Pharmacy Department, Alfred Health, Melbourne, Vic., Australia.
Department of Infectious Diseases, The Alfred and Central Clinical School, Monash University, Melbourne, Vic., Australia.
Transpl Infect Dis. 2021 Apr;23(2):e13510. doi: 10.1111/tid.13510. Epub 2020 Dec 4.
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.
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。