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Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics

BACKGROUND: In 1998, a process of centralisation was initiated for services for children born with a cleft lip or palate in the UK. We studied the timing of this process in England according to its impact on the number of hospitals and surgeons involved in primary surgical repairs. METHODS: All live...

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Autores principales: Fitzsimons, Kate J, Mukarram, Shumaila, Copley, Lynn P, Deacon, Scott A, van der Meulen, Jan H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464162/
https://www.ncbi.nlm.nih.gov/pubmed/22682355
http://dx.doi.org/10.1186/1472-6963-12-148
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author Fitzsimons, Kate J
Mukarram, Shumaila
Copley, Lynn P
Deacon, Scott A
van der Meulen, Jan H
author_facet Fitzsimons, Kate J
Mukarram, Shumaila
Copley, Lynn P
Deacon, Scott A
van der Meulen, Jan H
author_sort Fitzsimons, Kate J
collection PubMed
description BACKGROUND: In 1998, a process of centralisation was initiated for services for children born with a cleft lip or palate in the UK. We studied the timing of this process in England according to its impact on the number of hospitals and surgeons involved in primary surgical repairs. METHODS: All live born patients with a cleft lip and/or palate born between April 1997 and December 2008 were identified in Hospital Episode Statistics, the database of admissions to English National Health Service hospitals. Children were included if they had diagnostic codes for a cleft as well as procedure codes for a primary surgical cleft repair. Children with codes indicating additional congenital anomalies or syndromes were excluded as their additional problems could have determined when and where they were treated. RESULTS: We identified 10,892 children with a cleft. 21.0% were excluded because of additional anomalies or syndromes. Of the remaining 8,606 patients, 30.4% had a surgical lip repair only, 41.7% a palate repair only, and 28.0% both a lip and palate repair. The number of hospitals that carried out these primary repairs reduced from 49 in 1997 to 13, with 11 of these performing repairs on at least 40 children born in 2008. The number of surgeons responsible for repairs reduced from 98 to 26, with 22 performing repairs on at least 20 children born in 2008. In the same period, average length of hospital stay reduced from 3.8 to 3.0 days for primary lip repairs, from 3.8 to 3.3 days for primary palate repairs, and from 4.6 to 2.6 days for combined repairs with no evidence for a change in emergency readmission rates. The speed of centralisation varied with the earliest of the nine regions completing it in 2001 and the last in 2007. CONCLUSIONS: Between 1998 and 2007, cleft services in England were centralised. According to a survey among patients’ parents, the quality of cleft care improved in the same period. Surgical care became more consistent with current recommendations. However, key outcomes, including facial appearance and speech, can only be assessed many years after the initial surgical treatment.
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spelling pubmed-34641622012-10-05 Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics Fitzsimons, Kate J Mukarram, Shumaila Copley, Lynn P Deacon, Scott A van der Meulen, Jan H BMC Health Serv Res Research Article BACKGROUND: In 1998, a process of centralisation was initiated for services for children born with a cleft lip or palate in the UK. We studied the timing of this process in England according to its impact on the number of hospitals and surgeons involved in primary surgical repairs. METHODS: All live born patients with a cleft lip and/or palate born between April 1997 and December 2008 were identified in Hospital Episode Statistics, the database of admissions to English National Health Service hospitals. Children were included if they had diagnostic codes for a cleft as well as procedure codes for a primary surgical cleft repair. Children with codes indicating additional congenital anomalies or syndromes were excluded as their additional problems could have determined when and where they were treated. RESULTS: We identified 10,892 children with a cleft. 21.0% were excluded because of additional anomalies or syndromes. Of the remaining 8,606 patients, 30.4% had a surgical lip repair only, 41.7% a palate repair only, and 28.0% both a lip and palate repair. The number of hospitals that carried out these primary repairs reduced from 49 in 1997 to 13, with 11 of these performing repairs on at least 40 children born in 2008. The number of surgeons responsible for repairs reduced from 98 to 26, with 22 performing repairs on at least 20 children born in 2008. In the same period, average length of hospital stay reduced from 3.8 to 3.0 days for primary lip repairs, from 3.8 to 3.3 days for primary palate repairs, and from 4.6 to 2.6 days for combined repairs with no evidence for a change in emergency readmission rates. The speed of centralisation varied with the earliest of the nine regions completing it in 2001 and the last in 2007. CONCLUSIONS: Between 1998 and 2007, cleft services in England were centralised. According to a survey among patients’ parents, the quality of cleft care improved in the same period. Surgical care became more consistent with current recommendations. However, key outcomes, including facial appearance and speech, can only be assessed many years after the initial surgical treatment. BioMed Central 2012-06-10 /pmc/articles/PMC3464162/ /pubmed/22682355 http://dx.doi.org/10.1186/1472-6963-12-148 Text en Copyright ©2012 Fitzsimons et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Fitzsimons, Kate J
Mukarram, Shumaila
Copley, Lynn P
Deacon, Scott A
van der Meulen, Jan H
Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics
title Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics
title_full Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics
title_fullStr Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics
title_full_unstemmed Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics
title_short Centralisation of services for children with cleft lip or palate in England: a study of hospital episode statistics
title_sort centralisation of services for children with cleft lip or palate in england: a study of hospital episode statistics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464162/
https://www.ncbi.nlm.nih.gov/pubmed/22682355
http://dx.doi.org/10.1186/1472-6963-12-148
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