Natural history, angiographic presentation and outcomes of anterior cranial fossa dural arteriovenous fistulas.


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
Historique:
received: 14 05 2022
accepted: 28 07 2022
medline: 21 8 2023
pubmed: 10 8 2022
entrez: 9 8 2022
Statut: ppublish

Résumé

Anterior cranial fossa dural arteriovenous fistulas (ACF-dAVFs) are aggressive vascular lesions. The pattern of venous drainage is the most important determinant of symptoms. Due to the absence of a venous sinus in the anterior cranial fossa, most ACF-dAVFs have some degree of drainage through small cortical veins. We describe the natural history, angiographic presentation and outcomes of the largest cohort of ACF-dAVFs. The CONDOR consortium includes data from 12 international centers. Patients included in the study were diagnosed with an arteriovenous fistula between 1990-2017. ACF-dAVFs were selected from a cohort of 1077 arteriovenous fistulas. The presentation, angioarchitecture and treatment outcomes of ACF-dAVF were extracted and analyzed. 60 ACF-dAVFs were included in the analysis. Most ACF-dAVFs were symptomatic (38/60, 63%). The most common symptomatic presentation was intracranial hemorrhage (22/38, 57%). Most ACF-dAVFs drained through cortical veins (85%, 51/60), which in most instances drained into the superior sagittal sinus (63%, 32/51). The presence of cortical venous drainage predicted symptomatic presentation (OR 9.4, CI 1.98 to 69.1, p=0.01). Microsurgery was the most effective modality of treatment. 56% (19/34) of symptomatic patients who were treated had complete resolution of symptoms. Improvement of symptoms was not observed in untreated symptomatic ACF-dAVFs. Most ACF-dAVFs have a symptomatic presentation. Drainage through cortical veins is a key angiographic feature of ACF-dAVFs that accounts for their malignant course. Microsurgery is the most effective treatment. Due to the high risk of bleeding, closure of ACF-dAVFs is indicated regardless of presentation.

Sections du résumé

BACKGROUND BACKGROUND
Anterior cranial fossa dural arteriovenous fistulas (ACF-dAVFs) are aggressive vascular lesions. The pattern of venous drainage is the most important determinant of symptoms. Due to the absence of a venous sinus in the anterior cranial fossa, most ACF-dAVFs have some degree of drainage through small cortical veins. We describe the natural history, angiographic presentation and outcomes of the largest cohort of ACF-dAVFs.
METHODS METHODS
The CONDOR consortium includes data from 12 international centers. Patients included in the study were diagnosed with an arteriovenous fistula between 1990-2017. ACF-dAVFs were selected from a cohort of 1077 arteriovenous fistulas. The presentation, angioarchitecture and treatment outcomes of ACF-dAVF were extracted and analyzed.
RESULTS RESULTS
60 ACF-dAVFs were included in the analysis. Most ACF-dAVFs were symptomatic (38/60, 63%). The most common symptomatic presentation was intracranial hemorrhage (22/38, 57%). Most ACF-dAVFs drained through cortical veins (85%, 51/60), which in most instances drained into the superior sagittal sinus (63%, 32/51). The presence of cortical venous drainage predicted symptomatic presentation (OR 9.4, CI 1.98 to 69.1, p=0.01). Microsurgery was the most effective modality of treatment. 56% (19/34) of symptomatic patients who were treated had complete resolution of symptoms. Improvement of symptoms was not observed in untreated symptomatic ACF-dAVFs.
CONCLUSION CONCLUSIONS
Most ACF-dAVFs have a symptomatic presentation. Drainage through cortical veins is a key angiographic feature of ACF-dAVFs that accounts for their malignant course. Microsurgery is the most effective treatment. Due to the high risk of bleeding, closure of ACF-dAVFs is indicated regardless of presentation.

Identifiants

pubmed: 35944975
pii: jnis-2022-019160
doi: 10.1136/jnis-2022-019160
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

903-908

Commentaires et corrections

Type : CommentIn

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: LJK is a co-founder of Spi Surgical and reports compensation for consultant services from Microvention. IJA reports stock options in Remedy Robotics and compensation from Remedy Robotics and InNeuroCo for consultant services. MRL reports equity interest in Propio, Cerebrotech and Synchron, and grants from Stryker, Volcano Philips and Medtronic. MRL is part of the editorial board of JNIS. APK reports compensation from Penumbra and Microvention for consultant services. WB reports compensation for consultant services from Johnson & Johnson, Stryker, Medtronic Vascular and Microvention; compensation from MIVI Neurovascular for data and safety monitoring services; stock holdings from Marblehead Medical LLC. AJP reports compensation from DePuy Synthes Spine for consultant services. BG reports compensation from Microvention and Medtronic for consultant services. AA reports compensation from Johnson & Johnson and Cerenovous for consultant services. RMS reports consulting and teaching agreements with Penumbra, Abbott, Medtronic, InNeuroCo and Cerenovous. RD reports compensation from Grand Rounds for consultant services and compensation from NIH for other services. CD reports stock options from Euphrates Vascular; compensation from noNO and Penumbra, Inc for data and safety monitoring services. EAS is a proctor with Microvention and reports compensation from Medtronic and Rapid Medical for consultant services.

Auteurs

Sebastian Sanchez (S)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Ashrita Raghuram (A)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Linder Wendt (L)

Institute for Clinical and Translational Science, The University of Iowa, Iowa City, Iowa, USA.

Minako Hayakawa (M)

Department of Radiology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Ching-Jen Chen (CJ)

Department of Neurosurgery, The University of Texas Health Science Center at Houston, Houston, Texas, USA.

Jason P Sheehan (JP)

Department of Neurosurgery, University of Virginia Health System, Charlottesville, Virginia, USA.

Louis J Kim (LJ)

Department of Neurosurgery, University of Washington, Seattle, Washington, USA.

Isaac Josh Abecassis (IJ)

Department of Neurosurgery, University of Washington, Seattle, Washington, USA.

Michael R Levitt (MR)

Department of Neurosurgery, University of Washington, Seattle, Washington, USA.

R Michael Meyer (RM)

Department of Neurosurgery, University of Washington, Seattle, Washington, USA.

Ridhima Guniganti (R)

Department of Neurosurgery, Washington University School of Medicine in Saint Louis, St Louis, Missouri, USA.

Akash P Kansagra (AP)

Mallinckrodt Institute of Radiology, Washington University School of Medicine in Saint Louis, St Louis, Missouri, USA.

Giuseppe Lanzino (G)

Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.

Enrico Giordan (E)

Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.

Waleed Brinjikji (W)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Diederik O Bulters (DO)

Department of Neurosurgery, University Hospital Southampton NHS Foundation Trust, Southampton, Southampton, UK.

Andrew Durnford (A)

Department of Neurosurgery, University Hospital Southampton NHS Foundation Trust, Southampton, Southampton, UK.

W Christopher Fox (WC)

Department of Neurosurgery, Mayo Clinic Jacksonville Campus, Jacksonville, Florida, USA.

Jessica Smith (J)

Department of Neurosurgery, University of Florida, Gainesville, Florida, USA.

Adam J Polifka (AJ)

Department of Neurosurgery, University of Florida, Gainesville, Florida, USA.

Bradley Gross (B)

Department of Neurosurgery, University of Pittsburgh Medical Center Health System, Pittsburgh, Pennsylvania, USA.

Sepideh Amin-Hanjani (S)

Department of Neurosurgery, University of Illinois Chicago, Chicago, Illinois, USA.

Ali Alaraj (A)

Department of Neurosurgery, University of Illinois Chicago, Chicago, Illinois, USA.

Amanda Kwasnicki (A)

Department of Neurosurgery, University of Illinois Chicago, Chicago, Illinois, USA.

Robert M Starke (RM)

Department of Neurosurgery, University of Miami, Coral Gables, Florida, USA.

Stephanie H Chen (SH)

Department of Neurosurgery, University of Miami, Coral Gables, Florida, USA.

J Marc C van Dijk (JMC)

Department of Neurosurgery, University of Groningen, Groningen, Groningen, Netherlands.

Adriaan R E Potgieser (ARE)

Department of Neurosurgery, University of Groningen, Groningen, Groningen, Netherlands.

Junichiro Satomi (J)

Department of Neurosurgery, Tokushima University Hospital, Tokushima, Tokushima, Japan.

Yoshiteru Tada (Y)

Department of Neurosurgery, Tokushima University Hospital, Tokushima, Tokushima, Japan.

Ryan Phelps (R)

Department of Neurosurgery, University of California San Francisco, San Francisco, California, USA.

Adib Abla (A)

Department of Neurosurgery, University of California San Francisco, San Francisco, California, USA.

Ethan Winkler (E)

Department of Neurosurgery, University of California San Francisco, San Francisco, California, USA.

Rose Du (R)

Department of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Pui Man Rosalind Lai (PMR)

Department of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Gregory J Zipfel (GJ)

Department of Neurosurgery, Washington University School of Medicine in Saint Louis, St Louis, Missouri, USA.

Colin Derdeyn (C)

Department of Radiology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Edgar A Samaniego (EA)

Departments of Neurology, Radiology and Neurosurgery, The University of Iowa, Iowa City, Iowa, USA edgarsama@gmail.com.

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