Literature DB >> 28952886

Predictors of patient-related benefit, burden and feeling safe in relation to hospital admissions in palliative care: A cross-sectional survey.

Jackie Robinson1,2, Merryn Gott1, Rosemary Frey1, Clare Gardiner1, Christine Ingleton3.   

Abstract

BACKGROUND: Research exploring patient experience of palliative care in the hospital setting has previously been limited to negative aspects of care. However, recent studies have shown that patients with palliative care needs experience benefits being in hospital. Little is known about how experiences of benefit and burden vary according to socio-demographic and illness-related factors and how these experiences influence patient preferences to return to hospital. AIM: To identify factors influencing experiences of benefit and burden and the predictors associated with a preference to return to hospital in palliative care.
DESIGN: Cross-sectional design using a questionnaire survey. SETTING/PARTICIPANTS: In total, 116 hospital inpatients admitted with palliative care needs in an urban hospital in New Zealand. Recruitment was from an oncology ward, four general medical wards and a respiratory ward.
RESULTS: Those living in more deprived areas experienced more benefit being in hospital ( F(4, 109) = 3.15, p = 0.017), while younger people ( F(4, 109) = 4.44, p = 0.00) and those from Asian or Pacific cultures ( F(2, 111) = 7.78, p = 0.000) experienced more burden. Those with a non-cancer diagnosis felt less safe in hospital ( p = 0.04). 'Feeling safe' was a significant ( B = 0.14, p = 0.03) predictor for a preference to return to hospital.
CONCLUSION: Deprivation, diagnosis, age and ethnicity influenced experiences of benefit and burden in hospital. 'Feeling safe' was a significant predictor for a preference to return to hospital. Further research is needed to understand why certain patient factors influence experiences of hospitalisation and how 'feeling safe' can be replicated in other care environments.

Entities:  

Keywords:  Palliative care; hospital admissions; hospitalisations; patient preferences

Mesh:

Year:  2017        PMID: 28952886     DOI: 10.1177/0269216317731991

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  4 in total

1.  Residential aged care residents and components of end of life care in an Australian hospital.

Authors:  Laurence Jee Peng Leong; Gregory Brian Crawford
Journal:  BMC Palliat Care       Date:  2018-06-09       Impact factor: 3.234

2.  Exploring a New Model of End-of-Life Care for Older People That Operates in the Space Between the Life World and the Healthcare System: A Qualitative Case Study.

Authors:  Steven Dodd; Nancy Preston; Sheila Payne; Catherine Walshe
Journal:  Int J Health Policy Manag       Date:  2020-08-01

3.  Quality indicators for the evaluation of end-of-life care in Germany - a retrospective cross-sectional analysis of statutory health insurance data.

Authors:  Katharina van Baal; Sophie Schrader; Nils Schneider; Birgitt Wiese; Jona Theodor Stahmeyer; Sveja Eberhard; Siegfried Geyer; Stephanie Stiel; Kambiz Afshar
Journal:  BMC Palliat Care       Date:  2020-12-08       Impact factor: 3.234

Review 4.  ILIVE Project Volunteer study. Developing international consensus for a European Core Curriculum for hospital end-of-life-care volunteer services, to train volunteers to support patients in the last weeks of life: A Delphi study.

Authors:  Tamsin McGlinchey; Stephen R Mason; Ruthmarijke Smeding; Anne Goosensen; Inmaculada Ruiz-Torreras; Dagny Faksvåg Haugen; Miša Bakan; John E Ellershaw
Journal:  Palliat Med       Date:  2021-10-20       Impact factor: 4.762

  4 in total

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