Distal cerebral vasospasm treatment following aneurysmal subarachnoid hemorrhage using the Comaneci device: technical feasibility and single-center preliminary results.


Journal

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

Informations de publication

Date de publication:
Apr 2023
Historique:
received: 26 01 2022
accepted: 05 05 2022
pubmed: 19 5 2022
medline: 17 3 2023
entrez: 18 5 2022
Statut: ppublish

Résumé

Balloon-assisted mechanical angioplasty for cerebral vasospasm following aneurysmal subarachnoid hemorrhage (aSAH) has a number of limitations, including transient occlusion of the spastic blood vessel. Comaneci is an FDA-approved device for temporary coil embolization assistance which has recently also been approved for the treatment of distal symptomatic refractory vasospasm. We aimed to report the feasibility, efficacy and safety of our experience with Comaneci angioplasty for refractory distal vasospasm (up to the second segment of the cerebral arteries) following aSAH. This is a retrospective analysis of a prospective series of 18 patients included between April 2019 and June 2021 with aSAH and symptomatic vasospasm refractory to medical therapy, who were treated using Comaneci-17-asssisted mechanical distal angioplasty. Immediate angiographic results, procedure-related complications, and clinical outcomes were assessed. Inter-rater reliability of the scores was determined using the intraclass correlation coefficient. Comaneci-assisted distal angioplasty was performed in 18 patients, corresponding to 31 target arteries. All distal anterior segments were easily accessible with the Comaneci-17 device. Vasospasm improvement after Comaneci mechanical angioplasty was seen in 22 distal arteries (71%) (weighted Cohen's kappa (κ This initial experience suggests that distal mechanical angioplasty performed with the Comaneci-17 device for refractory vasospasm following aSAH seems to be safe, with good feasibility and efficacy.

Sections du résumé

BACKGROUND BACKGROUND
Balloon-assisted mechanical angioplasty for cerebral vasospasm following aneurysmal subarachnoid hemorrhage (aSAH) has a number of limitations, including transient occlusion of the spastic blood vessel. Comaneci is an FDA-approved device for temporary coil embolization assistance which has recently also been approved for the treatment of distal symptomatic refractory vasospasm. We aimed to report the feasibility, efficacy and safety of our experience with Comaneci angioplasty for refractory distal vasospasm (up to the second segment of the cerebral arteries) following aSAH.
METHODS METHODS
This is a retrospective analysis of a prospective series of 18 patients included between April 2019 and June 2021 with aSAH and symptomatic vasospasm refractory to medical therapy, who were treated using Comaneci-17-asssisted mechanical distal angioplasty. Immediate angiographic results, procedure-related complications, and clinical outcomes were assessed. Inter-rater reliability of the scores was determined using the intraclass correlation coefficient.
RESULTS RESULTS
Comaneci-assisted distal angioplasty was performed in 18 patients, corresponding to 31 target arteries. All distal anterior segments were easily accessible with the Comaneci-17 device. Vasospasm improvement after Comaneci mechanical angioplasty was seen in 22 distal arteries (71%) (weighted Cohen's kappa (κ
CONCLUSION CONCLUSIONS
This initial experience suggests that distal mechanical angioplasty performed with the Comaneci-17 device for refractory vasospasm following aSAH seems to be safe, with good feasibility and efficacy.

Identifiants

pubmed: 35584908
pii: neurintsurg-2022-018699
doi: 10.1136/neurintsurg-2022-018699
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

325-329

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: XC and J-FH are consultants for educational work with Rapid Medical.

Auteurs

Louis Thiery (L)

Department of Neuroradiology, APHM La Timone, Marseille, France louisthiery@hotmail.fr.

Xavier Carle (X)

Department of Neuroradiology, APHM La Timone, Marseille, France.

Benoit Testud (B)

Department of Neuroradiology, APHM La Timone, Marseille, France.
CEMEREM, Aix Marseille University, Marseille, France.
CNRS, CRMBM, Aix Marseille University, Marseille, France.

Gregoire Boulouis (G)

Department of Neuroradiology, CHRU Tours, Tours, France.

Paul Habert (P)

Department of Medical Imaging, APHM La Timone, Marseille, France.
LIIE, Aix Marseille University, Marseille, France.
CERIMED, Aix Marseille University, Marseille, France.

Farouk Tradi (F)

Department of Medical Imaging, APHM La Timone, Marseille, France.
LIIE, Aix Marseille University, Marseille, France.
CERIMED, Aix Marseille University, Marseille, France.

Anthony Reyre (A)

Department of Neuroradiology, APHM La Timone, Marseille, France.

Pierre Lehmann (P)

Department of Neuroradiology, APHM La Timone, Marseille, France.

Philippe Dory-Lautrec (P)

Department of Neuroradiology, APHM La Timone, Marseille, France.

Jan-Patrick Stellmann (JP)

Department of Neuroradiology, APHM La Timone, Marseille, France.
CEMEREM, Aix Marseille University, Marseille, France.
CNRS, CRMBM, Aix Marseille University, Marseille, France.

Nadine Girard (N)

Department of Neuroradiology, APHM La Timone, Marseille, France.

Herve Brunel (H)

Department of Neuroradiology, APHM La Timone, Marseille, France.

Jean-Francois Hak (JF)

Department of Neuroradiology, APHM La Timone, Marseille, France.
LIIE, Aix Marseille University, Marseille, France.
CERIMED, Aix Marseille University, Marseille, France.

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