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Mapping Two Decades of Paediatric Down Syndrome Research Literature.
BACKGROUND: While research has led to significant advancements in the health and life expectancy of children with Down Syndrome (DS), there remains a significant burden of disease and health inequity. Further research, focused on areas of greatest need, is imperative to address this. An understandin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Ulster Medical Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464630/ https://www.ncbi.nlm.nih.gov/pubmed/37649911 |
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author | McKenna, Caoimhe Schilder, Anne Lee, Rachel Xue Ning Manikam, Logan Venekamp, Roderick Lakhanpaul, Monica |
author_facet | McKenna, Caoimhe Schilder, Anne Lee, Rachel Xue Ning Manikam, Logan Venekamp, Roderick Lakhanpaul, Monica |
author_sort | McKenna, Caoimhe |
collection | PubMed |
description | BACKGROUND: While research has led to significant advancements in the health and life expectancy of children with Down Syndrome (DS), there remains a significant burden of disease and health inequity. Further research, focused on areas of greatest need, is imperative to address this. An understanding of what research has been undertaken, and any existing gaps, helps to guide future academic efforts. METHODS: We utilised an epistemological approach to summarise two decades of paediatric DS literature. Publications were categorised according to the country of origin, methodology, primary health themes and subcategory research themes. RESULTS: Across 5,800 paediatric DS publications we demonstrate a general increase in the number of publications in this field between 2000 and 2014, with a trending decline thereafter. The majority of publications were affiliated with Institutions based in Western countries. The majority of studies utilised a cross-sectional methodology (33.3%), while relatively few were interventional (5.6%), qualitative (2.7%) or mixed-method studies (1.6%). Most publications focused on development & cognition (13.1%), neurology (9.9%) and oncology (9.8%), with fewer focusing on genitourinary health (0.9%), growth (0.9%), mortality (0.9%) and child protection (0.2%). CONCLUSION: These findings highlight areas of relative paucity within the paediatric DS literature which may warrant increased academic attention. |
format | Online Article Text |
id | pubmed-10464630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Ulster Medical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104646302023-08-30 Mapping Two Decades of Paediatric Down Syndrome Research Literature. McKenna, Caoimhe Schilder, Anne Lee, Rachel Xue Ning Manikam, Logan Venekamp, Roderick Lakhanpaul, Monica Ulster Med J Clinical Paper BACKGROUND: While research has led to significant advancements in the health and life expectancy of children with Down Syndrome (DS), there remains a significant burden of disease and health inequity. Further research, focused on areas of greatest need, is imperative to address this. An understanding of what research has been undertaken, and any existing gaps, helps to guide future academic efforts. METHODS: We utilised an epistemological approach to summarise two decades of paediatric DS literature. Publications were categorised according to the country of origin, methodology, primary health themes and subcategory research themes. RESULTS: Across 5,800 paediatric DS publications we demonstrate a general increase in the number of publications in this field between 2000 and 2014, with a trending decline thereafter. The majority of publications were affiliated with Institutions based in Western countries. The majority of studies utilised a cross-sectional methodology (33.3%), while relatively few were interventional (5.6%), qualitative (2.7%) or mixed-method studies (1.6%). Most publications focused on development & cognition (13.1%), neurology (9.9%) and oncology (9.8%), with fewer focusing on genitourinary health (0.9%), growth (0.9%), mortality (0.9%) and child protection (0.2%). CONCLUSION: These findings highlight areas of relative paucity within the paediatric DS literature which may warrant increased academic attention. The Ulster Medical Society 2023-08-29 2023-05 /pmc/articles/PMC10464630/ /pubmed/37649911 Text en Copyright © 2023 Ulster Medical Society https://creativecommons.org/licenses/by-nc-sa/4.0/The Ulster Medical Society grants to all users on the basis of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Licence the right to alter or build upon the work non-commercially, as long as the author is credited and the new creation is licensed under identical terms. |
spellingShingle | Clinical Paper McKenna, Caoimhe Schilder, Anne Lee, Rachel Xue Ning Manikam, Logan Venekamp, Roderick Lakhanpaul, Monica Mapping Two Decades of Paediatric Down Syndrome Research Literature. |
title | Mapping Two Decades of Paediatric Down Syndrome Research Literature. |
title_full | Mapping Two Decades of Paediatric Down Syndrome Research Literature. |
title_fullStr | Mapping Two Decades of Paediatric Down Syndrome Research Literature. |
title_full_unstemmed | Mapping Two Decades of Paediatric Down Syndrome Research Literature. |
title_short | Mapping Two Decades of Paediatric Down Syndrome Research Literature. |
title_sort | mapping two decades of paediatric down syndrome research literature. |
topic | Clinical Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464630/ https://www.ncbi.nlm.nih.gov/pubmed/37649911 |
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