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连续肾脏替代治疗危重症患者利奈唑胺的药代动力学:残余肾功能对 PK/PD 目标达成的影响。

Pharmacokinetics of linezolid in critically ill patients on continuous renal replacement therapy: Influence of residual renal function on PK/PD target attainment.

机构信息

Intensive Care Unit, University Hospital Araba C/ Olaguibel n° 29, Vitoria-Gasteiz, Spain.

Pharmacokinetics, Nanotechnology and Gene Therapy Group, Faculty of Pharmacy, University of the Basque Country UPV/EHU, Paseo de la Universidad n° 7, Vitoria-Gasteiz, Spain; Centro de Investigación Lascaray ikergunea, University of the Basque Country UPV/EHU, Avenida Miguel de Unamuno, 3, Vitoria-Gasteiz, Spain.

出版信息

J Crit Care. 2019 Apr;50:69-76. doi: 10.1016/j.jcrc.2018.11.016. Epub 2018 Nov 17.

Abstract

PURPOSE

To assess the pharmacokinetics of linezolid in septic patients undergoing continuous renal replacement therapy (CRRT) and investigate whether residual renal function affects the probability of attaining the pharmacokinetic/pharmacodynamic (PK/PD) target.

MATERIAL AND METHODS

Prospective study conducted in three Spanish hospitals. Linezolid concentrations were measured in plasma and effluent samples and pharmacokinetic parameters were calculated. The probability of target attainment (PTA) and the cumulative fraction of response (CFR) were calculated considering AUC/MIC>80 and %T > 85% as the PK/PD indexes related to efficacy.

RESULTS

In anuric patients (CrCl<10 mL/min), the contribution of extracorporeal Cl to total Cl was higher (47% vs 16%) than in patients with residual renal function (CrCl≥10 mL/min). For an MIC of 2 mg/L, AUC/MIC>80 was achieved in >85% of the anuric patients, but in <15% of the patients with residual renal function.

CONCLUSIONS

The standard dose (600 mg q12h) ensures a moderately high probability of treatment success in anuric patients when the infection is due to microorganisms with MIC≤2 mg/L; although higher doses increase the probability of treatment success, the safety is compromised. In patients with residual renal function, the standard dose is insufficient, but 900 mg q8h provide higher probability of treatment success without compromising the safety.

摘要

目的

评估脓毒症患者接受连续肾脏替代治疗(CRRT)时利奈唑胺的药代动力学,并研究残余肾功能是否会影响达到药代动力学/药效学(PK/PD)目标的概率。

材料和方法

这是在西班牙的三家医院进行的前瞻性研究。测定血浆和洗脱液样本中的利奈唑胺浓度并计算药代动力学参数。考虑 AUC/MIC>80 和 %T > 85% 作为与疗效相关的 PK/PD 指标,计算目标达标率(PTA)和累积反应分数(CFR)。

结果

在无尿患者(CrCl<10 mL/min)中,体外 Cl 对总 Cl 的贡献高于(47% vs 16%)有残余肾功能的患者(CrCl≥10 mL/min)。对于 MIC 为 2 mg/L,>85%的无尿患者达到 AUC/MIC>80,但仅有<15%的有残余肾功能的患者达到该值。

结论

当感染由 MIC≤2 mg/L 的微生物引起时,标准剂量(600 mg q12h)可确保无尿患者获得较高的治疗成功率,但较高的剂量会增加治疗成功率,但会影响安全性。对于有残余肾功能的患者,标准剂量不足,但 900 mg q8h 提供了更高的治疗成功率而不会影响安全性。

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