Wang Zihan, Shao Chunhong, Shao Jing, Hao Yingying, Jin Yan
Department of Clinical Laboratory, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Front Microbiol. 2024 Apr 12;15:1355069. doi: 10.3389/fmicb.2024.1355069. eCollection 2024.
Infections caused by Carbapenem-resistant Enterobacterales (CRE) have high treatment costs, high mortality and few effective therapeutic agents. This study aimed to determine the risk factors for progression from intestinal colonization to infection in hematological patients and the risk factors for 30-day mortality in infected patients.
A retrospective case-control study was conducted in the Department of Hematology at Shandong Provincial Hospital affiliated to Shandong First Medical University from April 2018 to April 2022. Patients who developed subsequent infections were identified as the case group by electronic medical record query of patients with a positive rectal screen for CRE colonization, and patients who did not develop subsequent infections were identified as the control group by stratified random sampling. Univariate analysis and logistic regression analysis determined risk factors for developing CRE infection and risk factors for mortality in CRE-infected patients.
Eleven hematological patients in the study developed subsequent infections. The overall 30-day mortality rate for the 44 hematological patients in the case-control study was 11.4% (5/44). Mortality was higher in the case group than in the control group (36.5 vs. 3.0%, = 0.0026), and septic shock was an independent risk factor for death ( = 0.024). Univariate analysis showed that risk factors for developing infections were non-steroidal immunosuppressants, serum albumin levels, and days of hospitalization. In multivariable logistic regression analysis, immunosuppressants [odds ratio (OR), 19.132; 95% confidence interval (CI), 1.349-271.420; = 0.029] and serum albumin levels (OR, 0.817; 95% CI, 0.668-0.999; = 0.049) were independent risk factors for developing infections.
Our findings suggest that septic shock increases mortality in CRE-infected hematological patients. Hematological patients with CRE colonization using immunosuppressive agents and reduced serum albumin are more likely to progress to CRE infection. This study may help clinicians prevent the onset of infection early and take measures to reduce mortality rates.
耐碳青霉烯类肠杆菌科细菌(CRE)引起的感染治疗成本高、死亡率高且有效治疗药物少。本研究旨在确定血液系统患者从肠道定植进展为感染的危险因素以及感染患者30天死亡率的危险因素。
2018年4月至2022年4月在山东第一医科大学附属山东省立医院血液科进行了一项回顾性病例对照研究。通过对直肠筛查CRE定植呈阳性的患者进行电子病历查询,将随后发生感染的患者确定为病例组,通过分层随机抽样将未发生随后感染的患者确定为对照组。单因素分析和逻辑回归分析确定了发生CRE感染的危险因素以及CRE感染患者的死亡危险因素。
本研究中有11例血液系统患者随后发生了感染。病例对照研究中44例血液系统患者的总体30天死亡率为11.4%(5/44)。病例组的死亡率高于对照组(36.5%对3.0%,P = 0.0026),感染性休克是死亡的独立危险因素(P = 0.024)。单因素分析显示,发生感染的危险因素是非甾体类免疫抑制剂、血清白蛋白水平和住院天数。在多变量逻辑回归分析中,免疫抑制剂[比值比(OR),19.132;95%置信区间(CI),1.349 - 271.420;P = 0.029]和血清白蛋白水平(OR,0.817;95% CI,0.668 - 0.999;P = 0.049)是发生感染的独立危险因素。
我们的研究结果表明,感染性休克会增加CRE感染的血液系统患者的死亡率。使用免疫抑制剂且血清白蛋白降低的CRE定植血液系统患者更有可能进展为CRE感染。本研究可能有助于临床医生早期预防感染的发生并采取措施降低死亡率。