“If We Don’t Beat It, How Long Will It Take?” Worries and Concerns of Children with Advanced Cancer and Their Parents
<b><i>Background:</i></b> Navigating pediatric advanced cancer is challenging for children and parents, resulting in increased risk for psychological distress. While research has explored parent worries/concerns, few studies have included children's perspectives. <b><i>Objectives:</i></b> To explore worries/concerns in children with advanced cancer and their parents. <b><i>Design:</i></b> This was a part of a larger, mixed-methods study examining shared decision-making. <b><i>Setting/Subjects:</i></b> Children (of age 5-25) with advanced cancer (i.e., relapsed/refractory disease or physician estimated prognosis of <60%) and their parents in the Midwestern United States. <b><i>Measurements:</i></b> Children and parents completed the Response to Stress Questionnaire and individual semi-structured interviews. Coders analyzed the qualitative data via thematic analysis. <b><i>Results:</i></b> Parent and child worries/concerns included: (1) prognosis, (2) symptom burden and side effects of treatment, (3) emotional well-being, (4) impact on future, and (5) no concerns/uncertainty (child-only theme). Benefit-finding emerged as a minor theme. Many expressed concerns about treatment response, resulting in worries about death/dying. Others shared fear about managing current symptoms and the impact of long-term treatment side effects on the child's future. Parents reported worry about their child's emotional well-being, while children expressed worries about their families if they died. While all parents were able to identify worries/concerns, some children denied worries/concerns. Quantitatively, parents similarly identified worries about prognosis and symptom burden but also endorsed concern about being unable to help their child feel better. <b><i>Conclusions:</i></b> Our findings highlight similarities and differences in worries/concerns among children and parents as they navigate a child's advanced cancer journey. Early integration of palliative care may be helpful in mitigating these issues.
Authors
- Alexandra C. Himelhoch (ORCID: https://orcid.org/0000-0002-4122-0507)
- Megan R. Schaefer (ORCID: https://orcid.org/0000-0001-9512-7773)
- Micah Skeens (ORCID: https://orcid.org/0000-0001-6786-8128)
- Cynthia A. Gerhardt (ORCID: https://orcid.org/0000-0002-4376-3652)
- Malcolm Sutherland‐Foggio (ORCID: https://orcid.org/0000-0002-8739-3948)
- Molly Gardner
- Ansley E. Kenney (ORCID: https://orcid.org/0000-0002-0189-7740)
- Randal Olshefski (ORCID: https://orcid.org/0000-0002-6035-2695)
- Priyal Patel
- Lisa Humphrey
- Andrea Wojtowicz
Institutions
- Nationwide Children's Hospital (US)
- University of Florida (US)
- University of Wisconsin–Milwaukee (US)
- The Ohio State University (US)
Publication Details
- Journal
- Journal of Palliative Medicine
- Published
- 2024-11-28
- DOI
- https://doi.org/10.1089/jpm.2024.0307
- Primary Topic
- Childhood Cancer Survivors' Quality of Life
- Type
- article
- Field-Weighted Citation Impact
- 0.00