Filho S T, Cucé L C, Foss N T, Marques S A, Santamaria J R
Departamento de Dermatologia, Universidade Federal de São, R. Botucatu, São Paulo, Brazil.
J Eur Acad Dermatol Venereol. 1998 Sep;11(2):141-6.
Tinea capitis is a common skin disease seen predominantly in children. The standard therapies for this disease are griseofulvin and ketoconazole. Nevertheless, these drugs have drawbacks in that they are only fungistatic and require treatment for at least 6 weeks. Previous studies with oral terbinafine for the treatment of Tinea capitis have shown that this agent is effective when given for 4 weeks, comparable to an 8-week regimen with griseofulvin. To date there is no data on the use of oral terbinafine in Brazilian children.
To assess the efficacy, safety and tolerability of oral terbinafine in short-term treatments (1-, 2- and 4-week treatment) of Tinea capitis in children.
One hundred and thirty-two children aged 1-14 years were enrolled in this study, but only 107 were considered for the final efficacy analysis. Diagnosis included clinical assessment and examination by Wood's light. Confirmation was obtained by direct microscopy and culture for fungus. Terbinafine dosage (125 or 250 mg/day) was adjusted according to patient weight. Efficacy was evaluated both by clinical and mycological assessment. Safety and tolerability variables included data on adverse reaction and clinical laboratory evaluations.
Mycological evaluation in the follow-up visit at week 12 showed negative direct microscopy and culture results in 48.6, 60.5 and 69.7% patients in groups 1-, 2- and 4-week, respectively (n.s.). At week 12, 84.8% patients in group 4-week achieved clinical cure with a significant difference compared to groups 1- and 2-week, 54.3 and 60.5%, respectively (P < 0.01). Adverse reactions were present in 4.8, 6.8 and 10.9% of patients in groups 1-, 2- and 4-week, respectively. terbinafine was not associated with clinically relevant increases in liver function tests.
Terbinafine is an effective, well tolerated and safe antifungal agent for the treatment of Tinea capitis in children. The shorter duration of treatment resulted in lower cure rates. However, it is important to note that depending on the severity of the disease, a 1-week-only treatment can also be effective in this indication.
头癣是一种常见的皮肤病,主要见于儿童。该疾病的标准治疗药物是灰黄霉素和酮康唑。然而,这些药物存在缺点,即它们只是抑菌剂,且需要至少治疗6周。先前关于口服特比萘芬治疗头癣的研究表明,该药物给药4周时有效,与灰黄霉素8周治疗方案相当。迄今为止,尚无关于巴西儿童使用口服特比萘芬的数据。
评估口服特比萘芬在儿童头癣短期治疗(1周、2周和4周治疗)中的疗效、安全性和耐受性。
132名1至14岁的儿童参与了本研究,但最终疗效分析仅纳入107名儿童。诊断包括临床评估和伍德灯检查。通过直接显微镜检查和真菌培养进行确诊。特比萘芬剂量(125或250mg/天)根据患者体重进行调整。通过临床和真菌学评估来评价疗效。安全性和耐受性变量包括不良反应数据和临床实验室评估。
在第12周随访时的真菌学评估显示,1周、2周和4周治疗组分别有48.6%、60.5%和69.7%的患者直接显微镜检查和培养结果为阴性(无显著性差异)。在第12周时,4周治疗组84.8%的患者实现临床治愈,与1周和2周治疗组分别为54.3%和60.5%相比有显著差异(P<0.01)。1周、2周和4周治疗组分别有4.8%、6.8%和10.9%的患者出现不良反应。特比萘芬与肝功能检查的临床相关升高无关。
特比萘芬是一种治疗儿童头癣有效、耐受性良好且安全的抗真菌药物。较短的治疗疗程导致治愈率较低。然而,需要注意的是,根据疾病的严重程度,仅1周的治疗在该适应证中也可能有效。