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Evaluation of 3-Day Course of Doxycycline for the Treatment of Uncomplicated Chlamydia trachomatis Cervicitis

机译:多西环素3天疗程治疗单纯性沙眼衣原体宫颈炎的评价

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摘要

Objective: The purpose of this study was to compare the efficacy of a 3-day course of doxycycline to a standard 7-day course for treating uncomplicated chlamydia cervicitis.Methods: During an 18-month period, 77 women with uncomplicated chlamydia cervicitis were randomized to receive either a 3-day or a 7-day course of doxycycline (100 mg twice daily). Tests of cure were performed 3 weeks after completion of therapy with the Amplicor polymerase chain reaction (PCR) assay (Roche Molecular Systems, Branchburg, NJ). Demographics, therapeutic results, and side effects for the two groups were compared.Results: Seventy-three patients completed the study: 35 in the 3-day group and 38 in the 7-day group. There were no significant differences in age, gravidity, or parity between the groups. There was a 94% (33/35) cure rate in the 3-day group and a 95% (36/38) cure rate in the 7-day group (P = 1.0). Thirty-four percent and 32% of the patients in the 3- and 7-day groups reported side effects, respectively; there was no significant differences between the 3- and 7-day groups in regard to population demographics, patient compliance, therapeutic outcome, or side effects.Conclusions: A 3-day course of doxycycline appears to be as effective as a 7-day course of doxycycline for the treatment of uncomplicated chlamydia cervicitis.
机译:目的:本研究的目的是比较多西环素3天疗程与标准7天疗程治疗单纯性衣原体宫颈炎的疗效。方法:在18个月内,将77例患有单纯性衣原体宫颈炎的妇女随机分组接受强力霉素3天或7天疗程(每天两次100毫克)。治疗完成后的3周内,用Amplicor聚合酶链反应(PCR)分析(罗氏分子系统公司,新泽西州布兰奇堡)进行治愈测试。比较了两组的人口统计学,治疗结果和副作用。结果:73名患者完成了研究:3天组35例,7天组38例。两组之间的年龄,妊娠率或均等率无显着差异。 3天组的治愈率为94%(33/35),而7天组的治愈率为95%(36/38)(P = 1.0)。在3天和7天组中,分别有34%和32%的患者报告了副作用。 3天和7天组在人口统计学,患者依从性,治疗结果或副作用方面无显着差异。结论:强力霉素3天疗程似乎与7天疗程一样有效强力霉素用于治疗单纯性衣原体宫颈炎。

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