Symptomatic cerebral vasospasm after posterior fossa surgery in pediatric patients: single-center study and systematic literature review.

Childs Nerv Syst

Department of Pediatric Neurosurgery, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

Published: December 2024

AI Article Synopsis

  • The study investigates symptomatic vasospasm in pediatric patients who had surgery on the posterior fossa, noting that it’s a rare complication primarily linked to subarachnoid hemorrhage.
  • One patient out of 178 developed symptomatic diffuse vasospasm post-surgery, and literature reviews found only 9 additional cases involving various intra- and extra-axial lesions.
  • The findings suggest that while iatrogenic vasospasm in children post-surgery is uncommon, outcomes can vary widely, and more awareness is needed among medical professionals regarding this complication, though definitive risk factors remain unclear due to the limited number of cases.

Article Abstract

Purpose: The most common cause of cerebral vasospasm is subarachnoid hemorrhage, less frequently it occurs after trauma, infection, and tumor resection. Vasospasm in children is rare and has not been systematically investigated in posterior fossa surgery.

Methods: The authors undertook a single-center retrospective study of all the pediatric patients who underwent surgery on the posterior fossa and presented with postoperative symptomatic vasospasm in the period from January 2018 to February 2024. Subsequently, a systematic literature review in accordance with the PRISMA guidelines was performed in the PubMed and Scopus databases to identify the published papers on symptomatic vasospasm after posterior fossa surgery in children.

Results: Of the 178 patients who underwent surgery on the posterior fossa, only one patient was diagnosed with symptomatic diffuse vasospasm on postoperative day 21. The systematic literature review provided further 9 children. The underlying pathology comprised 8 intra-axial lesions with 4 medulloblastomas, 1 schwannoma in the medulla oblongata, 1 pilocytic astrocytoma, 1 primitive neuroectodermal tumor, and 1 arteriovenous malformation. The extra-axial lesions were 1 hypoglossal schwannoma and 1 oculomotor nerve schwannoma.

Conclusion: Iatrogenic symptomatic vasospasm after posterior fossa surgery in children is a rare complication with an outcome ranging from complete recovery to the death of the patient. It is important for all staff involved in the care of patients undergoing surgery on the posterior fossa to be aware of this rare postoperative complication. The small number of patients affected does not allow a substantiated conclusion to be drawn about predictive risk factors.

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Source
http://dx.doi.org/10.1007/s00381-024-06630-2DOI Listing

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