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Profile photo of a child looking pensive.

This project aims to address questions of health justice arising out of changes to service restrictions and innovative practice in the delivery of healthcare for children with chronic illness in the UK during the pandemic.

To respond to the pandemic the NHS deployed strategies (e.g. usual service restriction, changes in care delivery, redeployment of staff and clinic space) which had an immediate effect on children’s usual care. To date, the direct impact of Covid-19 infection on children’s physical health has been recorded as being far milder than for other groups. By contrast the indirect impact on children has been profound, with substantial reductions in urgent activity in hospitals. The extent to which health service restrictions and changes in care delivery are fair for children has not been ethically assessed.

This project, undertaken in collaboration with NHS child healthcare specialists, aims to address the omission of a children-related ethical dimension in Covid-19 related research and policy. It will achieve this by exploring which risks on children’s physical and mental health can be morally justified in health systems’ response to the pandemic.

It aims to provide accessible ethical guidance to medical authorities and government departments on how the needs of children with long-term conditions should feature in the prioritisation process required in the pandemic context. This guidance will be assessed, in context, in conjunction with a range of decision-makers who are responsible for making decisions about the allocation to resources and by working closely with the clinical-academic Children and Young People’s Health Partnership (CYPHP) in South East London.

Project Team

  • Jenny Greenwood Research Assistant, Institute of Women and Children’s Health, Kings Health Partners, King’s College London
  • Sapfo Lignou Senior Researcher in Bioethics, Ethox Centre, University of Oxford
  • Mark Sheehan Oxford Biomedical Research Centre Ethics Fellow, Ethox Centre, University of Oxford
  • Ingrid Wolfe Director, Institute for Women and Children's Health; Clinical Senior Lecturer, Consultant Paediatric Population Health King's College London

Focus groups

We are working with the National Children's Bureau to recruit parents/carers of children with chronic illness (asthma, diabetes, cancer, mental health, neurodiversity)  to join our focus group discussions. The aim of this study is to understand the impact of changes in healthcare delivery on the care of children with chronic illness.

This research is funded by a grant from UKRI/AHRC AH/W003945/1