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Diagnosis and treatment of Chiari malformation type 1 in children : the International Consensus Document

Authors :
Massimi, Luca
Peretta, Paola
Erbetta, Alessandra
Solari, Alessandra
Farinotti, Mariangela
Ciaramitaro, Palma
Saletti, Veronica
Caldarelli, Massimo
Canheu, Alexandre Casagrande
Celada, Carlo
Chiapparini, Luisa
Chieffo, Daniela
Cinalli, Giuseppe
Di Rocco, Federico
Furlanetto, Marika
Giordano, Flavio
Jallo, George
James, Syril
Lanteri, Paola
Lemarchand, Christian
Messing-Jünger, Martina
Parazzini, Cecilia
Paternoster, Giovanna
Piatelli, Gianluca
Poca Pastor, María Antonia
Prabahkar, Prab
Ricci, Federica
Righini, Andrea
Sala, Francesco
Sahuquillo Barris, Juan
Stoodley, Marcus
Talamonti, Giuseppe
Thompson, Dominic
Triulzi, Fabio
Zucchelli, Mino
Valentini, Laura
Universitat Autònoma de Barcelona
Institut Català de la Salut
[Massimi L] Pediatric Neurosurgery, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy. [Peretta P] Pediatric Neurosurgery, AOU Citta’ della Salute e della Scienza di Torino, Torino, Italy. [Erbetta A] Department of Neuroradiology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. [Solari A, Farinotti M] Neuroepidemiology Unit – Scientific Directorate, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. [Ciaramitaro P] Department of Neuroscience, AOU Citta’ della Salute e della Scienza di Torino, Torino, Italy. [Poca MA, Sahuquillo J] Unitat de Recerca en Neurotrauma i Neurocirurgia, Servei de Neurocirurgia i Neurocirurgia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
Vall d'Hebron Barcelona Hospital Campus
Source :
Dipòsit Digital de Documents de la UAB, Universitat Autònoma de Barcelona, Neurological Sciences, Scientia
Publication Year :
2021

Abstract

Background Chiari malformation type 1 (CM1) is a rare condition where agreed classification and treatment are still missing. The goal of this study is to achieve a consensus on the diagnosis and treatment of CM1 in children. Methods A multidisciplinary panel formulated 57 provisional statements based on a review of the literature. Thirty-four international experts (IE) participated in a Delphi study by independently rating each statement on a 4-point Likert scale (“strongly disagree,” “disagree,” “agree,” “strongly agree”). Statements that were endorsed (“agree” or “strongly agree”) by < 75% of raters were re-formulated, or new statements were added, and another Delphi round followed (up to a maximum of three). Results Thirty-five IE were contacted and 34 agreed to participate. A consensus was reached on 30/57 statements (52.6%) after round 1. Three statements were added, and one removed. After round 2, agreement was reached on 56/59 statements (94.9%). Finally, after round 3, which took place during the 2019 Chiari Consensus Conference (Milan, Italy), agreement was reached on 58/59 statements (98.3%) about four main sections (Definition and Classification, Planning, Surgery, Isolated Syringomyelia). Only one statement did not gain a consensus, which is the “definition of radiological failure 24 month post-surgery.” Conclusions The consensus document consists of 58 statements (24 on diagnosis, 34 on treatment), serving clinicians and researchers following children with CM1. There is a clear need for establishing an international network and registry and to promote collaborative studies to increase the evidence base and optimize the long-term care of this patient population.

Details

Language :
English
Database :
OpenAIRE
Journal :
Dipòsit Digital de Documents de la UAB, Universitat Autònoma de Barcelona, Neurological Sciences, Scientia
Accession number :
edsair.doi.dedup.....633247871cd24e5c56e459500a7f1d60