Unmet support needs in teenage and young adult childhood brain tumour survivors and their caregivers: 'it’s all the aftermath, and then you’re forgotten about'
Autor: | Miguel Debono, Emma Nicklin, Adam Glaser, Michelle Kwok-Williams, Florien W. Boele, Lucy Pointon, Naseem Sarwar, Galina Velikova |
---|---|
Rok vydání: | 2021 |
Předmět: |
Gerontology
Aging out Adolescent Pain medicine Survivorship Unmet needs Young Adult 03 medical and health sciences 0302 clinical medicine Quality of life (healthcare) Survivorship curve Humans Medicine Survivors Young adult Health Services Needs and Demand Brain Neoplasms Family caregivers business.industry Late effects Nursing research Teenage young adult Social Support Brain tumour Mental health Caregivers Oncology 030220 oncology & carcinogenesis Quality of Life Original Article Family caregiver business Supportive care 030217 neurology & neurosurgery |
Zdroj: | Supportive Care in Cancer |
ISSN: | 1433-7339 0941-4355 |
Popis: | Purpose Teenage and young adult (TYA) survivors of childhood brain tumours and their family caregivers can experience many late effects of treatment that can hamper the transition to living independent lives. Yet, their long-term supportive care needs are largely unknown. We investigated the supportive care needs of TYA survivors and their caregivers and explored the role and perceived use of support. Methods Face-to-face semi-structured interviews were conducted with survivors aged 16–30 (n = 11) who were ≥ 5 years after diagnosis and caregivers (n = 11). Interviews were recorded and transcriptions thematically analysed. Results Four themes emerged: (1) preferences for support and support services (unmet needs). Concerns regarding mental health, employment and financial uncertainty, the desire to live independently, and lack of support were emphasised. (2) Decline in support. Caregivers noted a drop-off in support available when transitioning to adult services. (3) Reasons for not obtaining adequate support. Several barriers to accessing support were raised, including distance and aging out of services. (4) The role of long-term hospital-based follow-up care. Participants highlighted the importance of, and reassurance from, long-term follow-up care but noted a more all-inclusive approach is required. Conclusions Even many years after diagnosis, TYA childhood brain tumour survivors and their caregivers continue to have unmet supportive care needs. Both TYA survivors and their caregivers can benefit from support to meet their unique needs and improve long-term quality of life. Understanding unmet needs and recognising what services are required due to the late effects of treatment is critical to improving long-term quality of survival. |
Databáze: | OpenAIRE |
Externí odkaz: |