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Published on: February 2, 2021
Acute Kidney Injury Associated with the Concomitant Use of Vancomycin and Piperacillin-Tazobactam
Dayu Chen1,2,3, Jingjing Kan2, Qiaoling Gu2
1Department of Pharmacy, Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, People's Republic of China.
Abstract:
In recent years, the increased use of vancomycin (VAN) in combination with piperacillin-tazobactam (TZP) has raised significant concerns in clinical practice regarding the heightened risk of acute kidney injury (AKI). This topic has become a focal point in clinical therapeutics due to the widespread application of VAN alongside TZP. The specific mechanisms underlying vancomycin and piperacillin-tazobactam (VPT) associated AKI remain unclear. In this review, we discuss several controversial or underexplored aspects of current research. While the majority of literature links VPT to an elevated risk of AKI, numerous studies present conflicting outcomes. Mechanisms proposed for the increased risk of AKI associated with VPT, based on clinical observations and animal studies, include additive toxic effects, increased VAN exposure due to concomitant use with TZP, exacerbated VAN-induced oxidative stress injury in proximal renal tubule by TZP, pseudo-nephrotoxicity mediated by VPT-induced impaired creatinine secretion, or a combination of the aforementioned mechanisms. Additionally, this review outlines potential strategies that might effectively mitigate the risk of VPT-induced AKI, offering insights and future implications in the realm of pharmacovigilance.
Insights
The combination of vancomycin (VAN) and piperacillin-tazobactam (TZP) may increase acute kidney injury (AKI) risk. Research explores mechanisms and mitigation strategies for vancomycin and piperacillin-tazobactam (VPT)-associated AKI.
Area of Science:
- Pharmacology
- Nephrology
- Clinical Therapeutics
Background:
- Increased co-administration of vancomycin (VAN) and piperacillin-tazobactam (TZP) is linked to acute kidney injury (AKI) concerns.
- The precise mechanisms driving vancomycin and piperacillin-tazobactam (VPT)-associated AKI are not fully understood.
- Conflicting outcomes exist in the literature regarding the association between VPT and AKI risk.
Purpose of the Study:
- To review controversial and underexplored aspects of VPT-associated AKI.
- To elucidate potential mechanisms contributing to VPT-induced AKI.
- To outline strategies for mitigating the risk of VPT-induced AKI.
Main Methods:
- Review of existing clinical observations and animal studies.
- Analysis of proposed mechanisms for VPT-associated AKI.
- Exploration of pharmacovigilance insights.
Main Results:
- Proposed mechanisms include additive toxic effects, increased VAN exposure, exacerbated oxidative stress, and impaired creatinine secretion.
- Multiple factors may contribute to VPT-induced AKI.
- Evidence suggests a potential link between VPT and increased AKI risk, though conflicting data exists.
Conclusions:
- Understanding the complex mechanisms of VPT-associated AKI is crucial.
- Further research is needed to clarify conflicting outcomes.
- Developing effective mitigation strategies is essential for patient safety and pharmacovigilance.
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