Bony decompression vs duraplasty for Chiari I malformation: does the eternal dilemma matter?


Journal

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
ISSN: 1433-0350
Titre abrégé: Childs Nerv Syst
Pays: Germany
ID NLM: 8503227

Informations de publication

Date de publication:
10 2019
Historique:
received: 26 04 2019
accepted: 21 05 2019
pubmed: 19 6 2019
medline: 24 10 2020
entrez: 19 6 2019
Statut: ppublish

Résumé

The management of Chiari I malformation (CIM) still raises the problem of the optimal surgical treatment, with special regard to the "eternal dilemma" of the posterior fossa bony decompression alone (PFBD) or with duraplasty (PFBDD). The goal of the present review is to update the results (outcome and complications) of both techniques to better understand the correct indication for each of them. A review of the literature has been performed, focusing on the articles and the meta-analyses specifically addressing the problem of PFBD vs PFBDD. Also, the personal authors' experience is briefly discussed. PFBD (usually with C1 laminectomy, often with delamination of the external dural layer) is the most commonly used technique in children, especially if syringomyelia is absent. It ensures a high success rate, with > 80% clinical improvement and about 75% reduction of the syringomyelia, and a very low risk of complications, hospital stay, and costs. A certain risk of recurrence is present (2-12%). PFBDD (with autologous tissues or dural substitutes), on the other hand, is mostly used not only in adults but also in children with large syringomyelia. It is burdened by a higher risk of complications (namely, the CSF-related ones), longer hospital stay, and higher costs; however, it warrants a better clinical improvement (> 85%) and a lower risk of reoperation (2-3.5%). Eight meta-analyses of the literature (three on pediatric series and five in adult series) and one prospective study in children, published in the last decade, largely confirm these findings. PFBD and PFBDD are different techniques that are indicated for different types of patients. In children, PFBD has been demonstrated to represent the best choice, although some patients may require a more aggressive treatment. Therefore, the success in the management of CIM, with or without syringomyelia, depends on the correct indication to surgery and on a patient-tailored choice rather than on the surgical technique.

Identifiants

pubmed: 31209642
doi: 10.1007/s00381-019-04218-9
pii: 10.1007/s00381-019-04218-9
doi:

Types de publication

Comparative Study Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1827-1838

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Auteurs

Luca Massimi (L)

Neurochirurgia Infantile, Fondazione Policlinico Gemelli IRCCS, Rome, Italy. lmassmi@email.it.
Università Cattolica del Sacro Cuore, Istituto Neurochirurgia, Rome, Italy. lmassmi@email.it.

P Frassanito (P)

Neurochirurgia Infantile, Fondazione Policlinico Gemelli IRCCS, Rome, Italy.

F Bianchi (F)

Neurochirurgia Infantile, Fondazione Policlinico Gemelli IRCCS, Rome, Italy.

G Tamburrini (G)

Neurochirurgia Infantile, Fondazione Policlinico Gemelli IRCCS, Rome, Italy.
Università Cattolica del Sacro Cuore, Istituto Neurochirurgia, Rome, Italy.

M Caldarelli (M)

Neurochirurgia Infantile, Fondazione Policlinico Gemelli IRCCS, Rome, Italy.
Università Cattolica del Sacro Cuore, Istituto Neurochirurgia, Rome, Italy.

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