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A systematic review and qualitative synthesis of the experiences of parents of individuals living with Duchenne muscular dystrophy
Some parents of children with DMD find their role challenging, affecting quality of life. To inform support methods, we aimed to understand the lived experiences of parents and how these interact with disease progression. PRISMA informed protocol development. Qualitative and mixed methods studies we...
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Published in: | Disability and rehabilitation 2023-04, Vol.45 (8), p.1285-1298 |
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container_title | Disability and rehabilitation |
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creator | Donnelly, Clare M. Quinlivan, Rosaline M. Herron, Aaron Graham, Christopher D. |
description | Some parents of children with DMD find their role challenging, affecting quality of life. To inform support methods, we aimed to understand the lived experiences of parents and how these interact with disease progression.
PRISMA informed protocol development. Qualitative and mixed methods studies were included. Four databases were searched and study quality was assessed using a standardised measure. Extracted data were analysed using thematic synthesis.
26 studies were included, comprising 362 parents. Seven descriptive themes were apparent: "Diagnostic Experiences", "Coping with the Caregiver Role", "Illness Trajectory and Associated Interventions", "Family Communication", "Network of Support", "Navigating Systems" and "Transition Experiences". Four analytical themes were then derived: "The Cyclical Nature of Grief", "Lifelong Expert in the Needs and Experiences of an Individual with DMD", "Navigating Deviation from Typical Life Course" and "Uncertainty as Ever Present".
The extant evidence suggests that the experience of parenting a child with DMD is often characterised by: a cycle of grief that begins at diagnosis, which runs parallel to the development of expertise in caregiving; within this parents notice deviations from their child's and their own expected life course and adjust to the emotions and uncertainty that this can bring.
IMPLICATIONS FOR REHABILITATION
Professionals should be cognisant to the complex grief process associated with DMD, which occurs from diagnosis onwards.
There should be continued support for parents following bereavement.
Peer support groups may also offer parents ways to maintain well-being.
The necessity for parents to function effectively within an uncertain context that induces challenging emotions suggests a role for psychological therapies. |
doi_str_mv | 10.1080/09638288.2022.2060336 |
format | article |
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PRISMA informed protocol development. Qualitative and mixed methods studies were included. Four databases were searched and study quality was assessed using a standardised measure. Extracted data were analysed using thematic synthesis.
26 studies were included, comprising 362 parents. Seven descriptive themes were apparent: "Diagnostic Experiences", "Coping with the Caregiver Role", "Illness Trajectory and Associated Interventions", "Family Communication", "Network of Support", "Navigating Systems" and "Transition Experiences". Four analytical themes were then derived: "The Cyclical Nature of Grief", "Lifelong Expert in the Needs and Experiences of an Individual with DMD", "Navigating Deviation from Typical Life Course" and "Uncertainty as Ever Present".
The extant evidence suggests that the experience of parenting a child with DMD is often characterised by: a cycle of grief that begins at diagnosis, which runs parallel to the development of expertise in caregiving; within this parents notice deviations from their child's and their own expected life course and adjust to the emotions and uncertainty that this can bring.
IMPLICATIONS FOR REHABILITATION
Professionals should be cognisant to the complex grief process associated with DMD, which occurs from diagnosis onwards.
There should be continued support for parents following bereavement.
Peer support groups may also offer parents ways to maintain well-being.
The necessity for parents to function effectively within an uncertain context that induces challenging emotions suggests a role for psychological therapies.</description><identifier>ISSN: 0963-8288</identifier><identifier>EISSN: 1464-5165</identifier><identifier>DOI: 10.1080/09638288.2022.2060336</identifier><identifier>PMID: 35435109</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Adaptation, Psychological ; caregiver role ; Child ; Duchenne muscular dystrophy ; Humans ; Muscular Dystrophy, Duchenne - psychology ; Parenting - psychology ; parents ; Parents - psychology ; psychology ; qualitative synthesis ; Quality of Life ; systematic review</subject><ispartof>Disability and rehabilitation, 2023-04, Vol.45 (8), p.1285-1298</ispartof><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-a6459d5ed0ffcbc28061084cdb33b0733215f37b7688fe338eded0eb0ca39fdd3</citedby><cites>FETCH-LOGICAL-c413t-a6459d5ed0ffcbc28061084cdb33b0733215f37b7688fe338eded0eb0ca39fdd3</cites><orcidid>0000-0003-1614-0318 ; 0000-0001-8456-9154</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35435109$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Donnelly, Clare M.</creatorcontrib><creatorcontrib>Quinlivan, Rosaline M.</creatorcontrib><creatorcontrib>Herron, Aaron</creatorcontrib><creatorcontrib>Graham, Christopher D.</creatorcontrib><title>A systematic review and qualitative synthesis of the experiences of parents of individuals living with Duchenne muscular dystrophy</title><title>Disability and rehabilitation</title><addtitle>Disabil Rehabil</addtitle><description>Some parents of children with DMD find their role challenging, affecting quality of life. To inform support methods, we aimed to understand the lived experiences of parents and how these interact with disease progression.
PRISMA informed protocol development. Qualitative and mixed methods studies were included. Four databases were searched and study quality was assessed using a standardised measure. Extracted data were analysed using thematic synthesis.
26 studies were included, comprising 362 parents. Seven descriptive themes were apparent: "Diagnostic Experiences", "Coping with the Caregiver Role", "Illness Trajectory and Associated Interventions", "Family Communication", "Network of Support", "Navigating Systems" and "Transition Experiences". Four analytical themes were then derived: "The Cyclical Nature of Grief", "Lifelong Expert in the Needs and Experiences of an Individual with DMD", "Navigating Deviation from Typical Life Course" and "Uncertainty as Ever Present".
The extant evidence suggests that the experience of parenting a child with DMD is often characterised by: a cycle of grief that begins at diagnosis, which runs parallel to the development of expertise in caregiving; within this parents notice deviations from their child's and their own expected life course and adjust to the emotions and uncertainty that this can bring.
IMPLICATIONS FOR REHABILITATION
Professionals should be cognisant to the complex grief process associated with DMD, which occurs from diagnosis onwards.
There should be continued support for parents following bereavement.
Peer support groups may also offer parents ways to maintain well-being.
The necessity for parents to function effectively within an uncertain context that induces challenging emotions suggests a role for psychological therapies.</description><subject>Adaptation, Psychological</subject><subject>caregiver role</subject><subject>Child</subject><subject>Duchenne muscular dystrophy</subject><subject>Humans</subject><subject>Muscular Dystrophy, Duchenne - psychology</subject><subject>Parenting - psychology</subject><subject>parents</subject><subject>Parents - psychology</subject><subject>psychology</subject><subject>qualitative synthesis</subject><subject>Quality of Life</subject><subject>systematic review</subject><issn>0963-8288</issn><issn>1464-5165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><recordid>eNp9kMFu1DAQhi0EotvCI4B85JJiZ2JvcqMqhSJV4gJny7HHrFHipLazy1775PV2txx78YxG3-9f-gj5wNklZy37zDoJbd22lzWr6_JIBiBfkRVvZFMJLsVrsjow1QE6I-cp_WWMcVg3b8kZiAYEZ92KPFzRtE8ZR529oRG3HndUB0vvFz34XK5bLETIG0w-0cnRslH8N2P0GAw-nWYdMeSn1Qfrt96WcKJD2cIfuvN5Q78uZoMhIB2XZJZBR2pLbZzmzf4deeMKju9P84L8_nbz6_q2uvv5_cf11V1lGg650rIRnRVomXOmN3XLZBHRGNsD9GwNUHPhYN2vZds6BGjRFhZ7ZjR0zlq4IJ-O_85xul8wZTX6ZHAYdMBpSaqWombAukYWVBxRE6eUIjo1Rz_quFecqYN-9axfHfSrk_6S-3iqWPoR7f_Us-8CfDkCPrgpjno3xcGqrPfDFF3Uwfik4OWOR90RmAc</recordid><startdate>20230410</startdate><enddate>20230410</enddate><creator>Donnelly, Clare M.</creator><creator>Quinlivan, Rosaline M.</creator><creator>Herron, Aaron</creator><creator>Graham, Christopher D.</creator><general>Taylor & Francis</general><scope>0YH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1614-0318</orcidid><orcidid>https://orcid.org/0000-0001-8456-9154</orcidid></search><sort><creationdate>20230410</creationdate><title>A systematic review and qualitative synthesis of the experiences of parents of individuals living with Duchenne muscular dystrophy</title><author>Donnelly, Clare M. ; Quinlivan, Rosaline M. ; Herron, Aaron ; Graham, Christopher D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-a6459d5ed0ffcbc28061084cdb33b0733215f37b7688fe338eded0eb0ca39fdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adaptation, Psychological</topic><topic>caregiver role</topic><topic>Child</topic><topic>Duchenne muscular dystrophy</topic><topic>Humans</topic><topic>Muscular Dystrophy, Duchenne - psychology</topic><topic>Parenting - psychology</topic><topic>parents</topic><topic>Parents - psychology</topic><topic>psychology</topic><topic>qualitative synthesis</topic><topic>Quality of Life</topic><topic>systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Donnelly, Clare M.</creatorcontrib><creatorcontrib>Quinlivan, Rosaline M.</creatorcontrib><creatorcontrib>Herron, Aaron</creatorcontrib><creatorcontrib>Graham, Christopher D.</creatorcontrib><collection>Taylor & Francis (Open access)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Disability and rehabilitation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Donnelly, Clare M.</au><au>Quinlivan, Rosaline M.</au><au>Herron, Aaron</au><au>Graham, Christopher D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A systematic review and qualitative synthesis of the experiences of parents of individuals living with Duchenne muscular dystrophy</atitle><jtitle>Disability and rehabilitation</jtitle><addtitle>Disabil Rehabil</addtitle><date>2023-04-10</date><risdate>2023</risdate><volume>45</volume><issue>8</issue><spage>1285</spage><epage>1298</epage><pages>1285-1298</pages><issn>0963-8288</issn><eissn>1464-5165</eissn><abstract>Some parents of children with DMD find their role challenging, affecting quality of life. To inform support methods, we aimed to understand the lived experiences of parents and how these interact with disease progression.
PRISMA informed protocol development. Qualitative and mixed methods studies were included. Four databases were searched and study quality was assessed using a standardised measure. Extracted data were analysed using thematic synthesis.
26 studies were included, comprising 362 parents. Seven descriptive themes were apparent: "Diagnostic Experiences", "Coping with the Caregiver Role", "Illness Trajectory and Associated Interventions", "Family Communication", "Network of Support", "Navigating Systems" and "Transition Experiences". Four analytical themes were then derived: "The Cyclical Nature of Grief", "Lifelong Expert in the Needs and Experiences of an Individual with DMD", "Navigating Deviation from Typical Life Course" and "Uncertainty as Ever Present".
The extant evidence suggests that the experience of parenting a child with DMD is often characterised by: a cycle of grief that begins at diagnosis, which runs parallel to the development of expertise in caregiving; within this parents notice deviations from their child's and their own expected life course and adjust to the emotions and uncertainty that this can bring.
IMPLICATIONS FOR REHABILITATION
Professionals should be cognisant to the complex grief process associated with DMD, which occurs from diagnosis onwards.
There should be continued support for parents following bereavement.
Peer support groups may also offer parents ways to maintain well-being.
The necessity for parents to function effectively within an uncertain context that induces challenging emotions suggests a role for psychological therapies.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>35435109</pmid><doi>10.1080/09638288.2022.2060336</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-1614-0318</orcidid><orcidid>https://orcid.org/0000-0001-8456-9154</orcidid><oa>free_for_read</oa></addata></record> |
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source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Adaptation, Psychological caregiver role Child Duchenne muscular dystrophy Humans Muscular Dystrophy, Duchenne - psychology Parenting - psychology parents Parents - psychology psychology qualitative synthesis Quality of Life systematic review |
title | A systematic review and qualitative synthesis of the experiences of parents of individuals living with Duchenne muscular dystrophy |
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