Giacoia G, Jusko W J, Menke J, Koup J R
J Pediatr. 1976 Nov;89(5):829-32. doi: 10.1016/s0022-3476(76)80818-9.
The pharmacokinetics of theophylline were examined in eight low-birth-weight infants (gestation: 26-32 weeks: birth-weight: 887-1,480 gm), who received the drug for treatment of primary apnea. The drug was assayed by high pressure liquid chromatography. The final dosage was 1 to 3 mg/kg/6 hour at 25 to 37 days of age. At the time, theophylline had a prolonged half-life ranging from 13 to 29 hours, a relatively large volume of distribution of 0.65 to 2.86 1/kg, and a small body clearance of 23 to 68 ml/hr/kg. The extremely slow and variable elimination of theophylline must be considered in treatment of apneic infants. The initial dosage regimen suggested is a loading dose of 6 mg/kg and a maintenance dose of 2 mg/kg/ 12 hours, with adjustments made based on monitoring of the serum concentration and on an increased biotransformation capability as maturation occurs.
对8名低体重婴儿(孕周:26 - 32周;出生体重:887 - 1480克)进行了茶碱的药代动力学研究,这些婴儿接受该药物治疗原发性呼吸暂停。通过高压液相色谱法对药物进行分析。最终剂量为在25至37日龄时1至3毫克/千克/6小时。当时,茶碱的半衰期延长,范围为13至29小时,分布容积相对较大,为0.65至2.86升/千克,机体清除率较小,为23至68毫升/小时/千克。在治疗呼吸暂停婴儿时,必须考虑到茶碱极其缓慢且多变的消除情况。建议的初始给药方案为负荷剂量6毫克/千克,维持剂量2毫克/千克/12小时,并根据血清浓度监测以及随着成熟发生的生物转化能力增加进行调整。