Endovascular treatment strategy, technique, and outcomes for dural arteriovenous fistulas of the marginal sinus region.


Journal

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

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 28 02 2021
accepted: 11 05 2021
pubmed: 28 5 2021
medline: 21 1 2022
entrez: 27 5 2021
Statut: ppublish

Résumé

Dural arteriovenous fistulas (AVF) of the foramen magnum region (FMR) are technically challenging lesions to treat. Transvenous (TV), transarterial (TA), and surgical approaches have been described, but the optimum treatment strategy is not defined. To report treatment strategies and outcomes for FMR-AVF at a single, high-volume referral center. A retrospective review from January 2010 to August 2020 identified patients with FMR-AVF at a single referral center. Angiographic features, treatment (observation, endovascular, surgical), and follow-up of angiographic and clinical results were recorded. The technical aspects of TV embolization are then presented in detail. 29 FMR-AVF were identified in 28 patients. Of these, 24/29 (82.8%) were treated and 5/29 (17.2%) were observed. Treatment was endovascular in 21/24 (87.5%), combined (endovascular+surgical) in 2/24 (8.3%), and surgical in 1/24 (4.2%). Endovascular treatments were 76.2% TV, 14.3% TA, and 9.5% combined TV/TA. Sufficient follow-up data were available for 20/28 (71.4%) with mean follow-up of 16.8 months. No AVF recurrence was seen for TA/TV, combined endovascular/surgical, or surgical groups, and there was one recurrence (7.1%) in the TV group. Symptomatic improvement was seen in all groups: TV (71.4% complete, 28.6% partial), TA (66.7% complete, 33.3% no follow-up), TV+TA (100% partial), endovascular/surgical (100% complete), and surgical (100% partial). Minor non-neurologic complications included 1/14 (7.1%) in the TV group and 1/3 (33.3%) in the TA/TV group. Endovascular treatment is safe and effective for most FMR-AVF. TV embolization has a high cure rate with few complications.

Sections du résumé

BACKGROUND BACKGROUND
Dural arteriovenous fistulas (AVF) of the foramen magnum region (FMR) are technically challenging lesions to treat. Transvenous (TV), transarterial (TA), and surgical approaches have been described, but the optimum treatment strategy is not defined.
OBJECTIVE OBJECTIVE
To report treatment strategies and outcomes for FMR-AVF at a single, high-volume referral center.
METHODS METHODS
A retrospective review from January 2010 to August 2020 identified patients with FMR-AVF at a single referral center. Angiographic features, treatment (observation, endovascular, surgical), and follow-up of angiographic and clinical results were recorded. The technical aspects of TV embolization are then presented in detail.
RESULTS RESULTS
29 FMR-AVF were identified in 28 patients. Of these, 24/29 (82.8%) were treated and 5/29 (17.2%) were observed. Treatment was endovascular in 21/24 (87.5%), combined (endovascular+surgical) in 2/24 (8.3%), and surgical in 1/24 (4.2%). Endovascular treatments were 76.2% TV, 14.3% TA, and 9.5% combined TV/TA. Sufficient follow-up data were available for 20/28 (71.4%) with mean follow-up of 16.8 months. No AVF recurrence was seen for TA/TV, combined endovascular/surgical, or surgical groups, and there was one recurrence (7.1%) in the TV group. Symptomatic improvement was seen in all groups: TV (71.4% complete, 28.6% partial), TA (66.7% complete, 33.3% no follow-up), TV+TA (100% partial), endovascular/surgical (100% complete), and surgical (100% partial). Minor non-neurologic complications included 1/14 (7.1%) in the TV group and 1/3 (33.3%) in the TA/TV group.
CONCLUSION CONCLUSIONS
Endovascular treatment is safe and effective for most FMR-AVF. TV embolization has a high cure rate with few complications.

Identifiants

pubmed: 34039683
pii: neurintsurg-2021-017476
doi: 10.1136/neurintsurg-2021-017476
pmc: PMC8722448
mid: NIHMS1766401
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-159

Subventions

Organisme : NHLBI NIH HHS
ID : R56 HL149124
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Michael Travis Caton (MT)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA travis.caton@gmail.com.

Kazim H Narsinh (KH)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.

Amanda Baker (A)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.

Steven W Hetts (SW)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.

Daniel L Cooke (DL)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.

Randall T Higashida (RT)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.
Departments of Neurological Surgery, Neurology, and Anesthesiology, University of California San Francisco, San Francisco, CA, USA.

Christopher F Dowd (CF)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.
Departments of Neurological Surgery, Neurology, and Anesthesiology, University of California San Francisco, San Francisco, CA, USA.

Van V Halbach (VV)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.
Departments of Neurological Surgery, Neurology, and Anesthesiology, University of California San Francisco, San Francisco, CA, USA.

Matthew R Amans (MR)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.

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Classifications MeSH