Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/14831
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dc.contributor.authorSiddiq, S-
dc.contributor.authorWilson, BJ-
dc.contributor.authorGraham, ID-
dc.contributor.authorLamoureux, M-
dc.contributor.authorKhangura, SD-
dc.contributor.authorTingley, K-
dc.contributor.authorTessier, L-
dc.contributor.authorChakraborty, P-
dc.contributor.authorCoyle, D-
dc.contributor.authorDyack, S-
dc.contributor.authorGillis, J-
dc.contributor.authorGreenberg, C-
dc.contributor.authorHayeems, RZ-
dc.contributor.authorJain-Ghai, S-
dc.contributor.authorKronick, JB-
dc.contributor.authorLaberge, A-M-
dc.contributor.authorLittle, J-
dc.contributor.authorMitchell, JJ-
dc.contributor.authorPrasad, C-
dc.contributor.authorSiriwardena, K-
dc.contributor.authorSparkes, R-
dc.contributor.authorSpeechley, KN-
dc.contributor.authorStockler, S-
dc.contributor.authorTrakadis, Y-
dc.contributor.authorWafa, S-
dc.contributor.authorWalia, J-
dc.contributor.authorWilson, K-
dc.contributor.authorYuskiv, N-
dc.contributor.authorPotter, BK-
dc.date.accessioned2017-06-28T12:17:10Z-
dc.date.available2016-12-07-
dc.date.available2017-06-28T12:17:10Z-
dc.date.issued2016-
dc.identifier.citationORPHANET JOURNAL OF RARE DISEASES, 2016, 11 pp. ? - ? (10)en_US
dc.identifier.issnhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000390318400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=f12c8c83318cf2733e615e54d9ed7ad5-
dc.identifier.issnARTN 168-
dc.identifier.issnhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000390318400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=f12c8c83318cf2733e615e54d9ed7ad5-
dc.identifier.issnARTN 168-
dc.identifier.issn1750-1172-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/14831-
dc.description.abstractAbstract Background: We sought to understand the experiences of parents/caregivers of children with inherited metabolic diseases (IMD) in order to inform strategies for supporting patients and their families. We investigated their experiences regarding the management of disease, its impact on child and family life, and interactions with the health care system. Methods: From four Canadian centres, we conducted semi-structured telephone interviews with parents/caregivers of children with an IMD who were born between 2006 and 2015 and who were participating in a larger cohort study. Participants were selected with the aim of achieving a diverse sample with respect to treatment centre, IMD, and age of the child. Interviews emphasized the impacts of the disease and its treatment on the child and family and explicitly queried perceptions of interactions with the health care system. We identified emergent themes from the interview data. Results: We completed interviews with 21 parents/caregivers. The 21 children were aged <1 to 7 years old with IMD that included amino acid disorders, urea cycle disorders, fatty acid oxidation disorders, and organic acid disorders or ‘other’ IMD. Most parents reported that they and their families had adapted well to their child’s diagnosis. Parents used proactive coping strategies to integrate complex disease management protocols into routine family life. An important source of stress was concern about the social challenges faced by their children. Participants reported positive interactions with their most involved health care providers within the metabolic clinic. However, they reported challenges associated with the health care system outside of disease-specific metabolic care, when encountering systems and providers unfamiliar with the child’s disease. Conclusions: The successful use of proactive coping strategies among parents of children with IMD in this study suggests the potential value of promoting positive coping and is an important direction for future study. Parents’ social concerns for their children were important stressors that warrant consideration by health care providers positioned to support families. Our results with respect to experiences with care highlight the important role of specialized metabolic clinics and point to a need for better coordination of the care that takes place outside the disease-specific management of IMD.en_US
dc.description.sponsorshipThis study was funded by the Canadian Institutes of Health Research (CIHR) Emerging Team Grant, TR3-119195.en_US
dc.format.extent? - ? (10)-
dc.languageEnglish-
dc.language.isoenen_US
dc.publisherBIOMED CENTRAL LTDen_US
dc.subjectScience & Technologyen_US
dc.subjectLife Sciences & Biomedicineen_US
dc.subjectGenetics & Heredityen_US
dc.subjectMedicine, Research & Experimentalen_US
dc.subjectResearch & Experimental Medicineen_US
dc.subjectExperiences with careen_US
dc.subjectInherited metabolic diseasesen_US
dc.subjectFamily supporten_US
dc.subjectCopingen_US
dc.subjectQualitative researchen_US
dc.subjectOF-LIFEen_US
dc.subjectINBORN-ERRORSen_US
dc.subjectPSYCHOSOCIAL-ASPECTSen_US
dc.subjectMEDICAL COMPLEXITYen_US
dc.subjectPARENTAL BELIEFSen_US
dc.subjectDATA SATURATIONen_US
dc.subjectOUTCOMESen_US
dc.subjectIMPACTen_US
dc.subjectDISABILITIESen_US
dc.subjectDISORDERSen_US
dc.titleExperiences of caregivers of children with inherited metabolic diseases: A qualitative studyen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1186/s13023-016-0548-2-
dc.relation.isPartOfORPHANET JOURNAL OF RARE DISEASES-
pubs.publication-statusPublished-
pubs.volume11-
Appears in Collections:Dept of Health Sciences Research Papers

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