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特比萘芬(兰美抒)成功治疗慢性足癣(拖鞋型)

Successful treatment of chronic tinea pedis (moccasin type) with terbinafine (Lamisil).

作者信息

Savin R

出版信息

Clin Exp Dermatol. 1989 Mar;14(2):116-9. doi: 10.1111/j.1365-2230.1989.tb00906.x.

Abstract

Terbinafine (Lamisil) is the first safe and effective orally active agent in a new family of antifungal drugs, the allylamines. The drug has a unique site of action on sterol synthesis due to its inhibition of squalene epoxidase. The drug is highly effective against dermatophytes in vitro, and in placebo controlled trials, it is effective both topically and orally against dermatophytes. In the study reported here, terbinafine has been compared to griseofulvin in patients with moccasin type tinea pedis. Terbinafine was given at 125 mg b.i.d. and griseofulvin was given at 250 mg (microsize) b.i.d. Thirty-six patients were enrolled in a randomized, double-blind study. Patients were evaluated weekly by mycological culture, microscopy and clinical signs and symptoms for 6 weeks during therapy and at follow-up 2 weeks later. Twenty-eight of the 36 patients were evaluable for drug efficacy. Twelve out of sixteen (75%) of the terbinafine group were mycologically and clinically cured by the end of therapy (6 weeks) and 14/16 (88%) were cured at the time of follow-up 2 weeks later. Two patients were mycologically cured, but moderate signs or symptoms were present at follow-up. In the griseofulvin-treated group 3/12 (27%) were cured at the end of treatment and 5/11 (45%) at follow-up evaluation. Follow-up after 6-15 months showed continued resolution of the terbinafine-treated patients, but relapse of infection in griseofulvin-treated patients. There were two side-effects during terbinafine treatment (one gastro-intestinal, one skin allergy), and no significant changes in haematological, hepatic enzyme or renal blood tests done weekly.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

特比萘芬(兰美抒)是新型抗真菌药烯丙胺类中首个安全有效的口服活性药物。由于其抑制角鲨烯环氧化酶,该药物在固醇合成方面具有独特的作用位点。此药在体外对皮肤癣菌高度有效,在安慰剂对照试验中,其局部和口服给药对皮肤癣菌均有效。在本报告的研究中,对患有拖鞋型足癣的患者,将特比萘芬与灰黄霉素进行了比较。特比萘芬给药剂量为125毫克,每日两次,灰黄霉素给药剂量为250毫克(微晶型),每日两次。36名患者参与了一项随机双盲研究。在治疗的6周期间及2周后的随访中,每周通过真菌培养、显微镜检查以及临床体征和症状对患者进行评估。36名患者中有28名可对药物疗效进行评估。特比萘芬组16名患者中有12名(75%)在治疗结束时(6周)真菌学和临床治愈,2周后的随访时14/16(88%)治愈。2名患者真菌学治愈,但随访时有中度体征或症状。在灰黄霉素治疗组,治疗结束时3/12(27%)治愈,随访评估时5/11(45%)治愈。6至15个月后的随访显示,特比萘芬治疗的患者病情持续缓解,而灰黄霉素治疗的患者感染复发。特比萘芬治疗期间出现了两例副作用(一例胃肠道反应,一例皮肤过敏),每周进行的血液学、肝酶或肾功检查无显著变化。(摘要截选至250字)

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