Dong Luyan, Huang Yingbin, Zhang Shengcen, Xu Binbin, Li Bin, Cao Yingping
Department of Clinical Laboratory, Fujian Medical University Union Hospital, Fuzhou, 350001, People's Republic of China.
Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, 350001, People's Republic of China.
Infect Drug Resist. 2025 Feb 18;18:979-991. doi: 10.2147/IDR.S495240. eCollection 2025.
() is a gram-negative opportunistic pathogen, which can cause acute and chronic infections, often resulting in high mortality. The aim of this study was to investigate the risk factors for the development and mortality of patients with carbapenem-resistant bloodstream infection (CRPA BSI).
A total of 112 patients with CRPA BSI and 112 patients with carbapenem-sensitive (CSPA) BSI were included from a Chinese teaching hospital from January 2017 to December 2023 in this retrospective cohort study. The detection rate, antimicrobial susceptibility of and clinical characteristics of these patients were investigated. Multivariable logistic regression analysis was used to identify risk factors for the development and outcomes of CRPA BSI.
In the past 7 years, 7480 blood samples of were cultured in the hospital. The detection rates of CRPA, multidrug resistant (MDRPA), and difficult-to-treat resistant (DTRPA) BSI increased annually (26% to 47%, 10% to 36% and 5% to 15%, respectively). CRPA showed high resistance to conventional antibiotics. Chronic lung disease (OR 3.953, 95% CI 1.131-13.812), transplantation (OR 2.837, 95% CI 1.036-7.770), multi-organ failure (OR 4.815, 95% CI 1.949-11.894), pre-infection within CRPA (OR 9.239, 95% CI 3.441-24.803), and exposure to carbapenems within 90 days (OR 2.734, 95% CI 1.052 -7.106) were independent risk factors for the development of CRPA bacteremia. Sepsis or septic shock (OR 8.774, 95% CI 3.140-24.515, = 0.001) were independent risk factors of mortality.
Chronic lung disease, transplantation, multi-organ failure, prior CRPA infection, and prior carbapenems exposure are independent risk factors for the development of CRPA bacteremia. Sepsis or septic shock increases 28-day mortality. To investigate the molecular mechanisms of carbapenem-resistance of , standardize antibiotic usage, and assess risk factors for the development and mortality of CRPA BSI are beneficial to control infection and reduce death.
(病原体名称)是一种革兰氏阴性机会致病菌,可引起急性和慢性感染,常导致高死亡率。本研究旨在调查耐碳青霉烯类血流感染(CRPA BSI)患者发生感染及死亡的危险因素。
本回顾性队列研究纳入了2017年1月至2023年12月期间来自一家中国教学医院的112例CRPA BSI患者和112例碳青霉烯类敏感(CSPA)BSI患者。调查了这些患者的检出率、抗菌药物敏感性及临床特征。采用多变量逻辑回归分析确定CRPA BSI发生及转归的危险因素。
在过去7年中,该医院共培养了7480份(病原体名称)血样。CRPA、多重耐药(MDRPA)和难治性耐药(DTRPA)BSI的检出率逐年上升(分别从26%升至47%、10%升至36%和5%升至15%)。CRPA对传统抗生素表现出高度耐药性。慢性肺病(OR 3.953,95%CI 1.131-13.812)、移植(OR 2.837,95%CI 1.036-7.77)、多器官功能衰竭(OR 4.815,95%CI 1.949-11.894)、CRPA感染前感染(OR 9.239,95%CI 3.441-24.803)以及90天内接触碳青霉烯类药物(OR 2.734,95%CI 1.052-7.106)是CRPA菌血症发生的独立危险因素。脓毒症或脓毒性休克(OR 8.774,95%CI 3.140-24.515,P = 0.001)是死亡的独立危险因素。
慢性肺病、移植、多器官功能衰竭、既往CRPA感染以及既往接触碳青霉烯类药物是CRPA菌血症发生的独立危险因素。脓毒症或脓毒性休克会增加28天死亡率。研究(病原体名称)耐碳青霉烯类的分子机制、规范抗生素使用以及评估CRPA BSI发生及死亡的危险因素,有利于控制感染和降低死亡率。