Referral to a specialist paediatric palliative care service in oncology patients

Lorna K Fraser1, Michael Miller, Patricia A McKinney

  • 1Paediatric Epidemiology Group, Centre for Epidemiology and Biostatistics, University of Leeds, Leeds, UK. l.k.fraser@leeds.ac.uk

Pediatric Blood & Cancer
|February 8, 2011
PubMed

Insights

Palliative care referrals for children with cancer in Yorkshire were low (37.6%). Referrals varied by cancer type, indicating potential to improve access to specialist palliative care for pediatric cancer patients.

Area of Science:

  • Pediatric oncology
  • Palliative care
  • Childhood cancer outcomes

Background:

  • Cancer is a leading cause of death in children and young people (0-19 years).
  • In 2005, cancer accounted for 16.2% of deaths in this age group in England and Wales.
  • Palliative care services aim to improve quality of life for patients with life-limiting illnesses.

Purpose of the Study:

  • To assess the referral rates of children and young people with cancer to a children's hospice.
  • To identify patterns in referrals based on cancer type.
  • To determine the potential for increasing access to specialist palliative care.

Main Methods:

  • Retrospective analysis of patient data.
  • Examination of referral records to Martin House Children's Hospice (MH).
  • Comparison of referral proportions with expected rates based on cancer diagnosis.

Main Results:

  • Only 37.6% of children and young people who died from cancer in Yorkshire were referred to MH between 1990-2005.
  • A higher proportion of patients with central nervous system tumors were referred.
  • A lower than expected proportion of patients with leukemia or lymphoma were referred.

Conclusions:

  • Referral rates to specialist palliative care for pediatric cancer patients in Yorkshire were suboptimal.
  • Significant variations in referral patterns exist based on cancer diagnosis.
  • There is a clear opportunity to enhance the integration of palliative care services for children with cancer.

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