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治疗头癣:酮康唑应取代灰黄霉素吗?

Treating tinea capitis: should ketoconazole replace griseofulvin?

作者信息

Tanz R R, Hebert A A, Esterly N B

机构信息

Division of General and Emergency Pediatrics, Northwestern University Medical School, Chicago, IL.

出版信息

J Pediatr. 1988 Jun;112(6):987-91. doi: 10.1016/s0022-3476(88)80232-4.

DOI:10.1016/s0022-3476(88)80232-4
PMID:3373408
Abstract

We undertook a randomized double-blind comparison of griseofulvin and ketoconazole for the treatment of tinea capitis. The outcome was based on fungal culture results and changes in clinical signs and symptoms determined by an assessment system that yielded a severity score. Patients were evaluated at 4-week intervals for 12 weeks. Seventy-nine patients were enrolled; 46 received griseofulvin, and 33 received ketoconazole. Forty-eight patients (26 griseofulvin, 22 ketoconazole) were considered evaluable. Pathogenic fungi were isolated from 78% of the enrolled and 87% of the evaluable patients. Trichophyton tonsurans was the predominant dermatophyte isolated. Potassium hydroxide preparation correlated poorly with culture results (sensitivity 59%). Of 22 evaluable ketoconazole patients, 16 (73%) were considered to have been treated successfully; 25 of 26 (96%) patients who received griseofulvin were successfully treated (chi-square = 3.54, p less than 0.10). The proportion of culture-positive patients at each follow-up visit appeared somewhat greater for the ketoconazole-treated group than for the griseofulvin-treated group, but the differences were not statistically significant. Analysis of severity scores revealed no significant differences between the groups (t test and Mann-Whitney U test). No significant hepatotoxicity or other adverse reactions were observed. We conclude that griseofulvin should remain the drug of choice for treating tinea capitis.

摘要

我们对灰黄霉素和酮康唑治疗头癣进行了一项随机双盲比较。结果基于真菌培养结果以及由一个产生严重程度评分的评估系统所确定的临床体征和症状的变化。患者每隔4周接受评估,为期12周。79名患者入组;46名接受灰黄霉素治疗,33名接受酮康唑治疗。48名患者(26名灰黄霉素治疗组,22名酮康唑治疗组)被认为可评估。从78%的入组患者和87%的可评估患者中分离出致病真菌。断发毛癣菌是分离出的主要皮肤癣菌。氢氧化钾制剂与培养结果的相关性较差(敏感性59%)。在22名可评估的酮康唑治疗患者中,16名(73%)被认为治疗成功;接受灰黄霉素治疗的26名患者中有25名(96%)治疗成功(卡方检验=3.54,p<0.10)。酮康唑治疗组每次随访时培养阳性患者的比例似乎比灰黄霉素治疗组略高,但差异无统计学意义。严重程度评分分析显示两组之间无显著差异(t检验和曼-惠特尼U检验)。未观察到明显的肝毒性或其他不良反应。我们得出结论,灰黄霉素应仍然是治疗头癣的首选药物。

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