Transient meningism in children after non-autologous duraplasty for Chiari Malformation surgery: A case series.


Journal

Neuro-Chirurgie
ISSN: 1773-0619
Titre abrégé: Neurochirurgie
Pays: France
ID NLM: 0401057

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 18 11 2022
revised: 14 01 2023
accepted: 31 01 2023
medline: 28 3 2023
pubmed: 13 2 2023
entrez: 12 2 2023
Statut: ppublish

Résumé

Increasing the posterior fossa volume is the mainstay of treatment for Chiari type 1 Malformation (C1M) and type 1.5 (C1.5M). Different options to restore CSF flow have been described but no consensus has been reached yet. Bony decompression of posterior cranial fossa with dural opening provides good results but at the price of complications such as pseudomeningocele and aseptic meningitis. A single center retrospective analysis was conducted to find any relationships between outcome and perioperative factors. As a second goal a specific analysis was conducted on the complications and their hypothetical causes. All the pediatric patients who underwent to posterior fossa bony decompression and dural opening for C1M or C1.5M in the period 2008-2020 were included in the study. A minimum period of three-months follow-up was considered among the inclusion criteria. A population of fifty-three consecutive patients was collected. Pseudomeningocele and a mild meningeal irritation resulted the most frequent complications. Considering preoperative and intraoperative factors, the type of dural graft showed a relatively strong correlation (P<.01) with pseudomeningocele appearance and the development of meningism. In the latter case, a short course of steroids was the only treatment required to control symptoms. Different factors could influence the outcome in Chiari Malformation surgery and eventually the development of complications. An adequate dural graft selection is of paramount importance when a dural opening for posterior fossa augmentation is planned. In case of mild meningeal irritation, a trial with short course steroids could avoid revision surgery.

Sections du résumé

BACKGROUND BACKGROUND
Increasing the posterior fossa volume is the mainstay of treatment for Chiari type 1 Malformation (C1M) and type 1.5 (C1.5M). Different options to restore CSF flow have been described but no consensus has been reached yet. Bony decompression of posterior cranial fossa with dural opening provides good results but at the price of complications such as pseudomeningocele and aseptic meningitis. A single center retrospective analysis was conducted to find any relationships between outcome and perioperative factors. As a second goal a specific analysis was conducted on the complications and their hypothetical causes.
METHODS METHODS
All the pediatric patients who underwent to posterior fossa bony decompression and dural opening for C1M or C1.5M in the period 2008-2020 were included in the study. A minimum period of three-months follow-up was considered among the inclusion criteria.
RESULTS RESULTS
A population of fifty-three consecutive patients was collected. Pseudomeningocele and a mild meningeal irritation resulted the most frequent complications. Considering preoperative and intraoperative factors, the type of dural graft showed a relatively strong correlation (P<.01) with pseudomeningocele appearance and the development of meningism. In the latter case, a short course of steroids was the only treatment required to control symptoms.
CONCLUSIONS CONCLUSIONS
Different factors could influence the outcome in Chiari Malformation surgery and eventually the development of complications. An adequate dural graft selection is of paramount importance when a dural opening for posterior fossa augmentation is planned. In case of mild meningeal irritation, a trial with short course steroids could avoid revision surgery.

Identifiants

pubmed: 36775120
pii: S0028-3770(23)00020-6
doi: 10.1016/j.neuchi.2023.101423
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101423

Informations de copyright

Copyright © 2023 Elsevier Masson SAS. All rights reserved.

Auteurs

R De Marco (R)

Department of Neurosurgery, Istituto Giannina Gaslini Children's Hospital, Genova, Italy; Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", "Città della Salute e della Scienza" University Hospital, University of Turin, Turin, Italy. Electronic address: r_dema@outlook.it.

G Piatelli (G)

Department of Neurosurgery, Istituto Giannina Gaslini Children's Hospital, Genova, Italy.

I Portonero (I)

Department of Neurosurgery, Istituto Giannina Gaslini Children's Hospital, Genova, Italy; Neurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", "Città della Salute e della Scienza" University Hospital, University of Turin, Turin, Italy.

P Fiaschi (P)

Section of Neurosurgery, IRCCS Ospedale Policlinico San Martino, Genova, Italy; Dipertimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze materno infantili (DINOGMI), IRCCS Ospedale Policlinico San Martino, Università di Genova, Genova, Italy.

F Secci (F)

Department of Neurosurgery, Istituto Giannina Gaslini Children's Hospital, Genova, Italy.

M Pacetti (M)

Department of Neurosurgery, Istituto Giannina Gaslini Children's Hospital, Genova, Italy.

M Pavanello (M)

Department of Neurosurgery, Istituto Giannina Gaslini Children's Hospital, Genova, Italy.

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Classifications MeSH