ABSTRACT Objectives The number of Canadian children living with serious illness is increasing. Access to specialist paediatric palliative care is recognized as essential for these children, their families, and their care providers, and yet programs remain under-resourced or non-existent in much of Canada. Health services planning requires current data. This study examined the initial experience of a specialist program established in 2015 at a tertiary paediatric centre in Canada. Methods A prospective database study of referred patients was conducted from 2015 to 2023 (prenatal referrals were first accepted in 2021). Data were collected at referral, consult, and discharge/death/end of pregnancy. Program clinician growth was tracked. The analysis included descriptive statistics and a Kaplan–Meier survival curve. Results The program received 650 unique paediatric referrals plus 55 prenatal referrals. The number of patients receiving care annually quadrupled over the course of the study. Two-hundred and twenty-seven children died: 99% with goal-concordant care at end-of-life and most frequently in hospital, although death at home was increasingly common. A rapid increase in program resources was required to meet care needs per modern standards of care. Conclusions This study demonstrates that a new paediatric palliative care program was met with demand akin to existing established comparator programs. These results are congruent with the increase in prevalence of children with serious illness and the evolution of care standards to incorporate specialist care provision. These findings can help advocacy and resource planning for modernizing Canada’s paediatric palliative care infrastructure.
Lysecki et al. (Mon,) studied this question.