Literature DB >> 20498169

A controlled, longitudinal study of the social functioning of youth with sickle cell disease.

Robert B Noll1, Raechel Kiska, Jennifer Reiter-Purtill, Cynthia A Gerhardt, Kathryn Vannatta.   

Abstract

OBJECTIVE: To assess the peer relationships of adolescents with sickle cell disease (SCD) and demographically similar comparison peers who did not have a chronic illness 2 years after an initial evaluation. As a result of ongoing medical challenges associated with SCD and the psychological demands of adolescence, we hypothesized that children with SCD would be viewed by peers as more sensitive and isolated, they would have fewer friends, and they would be less well liked than comparison peers. PATIENTS AND METHODS: At follow-up, peer (n = 2067) and teacher (n = 120) reports of social functioning were obtained for 60 children with SCD and 66 comparison peers. Social reputation (What is the child like?) and social acceptance (Is the child liked?) were evaluated cross-sectionally and longitudinally at the 2-year follow-up (ages 10-17).
RESULTS: Relative to comparison peers, children with SCD were perceived as less aggressive by peers and teachers. No significant differences were found between groups on measures of friendship or social acceptance. Results of longitudinal analyses indicated that teacher-reported levels of sensitive and isolated behavior increased over time for comparison peers but remained stable for children with SCD.
CONCLUSIONS: In general, the social functioning of children with SCD remained stable over time and was not suggestive of emergent social dysfunction. Findings are discussed within a developmental psychopathology framework, possible protective effect of SCD for youth from high-risk environments, and implications regarding pain management for these youth.

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Mesh:

Year:  2010        PMID: 20498169     DOI: 10.1542/peds.2009-2996

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  9 in total

1.  Social-environmental factors and cognitive and behavioral functioning in pediatric sickle cell disease.

Authors:  Sarah E Bills; Jeffrey Schatz; Steven J Hardy; Laura Reinman
Journal:  Child Neuropsychol       Date:  2019-02-21       Impact factor: 2.500

2.  Growing up with a chronic illness: social success, educational/vocational distress.

Authors:  Gary R Maslow; Abigail Haydon; Annie-Laurie McRee; Carol A Ford; Carolyn T Halpern
Journal:  J Adolesc Health       Date:  2011-02-04       Impact factor: 5.012

3.  Social skills and executive function among youth with sickle cell disease: a preliminary investigation.

Authors:  Molly Hensler; Kelly Wolfe; Jeffrey Lebensburger; Jilian Nieman; Margaux Barnes; William Nolan; Allison King; Avi Madan-Swain
Journal:  J Pediatr Psychol       Date:  2014-01-14

4.  PROMIS Pediatric Peer Relationships Scale: development of a peer relationships item bank as part of social health measurement.

Authors:  Darren A Dewalt; David Thissen; Brian D Stucky; Michelle M Langer; Esi Morgan Dewitt; Debra E Irwin; Jin-Shei Lai; Karin B Yeatts; Heather E Gross; Olivia Taylor; James W Varni
Journal:  Health Psychol       Date:  2013-06-17       Impact factor: 4.267

5.  Youth with Sickle Cell Disease: Genetic and Sexual Health Education Needs.

Authors:  Ashley J Housten; Regina A Abel; Joyce Dadekian; Kelly Schwieterman; Dawn Jason; Allison A King
Journal:  Am J Health Behav       Date:  2015-11

6.  Friendship Quality Over Time in Youth With Spina Bifida Compared to Peers.

Authors:  Colleen Stiles-Shields; Colleen F Bechtel Driscoll; Joseph R Rausch; Grayson N Holmbeck
Journal:  J Pediatr Psychol       Date:  2019-06-01

7.  Poor health related quality of life among patients of sickle cell disease.

Authors:  Vijay M Bhagat; Shubhangi R Baviskar; Abhay B Mudey; Ramchandra C Goyal
Journal:  Indian J Palliat Care       Date:  2014-05

8.  The lived experiences of adolescents with sickle cell disease in Kingston, Jamaica.

Authors:  Andrea Brown Forrester; Antoinette Barton-Gooden; Cynthia Pitter; Jascinth L M Lindo
Journal:  Int J Qual Stud Health Well-being       Date:  2015-09-03

9.  Depression and Anxiety as Moderators of the Pain-Social Functioning Relationship in Youth with Sickle Cell Disease.

Authors:  Cecelia Valrie; Alfonso Floyd; India Sisler; Rupa Redding-Lallinger; Beng Fuh
Journal:  J Pain Res       Date:  2020-04-08       Impact factor: 3.133

  9 in total

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