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非稳态条件下药物组织药代动力学间接评估的生理模型:肝手术中抗菌预防的实例

Physiological modeling for indirect evaluation of drug tissular pharmacokinetics under non-steady-state conditions: an example of antimicrobial prophylaxis during liver surgery.

作者信息

Lagneau Franck, Marty Jean, Beyne Pascale, Tod Michel

机构信息

Department of Anesthesia and Intensive Care, Henri-Mondor Hospital, 51, Avenue du Maréchal-de-Lattre-de-Tassigny, 94000, Créteil, France.

出版信息

J Pharmacokinet Pharmacodyn. 2005 Feb;32(1):1-32. doi: 10.1007/s10928-005-2101-0.

Abstract

Cefazolin, a time-dependent first-generation cephalosporin with non-linear binding to albumin, is widely recommended for antimicrobial prophylaxis during liver surgery to decrease the incidence of postoperative wound infections. The recommended protocol (2 g IV at anesthesia induction followed by 1 g 4 h later) is expected to maintain the free cefazolin concentration in exposed intratissular fluids above its minimal inhibitory concentration (MIC) for potentially encountered microorganisms, from skin incision to skin closure. Since this dosing protocol fails to take into account either of patients status (total body weight and renal function) or of surgical and anesthetic consequences (variations of cardiac output and regional blood flows, progressive decrease of plasma albumin concentration) on cefazolin tissular pharmacokinetics, a physiological modeling study was conducted to investigate protocol suitability for liver surgery in six populations: obese (body mass index >34), renal insufficiency (GFR = 10, 30 or 50 ml min(-1)) and high intraoperative blood loss (three times that usually observed during this surgery) and none of these features referred to as controls. A previously validated physiologically based pharmacokinetic (PB-PK) model for cefazolin in humans was used and then further adapted to simulate obese or renal insufficiency patients as well as the consequences of general anesthesia and liver surgery on cefazolin pharmacokinetics. Clinical data required for simulation (intraoperative kinetics of percent expired isoflurane and plasma albumin concentration, mean intraoperative blood loss) were obtained from 10 patients who underwent right hepatectomy in our institution. Using a fixed MIC of 2 microg ml(-1) against potentially encountered bacteria, it was concluded that the recommended dosing schedule was suitable in all tested populations, including obese patients, although prolongation of the interval between injections appeared advisable for renal insufficiency patients. Furthermore, when a MIC of 3 microg ml(-1) was considered, the recommended cefazolin-dosing regimen failed to maintain sufficient free cefazolin concentrations in the interstitial fluids during surgery in all tested populations except renal insufficiency patients (GFR < 50 ml min(-1)).

摘要

头孢唑林是一种时间依赖性的第一代头孢菌素,与白蛋白呈非线性结合,广泛推荐用于肝脏手术期间的抗菌预防,以降低术后伤口感染的发生率。推荐方案(麻醉诱导时静脉注射2g,4小时后再注射1g)预期可使暴露的组织内液中的游离头孢唑林浓度维持在对可能遇到的微生物的最低抑菌浓度(MIC)之上,从皮肤切开至皮肤缝合。由于该给药方案未考虑患者状态(总体重和肾功能)以及手术和麻醉后果(心输出量和局部血流变化、血浆白蛋白浓度逐渐降低)对头孢唑林组织药代动力学的影响,因此进行了一项生理建模研究,以调查该方案在六种人群中的肝脏手术适用性:肥胖(体重指数>34)、肾功能不全(肾小球滤过率=10、30或50ml·min⁻¹)以及术中失血量大(是该手术通常观察到的失血量的三倍),无这些特征的人群作为对照。使用先前验证的人体头孢唑林生理药代动力学(PB-PK)模型,然后进一步调整以模拟肥胖或肾功能不全患者以及全身麻醉和肝脏手术对头孢唑林药代动力学的影响。模拟所需的临床数据(异氟烷呼出百分比和血浆白蛋白浓度的术中动力学、平均术中失血量)来自在我们机构接受右半肝切除术的10名患者。针对可能遇到的细菌使用固定的MIC为2μg/ml,得出结论:推荐的给药方案在所有测试人群中均适用,包括肥胖患者,尽管对于肾功能不全患者,建议延长注射间隔。此外,当考虑MIC为3μg/ml时,除肾功能不全患者(肾小球滤过率<50ml·min⁻¹)外,在所有测试人群中,推荐的头孢唑林给药方案在手术期间未能在组织间液中维持足够的游离头孢唑林浓度。

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