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Published on: May 6, 2018
Incidence and predictors of vancomycin-associated nephrotoxicity
Hamzah Moh'd1, Fayez Kheir1, Lan Kong1
1From the Department of Medicine, Division of Infectious Diseases and Epidemiology, Penn State Hershey Milton S. Hershey Medical Center, Penn State College of Medicine, Hershey, Pennsylvania, the Department of Medicine, Section of Pulmonary Diseases, Critical Care, and Environmental Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana, the Department of Public Health Sciences, Penn State College of Medicine, Hershey, and the Department of Internal Medicine, Chicago Medical School at Rosalind Franklin University, Chicago, Illinois.
Vancomycin-associated nephrotoxicity (VAN) affects over 26% of patients, even with long treatment courses. Intensive care unit admission, loop diuretics, and cirrhosis are key risk factors for developing VAN.
Area of Science:
- Nephrology
- Infectious Diseases
- Clinical Pharmacology
Background:
- Vancomycin-associated nephrotoxicity (VAN) incidence varies, with recent studies showing over 30%.
- Predictors for VAN remain poorly defined, necessitating further investigation.
- This study focuses on a cohort with predominantly long vancomycin treatment durations.
Purpose of the Study:
- To accurately estimate the incidence of VAN in a diverse patient population.
- To identify and evaluate clinical predictors associated with VAN development.
- To analyze risk factors in patients undergoing extended vancomycin therapy.
Main Methods:
- Retrospective analysis of patients receiving vancomycin and monitored via the Outpatient Parenteral Antibiotic Therapy program.
- Nephrotoxicity defined as a ≥50% or 0.5 mg/dL increase in serum creatinine on two consecutive readings.
- Comparison of nephrotoxic vs. non-nephrotoxic groups based on vancomycin parameters, comorbidities, and concurrent treatments.
Main Results:
- Out of 579 patients, 154 (26.6%) experienced nephrotoxicity.
- Nephrotoxicity occurred within 14 days for 90 patients and after 14 days for 64 patients, with a median onset of 9 days.
- Independent predictors of nephrotoxicity included ICU admission, loop diuretic use, and cirrhosis; higher baseline creatinine showed a protective effect (P=0.0016).
Conclusions:
- VAN is a significant risk in both short and long vancomycin treatment courses.
- Key risk factors for VAN include ICU stay, concurrent loop diuretic use, cirrhosis, and initial vancomycin trough levels.
- Elevated baseline creatinine may be protective, possibly due to cautious vancomycin administration in such patients.
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