Department of Pediatrics, Duke University, Durham, North Carolina2Duke Clinical Research Institute, Duke University, Durham, North Carolina3Academic Medical Center, Department of Public Health, Amsterdam, the Netherlands.
Department of Pediatrics, Duke University, Durham, North Carolina2Duke Clinical Research Institute, Duke University, Durham, North Carolina.
JAMA Pediatr. 2015 Jul;169(7):678-85. doi: 10.1001/jamapediatrics.2015.132.
Obesity affects nearly one-sixth of US children and results in alterations to body composition and physiology that can affect drug disposition, possibly leading to therapeutic failure or toxic side effects. The depth of available literature regarding obesity's effect on drug safety, pharmacokinetics, and dosing in obese children is unknown.
To perform a systematic literature review describing the current evidence of the effect of obesity on drug disposition in children.
We searched the MEDLINE, Cochrane, and EMBASE databases (January 1, 1970-December 31, 2012) and included studies if they contained data on drug clearance, volume of distribution, or drug concentration in obese children (aged ≤18 years). We compared exposure and weight-normalized volume of distribution and clearance between obese and nonobese children. We explored the association between drug physicochemical properties and clearance and volume of distribution.
Twenty studies met the inclusion criteria and contained pharmacokinetic data for 21 drugs. The median number of obese children studied per drug was 10 (range, 1-112) and ages ranged from newborn to 29 years (1 study described pharmacokinetics in children and adults together). Dosing schema varied and were either a fixed dose (6 [29%]) or based on body weight (10 [48%]) and body surface area (4 [19%]). Clinically significant pharmacokinetic alterations were observed in obese children for 65% (11 of 17) of the studied drugs. Pharmacokinetic alterations resulted in substantial differences in exposure between obese and nonobese children for 38% (5 of 13) of the drugs. We found no association between drug lipophilicity or Biopharmaceutical Drug Disposition Classification System class and changes in volume of distribution or clearance due to obesity.
Consensus is lacking on the most appropriate weight-based dosing strategy for obese children. Prospective pharmacokinetic trials in obese children are needed to ensure therapeutic efficacy and enhance drug safety.
肥胖影响了近六分之一的美国儿童,导致身体成分和生理机能发生改变,可能影响药物处置,从而导致治疗失败或产生毒副作用。目前,肥胖对儿童药物安全性、药代动力学和肥胖儿童用药剂量的影响的相关文献深度尚不清楚。
进行系统文献综述,描述肥胖对儿童药物处置的影响的现有证据。
我们检索了 MEDLINE、Cochrane 和 EMBASE 数据库(1970 年 1 月 1 日-2012 年 12 月 31 日),如果研究包含肥胖儿童(年龄≤18 岁)的药物清除率、分布容积或药物浓度数据,则将其纳入研究。我们比较了肥胖和非肥胖儿童的暴露量和体重归一化分布容积和清除率。我们探讨了药物物理化学性质与清除率和分布容积之间的关系。
20 项研究符合纳入标准,包含 21 种药物的药代动力学数据。每种药物研究肥胖儿童的中位数为 10 例(范围为 1-112 例),年龄从新生儿到 29 岁(1 项研究同时描述了儿童和成人的药代动力学)。给药方案各不相同,要么是固定剂量(6 种[29%]),要么是基于体重(10 种[48%])和体表面积(4 种[19%])。在肥胖儿童中,65%(17 种中的 11 种)研究药物观察到明显的药代动力学改变。由于肥胖,38%(13 种中的 5 种)药物的肥胖儿童和非肥胖儿童之间的暴露量存在显著差异。我们没有发现药物亲脂性或生物药剂学药物处置分类系统分类与肥胖引起的分布容积或清除率变化之间存在关联。
对于肥胖儿童最合适的基于体重的给药策略尚未达成共识。需要在肥胖儿童中进行前瞻性药代动力学试验,以确保治疗效果并提高药物安全性。