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单剂量口服氟康唑与阴道用特康唑治疗念珠菌性阴道炎的比较及初步研究

Single dose oral fluconazole vs intravaginal terconazole in treatment of Candida vaginitis. Comparison and pilot study.

作者信息

Slavin M B, Benrubi G I, Parker R, Griffin C R, Magee M J

机构信息

Clinical Pharmacy Service, Prudential Company, Roseland, N.J.

出版信息

J Fla Med Assoc. 1992 Oct;79(10):693-6.

PMID:1460451
Abstract

Candida vaginitis develops in approximately one-fourth of women in their childbearing years. Conventional management consists of antifungal creams or tablets/suppositories administered intravaginally. Many patients have stated preferences for oral therapy. A randomized, double-blind placebo trial compared the efficacy of a single oral 200 mg dose of fluconazole with the application of terconazole 80 mg vaginal suppository daily for 3 days. Twenty-two patients (fluconazole = 12, terconazole = 10) were evaluated during a four-month period and favorable clinical responses were observed at both early and late evaluations. Mycologic cure was attained by 75% of the fluconazole group and 50% of the terconazole group at the early evaluation. At the late evaluation, mycologic cure was 75% and 100% respectively. The mean time to onset of symptom relief was 2.4 (1.7) days for the fluconazole group and 1.8 (1.8) days for the terconazole group. The mean time to complete relief of symptoms was 6.08 (2.84) and 6.6 (2.95) days respectively. A statistically significant difference did not exist for any of these measures. Seventy-three percent of the patients preferred oral therapy.

摘要

约四分之一育龄期女性会患念珠菌性阴道炎。传统治疗方法包括阴道内使用抗真菌乳膏或片剂/栓剂。许多患者表示倾向于口服治疗。一项随机、双盲安慰剂试验比较了单次口服200毫克氟康唑与每日使用80毫克特康唑阴道栓剂共3天的疗效。在四个月期间对22名患者(氟康唑组 = 12名,特康唑组 = 10名)进行了评估,在早期和晚期评估中均观察到了良好的临床反应。早期评估时,氟康唑组75%的患者和特康唑组50%的患者实现了真菌学治愈。晚期评估时,真菌学治愈率分别为75%和100%。氟康唑组症状缓解开始的平均时间为2.4(1.7)天,特康唑组为1.8(1.8)天。症状完全缓解的平均时间分别为6.08(2.84)天和6.6(2.95)天。这些指标均不存在统计学显著差异。73%的患者更喜欢口服治疗。

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