Skip to main content

Long-term outcomes of pediatric arteriovenous malformations: the 30-year Pittsburgh experience.

Publication ,  Journal Article
McDowell, MM; Agarwal, N; Mao, G; Johnson, S; Kano, H; Lunsford, LD; Greene, S
Published in: J Neurosurg Pediatr
September 1, 2020

OBJECTIVE: The study of pediatric arteriovenous malformations (pAVMs) is complicated by the rarity of the entity. Treatment choice has often been affected by the availability of different modalities and the experience of the providers present. The University of Pittsburgh experience of multimodality treatment of pAVMs is presented. METHODS: The authors conducted a retrospective cohort study examining 212 patients with pAVM presenting to the University of Pittsburgh between 1988 and 2018, during which patients had access to surgical, endovascular, and radiosurgical options. Univariate analysis was performed comparing good and poor outcomes. A poor outcome was defined as a modified Rankin Scale (mRS) score of ≥ 3. Multivariate analysis via logistic regression was performed on appropriate variables with a p value of ≤ 0.2. Seventy-five percent of the cohort had at least 3 years of follow-up. RESULTS: Five patients (2.4%) did not receive any intervention, 131 (61.8%) had GKRS alone, 14 (6.6%) had craniotomies alone, and 2 (0.9%) had embolization alone. Twenty-two (10.4%) had embolization and Gamma Knife radiosurgery (GKRS); 20 (9.4%) had craniotomies and GKRS; 8 (3.8%) had embolization and craniotomies; and 10 (4.7%) had embolization, craniotomies, and GKRS. Thirty-one patients (14.6%) were found to have poor outcome on follow-up. The multivariate analysis performed in patients with poor outcomes was notable for associations with no treatment (OR 18.9, p = 0.02), hemorrhage requiring craniotomy for decompression alone (OR 6, p = 0.03), preoperative mRS score (OR 2.1, p = 0.004), and Spetzler-Martin score (OR 1.8, p = 0.0005). The mean follow-up was 79.7 ± 62.1 months. The confirmed radiographic obliteration rate was 79.4% and there were 5 recurrences found on average 9.5 years after treatment. CONCLUSIONS: High rates of long-term functional independence (mRS score of ≤ 2) can be achieved with comprehensive multimodality treatment of pAVMs. At this center there was no difference in outcome based on treatment choice when accounting for factors such as Spetzler-Martin grade and presenting morbidity. Recurrences are rare but frequently occur years after treatment, emphasizing the need for long-term screening after obliteration.

Duke Scholars

Published In

J Neurosurg Pediatr

DOI

EISSN

1933-0715

Publication Date

September 1, 2020

Volume

26

Issue

3

Start / End Page

275 / 282

Location

United States

Related Subject Headings

  • Neurology & Neurosurgery
  • 3213 Paediatrics
  • 3209 Neurosciences
  • 1114 Paediatrics and Reproductive Medicine
 

Citation

APA
Chicago
ICMJE
MLA
NLM
McDowell, M. M., Agarwal, N., Mao, G., Johnson, S., Kano, H., Lunsford, L. D., & Greene, S. (2020). Long-term outcomes of pediatric arteriovenous malformations: the 30-year Pittsburgh experience. J Neurosurg Pediatr, 26(3), 275–282. https://doi.org/10.3171/2020.3.PEDS19614
McDowell, Michael M., Nitin Agarwal, Gordon Mao, Stephen Johnson, Hideyuki Kano, L Dade Lunsford, and Stephanie Greene. “Long-term outcomes of pediatric arteriovenous malformations: the 30-year Pittsburgh experience.J Neurosurg Pediatr 26, no. 3 (September 1, 2020): 275–82. https://doi.org/10.3171/2020.3.PEDS19614.
McDowell MM, Agarwal N, Mao G, Johnson S, Kano H, Lunsford LD, et al. Long-term outcomes of pediatric arteriovenous malformations: the 30-year Pittsburgh experience. J Neurosurg Pediatr. 2020 Sep 1;26(3):275–82.
McDowell, Michael M., et al. “Long-term outcomes of pediatric arteriovenous malformations: the 30-year Pittsburgh experience.J Neurosurg Pediatr, vol. 26, no. 3, Sept. 2020, pp. 275–82. Pubmed, doi:10.3171/2020.3.PEDS19614.
McDowell MM, Agarwal N, Mao G, Johnson S, Kano H, Lunsford LD, Greene S. Long-term outcomes of pediatric arteriovenous malformations: the 30-year Pittsburgh experience. J Neurosurg Pediatr. 2020 Sep 1;26(3):275–282.

Published In

J Neurosurg Pediatr

DOI

EISSN

1933-0715

Publication Date

September 1, 2020

Volume

26

Issue

3

Start / End Page

275 / 282

Location

United States

Related Subject Headings

  • Neurology & Neurosurgery
  • 3213 Paediatrics
  • 3209 Neurosciences
  • 1114 Paediatrics and Reproductive Medicine