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氨曲南在妇产科领域的基础与临床研究

[Fundamental and clinical studies on aztreonam in the field of obstetrics and gynecology].

作者信息

Yamamoto T, Yasuda J, Tomioka M, Kanao M, Okada H

出版信息

Jpn J Antibiot. 1985 Dec;38(12):3634-44.

PMID:3834149
Abstract

Fundamental and clinical studies on aztreonam (AZT), a new synthetic monobactam antibiotic, were performed and following results were obtained. Concentration of AZT was examined in serum, internal genital tissues and retroperitoneal fluid after a single intravenous administration of 1 g dose. The venous serum level of AZT was 114.0 micrograms/ml at 10 minutes after the administration, then decreased to 7.0 micrograms/ml at 3 hours. Since concentration of AZT in examined tissues showed wide variation, it was irrelevant to calculate transfer ratio. Concentration in retroperitoneal fluid made the peak of 40.0 +/- 22.6 micrograms/ml at 1 hour after the administration, then slowly decreased to 13.4 +/- 3.2 micrograms/ml at 6 hours. Judging from above data, the transfer of AZT to retroperitoneal fluid was favorable. In clinical trial, AZT was given to 17 cases with obstetrical and gynecological infections such as endometritis, uterine adnexitis, pelvic peritonitis, parametritis and lymphocystitis. The efficacy was evaluated as excellent in 2 cases, good in 12 and poor in 3, and efficacy rate was 82.4%. No side effects were observed in any of the cases. In laboratory findings, transient elevation of liver function in 2 cases and eosinophilia in 1 case were noticed.

摘要

对新型合成单环β-内酰胺抗生素氨曲南(AZT)进行了基础和临床研究,并获得了以下结果。单次静脉注射1g剂量后,检测了血清、内生殖器组织和腹膜后液中氨曲南的浓度。给药后10分钟时,静脉血清中氨曲南水平为114.0微克/毫升,3小时时降至7.0微克/毫升。由于所检测组织中氨曲南的浓度差异很大,因此计算转运率并无意义。腹膜后液中的浓度在给药后1小时达到峰值40.0±22.6微克/毫升,6小时时缓慢降至13.4±3.2微克/毫升。从上述数据判断,氨曲南向腹膜后液的转运情况良好。在临床试验中,对17例患有子宫内膜炎、子宫附件炎、盆腔腹膜炎、子宫旁组织炎和淋巴囊肿等妇产科感染的患者给予氨曲南。疗效评估为优2例、良12例、差3例,有效率为82.4%。所有病例均未观察到副作用。在实验室检查结果中,注意到2例患者肝功能短暂升高,1例患者嗜酸性粒细胞增多。

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