Turner R Brigg, Cumpston Aaron, Sweet Michael, Briggs Frank, Slain Douglas, Wen Sijin, Craig Michael, Hamadani Mehdi, Petros William
West Virginia University Healthcare, Morgantown, West Virginia, USA.
West Virginia University Healthcare, Morgantown, West Virginia, USA Mary Babb Randolph Cancer Center, Morgantown, West Virginia, USA
Antimicrob Agents Chemother. 2016 Jan 11;60(3):1830-3. doi: 10.1128/AAC.02010-15.
The current recommendations for intravenous (i.v.) acyclovir dosing in obese patients suggest using ideal body weight (IBW) rather than total body weight (TBW). To our knowledge, no pharmacokinetic analysis has validated this recommendation. This single-dose pharmacokinetic study was conducted in an inpatient oncology population. Enrollment was conducted by 1:1 matching of obese patients (>190% of IBW) to normal-weight patients (80 to 120% of IBW). All patients received a single dose of i.v. acyclovir, 5 mg/kg, infused over 60 min. Consistent with current recommendations, IBW was used for obese patients and TBW for normal-weight patients. Serial plasma concentrations were obtained and compared. Seven obese and seven normal-weight patients were enrolled, with mean body mass indexes of 45.0 and 22.5 kg/m(2), respectively. Systemic clearance was substantially higher in the obese than normal-weight patients (mean, 19.4 ± 5.3 versus 14.3 ± 5.4 liters/h; P = 0.047). Area under the concentration-time curve was lower in the obese patients (15.2 ± 2.9 versus 24.0 ± 9.4 mg · h/liter; P = 0.011), as was maximum concentration (5.8 ± 0.9 versus 8.2 ± 1.3 mg/liter; P = 0.031). Utilization of IBW for dose calculation of i.v. acyclovir in obese patients leads to lower systemic exposure than dosing by TBW in normal-weight patients. While not directly evaluated in this study, utilization of an adjusted body weight for dose determination appears to more closely approximate the exposure seen in normal-weight patients. (This study has been registered at ClinicalTrials.gov under registration no. NCT01714180.).
目前针对肥胖患者静脉注射阿昔洛韦剂量的建议是使用理想体重(IBW)而非总体重(TBW)。据我们所知,尚无药代动力学分析验证这一建议。这项单剂量药代动力学研究在住院肿瘤患者群体中进行。通过将肥胖患者(>IBW的190%)与正常体重患者(IBW的80%至120%)按1:1匹配进行入组。所有患者接受单剂量静脉注射阿昔洛韦,5mg/kg,输注60分钟。与当前建议一致,肥胖患者使用IBW,正常体重患者使用TBW。获取并比较系列血浆浓度。入组了7名肥胖患者和7名正常体重患者,平均体重指数分别为45.0和22.5kg/m²。肥胖患者的全身清除率显著高于正常体重患者(平均值分别为19.4±5.3与14.3±5.4升/小时;P = 0.047)。肥胖患者的浓度-时间曲线下面积较低(15.2±2.9与24.0±9.4mg·小时/升;P = 0.011),最大浓度也是如此(5.8±0.9与8.2±1.3mg/升;P = 0.031)。肥胖患者静脉注射阿昔洛韦剂量计算使用IBW导致的全身暴露低于正常体重患者使用TBW给药。虽然本研究未直接评估,但使用调整体重进行剂量确定似乎更接近正常体重患者的暴露情况。(本研究已在ClinicalTrials.gov注册,注册号为NCT01714180。)