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ESMO-EONS collaborative session: Caring for the carers

CN70 - Experiences and needs of carers of patients with head and neck cancer: A systematic review

Date

16 Sep 2024

Session

ESMO-EONS collaborative session: Caring for the carers

Topics

Multi-Disciplinary and Multi-Professional Cancer Care;  Psycho-Oncology;  Survivorship

Tumour Site

Head and Neck Cancers

Presenters

Cherith Semple

Citation

Annals of Oncology (2024) 35 (suppl_2): S1191-S1196. 10.1016/annonc/annonc1585

Authors

C.J. Semple1, M. Tsai2, G. Cherry3, J. Patterson4, S. Rogers5

Author affiliations

  • 1 Institute Of Nursing And Health Research / Cancer Services, Ulster University / South Eastern Health and Social Care Trust, BT15 1AP - Northern Irealnd/GB
  • 2 Oral And Maxillofacial Surgery, Royal Brisbane and Women’s Hospital, Brisbane, QLD 4006 - Brisbane/AU
  • 3 Department Of Primary Care And Mental Health, University of Liverpool, L69 3GF - Liverpool/GB
  • 4 School Of Health Sciences, Liverpool Head and Neck Centre, School of Health Science, L3 5TR - Liverpool/GB
  • 5 Oral And Maxillofacial Surgery, Wirral University Teaching Hospital NHS Foundation Trust, CH49 5PE - Metropolitan Borough of Wirral/GB

Resources

This content is available to ESMO members and event participants.

Abstract CN70

Background

The needs of head and neck cancer (HNC) carers tends to be poorly addressed as most support systems are directed towards patients. This systematic review synthesises the existing qualitative evidence from carers for HNC patients to explore their experiences and needs; to inform the initial development of an item prompt list for HNC carers for use in routine clinical practice.

Methods

Seven electronic databases were searched from their inception until November 2022, supplemented by citation chaining and snowballing. Primary qualitative or mixed-methods studies reporting the experiences of carers for HNC patients, elicited using interviews, were included. Screening, selection, data extraction and quality assessment were independently conducted by two researchers. Data were analysed using inductive thematic synthesis and confidence evaluated using GRADE CERQual.

Results

Thirty studies met the inclusion criteria. Two overarching themes and nine subthemes emerged: i) the experiences of loss associated with being a carer (loss of: role and everyday routine, certainty leading to emotional distress, security as fear of recurrence prevailed, finances, intimacy and togetherness, enjoyment from social activities); and ii) factors promoting coping and adjustment to role of carer (information, supportive mechanisms, personal attributes).

Conclusions

A more informed appreciation of the HNC carers experience of sense of loss and what they perceive promotes coping, allows healthcare providers to adapt and refine existing patient support initiatives, to target carers needs. It allows the formulation for items for a pilot prompt tool, and this will be a future project of codesign with HNC carers. More support targeted at the carer in conjunction with the patient will provide a platform for better outcomes.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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