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COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom
PURPOSE: Little is known about the impact of COVID-19 on children and young people (CYP) with hydrocephalus and their families. This study explored the experiences and support needs of CYP with hydrocephalus and parents who have a child with hydrocephalus during the COVID-19 pandemic. METHODS: CYP w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199430/ https://www.ncbi.nlm.nih.gov/pubmed/37209198 http://dx.doi.org/10.1007/s00381-023-05980-7 |
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author | Collaço, Nicole Campion, Anna McNicholas, Roisin Darlington, Anne-Sophie |
author_facet | Collaço, Nicole Campion, Anna McNicholas, Roisin Darlington, Anne-Sophie |
author_sort | Collaço, Nicole |
collection | PubMed |
description | PURPOSE: Little is known about the impact of COVID-19 on children and young people (CYP) with hydrocephalus and their families. This study explored the experiences and support needs of CYP with hydrocephalus and parents who have a child with hydrocephalus during the COVID-19 pandemic. METHODS: CYP with hydrocephalus and parents of CYP with hydrocephalus in the United Kingdom completed an online survey with open and closed questions exploring experiences, information, support needs and decision making processes. Qualitative thematic content analysis and descriptive quantitative analyses were undertaken. RESULTS: CYP aged 12-32 years (n=25) and parents of CYP aged 0-20 years (n=69) responded. Parents (63.5%) and CYP (40.9%) worried about the virus, and both were vigilant for virus symptoms (86.5% and 57.1%). Parents (71.2%) and CYP (59.1%) worried about their child/feeling more isolated during the virus outbreak. Parents felt concerned about having to take their child to hospital with a suspected shunt problem during the virus outbreak (64.0%). Qualitative findings reported the following themes: (1) Healthcare and treatment provision: delays and challenges to access and availability of care (2) Impact of COVID-19/lockdown on daily lives and routines, and (3) Provision of information and support for parents and CYP with hydrocephalus. CONCLUSION: The impact of COVID-19 and national measures to control the spread of the virus- no contact with anyone outside the household significantly impacted the daily lives and routines of CYP with hydrocephalus and parents. Social engagements were missed, families faced challenges to their work life, education and access to health care and support, which subsequently contributed negatively to their mental wellbeing. CYP and parents highlighted a need for clear, timely and targeted information to address their concerns. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00381-023-05980-7. |
format | Online Article Text |
id | pubmed-10199430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101994302023-11-14 COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom Collaço, Nicole Campion, Anna McNicholas, Roisin Darlington, Anne-Sophie Childs Nerv Syst Original Article PURPOSE: Little is known about the impact of COVID-19 on children and young people (CYP) with hydrocephalus and their families. This study explored the experiences and support needs of CYP with hydrocephalus and parents who have a child with hydrocephalus during the COVID-19 pandemic. METHODS: CYP with hydrocephalus and parents of CYP with hydrocephalus in the United Kingdom completed an online survey with open and closed questions exploring experiences, information, support needs and decision making processes. Qualitative thematic content analysis and descriptive quantitative analyses were undertaken. RESULTS: CYP aged 12-32 years (n=25) and parents of CYP aged 0-20 years (n=69) responded. Parents (63.5%) and CYP (40.9%) worried about the virus, and both were vigilant for virus symptoms (86.5% and 57.1%). Parents (71.2%) and CYP (59.1%) worried about their child/feeling more isolated during the virus outbreak. Parents felt concerned about having to take their child to hospital with a suspected shunt problem during the virus outbreak (64.0%). Qualitative findings reported the following themes: (1) Healthcare and treatment provision: delays and challenges to access and availability of care (2) Impact of COVID-19/lockdown on daily lives and routines, and (3) Provision of information and support for parents and CYP with hydrocephalus. CONCLUSION: The impact of COVID-19 and national measures to control the spread of the virus- no contact with anyone outside the household significantly impacted the daily lives and routines of CYP with hydrocephalus and parents. Social engagements were missed, families faced challenges to their work life, education and access to health care and support, which subsequently contributed negatively to their mental wellbeing. CYP and parents highlighted a need for clear, timely and targeted information to address their concerns. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00381-023-05980-7. Springer Berlin Heidelberg 2023-05-20 2023 /pmc/articles/PMC10199430/ /pubmed/37209198 http://dx.doi.org/10.1007/s00381-023-05980-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Collaço, Nicole Campion, Anna McNicholas, Roisin Darlington, Anne-Sophie COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom |
title | COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom |
title_full | COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom |
title_fullStr | COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom |
title_full_unstemmed | COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom |
title_short | COVID-19- Experiences and support needs of children and young people with Hydrocephalus and parents in the United Kingdom |
title_sort | covid-19- experiences and support needs of children and young people with hydrocephalus and parents in the united kingdom |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199430/ https://www.ncbi.nlm.nih.gov/pubmed/37209198 http://dx.doi.org/10.1007/s00381-023-05980-7 |
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