Efficacy and Safety Factors Related to Plasma Concentration-Optimized Polymyxin B Therapy in Treating Carbapenem-Resistant Gram-Negative Bacterial Infections in China

Abstract

Background Polymyxin B (PMB)-based combination therapies are used to treat severe carbapenem-resistant gram-negative bacterial (CR-GNB) infections. This observational study investigated the relationship between clinical factors, including PMB concentration, and clinical efficacy and safety. Patients and Methods Polymyxin B regimens were optimized through therapeutic drug monitoring (TDM) and area under the concentration-time curve (AUC). In all, 382 samples were tested from 130 patients. Logistic regression was used to analyze the relationships between variables with clinical efficacy and 30-day mortality factors were analyzed by Cox regression. The sensitivity and specificity of C min and AUC for the occurrence of acute kidney injury (AKI) were determined by ROC curve analysis. Results The clinical effectiveness of PMB was 65.4%. Multivariate logistic regression analysis revealed that lung infection, continuous renal replacement therapy, and C-reactive protein were independent factors significantly associated with efficacy. AKI occurred in 14.6% of the patients during treatment; age > 73 years (OR: 3.63; 95% CI: 1.035–12.727; P = 0.044), C min greater than 2.3 µg/mL (OR: 7.37; 95% CI: 1.571–34.580; P = 0.011), combined vancomycin (OR: 9.47; 95% CI: 1.732–51.731; P = 0.009), and combined piperacillin-tazobactam (OR: 21.87; 95% CI: 3.139–152.324; P = 0.002) were independent risk factors. The identified PMB cut-offs for predicting AKI were C min = 2.3 µg/mL and AUC = 82.0 mg h/L. Conclusion Polymyxin B-based combination regimens are effective in treating CR-GNB infections, particularly bloodstream infections, but have shown unsatisfactory for lung infections. C min ≥ 2.3 µg /mL and AUC ≥ 82.0 mg h/L may increase PMB-associated AKI incidence. PMB dose should be adjusted based on TDM to ensure efficacy.