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Epidemiology of pediatric chronic kidney disease/kidney failure: learning from registries and cohort studies

Authors :
Harada, Ryoko
Hamasaki, Yuko
Okuda, Yusuke
Hamada, Riku
Ishikura, Kenji
Source :
Pediatric Nephrology. June, 2022, Vol. 37 Issue 6, p1215, 15 p.
Publication Year :
2022

Abstract

Although the concept of chronic kidney disease (CKD) in children is similar to that in adults, pediatric CKD has some peculiarities, and there is less evidence and many factors that are not clearly understood. The past decade has witnessed several additional registry and cohort studies of pediatric CKD and kidney failure. The most common underlying disease in pediatric CKD and kidney failure is congenital anomalies of the kidney and urinary tract (CAKUT), which is one of the major characteristics of CKD in children. The incidence/prevalence of CKD in children varies worldwide. Hypertension and proteinuria are independent risk factors for CKD progression; other factors that may affect CKD progression are primary disease, age, sex, racial/genetic factors, urological problems, low birth weight, and social background. Many studies based on registry data revealed that the risk factors for mortality among children with kidney failure who are receiving kidney replacement therapy are younger age, female sex, non-White race, non-CAKUT etiologies, anemia, hypoalbuminemia, and high estimated glomerular filtration rate at dialysis initiation. The evidence has contributed to clinical practice. The results of these registry-based studies are expected to lead to new improvements in pediatric CKD care.<br />Author(s): Ryoko Harada [sup.1] , Yuko Hamasaki [sup.2] , Yusuke Okuda [sup.3] , Riku Hamada [sup.1] , Kenji Ishikura [sup.3] Author Affiliations: (1) grid.417084.e, 0000 0004 1764 9914, Department of [...]

Details

Language :
English
ISSN :
0931041X
Volume :
37
Issue :
6
Database :
Gale General OneFile
Journal :
Pediatric Nephrology
Publication Type :
Academic Journal
Accession number :
edsgcl.705979176
Full Text :
https://doi.org/10.1007/s00467-021-05145-1