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Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
Infantile dural arteriovenous fistula: a reconsideration
Soliman Oushy1,2, Darren B Orbach3
1Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Infantile-type dural arteriovenous shunts (IDAVS) are rare pediatric vascular lesions. Stepwise embolization offers favorable outcomes, suggesting a revised classification for better diagnosis and treatment.
Area of Science:
- Pediatric Neurology
- Vascular Surgery
- Neuroradiology
Background:
- Infantile-type dural arteriovenous shunts (IDAVS) are rare and heterogeneous vascular lesions.
- Current classification systems for pediatric dural arteriovenous shunts (DAVS) are inadequate due to variable presentations.
- The study aims to determine IDAVS prevalence and long-term outcomes after endovascular treatment (EVT).
Purpose of the Study:
- To estimate the prevalence of infantile-type dural arteriovenous shunts (IDAVS) in a pediatric population.
- To evaluate the long-term clinical and radiographic outcomes following endovascular treatment (EVT) for IDAVS.
- To propose a revised classification system for pediatric dural arteriovenous shunts (DAVS).
Main Methods:
- Retrospective review of a pediatric cerebrovascular database (2006-2023).
- Analysis of clinical and radiographic data for presentation and outcomes of IDAVS.
- Evaluation of endovascular treatment (EVT) strategies and outcomes.
Main Results:
- IDAVS identified in 0.5% of patients (8/1463), with a mean age of 34.7 months.
- Common presentations included macrocephaly (37.5%) and seizures (25%).
- EVT performed in 87.5% of cases, achieving 28.6% radiographic obliteration and 85.7% good clinical outcomes (mRS ≤2).
Conclusions:
- IDAVS are rare, heterogeneous pediatric cerebrovascular pathologies.
- Stepwise selective embolization is recommended over aggressive approaches for favorable outcomes.
- A revised classification bifurcating pediatric DAVS into dural sinus malformations and other DAVS enhances diagnostic clarity and therapeutic approaches.
Background:
Infantile-type dural arteriovenous shunts (IDAVS) are rare and heterogeneous vascular lesions, complicating their classification and management. The current tripartite classification of pediatric dural arteriovenous shunts (DAVS) into dural sinus malformation, infantile-type, and adult-type, does not stand up to scrutiny, given the variable presentations of the latter two types in children. We estimate the prevalence of IDAVS and evaluate the long term outcomes after endovascular treatment (EVT).
Methods:
A retrospective review of a pediatric cerebrovascular database between 2006 and 2023 was conducted. Clinical and radiographic data were analyzed to evaluate the presentation and long term outcomes of IDAVS.
Results:
IDAVS were identified in 8 (0.5%) of 1463 patients, with mean age at diagnosis of 34.7 months; male infants comprised 62.5%. The most common clinical presentations included macrocephaly (37.5%), seizures (25%), and dilated scalp veins (25%). EVT was performed in 87.5% of cases, averaging 5.8 procedures per patient. Radiographic obliteration was observed in 28.6%. Good clinical outcomes (modified Rankin Scale score of ≤2) were achieved in 85.7%. Our findings showcased discrepancies and limitations in the current classification of pediatric DAVS, prompting a re-evaluation.
Conclusion:
IDAVS accounted for a small proportion of pediatric cerebrovascular pathologies, with markedly heterogeneous presentations. Stepwise selective embolization was associated with favorable outcomes, and is recommended over an aggressive approach with the goal of complete angiographic obliteration. Our proposed revised classification system bifurcates pediatric DAVS into dural sinus malformations and all other DAVS that are manifest in children, thereby enhancing diagnostic clarity and therapeutic approaches.
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