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克林霉素阴道乳膏与口服甲硝唑治疗细菌性阴道病的疗效比较

Efficacy of clindamycin vaginal cream versus oral metronidazole in the treatment of bacterial vaginosis.

作者信息

Fischbach F, Petersen E E, Weissenbacher E R, Martius J, Hosmann J, Mayer H

机构信息

Frauenklinik, TU München, Germany.

出版信息

Obstet Gynecol. 1993 Sep;82(3):405-10.

PMID:8355942
Abstract

OBJECTIVE

To compare the efficacy and tolerance with 2% clindamycin vaginal cream versus oral metronidazole for the treatment of bacterial vaginosis.

METHODS

This was a multicenter, randomized, double-blind study in which patients were randomly assigned to one of the following two regimens in a 1:1 ratio: clindamycin phosphate vaginal cream 2% (5 g intravaginally at bedtime for 7 days) plus two placebo capsules (twice a day for 7 days) or metronidazole 500 mg (two 250-mg capsules orally twice a day for 7 days) plus placebo vaginal cream (5 g intravaginally at bedtime for 7 days). The patients were seen for follow-up at 5-10 days and 25-39 days after completion of therapy.

RESULTS

Seven investigators, four in Germany, two in Austria, and one in Switzerland, enrolled 407 patients. Four patients never received either protocol drug, leaving 403 evaluable for safety. Two hundred thirty-four patients were evaluable for efficacy. The analysis for all evaluable patients showed no significant difference between treatment groups. The cure or improvement rate at 1 month after therapy was 83% in the clindamycin group versus 78% in the metronidazole group. The incidence of drug-related adverse medical events was approximately 12% in both groups.

CONCLUSIONS

Oral metronidazole and intravaginal clindamycin cream had a similar efficacy of 78 to 83%. Both drugs were tolerated, with vaginal candidiasis developing in 8.5 and 4.7% of the patients in the clindamycin and metronidazole groups, respectively.

摘要

目的

比较2%克林霉素阴道乳膏与口服甲硝唑治疗细菌性阴道病的疗效及耐受性。

方法

这是一项多中心、随机、双盲研究,患者按1:1比例随机分配至以下两种治疗方案之一:2%克林霉素磷酸酯阴道乳膏(睡前阴道内给药5 g,共7天)加两粒安慰剂胶囊(每日两次,共7天)或甲硝唑500 mg(250 mg胶囊口服,每日两次,共7天)加安慰剂阴道乳膏(睡前阴道内给药5 g,共7天)。治疗结束后5 - 10天及25 - 39天对患者进行随访。

结果

7名研究者,德国4名、奥地利2名、瑞士1名,共纳入407例患者。4例患者从未接受任何一种方案药物治疗,403例患者可进行安全性评估。234例患者可进行疗效评估。对所有可评估患者的分析显示,治疗组之间无显著差异。治疗后1个月,克林霉素组的治愈或改善率为83%,甲硝唑组为78%。两组药物相关不良医疗事件的发生率均约为12%。

结论

口服甲硝唑和阴道内使用克林霉素乳膏的疗效相似,为78%至83%。两种药物耐受性良好,克林霉素组和甲硝唑组分别有8.5%和4.7%的患者发生阴道念珠菌病。

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