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阿奇霉素在妇科组织中的水平。

Gynaecological tissue levels of azithromycin.

作者信息

Krohn K

机构信息

Department of Gynaecology and Obstetrics, Centrallasarettet, Norrköping, Sweden.

出版信息

Eur J Clin Microbiol Infect Dis. 1991 Oct;10(10):864-8. doi: 10.1007/BF01975844.

Abstract

In an open study the concentrations of azithromycin in plasma, urine, peritoneal fluid and gynaecological tissue in 20 patients undergoing elective gynaecological surgery were compared. Patients were allocated to one of four groups and all patients received a single 500 mg oral dose of azithromycin prior to surgery. In Group I, the dose was administered 24 h before surgery. In Groups II, III and IV it was administered 48, 72 and 96 h, respectively, prior to surgery. A total of 19 patients completed the study; one patient had peri-operative complications and did not proceed to surgery. High concentrations of azithromycin were found in gynaecological tissue up to 96 h after administration. The mean maximum observed concentration 24 h after administration was 1.44 +/- 0.22 micrograms/g. Using all data, the depletion rate constant was 0.0104 h-1, equivalent to a half-life of approximately 67 h. The mean concentration of drug in peritoneal fluid was approximately 9% of the mean concentration in gynaecological tissue. Tissue and peritoneal fluid azithromycin concentrations were much higher than plasma levels at the time of surgery. Detectable plasma levels were only found in four patients from Groups I and II. Six percent of the total dose was excreted in the urine during the seven-day period after drug administration. The single dose of azithromycin was well tolerated by all the patients in this study and no treatment-related side effects or laboratory test abnormalities were seen. It is concluded that a single 500 mg oral dose of azithromycin produces high and sustained levels in gynaecological tissue up to 96 h after administration.

摘要

在一项开放性研究中,比较了20例行择期妇科手术患者血浆、尿液、腹腔液和妇科组织中阿奇霉素的浓度。患者被分为四组,所有患者在手术前均接受单次500mg口服阿奇霉素剂量。在第一组中,该剂量在手术前24小时给药。在第二、三、四组中,分别在手术前48、72和96小时给药。共有19名患者完成了研究;一名患者出现围手术期并发症,未进行手术。给药后96小时内,在妇科组织中发现了高浓度的阿奇霉素。给药后24小时观察到的平均最大浓度为1.44±0.22微克/克。使用所有数据,消除速率常数为0.0104 h-1,相当于半衰期约为67小时。腹腔液中药物的平均浓度约为妇科组织中平均浓度的9%。手术时组织和腹腔液中的阿奇霉素浓度远高于血浆水平。仅在第一组和第二组的四名患者中发现了可检测到的血浆水平。给药后七天内,总剂量的6%经尿液排出。本研究中所有患者对单次剂量的阿奇霉素耐受性良好,未观察到与治疗相关的副作用或实验室检查异常。结论是,单次口服500mg阿奇霉素在给药后96小时内在妇科组织中产生高且持续的水平。

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