| Literature DB >> 33217119 |
Kelly A Cairns1, Victoria Hall2, Genevieve E Martin2, David W J Griffin2, James D Stewart2, Sadid F Khan2, Iain J Abbott2, Zaal Meher-Homji2, Catherine O Morrissey2, Christopher Sia3, Jane Love3, Carmela E Corallo1, Peter Bergin4, Ashish Sharma3, Gopal Basu3,5, Andrew Spencer6, Anton Y Peleg2,7.
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.Entities:
Keywords: zzm321990E. cloacaezzm321990; MBL; antimicrobial resistance; antimicrobials; metallo-beta-lactamase
Year: 2020 PMID: 33217119 DOI: 10.1111/tid.13510
Source DB: PubMed Journal: Transpl Infect Dis ISSN: 1398-2273 Impact factor: 2.228