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Risks of Polymyxin B Nephrotoxicity and Its Precursors in the Intensive Care Unit: A Retrospective Cohort Study
Hüseyin Özkarakaş1, Yeliz Özdemir2, Selma Tosun2
1Intensive Care Unit, University of Health Sciences Izmir Bozyaka Training and Research Hospital, Izmir, TUR.
Background And Aim:
Polymyxin group antibiotics constitute a part of our limited arsenal in the treatment of multidrug-resistant gram-negative bacteria. However, their use is limited especially due to nephrotoxicity and other side effects. In this study, we primarily aimed to determine the effect of polymyxin B on the rate of nephrotoxicity in critically ill patients, and secondly to identify the factors that facilitate nephrotoxicity caused by polymyxin B.
Materials And Methods:
The study was designed as a retrospective cohort study and conducted by scanning patients aged 18 years or older who had been admitted to our intensive care unit (ICU) in 2022 and treated with polymyxin B for at least 72 hours. Patients without chronic renal failure and acute kidney injury (AKI) before starting polymyxin B therapy were included and AKI was examined after the use of polymyxin B. The patients were then divided into two groups, those with AKI and those without AKI. We tried to find factors that may facilitate AKI by comparing the two groups.
Results:
Of the patients, 26 were female and 34 were male. In 21 of the patients (35%), renal damage of varying degrees developed; these patients belonged to the nephrotoxicity (NT) group, while the rest belonged to the non-nephrotoxicity (non-NT) group. We found that advanced age (p=0.008), low baseline GFR (p=0.01), baseline creatinine (p=0.006), BMI (p=0.011), concomitant diseases (p<0.001), and days of use of polymyxin B (p=0.006) were statistically different between the two groups. In multivariate analysis of univariate analysis, we found that duration of polymyxin B use, BMI, and advanced age were independent risk factors for AKI development.
Conclusion:
We found that 21 (35%) of 60 intensive care unit patients who had no previous history of kidney injury developed kidney injury after being treated with polymyxin B. We identified advanced age, high BMI, and duration of polymyxin B use as independent risk factors. Therefore, we recommend close monitoring of renal function and prompt intervention, particularly in patients with risk factors, during polymyxin B use.
Insights
Polymyxin B caused kidney injury in 35% of critically ill patients. Advanced age, high BMI, and longer duration of use are key risk factors for nephrotoxicity.
Area of Science:
- Critical Care Medicine
- Nephrology
- Infectious Diseases
Background:
- Polymyxin antibiotics are crucial for treating multidrug-resistant gram-negative infections.
- Nephrotoxicity is a significant limitation of polymyxin use, necessitating further investigation.
- Understanding polymyxin B's renal impact is vital for optimizing patient care.
Purpose of the Study:
- To evaluate the incidence of nephrotoxicity associated with polymyxin B in critically ill patients.
- To identify independent risk factors contributing to polymyxin B-induced kidney injury.
- To inform clinical practice regarding safe polymyxin B administration.
Main Methods:
- Retrospective cohort study of adult ICU patients treated with polymyxin B for ≥72 hours.
- Exclusion of patients with pre-existing renal failure or acute kidney injury (AKI).
- Comparison of patient characteristics between groups with and without AKI post-treatment.
Main Results:
- 35% of patients (21/60) developed nephrotoxicity (NT) after polymyxin B treatment.
- Statistically significant differences observed in advanced age, low GFR, high creatinine, BMI, comorbidities, and duration of use.
- Multivariate analysis identified duration of use, BMI, and advanced age as independent risk factors for AKI.
Conclusions:
- Polymyxin B is associated with a 35% rate of kidney injury in critically ill patients without prior renal issues.
- Advanced age, elevated BMI, and prolonged polymyxin B exposure are independent predictors of nephrotoxicity.
- Close renal function monitoring and early intervention are recommended for patients receiving polymyxin B, especially those with identified risk factors.
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