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Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK

Objective: Paediatric scoliosis (PS) and Chiari malformation type 1 (CM-1) have been reported to be associated with each other. Scoliosis curvature is a common finding among patients operated for CM-1, and curve development has been related to it. We report a cohort of PS and CM-1 patients managed w...

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Autores principales: Hershkovich, Oded, Lotan, Raphael, Steinberg, Netanel, Katzouraki, Galateia, D’Aquino, Daniel, Tsegaye, Magnum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219386/
https://www.ncbi.nlm.nih.gov/pubmed/37240514
http://dx.doi.org/10.3390/jcm12103409
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author Hershkovich, Oded
Lotan, Raphael
Steinberg, Netanel
Katzouraki, Galateia
D’Aquino, Daniel
Tsegaye, Magnum
author_facet Hershkovich, Oded
Lotan, Raphael
Steinberg, Netanel
Katzouraki, Galateia
D’Aquino, Daniel
Tsegaye, Magnum
author_sort Hershkovich, Oded
collection PubMed
description Objective: Paediatric scoliosis (PS) and Chiari malformation type 1 (CM-1) have been reported to be associated with each other. Scoliosis curvature is a common finding among patients operated for CM-1, and curve development has been related to it. We report a cohort of PS and CM-1 patients managed with posterior fossa and upper cervical decompression (PFUCD) by a single surgeon, with an average of two years of follow-up. Methods: We present a retrospective cohort in a single referral centre for patients with CM-1 and PS. Results: From 2011 to 2018, we identified fifteen patients with CM-1 and PS; eleven underwent PFUCD, ten had symptomatic CM-1, and one had asymptomatic CM-1 but showed curve progression. The remaining four CM-1 patients were asymptomatic and were hence treated conservatively. The average follow-up post-PFUCD was 26.2 months. Scoliosis surgery was performed in seven cases; six patients underwent PFUCD prior to the scoliosis correction. One scoliosis case underwent surgery in the presence of mild CM-1 treated conservatively. The remaining four cases were scheduled for scoliosis correction surgery, while three were managed conservatively, with one case lost to follow-up. The average time between PFUCD and scoliosis surgery was 11 months. None of the cases had intraoperative neuromonitoring alerts or perioperative neurological complications. Conclusion: CM-1 with concomitant scoliosis can be found. Symptomatic CM-1 might require surgery, but as we discovered, PFUCD had negligible effect on curve progression and the future need for scoliosis surgery.
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spelling pubmed-102193862023-05-27 Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK Hershkovich, Oded Lotan, Raphael Steinberg, Netanel Katzouraki, Galateia D’Aquino, Daniel Tsegaye, Magnum J Clin Med Brief Report Objective: Paediatric scoliosis (PS) and Chiari malformation type 1 (CM-1) have been reported to be associated with each other. Scoliosis curvature is a common finding among patients operated for CM-1, and curve development has been related to it. We report a cohort of PS and CM-1 patients managed with posterior fossa and upper cervical decompression (PFUCD) by a single surgeon, with an average of two years of follow-up. Methods: We present a retrospective cohort in a single referral centre for patients with CM-1 and PS. Results: From 2011 to 2018, we identified fifteen patients with CM-1 and PS; eleven underwent PFUCD, ten had symptomatic CM-1, and one had asymptomatic CM-1 but showed curve progression. The remaining four CM-1 patients were asymptomatic and were hence treated conservatively. The average follow-up post-PFUCD was 26.2 months. Scoliosis surgery was performed in seven cases; six patients underwent PFUCD prior to the scoliosis correction. One scoliosis case underwent surgery in the presence of mild CM-1 treated conservatively. The remaining four cases were scheduled for scoliosis correction surgery, while three were managed conservatively, with one case lost to follow-up. The average time between PFUCD and scoliosis surgery was 11 months. None of the cases had intraoperative neuromonitoring alerts or perioperative neurological complications. Conclusion: CM-1 with concomitant scoliosis can be found. Symptomatic CM-1 might require surgery, but as we discovered, PFUCD had negligible effect on curve progression and the future need for scoliosis surgery. MDPI 2023-05-11 /pmc/articles/PMC10219386/ /pubmed/37240514 http://dx.doi.org/10.3390/jcm12103409 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Hershkovich, Oded
Lotan, Raphael
Steinberg, Netanel
Katzouraki, Galateia
D’Aquino, Daniel
Tsegaye, Magnum
Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK
title Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK
title_full Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK
title_fullStr Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK
title_full_unstemmed Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK
title_short Treatment of Chiari Malformation and Concomitant Paediatric Scoliosis Long-Term Follow-Up in One Major Referral Centre in the UK
title_sort treatment of chiari malformation and concomitant paediatric scoliosis long-term follow-up in one major referral centre in the uk
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219386/
https://www.ncbi.nlm.nih.gov/pubmed/37240514
http://dx.doi.org/10.3390/jcm12103409
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