Pudpong Korawan, Pattharachayakul Sutthiporn, Santimaleeworagun Wichai, Nwabor Ozioma F, Laohaprertthisan Varaporn, Hortiwakul Thanaporn, Charernmak Boonsri, Chusri Sarunyou
Department of Pharmacy, College of Pharmacotherapy Thailand, Nontaburi, 11000, Thailand.
Pharmaceutical Care Unit, Department of Pharmacy, Sunpasitthiprasong Hospital, Ubon Ratchathani, 34000, Thailand.
Infect Drug Resist. 2022 Jun 13;15:3025-3037. doi: 10.2147/IDR.S363588. eCollection 2022.
Compared with non-carbapenemase producing carbapenem-resistant Enterobacterales (non-CP-CRE), carbapenemase-producing carbapenem-resistant Enterobacterales (CP-CRE) are associated with considerable mortality. However, given that the patients are treated with various therapeutic options, it remains unclear whether differences in types of carbapenemase genes yield different mortality rates. Therefore, this study aims to identify carbapenemase genes and identify whether clinical outcomes differ according to the prevalence of genotype and phenotype of carbapenemase among Enterobacterales clinical isolated.
A retrospective cohort study was performed to determine whether types of carbapenemase genes have an impact on clinical outcomes. Carbapenem-resistant clinical isolates were collected at a tertiary care university hospital in Songkhla, Thailand, between June 2018 and February 2020. Demographic and microbiological data such as antimicrobial susceptibility, carbapenemase genes, and overall mortality were evaluated.
A total of 121 Enterobacterales clinical isolated were evaluated. The gene was detected in 44% of the isolates, followed by (28%) and (28%). NDM-1- or NDM-1/OXA-48- producing isolates were more likely to require meropenem MICs of ≥16 mg/L, while OXA-48-producing isolates were more likely to require meropenem MICs of <16 mg/L. The patients with NDM-1 or NDM-1/OXA-48 had a higher 14 days mortality rate than those with OXA-48 after treating with carbapenem-containing regimens (-value 0.001) or colistin-containing regimens (-value < 0.001).
Our findings suggest that the mortality for CP-CRE infection in patients with NDM-1 or NDM-1/OXA-48 was higher than the mortality in those with OXA-48, which It seems that the type of carbapenemase gene may affect meropenem MIC levels. Hence, in treatment decisions involving the use of either carbapenem-containing regiment or colistin-containing regiment in patients with CP-CRE infection, especially those in the NDM-1 and NDM-1/OXA-48 groups, the patient symptoms should be closely monitored.
与非产碳青霉烯酶的耐碳青霉烯类肠杆菌科细菌(非CP-CRE)相比,产碳青霉烯酶的耐碳青霉烯类肠杆菌科细菌(CP-CRE)与相当高的死亡率相关。然而,鉴于患者接受了各种治疗方案,目前尚不清楚碳青霉烯酶基因类型的差异是否会导致不同的死亡率。因此,本研究旨在鉴定碳青霉烯酶基因,并确定肠杆菌科临床分离株中碳青霉烯酶的基因型和表型流行率是否会导致临床结果的差异。
进行了一项回顾性队列研究,以确定碳青霉烯酶基因类型是否对临床结果有影响。2018年6月至2020年2月期间,在泰国宋卡的一家三级护理大学医院收集了耐碳青霉烯类临床分离株。评估了人口统计学和微生物学数据,如抗菌药物敏感性、碳青霉烯酶基因和总体死亡率。
共评估了121株肠杆菌科临床分离株。44%的分离株检测到 blaKPC 基因,其次是 blaNDM(28%)和 blaOXA-48(28%)。产NDM-1或NDM-1/OXA-48的分离株更有可能需要美罗培南最低抑菌浓度≥16mg/L,而产OXA-48的分离株更有可能需要美罗培南最低抑菌浓度<16mg/L。在用含碳青霉烯类方案治疗后(P值0.001)或含黏菌素方案治疗后(P值<0.001),NDM-1或NDM-1/OXA-48患者的14天死亡率高于OXA-48患者。
我们的研究结果表明,NDM-1或NDM-1/OXA-48患者的CP-CRE感染死亡率高于OXA-48患者,似乎碳青霉烯酶基因类型可能会影响美罗培南最低抑菌浓度水平。因此,在涉及CP-CRE感染患者使用含碳青霉烯类方案或含黏菌素方案的治疗决策中,尤其是NDM-1和NDM-1/OXA-48组的患者,应密切监测患者症状。