Literature DB >> 32743664

Patient- and parent proxy-reported outcome measures for life participation in children with chronic kidney disease: a systematic review.

Jasmijn Kerklaan1,2, Elyssa Hannan1,2, Amanda Baumgart1,2, Karine E Manera1,2, Angela Ju1,2, Mignon McCulloch3, Bashir Admani4, Amanda Dominello1,2, Christopher Esezobor5,6, Bethany Foster7, Alexander Hamilton8, Augustina Jankauskiene9, Rebecca J Johnson10, Isaac Liu11, Stephen D Marks12,13, Alicia Neu14, Franz Schaefer15, Shanna Sutton1, Sebastian Wolfenden1, Jonathan C Craig16, Jaap Groothoff17, Martin Howell1,2, Allison Tong1,2.   

Abstract

BACKGROUND: The burden of chronic kidney disease (CKD) and its treatment may severely limit the ability of children with CKD to do daily tasks and participate in family, school, sporting and recreational activities. Life participation is critically important to affected children and their families; however, the appropriateness and validity of available measures used to assess this outcome are uncertain. The aim of this study was to identify the characteristics, content and psychometric properties of existing measures for life participation used in children with CKD.
METHODS: We searched MEDLINE, Embase, PsychINFO, Cumulative Index to Nursing and Allied Health Literature and the Cochrane Kidney and Transplant register to August 2019 for all studies that used a measure to report life participation in children with CKD. For each measure, we extracted and analyzed the characteristics, dimensions of life participation and psychometric properties.
RESULTS: From 128 studies, we identified 63 different measures used to assess life participation in children with CKD. Twenty-five (40%) of the measures were patient reported, 7 (11%) were parent proxy reported and 31 (49%) had both self and parent proxy reports available. Twenty-two were used in one study only. The Pediatric Quality of Life Inventory version 4.0 generic module was used most frequently in 62 (48%) studies. Seven (11%) were designed to assess ability to participate in life, with 56 (89%) designed to assess other constructs (e.g. quality of life) with a subscale or selected questions on life participation. Across all measures, the three most frequent activities specified were social activities with friends and/or family, leisure activities and self-care activities. Validation data in the pediatric CKD population were available for only 19 (30%) measures.
CONCLUSIONS: Life participation is inconsistently measured in children with CKD and the measures used vary in their characteristics, content and validity. Validation data supporting these measures in this population are often incomplete and are sparse. A meaningful and validated measure for life participation in children with CKD is needed.
© The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

Entities:  

Keywords:  children; chronic kidney disease; chronic renal failure; life participation; patient-reported outcome measures

Mesh:

Year:  2020        PMID: 32743664     DOI: 10.1093/ndt/gfaa132

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  2 in total

Review 1.  Long-Term Care of the Pediatric Kidney Transplant Recipient.

Authors:  Hilda E Fernandez; Bethany J Foster
Journal:  Clin J Am Soc Nephrol       Date:  2021-05-12       Impact factor: 8.237

2.  Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease-are patient-centered outcomes our blind spot?

Authors:  Charlotte Gimpel; Max Christoph Liebau; Franz Schaefer
Journal:  Pediatr Nephrol       Date:  2021-08-12       Impact factor: 3.714

  2 in total

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