Suppr超能文献

病态肥胖个体的血清哌拉西林/他唑巴坦药代动力学

Serum piperacillin/tazobactam pharmacokinetics in a morbidly obese individual.

作者信息

Newman Diane, Scheetz Marc H, Adeyemi Oluwadamilola A, Montevecchi Mauro, Nicolau David P, Noskin Gary A, Postelnick Michael J

机构信息

Department of Pharmacy, Northwestern Memorial Hospital, Chicago, IL 60611, USA.

出版信息

Ann Pharmacother. 2007 Oct;41(10):1734-9. doi: 10.1345/aph.1K256. Epub 2007 Aug 28.

Abstract

OBJECTIVE

To report pharmacokinetic alterations and optimal dosing of piperacillin/tazobactam in an obese patient.

CASE SUMMARY

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.

DISCUSSION

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.

CONCLUSIONS

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.

摘要

目的

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。

病例摘要

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。

讨论

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%。

结论

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验