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The association between acute kidney injury and Polymyxin B treatment: A retrospective cohort study
Long Wen1, Xuefeng Yuan2, Xiaohui Liu3
1Department of Respiratory and Critical Care Medicine, The First Hospital of Changsha (The Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University), Changsha, Hunan, People's Republic of China.
Abstract:
PurposeThis retrospective study aimed to analyse the impact of polymyxin B (PMB) on nephrotoxicity parameters and identify associated variables.Patients and methodsThe study, which was conducted at a tertiary general hospital in China, included 84 patients over the age of 18 who had received PMB for a period of more than 48 h. Patients were divided into two groups based on the presence or absence of acute kidney injury (AKI) according to KDIGO standards. The identification of risk factors for PMB-associated AKI was facilitated by data collection and multivariate logistic regression analysis.ResultsThe majority of patients were male, with a median age of 80 years (interquartile range (IQR): 68.5, 87.0) and a median weight of 60.0 kg (IQR: 50.0, 65.0). PMB was administered with a median loading dose of 1.73 mg/kg (IQR: 1.67, 1.82) and a median daily maintenance dose of 1.82 mg/kg (IQR: 1.67, 2.22) over a median treatment duration of 7.75 days (IQR: 5.00, 10.38). The development of AKI was observed in 36 patients (42.9%), with a median time to onset of 5 days (IQR: 3, 6). In the cohort of patients who developed AKI, 11 (30.6%) patients discontinued PMB therapy, while 8 (16.7%) patients required renal replacement therapy (RRT). The study revealed that concurrent chronic kidney disease (CKD) (odds ratio (OR) = 5.47, 95% confidence interval (CI) 1.52-19.64, P = 0.01) and the daily maintenance dose (OR = 12.57, 95% CI 2.84-55.59, P = 0.00) were independently associated with AKI onset following PMB therapy.ConclusionsThe potential association between PMB therapy and AKI raises clinical concern. Concurrent CKD and higher PMB maintenance doses were identified as independent risk factors for AKI associated with PMB therapy. Consequently, rigorous monitoring of renal function indices and therapeutic drug concentrations is recommended to facilitate early detection of nephrotoxic risks, thereby minimizing renal injury and ensuring the safe administration of PMB.
Insights
Polymyxin B (PMB) treatment can cause acute kidney injury (AKI). Concurrent chronic kidney disease (CKD) and higher PMB doses increase AKI risk, necessitating careful monitoring.
Area of Science:
- Nephrology
- Pharmacology
- Infectious Diseases
Background:
- Polymyxin B (PMB) is a critical antibiotic for treating multidrug-resistant Gram-negative bacterial infections.
- Nephrotoxicity is a significant concern associated with PMB therapy, potentially leading to acute kidney injury (AKI).
- Identifying risk factors for PMB-induced AKI is crucial for patient safety and optimizing treatment strategies.
Purpose of the Study:
- To analyze the impact of Polymyxin B (PMB) on nephrotoxicity parameters.
- To identify variables associated with the development of AKI in patients receiving PMB.
- To determine independent risk factors for PMB-associated AKI.
Main Methods:
- Retrospective study of 84 adult patients receiving PMB for >48 hours at a tertiary hospital.
- Patients categorized into AKI and non-AKI groups based on KDIGO criteria.
- Multivariate logistic regression analysis employed to identify risk factors for PMB-associated AKI.
Main Results:
- 42.9% of patients developed AKI, with a median onset time of 5 days.
- Concurrent chronic kidney disease (CKD) (OR=5.47) and higher daily PMB maintenance doses (OR=12.57) were independently associated with AKI.
- 16.7% of AKI patients required renal replacement therapy (RRT).
Conclusions:
- PMB therapy is associated with a significant risk of AKI.
- Pre-existing CKD and elevated PMB maintenance doses are independent risk factors for PMB-induced nephrotoxicity.
- Close monitoring of renal function and drug levels is essential for safe PMB administration.
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