Pilková Alena, Hartinger Jan Miroslav
Vnitr Lek. 2020 Winter;66(8):465-471.
Pharmacokinetics of drugs in obese patients can be affected by changes in drug distribution and/or changes in elimination functions. Drug dosing based on patients weight or body surface area may not be satisfactory in terms of safety or efficacy, especially for patients with a higher degree of obesity. However, current knowledge about most drugs does not provide sufficient guidance for dose adjustment in this group of patients. This article provides an overview of factors influencing changes in pharmacokinetics of drugs in obese, including some examples (eg. analgesics, antibiotics, anticoagulants and others). Due to different changes in pharmacokinetics, which cannot always be estimated from the physical and chemical properties of drug molecular structure, it is important to assess pharmacokinetic properties of a particular drug rather than looking for general rules for the most appropriate dosing. In case of drugs with a narrow therapeutic index (aminoglycoside antibiotics and vancomycin, anticonvulsants, immunosuppressants, lithium, digoxin and theophylline), it is always advisable to measure drug plasma levels and use therapeutic drug monitoring.
肥胖患者体内药物的药代动力学可能会受到药物分布变化和/或消除功能变化的影响。基于患者体重或体表面积的给药在安全性或有效性方面可能并不理想,尤其是对于肥胖程度较高的患者。然而,目前关于大多数药物的知识并不能为这组患者的剂量调整提供足够的指导。本文概述了影响肥胖患者药物药代动力学变化的因素,包括一些实例(如镇痛药、抗生素、抗凝剂等)。由于药代动力学的变化不同,而这些变化不能总是从药物分子结构的物理和化学性质中估计出来,因此评估特定药物的药代动力学性质很重要,而不是寻找最合适给药的一般规则。对于治疗指数较窄的药物(氨基糖苷类抗生素和万古霉素、抗惊厥药、免疫抑制剂、锂、地高辛和茶碱),始终建议测量药物血浆水平并使用治疗药物监测。