Management of pediatric intracranial arteriovenous malformations: experience with multimodality therapy

Tim E Darsaut1, Raphael Guzman, Mary L Marcellus

  • 1Department of Neurosurgery, Stanford University School of Medicine, Stanford, California 94305-5325, USA.

Neurosurgery
|March 25, 2011
PubMed

Insights

Multimodality therapy improves obliteration rates for pediatric arteriovenous malformations (AVMs), reducing hemorrhage risk. Careful consideration of intervention risks is crucial for high-grade AVMs.

Area of Science:

  • Neurology
  • Vascular Surgery
  • Pediatric Neurosurgery

Background:

  • Pediatric arteriovenous malformations (AVMs) present complex management challenges.
  • Successful treatment often necessitates a combination of embolization, surgery, and radiosurgery.

Purpose of the Study:

  • To evaluate the efficacy and outcomes of multimodality treatment for pediatric AVMs.
  • To analyze factors influencing treatment success and clinical outcomes in this population.

Main Methods:

  • A retrospective analysis of 120 pediatric patients (<18 years) with AVMs treated between 1985 and 2009.
  • Patients received combined or single-modality treatments including radiosurgery, surgery, and endovascular techniques.
  • Outcomes assessed included AVM obliteration rates, hemorrhage risk, neurological complications, and functional status (modified Rankin Scale).

Main Results:

  • Multimodality therapy significantly improved AVM obliteration rates, especially for high-grade lesions (9% to 26%).
  • Disabling neurological complications were more frequent in high-grade AVMs (28%) compared to low-grade (5%).
  • Poor final outcomes (mRS ≥ 2) were associated with higher baseline mRS, left-sided location, and high AVM grade.

Conclusions:

  • Multimodality therapy offers substantial improvements in obliteration rates and may reduce hemorrhage risk for pediatric AVMs.
  • The inherent risks of intervention necessitate careful consideration, particularly for high-grade pediatric AVMs with a poor natural history.
Abstract