Gupta A K, Solomon R S, Adam P
Department of Medicine, Sunnybrook Health Science Center, Toronto, Ontario, Canada.
Br J Dermatol. 1998 Jul;139(1):104-6. doi: 10.1046/j.1365-2133.1998.02323.x.
Twenty-seven children (12 boys, 15 girls, age range 3-11 years, weight range 10-40 kg) were treated with itraconazole oral solution 10 mg/mL given as pulse therapy for tinea capitis. The dosage regimen was 3 mg/kg per day given once daily in a fasting state with each pulse lasting 1 week. The first two pulses were separated by a 2-week off-drug period, and the second and third pulses had a 3-week period without drug between them. For each patient a second and third pulse were administered if there was clinical evidence of tinea capitis at the time-point when the next pulse was due. The overall severity of tinea capitis at pretherapy was classified as mild, moderate or severe with the aetiology being: Trichophyton tonsurans, 24 patients; T. violaceum, two patients and Microsporum canis, one patient. In 19 evaluable patients, 12 weeks after starting therapy, the numbers of pulses of itraconazole oral solution required to produce complete cure were, according to the severity of disease, mild tinea capitis (one pulse: four patients; two pulses: five), moderate disease (one pulse: two patients; two pulses: two; three pulses: two), and severe disease (three pulses: three patients). One patient with moderate severity tinea capitis was clinically clear after three pulses of therapy but mycological examination was positive. Seven patients were lost to follow-up and one discontinued therapy because of nausea. Itraconazole oral solution 3 mg/kg per day was generally well tolerated. Three children developed gastrointestinal adverse effects which were considered to be minor or 'nuisance' effects. The data from this preliminary report need to be confirmed in a larger group of patients. It remains to be seen whether itraconazole oral solution will become a practical alternative to the antifungal agents available in a liquid preparation for the treatment of tinea capitis.
27名儿童(12名男孩,15名女孩,年龄范围3至11岁,体重范围10至40千克)接受了10mg/mL伊曲康唑口服溶液治疗头癣的脉冲疗法。给药方案为每日3mg/kg,空腹状态下每日给药一次,每个脉冲疗程持续1周。前两个脉冲疗程之间有2周的停药期,第二个和第三个脉冲疗程之间有3周的停药期。对于每位患者,如果在下一个脉冲疗程预定时间点有头癣的临床证据,则给予第二个和第三个脉冲疗程。治疗前头癣的总体严重程度分为轻度、中度或重度,病因如下:断发毛癣菌,24例患者;紫色毛癣菌,2例患者;犬小孢子菌,1例患者。在19例可评估患者中,治疗开始12周后,根据疾病严重程度,治愈所需伊曲康唑口服溶液的脉冲疗程数为:轻度头癣(一个脉冲疗程:4例患者;两个脉冲疗程:5例),中度疾病(一个脉冲疗程:2例患者;两个脉冲疗程:2例;三个脉冲疗程:2例),重度疾病(三个脉冲疗程:3例患者)。1例中度头癣患者在三个脉冲疗程治疗后临床症状消失,但真菌学检查呈阳性。7例患者失访,1例因恶心停药。每日3mg/kg的伊曲康唑口服溶液总体耐受性良好。3名儿童出现胃肠道不良反应,被认为是轻微或“烦扰性”反应。本初步报告的数据需要在更大规模的患者群体中得到证实。伊曲康唑口服溶液是否会成为治疗头癣的液体制剂中现有抗真菌药物的实用替代品,仍有待观察。