Literature DB >> 32472121

Racism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and Support.

Ifigenia Mougianis1, Lindsey L Cohen2, Sarah Martin3, Caitlin Shneider2, Meredith Bishop2.   

Abstract

INTRODUCTIONS: Sickle cell disease (SCD) is the most commonly inherited blood disorder in the United States, and it predominately affects the Black community. SCD is characterized by a number of symptoms, including unpredictable pain, which can lead to hospitalizations. Data indicate that people with SCD experience racism and ample data indicate that racism predicts depressive symptoms and impaired health-related quality of life (HRQOL). In contrast, research suggests that social support might buffer the impact of racism on depression. The aim of this study was to explore associations among perceived racism, depressive symptoms, and HRQOL in adolescents with SCD. Consistent with the literature, it was predicted that perceived racism would predict HRQOL through depression, and social support would moderate the negative impact of racism on depression.
METHODS: In a cross-sectional design, 75 inpatient adolescents with SCD completed measures of perceived racism, depressive symptoms, HRQOL, and social support.
RESULTS: This results indicated a moderated mediation model with greater perceived racism predicting more depressive symptoms, which in turn related to poorer HRQOL; greater access to social support from individuals with SCD strengthened the perceived racism-depressive symptom association.
CONCLUSIONS: Findings suggest a model for how racism, depressive symptoms, HRQOL, and social support might interact in hospitalized adolescents with SCD. Longitudinal or experimental designs are needed to substantiate directionality among these variables. Results highlight several areas for future research and clinical avenues to improve the welfare of youth with SCD.
© The Author(s) 2020. Published by Oxford University Press on behalf of the Society of Pediatric Psychology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  depression; quality of life; race/ethnicity; sickle cell disease; social support

Mesh:

Year:  2020        PMID: 32472121     DOI: 10.1093/jpepsy/jsaa035

Source DB:  PubMed          Journal:  J Pediatr Psychol        ISSN: 0146-8693


  4 in total

1.  Health-related quality of life in hemoglobinopathies: A systematic review from a global perspective.

Authors:  Francesca Rodigari; Giorgia Brugnera; Raffaella Colombatti
Journal:  Front Pediatr       Date:  2022-08-25       Impact factor: 3.569

2.  Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation.

Authors:  Megan M Miller; Deanna D Rumble; Adam T Hirsh; Tine Vervoort; Lori E Crosby; Avi Madan-Swain; Jeffrey Lebensburger; Anna M Hood; Zina Trost
Journal:  Pain Med       Date:  2021-10-08       Impact factor: 3.750

3.  Introduction to the Special Issue: Addressing Health Disparities in Pediatric Psychology.

Authors:  Cecelia Valrie; Idia Thurston; Melissa Santos
Journal:  J Pediatr Psychol       Date:  2020-09-01

Review 4.  Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority.

Authors:  Raffaella Colombatti; Maddalena Casale; Giovanna Russo
Journal:  Ital J Pediatr       Date:  2021-07-29       Impact factor: 2.638

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.