针对由产扩展谱β-内酰胺酶肠杆菌科细菌引起的菌血症患者的非碳青霉烯类药物:哌拉西林-他唑巴坦

Hyunjoo Oh, Seunghee Lee, Misun Kim, S. Heo, J. Yoo
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引用次数: 0

摘要

背景/目的:碳青霉烯类被推荐用于治疗由产扩展谱β-内酰胺酶(ESBL)肠杆菌科细菌(ESBL-E)引起的菌血症。然而,这也导致了在 ESBL-E 感染病例中碳青霉烯类药物使用率的显著上升。我们评估了使用非碳青霉烯类抗菌药物治疗 ESBL-E 菌血症患者的临床疗效:我们对 2021 年 1 月至 2021 年 12 月期间记录在案的 ESBL-E 菌血症患者队列进行了一项回顾性病例对照研究。根据患者接受的是非碳青霉烯类治疗还是碳青霉烯类治疗,将其分为两组。比较了两组患者的治疗失败率、30 天死亡率和微生物学失败率,以及住院时间和抗菌治疗时间。使用 Vitek 2 系统对 ESBL-E 进行抗菌药物药敏试验和表型鉴定:118名ESBL-E菌血症患者中,54人接受了非碳青霉烯类药物治疗(非碳青霉烯类组 [NCG]),64人接受了碳青霉烯类药物治疗(碳青霉烯类组 [CG])。在 30 天内治疗失败的患者中,NCG 组为 16.7%,CG 组为 18.8%(P = 0.65)。NCG组的30天死亡率为14.8%,CG组为17.2%(P = 0.63)。ESBL-E菌血症患者尿路外感染和30天内曾接受抗菌治疗是治疗失败的风险因素。两组患者的临床结果无明显差异,这对目前治疗ESBL-E菌血症时首选碳青霉烯类抗生素的观点提出了质疑:结论:韩国建议对轻度ESBL-E菌血症患者使用哌拉西林/他唑巴坦等非碳青霉烯类抗菌药物。
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Non-carbapenem Drugs for Patients with Bacteremia caused by Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae: Piperacillin-Tazobactam
Background/Aims: Carbapenems are recommended for treating bacteremia caused by extended-spectrum β-lactamase (ESBL) producing Enterobacteriaceae (ESBL-E). However, this has resulted in a significant rise in the utilization of carbapenems in cases of ESBL-E infection. We evaluated the clinical outcomes of patients with ESBL-E bacteremia treated with non-carbapenem antimicrobials.Methods: We conducted a retrospective case-control study of a cohort of patients with documented ESBL-E bacteremia from January 2021 to December 2021. The patients were divided into two groups according to whether they received non-carbapenem or carbapenem therapy. The rates of treatment failure, 30-day mortality and microbiologic failure, and the durations of hospitalization and of antimicrobial therapy were compared between the two groups. Antimicrobial susceptibility testing and phenotypic identification of ESBL-E were performed using the Vitek 2 system.Results: Of 118 patients with ESBL-E bacteremia, 54 received non-carbapenem drugs (non-carbapenem group [NCG]) and 64 received carbapenems (carbapenem group [CG]). Treatment failure at 30 days occurred in 16.7% of the patients in the NCG and in 18.8% in the CG (p = 0.65). The 30-day mortality rate was 14.8% in the NCG and 17.2% in the CG (p = 0.63). Extra-urinary tract infection and prior antimicrobial therapy within 30 days were risk factors for treatment failure in patients with ESBL-E bacteremia. The clinical outcomes did not differ significantly between the two groups, challenging the prevailing preference for carbapenems in the treatment of ESBL-E bacteremia.Conclusions: Non-carbapenem antimicrobials such as piperacillin/tazobactam are recommended for patients with mild ESBL-E bacteremia in South Korea.
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