Bulitta J B, Duffull S B, Kinzig-Schippers M, Holzgrabe U, Stephan U, Drusano G L, Sörgel F
Institute for Biomedical and Pharmaceutical Research, Nürnberg-Heroldsberg, Germany.
Antimicrob Agents Chemother. 2007 Jul;51(7):2497-507. doi: 10.1128/AAC.01477-06. Epub 2007 May 7.
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.
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%。