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Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study

PURPOSE: The aim of this study was to identify risk factors for ankle valgus in children with hereditary multiple exostoses (HME). METHODS: We retrospectively reviewed the medical records of patients with HME who were examined at our hospital between 2010 and 2020. Patients’ age and sex were recorde...

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Autores principales: Zhang, Wanglin, Wang, Zhigang, Chen, Mu, Li, Yuchan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Editorial Society of Bone & Joint Surgery 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381398/
https://www.ncbi.nlm.nih.gov/pubmed/34476027
http://dx.doi.org/10.1302/1863-2548.15.210032
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author Zhang, Wanglin
Wang, Zhigang
Chen, Mu
Li, Yuchan
author_facet Zhang, Wanglin
Wang, Zhigang
Chen, Mu
Li, Yuchan
author_sort Zhang, Wanglin
collection PubMed
description PURPOSE: The aim of this study was to identify risk factors for ankle valgus in children with hereditary multiple exostoses (HME). METHODS: We retrospectively reviewed the medical records of patients with HME who were examined at our hospital between 2010 and 2020. Patients’ age and sex were recorded along with radiographic variables including mechanical axis deviation (MAD), mechanical lateral distal tibia angle (LDTA), fibula/tibia length ratio (F/T); distal fibula station according to Malhotra’s classification, location of exostoses at the ankle joint and fibular neck/physis width (N/P) ratio, which were measured from radiographs. Binary logistic regression analysis was performed to identify significant independent risk factors for ankle valgus. RESULTS: There were 61 children (20 girls and 41 boys; 122 ankles) who met the inclusion criteria. The mean age was 10.4 years (sd 3.4) and mean LDTA was 83° (sd 7°). Ankle valgus was found in 64 ankles (52%). In addition to younger age, exostoses involving the lateral aspects of the distal tibial and the medial aspect of the distal fibula (odds ratio (OR) = 4.091; 95% confidence interval (CI) 1.065 to 15.712; p = 0.040), F/T ratio < 0.96 (OR = 4.457; 95% CI 1.498 to 13.261; p = 0.007) and N/P ratio > 1.6 (OR = 2.855; 95% CI 1.031 to 7.907; p = 0.043) were associated with an increased risk of developing ankle valgus, while sex and MAD were unrelated to its occurrence. CONCLUSION: Young age, exostoses involving both the distal tibia and fibula, the F/T ratio < 0.96 and fibular N/P width ratio > 1.6 seemed to be risk factors of developing ankle valgus. LEVELS OF EVIDENCE: Prognostic studies, IV
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spelling pubmed-83813982021-09-01 Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study Zhang, Wanglin Wang, Zhigang Chen, Mu Li, Yuchan J Child Orthop Original Clinical Article PURPOSE: The aim of this study was to identify risk factors for ankle valgus in children with hereditary multiple exostoses (HME). METHODS: We retrospectively reviewed the medical records of patients with HME who were examined at our hospital between 2010 and 2020. Patients’ age and sex were recorded along with radiographic variables including mechanical axis deviation (MAD), mechanical lateral distal tibia angle (LDTA), fibula/tibia length ratio (F/T); distal fibula station according to Malhotra’s classification, location of exostoses at the ankle joint and fibular neck/physis width (N/P) ratio, which were measured from radiographs. Binary logistic regression analysis was performed to identify significant independent risk factors for ankle valgus. RESULTS: There were 61 children (20 girls and 41 boys; 122 ankles) who met the inclusion criteria. The mean age was 10.4 years (sd 3.4) and mean LDTA was 83° (sd 7°). Ankle valgus was found in 64 ankles (52%). In addition to younger age, exostoses involving the lateral aspects of the distal tibial and the medial aspect of the distal fibula (odds ratio (OR) = 4.091; 95% confidence interval (CI) 1.065 to 15.712; p = 0.040), F/T ratio < 0.96 (OR = 4.457; 95% CI 1.498 to 13.261; p = 0.007) and N/P ratio > 1.6 (OR = 2.855; 95% CI 1.031 to 7.907; p = 0.043) were associated with an increased risk of developing ankle valgus, while sex and MAD were unrelated to its occurrence. CONCLUSION: Young age, exostoses involving both the distal tibia and fibula, the F/T ratio < 0.96 and fibular N/P width ratio > 1.6 seemed to be risk factors of developing ankle valgus. LEVELS OF EVIDENCE: Prognostic studies, IV The British Editorial Society of Bone & Joint Surgery 2021-08-20 /pmc/articles/PMC8381398/ /pubmed/34476027 http://dx.doi.org/10.1302/1863-2548.15.210032 Text en Copyright © 2021, The author(s) https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 International (CC BY-NC 4.0) licence (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed.
spellingShingle Original Clinical Article
Zhang, Wanglin
Wang, Zhigang
Chen, Mu
Li, Yuchan
Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
title Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
title_full Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
title_fullStr Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
title_full_unstemmed Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
title_short Risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
title_sort risk factors for ankle valgus in children with hereditary multiple exostoses: a retrospective cross-sectional study
topic Original Clinical Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381398/
https://www.ncbi.nlm.nih.gov/pubmed/34476027
http://dx.doi.org/10.1302/1863-2548.15.210032
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