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首页> 外文期刊>Infectious diseases in obstetrics and gynecology >An evaluation of butoconazole nitrate 2% site release vaginal cream (Gynazole-1) compared to fluconazole 150 mg tablets (Diflucan) in the time to relief of symptoms in patients with vulvovaginal candidiasis.
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An evaluation of butoconazole nitrate 2% site release vaginal cream (Gynazole-1) compared to fluconazole 150 mg tablets (Diflucan) in the time to relief of symptoms in patients with vulvovaginal candidiasis.

机译:在缓解阴道念珠菌病患者症状时,与150毫克氟康唑(Diflucan)相比,对硝酸丁康康唑2%部位释放阴道乳膏(Gynazole-1)进行了评估。

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BACKGROUND: It is estimated that as many as 13 million cases of vulvovaginal infection occur in the United States annually, the majority of which are the result of Candida albicans infection. The symptoms of vulvovaginal infections are often painful and distressing to the patient. The objective of this study was to compare the time to symptomatic relief of vulvovaginal candidiasis (VVC) with butoconazole nitrate 2% Site Release vaginal cream (Gynazole-1) and oral fluconazole 150 mg tablets (Diflucan). METHODS: This randomized, open-label, parallel study evaluated 181 female patients with moderate to severe symptoms of VVC. Patients were randomized to single-dose therapy with either butoconazole nitrate 2% Site Release vaginal cream or fluconazole. The primary outcome measure was the time to onset of first relief of symptoms. Secondary measures included the time to overall relief of symptoms and the reinfection rate over the first 30 days following treatment. The overall safety of both products was investigated through the collection of adverse event reports. RESULTS: The median time to first relief of symptoms occurred at 17.5 h for butoconazole patients as compared to 22.9 h for fluconazole patients (p < 0.001). The time at which 75% of patients experienced first relief of symptoms was 24.5 h versus 46.3 h for butoconazole and fluconazole, respectively (p < 0.001). By 12- and 24-h post-treatment, 44.4% and 72.8% of patients in the butoconazole treatment group reported first relief of symptoms versus 29.1% and 55.7% of patients in the fluconazole group (p = 0.044 and p = 0.024 respectively). In patients experiencing first relief of symptoms within 48 h of dosing, the median time to first relief of symptoms in the butoconazole treatment group was significantly shorter at 12.9 h compared to 20.7 h for the fluconazole treatment group (p = 0.048). There were no significant differences between the two groups with respect to time to total relief of symptoms or reoccurrence of infection within 30 days of treatment. Butoconazole therapy was shown to have fewer reported adverse events, including drug-related adverse events, than fluconazole therapy. Vulvovaginal pruritis and vulvovaginal burning were the most common drug-related adverse events attributed to butoconazole. Headache, diarrhea, nausea, upset stomach and skin sensitivity were the most common drug-related adverse events attributable to fluconazole. CONCLUSIONS: Single-dose butoconazole nitrate 2% Site Release vaginal cream provides statistically significant improvement in time to first relief of symptoms in the treatment of VVC compared to fluconazole. There is no difference between these two treatments with respect to total relief of symptoms or reinfection rate. Although there was no significant difference in the incidence of adverse events judged by the investigator to be treatment-related, butoconazole treatment did result in fewer patients experiencing adverse events than fluconazole.
机译:背景:据估计,美国每年发生多达1300万例外阴阴道感染,其中大多数是白色念珠菌感染的结果。外阴阴道感染的症状通常使患者痛苦不堪。这项研究的目的是比较使用2%硝酸丁康康唑阴道释放乳膏(Gynazole-1)和口服氟康唑150 mg片剂(Diflucan)来缓解外阴念珠菌病(VVC)症状的时间。方法:这项随机,开放标签,平行研究评估了181例具有中度至重度VVC症状的女性患者。患者被随机分配接受2%硝酸丁康康唑阴道释放乳膏或氟康唑的单剂量治疗。主要结果指标是症状首次缓解的时间。次要措施包括治疗后最初30天内症状总体缓解的时间和再感染率。通过收集不良事件报告,对这两种产品的总体安全性进行了调查。结果:布托康唑患者首次缓解症状的中位时间为17.5 h,而氟康唑患者为22.9 h(p <0.001)。 75%的患者首次缓解症状的时间为24.5小时,而丁康康唑和氟康唑的时间分别为46.3小时(p <0.001)。到治疗后12小时和24小时,布康唑治疗组的患者首次缓解症状的比例分别为44.4%和72.8%,而氟康唑组的患者分别为29.1%和55.7%(分别为p = 0.044和p = 0.024) 。在给药后48小时内症状首次缓解的患者中,布康唑治疗组中症状首次缓解的中位时间为12.9 h,而氟康唑治疗组为20.7 h(p = 0.048)。两组在治疗30天内症状完全缓解或感染再次发作的时间方面无显着差异。与氟康唑治疗相比,布托康唑治疗的不良事件(包括药物相关不良事件)的报道更少。外阴阴道炎和外阴灼热是丁康康唑最常见的药物相关不良事件。头痛,腹泻,恶心,胃部不适和皮肤敏感性是氟康唑最常见的药物相关不良事件。结论:与氟康唑相比,单剂量硝酸2%硝酸布托康唑定点释放阴道乳膏在VVC治疗中首次缓解症状的时间具有统计学上的显着改善。完全缓解症状或再感染率方面,这两种治疗之间没有差异。尽管研究者认为与治疗有关的不良事件发生率没有显着差异,但是与氟康唑相比,丁康唑治疗的确有较少的患者发生不良事件。

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