Newman Diane, Scheetz Marc H, Adeyemi Oluwadamilola A, Montevecchi Mauro, Nicolau David P, Noskin Gary A, Postelnick Michael J
Department of Pharmacy, Northwestern Memorial Hospital, Chicago, IL 60611, USA.
Ann Pharmacother. 2007 Oct;41(10):1734-9. doi: 10.1345/aph.1K256. Epub 2007 Aug 28.
To report pharmacokinetic alterations and optimal dosing of piperacillin/tazobactam in an obese patient.
A 39-year-old morbidly obese (weight 167 kg, body mass index 50 kg/m2) man was treated with piperacillin/tazobactam 3.375 g every 4 hours for recurrent cellulitis. The wound culture grew Groups A and B Streptococcus and rare Pseudomonas aeruginosa. Blood samples were obtained at steady-state from a peripheral venous catheter at 0, 0.5, 1, 2, 3, and 4 hours after the start of the infusion. Population pharmacokinetics were generated from a previously published data set. The serum concentrations of piperacillin/tazobactam obtained in the patient were compared with the 95% confidence interval from the representative population. Pharmacokinetic parameters such as maximal serum concentration, minimal serum concentration, average steady-state concentration, half-life, elimination rate constant, volume of distribution (V(d)), clearance, area under the curve at steadystate, and percent of time greater than the minimum inhibitory concentration (%t>MIC) were calculated and qualitatively compared between the sample and the population.
Substantial differences were noted in both the absolute values at the times of sample collection and the overall concentration-versus-time profile of both compounds. The morbidly obese individual compared with the population demonstrated a reduced average serum steady-state concentration: 39.8 mg/L versus 123.6 mg/L, an increased V(d): 54.3 L versus 12.7 L, and an increased half-life: 1.4 hours versus 0.6 hours, respectively. The %t >MIC of piperacillin for the patient, assuming MICs of 2, 4, 8, 16, 32, 64, and 128 mg/L, was 100%, 100%, 90.9%, 55.4%, 19.9%, 0%, and 0%, respectively.
Pathogens with elevated MICs may require altered dosing schemes with piperacillin/tazobactam. Future studies are warranted to assess increased dosages, more frequent dosing intervals, or continuous infusion dosing schemes for obese individuals with serious infections.
报告肥胖患者哌拉西林/他唑巴坦的药代动力学改变及最佳给药剂量。
一名39岁的病态肥胖男性(体重167千克,体重指数50千克/平方米)因复发性蜂窝织炎接受每4小时3.375克哌拉西林/他唑巴坦治疗。伤口培养物中分离出A组和B组链球菌以及罕见的铜绿假单胞菌。在输注开始后0、0.5、1、2、3和4小时从外周静脉导管采集稳态血样。群体药代动力学数据来自先前发表的数据集。将患者获得的哌拉西林/他唑巴坦血清浓度与代表性群体的95%置信区间进行比较。计算药代动力学参数,如最大血清浓度、最小血清浓度、平均稳态浓度、半衰期、消除速率常数、分布容积(V(d))、清除率、稳态曲线下面积以及高于最低抑菌浓度的时间百分比(%t>MIC),并对样本与群体之间进行定性比较。
在样本采集时间的绝对值以及两种化合物的总体浓度-时间曲线方面均发现了显著差异。与群体相比,病态肥胖个体的平均血清稳态浓度降低:39.8毫克/升对123.6毫克/升,分布容积增加:54.3升对12.7升,半衰期增加:1.4小时对0.6小时。假设最低抑菌浓度分别为2、4、8、16、32、64和128毫克/升,该患者哌拉西林的%t>MIC分别为100%、100%、90.9%、55.4%、19.9%、0%和0%。
对于最低抑菌浓度升高的病原体,可能需要调整哌拉西林/他唑巴坦的给药方案。有必要开展进一步研究,以评估增加剂量、缩短给药间隔或采用持续输注给药方案对严重感染肥胖个体的疗效。