Literature DB >> 9782678

Psychological adjustment of adolescents with sickle cell disease: relations with demographic, medical, and family competence variables.

R S Kell1, W Kliewer, M T Erickson, K Ohene-Frempong.   

Abstract

OBJECTIVE: Investigate the hypothesis that family competence in addressing challenges associated with sickle cell disease (SCD) contributes to adolescents' adjustment.
METHOD: During routine clinic appointments, 80 adolescents (M age = 14.4 years) and their parents independently completed the Self-Report Family Inventory (SFI), which assesses family competence, and measures of adolescent adjustment problems. Information related to disease severity was obtained from clinic files.
RESULTS: Regression analyses controlling for demographic and medical variables revealed that higher family competence was associated with fewer internalizing and externalizing behaviors by the adolescent; these relations were particularly true for younger adolescents and for girls. Parental reports of somatic complaints in girls were predicted by parental ratings of family competence. DISCUSSION: Interventions for adolescents with SCD should be family-centered and should focus on strengthening the family's ability to manage stressors associated with parenting an adolescent with a chronic illness.

Entities:  

Mesh:

Year:  1998        PMID: 9782678     DOI: 10.1093/jpepsy/23.5.301

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


  11 in total

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3.  Influence of single parenthood on cardiopulmonary function in pediatric patients with sickle cell anemia.

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4.  Health-related quality of life in children with sickle cell disease using the child health questionnaire.

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5.  Autonomic nervous system reactivity: children with and without sickle cell disease.

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6.  Health-related stigma in young adults with sickle cell disease.

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7.  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
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8.  Parental report of health-related quality of life in children with sickle cell disease.

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9.  Disease Knowledge, Illness Perceptions, and Quality of Life in Adolescents With Sickle Cell Disease: Is There a Link?

Authors:  Monika Rani Asnani; Antoinette Barton-Gooden; Marlyn Grindley; Jennifer Knight-Madden
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10.  Quality of life among caregivers of sickle cell disease patients: a cross sectional study.

Authors:  Badr M Madani; Rajaa Al Raddadi; Soad Al Jaouni; Mohab Omer; Marie-Isabelle Al Awa
Journal:  Health Qual Life Outcomes       Date:  2018-09-10       Impact factor: 3.186

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