Literature DB >> 23701707

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

William T Zempsky1, Emily A O'Hara, James P Santanelli, Tonya M Palermo, Tamara New, Kim Smith-Whitley, James F Casella.   

Abstract

UNLABELLED: The purpose of this study was to develop and validate a brief, clinically relevant, multidimensional interview to assess pain burden among children and adolescents with sickle cell disease (SCD). The Sickle Cell Disease Pain Burden Interview-Youth (SCPBI-Y) was developed using a panel of experts, patients, and caregivers. Validation was undertaken with children and youth with SCD, ages 7 to 21 years (N = 129), recruited from 4 urban children's hospitals. Participants were recruited from inpatient (n = 62) and outpatient (n = 67) settings. The SCPBI-Y demonstrated strong internal consistency reliability, cross-informant concordance (child-caregiver), and test-retest reliability (outpatient setting). Moderate construct validity was found with validated measures of functional ability, pain, and quality of life. The SCPBI-Y demonstrated construct validity using a contrasted group approach between youth in inpatient versus outpatient settings and by severity of SCD symptoms, suggesting that youth in inpatient settings and with higher disease severity exhibited greater pain burden. Discriminant validity was found between SCPBI-Y and mood. Our preliminary findings suggest that the SCPBI-Y is a valid and reliable multidimensional interview that can be used in different clinical settings to evaluate pain burden among children and adolescents with SCD. PERSPECTIVE: Multifaceted pain assessments are salient in providing optimal care to children and adolescents with SCD; however, current evaluations are lengthy and cumbersome to administer clinically. The current study introduces and validates a brief, clinically useful multidimensional interview to evaluate pain burden specific to youth with SCD.
Copyright © 2013 American Pain Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Sickle cell disease; adolescents; functional assessment; pain

Mesh:

Year:  2013        PMID: 23701707      PMCID: PMC3759569          DOI: 10.1016/j.jpain.2013.03.007

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.820


  37 in total

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4.  Pain intensity and home pain management of children with sickle cell disease.

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Journal:  Issues Compr Pediatr Nurs       Date:  1996 Jul-Sep

5.  Daily changes in pain, mood and physical function in children hospitalized for sickle cell disease pain.

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8.  Correlates of pain-rating concordance for adolescents with sickle cell disease and their caregivers.

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9.  The performance of the PedsQL generic core scales in children with sickle cell disease.

Authors:  Julie A Panepinto; Nicholas M Pajewski; Lisa M Foerster; Raymond G Hoffmann
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10.  Caregiver report of pain in infants and toddlers with sickle cell disease: reliability and validity of a daily diary.

Authors:  Beth Ely; Carlton Dampier; Miriam Gilday; Patricia O'Neal; Darcy Brodecki
Journal:  J Pain       Date:  2002-02       Impact factor: 5.820

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  13 in total

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.

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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.  Development and validation of the Youth Acute Pain Functional Ability Questionnaire (YAPFAQ).

Authors:  William T Zempsky; Emily A O'Hara; James P Santanelli; Tamara New; Kim Smith-Whitley; James Casella; Tonya M Palermo
Journal:  J Pain       Date:  2014-09-30       Impact factor: 5.820

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

Authors:  Alyssa M Schlenz; Jeffrey Schatz; Carla W Roberts
Journal:  J Pediatr Psychol       Date:  2016-02-10

6.  Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study.

Authors:  Soumitri Sil; Lindsey L Cohen; Nitya Bakshi; Amanda Watt; Morgan Hathaway; Farida Abudulai; Carlton Dampier
Journal:  Clin J Pain       Date:  2020-06       Impact factor: 3.442

Review 7.  Managing Chronic Pain in Special Populations with Emphasis on Pediatric, Geriatric, and Drug Abuser Populations.

Authors:  Kyle M Baumbauer; Erin E Young; Angela R Starkweather; Jessica W Guite; Beth S Russell; Renee C B Manworren
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8.  Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia.

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9.  Overnight auto-adjusting continuous airway pressure + standard care compared with standard care alone in the prevention of morbidity in sickle cell disease phase II (POMS2b): study protocol for a randomised controlled trial.

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Journal:  Trials       Date:  2018-01-22       Impact factor: 2.279

10.  Prevention of Morbidity in sickle cell disease--qualitative outcomes, pain and quality of life in a randomised cross-over pilot trial of overnight supplementary oxygen and auto-adjusting continuous positive airways pressure (POMS2a): study protocol for a randomised controlled trial.

Authors:  Jo Howard; Baba Inusa; Christina Liossi; Eufemia Jacob; Patrick B Murphy; Nicholas Hart; Johanna Gavlak; Sati Sahota; Maria Chorozoglou; Carol Nwosu; Maureen Gwam; Atul Gupta; David C Rees; Swee Lay Thein; Isabel C Reading; Fenella J Kirkham; Man Yeung Edith Cheng
Journal:  Trials       Date:  2015-08-25       Impact factor: 2.279

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