Xiao Shuzhen, Zhu Deyong, Liang Xianghui, Han Lizhong, Zhao Shengyuan
Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Laboratory Medicine, The People's Hospital of Wenshan Prefecture, The Affiliated Hospital of Kunming University of Science and Technology, Wenshan, Yunnan, China.
Sci Rep. 2025 Jul 1;15(1):20719. doi: 10.1038/s41598-025-07820-x.
Bloodstream infections (BSIs) caused by multidrug resistant Pseudomonas aeruginosa (MDRPA) and carbapenem resistant Pseudomonas aeruginosa (CRPA) accounted for high morbidity and mortality. This retrospective cohort study aimed to determine risk factors for MDRPA and CRPA BSIs by examining both clinical and laboratory data of inpatients with MDRPA and CRPA BSIs at two tertiary care hospitals in 2017-2021. Generalized linear mixed models were used to identify risk factors for MDRPA and CRPA BSIs. Factors significantly associated with both MDRPA BSIs and CRPA BSIs included central venous catheter, invasive ventilation including duration of use, urinary catheterization, gastric tube insertion, vancomycin use including quantity of usage, imipenem use including quantity of usage, and tigecycline use. Respiratory infection [adjusted odds ratio (aOR) 2.10, 95% confidence interval (95% CI) 1.00-4.42; P = 0.049] was identified as an independent risk factor for MDRPA BSIs. For CRPA BSIs, independent risk factors included the use of invasive ventilation [aOR 2.82, 95% CI 1.36-5.84; P = 0.005] and a history of tigecycline use [aOR 3.34, 95% CI 1.16-9.58; P = 0.025]. Conversely, circulatory system diseases [aOR 0.41, 95% CI 0.22-0.77; P = 0.006] and quantity of piperacillin-tazobactam use [aOR 0.83, 95% CI 0.72-0.96; P = 0.013] were identified as independent protective factors for CRPA BSIs. Inpatients with respiratory infection, invasive ventilation and a history of tigecycline use are at higher risk of MDRPA and CRPA BSIs. More prudent clinical interventions and antimicrobial therapy should be implemented to inpatients with these factors to prevent and control MDRPA and CRPA BSIs.
由多重耐药铜绿假单胞菌(MDRPA)和碳青霉烯耐药铜绿假单胞菌(CRPA)引起的血流感染(BSIs)导致了高发病率和死亡率。这项回顾性队列研究旨在通过检查2017年至2021年两家三级护理医院中患有MDRPA和CRPA血流感染的住院患者的临床和实验室数据,来确定MDRPA和CRPA血流感染的危险因素。使用广义线性混合模型来识别MDRPA和CRPA血流感染的危险因素。与MDRPA血流感染和CRPA血流感染均显著相关的因素包括中心静脉导管、有创通气(包括使用持续时间)、导尿、胃管插入、万古霉素使用(包括使用量)、亚胺培南使用(包括使用量)以及替加环素使用。呼吸道感染[调整优势比(aOR)2.10,95%置信区间(95%CI)1.00 - 4.42;P = 0.049]被确定为MDRPA血流感染的独立危险因素。对于CRPA血流感染,独立危险因素包括有创通气的使用[aOR 2.82,95%CI 1.36 - 5.84;P = 0.005]和替加环素使用史[aOR 3.34,95%CI 1.16 - 9.58;P = 0.025]。相反,循环系统疾病[aOR 0.41,95%CI 0.22 - 0.77;P = 0.006]和哌拉西林 - 他唑巴坦使用量[aOR 0.83,95%CI 0.72 - 0.96;P = 0.013]被确定为CRPA血流感染的独立保护因素。患有呼吸道感染、有创通气和有替加环素使用史的住院患者发生MDRPA和CRPA血流感染的风险更高。对于有这些因素的住院患者,应实施更谨慎的临床干预和抗菌治疗,以预防和控制MDRPA和CRPA血流感染。