“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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

“If We Don’t Beat It, How Long Will It Take?” Worries and Concerns of Children with Advanced Cancer and Their Parents

Alexandra C. Himelhoch, Megan R. Schaefer, Micah Skeens, Cynthia A. Gerhardt et al.
Journal of Palliative Medicine
Childhood Cancer Survivors' Quality of Life
article

“If We Don’t Beat It, How Long Will It Take?” Worries and Concerns of Children with Advanced Cancer and Their Parents

Alexandra C. Himelhoch, Megan R. Schaefer, Micah Skeens, Cynthia A. Gerhardt, Malcolm Sutherland‐Foggio, Molly Gardner, Ansley E. Kenney, Randal Olshefski, Priyal Patel, Lisa Humphrey, Andrea Wojtowicz
article en

Abstract

<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.

Journal of Palliative MedicineVol. 28(2)
Nationwide Children's Hospital (US), University of Florida (US), University of Wisconsin–Milwaukee (US), The Ohio State University (US)
Openalex Percentile: Top 67%
Childhood Cancer Survivors' Quality of Life
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.