Fersiynau electronig

Dogfennau

Dangosydd eitem ddigidol (DOI)

  • Andrew Papworth
    University of York
  • Julia Hackett
    University of York
  • Bryony Beresford
    University of York
  • Fliss Murtagh
    Hull University
  • Helen Weatherly
    University of York
  • Sebastian Hinde
    University of York
  • Andre Bedendo
    University of York
  • Gabriella Walker
    Parent Advisory Panel Member
  • Jane Noyes
  • Sam Oddie
    Bradford Hospitals National Health Service Trust
  • Chakrapani Vasudevan
    Bradford Hospitals National Health Service Trust
  • Richard Feltbower
    School of Geography, University of Leeds, UK
  • Bob Phillips
    University of York
  • Richard Hain
    Cardiff and Vale University Health BoardSwansea University
  • Gayathri Subramanian
    Manchester University National Health Service Foundation Trust
  • Andrew Haynes
    University of York
  • Lorna K Fraser
    University of York

Background: Although child mortality has decreased over the last few decades, around 4,500 infants and children die in the UK every year, many of whom require palliative care. There is, however, little evidence on paediatric end-of-life care services. The current National Institute for Health and Care Excellence (NICE) guidance provides recommendations about what should be offered, but these are based on low quality evidence. The ENHANCE study aims to identify and investigate the different models of existing end-of-life care provision for infants, children, and young people in the UK, including an assessment of the outcomes and experiences for children and parents, and the cost implications to families and healthcare providers.

Methods: This mixed methods study will use three linked workstreams and a cross-cutting health economics theme to examine end-of-life care models in three exemplar clinical settings: infant, children and young adult cancer services (PTCs), paediatric intensive care units (PICUs), and neonatal units (NNUs).Workstream 1 (WS1) will survey current practice in each setting and will result in an outline of the different models of care used. WS2 is a qualitative comparison of the experiences of staff, parents and patients across the different models identified. WS3 is a quantitative assessment of the outcomes, resource use and costs across the different models identified.

Discussion: Results from this study will contribute to an understanding of how end-of-life care can provide the greatest benefit for children at the end of their lives. It will also allow us to understand the likely benefits of additional funding in end-of-life care in terms of patient outcomes.

Iaith wreiddiolSaesneg
Rhif yr erthygl37
Nifer y tudalennau17
CyfnodolynNIHR open research
Cyfrol2
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - 13 Mai 2022

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