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Assessment of Causality in Hospitalized Children With Aminoglycoside-Related Nephrotoxicity
Madhileti Sravani1, Sriram Krishnamurthy2, Narayanan Parameswaran1
1Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry.
Insights
Aminoglycoside antibiotics can cause kidney injury in children. This study found that while many children experienced acute kidney injury (AKI), only a small percentage had it definitively linked to the drug, suggesting other factors may be involved.
Area of Science:
- Pediatric Nephrology
- Pharmacovigilance
- Adverse Drug Reactions
Background:
- Aminoglycosides are crucial antibiotics for treating severe pediatric infections.
- Nephrotoxicity is a known, but often poorly quantified, adverse effect of aminoglycoside therapy in children.
Purpose of the Study:
- To determine the incidence of aminoglycoside-induced nephrotoxicity in pediatric patients.
- To establish drug causality for observed kidney injury.
- To identify risk factors associated with aminoglycoside-related nephrotoxicity.
Main Methods:
- Prospective study of 110 children (1 month-12 years) receiving aminoglycosides for ≥4 days.
- Utilized the Liverpool adverse drug reaction causality assessment tool to evaluate drug causality.
- Monitored for acute kidney injury (AKI) and tubular dysfunction.
Main Results:
- 38.2% of children developed AKI; 64.5% had composite nephrotoxicity.
- Only 15.5% of AKI cases were definitively attributed to aminoglycosides.
- Hypotension, high PRISM-III scores (20-29%), and post-surgery status were independent predictors of AKI.
Conclusions:
- A small proportion of pediatric AKI cases in patients receiving aminoglycosides are definitively attributable to the drug.
- Risk factors like hypotension and critical illness scores are associated with AKI in this population.
- Further research is needed to elucidate the precise mechanisms and contributing factors to aminoglycoside nephrotoxicity.
Objective:
To evaluate the incidence of aminoglycoside-related nephrotoxicity and ascertain drug causality and its risk factors.
Methods:
This prospective study was conducted from January, 2019 to January, 2021, and recruited 110 consecutively admitted children aged 1 month to 12 years, receiving aminoglycosides for ≥4 days. Drug causality was assessed using Liverpool adverse drug reaction causality assessment tool.
Results:
42 (38.2%) children developed acute kidney injury (AKI), with 71 (64.5%) having composite nephrotoxicity (AKI and/or tubular-dysfunction). Only 17 (15.5%) had AKI definitively attributable to aminoglycosides. Hypotension [OR 0.016 (95% CI 0.01-0.71), P=0.03], PRISM-III score 20-29% [OR 55.48 (95% CI 3.66-840.53), P=0.004] and post-surgery patients [OR 3.2 (95% CI 1.01-10.1), P=0.047] were independent predictors of AKI.
Conclusions:
Only a small proportion of children receiving aminoglycosides had AKI definitively attributable to the drug.
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