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

被引:2
作者
Herrera-Abian, Maria [1 ]
Castaneda-Vozmediano, Raul [2 ,10 ]
Anton-Rodriguez, Cristina [2 ]
Palacios-Cena, Domingo [3 ,4 ]
Gonzalez-Morales, Luz Maria [5 ,6 ]
Pfang, Bernadette [7 ,8 ]
Noguera, Antonio [1 ,9 ]
机构
[1] Infanta Elena Univ Hosp, Palliat Care Unit, Madrid, Spain
[2] Univ Francisco de Vitoria, Fac Med, Madrid, Spain
[3] Rey Juan Carlos Univ Hum & QRinHS, Dept Phys Therapy Occupat Therapy Phys Med & Reha, Alcorcon, Spain
[4] Rey Juan carlos Univ Hum & QRinHS, Humanities & Qualitat Res Hlth Sci Res Grp, Alcorcon, Spain
[5] Hosp Univ Infanta Elena, Bioeth Dept, Madrid, Spain
[6] Hosp Univ infanta elena, support Team, Madrid, Spain
[7] Clin & Org Innovat Unit UICO, Madrid, Spain
[8] Fdn Jimenez Diaz Univ Hosp, Healthcare Res Inst, Madrid, Spain
[9] Fdn Jimenez Diaz Univ Hosp, Palliat Care, Madrid, Spain
[10] Francisco de Vitoria Univ, Fac Med, carretera Pozuelo,Km 1800, Madrid 28223, Spain
关键词
Caregivers; palliative care; palliative medicine; qualitative research; CANCER-PATIENTS; SATISFACTION; OUTCOMES; PATIENT; COMMUNICATION;
D O I
10.1080/07853890.2023.2260400
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. This article describes a qualitative case study focusing on family caregivers' perception of end-of-life care during their loved ones' dying process in their last hospital admission. Differences were observed between palliative care and non-palliative care groups regarding the perception of scientific appropriateness of care and person-centered nature of care as reported by caregivers.
引用
收藏
页数:11
相关论文
共 58 条
  • [1] Integrated Primary Palliative Care in Nigeria- Perspectives of Patients, Families and Providers
    Afolabi, Oladayo A.
    Nkhoma, Kennedy
    Soyannwo, Olaitan
    Aje, Akinyemi
    Ogunniyi, Adesola
    Harding, Richard
    Maddocks, Matthew
    [J]. JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2022, 64 (04) : 319 - 329
  • [2] Patient & Caregiver Experiences: Qualitative Study Comparison Before and After Implementation of Early Palliative Care for Advanced Colorectal Cancer
    Ahmed, Sadia
    Naqvi, Syeda Farwa
    Sinnarajah, Aynharan
    McGhan, Gwen
    Simon, Jessica
    Santana, Maria J.
    [J]. CANADIAN JOURNAL OF NURSING RESEARCH, 2023, 55 (01) : 110 - 125
  • [3] How Caregivers Cope and Adapt When a Family Member Is Diagnosed With a Hematologic Malignancy: Informing Supportive Care Needs
    Albrecht, Tara A.
    Hoppe, Rebecca
    Winter, Marcia A.
    [J]. CANCER NURSING, 2022, 45 (06) : E849 - E855
  • [4] Arias-Casais N., 2019, EAPC Atlas of Palliative Care in Europe 2019
  • [5] Arias-Casais N., 2019, EAPCU Atlas of Palliative Care in Europe 2019
  • [6] Baxter P, 2008, QUAL REP, V13, P544
  • [7] Benitez Del Rosario M A, 2002, Aten Primaria, V29, P50
  • [8] An international prospective study of the EORTC cancer in-patient satisfaction with care measure (EORTC IN-PATSAT32)
    Brédart, A
    Bottomley, A
    Blazeby, JM
    Conroy, T
    Coens, C
    D'Haese, S
    Chie, WC
    Hammerlid, E
    Arraras, JI
    Efficace, F
    Rodary, C
    Schraub, S
    Costantini, M
    Costantini, A
    Joly, F
    Sezer, O
    Razavi, D
    Mehlitz, M
    Bielska-Lasota, M
    Aaronson, NK
    [J]. EUROPEAN JOURNAL OF CANCER, 2005, 41 (14) : 2120 - 2131
  • [9] Communication in palliative care: talking about the end of life, before the end of life
    Brighton, Lisa Jane
    Bristowe, Katherine
    [J]. POSTGRADUATE MEDICAL JOURNAL, 2016, 92 (1090) : 466 - 470
  • [10] Carpenter C., 2008, QUALITATIVE RES OCCU