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Published on: June 4, 2012
Initial low-dose gentamicin for Staphylococcus aureus bacteremia and endocarditis is nephrotoxic
Sara E Cosgrove1, Gloria A Vigliani, Vance G Fowler
1Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA. scosgro1@jhmi.edu
Background:
The safety of adding initial low-dose gentamicin to antistaphylococcal penicillins or vancomycin for treatment of suspected Staphylococcus aureus native valve endocarditis is unknown. This study evaluated the association between this practice and nephrotoxicity.
Methods:
We performed a prospective cohort study of safety data from a randomized, controlled trial of therapy for S. aureus bacteremia and native valve infective endocarditis involving 236 patients from 44 hospitals in 4 countries. Patients either received standard therapy (antistaphylococcal penicillin or vancomycin) plus initial low-dose gentamicin (n=116) or received daptomycin monotherapy (n = 120). We measured renal adverse events and clinically significant decreased creatinine clearance in patients (1) in the original randomized study arms and (2) who received any initial low-dose gentamicin either, as a study medication or
Results:
Renal adverse events occurred in 8 (7%) of 120 daptomycin recipients, 10 (19%) of 53 vancomycin recipients, and 11 (17%) of 63 antistaphylococcal penicillin recipients. Decreased creatinine clearance occurred in 9 (8%) of 113 of evaluable daptomycin recipients, 10 (22%) of 46 vancomycin recipients, and 16 (25%) of 63 antistaphylococcal penicillin recipients. An additional 21 patients received initial low-dose gentamicin
Conclusions:
Initial low-dose gentamicin as part of therapy for S. aureus bacteremia and native valve infective endocarditis is nephrotoxic and should not be used routinely, given the minimal existing data supporting its benefit.
Insights
Adding low-dose gentamicin to Staphylococcus aureus endocarditis treatment increases nephrotoxicity. This practice should be avoided due to potential kidney damage, especially in older patients.
Area of Science:
- Infectious Diseases
- Nephrology
- Clinical Pharmacology
Background:
- The safety of combining initial low-dose gentamicin with antistaphylococcal penicillins or vancomycin for Staphylococcus aureus native valve endocarditis is not well-established.
- This study aimed to assess the association between this therapeutic approach and the incidence of nephrotoxicity.
Purpose of the Study:
- To evaluate the nephrotoxic potential of adding initial low-dose gentamicin to standard therapies for Staphylococcus aureus native valve endocarditis.
- To identify risk factors for decreased creatinine clearance in patients with S. aureus bacteremia and native valve endocarditis.
Main Methods:
- A prospective cohort study was conducted using safety data from a randomized controlled trial involving 236 patients with S. aureus bacteremia and native valve endocarditis.
- Patients received either standard therapy plus initial low-dose gentamicin or daptomycin monotherapy.
- Renal adverse events and clinically significant decreases in creatinine clearance were measured, including patients who received gentamicin shortly before enrollment.
Main Results:
- Nephrotoxicity, indicated by decreased creatinine clearance, was significantly higher in patients receiving initial low-dose gentamicin (22%) compared to those who did not (8%).
- Independent predictors of decreased creatinine clearance included advanced age (≥65 years) and the administration of any initial low-dose gentamicin.
- Specific rates of renal adverse events and decreased creatinine clearance varied among vancomycin and antistaphylococcal penicillin recipients when combined with gentamicin.
Conclusions:
- Initial low-dose gentamicin, when used as part of the therapy for Staphylococcus aureus bacteremia and native valve endocarditis, is associated with significant nephrotoxicity.
- Routine use of initial low-dose gentamicin in this context is not recommended due to the observed renal risks and limited supporting evidence of benefit.
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