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Parental understanding of relapsing idiopathic nephrotic syndrome—Where are the knowledge gaps?
Author(s) -
Lo Cao Edward,
Amir Noa,
McKay Ashlene,
Durkan Anne M.
Publication year - 2020
Publication title -
acta paediatrica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 115
eISSN - 1651-2227
pISSN - 0803-5253
DOI - 10.1111/apa.15111
Subject(s) - medicine , nephrotic syndrome , disease , pediatrics , disease management , family medicine , parkinson's disease
Abstract Aim To assess parental understanding of idiopathic nephrotic syndrome (INS) and its management, to enable targeted education in areas of deficit. Methods Families of children with at least one relapse of INS were interviewed, following a template covering key domains of (a) disease understanding, (b) management of INS and (c) access to information. Common trends and responses were identified and notable observations recorded. Results Twenty‐one parents were interviewed. The mean duration of INS was 4.4 years (range 0.5‐14.5 years), with a mean of two steroid‐sparing agents used. Although 90% parents self‐reported that they understood INS, only 29% could appropriately define relapse and 24% name potential complications. The management of INS was generally good, with most parents appropriately testing urine (81%) and managing relapses (90%). Unnecessary dietary restrictions were imposed on 57% during remission. The Internet was searched by 90% of parents for disease and drug information. Further information was desired in paper form (71%), hospital website (81%) and face‐to‐face workshop (90%), plus educational materials for schools. Conclusion Parents overestimated their understanding of INS; however, their management was generally well done. Parents desired more information and support in various forms.