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每周口服一次150毫克氟康唑治疗体癣/股癣和皮肤念珠菌病。

Once-weekly oral doses of fluconazole 150 mg in the treatment of tinea corporis/cruris and cutaneous candidiasis.

作者信息

Suchil P, Gei F M, Robles M, Perera-Ramírez A, Welsh O, Male O

机构信息

Centro Dermatológico Pascua, Mexico City, Mexico.

出版信息

Clin Exp Dermatol. 1992 Nov;17(6):397-401. doi: 10.1111/j.1365-2230.1992.tb00246.x.

DOI:10.1111/j.1365-2230.1992.tb00246.x
PMID:1486705
Abstract

Ninety-five adult out-patients with tinea corporis and/or tinea cruris participated in a multicentre open non-comparative study investigating the safety and efficacy of 1-4 once-weekly doses of oral fluconazole 150 mg. Trichophyton rubrum was isolated most frequently (67 of 86 mycologically evaluable patients). A mean of 2.6 doses of fluconazole was administered; patients infected with Candida albicans or Epidermophyton floccosum required an average of 2 doses compared to 3-4 doses in patients infected with other organisms. Clinical cure was obtained in 85 of 92 (92%) patients at the last post-treatment evaluation, with the remaining seven patients being substantially improved. At long-term follow-up, 28-30 days after the last dose, 80 of 91 (88%) patients were assessed as clinically cured, three (3%) patients were improved and eight (9%) patients failed. Among the long-term clinical failures, there was one diagnosis of tinea corporis (3% failure rate) and seven diagnoses of tinea cruris (12% failure rate). Mycological evidence of infection occurred in only 1 of 86 patients assessed at the last post-treatment follow-up. Mycological relapse occurred in nine (11%) patients at long-term follow-up; one patient was infected with Trichophyton mentagrophytes and eight patients were infected with T. rubrum. Relapse occurred in 2 of 29 (7%) patients with tinea corporis and eight of 57 (14%) patients with tinea cruris (one patient who relapsed had both tinea corporis and cruris). There was no correlation between the number of doses received and the mycological response or relapse rates at long-term follow-up.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

95名患有体癣和/或股癣的成年门诊患者参与了一项多中心开放性非对照研究,该研究旨在调查每周1次、每次口服150mg氟康唑,共服用1 - 4剂的安全性和疗效。红色毛癣菌分离率最高(86例可进行真菌学评估的患者中有67例)。平均给予2.6剂氟康唑;白色念珠菌或絮状表皮癣菌感染的患者平均需要2剂,而感染其他真菌的患者平均需要3 - 4剂。在最后一次治疗后评估时,92例患者中有85例(92%)获得临床治愈,其余7例患者有显著改善。在最后一剂后28 - 30天的长期随访中,91例患者中有80例(88%)被评估为临床治愈,3例(3%)患者病情改善,8例(9%)患者治疗失败。在长期临床治疗失败的患者中,有1例体癣诊断(失败率3%)和7例股癣诊断(失败率12%)。在最后一次治疗后随访评估的86例患者中,只有1例有感染的真菌学证据。长期随访中有9例(11%)患者出现真菌学复发;1例患者感染须癣毛癣菌,8例患者感染红色毛癣菌。29例体癣患者中有2例(7%)复发,57例股癣患者中有8例(14%)复发(1例复发患者同时患有体癣和股癣)。长期随访中,接受的剂量数与真菌学反应或复发率之间无相关性。(摘要截选至250字)

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