Literature DB >> 8625722

Peer relationships and emotional well-being of youngsters with sickle cell disease.

R B Noll1, K Vannatta, K Koontz, K Kalinyak, W M Bukowski, W H Davies.   

Abstract

Comparisons with measures of peer relationships and emotional well-being were made between youngsters with sickle cell disease (SCD) and same-classroom comparison peers. Relative to the comparison subjects, females with SCD were perceived by peers as being less sociable and less well accepted; males with SCD were perceived as being less aggressive than comparison peers. For both males and females with SCD, no other differences were identified on numerous measures of emotional well-being. None of the multiple measures of illness severity were significantly related to measures of psychological adjustment. The common side effects of SCD, chronic fatigue and small physical size, may divert males with the illness from manifesting difficulties related to aggressive behavior with peers. For females with the illness, the common side effects of the illness may hinder the development of normal social relationships. Despite chronic exposure to numerous stressful life events associated with SCD, the youngsters with the illness were remarkably similar to comparison peers, showing evidence of considerable hardiness.

Entities:  

Mesh:

Year:  1996        PMID: 8625722     DOI: 10.1111/j.1467-8624.1996.tb01743.x

Source DB:  PubMed          Journal:  Child Dev        ISSN: 0009-3920


  19 in total

Review 1.  Applying the transactional stress and coping model to sickle cell disorder and insulin-dependent diabetes mellitus: identifying psychosocial variables related to adjustment and intervention.

Authors:  Matthew C Hocking; John E Lochman
Journal:  Clin Child Fam Psychol Rev       Date:  2005-09

Review 2.  A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

Authors:  Christopher L Edwards; Mischca T Scales; Charles Loughlin; Gary G Bennett; Shani Harris-Peterson; Laura M De Castro; Elaine Whitworth; Mary Abrams; Miriam Feliu; Stephanie Johnson; Mary Wood; Ojinga Harrison; Alvin Killough
Journal:  Int J Behav Med       Date:  2005

3.  Health-related quality of life and adaptive behaviors of adolescents with sickle cell disease: stress processing moderators.

Authors:  Maisa S Ziadni; Chavis A Patterson; Elizabeth R Pulgarón; M Renée Robinson; Lamia P Barakat
Journal:  J Clin Psychol Med Settings       Date:  2011-12

4.  Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease.

Authors:  Steven K Reader; Laura M Rockman; Katherine M Okonak; Nicole M Ruppe; Colleen N Keeler; Anne E Kazak
Journal:  J Clin Psychol Med Settings       Date:  2020-06

5.  Quality of life and psychosocial functioning of children with cardiac arrhythmias.

Authors:  Elizabeth R Pulgaron; Diana Wile; Kerri Schneider; Ming-Lon Young; Alan M Delamater
Journal:  Cardiol Young       Date:  2012-04-18       Impact factor: 1.093

6.  Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study.

Authors:  Soumitri Sil; Lindsey L Cohen; Nitya Bakshi; Amanda Watt; Morgan Hathaway; Farida Abudulai; Carlton Dampier
Journal:  Clin J Pain       Date:  2020-06       Impact factor: 3.442

7.  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

8.  Double disadvantage: a case control study on health-related quality of life in children with sickle cell disease.

Authors:  Channa T Hijmans; Karin Fijnvandraat; Jaap Oosterlaan; Harriët Heijboer; Marjolein Peters; Martha A Grootenhuis
Journal:  Health Qual Life Outcomes       Date:  2010-10-26       Impact factor: 3.186

9.  Negative thinking as a coping strategy mediator of pain and internalizing symptoms in adolescents with sickle cell disease.

Authors:  Lamia P Barakat; Lisa A Schwartz; Katherine Simon; Jerilynn Radcliffe
Journal:  J Behav Med       Date:  2007-04-24

10.  Parental report of health-related quality of life in children with sickle cell disease.

Authors:  Tonya Mizell Palermo; Lisa Schwartz; Dennis Drotar; Kathryn McGowan
Journal:  J Behav Med       Date:  2002-06
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