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dc.contributor.authorHerrera-Abiána, María
dc.contributor.authorCastañeda-Vozmediano, Raul
dc.contributor.authorAntón Rodríguez, Cristina 
dc.contributor.authorPalacios-Ceña, Domingo
dc.contributor.authorGonzález-Morales, Luz María
dc.contributor.authorPfang, Bernadette
dc.contributor.authorNoguera, Antonio
dc.date.accessioned2023-12-13T09:23:53Z
dc.date.available2023-12-13T09:23:53Z
dc.date.issued2023
dc.identifier.issn1365-2060spa
dc.identifier.urihttps://hdl.handle.net/10641/3570
dc.description.abstractIntroduction: Understanding patient and caregiver experience is key to providing person-centered care. The palliative care approach includes holistic assessment and whole-person care at the end of life, that also involves the patient’s family and loved ones. The aim of this study was to describe the way that family caregivers experienced patients’ deaths during their loved ones’ last hospital admission, comparing inpatient palliative care (PCU) and non-palliative care (Non-PCU) units. Methods: A qualitative case study approach was implemented. Family caregivers of terminally ill patients admitted to the Infanta Elena Hospital (Madrid, Spain) between 2016 and 2018 were included using purposeful sampling. Eligible caregivers were first-degree relatives or spouses present during the patient’s last hospital admission. Data were collected via in-depth interviews and researchers’ field notes. Semi-structured interviews with a question guide were used. A thematic inductive analysis was performed. The group of caregivers of patients admitted to the PCU unit and the group of caregivers of patients admitted to Non-PCU were analyzed separately, through a matrix. Results: In total 24 caregivers (12 from the PCU and 12 from Non-PCU units) were included. Two main themes were identified: caregivers’ perception of scientific and technical appropriateness of care, and perception of person-centred care. Scientific appropriateness of care was subdivided into two categories: diagnostic tests and treatment, and symptom control. Perception of person-centred care was subdivided as: communication, emotional support, and facilitating the farewell process. Caregivers of patients admitted to a PCU unit described their experience of end-of-life care as positive, while their Non-PCU unit counterparts described largely negative experiences. Conclusions: PCU provides a person-centered approach to care at the end of life, optimizing treatment for patients with advanced disease, ensuring effective communication, establishing a satisfactory professional relationship with both patients and their loved ones, and facilitating the farewell process for family caregivers.spa
dc.language.isoengspa
dc.publisherAnnals of Medicinespa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectCaregiversspa
dc.subjectPalliative carespa
dc.subjectPalliative medicinespa
dc.subjectQualitative researchspa
dc.titleThe caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study.spa
dc.typejournal articlespa
dc.type.hasVersionAMspa
dc.rights.accessRightsopen accessspa
dc.description.extent1,34 MBspa
dc.identifier.doi10.1080/07853890.2023.2260400spa
dc.relation.publisherversionhttps://www.tandfonline.com/doi/full/10.1080/07853890.2023.2260400spa


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