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.
Resources from the same session
Optimising well-being and tackling burnout in oncology
Presenter: Kok Haw Jonathan Lim
Session: ESMO-EONS collaborative session: Caring for the carers
Resources:
Slides
Webcast
Cancer is a family affair
Presenter: Karin Dieperink
Session: ESMO-EONS collaborative session: Caring for the carers
Resources:
Slides
Webcast
CN30 - Scoping review of the interventions for promoting dyadic adjustment in adult cancer patients and their partners
Presenter: Reyyan Gürel
Session: ESMO-EONS collaborative session: Caring for the carers
Resources:
Abstract
Slides
Webcast
CN4 - Parents’ lived experience of children with leukemia
Presenter: Qasem Alnasser
Session: ESMO-EONS collaborative session: Caring for the carers
Resources:
Abstract
Slides
Webcast
Q&A and discussion
Session: ESMO-EONS collaborative session: Caring for the carers
Resources:
Webcast