Evidence map›Paper›PMID 41582201›Full record

ArticleBMC pediatrics2026

Prevalence of acute kidney injury and nephrotoxic drug exposure in premature and low birth weight neonates admitted to intensive care units at Muhimbili National Hospital, Dar es Salaam.

Helfrid B Ilomo, Rajabu H Mnkugwe, Raphael C Kambona, Mwanaidi A Msuya, Joram A Sungura, Jonathan Mngumi, Ritah F Mutagonda

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Article in BMC pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Helfrid B IlomoMuhimbili National Hospital, Dar es Salaam, Tanzania. ilomohb@gmail.com.
Rajabu H MnkugweMuhimbili University of Health and Allied Sciences, Dar Es Salaam, Tanzania.
Raphael C KambonaSimiyu Regional Referral Hospital, Simiyu, Tanzania.
Mwanaidi A MsuyaMuhimbili National Hospital, Dar es Salaam, Tanzania.
Joram A SunguraMaweni Regional Referral Hospital, Kigoma, Tanzania.
Jonathan MngumiMuhimbili National Hospital, Dar es Salaam, Tanzania.
Ritah F MutagondaMuhimbili University of Health and Allied Sciences, Dar Es Salaam, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) poses a significant threat to premature and low birth weight (LBW) neonates in neonatal intensive care units (NICUs), driven by immature renal function and frequent exposure to nephrotoxic medications. Understanding its prevalence and risk factors is critical for improving outcomes in vulnerable populations.

objectiveTo determine the prevalence of AKI, exposure to potential nephrotoxic drugs and identify associated risk factors, among premature and LBW neonates admitted to NICUs at Muhimbili National Hospital (MNH), Dar es Salaam, Tanzania.

methodsA cross-sectional study was conducted from February to June 2024 at MNH Upanga and Mloganzila, enrolling 144 premature and LBW neonates via non-probability consecutive sampling. Serum creatinine levels were measured at admission, 48 h, and day seven or pre-discharge to diagnose AKI using KDIGO criteria. Data were analyzed with SPSS v26.0, employing chi-square tests for associations and robust Poisson regression for risk factor identification (p < 0.20 for univariable inclusion, p < 0.05 for significance).

resultsAmong 144 neonates (61.8% female, median age 5 days [IQR 3-12]), 65.3% received nephrotoxic drugs, primarily ampicillin-cloxacillin (58.3%) and gentamicin (54.9%). AKI was diagnosed in 26.4% of neonates, with 18.8% in stage 1, 6.3% in stage 2, and 1.4% in stage 3. Multivariable analysis identified male sex (aPR = 1.68, 95% CI: 1.01-2.89, p = 0.049) and exposure to two nephrotoxic drugs (aPR = 2.58, 95% CI: 1.20-5.55, p = 0.015) as independent risk factors for AKI.

conclusionAKI affects over a quarter of premature and LBW neonates in NICUs, with male sex and multiple nephrotoxic drug exposures as key risk factors. Implementing routine renal monitoring and optimizing pharmacotherapy are essential to reduce AKI incidence and improve neonatal outcomes in resource-constrained settings.

Indexed as

Acute Kidney InjuryInfant, Low Birth WeightCreatinineCross-Sectional StudiesFemaleHumansInfant, NewbornInfant, PrematureIntensive Care Units, NeonatalMalePrevalenceRisk FactorsTanzaniaCreatinineAcute kidney injuryLow birth weight and intensive care unitNeonateNephrotoxic drug exposurePremature

Identifiers

PMID41582201
PMCPMC12918346

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