Antibiotic Management Program, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Department of Pharmacy, Allegheny Health Network, Pittsburgh, PA, United States.
J Infect Chemother. 2022 Jan;28(1):87-90. doi: 10.1016/j.jiac.2021.08.013. Epub 2021 Sep 15.
We describe a case of a 48 years old male with left sided endocarditis and septic emboli secondary to a Pseudomonas aeruginosa strain that developed resistance to other β-lactam antibiotics during therapy resulting in prolonged bacteremia. Blood cultures sterilized within 1 day of initiating ceftolozane/tazobactam 3 g every 8 hours in combination with ciprofloxacin. Steady state free ceftolozane plasma Cmax and Cmin concentrations were calculated to be 122.2μg/mL and 24.3μg/mL, respectively. The multidrug-resistant strain harbored chromosomal β-lactamases OXA-486 and PDC-3, mutations in ampD and dacB predicted to lead to ampC over-expression, and mutations in OprD predicted to decrease outer membrane permeability. Following completion of a 42 day course and aortic valve replacement, the patient was deemed clinically cured without recurrence of infection at follow up 2 years later. To our knowledge, this is the first reported case to measure ceftolozane concentrations during the treatment of endocarditis which supports dose optimization approaches of severe endovascular disease due to multidrug resistant pathogens.
我们描述了一例 48 岁男性患者,其左侧心内膜炎和脓毒性栓子继发于铜绿假单胞菌菌株,该菌株在治疗过程中对其他β-内酰胺抗生素产生耐药性,导致长时间菌血症。在开始使用头孢他唑巴坦/他唑巴坦 3 g 每 8 小时联合环丙沙星治疗后,1 天内血培养即无菌。稳态游离头孢他唑巴坦血浆 Cmax 和 Cmin 浓度分别计算为 122.2μg/mL 和 24.3μg/mL。多药耐药株携带染色体β-内酰胺酶 OXA-486 和 PDC-3、ampD 和 dacB 突变,预计导致 ampC 过度表达,以及 OprD 突变,预计降低外膜通透性。在完成 42 天疗程和主动脉瓣置换术后,患者被认为临床治愈,2 年后随访未再发生感染。据我们所知,这是首例报道在心内膜炎治疗期间测量头孢他唑巴坦浓度的病例,支持针对多药耐药病原体引起的严重血管内疾病的剂量优化方法。