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The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme

AIMS: Early detection of developmental dysplasia of the hip (DDH) is associated with improved outcomes of conservative treatment. Therefore, we aimed to evaluate a novel screening programme that included both the primary risk factors of breech presentation and family history, and the secondary risk...

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Autores principales: Poacher, Arwel T., Froud, Joseph L. J., Caterson, Jessica, Crook, Daniel L., Ramage, Gregor, Marsh, Luke, Poacher, Gethin, Carpenter, Eleanor C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Editorial Society of Bone & Joint Surgery 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067325/
https://www.ncbi.nlm.nih.gov/pubmed/37051819
http://dx.doi.org/10.1302/2633-1462.44.BJO-2022-0135.R1
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author Poacher, Arwel T.
Froud, Joseph L. J.
Caterson, Jessica
Crook, Daniel L.
Ramage, Gregor
Marsh, Luke
Poacher, Gethin
Carpenter, Eleanor C.
author_facet Poacher, Arwel T.
Froud, Joseph L. J.
Caterson, Jessica
Crook, Daniel L.
Ramage, Gregor
Marsh, Luke
Poacher, Gethin
Carpenter, Eleanor C.
author_sort Poacher, Arwel T.
collection PubMed
description AIMS: Early detection of developmental dysplasia of the hip (DDH) is associated with improved outcomes of conservative treatment. Therefore, we aimed to evaluate a novel screening programme that included both the primary risk factors of breech presentation and family history, and the secondary risk factors of oligohydramnios and foot deformities. METHODS: A five-year prospective registry study investigating every live birth in the study’s catchment area (n = 27,731), all of whom underwent screening for risk factors and examination at the newborn and six- to eight-week neonatal examination and review. DDH was diagnosed using ultrasonography and the Graf classification system, defined as grade IIb or above or rapidly regressing IIa disease (≥4(o) at four weeks follow-up). Multivariate odds ratios were calculated to establish significant association, and risk differences were calculated to provide quantifiable risk increase with DDH, positive predictive value was used as a measure of predictive efficacy. The cost-effectiveness of using these risk factors to predict DDH was evaluated using NHS tariffs (January 2021). RESULTS: The prevalence of DDH that required treatment within our population was 5/1,000 live births. The rate of missed presentation of DDH was 0.43/1000 live births. Breech position, family history, oligohydramnios, and foot deformities demonstrated significant association with DDH (p < 0.0001). The presence of breech presentation increased the risk of DDH by 1.69% (95% confidence interval (CI) 0.93% to 2.45%), family history by 3.57% (95% CI 2.06% to 5.09%), foot deformities by 8.95% (95% CI 4.81% to 13.1%), and oligohydramnios nby 11.6% (95 % CI 3.0% to 19.0%). Primary risk factors family history and breech presentation demonstrated an estimated cost-per-case detection of £6,276 and £11,409, respectively. Oligohydramnios and foot deformities demonstrated a cost-per-case detected less than the cost of primary risk factors of £2,260 and £2,670, respectively. CONCLUSION: The inclusion of secondary risk factors within a national screening programme was clinically successful as they were more cost and resource-efficient predictors of DDH than primary risk factors, suggesting they should be considered in the national guidance. Cite this article: Bone Jt Open 2023;4(4):234–240.
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spelling pubmed-100673252023-04-03 The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme Poacher, Arwel T. Froud, Joseph L. J. Caterson, Jessica Crook, Daniel L. Ramage, Gregor Marsh, Luke Poacher, Gethin Carpenter, Eleanor C. Bone Jt Open Children’s Orthopaedics AIMS: Early detection of developmental dysplasia of the hip (DDH) is associated with improved outcomes of conservative treatment. Therefore, we aimed to evaluate a novel screening programme that included both the primary risk factors of breech presentation and family history, and the secondary risk factors of oligohydramnios and foot deformities. METHODS: A five-year prospective registry study investigating every live birth in the study’s catchment area (n = 27,731), all of whom underwent screening for risk factors and examination at the newborn and six- to eight-week neonatal examination and review. DDH was diagnosed using ultrasonography and the Graf classification system, defined as grade IIb or above or rapidly regressing IIa disease (≥4(o) at four weeks follow-up). Multivariate odds ratios were calculated to establish significant association, and risk differences were calculated to provide quantifiable risk increase with DDH, positive predictive value was used as a measure of predictive efficacy. The cost-effectiveness of using these risk factors to predict DDH was evaluated using NHS tariffs (January 2021). RESULTS: The prevalence of DDH that required treatment within our population was 5/1,000 live births. The rate of missed presentation of DDH was 0.43/1000 live births. Breech position, family history, oligohydramnios, and foot deformities demonstrated significant association with DDH (p < 0.0001). The presence of breech presentation increased the risk of DDH by 1.69% (95% confidence interval (CI) 0.93% to 2.45%), family history by 3.57% (95% CI 2.06% to 5.09%), foot deformities by 8.95% (95% CI 4.81% to 13.1%), and oligohydramnios nby 11.6% (95 % CI 3.0% to 19.0%). Primary risk factors family history and breech presentation demonstrated an estimated cost-per-case detection of £6,276 and £11,409, respectively. Oligohydramnios and foot deformities demonstrated a cost-per-case detected less than the cost of primary risk factors of £2,260 and £2,670, respectively. CONCLUSION: The inclusion of secondary risk factors within a national screening programme was clinically successful as they were more cost and resource-efficient predictors of DDH than primary risk factors, suggesting they should be considered in the national guidance. Cite this article: Bone Jt Open 2023;4(4):234–240. The British Editorial Society of Bone & Joint Surgery 2023-04-03 /pmc/articles/PMC10067325/ /pubmed/37051819 http://dx.doi.org/10.1302/2633-1462.44.BJO-2022-0135.R1 Text en © 2023 Author(s) et al. https://creativecommons.org/licenses/by-nc-nd/4.0/https://online.boneandjoint.org.uk/TDMThis is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND 4.0) licence, which permits the copying and redistribution of the work only, and provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Children’s Orthopaedics
Poacher, Arwel T.
Froud, Joseph L. J.
Caterson, Jessica
Crook, Daniel L.
Ramage, Gregor
Marsh, Luke
Poacher, Gethin
Carpenter, Eleanor C.
The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
title The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
title_full The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
title_fullStr The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
title_full_unstemmed The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
title_short The cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
title_sort cost effectiveness of potential risk factors for developmental dysplasia of the hip within a national screening programme
topic Children’s Orthopaedics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067325/
https://www.ncbi.nlm.nih.gov/pubmed/37051819
http://dx.doi.org/10.1302/2633-1462.44.BJO-2022-0135.R1
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