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The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study

INTRODUCTION: 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...

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Autores principales: Herrera-Abián, María, Castañeda-Vozmediano, Raul, Antón-Rodríguez, Cristina, Palacios-Ceña, Domingo, González-Morales, Luz María, Pfang, Bernadette, Noguera, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519265/
https://www.ncbi.nlm.nih.gov/pubmed/37738527
http://dx.doi.org/10.1080/07853890.2023.2260400
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author Herrera-Abián, María
Castañeda-Vozmediano, Raul
Antón-Rodríguez, Cristina
Palacios-Ceña, Domingo
González-Morales, Luz María
Pfang, Bernadette
Noguera, Antonio
author_facet Herrera-Abián, María
Castañeda-Vozmediano, Raul
Antón-Rodríguez, Cristina
Palacios-Ceña, Domingo
González-Morales, Luz María
Pfang, Bernadette
Noguera, Antonio
author_sort Herrera-Abián, María
collection PubMed
description INTRODUCTION: 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.
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spelling pubmed-105192652023-09-26 The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study Herrera-Abián, María Castañeda-Vozmediano, Raul Antón-Rodríguez, Cristina Palacios-Ceña, Domingo González-Morales, Luz María Pfang, Bernadette Noguera, Antonio Ann Med Primary Care INTRODUCTION: 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. Taylor & Francis 2023-09-22 /pmc/articles/PMC10519265/ /pubmed/37738527 http://dx.doi.org/10.1080/07853890.2023.2260400 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Primary Care
Herrera-Abián, María
Castañeda-Vozmediano, Raul
Antón-Rodríguez, Cristina
Palacios-Ceña, Domingo
González-Morales, Luz María
Pfang, Bernadette
Noguera, Antonio
The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
title The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
title_full The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
title_fullStr The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
title_full_unstemmed The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
title_short The caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
title_sort caregiver’s perspective on end-of-life inpatient palliative care: a qualitative study
topic Primary Care
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10519265/
https://www.ncbi.nlm.nih.gov/pubmed/37738527
http://dx.doi.org/10.1080/07853890.2023.2260400
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