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Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention

Hip dysplasia is a common cause of hip pain and a known risk factor for hip osteoarthritis (OA) and early total hip arthroplasty (THA). Unfortunately, little is known about the specific factors associated with an increased risk of OA. The purpose was (i) to report the overall rate of symptomatic hip...

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Autores principales: Melugin, Heath P, Hale, Rena F, Lee, Dustin R, LaPrade, Matthew D, Okoroha, Kelechi R, Sierra, Rafael J, Trousdale, Robert T, Levy, Bruce A, Krych, Aaron J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142191/
https://www.ncbi.nlm.nih.gov/pubmed/35651707
http://dx.doi.org/10.1093/jhps/hnac007
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author Melugin, Heath P
Hale, Rena F
Lee, Dustin R
LaPrade, Matthew D
Okoroha, Kelechi R
Sierra, Rafael J
Trousdale, Robert T
Levy, Bruce A
Krych, Aaron J
author_facet Melugin, Heath P
Hale, Rena F
Lee, Dustin R
LaPrade, Matthew D
Okoroha, Kelechi R
Sierra, Rafael J
Trousdale, Robert T
Levy, Bruce A
Krych, Aaron J
author_sort Melugin, Heath P
collection PubMed
description Hip dysplasia is a common cause of hip pain and a known risk factor for hip osteoarthritis (OA) and early total hip arthroplasty (THA). Unfortunately, little is known about the specific factors associated with an increased risk of OA. The purpose was (i) to report the overall rate of symptomatic hip OA and THA and (ii) to identify radiographic features and patient characteristics associated with the development of symptomatic hip OA. A geographic database was used to identify all patients aged 14–50 years old diagnosed with symptomatic hip dysplasia between 2000 and 2016. Kaplan–Meier analysis was used to determine the rate of symptomatic hip OA, defined as a Tönnis grade of ≥1 on hip radiograph. Univariate and multivariate proportional hazard regression models were performed to determine risk factors for OA. One hundred and fifty-nine hips (144 patients) with hip dysplasia (52 F:107 M) out of 1893 patients with hip pain were included. Of these, 45 (28%) had severe hip dysplasia with a lateral center-edge angle ≤18°. Mean age at time of presentation was 26.1 (±10.1) years. Mean follow-up time was 8.2 (±5) years. The rate of OA was 20%. THA was performed in 11% of patients. Body mass index >29 (P = 0.03) and increased age (P < 0.01) were risk factors for OA. Patients with symptomatic hip dysplasia are at significant risk of developing hip OA. Body mass index >29 and age ≥35 years at the time of presentation with hip pain were risk factors for hip OA.
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spelling pubmed-91421912022-05-31 Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention Melugin, Heath P Hale, Rena F Lee, Dustin R LaPrade, Matthew D Okoroha, Kelechi R Sierra, Rafael J Trousdale, Robert T Levy, Bruce A Krych, Aaron J J Hip Preserv Surg Research Article Hip dysplasia is a common cause of hip pain and a known risk factor for hip osteoarthritis (OA) and early total hip arthroplasty (THA). Unfortunately, little is known about the specific factors associated with an increased risk of OA. The purpose was (i) to report the overall rate of symptomatic hip OA and THA and (ii) to identify radiographic features and patient characteristics associated with the development of symptomatic hip OA. A geographic database was used to identify all patients aged 14–50 years old diagnosed with symptomatic hip dysplasia between 2000 and 2016. Kaplan–Meier analysis was used to determine the rate of symptomatic hip OA, defined as a Tönnis grade of ≥1 on hip radiograph. Univariate and multivariate proportional hazard regression models were performed to determine risk factors for OA. One hundred and fifty-nine hips (144 patients) with hip dysplasia (52 F:107 M) out of 1893 patients with hip pain were included. Of these, 45 (28%) had severe hip dysplasia with a lateral center-edge angle ≤18°. Mean age at time of presentation was 26.1 (±10.1) years. Mean follow-up time was 8.2 (±5) years. The rate of OA was 20%. THA was performed in 11% of patients. Body mass index >29 (P = 0.03) and increased age (P < 0.01) were risk factors for OA. Patients with symptomatic hip dysplasia are at significant risk of developing hip OA. Body mass index >29 and age ≥35 years at the time of presentation with hip pain were risk factors for hip OA. Oxford University Press 2022-01-19 /pmc/articles/PMC9142191/ /pubmed/35651707 http://dx.doi.org/10.1093/jhps/hnac007 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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 Research Article
Melugin, Heath P
Hale, Rena F
Lee, Dustin R
LaPrade, Matthew D
Okoroha, Kelechi R
Sierra, Rafael J
Trousdale, Robert T
Levy, Bruce A
Krych, Aaron J
Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
title Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
title_full Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
title_fullStr Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
title_full_unstemmed Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
title_short Risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
title_sort risk factors for long-term hip osteoarthritis in patients with hip dysplasia without surgical intervention
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142191/
https://www.ncbi.nlm.nih.gov/pubmed/35651707
http://dx.doi.org/10.1093/jhps/hnac007
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