Standards of psychosocial care for parents of children with cancer
Open accessAbstract
Parents and caregivers of children with cancer are both resilient and deeply affected by the child's cancer. A systematic review of published research since 1995 identified 138 studies of moderate quality indicating that parent distress increases around diagnosis, then returns to normal levels. Post-traumatic symptoms are common. Distress may be impairing for vulnerable parents and may impact a child's coping and adjustment. Moderate quality evidence and expert consensus informed a strong recommendation for parents and caregivers to receive early and ongoing assessment of their mental health needs with access to appropriate interventions facilitated to optimize parent, child, and family well being.
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International standards of care state that parents should have early and ongoing access to psychosocial support and evidence-based interventions throughout their child's cancer trajectory.
“Given parents’ risk of psychological difficulties, international standards of care state that parents should have early and ongoing access to psychosocial support and evidence-based interventions throughout their child’s cancer trajectory [21].”
From Providing psychological support to parents of childhood cancer survivors: ‘cascade’ intervention trial results and lessons for the future (2021) · cites this paper as [21]
The Discussion (page unavailable) recommends early and ongoing assessment of parents’ mental health needs and facilitating access to appropriate interventions. It does not specify early and ongoing access to evidence-based interventions throughout the child’s cancer trajectory; it notes that evidence-based interventions are not yet routinely available. (LLM, conf=0.86)
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- Authors
- Kearney, J. A., Salley, C. G., & Muriel, A. C.
- Affiliations
- Memorial Sloan Kettering Cancer Center (US)
- Boston Children's Hospital (US)
- Corresponding author
- Kearney, Julia A.
- Venue
- Pediatric Blood & Cancer
- Publisher
- Wiley
- Published
- 2015-12
- Volume
- 62
- Issue
- S5
- Pages
- S632-83
- ISSN
- 1545-5009 (ISSN-L)
- 1545-5017
- PMC
- PMC5066591
- OpenAlex
- W2267098927
- Cited by
- 356
- References
- 132
- Citations by year
- 2026: 23 · 2025: 37 · 2024: 41 · 2023: 33 · 2022: 51 · 2021: 44 · 2020: 35 · 2019: 40 · 2018: 22 · 2017: 20 · 2016: 6 · 2015: 2
- FWCI
- 2.54
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Pediatric Blood & Cancer (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Memorial Sloan-Kettering Cancer Center
- Royal Bank of Canada
- National Cancer Institute (P30CA008748)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Childhood Cancer Survivors' Quality of Life
- Social Sciences › Sociology and Political Science › Family Support in Illness
- Health Sciences › Medicine › Oncology › Cancer survivorship and care
- Keywords
- psychosocial care, parents of children with cancer, caregiver distress, post-traumatic stress, mental health assessment, early intervention, family well-being, childhood cancer
- MeSH terms
- Child, Humans, Neoplasms, Parents, Psychology, Stress, Psychological, Standard of Care
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