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Clinical characteristics and risk factors of colistin-induced nephrotoxicity
Jieun Kim1, Kyoung-Ho Lee, Sunmi Yoo
1Department of Internal Medicine, Hanyang University College of Medicine, 17 Haengdang-dong, Sungdong-gu, Seoul 133-792, South Korea.
Abstract:
Since multidrug-resistant gram-negative organisms have been increasing, polymyxin E (colistin) has been reintroduced despite its nephrotoxicity. A case-control study was performed to investigate the incidence, clinical characteristics and risk factors of colistin-induced nephrotoxicity. From August 2006 to June 2008, 47 cases receiving at least one defined daily dose (DDD) of intravenous colistin were included; 15 (31.9%) of the 47 cases developed nephrotoxicity with preserved urine output, 3 (20%) of whom underwent renal replacement therapy. The mean dosage of colistimethate sodium was 2.25 g (22.5 DDD; range 0.6-8.7 g) at the time of nephrotoxicity. Of 10 patients who were re-assessed for renal function after 1 month, 9 (90%) recovered their renal function. In the univariate analysis, site of infection, hypoalbuminaemia and cumulative dosage of the second-generation fluoroquinolones, aminoglycosides and non-steroidal anti-inflammatory drugs (NSAIDs) co-administered during colistin treatment as well as concomitant use of NSAIDs were risk factors for nephrotoxicity. However, in the logistic regression hypoalbuminaemia and the use of NSAIDs were significant risk factors for increased nephrotoxicity during colistin administration, suggesting that free colistin might cause renal toxicity. In conclusion, colistin-induced nephrotoxicity occurred at a high rate, and hypoalbuminaemia and concomitant use of NSAIDs were significant risk factors.
Insights
Colistin reintroduction for multidrug-resistant infections led to high nephrotoxicity rates. Hypoalbuminemia and NSAID use were identified as significant risk factors for this colistin-induced kidney damage.
Area of Science:
- Nephrology
- Infectious Diseases
- Pharmacology
Background:
- Increasing prevalence of multidrug-resistant gram-negative organisms necessitates the re-emergence of polymyxin E (colistin) as a critical therapeutic option.
- Colistin's reintroduction is tempered by its known nephrotoxicity, prompting further investigation into its renal impact.
Purpose of the Study:
- To investigate the incidence, clinical characteristics, and risk factors associated with colistin-induced nephrotoxicity.
- To identify patient-specific and treatment-related factors that predispose individuals to kidney damage during colistin therapy.
Main Methods:
- A case-control study design was employed, including 47 patients who received at least one defined daily dose (DDD) of intravenous colistin between August 2006 and June 2008.
- Data collection focused on incidence of nephrotoxicity, clinical presentation, co-administered medications, and patient factors such as hypoalbuminemia.
Main Results:
- Colistin-induced nephrotoxicity was observed in 31.9% of patients (15 out of 47), with 20% of these requiring renal replacement therapy.
- Hypoalbuminemia and the concomitant use of non-steroidal anti-inflammatory drugs (NSAIDs) were identified as significant independent risk factors for nephrotoxicity in logistic regression analysis.
- A high rate of renal function recovery (90%) was noted in patients reassessed after one month.
Conclusions:
- Colistin-induced nephrotoxicity occurs frequently and is associated with significant risk factors.
- Hypoalbuminemia and concurrent NSAID administration are critical factors that increase the risk of nephrotoxicity during colistin treatment.
- These findings suggest that careful patient selection and monitoring, particularly regarding albumin levels and NSAID use, are crucial when administering colistin.
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