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Published in: Pediatric Nephrology 10/2008

01-10-2008 | Original Article

The spectrum of chronic kidney disease (stages 2–5) in KwaZulu-Natal, South Africa

Authors: Rajendra Bhimma, Miriam Adhikari, Kareshma Asharam, Catherine Connolly

Published in: Pediatric Nephrology | Issue 10/2008

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Abstract

The burden of chronic kidney disease (CKD) in children in developing countries remains unknown, due to the lack of a national data-reporting system. We undertook a retrospective study of all children < 16 years old in our hospital, which is the tertiary referral centre for children with complex kidney disorders, to analyse the spectrum of CKD (stages 2–5) from 1994–2006. Six hundred and fifty-three children with kidney disorders were screened for CKD; 286 (44.0%) were < 5 years old. Of these, 177 (62%) were male, 202 (70.6%) were black, 77 (26.9%) were Indian, five (1.8%) were mixed race and two (0.7%) were white. One hundred and twenty-six children had CKD (stages 2–5); 55 (43.7%) were < 5 years olds; 41 (74.5%) were male. There were 71 (56.3%) that were > 5 years old, 42 (59.2%) were male. The commonest cause of CKD (stages 2–5) in all children was nephrotic syndrome, comprising 30.9% in children < 5 years old and 40.8% in children > 5 years old. Within the observation period of 11 years, end-stage kidney disease was diagnosed in 20 children; only nine had been on long-term dialysis, and seven qualified for transplantation. Five (25%) children had died, four from sepsis during dialysis and one from tuberculosis after receiving a transplant. We concluded that lack of resources, late referrals, and high cost of renal replacement therapy in developing countries leads to poor outcome in CKD.
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Metadata
Title
The spectrum of chronic kidney disease (stages 2–5) in KwaZulu-Natal, South Africa
Authors
Rajendra Bhimma
Miriam Adhikari
Kareshma Asharam
Catherine Connolly
Publication date
01-10-2008
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Nephrology / Issue 10/2008
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-008-0871-5

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