Ross Ashley L, Tharp Jennifer L, Hobbs Gerald R, McKnight Richard, Cumpston Aaron
Department of Pharmacy, Jewish Hospital, 200 Abraham Flexner Way, Louisville, KY 40202, USA.
Adv Pharmacol Sci. 2013;2013:194389. doi: 10.1155/2013/194389. Epub 2013 Aug 19.
Aminoglycoside dosing has been studied in the obese population, typically recommending an adjusted weight utilizing a 40% dosing weight correction factor (IBW + 0.4 × (TBW-IBW)). These studies included limited numbers of morbidly obese patients and were not done in the era of extended interval aminoglycoside dosing. Here, we report a retrospective evaluation of morbidly obese patients receiving gentamicin or tobramycin at our hospital. The objective of this study was to evaluate the accuracy of the commonly recommended adjusted weight for weight-based dosing. There were 31 morbidly obese patients who received gentamicin or tobramycin 5-7 mg/kg every 24 hours using a 40% dosing weight correction factor. Our institution utilizes 16-hour postdose concentrations to monitor extended interval aminoglycosides. Twenty-two of the 31 patients (71%) achieved an appropriate serum drug concentration. Four patients (13%) were found to be supratherapeutic and 5 patients (16%) subtherapeutic. The only variable that correlated with supratherapeutic levels was older age (P = 0.0378). Our study helps to validate the current dosing weight correction factor (40%) in the morbidly obese population. We recommend caution when dosing aminoglycosides in morbidly obese patients who are of older age.
氨基糖苷类药物的给药方案已在肥胖人群中进行了研究,通常建议使用40%的给药体重校正因子(理想体重+0.4×(实际体重-理想体重))来调整体重。这些研究纳入的病态肥胖患者数量有限,且并非在延长给药间隔的氨基糖苷类药物给药时代进行的。在此,我们报告了对我院接受庆大霉素或妥布霉素治疗的病态肥胖患者的回顾性评估。本研究的目的是评估常用的基于体重给药的调整体重建议的准确性。有31例病态肥胖患者使用40%的给药体重校正因子,每24小时接受5-7mg/kg的庆大霉素或妥布霉素治疗。我院利用给药后16小时的血药浓度来监测延长给药间隔的氨基糖苷类药物。31例患者中有22例(71%)达到了合适的血药浓度。4例患者(13%)血药浓度高于治疗水平,5例患者(16%)血药浓度低于治疗水平。与血药浓度高于治疗水平相关的唯一变量是年龄较大(P=0.0378)。我们的研究有助于验证目前病态肥胖人群的给药体重校正因子(40%)。我们建议在给年龄较大的病态肥胖患者使用氨基糖苷类药物时要谨慎。