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Published in: Pediatric Nephrology 7/2003

01-07-2003 | Original Article

Chronic renal failure in children: a report from Port Harcourt, Nigeria (1985–2000)

Authors: Ifeoma Anochie, Felicia Eke

Published in: Pediatric Nephrology | Issue 7/2003

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Abstract

A 15-year review of children who presented with chronic renal failure (CRF) to the University of Port Harcourt Teaching Hospital, Rivers State of Nigeria, was carried out. Forty-five children (28 boys, 17 girls) with CRF, defined as a glomerular filtration rate below 30 ml/min per 1.73 m2 body surface area or a rise in serum creatinine above 120 µmol/l for at least 6 months, often accompanied by other biochemical abnormalities, were identified. The median annual incidence of CRF was 3.0 per million children. The prevalence of CRF increased from 12.5 in the 1985–1990 periods to 15 per million children after 1995. Acquired disorder was the major cause of CRF. Glomerulopathies were the cause in 53.3% of patients, mainly chronic glomerulonephritis (56.5%) and nephrotic syndrome (30.4%). Hepatitis B surface antigen was positive in 2 patients. Congenital disorders accounted for 28.9% of all cases of CRF, which is lower than data from other countries. Posterior urethral valve was the only congenital disorder causing CRF in the study. No child with hereditary renal disorder as a cause of CRF was identified. Children with congenital disorders were diagnosed at an earlier age. The mortality rate was high (46.7%), as most patients were managed conservatively, since there were no permanent facilities for chronic dialysis or renal transplantation in Nigeria. The study shows that CRF is common in Nigerian children, and there is an urgent need for the establishment of facilities for renal replacement therapy.
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Metadata
Title
Chronic renal failure in children: a report from Port Harcourt, Nigeria (1985–2000)
Authors
Ifeoma Anochie
Felicia Eke
Publication date
01-07-2003
Publisher
Springer-Verlag
Published in
Pediatric Nephrology / Issue 7/2003
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-003-1150-0

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