Cho N, Fukunaga K, Kunii K
Jpn J Antibiot. 1981 Jun;34(6):915-24.
The fundamental study of cefmetazole treatment in a clinical situation during the perinatal period were made, and the following results were obtained. Absorption of CMZ in pregnant women is rapid; and the intravenous injection intravenous drip infusion and intramuscular injection of CMZ all reached their peak serum levels in a short time with a half-life of approximately 1 hour or so. The transference of CMZ to the fetus through placenta is good. It is so good that a single dose of 0.5 approximately equal to 1.0 g by intravenous injection, intravenous drip infusion or intramuscular injection can obtain desired concentration levels covering MIC of main causative pathogenic organisms in the cord blood, amniotic fluid and blood in the fetus. Therefore, the administration of CMZ with this dose and method of administration once or twice daily can prevent or treat intrauterine infection. The transition of CMZ to mother's milk is a small quantity and the transition of CMZ through mother's milk to a neonate is considered to be a very small amount. The absorption of CMZ in neonate is rapid. It reaches a peak serum concentration 15 minutes after the intravenous injection. The half-life varies depending on the number days after birth. With the administration of 20 mg/Kg, the half-life at 0 day after birth is 6.32 approximately 6.78 hours, 3.79 hours at 1st day after birth and 2.27 approximately 2.72 hours at 5th-6th day after birth. Excretion into the urine is slow on 0 day after birth and becomes rapid on the 6th day after birth, coinciding with the maintained level of CMZ in the blood. Positive results were obtained from the overview of CMZ administration in the prophpylaxis or treatment of intrauterine infection during the perinatal period. No abnormalities were noted from the examinations performed on a neonate delivered from a mother who had received CMZ during perinatal period. Judging from the various results mentioned above, 20 mg/kg of CMZ administered to a neonate twice a day at 12 hour intervals would be sufficient to attain therapeutic efficacy.
我们对头孢美唑在围产期临床情况下的治疗进行了基础研究,并取得了以下结果。孕妇对头孢美唑的吸收迅速;静脉注射、静脉滴注和肌内注射头孢美唑后,血清水平均在短时间内达到峰值,半衰期约为1小时左右。头孢美唑通过胎盘向胎儿的转运良好。单次静脉注射、静脉滴注或肌内注射0.5 - 1.0g剂量,可在脐血、羊水和胎儿血液中获得覆盖主要致病病原体最低抑菌浓度(MIC)的理想浓度水平。因此,采用该剂量和给药方法,每日1 - 2次给药可预防或治疗宫内感染。头孢美唑向母乳中的转移量较少,通过母乳向新生儿的转移量被认为非常少。新生儿对头孢美唑的吸收迅速。静脉注射后15分钟达到血清浓度峰值。半衰期随出生后天数而异。给予20mg/Kg剂量时,出生0天时半衰期为6.32 - 6.78小时,出生第1天时为3.79小时,出生第5 - 6天时为2.27 - 2.72小时。出生0天时尿液排泄缓慢,出生第6天时加快,这与血液中头孢美唑的维持水平一致。在围产期预防或治疗宫内感染时使用头孢美唑的概述获得了阳性结果。对围产期接受头孢美唑治疗的母亲所分娩的新生儿进行检查,未发现异常。从上述各种结果判断,以12小时间隔每天给新生儿两次20mg/kg的头孢美唑足以达到治疗效果。