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‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy

INTRODUCTION: Sleep problems in children with epilepsy (CWE) are common. However, little is known about parental experiences and feelings about managing sleep in their CWE. To provide the most appropriate services' provision, it is essential that the lived experience of parents of this patient...

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Autores principales: Cook, Georgia, Gringras, Paul, Hiscock, Harriet, Pal, Deb K., Wiggs, Luci
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010080/
https://www.ncbi.nlm.nih.gov/pubmed/36606569
http://dx.doi.org/10.1111/hex.13694
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author Cook, Georgia
Gringras, Paul
Hiscock, Harriet
Pal, Deb K.
Wiggs, Luci
author_facet Cook, Georgia
Gringras, Paul
Hiscock, Harriet
Pal, Deb K.
Wiggs, Luci
author_sort Cook, Georgia
collection PubMed
description INTRODUCTION: Sleep problems in children with epilepsy (CWE) are common. However, little is known about parental experiences and feelings about managing sleep in their CWE. To provide the most appropriate services' provision, it is essential that the lived experience of parents of this patient group and the issues and problems that they face in managing their child's sleep is understood. METHOD: In 2018, nine mothers of CWE (aged 5–15 years) were interviewed about their perceptions and experiences around their child's sleep, sleep problems and their management, the impact of sleep difficulties on the child and their family and available support. RESULTS: Four themes were identified that represented the nature of the child's sleep problems, including settling and night‐waking issues, parasomnias and child anxiety around sleep. Seven themes represented mothers' experiences of managing their child's sleep and any associated problems, including the longstanding challenging nature of child sleep issues, management strategies adopted, challenges related to managing sleep over time, the link between sleep and seizures, the negative impact of poor sleep on daytime functioning, role of antiseizure medication and maternal concerns about child sleep. One theme represented the perceived lack of information, help and support available. CONCLUSIONS: Findings suggest there are unmet needs in supporting parents to deal with sleep, sleep problems and their management in CWE. PATIENT OR PUBLIC CONTRIBUTION: This individual study was conducted under the umbrella of the CASTLE research programme (see https://castlestudy.org.uk/). Parents who have lived experience of parenting a child with epilepsy were co‐applicants for the programme and were involved in the original conception, aims, design and funding application for the research programme (including the project reported in this paper) and advised on project design. Mothers of CWE who have lived experience of managing sleep and sleep problems in their child were participants who shared their experiences through the interviews, which formed the data of the current study.
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spelling pubmed-100100802023-03-14 ‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy Cook, Georgia Gringras, Paul Hiscock, Harriet Pal, Deb K. Wiggs, Luci Health Expect Original Articles INTRODUCTION: Sleep problems in children with epilepsy (CWE) are common. However, little is known about parental experiences and feelings about managing sleep in their CWE. To provide the most appropriate services' provision, it is essential that the lived experience of parents of this patient group and the issues and problems that they face in managing their child's sleep is understood. METHOD: In 2018, nine mothers of CWE (aged 5–15 years) were interviewed about their perceptions and experiences around their child's sleep, sleep problems and their management, the impact of sleep difficulties on the child and their family and available support. RESULTS: Four themes were identified that represented the nature of the child's sleep problems, including settling and night‐waking issues, parasomnias and child anxiety around sleep. Seven themes represented mothers' experiences of managing their child's sleep and any associated problems, including the longstanding challenging nature of child sleep issues, management strategies adopted, challenges related to managing sleep over time, the link between sleep and seizures, the negative impact of poor sleep on daytime functioning, role of antiseizure medication and maternal concerns about child sleep. One theme represented the perceived lack of information, help and support available. CONCLUSIONS: Findings suggest there are unmet needs in supporting parents to deal with sleep, sleep problems and their management in CWE. PATIENT OR PUBLIC CONTRIBUTION: This individual study was conducted under the umbrella of the CASTLE research programme (see https://castlestudy.org.uk/). Parents who have lived experience of parenting a child with epilepsy were co‐applicants for the programme and were involved in the original conception, aims, design and funding application for the research programme (including the project reported in this paper) and advised on project design. Mothers of CWE who have lived experience of managing sleep and sleep problems in their child were participants who shared their experiences through the interviews, which formed the data of the current study. John Wiley and Sons Inc. 2023-01-06 /pmc/articles/PMC10010080/ /pubmed/36606569 http://dx.doi.org/10.1111/hex.13694 Text en © 2023 The Authors. Health Expectations published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Cook, Georgia
Gringras, Paul
Hiscock, Harriet
Pal, Deb K.
Wiggs, Luci
‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy
title ‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy
title_full ‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy
title_fullStr ‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy
title_full_unstemmed ‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy
title_short ‘No one's ever said anything about sleep’: A qualitative investigation into mothers' experiences of sleep in children with epilepsy
title_sort ‘no one's ever said anything about sleep’: a qualitative investigation into mothers' experiences of sleep in children with epilepsy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010080/
https://www.ncbi.nlm.nih.gov/pubmed/36606569
http://dx.doi.org/10.1111/hex.13694
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