舒巴坦钠
鲍曼不动杆菌
微生物学
药代动力学
不动杆菌
钙不动杆菌
肾毒性
药理学
生物
医学
抗生素
细菌
亚胺培南
毒性
内科学
抗生素耐药性
铜绿假单胞菌
遗传学
作者
Rodrigo M Burgos,Yifan Wang,Jysheng Hou,Larry H. Danziger
标识
DOI:10.1080/17425255.2025.2567533
摘要
S/D has the potential to replace polymyxin-based therapy for directed CRAB therapy due to its targeted spectrum of activity and renal safety. Notably, S/D is inappropriate for isolates harboring class B metallo-β-lactamases and/or certain penicillin-binding proteins-3 (PBP3) mutations, those with S/D minimum inhibitory concentration (MIC) ≥4 mcg/mL and in populations with data gaps. Pharmacovigilance, studies of use in broader populations, and cost-effectiveness will be critical to maximize its clinical and stewardship value.
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