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Increasing vancomycin serum trough concentrations and incidence of nephrotoxicity
Lindsey Pritchard1, Catherine Baker, James Leggett
1St. Louis College of Pharmacy, St. Louis, MO 63110-1088, USA. lprichard@stlcop.edu
Background:
conflicting evidence regarding the association of vancomycin serum concentrations with efficacy and toxicity has resulted in controversy regarding optimal target concentrations. Recent publications recommend attaining higher vancomycin trough concentrations of 15 to 20 mg/L for target infections, yet limited research is available assessing the correlation of vancomycin serum concentrations with toxicity. The aim of this study was to evaluate the association between vancomycin serum trough concentrations and nephrotoxicity.
Methods:
a 2-phase retrospective analysis was completed. Phase 1 evaluated 2493 courses of vancomycin completed between January 2003 and December 2007. The analysis describes a 5-year trend in vancomycin prescribing practices and assesses the association of nephrotoxicity with baseline serum creatinine, vancomycin serum trough concentrations, and duration of vancomycin therapy. Phase 2 examined patients receiving vancomycin therapy during 2007 to evaluate specific risk factors for development of nephrotoxicity.
Results:
the proportion of vancomycin serum trough concentrations ≥ 15 mg/L and ≥ 20 mg/L increased significantly over time. Statistical analysis identified vancomycin serum trough concentrations ≥ 14 mg/L, duration of vancomycin therapy ≥ 7 days, and baseline serum creatinine levels ≥ 1.7 mg/dL as independent predictors of nephrotoxicity. Phase 2 analysis again implicated mean vancomycin serum trough concentration as a significant predictor of nephrotoxicity. Nephrotoxicity resolved in 81% (17/21) of cases evaluated.
Conclusions:
a higher vancomycin serum trough concentration and prolonged vancomycin therapy are associated with an increased risk of nephrotoxicity. The decision to target increased vancomycin trough concentrations should be based on an assessment of the severity of the infection and must consider the nephrotoxicity risk associated with increased vancomycin levels.
Insights
Higher vancomycin trough concentrations and longer treatment durations increase the risk of vancomycin-associated nephrotoxicity. Careful patient assessment is crucial when targeting higher drug levels.
Area of Science:
- Pharmacology
- Nephrology
- Infectious Diseases
Background:
- Conflicting evidence exists on optimal vancomycin concentrations, with recent recommendations for higher trough levels (15-20 mg/L).
- Limited research has correlated vancomycin serum concentrations with toxicity, specifically nephrotoxicity.
- This study aimed to evaluate the association between vancomycin serum trough concentrations and nephrotoxicity.
Purpose of the Study:
- To investigate the relationship between vancomycin serum trough concentrations and the incidence of nephrotoxicity.
- To identify predictors of vancomycin-induced nephrotoxicity.
- To analyze trends in vancomycin prescribing and associated toxicity.
Main Methods:
- A 2-phase retrospective analysis of vancomycin therapy courses.
- Phase 1: Assessed 2493 courses (2003-2007) for trends and associations between nephrotoxicity, serum creatinine, vancomycin trough concentrations, and therapy duration.
- Phase 2: Examined patients receiving vancomycin in 2007 to identify specific nephrotoxicity risk factors.
Main Results:
- Vancomycin trough concentrations ≥ 15 mg/L and ≥ 20 mg/L increased significantly over the study period.
- Independent predictors of nephrotoxicity included vancomycin trough concentrations ≥ 14 mg/L, therapy duration ≥ 7 days, and baseline serum creatinine ≥ 1.7 mg/dL.
- Mean vancomycin serum trough concentration was a significant predictor of nephrotoxicity; 81% of cases resolved.
Conclusions:
- Elevated vancomycin serum trough concentrations and prolonged therapy duration are linked to increased nephrotoxicity risk.
- Targeting higher vancomycin trough concentrations requires careful consideration of infection severity and potential nephrotoxicity.
- Clinical decisions on vancomycin dosing should balance efficacy with patient safety and renal function.
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