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The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists

BACKGROUND: Developmental dysplasia of the hip (DDH) is the most common orthopaedic disorder in newborns. Despite this considerable variation in practice exists. The aim of this study was to determine the clinical relevance and a ranking order for the diagnostic criteria in DDH amongst paediatric or...

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Autores principales: Williams, Daniel, Protopapa, Evangelia, Stohr, Kuldeep, Hunter, James B., Roposch, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719727/
https://www.ncbi.nlm.nih.gov/pubmed/26787538
http://dx.doi.org/10.1186/s12891-016-0867-4
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author Williams, Daniel
Protopapa, Evangelia
Stohr, Kuldeep
Hunter, James B.
Roposch, Andreas
author_facet Williams, Daniel
Protopapa, Evangelia
Stohr, Kuldeep
Hunter, James B.
Roposch, Andreas
author_sort Williams, Daniel
collection PubMed
description BACKGROUND: Developmental dysplasia of the hip (DDH) is the most common orthopaedic disorder in newborns. Despite this considerable variation in practice exists. The aim of this study was to determine the clinical relevance and a ranking order for the diagnostic criteria in DDH amongst paediatric orthopaedic surgeons practicing in the UK. METHOD: One hundred members of the British Society of Children’s Orthopaedic Surgery (BSCOS) were asked to rate the importance of 37 criteria useful in the diagnosis of DDH in newborns, using a 10 cm visual analogue scale. We determined the consistency among specialists in rating the criteria with the intraclass correlation coefficient (ICC) and compared the results to a group of international peers. RESULTS: Ortolani/Barlow tests, asymmetry in abduction ≥20° and a first-degree relative treated for DDH ranked among the top ten. Participants demonstrated poor consistency in rating the 37 criteria (ICC 0.39; 95 % CI 0.29, 0.52), but for clinical examination criteria alone their consistency improved (ICC 0.52; 0.35, 0.75). The importance ratings of members of BSCOS and members of the European Paediatric Orthopaedic Society differed for 15/37 (41 %) criteria (p <0.05). CONCLUSIONS: Members of BSCOS had a preference for criteria relating to clinical examination and ultrasound. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12891-016-0867-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-47197272016-01-21 The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists Williams, Daniel Protopapa, Evangelia Stohr, Kuldeep Hunter, James B. Roposch, Andreas BMC Musculoskelet Disord Research Article BACKGROUND: Developmental dysplasia of the hip (DDH) is the most common orthopaedic disorder in newborns. Despite this considerable variation in practice exists. The aim of this study was to determine the clinical relevance and a ranking order for the diagnostic criteria in DDH amongst paediatric orthopaedic surgeons practicing in the UK. METHOD: One hundred members of the British Society of Children’s Orthopaedic Surgery (BSCOS) were asked to rate the importance of 37 criteria useful in the diagnosis of DDH in newborns, using a 10 cm visual analogue scale. We determined the consistency among specialists in rating the criteria with the intraclass correlation coefficient (ICC) and compared the results to a group of international peers. RESULTS: Ortolani/Barlow tests, asymmetry in abduction ≥20° and a first-degree relative treated for DDH ranked among the top ten. Participants demonstrated poor consistency in rating the 37 criteria (ICC 0.39; 95 % CI 0.29, 0.52), but for clinical examination criteria alone their consistency improved (ICC 0.52; 0.35, 0.75). The importance ratings of members of BSCOS and members of the European Paediatric Orthopaedic Society differed for 15/37 (41 %) criteria (p <0.05). CONCLUSIONS: Members of BSCOS had a preference for criteria relating to clinical examination and ultrasound. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12891-016-0867-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-19 /pmc/articles/PMC4719727/ /pubmed/26787538 http://dx.doi.org/10.1186/s12891-016-0867-4 Text en © Williams et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Williams, Daniel
Protopapa, Evangelia
Stohr, Kuldeep
Hunter, James B.
Roposch, Andreas
The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists
title The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists
title_full The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists
title_fullStr The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists
title_full_unstemmed The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists
title_short The most relevant diagnostic criteria for developmental dysplasia of the hip: a study of British specialists
title_sort most relevant diagnostic criteria for developmental dysplasia of the hip: a study of british specialists
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719727/
https://www.ncbi.nlm.nih.gov/pubmed/26787538
http://dx.doi.org/10.1186/s12891-016-0867-4
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