Literature DB >> 31463865

Brief Screening Measures Identify Risk for Psychological Difficulties Among Children with Sickle Cell Disease.

Anna M Hood1,2, Ilana Reife3, Allison A King4, Desiree A White5.   

Abstract

Children with sickle cell disease (SCD) experience disproportionately high rates of psychological problems. Our goal was to examine the clinical utility of psychological screening measures to identify children with such problems in medical settings. Caregivers completed screening measures assessing social-emotional problems, ADHD symptoms, executive dysfunction, and health-related quality of life for children with SCD (receiving either chronic blood transfusion or hydroxyurea) and their siblings. Our findings demonstrated that screening measures identified clinically elevated symptoms in children with SCD that had not been previously reported. Scores for siblings were for the most part in the normal range. The number of days hospitalized (but not cerebral infarct status) predicted higher scores, emphasizing the challenges associated with SCD complications. Overall, our findings support the notion that screening measures reduce the need for reliance on medical provider judgment for psychological referrals and increase equitability in access to services. Early identification resulting in early intervention has contributed substantially to improved psychological functioning in many contexts, and it is thus likely that such improvements would also be achieved in this uniquely vulnerable population.

Entities:  

Keywords:  Behavior; Children; Executive dysfunction; Hydroxyurea; Quality of life; Sickle cell disease; Transfusion

Mesh:

Year:  2020        PMID: 31463865      PMCID: PMC7047601          DOI: 10.1007/s10880-019-09654-y

Source DB:  PubMed          Journal:  J Clin Psychol Med Settings        ISSN: 1068-9583


  34 in total

1.  Primary care pediatricians' roles and perceived responsibilities in the identification and management of depression in children and adolescents.

Authors:  A L Olson; K J Kelleher; K J Kemper; B S Zuckerman; C S Hammond; A J Dietrich
Journal:  Ambul Pediatr       Date:  2001 Mar-Apr

Review 2.  Psychological interventions for mental health disorders in children with chronic physical illness: a systematic review.

Authors:  Sophie Bennett; Roz Shafran; Anna Coughtrey; Susan Walker; Isobel Heyman
Journal:  Arch Dis Child       Date:  2015-04       Impact factor: 3.791

Review 3.  Strategies to improve the management of depression in primary care.

Authors:  Jürgen Unützer; Mijung Park
Journal:  Prim Care       Date:  2012-06       Impact factor: 2.907

4.  Psychiatric diagnosis in adolescents with sickle cell disease: a preliminary report.

Authors:  Tami D Benton; Rhonda Boyd; Judith Ifeagwu; Emily Feldtmose; Kim Smith-Whitley
Journal:  Curr Psychiatry Rep       Date:  2011-04       Impact factor: 5.285

5.  Health-related quality of life in children with sickle cell disease: a report from the Comprehensive Sickle Cell Centers Clinical Trial Consortium.

Authors:  Carlton Dampier; Susan Lieff; Petra LeBeau; Seungshin Rhee; Marsha McMurray; Zora Rogers; Kim Smith-Whitley; Winfred Wang
Journal:  Pediatr Blood Cancer       Date:  2010-09       Impact factor: 3.167

Review 6.  Sickle-cell disease.

Authors:  David C Rees; Thomas N Williams; Mark T Gladwin
Journal:  Lancet       Date:  2010-12-03       Impact factor: 79.321

7.  Responsiveness of PROMIS® Pediatric Measures to Hospitalizations for Sickle Pain and Subsequent Recovery.

Authors:  Carlton Dampier; Byron Jaeger; Heather E Gross; Vaughn Barry; Lloyd Edwards; Yang Lui; Darren A DeWalt; Bryce B Reeve
Journal:  Pediatr Blood Cancer       Date:  2016-02-08       Impact factor: 3.167

Review 8.  Anxiety and depression in children and adolescents with sickle cell disease.

Authors:  Tami D Benton; Judith A Ifeagwu; Kim Smith-Whitley
Journal:  Curr Psychiatry Rep       Date:  2007-04       Impact factor: 5.285

9.  PedsQL™ sickle cell disease module: feasibility, reliability, and validity.

Authors:  Julie A Panepinto; Sylvia Torres; Cristiane B Bendo; Timothy L McCavit; Bogdan Dinu; Sandra Sherman-Bien; Christy Bemrich-Stolz; James W Varni
Journal:  Pediatr Blood Cancer       Date:  2013-02-25       Impact factor: 3.167

10.  Clinically meaningful interpretation of pediatric health-related quality of life in sickle cell disease.

Authors:  Lauren M Beverung; James W Varni; Julie A Panepinto
Journal:  J Pediatr Hematol Oncol       Date:  2015-03       Impact factor: 1.289

View more
  3 in total

Review 1.  Considerations for Selecting Cognitive Endpoints and Psychological Patient-Reported Outcomes for Clinical Trials in Pediatric Patients With Sickle Cell Disease.

Authors:  Anna M Hood; Lori E Crosby; Hanne Stotesbury; Melanie Kölbel; Fenella J Kirkham
Journal:  Front Neurol       Date:  2022-06-21       Impact factor: 4.086

2.  Academic Challenges and School Service Utilization in Children with Sickle Cell Disease.

Authors:  Kristine A Karkoska; Kenneth Haber; Megan Elam; Sarah Strong; Patrick T McGann
Journal:  J Pediatr       Date:  2020-12-01       Impact factor: 4.406

3.  The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease.

Authors:  Anna M Hood; Lori E Crosby; Eva Hanson; Lisa M Shook; Jeffrey D Lebensburger; Avi Madan-Swain; Megan M Miller; Zina Trost
Journal:  Ethn Health       Date:  2020-09-08       Impact factor: 2.732

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.