Clinical Outcomes Associated with Co-infection of Carbapenem-Resistant Enterobacterales and other Multidrug-Resistant Organisms

被引:1
|
作者
Tadese, Bekana K. [1 ,2 ]
DeSantis, Stacia M. [1 ]
Mgbere, Osaro [4 ,5 ]
Fujimoto, Kayo [1 ]
Darkoh, Charles [1 ,3 ,6 ]
机构
[1] Univ Texas Hlth Sci Ctr, Sch Publ Hlth, Houston, TX USA
[2] Ft Bend Cty Hlth & Human Serv, Ft Bend, TX USA
[3] MD Anderson Canc Ctr UTHealth Grad Sch Biomed Sci, Microbiol & Infect Dis Program, Houston, TX USA
[4] Houston Hlth Dept, Dis Prevent & Control Div, Houston, TX USA
[5] Univ Houston Coll Pharm, Inst Community Hlth, Houston, TX USA
[6] 1200 Pressler St, RAS E715, Houston, TX 77030 USA
关键词
CRE; Carbapenem-resistance; Pseudomonas aeruginosa; Antimicrobial; -resistance; Enterobacterales; Carbapenemase; INFECTIONS; MORTALITY;
D O I
10.1016/j.infpip.2022.100255
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Infections with carbapenem-resistant Enterobacterales (CRE) are associated with increased risk of death. Polymicrobial infections with antimicrobial-resistance may add to the burden of clinical care and patients' clinical prognosis. Aim: To examine the impact of CRE co-infection with other multi-drug resistant organisms (MDRO) on patient clinical outcomes. Study Design: A retrospective observational study was conducted to compare the clinical outcomes of CRE patients who were co-infected with carbapenem-resistant Pseudomonas aeruginosa (CRPA), multidrug-resistant Acinetobacter baumannii (MDRA) and Methicillinresistant Staphylococcus aureus (MRSA). Results: A total of 224 CRPA and 209 MDRA co-infections with CRE were identified from 4,236 cases from 2015-2020. The overall 90-day all-cause mortality was 21.6% but increased to 35.0% and 33.5% among patients who were co-infected with CRPA and MDRA, respectively. The odds of all-cause mortality among CRE patients who were co-infected with CRPA was twice that of patients identified with CRE alone [adjusted odds ratio (AOR) = 2.02, 95% confidence interval (CI): 1.18-3.46]. Further, the odds of all-cause mortality among CRE patients who were concomitantly identified with MRSA was more than twice that of patients who were not identified with MRSA [AOR = 2.16, 95%CI:1.31 -3.56]. The clinical outcome of patients with CRE did not differ significantly depending on the presence of carbapenemase genes. Conclusion: The results show that CRPA and CRE co-infections have synergistic effects on clinical outcomes. Further investigation is necessary to understand the mechanism. Screening high risk patients for concomitant antimicrobial-resistant infections may have a
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页数:8
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