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伊曲康唑脉冲疗法与特比萘芬连续给药治疗趾甲甲真菌病的比较

Itraconazole pulse therapy vs continuous terbinafine dosing for toenail onychomycosis.

作者信息

Kejda J

机构信息

Thomayer Hospital, Department of Dermatovernercology, Prague, Czech Republic.

出版信息

Postgrad Med. 1999 Jul;Spec No:12-5.

Abstract

In this open, randomized, parallel-group, the efficacy and safety of itraconazole pulse therapy (1 week 400 mg daily, 3 months) was evaluated in comparison with continuous terbinafine dosing (250 mg daily, 3 months) for the treatment of toenail onychomycosis. The study included a total of 51 patients with distal subungual onychomycosis of the toenails confirmed by microscopy and positive culture. Twenty-six patients received itraconazole pulse therapy and 25 patients received continuous terbinafine therapy. A minimum of 50% nail involvement was a requirement for inclusion. In total, 153 nails (121 toenails) were treated with itraconazole pulse therapy and 162 nails (122 toenails) were treated with continuous terbinafine therapy. Patients were evaluated every third month for 9 months after treatment. Photographs were taken at each visit. Clinical success and mycologic cure (negative potassium hydroxide preparation and culture) were the main outcome measures. Mycologic cure rates were 75% in the itraconazole pulse group and 76% in the continuous terbinafine group at month 12; the corresponding clinical response rates were 77% and 68%, respectively. Six (23%) patients in the itraconazole group reported 7 adverse events and 13 (52%) patients in the terbinafine group reported 19 adverse events. In the terbinafine group, 12% discontinued therapy due to adverse events; no patients in the itraconazole arm discontinued. Both therapies showed comparable efficacy, though baseline nail severity was greater in the itraconazole group, and adverse effects were greater in the terbinafine group.

摘要

在这项开放性、随机、平行组研究中,比较了伊曲康唑冲击疗法(每日400mg,共1周,持续3个月)与特比萘芬连续给药(每日250mg,共3个月)治疗趾甲甲真菌病的疗效和安全性。该研究共纳入51例经显微镜检查和培养阳性确诊为远端甲下型趾甲甲真菌病的患者。26例患者接受伊曲康唑冲击疗法,25例患者接受特比萘芬连续疗法。纳入标准为至少50%的趾甲受累。总计,153枚指甲(其中121枚趾甲)接受了伊曲康唑冲击疗法,162枚指甲(其中122枚趾甲)接受了特比萘芬连续疗法。治疗后每三个月对患者进行一次评估,为期9个月。每次就诊时均拍摄照片。主要观察指标为临床治愈和真菌学治愈(氢氧化钾制剂和培养阴性)。在第12个月时,伊曲康唑冲击组的真菌学治愈率为75%,特比萘芬连续组为76%;相应的临床有效率分别为77%和68%。伊曲康唑组有6例(23%)患者报告了7起不良事件,特比萘芬组有13例(52%)患者报告了19起不良事件。在特比萘芬组中,12%的患者因不良事件而停药;伊曲康唑组无患者停药。两种疗法疗效相当,尽管伊曲康唑组的基线趾甲严重程度更高,且特比萘芬组的不良反应更多。

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