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Determining the optimal vancomycin daily dose for pediatrics: a meta-analysis
Geisa Cristina da Silva Alves1,2, Samuel Dutra da Silva3, Virginia Paula Frade3
1Federal University of São João del Rei, Divinópolis, MG, Brazil. geisa.cristina@gmail.com.
Insights
Pediatric vancomycin dosing requires careful consideration. Doses below 60 mg/kg/day are often insufficient for achieving therapeutic vancomycin targets in children.
Area of Science:
- Pharmacology
- Pediatric Infectious Diseases
- Clinical Pharmacy
Background:
- Vancomycin is a critical antibiotic for treating serious Gram-positive bacterial infections in children.
- Establishing optimal dosing regimens is essential to maximize efficacy and minimize toxicity.
- Current pediatric dosing guidelines require evaluation to ensure therapeutic targets are met.
Purpose of the Study:
- To determine the appropriate initial vancomycin dose required to achieve therapeutic targets in pediatric patients.
- To analyze existing literature to identify effective vancomycin dosing strategies for children.
Main Methods:
- A systematic literature search was conducted across PubMed, Cochrane Library, and Embase (1980-2017).
- Key terms included pediatric populations and vancomycin pharmacokinetics/pharmacodynamics.
- Data from eligible studies were analyzed using RevMan V 5.2, calculating confidence intervals and odds ratios.
Main Results:
- Out of 704 identified studies, 40 were eligible, with 20 included in the final statistical analysis.
- Vancomycin doses in the reviewed studies ranged from 40 mg/kg/day to 120 mg/kg/day.
- Significant clinical heterogeneity (I²=84%) was observed across the studies.
Conclusions:
- The meta-analysis indicated that vancomycin doses below 60 mg/kg/day were frequently inadequate.
- Lower doses often failed to achieve the desired vancomycin plasma concentrations (AUC0-24/MIC >400 or trough 10-20 mg/L).
- Higher initial doses may be necessary to effectively control pediatric bacterial infections with vancomycin.
Objective:
The objective of this study was to check which initial dose of vancomycin is needed to achieve the therapeutic target that is currently used in pediatrics.
Methods:
The search was conducted in the following data sources: Pubmed (1980-2017), the Cochrane Library, and Embase (1986-2017) and the references of the published studies; searches were performed using the key terms: child, children, pediatrics, infants and adolescents, vancomycin, pharmacokinetics, and pharmacodynamics. The data extracted from the studies were analyzed and grouped using RevMan V 5.2 software. The confidence interval (CI) 95% and the odds ratio (OR) were calculated considering the Mantel-Haenszel random effect.
Results:
From the 704 studies identified, 40 revealed eligibility for this review and only 20 presented enough data to be included in the statistical analysis. The articles found in this review were published between 1980 and 2017. The vancomycin doses varied between 40 mg/kg/day to 120 mg/kg/day. The statistical tests demonstrated significant clinical heterogeneity of I2 (84%).
Conclusions:
The meta-analysis study revealed in the majority of studies that doses lower than 60 mg/kg/day were not enough to achieve desirable vancomycin plasma concentrations "area under the curve in 24 h/minimum inhibitory concentration >400 (AUC0-24/MIC>400) or trough 10-20 mg/L" to control bacterial infections in pediatrics.
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