Literature DB >> 26869665

Examining Biopsychosocial Factors in Relation to Multiple Pain Features in Pediatric Sickle Cell Disease.

Alyssa M Schlenz1, Jeffrey Schatz2, Carla W Roberts3.   

Abstract

OBJECTIVE: To examine biopsychosocial variables in relation to multiple pain features in pediatric sickle cell disease (SCD).
METHODS: 76 children with SCD (M = 14.05, SD = 3.26), ages 8-19 years, and 70 caregivers completed measures of coping, mood, and family functioning and reported on multiple pain features via retrospective interviews during routine hematological visits. Sickle cell genotype and health care utilization were collected via medical record review. Using hierarchical regression, biological (genotype), child psychological (coping and mood), and social factors (caregiver coping and family functioning) were evaluated in relation to multiple pain features.
RESULTS: Genotype was associated with pain intensity, and child psychological factors were associated with pain frequency. Multiple biopsychosocial factors were related to health care utilization.
CONCLUSIONS: Biopsychosocial factors may have distinct relationships with pain features in pediatric SCD. Understanding these relationships may refine the biopsychosocial model and inform integrated medical and psychosocial approaches in SCD.
© The Author 2016. 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:  children; pain; sickle cell disease

Mesh:

Year:  2016        PMID: 26869665      PMCID: PMC4982540          DOI: 10.1093/jpepsy/jsw003

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


  40 in total

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2.  A prospective study of the role of coping and family functioning in health outcomes for adolescents with sickle cell disease.

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Review 3.  A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

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7.  Role of child and maternal processes in the psychological adjustment of children with sickle cell disease.

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8.  Validation of the sickle cell disease pain burden interview-youth.

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Review 9.  Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease.

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Review 1.  Psychological Predictors of Pain in Children and Adolescents With Sickle Cell Disease: A Scoping Review.

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2.  Feasibility and Acceptability of Internet-delivered Cognitive Behavioral Therapy for Chronic Pain in Adolescents With Sickle Cell Disease and Their Parents.

Authors:  Tonya M Palermo; Joanne Dudeney; James P Santanelli; Alexie Carletti; William T Zempsky
Journal:  J Pediatr Hematol Oncol       Date:  2018-03       Impact factor: 1.289

3.  iCanCope with Sickle Cell Pain: Design of a randomized controlled trial of a smartphone and web-based pain self-management program for youth with sickle cell disease.

Authors:  Tonya M Palermo; William T Zempsky; Carlton D Dampier; Chitra Lalloo; Amos S Hundert; Lexa K Murphy; Nitya Bakshi; Jennifer N Stinson
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4.  Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease.

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5.  Emotion-Focused Avoidance Coping Mediates the Association Between Pain and Health-Related Quality of Life in Children With Sickle Cell Disease.

Authors:  Crystal S Lim; Cynthia Karlson; Sara N Edmond; Josie S Welkom; Ifeyinwa Osunkwo; Lindsey L Cohen
Journal:  J Pediatr Hematol Oncol       Date:  2019-04       Impact factor: 1.289

6.  Pica in Pediatric Sickle Cell Disease.

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7.  The Problem of Pain in Systemic Lupus Erythematosus: An Explication of the Role of Biopsychosocial Mechanisms.

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8.  Severe Pain Profiles and Associated Sociodemographic and Clinical Characteristics in Individuals With Sickle Cell Disease.

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10.  Depression and Anxiety as Moderators of the Pain-Social Functioning Relationship in Youth with Sickle Cell Disease.

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