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持续输注替莫西林在伴有腹腔内感染和腹水渗出的感染性休克患者中的群体药代动力学

Population Pharmacokinetics of Temocillin Administered by Continuous Infusion in Patients with Septic Shock Associated with Intra-Abdominal Infection and Ascitic Fluid Effusion.

作者信息

Ngougni Pokem Perrin, Wittebole Xavier, Collienne Christine, Rodriguez-Villalobos Hector, Tulkens Paul M, Elens Laure, Van Bambeke Françoise, Laterre Pierre-François

机构信息

Pharmacologie Cellulaire et Moléculaire, Louvain Drug Research Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.

Integrated PharmacoMetrics, PharmacoGenomics and PharmacoKinetics, Louvain Drug Research Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.

出版信息

Antibiotics (Basel). 2022 Jul 5;11(7):898. doi: 10.3390/antibiotics11070898.

Abstract

Temocillin is active against Gram-negative bacteria, including many extended-spectrum β-lactamase (ESBL)-producing Enterobacterales. We studied its pharmacokinetics in plasma and ascitic fluid after intravenous administration of a loading dose of 2 g over 30 min, followed by continuous infusion of 6 g/24 h, to 19 critically-ill patients with septic shock associated with complicated intra-abdominal infection. We established a pharmacokinetic model describing unbound temocillin concentrations in plasma and ascitic fluid and performed Monte-Carlo simulations to evaluate the probability of target attainment (PTA) of unbound concentrations (100% fT > MIC, i.e., unbound concentrations remaining above the MIC during 100% of the time) for the applied and hypothetical dosing regimens. The temocillin AUC in ascitic fluid was 46% of the plasma AUC. Plasma unbound concentrations were best described by a two-compartment model, and an additional compartment was added to describe unbound concentration in ascitic fluid, with renal clearance as a covariate. Dosing simulations showed that 90% PTA was achieved in the plasma with the current dosing regimen for MIC ≤ 16 mg/L (EUCAST susceptibility breakpoint) but not in the ascitic fluid if renal clearance was ≥40 mL/min. Hypothetical dosing with a higher (a) loading dose or (b) infused dose allowed to reach target concentrations in ascitic fluid (a) more rapidly or (b) sustainably, but these simulations need to be evaluated in the clinics for safety and efficacy.

摘要

替莫西林对革兰氏阴性菌具有活性,包括许多产超广谱β-内酰胺酶(ESBL)的肠杆菌科细菌。我们对19例患有与复杂性腹腔内感染相关的感染性休克的重症患者进行了研究,在30分钟内静脉注射2g负荷剂量,随后以6g/24h持续输注,研究替莫西林在血浆和腹水中的药代动力学。我们建立了一个药代动力学模型,描述血浆和腹水中未结合的替莫西林浓度,并进行蒙特卡洛模拟,以评估应用和假设给药方案下未结合浓度(100% fT > MIC,即在100%的时间内未结合浓度保持高于MIC)达到目标的概率(PTA)。腹水中替莫西林的AUC为血浆AUC的46%。血浆未结合浓度最好用二室模型描述,并增加一个室来描述腹水中的未结合浓度,以肾脏清除率作为协变量。给药模拟表明,对于MIC≤16mg/L(EUCAST敏感性断点)的当前给药方案,血浆中可实现90%的PTA,但如果肾脏清除率≥40mL/min,则腹水中无法实现。假设使用更高的(a)负荷剂量或(b)输注剂量给药,可以(a)更快或(b)持续地在腹水中达到目标浓度,但这些模拟需要在临床上评估其安全性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3dc/9311849/d40be03f10e0/antibiotics-11-00898-g001.jpg

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