Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa
Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Antimicrob Agents Chemother. 2018 Jan 25;62(2). doi: 10.1128/AAC.01521-17. Print 2018 Feb.
Levofloxacin is increasingly used in the treatment of multidrug-resistant tuberculosis (MDR-TB). There are limited pediatric pharmacokinetic data to inform dose selection for children. Children routinely receiving levofloxacin (250-mg adult tablets) for MDR-TB prophylaxis or disease in Cape Town, South Africa, underwent pharmacokinetic sampling following receipt of a dose of 15 or 20 mg/kg of body weight given as a whole or crushed tablet(s) orally or via a nasogastric tube. Pharmacokinetic parameters were estimated using nonlinear mixed-effects modeling. Model-based simulations were performed to estimate the doses across weight bands that would achieve adult exposures with 750-mg once-daily dosing. One hundred nine children were included. The median age was 2.1 years (range, 0.3 to 8.7 years), and the median weight was 12 kg (range, 6 to 22 kg). Levofloxacin followed 2-compartment kinetics with first-order elimination and absorption with a lag time. After inclusion of allometric scaling, the model characterized the age-driven maturation of clearance (CL), with the effect reaching 50% of that at maturity at about 2 months after birth and 100% of that at maturity by 2 years of age. CL in a typical child (weight, 12 kg; age, 2 years) was 4.7 liters/h. HIV infection reduced CL by 16%. By use of the adult 250-mg formulation, levofloxacin exposures were substantially lower than those reported in adults receiving a similar dose on a milligram-per-kilogram basis. To achieve adult-equivalent exposures at a 750-mg daily dose, higher levofloxacin pediatric doses of from 18 mg/kg/day for younger children with weights of 3 to 4 kg (due to immature clearance) to 40 mg/kg/day for older children may be required. The doses of levofloxacin currently recommended for the treatment of MDR-TB in children result in exposures considerably lower than those in adults. The effects of different formulations and formulation manipulation require further investigation. We recommend age- and weight-banded doses of 250-mg tablets of the adult formulation most likely to achieve target concentrations for prospective evaluation.
左氧氟沙星在治疗耐多药结核病(MDR-TB)中的应用日益增多。目前针对儿童人群,其药代动力学数据十分有限,无法为剂量选择提供参考。在南非开普敦,儿童常规接受左氧氟沙星(250mg 成人片剂)作为 MDR-TB 预防或治疗药物。在接受 15 或 20mg/kg 体重剂量的全或碎片剂(经口或经鼻胃管)给药后,进行药代动力学采样。采用非线性混合效应模型估算药代动力学参数。基于模型的模拟用于估算在不同体重范围内的剂量,以实现 750mg 每日一次给药的成人暴露量。共纳入 109 例儿童。中位年龄为 2.1 岁(范围:0.3 至 8.7 岁),中位体重为 12kg(范围:6 至 22kg)。左氧氟沙星遵循二室模型动力学,具有一级消除和吸收时的滞后时间。纳入比例房室模型后,该模型描述了清除率(CL)随年龄的成熟变化,大约在出生后 2 个月时达到成熟的 50%,2 岁时达到成熟的 100%。典型儿童(体重 12kg,年龄 2 岁)的 CL 为 4.7L/h。HIV 感染使 CL 降低 16%。使用成人 250mg 剂型,以毫克/千克为基础,左氧氟沙星的暴露量远低于接受类似剂量的成人报告的暴露量。为了在 750mg 每日剂量下实现成人等效暴露,可能需要为体重 3 至 4kg 的年幼儿童(由于清除不成熟)给予 18mg/kg/天的较高剂量,或为年龄较大的儿童给予 40mg/kg/天的较高剂量。目前推荐的儿童 MDR-TB 治疗剂量,导致的暴露量远低于成人。不同剂型和剂型处理的影响需要进一步研究。我们建议使用最有可能达到目标浓度的成人剂型 250mg 片剂,根据年龄和体重进行分组给药,以供前瞻性评估。