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氨曲南在妇产科围产期感染中的药代动力学及临床评价。围产期联合研究组对氨曲南的一项研究

[Pharmacokinetics and clinical evaluations on aztreonam in perinatal infections in obstetrics and gynecology. A study of aztreonam in the perinatal co-research group].

作者信息

Matsuda S, Oh K, Hirayama H, Shimizu T, Sengoku K, Haga H, Inoue R, Yamazaki T, Mizoguchi H, Tori-i Y

机构信息

Department of Obstetrics and Gynecology, Juntendo University School of Medicine, Kotoh Hospital.

出版信息

Jpn J Antibiot. 1990 Apr;43(4):736-53.

PMID:2199691
Abstract

Pharmacokinetics and clinical studies on an injectable monobactam antibiotic aztreonam (AZT), were carried out in perinatal infections in obstetrics and gynecology and the obtained results are summarized as follows. 1. Pharmacokinetic study (1) Upon one-shot intravenous injection of AZT 1 g before delivery, maternal serum concentration of AZT was 89.0 micrograms/ml immediately after the injection and a half-life (T 1/2) of 0.96 hour was observed. Umbilical-cord serum concentration showed a peak value of 16.5 micrograms/ml at 1.26 hours after the injection and gradually decreased with a T 1/2 of 1.91 hours. The transfer into amniotic fluid was observed and the peak value of AZT in amniotic fluid reached 12.9 micrograms/ml at 5.57 hours after the injection and slowly decreased thereafter with a T 1/2 of 4.42 hours. Transfer and disappearance in one-shot 2 g intravenous injection and 1 g intravenous drip infusion (1 hour) of AZT were very similar to the results obtained with the one-shot 1 g intravenous injection. (2) The residual serum concentration in neonates after one-shot 1 g intravenous injection of AZT to the mother was almost below the detectable limit. Transfer of AZT into milk was scarcely recognized. 2. Clinical studies (1) AZT was injected to 47 cases with various perinatal infections and it was more than "effective" in 45 cases with an efficacy rate of 95.7%. Also, all the 12 cases to which AZT was administered for prophylaxis of infections showed prophylactic effect. Bacterial eradication was obtained with 25 strains out of 29 aerobic Gram-negative bacteria, but 1 strain "persisted" and for 3 strains results were "unknown", hence an eradication rate of 96.2% was obtained. However, AZT treatment resulted in a little lower eradication rate against Gram-positive bacteria. (2) One case (1.3%) of minor degree of urticaria was found as a side effect, and one case each of eosinophilia and elevation of GOT, GPT and Al-P was observed as abnormal laboratory value. From the above results of pharmacokinetics and clinical evaluation, it has been concluded that AZT is a useful and highly safe drug in various perinatal infections and prophylaxis.

摘要

对一种注射用单环β-内酰胺类抗生素氨曲南(AZT)进行了妇产科围产期感染方面的药代动力学和临床研究,所得结果总结如下。1. 药代动力学研究(1)在分娩前单次静脉注射1g氨曲南后,注射后即刻母体血清中氨曲南浓度为89.0微克/毫升,观察到半衰期(T1/2)为0.96小时。脐带血清浓度在注射后1.26小时达到峰值16.5微克/毫升,随后逐渐下降,半衰期为1.91小时。观察到药物向羊水转移,羊水中氨曲南的峰值在注射后5.57小时达到12.9微克/毫升,此后缓慢下降,半衰期为4.42小时。单次静脉注射2g和静脉滴注1g(1小时)氨曲南后的转移和消除情况与单次静脉注射1g的结果非常相似。(2)母亲单次静脉注射1g氨曲南后,新生儿的残余血清浓度几乎低于检测限。几乎未观察到氨曲南向乳汁的转移。2. 临床研究(1)对47例各种围产期感染患者注射了氨曲南,45例有效,有效率为95.7%。此外,所有12例接受氨曲南预防感染的患者均显示出预防效果。29株需氧革兰氏阴性菌中有25株细菌被清除,但有1株“持续存在”,3株结果“未知”,因此清除率为96.2%。然而,氨曲南治疗对革兰氏阳性菌的清除率略低。(2)发现1例(1.3%)出现轻度荨麻疹作为副作用,各有1例出现嗜酸性粒细胞增多以及谷草转氨酶、谷丙转氨酶和碱性磷酸酶升高作为异常实验室值。从上述药代动力学和临床评估结果得出结论,氨曲南在各种围产期感染和预防中是一种有用且高度安全的药物。

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