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A novel and simple classification for ligamentum teres pathology based on joint hypermobility

Ligamentum teres (LT) pathology (including synovitis, partial and complete tears) is common at the time of hip arthroscopy with a reported prevalence of 51–90%. Currently, there are four published classifications of LT injuries and tears. The majority focuses on differentiating partial from full thi...

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Autores principales: O’Donnell, John M, Arora, Manit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961003/
https://www.ncbi.nlm.nih.gov/pubmed/29876126
http://dx.doi.org/10.1093/jhps/hnx039
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author O’Donnell, John M
Arora, Manit
author_facet O’Donnell, John M
Arora, Manit
author_sort O’Donnell, John M
collection PubMed
description Ligamentum teres (LT) pathology (including synovitis, partial and complete tears) is common at the time of hip arthroscopy with a reported prevalence of 51–90%. Currently, there are four published classifications of LT injuries and tears. The majority focuses on differentiating partial from full thickness tears, whereas a more recently published classification also incorporates the presumed underlying mechanism of pathology. A recent review of the current classification systems found that all are deficient for lack of inclusion of what constitutes a normal ligament, lack of inclusion of synovitis as a source of pathology and lack of inclusion of hypermobility as part of the treatment algorithm. Also, the two most commonly used classification systems have only fair inter-observer reliability. Recent work has found that underlying joint hypermobility plays an important role in LT pathology and that the addition of capsular plication/suture at the time of surgery for LT pathology improves outcomes and reduces re-tear rates. In order to address these problems which have been identified with the currently available classification systems, we propose a novel and simple classification for LT pathology based on underlying joint hypermobility [as assessed by the Beighton test score (BTS)]. LT pathology is used to divide all patients into four types: 0 normal (which includes minor fraying), 1 synovitis (which would also include minor fraying), 2 partial tear and 3 complete tear. Further, all types are subdivided into two groups: Group A patients have no clinical evidence of joint hypermobility (BTS < 3), whereas Group B patients do have clinical evidence of joint hypermobility (BTS ≥ 4). On the basis of this classification system and the available literature, we have also developed a treatment algorithm for LT pathology.
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spelling pubmed-59610032018-06-06 A novel and simple classification for ligamentum teres pathology based on joint hypermobility O’Donnell, John M Arora, Manit J Hip Preserv Surg Review Articles Ligamentum teres (LT) pathology (including synovitis, partial and complete tears) is common at the time of hip arthroscopy with a reported prevalence of 51–90%. Currently, there are four published classifications of LT injuries and tears. The majority focuses on differentiating partial from full thickness tears, whereas a more recently published classification also incorporates the presumed underlying mechanism of pathology. A recent review of the current classification systems found that all are deficient for lack of inclusion of what constitutes a normal ligament, lack of inclusion of synovitis as a source of pathology and lack of inclusion of hypermobility as part of the treatment algorithm. Also, the two most commonly used classification systems have only fair inter-observer reliability. Recent work has found that underlying joint hypermobility plays an important role in LT pathology and that the addition of capsular plication/suture at the time of surgery for LT pathology improves outcomes and reduces re-tear rates. In order to address these problems which have been identified with the currently available classification systems, we propose a novel and simple classification for LT pathology based on underlying joint hypermobility [as assessed by the Beighton test score (BTS)]. LT pathology is used to divide all patients into four types: 0 normal (which includes minor fraying), 1 synovitis (which would also include minor fraying), 2 partial tear and 3 complete tear. Further, all types are subdivided into two groups: Group A patients have no clinical evidence of joint hypermobility (BTS < 3), whereas Group B patients do have clinical evidence of joint hypermobility (BTS ≥ 4). On the basis of this classification system and the available literature, we have also developed a treatment algorithm for LT pathology. Oxford University Press 2017-10-16 /pmc/articles/PMC5961003/ /pubmed/29876126 http://dx.doi.org/10.1093/jhps/hnx039 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Review Articles
O’Donnell, John M
Arora, Manit
A novel and simple classification for ligamentum teres pathology based on joint hypermobility
title A novel and simple classification for ligamentum teres pathology based on joint hypermobility
title_full A novel and simple classification for ligamentum teres pathology based on joint hypermobility
title_fullStr A novel and simple classification for ligamentum teres pathology based on joint hypermobility
title_full_unstemmed A novel and simple classification for ligamentum teres pathology based on joint hypermobility
title_short A novel and simple classification for ligamentum teres pathology based on joint hypermobility
title_sort novel and simple classification for ligamentum teres pathology based on joint hypermobility
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961003/
https://www.ncbi.nlm.nih.gov/pubmed/29876126
http://dx.doi.org/10.1093/jhps/hnx039
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