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Published on: July 17, 2016
Comprehensive Assessment of Colistin Induced Nephrotoxicity: Incidence, Risk Factors and Time Course
Razan Rabi1, Ahmad Enaya1, Mamoun W Sweileh1
1Department of Internal Medicine, An-Najah National University Hospital, Nablus, Palestine.
Purpose:
In recent years, the emergence of multidrug-resistant (MDR) microorganisms had caused the resurgence of colistin use after it was previously abandoned due to its side effects, nephrotoxicity in particular. However, the specific incidence of colistin-induced nephrotoxicity varies in reports with different populations. This study aims to assess the incidence of colistin-associated nephrotoxicity and the associated risk factors.
Patients And Methods:
This study was on 178 patients who received colistin for more than 48 hours during the years 2019-2022, who were followed up for 14 days after the initiation of colistin, and demographic and clinical data were gained from medical reports. Logistic regression was used to assess the relationship between nephrotoxicity and study variables.
Results:
The incidence of nephrotoxicity was 44.9% (95% confidence interval (CI); 37% to 53%), and the overall mortality was 33%, with a significantly higher level among patients with nephrotoxicity. The significant risk factors for nephrotoxicity after adjustment were; higher weights (OR = 1.1, 95% CI; 0.03-1.2), P-value: 0.006, and the combination with carbapenem showed a significant protective effect (OR = 0.09, 95% CI; 0.01-0.8), P-value: 0.03. The severity, according to KDIGO classification, was stage 1 (47%), stage 2 (21%), and stage 3 (31%). Higher stages had earlier onset acute kidney injury, a lower percentage of returning to baseline, and exposure to a higher colistin dose.
Conclusion:
Colistin-induced nephrotoxicity was a frequent issue associated with higher weights, mitigated by the combination with carbapenems. While higher colistin dosages, and earlier onset AKI, were linked to the progression to higher AKI stages and the need for dialysis.
Insights
Colistin use, driven by multidrug-resistant organisms, frequently causes nephrotoxicity, especially in heavier patients. Combining colistin with carbapenems may offer protection against kidney injury.
Area of Science:
- Pharmacology and Nephrology
- Infectious Diseases and Critical Care Medicine
Background:
- The rise of multidrug-resistant (MDR) microorganisms has led to the re-emergence of colistin use.
- Colistin's previous abandonment was due to adverse effects, particularly nephrotoxicity.
- The incidence of colistin-induced nephrotoxicity varies across different patient populations.
Purpose of the Study:
- To determine the incidence of colistin-associated nephrotoxicity.
- To identify risk factors associated with colistin-induced nephrotoxicity.
Main Methods:
- A retrospective study of 178 patients receiving colistin for over 48 hours between 2019-2022.
- Data collected included demographic and clinical information, with a 14-day follow-up post-colistin initiation.
- Logistic regression analysis was employed to identify risk factors for nephrotoxicity.
Main Results:
- The incidence of nephrotoxicity was 44.9%, with overall mortality at 33%.
- Higher patient weight (OR=1.1) was a significant risk factor for nephrotoxicity.
- Combination therapy with carbapenems demonstrated a protective effect (OR=0.09).
- Nephrotoxicity severity (KDIGO stages 1-3) correlated with earlier acute kidney injury (AKI) onset, reduced recovery, and higher colistin doses.
Conclusions:
- Colistin-induced nephrotoxicity is a significant concern, particularly in patients with higher body weight.
- Carbapenem combination therapy may mitigate the risk of colistin-induced nephrotoxicity.
- Higher colistin doses and early AKI onset are associated with increased severity and potential need for dialysis.
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