Validation of Patient-Reported Outcome measure in pediatric chronic Kidney disease (PRO-Kid)

Author:

Matsuda-Abedini Mina12ORCID,Zappitelli Michael345ORCID,Widger Kimberley67ORCID,Rapoport Adam836ORCID,Dionne Janis M12ORCID,Chanchlani Rahul9ORCID,Samuel Susan10,Davison Sara N.11ORCID,Bei Ke Fan12ORCID,Wai Lai Veronica Ka13ORCID,Dufault Brenden14ORCID,Dart Allison B.1315ORCID

Affiliation:

1. Division of Nephrology, BC Children’s Hospital, Vancouver, British Columbia, Canada

2. Department of Paediatrics, Faculty of Medicine, University of British Columbia

3. Department of Paediatrics, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada

4. Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada

5. Division of Nephrology, The Hospital for Sick Children, Toronto, Ontario, Canada

6. Pediatric Advanced Care Team, Hospital for Sick Children, Toronto, Ontario, Canada

7. Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, Ontario, Canada

8. Emily House Children’s Hospice, Toronto, Ontario, Canada

9. Division of Pediatric Nephrology, McMaster Children's Hospital, Hamilton, ON, Canada

10. University of Calgary, and Alberta Children’s Hospital, Calgary, Alberta, Canada

11. Division of Nephrology and Immunology, University of Alberta, Edmonton, Alberta, Canada

12. Department of Immunology, University of Toronto, Canada

13. Children’s Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada

14. George & Fay Yee Centre for Healthcare Innovation, Winnipeg, Canada

15. Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba, Canada

Abstract

Background: Measuring the burden of symptoms that matter most to children and adolescents with chronic kidney disease (CKD) is essential for optimizing patient-centered care. We developed a novel CKD-specific Patient-Reported Outcome measure (PRO-Kid) to assess both frequency and impact of symptoms in children. In the current study, we further assessed the validity and internal consistency of PRO-Kid. Methods: In this multicenter study, children age 8 to 18 years with stages 3-5 CKD, including those on dialysis, were recruited from five pediatric centers. Children completed the 14-item PRO-Kid questionnaire and the validated Pediatric Quality of Life Inventory (PedsQL™ 4.0). We explored the dimensionality of the PRO-kid scale using exploratory and confirmatory factor analysis, to either establish that it is a unidimensional construct or identify evidence of subfactors. We then assessed internal consistency (Cronbach’s alpha [Cα]) and construct validity (Pearson correlations). Results: In total, 100 children were included. The median eGFR was 27.4 ml/min/1.73m2 [7.43, 63.4], and 26 children (26%) were on dialysis. Both the PRO-Kid frequency and the impact scales were unidimensional. Cα was high for both the PRO-Kid frequency and impact scales, 0.83 (95% CI = 0.78 to 0.88) and 0.84 (95% CI = 0.80 to 0.89) respectively, showing strong internal consistency. Pearson correlations between PRO-Kid and PedsQL™ scores were also strong: -0.78 (95% confidence interval [CI] = -0.85 to -0.70) for the frequency score and -0.69 (95% CI = -0.78 to -0.56) for the impact score, reflecting the association between poorer quality of life and higher symptom burden. Conclusions: PRO-Kid is a novel patient-reported symptom burden tool for children 8-18 years of age with CKD that correlates strongly in the expected direction with PedsQL™, supporting its validity. Future work will evaluate changes in PRO-Kid score with progression of CKD, and implementation of the tool into clinical care.

Funder

Children's Hospital Research Institute of Manitoba

Canadian Institutes of Health Research

Publisher

Ovid Technologies (Wolters Kluwer Health)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Patient and Caregiver Perspective on PRO-Kid Quality of Life Tool;Clinical Journal of the American Society of Nephrology;2024-06-12

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