P=0.02) at 90 days. Endovascular therapy in DAO appears to result in a comparable safety and technical success profile as in PAO. The potential benefits of DAO thrombectomy should be investigated in future randomized trials.

Sections du résumé

BACKGROUND BACKGROUND
There is a paucity of data regarding mechanical thrombectomy (MT) in distal arterial occlusions (DAO). We aim to evaluate the safety and efficacy of MT in patients with DAO and compare their outcomes with proximal arterial occlusion (PAO) strokes.
METHODS METHODS
The Trevo Registry was a prospective open-label MT registry including 2008 patients from 76 sites across 12 countries. Patients were categorized into: PAO: intracranial ICA, and MCA-M1; and DAO: MCA-M2, MCA-M3, ACA, and PCA. Baseline and outcome variables were compared across the PAO vs DAO patients with pre-morbid mRS 0-2.
RESULTS RESULTS
Among 407 DAOs including 350 (86.0%) M2, 25 (6.1%) M3, 10 (2.5%) ACA, and 22 (5.4%) PCA occlusions, there were 376 DAO with pre-morbid mRS 0-2 which were compared with 1268 PAO patients. The median baseline NIHSS score was lower in DAO (13 [8-18] vs 16 [12-20], P<0.001). There were no differences in terms of age, sex, IV-tPA use, co-morbidities, or time to treatment across DAO vs PAO. The rates of post-procedure reperfusion, symptomatic intracranial hemorrhage (sICH), and 90-mortality were comparable between both groups. DAO showed significantly higher rates of 90-day mRS 0-2 (68.3% vs 56.5%, P<0.001). After adjustment for potential confounders, the level of arterial occlusion was not associated with the chances of excellent outcome (DAO for 90-day mRS 0-1: OR; 1.18, 95% CI [0.90 to 1.54], P=0.225), successful reperfusion or SICH. However, DAO patients were more likely to be functionally independent (mRS 0-2: OR; 1.45, 95% CI [1,09 to 1.92], P=0.01) or dead (OR; 1.54, 95% CI [1.06 to 2.27], P=0.02) at 90 days.
CONCLUSION CONCLUSIONS
Endovascular therapy in DAO appears to result in a comparable safety and technical success profile as in PAO. The potential benefits of DAO thrombectomy should be investigated in future randomized trials.

Identifiants

pubmed: 33323503
pii: neurintsurg-2020-016851
doi: 10.1136/neurintsurg-2020-016851
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

979-984

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: RGN reports consulting fees for advisory roles with Stryker Neurovascular, Cerenovus, Medtronic, Phenox, Anaconda, Genentech, Biogen, Prolong Pharmaceuticals, and Imperative Care, and stock options for advisory roles with Brainomix, Viz-AI, Corindus Vascular Robotics, Vesalio, Ceretrieve, Astrocyte, and Cerebrotech. DCH is a consultant for Stryker and Vesalio, and holds stock options at Viz.AI. RG has ownership interest/royalties from UpToDate and is a consultant for Stryker, Medtronic, and Rapid Medical. AK is a consultant for Stryker. JDE is a consultant for Penumbra, Medtronic, and Stryker. ARM is a proctor for Stryker and consultant for InNeuroCo. AS reports research grants from, and is consultant for, Stryker. MAT is a consultant for Stryker, Rapid Medical, Balt USA, and Medtronic. MRF is a consultant for Nico Corporation. BWB is a consultant for Stryker, Penumbra, Medtronic, Cerenovus, Route 92 Medical, and Artio Medical, and has stock/stock options/equity in Penumbra, Viz.ai, Rapid Medical, Route 92 Medical, Artio Medical, 880 Medical, and Marblehead Medical. PJ is a consultant for Stryker. BMB, is a consultant for Stryker. DL is a consultant for Cerenovus, Genentech, Medtronic, Rapid Medical, Stryker, and Vesalio. EV is a consultant for Stryker, patent holder and scientific advisor for Penumbra, is a Trice consultant, and holds a Mizuho patent.

Auteurs

Raul G Nogueira (RG)

Department of Neurology, Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Emory University School of Medicine, Atlanta, Georgia, USA raul.g.nogueira@emory.edu.

Mahmoud H Mohammaden (MH)

Department of Neurology, Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Emory University School of Medicine, Atlanta, Georgia, USA.

Diogo C Haussen (DC)

Department of Neurology, Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Emory University School of Medicine, Atlanta, Georgia, USA.

Ronald F Budzik (RF)

Department of Neuroradiology, Riverside Methodist Hospital, Columbus, Ohio, USA.

Rishi Gupta (R)

Department of Neurosciences, WellStar Health System, Atlanta, Georgia, USA.

Antonin Krajina (A)

Department of Neuroradiology, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.

Joey D English (JD)

Department of Neurology, California Pacific Medical Center, San Francisco, California, USA.

Ali R Malek (AR)

Neurointerventional & Comprehensive Stroke Program, Saint Mary Medical Center, Long Beach, California, USA.

Amrou Sarraj (A)

Neurology, University of Texas McGovern Medical School, Houston, Texas, USA.

Ana Paula Narata (AP)

Department of Radiology, Diagnostic and Interventional Neuroradiology Section, Regional University Hospital Centre Tours, Tours, Centre, France.

Muhammad Asif Taqi (MA)

Department of Neurology, Vascular Neurology of Southern California, Thousand Oaks, California, USA.

Michael R Frankel (MR)

Department of Neurology, Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Emory University School of Medicine, Atlanta, Georgia, USA.

Timothy Ryan Miller (TR)

Department of Radiology, University of Maryland School of Medicine, Baltimore, Maryland, USA.

Thomas Grobelny (T)

Advocate Neurovascular Center, Advocate Health Care Library Network, Park Ridge, Illinois, USA.

Blaise W Baxter (BW)

Department of Radiology, University of Tennessee, Chattanooga, TN, USA.

Bruno Mario Bartolini (BM)

Department of Neuroradiology, CHUV, Lausanne, VD, Switzerland.

Paul Jenkins (P)

Division of Biostatistics, Stryker Neurovascular, Fremont, California, USA.

Laurent Estrade (L)

Department of Interventional Neuroradiology, Centre Hospitalier Regional Universitaire de Lille, Lille, France.

David Liebeskind (D)

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

Erol Veznedaroglu (E)

Department of Neurosciences, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.

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