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Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate
BACKGROUND: The objective of the Swedish cleft lip and palate (CLP) registry is to promote quality control, research and improvement of treatment, by comparison of the long-term results of surgery, orthodontics and speech from all six Swedish CLP centres. The purpose of the study was to investigate...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288403/ https://www.ncbi.nlm.nih.gov/pubmed/32522189 http://dx.doi.org/10.1186/s12913-020-05389-x |
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author | Klintö, Kristina Karsten, Agneta Marcusson, Agneta Paganini, Anna Rizell, Sara Cajander, Jenny Brunnegård, Karin Hakelius, Malin Okhiria, Åsa Peterson, Petra Abdiu, Avni Havstam, Christina Mark, Hans Hagberg, Emilie Björnström, Lena Wiedel, Anna-Paulina Becker, Magnus |
author_facet | Klintö, Kristina Karsten, Agneta Marcusson, Agneta Paganini, Anna Rizell, Sara Cajander, Jenny Brunnegård, Karin Hakelius, Malin Okhiria, Åsa Peterson, Petra Abdiu, Avni Havstam, Christina Mark, Hans Hagberg, Emilie Björnström, Lena Wiedel, Anna-Paulina Becker, Magnus |
author_sort | Klintö, Kristina |
collection | PubMed |
description | BACKGROUND: The objective of the Swedish cleft lip and palate (CLP) registry is to promote quality control, research and improvement of treatment, by comparison of the long-term results of surgery, orthodontics and speech from all six Swedish CLP centres. The purpose of the study was to investigate the coverage and reporting degree of the Swedish CLP registry, and to describe the design of the registry and discuss questions of reliability and validity of the data included. METHODS: All six Swedish CLP centres participate in the registry. All children in Sweden with cleft lip and/or cleft palate, born from 2009 onwards, are included in the registry. Baseline data such as cleft type (ICD-10 diagnosis), heredity, birth weight and additional deformities and/or syndromes, as well as pre-surgical treatment, are recorded at first visit. Data on surgical treatment are recorded continuously. Treatment outcome regarding dentofacial development and speech are recorded at follow-ups at 5, 10, 16 and 19 years of age. Data on dentofacial development are also recorded 1 year after orthognathic surgery. In addition, data on babbling and speech are recorded at 18 months of age. Coverage degree and reporting degree of surgery was assessed by comparison with registrations in the Swedish Central patient registry. Reporting degree of orthodontic and speech registrations at 5 years of age was assessed by comparison with registrations at baseline. RESULTS: The average coverage degree for children born 2009 to 2018 was 95.1%. For cleft-related surgeries, the average reporting degree was 92.4%. Average reporting degree of orthodontic registrations and speech registrations at age 5 years was 92 and 97.5% respectively. CONCLUSION: In order to achieve valid and reliable data in a healthcare quality registry, the degree of coverage and reporting needs to be high, the variables included should be limited and checked for reliability, and the professionals must calibrate themselves regularly. The Swedish CLP registry fulfils these requirements. |
format | Online Article Text |
id | pubmed-7288403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72884032020-06-11 Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate Klintö, Kristina Karsten, Agneta Marcusson, Agneta Paganini, Anna Rizell, Sara Cajander, Jenny Brunnegård, Karin Hakelius, Malin Okhiria, Åsa Peterson, Petra Abdiu, Avni Havstam, Christina Mark, Hans Hagberg, Emilie Björnström, Lena Wiedel, Anna-Paulina Becker, Magnus BMC Health Serv Res Research Article BACKGROUND: The objective of the Swedish cleft lip and palate (CLP) registry is to promote quality control, research and improvement of treatment, by comparison of the long-term results of surgery, orthodontics and speech from all six Swedish CLP centres. The purpose of the study was to investigate the coverage and reporting degree of the Swedish CLP registry, and to describe the design of the registry and discuss questions of reliability and validity of the data included. METHODS: All six Swedish CLP centres participate in the registry. All children in Sweden with cleft lip and/or cleft palate, born from 2009 onwards, are included in the registry. Baseline data such as cleft type (ICD-10 diagnosis), heredity, birth weight and additional deformities and/or syndromes, as well as pre-surgical treatment, are recorded at first visit. Data on surgical treatment are recorded continuously. Treatment outcome regarding dentofacial development and speech are recorded at follow-ups at 5, 10, 16 and 19 years of age. Data on dentofacial development are also recorded 1 year after orthognathic surgery. In addition, data on babbling and speech are recorded at 18 months of age. Coverage degree and reporting degree of surgery was assessed by comparison with registrations in the Swedish Central patient registry. Reporting degree of orthodontic and speech registrations at 5 years of age was assessed by comparison with registrations at baseline. RESULTS: The average coverage degree for children born 2009 to 2018 was 95.1%. For cleft-related surgeries, the average reporting degree was 92.4%. Average reporting degree of orthodontic registrations and speech registrations at age 5 years was 92 and 97.5% respectively. CONCLUSION: In order to achieve valid and reliable data in a healthcare quality registry, the degree of coverage and reporting needs to be high, the variables included should be limited and checked for reliability, and the professionals must calibrate themselves regularly. The Swedish CLP registry fulfils these requirements. BioMed Central 2020-06-11 /pmc/articles/PMC7288403/ /pubmed/32522189 http://dx.doi.org/10.1186/s12913-020-05389-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Klintö, Kristina Karsten, Agneta Marcusson, Agneta Paganini, Anna Rizell, Sara Cajander, Jenny Brunnegård, Karin Hakelius, Malin Okhiria, Åsa Peterson, Petra Abdiu, Avni Havstam, Christina Mark, Hans Hagberg, Emilie Björnström, Lena Wiedel, Anna-Paulina Becker, Magnus Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate |
title | Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate |
title_full | Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate |
title_fullStr | Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate |
title_full_unstemmed | Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate |
title_short | Coverage, reporting degree and design of the Swedish quality registry for patients born with cleft lip and/or palate |
title_sort | coverage, reporting degree and design of the swedish quality registry for patients born with cleft lip and/or palate |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288403/ https://www.ncbi.nlm.nih.gov/pubmed/32522189 http://dx.doi.org/10.1186/s12913-020-05389-x |
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