Literature DB >> 24147272

Patient versus parental perceptions about pain and disability in children and adolescents with a variety of chronic pain conditions.

Thomas R Vetter, Cynthia L Bridgewater, Lee I Ascherman, Avi Madan-Swain, Gerald L McGwin.   

Abstract

BACKGROUND: Cross-informant variance is often observed in patient self-reports versus parent proxy reports of pediatric chronic pain and disability.
OBJECTIVE: To assess the relationship and merit of the child versus parent perspective.
METHODS: A total of 99 patients (eight to 17 years of age [mean 13.2 years]; 71% female, 81% Caucasian) and parents completed the Pediatric Pain Questionnaire and Functional Disability Inventory at their initial clinic visit. Patients' and parents' pain intensity and disability scores were analyzed using an intraclass correlation coefficient (ICC), Wilcoxon signed-rank test, Bland-Altman plot and Spearman's correlation coefficient. The association between clinical⁄demographic variables and differences in patient⁄parent pain intensity and disability scores was assessed using multivariable regression.
RESULTS: There was significant agreement between patients' self-reports and parents' proxy reports of their child's pain intensity (ICC=0.52; P<0.001) and disability (ICC=0.57; P=0.004) at the individual level. There were no significant group differences in patient versus parent-proxy pain intensity scores (P=0.40) and disability scores (P=0.54). The difference between patient and parent-proxy pain intensity was associated with patients' self-reported pain intensity (P<0.001). The difference between patient and parent-proxy disability was associated with patient's self-reported pain disability (P<0.001). Bland-Altman plots revealed major inter-rater variation in the Pediatric Pain Questionnaire and Functional Disability Inventory across their score ranges. A significant relationship (r=0.38; P<0.001) was observed between patients' self-reported pain intensity and disability.
CONCLUSIONS: While equal merit should ideally be given to pediatric chronic pain patients' self-reports and their parents' proxy reports of pain intensity and disability, it would appear that, as needed, pediatric patients or parents can offer a clinically valid, single clinical perspective.

Entities:  

Mesh:

Year:  2013        PMID: 24147272      PMCID: PMC3938337          DOI: 10.1155/2014/736053

Source DB:  PubMed          Journal:  Pain Res Manag        ISSN: 1203-6765            Impact factor:   3.037


  48 in total

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3.  The impact of pediatric chronic pain on parents' health-related quality of life and family functioning: reliability and validity of the PedsQL 4.0 Family Impact Module.

Authors:  Kristen E Jastrowski Mano; Kimberly Anderson Khan; Renee J Ladwig; Steven J Weisman
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Authors:  Deirdre E Logan; Laura E Simons; Karen J Kaczynski
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6.  Association of parental chronic pain with chronic pain in the adolescent and young adult: family linkage data from the HUNT Study.

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Review 7.  Association between self-report pain ratings of child and parent, child and nurse and parent and nurse dyads: meta-analysis.

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9.  An observational study of patient versus parental perceptions of health-related quality of life in children and adolescents with a chronic pain condition: who should the clinician believe?

Authors:  Thomas R Vetter; Cynthia L Bridgewater; Gerald McGwin
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Journal:  J Pediatr Hematol Oncol       Date:  2019-04       Impact factor: 1.289

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Review 4.  Chronic Pain Assessments in Children and Adolescents: A Systematic Literature Review of the Selection, Administration, Interpretation, and Reporting of Unidimensional Pain Intensity Scales.

Authors:  Rebecca Rachael Lee; Amir Rashid; Daniela Ghio; Wendy Thomson; Lis Cordingley
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Review 5.  Cutting the cord? Parenting emerging adults with chronic pain.

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6.  Consistency of pediatric pain ratings between dyads: an updated meta-analysis and metaregression.

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  6 in total

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