Literature DB >> 32020725

Level of agreement between adolescents' self-assessment and parent proxy report of health-related quality of life in adolescents with sickle cell disease.

Alphanso Blake1, Natalie Guthrie-Dixon2, Marlyn Grindley1, Antoinette Barton-Gooden3, Jennifer Knight-Madden1, Monika Asnani1.   

Abstract

BACKGROUND: We aim to assess the levels of agreement between parents, as proxies, and Jamaican adolescents living with sickle cell disease (SCD) in the reporting of the adolescent's quality of life. PROCEDURES: This cross-sectional study assessed 102 patient/proxy pairs on quality of life of adolescents with SCD using the PedsQL-SCD module. The level of agreement among pairs was assessed starting with broad group-level approaches (the Wilcoxon signed-rank test augmented by exploring percentage agreement) tapering to individual-level approaches (intraclass correlation coefficients [ICCs] supplemented with Bland-Altman plots).
RESULTS: Most patients (76.5%) had homozygous SS disease (45.1% females; mean age 15.2 ± 1.5 years). Median total pediatric quality of life (PedsQL) scores were 79.1 (adolescent report) and 80.2 (parental report) (P = .60). There were 11.8% underestimation and 12.7% overestimation of overall health-related quality of life (HRQOL) by parents. The highest perfect agreement existed on the "pain and hurt" domain for both male and female adolescents (85.7% and 84.4%, respectively). Overestimation was highest on the "social communication" domain for both male and female adolescents (19.6% and 34.8%, respectively). Parents exhibited good agreement on total PedsQL scores in male adolescents (ICC = 0.70), but moderate agreement (ICC = 0.43) in female adolescents. Generally, parents underestimated their male child's functioning and overestimated the female child's functioning on the various domains.
CONCLUSIONS: Parents and adolescents exhibit fair agreement in assessment of the adolescent's overall HRQOL but differ on subjective domains. Agreement varies by sex of the affected teen where girls' HRQOL is generally overestimated by the parental proxy. Interventions to improve parents' understanding of their children's psychosocial needs are needed.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  Jamaica; PedsQL-SCD; adolescents; health-related quality of life; level of agreement; sickle cell disease

Mesh:

Year:  2020        PMID: 32020725     DOI: 10.1002/pbc.28198

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  6 in total

Review 1.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

2.  Quality of life assessments in a cohort of Mozambican children with sickle cell disease.

Authors:  Faiaz Issa; Brian Norman Dang; W Chris Buck; Sérgio Chicumbe; Nelsa Nicolau; Chana Virate; Naya Cassamo; Angelina Dias; Faizana Amodo
Journal:  Pan Afr Med J       Date:  2020-08-25

3.  Sex differences in children's health status as measured by the Pediatric Quality of Life Inventory (PedsQL)™: cross-sectional findings from a large school-based sample in the Netherlands.

Authors:  Annelieke Hijkoop; Chantal A Ten Kate; Marlous J Madderom; Hanneke IJsselstijn; Julie A Reuser; Hendrik Koopman; Joost van Rosmalen; André B Rietman
Journal:  BMC Pediatr       Date:  2021-12-18       Impact factor: 2.125

4.  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

5.  Risk mitigation behaviors to prevent infection in the mitochondrial disease community during the COVID-19 pandemic.

Authors:  Eliza Gordon-Lipkin; Shannon Kruk; Elizabeth Thompson; Philip Yeske; Lori Martin; Michio Hirano; Bruce H Cohen; Christopher Steven Marcum; Peter J McGuire
Journal:  Mol Genet Metab Rep       Date:  2021-12-18

Review 6.  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

  6 in total

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