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: Current guidelines for the therapeutic monitoring of vancomycin recommend dosing based on the area under the concentration-time curve (AUC) to achieve clinical efficacy while reducing nephrotoxicity. Although, a wide range of nephrotoxicity thresholds have been reported, few studies have documented clinical outcomes based on AUC-guided vancomycin dosing in Korea. : The aim of the study was to evaluate whether a relationship exists between AUC and treatment outcomes in vancomycin treated patients in MRSA (methicillin-resistant Staphylococcus aureus) bacteremia. Furthermore, this study tries to estimate AUC threshold for treatment failure and nephrotoxicity. : The records of adult patients with MRSA bacteremia treated with vancomycin for ≥72 hrs without dialysis between April 2013 and April 2021, were reviewed retrospectively. Treatment success was defined as defervescence and blood culture sterilization by day 7. Nephrotoxicity was defined as an increase in serum creatinine (SCr) levels ≥0.3 mg/dL or a 50% increase from baseline on two consecutive days. Bayesian estimation was used to predict individual vancomycin AUC. Both classification and regression tree (CART) and receiver operating characteristic (ROC) curve analyses were performed to estimate the optimal AUC thresholds for vancomycin efficacy and nephrotoxicity. : Of 118 patients, 61 (51.7%) experienced treatment failure and 42 (35.6%) developed acute kidney injury (AKI). The vancomycin AUC threshold for predicting AKI was 615.0 mg∙hr/L. In the multivariate analysis, AUC ≥ 615.0 mg∙hr/L was a significant risk factor for nephrotoxicity (adjusted Odds Ratio [aOR] = 5.24, 95% confidence interval [CI] 1.8–14.65). The lower threshold for treatment failure was not defined since it was not statistically significant. Risk factors for treatment failure included low BMI (aOR=0.82, 95% CI 0.70-0.96), severity of acute illness represented by complicated infection (aOR=77.56, 95% CI 16.7–359.4) and comorbidities, such as solid organ tumors (aOR=6.61, 95% CI 1.19–36.81) and cerebrovascular disease (aOR=6.05, 95% CI 1.17–31.23). : Although AUC-guided vancomycin dosing was associated with a reduced risk of AKI, its ability to predict clinical outcomes was modest. Further studies are needed to define the AUC therapeutic range to maximize efficacy and minimize nephrotoxicity.
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Kim et al. (2022) studied this question.
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