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.
Massimi, L., Peretta, P., Erbetta, A., Solari, A., Farinotti, M., Ciaramitaro, P., Saletti, V., Caldarelli, M., Canheu, A. C., Celada, C., Chiapparini, L., Chieffo, D. P. R., Cinalli, G., Di Rocco, F., Furlanetto, M., Giordano, F., Jallo, G., James, S., Lanteri, P., Lemarchand, C., Messing-Junger, M., Parazzini, C., Paternoster, G., Piatelli, G., Poca, M. A., Prabahkar, P., Ricci, F., Righini, A., Sala, F., Sahuquillo, J., Stoodley, M., Talamonti, G., Thompson, D., Triulzi, F., Zucchelli, M., Valentini, L., Diagnosis and treatment of Chiari malformation type 1 in children: the International Consensus Document, <<NEUROLOGICAL SCIENCES>>, 2022; 43 (2): 1311-1326. [doi:10.1007/s10072-021-05317-9] [https://hdl.handle.net/10807/326914]
Diagnosis and treatment of Chiari malformation type 1 in children: the International Consensus Document
Massimi, Luca;Chieffo, Daniela Pia Rosaria;Lanteri, Paola;
2022
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.| File | Dimensione | Formato | |
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