Literature DB >> 25556914

A controlled study of internalizing symptoms in older adolescents with sickle cell disease.

Adia D Kelly1, Anna M Egan, Jennifer Reiter-Purtill, Cynthia A Gerhardt, Kathryn Vannatta, Robert B Noll.   

Abstract

BACKGROUND: Due to the ongoing medical challenges we hypothesized that older adolescents with sickle cell disease (SCD) would report greater rates of internalizing symptoms and diagnoses. This study is a follow-up to a previous study [1] that found few differences between the emotional well-being of children ages 8-15 with SCD and comparison peers. Our aim is to re-assess internalizing symptoms of youth with SCD and comparison peers at age 18. PROCEDURE: At follow-up, trained staff members administered semi-structured psychiatric interviews and widely use behavioral health questionnaires to adolescents with SCD (n = 48), their comparison peers (COMP; n = 51) and a caregiver. Mood, internalizing symptoms and diagnoses, were evaluated cross-sectionally at the follow-up (age 18).
RESULTS: Psychiatric interview data showed that COMP reported more phobias relative to adolescents with SCD; no significant differences were reported for any other current symptoms (depression, anxiety, or mania). Questionnaire data showed all scores in the normal range with two significant differences: older adolescents with SCD reported more symptoms of tension-anxiety and fatigue-inertia. Both groups reported significant rates of internalizing disorders with 31% of youth with SCD and 35% of COMP having a DSM-IV diagnosis.
CONCLUSIONS: Psychiatric interview data for both groups of older adolescents suggested considerable psychopathology; questionnaire data for both groups were in the normal range. We report few significant differences-more phobias in comparisons peers; more tension-anxiety and fatigue-inertia reported by youth with SCD. The overall findings suggest considerable resilience for youth with SCD, but both groups of adolescents report significant rates of psychopathology similar to national rates.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  psychosocial; quality of Life; sickle cell disease

Mesh:

Year:  2014        PMID: 25556914     DOI: 10.1002/pbc.25325

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


  1 in total

1.  Sickle Cell Disease and Psychosocial Well-Being: Comparison of Patients With Preclinical and Clinical Avascular Necrosis of the Femoral Head.

Authors:  Ozlem Tezol; Feryal Karahan; Selma Unal
Journal:  Turk Arch Pediatr       Date:  2021-07-01
  1 in total

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