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肥胖成年患者的抗菌药物剂量考量

Antimicrobial dosing considerations in obese adult patients.

作者信息

Pai Manjunath P, Bearden David T

机构信息

Division of Pharmacy Practice, College of Pharmacy, University of New Mexico, Albuquerque, New Mexico, USA.

出版信息

Pharmacotherapy. 2007 Aug;27(8):1081-91. doi: 10.1592/phco.27.8.1081.

Abstract

As obesity continues to increase in prevalence throughout the world, it becomes important to explore the effects that obesity has on antimicrobial disposition. Physiologic changes in obesity can alter both the volume of distribution and clearance of many commonly used antimicrobials. These changes often present challenges such as estimation of creatinine clearance to predict drug clearance. Although these physiologic changes are increasingly being characterized, few studies assessing alterations in tissue drug distribution and the effects of obesity on antimicrobial pharmacokinetics have been published. The available data are most plentiful for antibiotics that historically have included clinical therapeutic drug monitoring. These data suggest that dosing of vancomycin and aminoglycosides be based on total body weight and adjusted body weight, respectively. Obese patients may require larger doses of beta-lactams to achieve similar concentrations as those of patients who are not obese. Fluoroquinolone pharmacokinetics are variably altered by obesity, which prevents a uniform approach. Data on the pharmacokinetics of drugs that have activity against gram-positive organisms-quinupristin-dalfopristin, linezolid, and daptomycin-reveal that they are altered in the presence of obesity, but more data are needed to solidify dosing recommendations. Limited data are available on nonantibacterials. An understanding of the physiologic changes in obesity and the available literature on specific antibiotics is valuable in providing a framework for rational selection of dosages in this increasingly common population of obese patients.

摘要

随着肥胖在全球的患病率持续上升,探究肥胖对抗菌药物处置的影响变得至关重要。肥胖引起的生理变化可改变许多常用抗菌药物的分布容积和清除率。这些变化常常带来挑战,比如估算肌酐清除率以预测药物清除率。尽管这些生理变化正越来越多地得到描述,但评估组织药物分布改变以及肥胖对抗菌药物药代动力学影响的研究却鲜有发表。对于历史上一直包含临床治疗药物监测的抗生素,现有数据最为丰富。这些数据表明,万古霉素和氨基糖苷类药物的给药应分别基于总体重和校正体重。肥胖患者可能需要更大剂量的β-内酰胺类药物才能达到与非肥胖患者相似的血药浓度。肥胖对氟喹诺酮类药物药代动力学的影响各不相同,这使得无法采用统一的方法。针对革兰氏阳性菌有活性的药物——奎奴普丁-达福普汀、利奈唑胺和达托霉素——的药代动力学数据显示,在肥胖情况下它们会发生改变,但还需要更多数据来确定给药建议。关于非抗菌药物的可用数据有限。了解肥胖引起的生理变化以及特定抗生素的现有文献,对于为这个日益常见的肥胖患者群体合理选择用药剂量提供一个框架很有价值。

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