4.4 Article

Characteristics of good home-based end-of-life care: analysis of 5-year data from a nationwide mortality follow-back survey in England

Journal

BRITISH JOURNAL OF GENERAL PRACTICE
Volume 73, Issue 731, Pages E443-E450

Publisher

ROYAL COLL GENERAL PRACTITIONERS
DOI: 10.3399/BJGP.2022.0315

Keywords

general practice; health inequities; palliative medicine; quality indicators; terminal care

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Receiving good continuity of primary care and palliative care support, as well as dying outside of hospital, are characteristics of good-quality end-of-life care for patients living at home. Being older, female, from areas with less socioeconomic deprivation, and being White are associated with better overall end-of-life care. However, disparities still exist for patients from minority ethnic groups and living in areas of socioeconomic deprivation.
Background Recently, there has been an emphasis on providing good-quality end-of-life care; however, little is known about it and its determinants for patients living at home. Aim To determine what characterises good-quality end-of-life care for patients living at home. Design and setting An observational study using 5-year data from the National Survey of Bereaved People (Views of Informal Carers Evaluation of Services [VOICES]) in England. Method Analysis was based on data for 63 598 decedents, who were cared for at home in the last 3 months of life. Data were drawn from 110 311 completed mortality follow-back surveys of a stratified sample of 246 763 deaths registered in England between 2011 and 2015. Logistic regression analyses were used to identify independent variables associated with overall quality of end-of-life care and other indicators of end-of-life care quality. Results Patients who received good continuity of primary care (adjusted odds ratio [AOR] 2.03; 95% confidence interval [CI] = 2.01 to 2.06) and palliative care support (AOR 1.86; 95% CI = 1.84 to 1.89) experienced better overall quality of end-of-life care than those who did not, as perceived by relatives. Decedents who died from cancer (AOR 1.05; 95% CI = 1.03 to 1.06) or outside of hospital were more likely to receive good end-of-life care, as perceived by relatives. Being older, female (AOR 1.16; 95% CI = 1.15 to 1.17), from areas with least socioeconomic deprivation, and White (AOR 1.09; 95% CI = 1.06 to 1.12) were associated with better overall end-of-life care, as perceived by relatives. Conclusion Better quality of end-of-life care was associated with good continuity of primary care, specialist palliative care support, and death outside of hospital. Disparities still exist for those from minority ethnic groups and those living in areas of socioeconomic deprivation. Future commissioning and initiatives must consider these variables to provide a more-equitable service.

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