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囊性纤维化患者和健康志愿者中哌拉西林群体药代动力学和药效学的系统比较。

Systematic comparison of the population pharmacokinetics and pharmacodynamics of piperacillin in cystic fibrosis patients and healthy volunteers.

作者信息

Bulitta J B, Duffull S B, Kinzig-Schippers M, Holzgrabe U, Stephan U, Drusano G L, Sörgel F

机构信息

Institute for Biomedical and Pharmaceutical Research, Nürnberg-Heroldsberg, Germany.

出版信息

Antimicrob Agents Chemother. 2007 Jul;51(7):2497-507. doi: 10.1128/AAC.01477-06. Epub 2007 May 7.

Abstract

Respiratory tract infections cause 90% of premature mortality in patients with cystic fibrosis (CF). Treatment of Pseudomonas aeruginosa infection is often very problematic. Piperacillin-tazobactam has good activity against P. aeruginosa, but its pharmacokinetics (PK) in CF patients has not been compared to the PK in healthy volunteers in a controlled clinical study. Therefore, we compared the population PK and pharmacodynamics (PD) of piperacillin between CF patients and healthy volunteers. We studied 8 adult (median age, 20 years) CF patients (average total body weight [WT], 43.1 +/- 7.8 kg) and 26 healthy volunteers (WT, 71.1 +/- 11.8 kg) who each received 4 g piperacillin as a 5-min intravenous infusion. We determined piperacillin levels by high-performance liquid chromatography, and we used NONMEM for population PK and Monte Carlo simulation. We used a target time of nonprotein-bound concentration above the MIC of 50%, which represents near-maximal bacterial killing. Unscaled total clearance was 25% lower, and the volume of distribution was 31% lower in CF patients. Allometric scaling by lean body mass reduced the unexplained (random) between-subject variability in clearance by 26% compared to the variability of linear scaling by WT. A standard dosage regimen of 3 g/70 kg body WT every 4 h as a 30-min infusion (daily dose, 18 g) achieved a robust (> or =90%) probability-of-target attainment (PTA) for MICs of < or =12 mg/liter in CF patients and < or =16 mg/liter in healthy volunteers. Alternative modes of administration allowed a marked dose reduction to 9 g daily. Prolonged (4-h) infusions of 3 g/70 kg WT every 8 h and continuous infusion (daily dose, 9 g), achieved a robust PTA for MICs of < or =16 mg/liter in both groups. Piperacillin achieved PTA expectation values of 64% and 89% against P. aeruginosa infection in CF patients, based on susceptibility data from two German CF clinics.

摘要

呼吸道感染导致囊性纤维化(CF)患者90%的过早死亡。铜绿假单胞菌感染的治疗通常非常棘手。哌拉西林 - 他唑巴坦对铜绿假单胞菌具有良好的活性,但在一项对照临床研究中,其在CF患者中的药代动力学(PK)尚未与健康志愿者的PK进行比较。因此,我们比较了CF患者和健康志愿者中哌拉西林的群体PK和药效学(PD)。我们研究了8名成年(中位年龄20岁)CF患者(平均总体重[WT],43.1±7.8 kg)和26名健康志愿者(WT,71.1±11.8 kg),他们每人接受4 g哌拉西林作为5分钟静脉输注。我们通过高效液相色谱法测定哌拉西林水平,并使用NONMEM进行群体PK和蒙特卡罗模拟。我们使用非蛋白结合浓度高于MIC的50%的目标时间,这代表近乎最大的细菌杀灭。CF患者的未标化总清除率低25%,分布容积低31%。与按WT进行线性标度的变异性相比,按瘦体重进行异速标度使清除率中无法解释的(随机)受试者间变异性降低了26%。每4小时以30分钟输注给予3 g/70 kg体重WT的标准给药方案(每日剂量18 g),对于CF患者中MIC≤12 mg/L和健康志愿者中MIC≤16 mg/L的情况,实现了较高的(≥90%)目标达成概率(PTA)。替代给药方式可使每日剂量显著降低至9 g。每8小时延长(4小时)输注3 g/70 kg WT以及持续输注(每日剂量9 g),在两组中对于MIC≤16 mg/L的情况均实现了较高的PTA。根据来自两家德国CF诊所的药敏数据,哌拉西林在CF患者中针对铜绿假单胞菌感染实现的PTA期望值分别为64%和89%。

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