When Dialysis “Becomes Life”: Pediatric Caregivers' Lived Experiences Obtained From Patient-Reported Outcomes Measures

Daniella Levy Erez*, Melissa R. Meyers*, Swathi Raman, Melissa Thomas, Susan Furth, Christopher B. Forrest, Michelle Denburg

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Introduction: Qualitative research reveals significant caregiver impact resulting from managing children requiring chronic dialysis but offers few quantitative measures of their lived experiences. Materials and Methods: This cross-sectional study included 25 caregivers of children on chronic peritoneal dialysis (PD) and hemodialysis (HD) enrolled from 2018 to 2019 at a large pediatric dialysis program in the U.S. Patient Reported Outcomes Measures Information System (PROMIS) measures and free text commentary were collected and analyzed to evaluate the self-reported impact and wellbeing of these caregivers. Results: Among all dialysis modalities, caregivers' positive affect (43.4 ± 10) and general life satisfaction (45.1 ± 11.5) were significantly lower than the general adult population. Compared with HD caregivers, PD caregivers demonstrated significantly more fatigue and sleep disturbance and less positive affect and life satisfaction. Amongst HD caregivers, sleep disturbance, positive affect, and meaning/purpose differed significantly from the general population. Analyses of text commentary revealed that caregivers also expressed the feelings of loss, importance of knowing the impact of dialysis prior to initiation, need for a support group, and value of home nursing. Conclusions: Caregivers of children on chronic dialysis had significantly poorer self-rated health and wellbeing compared with the general adult population. This may be due in part to their feelings of social isolation. Our findings highlight opportunities to improve caregivers' lived experiences.

Original languageEnglish
Article number864134
JournalFrontiers in Pediatrics
Volume10
DOIs
StatePublished - 23 May 2022
Externally publishedYes

Funding

FundersFunder number
PROMIS Measures in Chronically Ill ChildrenT32-DK007006-43, U19AR069525, T32-DK007785
Sherrin Meloni MBA
National Institutes of Health

    Keywords

    • caregiver
    • child
    • chronic dialysis
    • patient reported clinical outcomes
    • patient-reported outcomes measurement information system (PROMIS)
    • quality of life

    Fingerprint

    Dive into the research topics of 'When Dialysis “Becomes Life”: Pediatric Caregivers' Lived Experiences Obtained From Patient-Reported Outcomes Measures'. Together they form a unique fingerprint.

    Cite this