{"title":"Predictive factors for 30-day mortality after polymyxin B treatment of carbapenem-resistant Gram-negative bacilli infections.","authors":"Simin Zhou, Xuemei Luo, Shuo Cheng, Xinyue ShuLai, Huimin Zhou, Weihong Ge","doi":"10.1016/j.ijid.2025.107844","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to investigate the associated factors predicting 30-day mortality of carbapenem-resistant Gram-negative bacilli (CR-GNB) infections, with focus on polymyxin B AUC<sub>ss,24h</sub>/MIC.</p><p><strong>Methods: </strong>This prospective cohort study included patients with CR-GNB infections from January 2022 to January 2024. The primary outcome was 30-day mortality. Classification and regression tree (CART) analysis was used to calculate the AUC<sub>ss,24h</sub>/MIC threshold for 30-day mortality. Multivariate analysis was conducted to assess risk factors affecting this outcome.</p><p><strong>Results: </strong>We enrolled 107 patients, among which 30-day mortality occurred in 31 (29.0%) cases. The CART-derived AUC<sub>ss,24h</sub>/MIC breakpoint was 51.3, and patients in the below-breakpoint group had 3.4-fold higher 30-day mortality than those in the above-breakpoint group (58.1% vs 17.1%, P < 0.001). On multivariate analysis, polymyxin B AUC<sub>ss,24h</sub>/MIC of ≥ 51.3 (aOR 0.08, P = 0.001) predicted a lower risk for 30-day mortality. In subgroup analysis, the survival benefit of AUC<sub>ss,24h</sub>/MIC target attainment remained in patients with high risk of mortality or carbapenem-resistant Acinetobacter baumannii infections.</p><p><strong>Conclusions: </strong>Polymyxin B AUC<sub>ss,24h</sub>/MIC of ≥ 51.3 independently predicted lower 30-day mortality in treating CR-GNB infections. Further studies should verify the AUC<sub>ss,24h</sub>/MIC target associated with survival outcomes in larger randomized controlled trials.</p>","PeriodicalId":14006,"journal":{"name":"International Journal of Infectious Diseases","volume":" ","pages":"107844"},"PeriodicalIF":4.8000,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ijid.2025.107844","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: This study aimed to investigate the associated factors predicting 30-day mortality of carbapenem-resistant Gram-negative bacilli (CR-GNB) infections, with focus on polymyxin B AUCss,24h/MIC.
Methods: This prospective cohort study included patients with CR-GNB infections from January 2022 to January 2024. The primary outcome was 30-day mortality. Classification and regression tree (CART) analysis was used to calculate the AUCss,24h/MIC threshold for 30-day mortality. Multivariate analysis was conducted to assess risk factors affecting this outcome.
Results: We enrolled 107 patients, among which 30-day mortality occurred in 31 (29.0%) cases. The CART-derived AUCss,24h/MIC breakpoint was 51.3, and patients in the below-breakpoint group had 3.4-fold higher 30-day mortality than those in the above-breakpoint group (58.1% vs 17.1%, P < 0.001). On multivariate analysis, polymyxin B AUCss,24h/MIC of ≥ 51.3 (aOR 0.08, P = 0.001) predicted a lower risk for 30-day mortality. In subgroup analysis, the survival benefit of AUCss,24h/MIC target attainment remained in patients with high risk of mortality or carbapenem-resistant Acinetobacter baumannii infections.
Conclusions: Polymyxin B AUCss,24h/MIC of ≥ 51.3 independently predicted lower 30-day mortality in treating CR-GNB infections. Further studies should verify the AUCss,24h/MIC target associated with survival outcomes in larger randomized controlled trials.
期刊介绍:
International Journal of Infectious Diseases (IJID)
Publisher: International Society for Infectious Diseases
Publication Frequency: Monthly
Type: Peer-reviewed, Open Access
Scope:
Publishes original clinical and laboratory-based research.
Reports clinical trials, reviews, and some case reports.
Focuses on epidemiology, clinical diagnosis, treatment, and control of infectious diseases.
Emphasizes diseases common in under-resourced countries.