Publication:
Clinical and Laboratory Predictors of Acute Kidney Injury in Childhood Severe Malaria

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorIbrahim, Olayinka Rasheed
dc.contributor.authorAlao, Michael Abel
dc.contributor.authorAdeboye, Muhammed Nurudeen
dc.date.accessioned2025-10-14T09:56:06Z
dc.date.available2025-10-14T09:56:06Z
dc.date.issued2024
dc.descriptionOlayinka Rasheed Ibrahim Department of Paediatrics, Federal Teaching Hospital, Katsina, Nigeria and Department of Paediatrics, University of Ilorin Teaching Hospital, Ilorin, Nigeria. Michael Abel Alao Department of Paediatrics, University College Hospital and University of Ibadan, Ibadan, Nigeria. Muhammed Nurudeen Adeboye Department of Paediatrics, University of Ilorin Teaching Hospital, Ilorin, Nigeria.
dc.description.abstractAbstract: Introduction: Despite being responsible for the highest burden of global malaria infection, there are limited data on malaria-associated acute kidney injury (MAKI) among Nigerian children for informed decisions. This study described the incidence and predictors of malaria-associated AKI among a cohort of 541 children in northwestern Nigeria. Method: This was a retrospective review of malaria cases from 1st January 2019 to December 31, 2020. We extracted socio-demographics, clinical features, and laboratory parameters from the records of the children with confirmed cases of severe malaria. AKI was defined and staged according to the 2012 Kidney Disease: Improving Global Outcomes (KDIGO) criteria. We carried out bivariate analysis and entered variables that were significant into binary logistic regression in order to determine predictors of AKI. Result: Out of the 541 children, 208 (38.4%) had MAKI. Of the 208, 165 (79.3%) were in stage 1, 26 (12.5%) were in stage 2, and 17 (8.2%) were in stage 3. Clinical features associated with AKI included hypoxemia, respiratory distress, loss of consciousness, prostration, passage of dark-colored urine, and shock (p<0.05). Laboratory parameters associated with AKI included acidosis, leukocytosis, hyponatremia, and hyperkalemia (p<0.05). Factors that independently predicted AKI included the passage of dark-colored urine with an adjusted odds ratio (AOR)-3.853 (95% CI 2.417, 6.143), hyponatremia-AOR 2.346, (95% CI 1.287, 4.277), and hyperkalemia-AOR 3.122, (95% CI 1.031, 9.393). Conclusion: The incidence of malaria-associated AKI is high among children in northwestern Nigeria. The presence of dark-colored urine, hyponatremia, and hyperkalemia strongly predict the risk for AKI.
dc.identifierhttps://doi.org/10.60086/jnps1032
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2684
dc.language.isoen_US
dc.publisherPerinatal Society of Nepal (PESON)
dc.titleClinical and Laboratory Predictors of Acute Kidney Injury in Childhood Severe Malaria
dc.typeArticle
dspace.entity.typePublication
local.article.typeOriginal Article
oaire.citation.endPage30
oaire.citation.startPage24
relation.isJournalIssueOfPublication55586c20-6e34-4f8f-a3a3-2c9de99bab0e
relation.isJournalIssueOfPublication.latestForDiscovery55586c20-6e34-4f8f-a3a3-2c9de99bab0e
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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