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dc.contributor.authorMc Carron, Mary
dc.contributor.authorBurke, Eilish
dc.contributor.authorTimmins, Fiona
dc.contributor.authorMc Callion, Philip
dc.date.accessioned2025-03-04T17:19:30Z
dc.date.available2025-03-04T17:19:30Z
dc.date.issued2024
dc.date.submitted2024en
dc.identifier.citationMcCarron, M., Burke, E., McCallion, P. Timmins, F., A Qualitative Exploration of Healthcare Workers' Experiences of End of Life Care for People With an Intellectual Disability, Journal of Advanced Nursing, 2024en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractAim: To explore healthcare workers' experiences of end of life care for people with an intellectual disability. Design: A descriptive qualitative study. Method: Semi-structured interviews were conducted with 28 healthcare workers who cared for older people with an intellectual disability at their end of life. Data were analysed using thematic analysis and reported according to the COREQ guidelines. Results: Three major themes emerged: not joining up the dots, living the life desired in one's last days and dealing with death and beyond. Conclusion: Gaps emerged in the care of the person with intellectual disability. Pain assessment and pain management were particular challenges. End of life care was not always effectively planned, and earlier intervention, including end of life conver- sations, were needed. More needs to be done in terms of education for healthcare workers, and especially those in the acute care setting and palliative care services who may be unfamiliar with the needs of this cohort. Implications for the Profession and/or Patient Care: There is little consensus or understanding about the palliative care needs of those with intellectual disability. There are often specific challenges around providing palliative care particularly in relation to healthcare staffs' knowledge and confidence in understanding palliative care needs of this group and indeed com- municating and assessing particular needs. Staff require educational preparation and training in palliative care to address the particular needs of this cohort. Impact: This study revealed that there are gaps emerging in the care of the person with intellectual disability at the end of life. Pain assessment and pain management are particular challenges that require urgent attention. Patient or Public Contribution: There was no patient or publication contribution in this specific study, although IDS-TILDA has a client representative and advisory committee that advise on all aspects of project design and management.en
dc.language.isoenen
dc.relation.ispartofseriesJournal of Advanced Nursing;
dc.rightsYen
dc.subjectage-specific care || death || developmental disability || hospice and palliative nursing || intellectual disability || interviews || palliative care || semi- structured interviewsen
dc.titleA Qualitative Exploration of Healthcare Workers' Experiences of End of Life Care for People With an Intellectual Disabilityen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mccarrm
dc.identifier.peoplefinderurlhttp://people.tcd.ie/timminsf
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mccallip
dc.identifier.peoplefinderurlhttp://people.tcd.ie/eburke7
dc.identifier.rssinternalid275561
dc.identifier.doihttps://doi.org/10.1111/jan.16556
dc.rights.ecaccessrightsopenAccess
dc.relation.doihttps://doi.org/10.1111/jan.16556en
dc.relation.citesCitesen
dc.subject.TCDThemeAgeingen
dc.identifier.orcid_id0000-0002-2531-0422
dc.status.accessibleNen
dc.contributor.sponsorHealth Research Board (HRB)en
dc.identifier.urihttps://hdl.handle.net/2262/111243


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