Supporting friends and family of adults with a primary brain tumour: A systematic review
- PMID: 34633723
- DOI: 10.1111/hsc.13586
Supporting friends and family of adults with a primary brain tumour: A systematic review
Abstract
Expanding on the limited work in supportive care for friends and family caregivers of adults with a primary brain tumour, this review sought to examine all available evidence since 2010 on the efficacy and feasibility of supportive interventions for this population including non-controlled studies. A systematic review of the literature was conducted on the feasibility and effectiveness/efficacy of supportive interventions for brain cancer caregivers in line with PRISMA guidelines. 13 studies met the eligibility criteria and were identified for inclusion. Most interventions employed tailored psychoeducation, and expert involvement via psychotherapy or care coordination. Only two interventions demonstrated clinically significant improvements. Findings indicate that dyadic yoga programs, and programs that enhance caregiver mastery to manage patient behavioural problems, may lead to improvements in some clinical outcomes. Results highlight the diverse nature of supportive interventions and indicate that support for primary brain tumour caregivers is currently suboptimal. Our findings illustrate an overall low certainty of evidence, with a need for more adequately powered randomised controlled trials. As the complexities of brain cancer care-giving are an obstacle to standardised interventions, this review underscores the need for future trials to incorporate complimentary qualitative research methodologies.
Keywords: brain tumour; caregivers; carers; family; neuro-oncology; supportive care.
© 2021 John Wiley & Sons Ltd.
References
REFERENCES
-
- Andersen, N. I., Nielsen, C. I., Danbjørg, D. B., Møller, P. K., & Dieperink, K. B. (2019). Caregivers’ need for support in an outpatient cancer setting. Oncology Nursing Forum, 46(6), 757-767. https://doi.org/10.1188/19.onf.757-767
-
- Aoun, S. M., Deas, K., Howting, D., & Lee, G. (2015). Exploring the support needs of family caregivers of patients with brain cancer using the CSNAT: A comparative study with other cancer groups. PLoS One, 10(12), e0145106. https://doi.org/10.1371/journal.pone.0145106
-
- Arber, A., Hutson, M., de Vries, K., & Guerrero, D. (2013). Finding the right kind of support: A study of carers of those with a primary malignant brain tumour. European Journal of Oncology Nursing, 17(1), 52-58. https://doi.org/10.1016/j.ejon.2012.01.008
-
- Baumstarck, K., Chinot, O., Tabouret, E., Farina, P., Barrié, M., Campello, C., Patrirena, G., Hamidou, Z., & Auquier, P. (2018). Coping strategies and quality of life: A longitudinal study of high-grade glioma patient-caregiver dyads. Health and Quality of Life Outcomes, 16(1), 157. https://doi.org/10.1186/s12955-018-0983-7
-
- Boele, F. W., Hoeben, W., Hilverda, K., Lenting, J., Calis, A., Sizoo, E. M., Collette, E. H., Heimans, J. J., Taphoorn, M. J. B., Reijneveld, J. C., & Klein, M. (2013). Enhancing quality of life and mastery of informal caregivers of high-grade glioma patients: A randomized controlled trial. Journal of Neuro-Oncology, 111(3), 303-311. https://doi.org/10.1007/s11060-012-101203
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous
