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Vancomycin associated acute kidney injury in patients with infectious endocarditis: a large retrospective cohort
Pan Kunming1, Huang Ying2,3,4, Xu Chenqi2,3
1Department of Pharmacy, Zhongshan Hospital, Fudan University, Shanghai, China.
Abstract:
Background: Vancomycin remains the cornerstone antibiotic for the treatment of infective endocarditis (IE). Vancomycin has been associated with significant nephrotoxicity. However, vancomycin associated acute kidney injury (AKI) has not been evaluated in patients with IE. We conducted this large retrospective cohort study to reveal the incidence, risk factors, and prognosis of vancomycin-associated acute kidney injury (VA-AKI) in patients with IE. Methods: Adult patients diagnosed with IE and receiving vancomycin were included. The primary outcome was VA-AKI. Results: In total, 435 of the 600 patients were enrolled. Of these, 73.6% were male, and the median age was 52 years. The incidence of VA-AKI was 17.01% (74). Only 37.2% (162) of the patients received therapeutic monitoring of vancomycin, and 30 (18.5%) patients had reached the target vancomycin trough concentration. Multiple logistic regression analysis revealed that body mass index [odds ratio (OR) 1.088, 95% CI 1.004, 1.179], duration of vancomycin therapy (OR 1.030, 95% CI 1.003, 1.058), preexisting chronic kidney disease (OR 2.291, 95% CI 1.018, 5.516), admission to the intensive care unit (OR 2.291, 95% CI 1.289, 3.963) and concomitant radiocontrast agents (OR 2.085, 95% CI 1.093, 3.978) were independent risk factors for VA-AKI. Vancomycin variety (Lai Kexin vs. Wen Kexin, OR 0.498, 95% CI 0.281, 0.885) were determined to be an independent protective factor for VI-AKI. Receiver operator characteristic curve analysis revealed that duration of therapy longer than 10.75 days was associated with a significantly increased risk of VA-AKI (HR 1.927). Kidney function was fully or partially recovered in 73.0% (54) of patients with VA-AKI. Conclusion: The incidence of VA-AKI in patients with IE was slightly higher than in general adult patients. Concomitant contrast agents were the most alarmingly nephrotoxic in patients with IE, adding a 2-fold risk of VA-AKI. In patients with IE, a course of vancomycin therapy longer than 10.75 days was associated with a significantly increased risk of AKI. Thus, closer monitoring of kidney function and vancomycin trough concentrations was recommended in patients with concurrent contrast or courses of vancomycin longer than 10.75 days.
Insights
Vancomycin-associated acute kidney injury (VA-AKI) occurred in 17% of infective endocarditis patients. Risk factors include contrast agents and longer vancomycin therapy, necessitating closer monitoring.
Area of Science:
- Nephrology
- Infectious Diseases
- Pharmacology
Background:
- Vancomycin is a primary treatment for infective endocarditis (IE).
- Vancomycin is linked to nephrotoxicity, but its impact on acute kidney injury (AKI) in IE patients is not well-defined.
- This study investigates vancomycin-associated AKI (VA-AKI) in IE patients.
Purpose of the Study:
- To determine the incidence, risk factors, and prognosis of VA-AKI in patients with IE.
- To identify specific patient characteristics and treatment parameters associated with VA-AKI development.
Main Methods:
- A large retrospective cohort study.
- Included adult patients diagnosed with IE receiving vancomycin.
- Primary outcome was the development of VA-AKI.
Main Results:
- The incidence of VA-AKI was 17.01% among 435 enrolled IE patients.
- Independent risk factors for VA-AKI included higher BMI, longer vancomycin duration, pre-existing CKD, ICU admission, and concomitant radiocontrast agents.
- Vancomycin variety (Lai Kexin vs. Wen Kexin) was a protective factor; therapy >10.75 days increased VA-AKI risk.
Conclusions:
- VA-AKI incidence in IE patients is notable, slightly higher than in the general population.
- Concomitant contrast agents significantly elevate nephrotoxicity risk (2-fold) in IE patients.
- Extended vancomycin therapy (>10.75 days) and contrast use warrant closer renal function and vancomycin level monitoring.
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