Bearden D T, Rodvold K A
Colleges of Pharmacy and Medicine, University of Illinois at Chicago, 60612, USA.
Clin Pharmacokinet. 2000 May;38(5):415-26. doi: 10.2165/00003088-200038050-00003.
Obesity is associated with physiological changes that can alter the pharmacokinetic parameters of many drugs. Vancomycin and the aminoglycosides are the only antibacterials that have been extensively investigated in the obese population. The apparent volume of distribution (Vd) and total body clearance of vancomycin are increased in obese patients and have a better correlation with total bodyweight (TBW) than with ideal bodyweight (IBW). The Vd of aminoglycosides is increased in obesity and can be estimated from an adjusted bodyweight that accounts for a fraction of the excess bodyweight (TBW - IBW). These observed changes in pharmacokinetic parameters of vancomycin and aminoglycosides in obese patients may necessitate a deviation from the commonly recommended dosages administered to non-obese individuals. There are limited data regarding the pharmacokinetics of other antibacterial classes in obese patients. The available information for cephalosporins suggests that dosages may need to be increased in obese patients in order to obtain similar serum and tissue concentrations as in non-obese patients. Additional pharmacokinetic studies of other antibacterial classes are required in this special patient population.
肥胖与一些生理变化相关,这些生理变化会改变许多药物的药代动力学参数。万古霉素和氨基糖苷类是仅有的在肥胖人群中得到广泛研究的抗菌药物。肥胖患者体内万古霉素的表观分布容积(Vd)和全身清除率增加,且与总体重(TBW)的相关性优于与理想体重(IBW)的相关性。肥胖患者体内氨基糖苷类的Vd增加,可根据考虑了部分超重体重(TBW - IBW)的调整体重来估算。肥胖患者中观察到的万古霉素和氨基糖苷类药代动力学参数的这些变化,可能需要偏离通常推荐给非肥胖个体的剂量。关于肥胖患者中其他抗菌药物类别药代动力学的数据有限。头孢菌素类的现有信息表明,肥胖患者可能需要增加剂量,以获得与非肥胖患者相似的血清和组织浓度。在这一特殊患者群体中,需要对其他抗菌药物类别进行更多的药代动力学研究。