Literature DB >> 31876791

Factors Related to Agreement Between Child and Caregiver Report of Child Functioning With Chronic Pain: PROMIS Pediatric and Parent Proxy Report.

Kathryn A Birnie1, Patricia A Richardson2, Adithi V Rajagopalan2, Rashmi P Bhandari2.   

Abstract

OBJECTIVES: Valid and efficient assessment of patient-reported outcomes remains a priority to guide pain treatment and research. PROMIS pediatric self-report and parent proxy measures offer feasible and rigorous evaluation of functioning in children with chronic conditions, including pain. A key challenge is determining the usefulness of multisource information from children and caregivers for understanding pain and function. Our primary aim examined child-caregiver agreement across child functioning domains. Our secondary aim examined child and caregiver factors associated with the child-caregiver agreement.
MATERIALS AND METHODS: A sample of 806 children with chronic pain (Mage=14.50 y; 72% female individuals) and a caregiver (Mage=45.82 y; 85% mothers) completed PROMIS pediatric self-report and parent proxy measures of anxiety, depression, fatigue, pain interference, and mobility before intake in an interdisciplinary outpatient pediatric chronic pain program.
RESULTS: The agreement was poor to good depending on the evaluation method (effect size, intraclass correlation, and clinical significance interpretation). Caregivers generally reported worse child symptoms across domains compared with child self-report. The greatest discrepancy was observed for child anxiety, pain interference, and peer relations, with the greatest agreement for child mobility. The greater caregiver-child discrepancy was found for younger children, girls, with a higher child or caregiver pain catastrophizing, and poorer caregiver physical or mental health. DISCUSSION: Findings are discussed within the interpersonal context of pain and indicate the relevance of both child and caregiver perspectives to personalize chronic pain assessment and treatment. Findings can be used by clinicians and researchers to guide whether and how to integrate multi-informant reports about child chronic pain functioning.

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Year:  2020        PMID: 31876791     DOI: 10.1097/AJP.0000000000000794

Source DB:  PubMed          Journal:  Clin J Pain        ISSN: 0749-8047            Impact factor:   3.442


  6 in total

Review 1.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

2.  Using the Parent Risk Screening Measure (PRISM) to Assess Pain-Related Risk Factors in Parents of Youth Seeking Treatment for Acute Musculoskeletal Pain.

Authors:  Amy L Holley; Wendy Gaultney; Anna C Wilson
Journal:  Clin J Pain       Date:  2022-08-01       Impact factor: 3.423

3.  Comparison of pain and psychosocial correlates among Hispanic and Non-Hispanic White youth with chronic pain.

Authors:  Ana B Goya Arce; Patricia A Richardson; Susan T Tran; Rashmi P Bhandari
Journal:  Pain Rep       Date:  2022-07-18

4.  COVID-19-Related Anxiety Symptoms among Quarantined Adolescents and Its Impact on Sleep Pattern Changes and Somatic Symptoms.

Authors:  Yulia Gendler; Ayala Blau
Journal:  Children (Basel)       Date:  2022-05-17

5.  Agreement between older adult patient and caregiver proxy symptom reports.

Authors:  Kurt Kroenke; Timothy E Stump; Patrick O Monahan
Journal:  J Patient Rep Outcomes       Date:  2022-05-14

6.  Parental Catastrophizing and Goal Pursuit in the Context of Child Chronic Pain: A Daily Diary Study.

Authors:  Line Caes; Cynthia van Gampelaere; Eline Van Hoecke; Myriam Van Winckel; Kristien Kamoen; Liesbet Goubert
Journal:  Front Psychol       Date:  2021-07-01
  6 in total

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