首页> 美国卫生研究院文献>Infectious Diseases in Obstetrics and Gynecology >Daily oral grepafloxacin vs. twice daily oral doxycycline in the treatment of Chlamydia trachomatis endocervical infection.
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Daily oral grepafloxacin vs. twice daily oral doxycycline in the treatment of Chlamydia trachomatis endocervical infection.

机译:每日口服格雷帕沙星与每日两次口服强力霉素治疗沙眼衣原体宫颈宫颈感染的比较。

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摘要

OBJECTIVE: To compare the efficacy and safety of a 7-day course of treatment with oral grepafloxacin, 400 mg once daily, and oral doxycycline, 100 mg twice daily, in patients with chlamydial cervicitis. METHODS: Women aged 18 years or older attending 17 sexually transmitted disease clinics in the United States who had clinical signs of mucopurulent cervicitis or who had a recent positive culture or nonculture test for Chlamydia trachomatis or who had contact with a male partner with a positive culture for C. trachomatis were enrolled into this randomized, double-blind, active-controlled clinical study. The diagnosis of chlamydial cervicitis was based on culture for C. trachomatis. Patients were randomized to receive a 7-day course of treatment with either oral grepafloxacin, 400 mg once daily, or oral doxycycline, 100 mg twice daily. Response to therapy was assessed 3-8 days and 21-28 days after completion of treatment. The primary measure of efficacy was eradication of C. trachomatis at the 21-28 day follow-up visit. Clinical success, defined as improvement or complete resolution of the signs and symptoms of cervicitis, was a secondary measure of efficacy. RESULTS: Of the 451 female patients enrolled, 228 received grepafloxacin and 223 received doxycycline. In all, 154/451 (35%) patients were evaluable at the 21-28 day follow-up (81 who received grepafloxacin and 73 who received doxycycline). Microbiologic and clinical success rates demonstrated the equivalence of the two treatments. The C. trachomatis eradication rates were 96.3% (78/81) and 98.6% (72/73) for patients receiving grepafloxacin or doxycycline, respectively. The two study drugs were also equivalent in resolving clinical signs and symptoms, with clinical success rates of 88.9% (64/72) and 89.5% (51/57) for patients treated with grepafloxacin and doxycycline, respectively. Both drugs were well tolerated, with 47% of patients receiving grepafloxacin and 46% of patients receiving doxycycline experiencing drug-related adverse events, none of which was serious. CONCLUSIONS: Seven days of treatment with oral grepafloxacin, 400 mg once daily, was as effective as 7 days of treatment with oral doxycycline, 100 mg twice daily, in patients with cervicitis caused by C. trachomatis. Both agents were well tolerated and had comparable safety profiles. Grepafloxacin's once-daily dosing regimen may offer advantages in terms of patient compliance.
机译:目的:比较在衣原体宫颈炎患者中每天口服一次400 mg格哌沙星和每天两次口服口服多西环素100 mg的7天疗程的疗效和安全性。方法:18岁或以上的妇女在美国的17家性传播疾病诊所就诊,他们有粘液性宫颈炎的临床体征或近期对沙眼衣原体进行了阳性培养或非培养检测,或者与具有阳性培养力的男性伴侣接触沙眼衣原体的研究被纳入这项随机,双盲,主动对照的临床研究中。衣原体宫颈炎的诊断基于沙眼衣原体的培养。患者被随机分配接受7天的疗程,口服400mg格列沙星每天一次,或口服强力霉素100mg每天两次。在治疗完成后3-8天和21-28天评估对治疗的反应。疗效的主要指标是在21-28天的随访中根除沙眼衣原体。定义为改善或完全缓解宫颈炎症状和体征的临床成功是疗效的次要指标。结果:在451名女性患者中,有228名接受了格列沙星治疗,而223名接受了强力霉素治疗。在21-28天的随访中,共有154/451(35%)位患者可评估(81位接受格列沙星治疗的患者和73位接受强力霉素的患者)。微生物学和临床成功率证明了两种治疗的等效性。接受格列沙星或强力霉素治疗的患者的沙眼衣原体根除率分别为96.3%(78/81)和98.6%(72/73)。两种研究药物在解决临床体征和症状方面也相当,用格列沙星和强力霉素治疗的患者的临床成功率分别为88.9%(64/72)和89.5%(51/57)。两种药物均具有良好的耐受性,其中47%的患者接受格列沙星治疗,而46%的强力霉素患者发生药物相关的不良事件,但没有一例是严重的。结论:对于由沙眼衣原体引起的宫颈炎患者,口服格列沙星400 mg每天一次,治疗7天与口服强力霉素100 mg,每天两次,每天7次治疗效果相同。两种药物都具有良好的耐受性,并且具有可比的安全性。格雷帕沙星的每日一次给药方案可能在患者依从性方面提供优势。

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