Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session 3

5084 - The BRIGHTLIGHT national survey of the impact of specialist teenage and young adult cancer care on caregivers’ information and support needs

Date

30 Sep 2019

Session

Poster Display session 3

Presenters

Rachel Taylor

Citation

Annals of Oncology (2019) 30 (suppl_5): v829-v835. 10.1093/annonc/mdz275

Authors

R.M. Taylor1, A. Martins2, J. Alvarez-Galvez3, L.A. Fern1, C. Vindrola-Padros4, J.A. Barber5, F. Gibson6, J. Whelan7

Author affiliations

  • 1 Cancer Division, University College London Hospital UCLH NHS Foundation Trust, NW1 2PG - London/GB
  • 2 Cancer Clinical Trials Unit, University College London Hospital UCLH NHS Foundation Trust, NW1 2PG - London/GB
  • 3 Department Of Biomedicine, Biotechnology And Public Health, University of Cadiz, 11001 - Cadiz/ES
  • 4 Faculty Of Pop Health Sciences, University College London, WC1E 7HB - London/GB
  • 5 Department Of Statistical Science, University College London, WC1E 7HB - London/GB
  • 6 Centre For Outcomes And Experience Research In Children’s Health, Illness And Disability (orchid), Great Ormond Street Hospital for Children NHS Foundation Trust, WC1N 3JH - London/GB
  • 7 Oncology, University College London Hospital UCLH NHS Foundation Trust, NW1 2PG - London/GB

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 5084

Background

Teenage and young adult cancer services in England are centralised in 13 principal treatment centres (TYA PTC). We sought to evaluate whether caregivers of young people with cancer had fewer unmet information and support needs if cancer care was provided in a TYA PTC.

Methods

Participants in the cohort study of young people with cancer nominated their main carer to complete the BRIGHTLIGHT Carer Questionnaire. Questionnaires were completed six months after diagnosis. Comparisons were made according to where young people’s care was delivered: all, some or no care in a TYA PTC. Principal component analysis reduced the questionnaire to five dimensions, which were used as dependent variables in subsequent regression analysis.

Results

A total of 830 young people were part of the BRIGHTLIGHT Cohort, of which 514 (62%) caregivers returned a questionnaire. Four hundred and seventy-six responses out of 514 returned questionnaires (92%) could be linked to the location of young people’s care and were included in the analysis. The majority of caregivers were white (89.7%), middle aged (71.1%), married/cohabiting (78%) mothers (80.2%). The Adjusted analysis indicated that caregivers of young people who had all or some of their care in a TYA PTC had more satisfaction with support and also with services specifically provided for carers. Those who had some care in a TYA PTC had greater satisfaction with information but less opportunity to be involved in decisions.

Conclusions

Caregivers of young people who had no TYA PTC, i.e. treated solely in adult or children’s cancer units have the most unmet information and support needs.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

UCLH.

Funding

National Institute for Health Research (NIHR).

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.