Kurashige T, Morita H, Araki K, Ogura H, Morioka N, Kitamura I
Jpn J Antibiot. 1986 Apr;39(4):1157-65.
We have evaluated cefixime (CFIX) fine granules for pharmacokinetics and therapeutic effectiveness in children with infections. The results were summarized as follows. Pharmacokinetic parameters after the oral administration of single doses of 1.5 mg and 6.0 mg per kg body weight in a cross-over design in 1 child were as follows: The peak serum CFIX concentrations were 0.65 microgram/ml at 2 to 3 hours and 3.33 micrograms/ml at 4 hours for the low and the high doses, respectively; the respective biological half-lives were 2.4 hours and 2.5 hours, and urinary recovery was 10.3% at 8 hours and 5.2% at 12 hours, respectively. A clinical study was performed on 19 children with infections, including 7 with bronchitis; 3 each with tonsillitis, UTI, and cervical lymphadenitis; and 1 each with pharyngitis, retroauricular lymphadenitis, and enteritis. Doses ranging from 1.8 to 7.8 mg/kg body weight were given b.i.d. or t.i.d. The period of treatment ranged from 3 to 13 days. The therapeutic response was considered "excellent" in 15 and "good" in 4, with an effectiveness rate of 100%. No side effects were observed. The only abnormal laboratory findings was a slight elevation of GOT and GTP recorded in 1 child. It was concluded that CFIX was a promising drug for the treatment of bacterial infections in children.
我们评估了头孢克肟(CFIX)细颗粒剂在感染儿童中的药代动力学和治疗效果。结果总结如下。在1名儿童中采用交叉设计口服单剂量每千克体重1.5毫克和6.0毫克后的药代动力学参数如下:低剂量和高剂量的血清CFIX峰值浓度分别在2至3小时时为0.65微克/毫升和在4小时时为3.33微克/毫升;各自的生物半衰期分别为2.4小时和2.5小时,8小时时尿回收率分别为10.3%和12小时时为5.2%。对19名感染儿童进行了临床研究,其中包括7名支气管炎患儿;3名扁桃体炎、尿路感染和颈淋巴结炎患儿;以及1名咽炎、耳后淋巴结炎和肠炎患儿。给予每千克体重1.8至7.8毫克的剂量,每日两次或每日三次。治疗期为3至13天。治疗反应被认为“优秀”的有15例,“良好”的有4例,有效率为100%。未观察到副作用。唯一的实验室异常发现是1名儿童记录到谷草转氨酶(GOT)和谷氨酰转肽酶(GTP)略有升高。得出的结论是,CFIX是治疗儿童细菌感染的一种有前景的药物。