Service de médecine Intensive Réanimation, Sorbonne Université, Groupe Hospitalier Pitié-Salpêtrière, Institut de Cardiologie, Assistance Publique-Hôpitaux de Paris, Paris, France.
Sorbonne Université, GRC 30, RESPIRE, UMRS 1166, ICAN Institute of Cardiometabolism and Nutrition, Paris, France.
J Antimicrob Chemother. 2024 May 2;79(5):1182-1186. doi: 10.1093/jac/dkae091.
The use of extracorporeal membrane oxygenation (ECMO) may alter blood levels of several drugs, including antibiotics, leading to under dosing of these drugs and thus to potential treatment failure. No data exist on pharmacokinetics of new antimicrobial, in particular ceftazidime/avibactam. We therefore perform this study to evaluate ceftazidime/avibactam blood levels in ECMO patients and find factors associated with underdosing.
Retrospective observational study of patients on ECMO having received ceftazidime/avibactam and in whom trough blood levels of ceftazidime and avibactam were available. Main outcome measurement was the number of patients with ceftazidime and avibactam blood levels above predefined cut-off values, derived from the European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints for Enterobacteriaceae and Pseudomonas aeruginosa, namely 8 mg/L for ceftazidime and 4 mg/L for avibactam, and explored factors associated with underdosing.
Twenty-three ceftazidime/avibactam trough levels were available in 14 ECMO patients, all of them having received veno-venous ECMO for SARS-CoV-2-associated pneumonia. Although ceftazidime levels were above 8 mg/L in all except one patient, nine (39%) of the avibactam dosages were below 4 mg/L. Increased renal clearance (creatinine clearance > 130 mL/min) was the main factor associated with under dosing, since 7 out of the 10 dosages below the predefined cut-offs were measured in patients with this condition.
In ECMO patients receiving ceftazidime/avibactam, ceftazidime and avibactam serum levels are above EUCAST breakpoints in most cases, justifying the use of normal dosing in ECMO patients. Increased renal clearance may lead to ceftazidime and avibactam under dosing.
体外膜肺氧合(ECMO)的使用可能会改变几种药物的血药水平,包括抗生素,导致这些药物的剂量不足,从而潜在地导致治疗失败。目前尚无新型抗菌药物(特别是头孢他啶/阿维巴坦)药代动力学的数据。因此,我们进行了这项研究,以评估 ECMO 患者的头孢他啶/阿维巴坦血药水平,并发现与剂量不足相关的因素。
这是一项回顾性观察研究,纳入了接受头孢他啶/阿维巴坦治疗且有头孢他啶和阿维巴坦血药谷浓度的 ECMO 患者。主要观察指标是达到欧洲抗菌药物敏感性测试委员会(EUCAST)针对肠杆菌科和铜绿假单胞菌设定的折点(头孢他啶 8mg/L,阿维巴坦 4mg/L)以上的患者人数,并探讨与剂量不足相关的因素。
14 例接受 SARS-CoV-2 相关性肺炎 veno-venous ECMO 的患者共获得 23 个头孢他啶/阿维巴坦血药谷浓度。除 1 例患者外,所有患者的头孢他啶水平均超过 8mg/L,而 9 例(39%)的阿维巴坦剂量低于 4mg/L。增加的肾清除率(肌酐清除率>130mL/min)是剂量不足的主要相关因素,因为在这种情况下,有 7 个低于预设截止值的剂量是在患者中测量的。
在接受头孢他啶/阿维巴坦治疗的 ECMO 患者中,头孢他啶和阿维巴坦的血清水平在大多数情况下超过 EUCAST 折点,这证明 ECMO 患者可以使用常规剂量。增加的肾清除率可能导致头孢他啶和阿维巴坦剂量不足。