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Nephrotoxicity With Vancomycin in the Pediatric Population: A Systematic Review and Meta-Analysis
Theresa M Fiorito1,2, Megan K Luther3,4, Penelope H Dennehy1,2
1From the Department of Pediatrics, Hasbro Children's Hospital.
Insights
High vancomycin trough levels (≥15 mg/L) significantly increase the risk of nephrotoxicity in pediatric patients. Other factors like ICU admission and concurrent nephrotoxic medications also contribute to kidney damage.
Area of Science:
- Pharmacology
- Nephrology
- Pediatric Medicine
Background:
- Vancomycin is a critical antibiotic for treating methicillin-resistant Staphylococcus aureus (MRSA) infections in children.
- Vancomycin exposure is associated with an increased risk of nephrotoxicity, necessitating careful monitoring.
- Predicting and mitigating vancomycin-induced nephrotoxicity in pediatric populations is crucial for patient safety.
Purpose of the Study:
- To systematically review predictors of vancomycin-associated nephrotoxicity in pediatric patients.
- To conduct a meta-analysis evaluating the impact of vancomycin trough concentrations ≥15 mg/L on nephrotoxicity.
- To identify key risk factors contributing to vancomycin-induced kidney injury in children.
Main Methods:
- A comprehensive literature search was conducted across major databases (PubMed, Cochrane Library, Embase, Web of Sciences).
- Included studies were randomized clinical trials and observational studies focusing on pediatric patients, vancomycin troughs, and nephrotoxicity.
- Studies were excluded if they did not measure troughs or used a different threshold than 15 mg/L for vancomycin levels.
Main Results:
- Ten studies were included in the meta-analysis, all with normal baseline serum creatinine.
- Elevated vancomycin trough levels (≥15 mg/L) were a significant predictor of nephrotoxicity, increasing risk by 2.7-fold (OR, 2.71).
- Nephrotoxicity risk was further elevated in pediatric intensive care unit (PICU) patients (OR, 3.61).
Conclusions:
- Higher vancomycin trough levels are linked to increased nephrotoxicity in pediatric patients.
- Other contributing factors to vancomycin-induced nephrotoxicity include ICU admission, hypovolemia, and concurrent use of nephrotoxic drugs.
- Optimizing vancomycin dosing and monitoring for these risk factors are essential in pediatric care.
Background:
Vancomycin is frequently used to treat methicillin-resistant Staphylococcus aureus infections in pediatric patients. Vancomycin exposure may lead to an increase in frequency of nephrotoxicity. Our aim was to conduct a systematic review to describe predictors of nephrotoxicity associated with vancomycin, including documented trough concentrations ≥15 mg/L. We also aimed to use a meta-analysis to assess the impact of a vancomycin trough ≥15 mg/L on nephrotoxicity.
Methods:
A literature search was performed using PubMed, Cochrane Library, Embase and Web of Sciences database. We included randomized clinical trials and observational studies evaluating the relationship between vancomycin troughs and nephrotoxicity in pediatric-age patients. Studies not measuring troughs or defining a different cut-off point than 15 mg/L were excluded. Data on age, exclusion criteria, nephrotoxicity definition, risk factors for nephrotoxicity and vancomycin trough levels were extracted from selected papers.
Results:
Ten studies were identified for meta-analysis. All subjects had comparatively normal baseline serum creatinine values. Common risk factors identified included elevated (≥15 mg/L) trough levels, renal impairment, hypovolemia and concurrent use of nephrotoxic medications. Troughs ≥15 mg/L increased nephrotoxicity by 2.7-fold (odds ratio (OR), 2.71; 95% confidence interval: 1.82-4.05; I(2) = 40%; Q = 0.09). These odds were further increased among patients in the pediatric intensive care unit (OR, 3.61; 95% confidence interval: 1.21-10.74; I(2) = 45%; Q = 0.18).
Conclusions:
Though the rate of vancomycin-induced nephrotoxicity is increased in pediatric patients with higher vancomycin troughs, other factors such as intensive care unit admission, hypovolemia and concurrent nephrotoxic drug use appear to contribute to the development of nephrotoxicity.
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