Schaad U B, Hayton W L, Stoeckel K
Clin Pharmacol Ther. 1985 May;37(5):522-8. doi: 10.1038/clpt.1985.82.
Ceftriaxone kinetics were characterized after a single, 2-minute, intravenous infusion of 50 mg/kg to 20 sick infants 1 to 8 days old who weighed 1.78 to 4.36 kg. Plasma binding parameters could be determined by equilibrium dialysis in 16 of the infants, in whom kinetic parameters for free ceftriaxone in plasma were also determined. Compared with corresponding values in adults, the elimination t1/2 was longer in infants (19 and 8.4 hours) because of reduced total systemic clearance (4.48 and 8.51 ml/min/m2). The apparent steady-state volume of distribution was of the same order in infants and adults (5,130 and 5,350 ml/m2). Both renal and nonrenal clearance of free ceftriaxone were reduced in infants, but these decreases were partially offset by an increased free fraction; plasma binding affinity and capacity constants for infants were about half the adult values. The mean fraction of dose excreted unchanged in urine was estimated at 70% in the neonates and 46% in adults. There were no clinically significant correlations between the kinetic parameters and either age since birth or age since conception. The fraction of free ceftriaxone in plasma inversely correlated with age since conception and was lower in female infants, which decreased the systemic clearance and volume of distribution of total drug in the female infants compared with the male infants. Values for the volume of distribution and clearance parameters were not related to body size (weight or body surface area). From our results, a ceftriaxone dosage of 50 to 100 mg/day is recommended during the first week of life for newborn infants who weigh between 1.8 and 4.4 kg. Impaired renal function may require a reduction in dosage.
对20名年龄为1至8天、体重为1.78至4.36千克的患病婴儿单次静脉输注50毫克/千克(输注时间为2分钟)后,对头孢曲松的动力学特征进行了研究。16名婴儿可通过平衡透析测定血浆结合参数,同时还测定了这些婴儿血浆中游离头孢曲松的动力学参数。与成人的相应值相比,婴儿的消除半衰期更长(分别为19小时和8.4小时),这是由于总全身清除率降低(分别为4.48毫升/分钟/平方米和8.51毫升/分钟/平方米)。婴儿和成人的表观稳态分布容积处于同一数量级(分别为5130毫升/平方米和5350毫升/平方米)。婴儿游离头孢曲松的肾脏清除率和非肾脏清除率均降低,但这些降低被游离分数增加部分抵消;婴儿的血浆结合亲和力和容量常数约为成人值的一半。估计新生儿尿液中以原形排泄的剂量平均比例为70%,成人为46%。动力学参数与出生后的年龄或受孕后的年龄之间均无临床显著相关性。血浆中游离头孢曲松的比例与受孕后的年龄呈负相关,且女婴较低,这使得女婴与男婴相比,总药物的全身清除率和分布容积降低。分布容积和清除参数的值与体型(体重或体表面积)无关。根据我们的研究结果,对于体重在1.8至4.4千克之间的新生儿,建议在出生后第一周给予50至100毫克/天的头孢曲松剂量。肾功能受损可能需要减少剂量。