Literature DB >> 30629003

Impact of Race and Socioeconomic Status on Psychologic Outcomes in Childhood Cancer Patients and Caregivers.

Logan H Ramsey1, Patricia E Graves1, Katianne M Howard Sharp2,3, Samantha R Seals4,5, Anderson B Collier1, Cynthia W Karlson1,2.   

Abstract

Complex relationships between race and socioeconomic status have a poorly understood influence on psychologic outcomes in pediatric oncology. The Family Symptom Inventory was used to assess symptoms of depression and anxiety in pediatric patients with cancer and their caregivers. Separate hierarchical linear regression models examined the relationship between demographic variables, cancer characteristics, socioeconomic status, and access to care and patient or caregiver depression/anxiety. Participants included 196 pediatric patients with cancer (mean age, 11.21 y; 49% African American) and their caregivers. On average, caregivers reported low levels of depression/anxiety. Symptoms of depression and anxiety in patients were correlated with poorer mental health in caregivers (r=0.62; P<0.01). Self-reported financial difficulty (β=0.49; P<0.001) and brain cancer diagnosis for their child (β=0.42; P=0.008) were significantly associated with depression and anxiety in caregivers. Analysis did not reveal significant associations between race, household income, or access to care and patient or caregiver depression/anxiety. Perception of financial hardship can adversely impact mental health in caregivers of children with cancer. Psychosocial assessment and interventions may be especially important for caregivers of patients with brain tumors and caregivers who report feeling financial difficulty.

Entities:  

Mesh:

Year:  2019        PMID: 30629003     DOI: 10.1097/MPH.0000000000001405

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  5 in total

1.  Racial and ethnic disparities in neurocognitive, emotional, and quality-of-life outcomes in survivors of childhood cancer: A report from the Childhood Cancer Survivor Study.

Authors:  Stephanie B Dixon; Nan Li; Yutaka Yasui; Smita Bhatia; Jacqueline N Casillas; Todd M Gibson; Kirsten K Ness; Jerlym S Porter; Rebecca M Howell; Wendy M Leisenring; Leslie L Robison; Melissa M Hudson; Kevin R Krull; Gregory T Armstrong
Journal:  Cancer       Date:  2019-07-10       Impact factor: 6.860

2.  The Relationship between the Unmet Needs of Chinese Family Caregivers and the Quality of Life of Childhood Cancer Patients Undergoing Inpatient Treatment: A Mediation Model through Caregiver Depression.

Authors:  Jiamin Wang; Peter C Coyte; Di Shao; Xuemei Zhen; Ni Zhao; Chen Sun; Xiaojie Sun
Journal:  Int J Environ Res Public Health       Date:  2022-08-17       Impact factor: 4.614

3.  Pediatric Palliative Care Parents' Distress, Financial Difficulty, and Child Symptoms.

Authors:  Jackelyn Y Boyden; Douglas L Hill; Russell T Nye; Kira Bona; Emily E Johnston; Pamela Hinds; Sarah Friebert; Tammy I Kang; Ross Hays; Matt Hall; Joanne Wolfe; Chris Feudtner
Journal:  J Pain Symptom Manage       Date:  2021-08-20       Impact factor: 3.612

4.  Systematic review of financial burden assessment in cancer: Evaluation of measures and utility among adolescents and young adults and caregivers.

Authors:  John M Salsman; Suzanne C Danhauer; Justin B Moore; Edward H Ip; Laurie E McLouth; Chandylen L Nightingale; Christabel K Cheung; Kristin M Bingen; Reginald D Tucker-Seeley; Denisha Little-Greene; Dianna S Howard; Bryce B Reeve
Journal:  Cancer       Date:  2021-04-13       Impact factor: 6.921

5.  Subjective Toxicity Profiles of Children in Treatment for Cancer: A New Guide to Supportive Care?

Authors:  Pamela S Hinds; Meaghann S Weaver; Janice S Withycombe; Justin N Baker; Shana S Jacobs; Jennifer W Mack; Scott H Maurer; Molly McFatrich; Laura C Pinheiro; Bryce B Reeve; Jichuan Wang
Journal:  J Pain Symptom Manage       Date:  2020-10-20       Impact factor: 5.576

  5 in total

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