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使用头孢他啶/阿维巴坦联合氨曲南治疗移植受者侵袭性 IMP-4 阴沟肠杆菌感染:病例系列和文献复习。

Treatment of invasive IMP-4 Enterobacter cloacae infection in transplant recipients using ceftazidime/avibactam with aztreonam: A case series and literature review.

机构信息

Pharmacy Department, Alfred Health, Melbourne, Vic., Australia.

Department of Infectious Diseases, The Alfred and Central Clinical School, Monash University, Melbourne, Vic., Australia.

出版信息

Transpl Infect Dis. 2021 Apr;23(2):e13510. doi: 10.1111/tid.13510. Epub 2020 Dec 4.

Abstract

Infections caused by carbapenemase-producing Enterobacteriaceae (CPE) are an emerging threat in both solid organ and stem cell transplant recipients. Invasive CPE infections in transplant recipients are associated with a high mortality, often due to limited therapeutic options and antibacterial toxicities. One of the most therapeutically challenging group of CPE are the metallo-β-lactamase (MBL)-producing Gram-negative bacteria, which are now found worldwide, and often need treatment with older, highly toxic antimicrobial regimens. Newer β-lactamase inhibitors such as avibactam have well-established activity against certain carbapenemases such as Klebsiella pneumoniae carbapenemases (KPC), but have no activity against MBL-producing organisms. Conversely, aztreonam has activity against MBL-producing organisms but is often inactivated by other co-existing β-lactamases. Here, we report four cases of invasive MBL-CPE infections in transplant recipients caused by IMP-4-producing Enterobacter cloacae who were successfully treated with a new, mechanism-driven antimicrobial combination of ceftazidime/avibactam with aztreonam. This novel antimicrobial combination offers a useful treatment option for high-risk patients with CPE infection, with reduced drug interactions and toxicity.

摘要

产碳青霉烯酶肠杆菌科(CPE)引起的感染在实体器官和干细胞移植受者中是一种新出现的威胁。移植受者中侵袭性 CPE 感染与高死亡率相关,这通常是由于治疗选择有限和抗菌药物毒性。治疗最具挑战性的一组 CPE 之一是产金属β-内酰胺酶(MBL)的革兰氏阴性菌,这些细菌现在在全球范围内都有发现,通常需要使用旧的、高度毒性的抗菌方案进行治疗。新型β-内酰胺酶抑制剂,如阿维巴坦,对某些碳青霉烯酶(如肺炎克雷伯菌碳青霉烯酶(KPC))具有良好的活性,但对产 MBL 的生物体没有活性。相反,氨曲南对产 MBL 的生物体具有活性,但通常被其他共存的β-内酰胺酶失活。在这里,我们报告了 4 例由产 IMP-4 的阴沟肠杆菌引起的移植受者侵袭性 MBL-CPE 感染病例,这些患者成功地接受了头孢他啶/阿维巴坦联合氨曲南这一新的、基于机制的抗菌联合治疗。这种新型抗菌联合治疗为 CPE 感染的高危患者提供了一种有用的治疗选择,减少了药物相互作用和毒性。

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