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April 14, 2026Journal of Antimicrobial Chemotherapy0 citations

Pathophysiology, risk factors and clinical management for polymyxin-associated acute kidney injury

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SZSai ZhaoGMGe MuXLXiao Liu

Key Points

  • The review aims to explore the mechanisms, risk factors, and management strategies for polymyxin-associated acute kidney injury.
  • Review of current literature on polymyxin and acute kidney injury.
  • Evaluation of risk factors and biomarkers for predicting acute kidney injury.
  • Discussion on clinical management strategies to reduce nephrotoxicity.
  • Highlighting the importance of monitoring serum creatinine and urine volume.
  • Identifying several promising biomarkers for early detection, though lacking validation.
  • Emphasizing the need for real-world evidence in clinical guidelines.

Abstract

Polymyxins serve as a 'last-line' defence against Gram-negative bacterial infections and are frequently used in critically ill patients with multidrug-resistant pathogens. However, polymyxin-associated acute kidney injury (PA-AKI) remains a major factor limiting their clinical application. This review examines the pathophysiology, risk factors and clinical management of PA-AKI, providing updated perspectives on its prevention and treatment. Reducing exposure to concomitant nephrotoxic agents, together with timely and standardized monitoring of serum creatinine, urine volume and polymyxin concentrations, plays a key role in mitigating the risk and progression of PA-AKI. Although several biomarkers show promise for the early prediction of PA-AKI and may enable earlier intervention, many have not yet undergone extensive clinical validation. There is a clear need to incorporate real-world evidence into clinical practice guidelines for polymyxin use. Further research should focus on identifying genetic risk factors for PA-AKI and developing novel polymyxin analogues with reduced nephrotoxicity.

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Cite This Study

Zhao et al. (2026) studied this question.

synapsesocial.com/papers/69ddd9cae195c95cdefd7198https://doi.org/10.1093/jac/dkag132
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