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Background: Intracranial dural arteriovenous fistulas (DAVFs) are rare lesions, making it challenging to fully understand and improve their management. Globally, only two major large-scale studies have focused on DAVFs. This report outlines the design of the DREAM-INI (Dural arteriovenous fistula research and management in China) project and provides an overview of the 1101-patient cohort it includes.
Methods: Patient data were sourced from the DREAM-INI database, a retrospective, single-center observational study conducted from January 2001 to December 2022, encompassing a total of 1101 DAVF patients.
Results: The cohort consists of 367 patients diagnosed with Borden type I DAVFs, 172 patients with Borden type II fistulas, and 562 patients with Borden type III fistulas. 565 patients exhibited flow-related symptoms, 176 patients presented with intracranial hemorrhage, and 275 patients had non-hemorrhagic neurological deficits. A large proportion of patients (95.6%, 1053/1101) underwent treatment through endovascular embolization (83.7%, 922/1101), surgery (8.7%, 96/1101), or multimodal therapy (3.2%, 35/1101). The overall immediate angiographic cure rate was 85.2% (897/1053 treated cases), and the rate of treatment-related permanent neurological morbidity was 3.4% (45/1328 total procedures). The median duration from the final treatment to the last follow-up for DAVF was 39 months. The predictive factors for aggressive symptoms, initial angiographic cure, and complications in DAVFs have also been preliminarily explored.
Conclusions: With over 1100 patients, DREAM-INI represents a large and relatively well-documented registry of DAVF patient data in China and even globally. This database will enable numerous future studies, further advancing our understanding of this rare disease.
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http://dx.doi.org/10.1136/jnis-2024-023014 | DOI Listing |
Cureus
July 2025
General Internal Medicine, King's Mill Hospital, Sherwood Forest Hospitals NHS Foundation Trust, Sutton-in-Ashfield, GBR.
A man in his 70s with known vascular risk factors presented with acute onset of bilateral lower limb weakness and urinary retention. Initial spinal magnetic resonance imaging (MRI) revealed a longitudinally extensive myelopathy. It was initially interpreted as transverse myelitis, prompting treatment with high-dose corticosteroids.
View Article and Find Full Text PDFNMC Case Rep J
August 2025
Department of Neurosurgery, Osaka Neurological Institute, Toyonaka, Osaka, Japan.
Dural arteriovenous fistula can present with cerebral venous sinus thrombosis and retrograde leptomeningeal venous drainage. Given the associated intracranial hemorrhage risk, immediate retrograde leptomeningeal venous drainage obliteration is desirable. Herein, we report a case of dural arteriovenous fistula with acute cerebral venous sinus thrombosis and intracranial hemorrhage that was successfully managed using sinus thrombectomy alone.
View Article and Find Full Text PDFWorld Neurosurg
August 2025
Section of Neurosurgery, Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Jeddah, Saudi Arabia. Electronic address:
Background: Spinal dural arteriovenous fistulas (SDAVFs) are the most prevalent type of spinal vascular malformation and can lead to progressive neurological impairments if left untreated. Endovascular embolization and microsurgical resection are treatment options, although the optimal treatment method remains a subject of debate.
Objective: A comprehensive systematic review and meta-analysis to compare the endovascular and microsurgical treatment outcomes of SDAVFs.
Neurosurg Rev
August 2025
Department of Neurology, First Hospital of Shanxi Medical University, No. 85, Jiefangnan Street, Yingze District, Taiyuan City, 030001, Shanxi Province, China.
Dural arteriovenous fistulas (DAVFs) are abnormal arteriovenous shunts that occur between intracranial arteries and venous sinuses, meningeal veins, or cortical veins. These lesions can lead to pathological changes such as cerebral edema, increased intracranial pressure, metabolic dysfunction in the brain, venous sinus thrombosis, and vascular rupture with hemorrhage. Clinically, DAVFs rarely present as Parkinsonism, often coexisting with dementia.
View Article and Find Full Text PDFRinsho Shinkeigaku
August 2025
Department of Neurology, Dokkyo Medical University Saitama Medical Center.
A 65-year-old man was admitted to our hospital following a sudden loss of consciousness and seizures. He presented with fever, and a head MRI revealed lesions in the left medial and lateral temporal lobes, as well as the thalamus. Initially, he was treated for suspected limbic encephalitis, including herpes simplex encephalitis (HSE).
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