Abstract
BackgroundColistin is widely used for the treatment of nosocomial infections caused by carbapenem-resistant gram-negative bacilli (CR-GNB). Colistin-induced nephrotoxicity is one of the major adverse reactions during colistin treatment. Comparisons of colistin-induced nephrotoxicity between different formulations of colistin are rarely reported. MethodsWe conducted a retrospective cohort study that enrolled ICU-admitted patients with cultured isolates of CR-GNB and treatment with intravenous colistin. Occurrences of acute kidney injury (AKI) during treatment with intravenous colistin were recorded. Colistin-induced nephrotoxicity between two formulations of colistin, Locolin® and Colimycin®, were compared. The treatment outcomes associated with the occurrence of colistin-induced nephrotoxicity were also investigated.ResultsA total of 195 patients, 95 treated with Locolin® and 100 treated with Colimycin®, were included for analysis. Patients treated with Locolin® had a higher rate of occurrence of stage 2 (46.3% vs. 32%, p=0.040) and stage 3 (29.5% vs. 13%, p=0.005) AKI than did those treated with Colimycin®. In multivariate analysis, the presence of septic shock (adjusted odds ratio (aOR) 2.07, 95% confidence interval (CI) 1.05–4.06), and inappropriate colistin dosage (aOR 2.49, 95% CI 1.01–60.16) were clinical factors associated with colistin-induced nephrotoxicity. Treatment with Colimycin® was an independent factor associated with a lower risk of colistin-induced nephrotoxicity (aOR 0.36, 95% CI 0.17-0.74). Other clinical factors associated with colistin-induced nephrotoxicity included the presence of septic shock (aOR 2.17, 95% CI 1.10-4.26) and inappropriate colistin dosage (aOR 2.52, 95% CI 1.00-6.33). A comparable mortality rate was noted between patients with and without colistin-induced nephrotoxicity. ConclusionsThe risk of colistin-induced nephrotoxicity significantly varied in different formulations of colistin in critically ill patients. Colistin-induced nephrotoxicity was not associated with increased mortality.