Literature DB >> 26275975

Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.

Lori E Crosby1, Naomi E Joffe2, Nina Reynolds3, James L Peugh2, Ellen Manegold4, Ahna L H Pai2.   

Abstract

OBJECTIVES: Adolescents and young adults (AYAs) with sickle cell disease (SCD) experience psychosocial factors that increase their risk for poor disease management and health outcomes. Routine assessment of psychosocial factors that perpetuate health disparities is recommended. The Psychosocial Assessment Tool 2.0_General (PAT2.0_GEN) AYA is a psychosocial screener with potential clinical utility in AYAs with SCD. This article is a preliminary examination of the internal consistency and predictive validity of this measure in a sample of 45 AYAs with SCD.
METHODS: Participants completed the PAT2.0_GEN AYA, Pediatric Quality of Life Inventory, and a demographics form; psychosocial referral data were also collected.
RESULTS: Internal consistency for the PAT2.0_GEN AYA was acceptable except for the Family Beliefs (0.67) and Structure and Resources subscales (0.37). PAT2.0_GEN AYA scores were associated with an increased likelihood of referral for intervention within 4 months.
CONCLUSIONS: The PAT2.0_GEN AYA holds promise as a screener to identify psychosocial risk factors that may compromise health outcomes in AYAs with SCD.
© The Author 2015. Published by Oxford University Press on behalf of the Society of Pediatric Psychology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  chronic illness; family; pediatric; psychosocial risk; quality of life; screening.

Mesh:

Year:  2015        PMID: 26275975      PMCID: PMC5009452          DOI: 10.1093/jpepsy/jsv073

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


  42 in total

1.  Too sick for school? Parent influences on school functioning among children with chronic pain.

Authors:  Deirdre E Logan; Laura E Simons; Elizabeth A Carpino
Journal:  Pain       Date:  2011-12-09       Impact factor: 6.961

2.  Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007.

Authors:  Hussain R Yusuf; Hani K Atrash; Scott D Grosse; Christopher S Parker; Althea M Grant
Journal:  Am J Prev Med       Date:  2010-04       Impact factor: 5.043

Review 3.  Health inequity in children and youth with chronic health conditions.

Authors:  Jay G Berry; Sheila Bloom; Susan Foley; Judith S Palfrey
Journal:  Pediatrics       Date:  2010-12       Impact factor: 7.124

4.  Relationships between family and parent characteristics and functional abilities in children with recurrent pain syndromes: an investigation of moderating effects on the pathway from pain to disability.

Authors:  Deirdre E Logan; Lisa Scharff
Journal:  J Pediatr Psychol       Date:  2005-08-10

5.  US Housing insecurity and the health of very young children.

Authors:  Diana Becker Cutts; Alan F Meyers; Maureen M Black; Patrick H Casey; Mariana Chilton; John T Cook; Joni Geppert; Stephanie Ettinger de Cuba; Timothy Heeren; Sharon Coleman; Ruth Rose-Jacobs; Deborah A Frank
Journal:  Am J Public Health       Date:  2011-06-16       Impact factor: 9.308

6.  Neuropsychological dysfunction and neuroimaging abnormalities in neurologically intact adults with sickle cell anemia.

Authors:  Elliott P Vichinsky; Lynne D Neumayr; Jeffrey I Gold; Michael W Weiner; Randall R Rule; Diana Truran; Jeffrey Kasten; Barry Eggleston; Karen Kesler; Lillian McMahon; Eugene P Orringer; Thomas Harrington; Karen Kalinyak; Laura M De Castro; Abdullah Kutlar; Cynthia J Rutherford; Cage Johnson; Joel David Bessman; Lanetta B Jordan; F Daniel Armstrong
Journal:  JAMA       Date:  2010-05-12       Impact factor: 56.272

Review 7.  Health-related quality of life in sickle cell disease: past, present, and future.

Authors:  Julie A Panepinto; Melanie Bonner
Journal:  Pediatr Blood Cancer       Date:  2012-04-22       Impact factor: 3.167

8.  Definitions of the phenotypic manifestations of sickle cell disease.

Authors:  Samir K Ballas; Susan Lieff; Lennette J Benjamin; Carlton D Dampier; Matthew M Heeney; Carolyn Hoppe; Cage S Johnson; Zora R Rogers; Kim Smith-Whitley; Winfred C Wang; Marilyn J Telen
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

9.  Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease.

Authors:  Carlton Haywood; Sophie Lanzkron; Shawn Bediako; John J Strouse; Jennifer Haythornthwaite; C Patrick Carroll; Marie Diener-West; Gladys Onojobi; Mary Catherine Beach
Journal:  J Gen Intern Med       Date:  2014-09-10       Impact factor: 5.128

10.  Parental beliefs and worries regarding adolescent chronic pain.

Authors:  Jessica W Guite; Deirdre E Logan; Rebecca McCue; David D Sherry; John B Rose
Journal:  Clin J Pain       Date:  2009 Mar-Apr       Impact factor: 3.442

View more
  7 in total

1.  Introduction to the Special Issue on Diversity and Health Disparities: Where Have We Been and Where Are We Going?

Authors:  Celia M Lescano; Daphne Koinis-Mitchell; Elizabeth L McQuaid
Journal:  J Pediatr Psychol       Date:  2016-05

2.  Identifying Chronic Pain Subgroups in Pediatric Sickle Cell Disease: A Cluster-Analytic Approach.

Authors:  Soumitri Sil; Alison Manikowski; Mallory Schneider; Lindsey L Cohen; Carlton Dampier
Journal:  Clin J Pain       Date:  2022-10-01       Impact factor: 3.423

3.  Psychosocial Screening in Sickle Cell Disease: Validation of the Psychosocial Assessment Tool.

Authors:  Steven K Reader; Colleen N Keeler; Fang Fang Chen; Nicole M Ruppe; Diana L Rash-Ellis; Jean R Wadman; Robin E Miller; Anne E Kazak
Journal:  J Pediatr Psychol       Date:  2020-05-01

4.  Psychosocial risk and health care utilization in pediatric sickle cell disease.

Authors:  Kerri E Woodward; Yelena L Johnson; Lindsey L Cohen; Carlton Dampier; Soumitri Sil
Journal:  Pediatr Blood Cancer       Date:  2021-05-24       Impact factor: 3.167

5.  Sociodemographic factors and health-related, neuropsychological, and psychosocial functioning in youth with spina bifida.

Authors:  Jaclyn Lennon Papadakis; Grayson N Holmbeck
Journal:  Rehabil Psychol       Date:  2021-05-27

6.  Comprehensive neuropsychological evaluation of children and adolescents with sickle cell anemia: a hospital-based sample.

Authors:  Samantha Nunes; Nayara Argollo; Marivania Mota; Camilo Vieira; Eduardo Pondé de Sena
Journal:  Rev Bras Hematol Hemoter       Date:  2016-10-07

7.  Psychosocial assessment of families caring for a child with acute lymphoblastic leukemia, epilepsy or asthma: Psychosocial risk as network of interacting symptoms.

Authors:  Chiara Colliva; Monica Cellini; Francesca Dalla Porta; Martina Ferrari; Barbara Maria Bergamini; Azzurra Guerra; Silvia Di Giuseppe; Annamaria Pinto; Roberto Capasso; Daniela Caprino; Marta Ferrari; Cristina Benatti; Fabio Tascedda; Johanna M C Blom
Journal:  PLoS One       Date:  2020-03-23       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.