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Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe
BACKGROUND: The pattern of paediatric kidney diseases across different regions is influenced by genetic, racial, and environmental differences. OBJECTIVES: The aim of this study was to review the current spectrum and outcome of childhood kidney diseases at Parirenyatwa Group of Hospitals and highlig...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403983/ https://www.ncbi.nlm.nih.gov/pubmed/37545479 http://dx.doi.org/10.1177/11795565231188940 |
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author | Makanda-Charambira, PD Mujuru, HA Ticklay, I Muchemwa, L |
author_facet | Makanda-Charambira, PD Mujuru, HA Ticklay, I Muchemwa, L |
author_sort | Makanda-Charambira, PD |
collection | PubMed |
description | BACKGROUND: The pattern of paediatric kidney diseases across different regions is influenced by genetic, racial, and environmental differences. OBJECTIVES: The aim of this study was to review the current spectrum and outcome of childhood kidney diseases at Parirenyatwa Group of Hospitals and highlight the challenges of care. DESIGN: Retrospective observational study. METHODS: Data on all children below 16 years of age hospitalised for any kidney disease over an 8-month period (1 January-31 August 2022) were retrieved and retrospectively analysed. Kidney diseases were categorised as per standard definitions. RESULTS: Kidney disease accounted for 2.2% (n = 50) of all 2264 admissions in the paediatric unit, with males constituting 60% (n = 30). Age ranged from 2 weeks to 13 years (mean 5.5 ± 3.5 years) with 58.0% being under 5 years. The commonest diagnoses in the unit were acute kidney injury (AKI) (n = 16, 32%) nephrotic syndrome (n = 16, 32%), hypertension (n = 12, 24%) and end stage kidney disease (ESKD) (n = 11, 22%) with some children presenting with more than 1 diagnosis. Only 3 out of 11 children with ESKD and 3 out of 8 children with AKI who required dialysis could be offered dialysis due to limited resources. Overall mortality rate was 32% (16/50): 5 children with AKI, 2 with nephrotic syndrome and normal kidney function, 8 with ESKD and 1 with Fanconi syndrome. CONCLUSION: Childhood kidney disease contributes significantly to hospitalisations at our institution with highest mortality among children with ESKD. The study highlighted the need for provision of essential drugs and kidney replacement therapy for children with kidney disease at our institution. |
format | Online Article Text |
id | pubmed-10403983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-104039832023-08-06 Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe Makanda-Charambira, PD Mujuru, HA Ticklay, I Muchemwa, L Clin Med Insights Pediatr Original Research BACKGROUND: The pattern of paediatric kidney diseases across different regions is influenced by genetic, racial, and environmental differences. OBJECTIVES: The aim of this study was to review the current spectrum and outcome of childhood kidney diseases at Parirenyatwa Group of Hospitals and highlight the challenges of care. DESIGN: Retrospective observational study. METHODS: Data on all children below 16 years of age hospitalised for any kidney disease over an 8-month period (1 January-31 August 2022) were retrieved and retrospectively analysed. Kidney diseases were categorised as per standard definitions. RESULTS: Kidney disease accounted for 2.2% (n = 50) of all 2264 admissions in the paediatric unit, with males constituting 60% (n = 30). Age ranged from 2 weeks to 13 years (mean 5.5 ± 3.5 years) with 58.0% being under 5 years. The commonest diagnoses in the unit were acute kidney injury (AKI) (n = 16, 32%) nephrotic syndrome (n = 16, 32%), hypertension (n = 12, 24%) and end stage kidney disease (ESKD) (n = 11, 22%) with some children presenting with more than 1 diagnosis. Only 3 out of 11 children with ESKD and 3 out of 8 children with AKI who required dialysis could be offered dialysis due to limited resources. Overall mortality rate was 32% (16/50): 5 children with AKI, 2 with nephrotic syndrome and normal kidney function, 8 with ESKD and 1 with Fanconi syndrome. CONCLUSION: Childhood kidney disease contributes significantly to hospitalisations at our institution with highest mortality among children with ESKD. The study highlighted the need for provision of essential drugs and kidney replacement therapy for children with kidney disease at our institution. SAGE Publications 2023-08-04 /pmc/articles/PMC10403983/ /pubmed/37545479 http://dx.doi.org/10.1177/11795565231188940 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Makanda-Charambira, PD Mujuru, HA Ticklay, I Muchemwa, L Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe |
title | Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe |
title_full | Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe |
title_fullStr | Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe |
title_full_unstemmed | Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe |
title_short | Burden of Paediatric Kidney Diseases in a Tertiary Care Hospital in Harare, Zimbabwe |
title_sort | burden of paediatric kidney diseases in a tertiary care hospital in harare, zimbabwe |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403983/ https://www.ncbi.nlm.nih.gov/pubmed/37545479 http://dx.doi.org/10.1177/11795565231188940 |
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