Lee How Sung, Khoo Yok Moi, Chirino-Barcelo Yazmin, Tan Kim Leong, Ong Dorothy
Department of Pharmacology National University of Singapore, Singapore.
Br J Clin Pharmacol. 2002 Jul;54(1):31-7. doi: 10.1046/j.1365-2125.2002.01589.x.
To monitor plasma caffeine concentrations and adverse effects and to study the pharmacokinetics of caffeine in neonatal apnoea in the local Asian population after intravenous administration of caffeine.
Eighteen neonates with apnoea were treated with caffeine citrate at a loading dose of 10 mg caffeine base kg-1 and a maintenance dose of 2.5 mg kg-1 day-1. Blood samples, three after loading and two after the maintenance dose on day 2, 3, 7, 14 and 21 were taken and analysed for caffeine and its main metabolites using solid phase extraction and h.p.l.c. Adverse effects were monitored. Sparse data pharmacokinetic analysis was performed using P-Pharm.
Mean caffeine concentrations varied from 10 to 20 mg l-1 throughout treatment (range 3.6-28.4 mg l-1). These concentrations were efficacious; less so in those with lower concentrations. Adverse effects included gastrointestinal disturbances, diuresis and hyperglycaemia. Pharmacokinetic parameter estimates [mean (coefficient of variation%)] were CL=0.00628 (17.5%) l h-1 and V=0.961 (20.3%) l. CL (l h-1)=0.004248 * wt(kg)+0.00154; r=0.8, P<0.01, explained 64% of the variation. V (l)=0.6299 * wt(kg)+0.259; r=0.67, P<0.01, explained 45% of variation. Model-predicted compared with observed plasma concentrations in a separate group of 10 neonates were unbiased and of good precision.
The dosing regimen studied was suitable for our local Asian neonates as it resulted in therapeutic caffeine concentrations for adequate treatment of apnoea. Adverse effects were tolerable. Therefore, to avoid a higher incidence of adverse effects, this regimen should be retained and not increased as proposed by other workers. CL and V were within values of those reported for neonatal apnoea. Sparse data analysis showed that weight alone was adequate as the influential variable for the accurate prediction of individual pharmacokinetic parameters, plasma concentrations and for dosage adjustment if required.
监测血浆咖啡因浓度及不良反应,并研究在亚洲当地人群中静脉注射咖啡因后新生儿呼吸暂停时咖啡因的药代动力学。
18例呼吸暂停新生儿接受枸橼酸咖啡因治疗,负荷剂量为10mg咖啡因碱基/kg,维持剂量为2.5mg/kg/天。在负荷剂量后采集3份血样,在第2、3、7、14和21天维持剂量后采集2份血样,采用固相萃取和高效液相色谱法分析咖啡因及其主要代谢产物。监测不良反应。使用P-Pharm进行稀疏数据药代动力学分析。
整个治疗过程中咖啡因平均浓度在10至20mg/L之间(范围为3.6 - 28.4mg/L)。这些浓度是有效的;浓度较低者效果稍差。不良反应包括胃肠道紊乱、利尿和高血糖。药代动力学参数估计值[平均值(变异系数%)]为CL = 0.00628(17.5%)L/h,V = 0.961(20.3%)L。CL(L/h)= 0.004248×体重(kg)+ 0.00154;r = 0.8,P < 0.01,解释了64%的变异。V(L)= 0.6299×体重(kg)+ 0.259;r = 0.67,P < 0.01,解释了45%的变异。在另一组10例新生儿中,模型预测的血浆浓度与观察到的血浆浓度相比无偏差且精度良好。
所研究的给药方案适用于当地亚洲新生儿,因为它能产生治疗呼吸暂停的有效咖啡因浓度。不良反应是可耐受的。因此,为避免更高的不良反应发生率,应保留该方案,而不应像其他研究者提议的那样增加剂量。CL和V在新生儿呼吸暂停报道的值范围内。稀疏数据分析表明,仅体重就足以作为准确预测个体药代动力学参数、血浆浓度以及必要时进行剂量调整的影响变量。