首页> 外文期刊>Journal of infection and chemotherapy: official journal of the Japan Society of Chemotherapy >Clinical efficacy of clarithromycin against uterine cervical and pharyngeal Chlamydia trachomatis and the sensitivity of polymerase chain reaction to detect C. trachomatis at various time points after treatment.
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Clinical efficacy of clarithromycin against uterine cervical and pharyngeal Chlamydia trachomatis and the sensitivity of polymerase chain reaction to detect C. trachomatis at various time points after treatment.

机译:克拉霉素对子宫宫颈和咽部沙眼衣原体的临床疗效以及聚合酶链反应在治疗后各个时间点检测沙眼衣原体的敏感性。

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摘要

The detection and eradication of pharyngeal Chlamydia trachomatis in patients with chlamydial uterine cervicitis (commercial sex workers and others) were investigated. Pharyngeal C. trachomatis was detected in 75.0% of the commercial sex workers and in 21.9% of the other subjects. All the pharyngeal C. trachomatis-positive patients had a past history of orogenital contact. Chlamydial infection was treated with clarithromycin for 7 or 14 days. The presence of C. trachomatis was determined by polymerase chain reaction (PCR) on days 8, 15, and 22 after completion of the treatment. In the 7-day treatment group, the eradication rate of pharyngeal C. trachomatis was 53.3%, 56.7%, and 60.0% on days 8, 15, and 22, respectively, after completion of the treatment, while the eradication rate of cervical C. trachomatis was 83.3%, 96.7%, and 100% on days 8, 15, and 22, respectively. The eradication rate of pharyngeal C. trachomatis in the 7-day treatment was significantly lower than that of cervical C. trachomatis, while there was no significant difference in the 14-day treatment. The eradication rate of pharyngeal C. trachomatis in the 14-day treatment was significantly higher than that in the 7-day treatment. Since the DNA of dead organisms may be detected because of high PCR sensitivity, appropriate therapeutic judgment by PCR could be done around day 22 after completion of the treatment.
机译:研究了沙眼衣原体宫颈炎患者(商业性工作者和其他人)的沙眼衣原体沙眼衣原体的检测和根除。在商业性工作者中有75.0%检出沙眼衣原体,在其他受试者中检出了21.9%。所有咽部沙眼衣原体阳性患者都有生殖器接触史。用克拉霉素治疗衣原体感染7或14天。治疗完成后第8、15和22天通过聚合酶链反应(PCR)确定沙眼衣原体的存在。在第7天的治疗组中,完成治疗后第8、15和22天,咽炎沙眼衣原体的根除率分别为53.3%,56.7%和60.0%,而宫颈C根除率在第8、15和22天,沙眼衣原体分别为83.3%,96.7%和100%。 7天治疗中咽炎沙眼衣原体的根除率显着低于宫颈沙眼衣原体,而14天治疗中的根除率无显着差异。 14天治疗中咽炎沙眼衣原体的根除率显着高于7天治疗。由于可以通过高PCR敏感性检测到死亡生物的DNA,因此可以在治疗完成后第22天左右通过PCR进行适当的治疗判断。

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