Palliative care in Yorkshire, UK 1987-2008: Survival and mortality in a hospice

Abstract

Objective: To provide new epidemiological evidence base of information on models of hospice care for children and young adults. Design: Retrospective cohort study of children referred to a hospice. Setting: Martin House Children's and Young Person's Hospice in Boston Spa, North Yorkshire, UK. Participants: All children who had been referred for care at Martin House Children's Hospice since it opened in August 1987, until May 2008. Main outcome measures: Demographic profiles and survival times overall and by diagnostic group classified by the Association of Children's Palliative Care (ACT) Diagnostic Categories, calculated using the Kaplan-Meier and log rank pair-wise methodology. Results: Over a 20-year period, 1554 children aged from birth to 19 years were referred to Martin House, of whom 89.5% (mean age 7.45 years) were accepted. The deprivation profile, referral source and distribution of diagnoses of these children have changed over time with recently increasing numbers of non-progressive disorders (ACT category 4). The ethnicity profile has changed with an increase in the numbers of South Asian children. The overall mean survival time was 5.6 years (95% CI 5.1 to 6.1) but this differed by ACT category. Diagnostic category was significantly associated with differing survival patterns. Conclusions: There are a disproportionate number of children from areas of higher deprivation being referred for palliative care services. There has been a recent increase in the number of children from South Asian families being referred to palliative care services in Yorkshire. Survival times for children and young people receiving care from a hospice can vary from hours and days to more than 20 years.