Ahmed-Jushuf I H, Arya O P, Hobson D, Pratt B C, Hart C A, How S J, Tait I A, Rao P M
Department of Genitourinary Medicine, Royal Hospital, Liverpool.
Genitourin Med. 1988 Feb;64(1):14-7. doi: 10.1136/sti.64.1.14.
Ciprofloxacin was evaluated in chlamydial infections of the urogenital tracts of women treated with a dosage regimen of 500 mg orally twice a day for seven days. Of the 40 women evaluated, 30 were infected with Chlamydia trachomatis only, two were infected with Neisseria gonorrhoeae only, and a further eight had combined gonococcal and chlamydial infections. Ten were found to be harbouring Chlamydia trachomatis in the urethra as well as the cervix. Neisseria gonorrhoeae was eradicated from all patients with or without concomitant chlamydial infection. The overall chlamydial reisolation rates were 14% (5/35) four weeks after treatment and 23% (6/26) 11 weeks after treatment. The organism was not reisolated from the urethra of any of the patients after treatment. Ciprofloxacin was effective against Mycoplasma hominis, but almost completely ineffective against Ureaplasma urealyticum.
对患有泌尿生殖道衣原体感染的女性采用每天口服两次、每次500毫克、连续服用七天的给药方案,对环丙沙星进行了评估。在接受评估的40名女性中,30名仅感染沙眼衣原体,2名仅感染淋病奈瑟菌,另有8名同时患有淋病和衣原体感染。发现10名患者的尿道和宫颈中均携带沙眼衣原体。所有患有或未患有衣原体感染的患者中的淋病奈瑟菌均被根除。治疗四周后的衣原体重新分离率为14%(5/35),治疗11周后的重新分离率为23%(6/26)。治疗后未从任何患者的尿道中重新分离出该病原体。环丙沙星对人型支原体有效,但对解脲脲原体几乎完全无效。