Clinical features and outcome in pediatric arteriovenous malformation: institutional multimodality treatment
- PMID: 36580118
- DOI: 10.1007/s00381-022-05800-4
Clinical features and outcome in pediatric arteriovenous malformation: institutional multimodality treatment
Abstract
Purpose: Intracranial arteriovenous-malformation (AVM) is a relatively rare condition in pediatrics, yet is a major cause of spontaneous intracranial hemorrhage with a risk of fatal hemorrhage reported to be between 4 and 29%. Little is known about vessel morphology and optimum treatment modalities including multimodality combination therapy and prognosis in children.
Methods: A retrospective review of all children presenting to our institution from 2006 to 2020 that had an AVM was undertaken.
Results: A total of 50 children were identified with median age of 11 (range 1-16) years. The mean follow-up was 7.6 years. Forty-one children presented as an emergency and of those, 40 had hemorrhage identified on initial brain imaging. The average nidus size was 25 mm, drainage was superficial in 51% of cases, and located in eloquent cortex in 56%. The supplemental Spetzler-Martin grading indicated 78% (39/50) were grade 4 and above (moderate to high risk). Primary treatment modalities included embolization in 50% (25) or SRS in 30% (15) and surgery in 20% (10).The AVM was obliterated on follow-up DSA in 66% children. Three children had post-treatment hemorrhage, two related to embolization and one the day following SRS, giving a re-bleed rate of 6%. The GOSE was available for 32 children at long term follow and 94% had a good outcome (GOSE 5-8). Two children died due to acute hemorrhage (4%).
Conclusion: The majority of children with AVM present with hemorrhage. The rebleed rate during definitive treatment is low at 6% over the study period. The selective use of the 3 modalities of treatment has significantly reduced mortality and severe disability.
Keywords: AVM; Arteriovenous malformation; Embolization; Pediatric; Stereotactic radiosurgery; Surgery.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Comment in
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Correspondence regarding "Clinical features and outcome in pediatric arteriovenous malformation: institutional multimodality treatment".Childs Nerv Syst. 2023 Dec;39(12):3337-3338. doi: 10.1007/s00381-023-06207-5. Epub 2023 Oct 30. Childs Nerv Syst. 2023. PMID: 37902888 No abstract available.
References
-
- Fullerton HJ, Wu YW, Zhao S, Johnston SC (2003) Risk of stroke in children: ethnic and gender disparities. Neurology 61:189–194. https://doi.org/10.1212/01.wnl.0000078894.79866.95 - DOI - PubMed
-
- Beslow LA, Licht DJ, Smith SE et al (2010) Predictors of outcome in childhood intracerebral hemorrhage: a prospective consecutive cohort study. Stroke 41:313–318. https://doi.org/10.1161/STROKEAHA.109.568071 - DOI - PubMed
-
- Di Rocco C, Tamburrini G, Rollo M (2000) Cerebral arteriovenous malformations in children. Acta Neurochir (Wien) 142:145–158. https://doi.org/10.1007/s007010050017 - DOI - PubMed
-
- Kumar R, Shukla D, Mahapatra AK (2009) Spontaneous intracranial hemorrhage in children. Pediatr Neurosurg 45:37–45. https://doi.org/10.1159/000202622 - DOI - PubMed
-
- Meyer-Heim AD, Boltshauser E (2003) Spontaneous intracranial haemorrhage in children: aetiology, presentation and outcome. Brain Dev 25:416–421. https://doi.org/10.1016/s0387-7604(03)00029-9 - DOI - PubMed
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