伊曲康唑治疗皮肤癣的随机对照试验:三种不同剂量方案的比较

IF 0.1 Q4 DERMATOLOGY
Abhishek Lachure, Bhabani S T P Singh, B. Kar, Liza Mohapatra, Nibedita Dixit
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引用次数: 0

摘要

简介:皮肤真菌病是由皮肤真菌引起的角化组织的浅表真菌感染。按标准剂量和时间使用伊曲康唑通常导致治疗失败。目的:比较伊曲康唑三种不同剂量方案治疗皮肤癣的疗效和安全性。材料与方法:在征得患者同意后,将患者随机分为A、B、C三组。在四周的时间里,A、B、C组患者分别接受伊曲康唑100mg / d, 200mg / d, 5mg /kg或400mg / d(以较轻者为准),分两次服用。所有患者建议使用外用埃伯康唑乳膏每日2次,左西替利嗪每日5毫克。在基线就诊时进行氢氧化钾(KOH)、真菌培养、全血细胞计数(CBC)和肝功能检查(LFT),并在4周内重复。两次就诊均进行临床评估。结果:治疗结束后,A、B、C组患者真菌成分KOH阴性的比例分别为21.4%、19%、17%。治疗后,A组、B组和C组分别有19%、17.5%和19.5%的患者培养真菌元素阴性。在四周结束时,三组的病变计数、体表面积受累、红斑和瘙痒均有统计学意义上的显著减少。然而,治疗4周后,三组患者的临床结局和真菌学状况无显著差异。结论:我们的研究表明,在4周结束时,较高剂量的伊曲康唑并不比常规剂量更有效,也没有比常规剂量更有优势。因此,我们建议长期(4周以上)依曲康唑常规剂量治疗,以达到充分治愈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Randomized control trial of itraconazole in the treatment of dermatophytosis: comparison of three different dose regimens
Introduction: Dermatophytosis is a superficial fungal infection of keratinized tissue caused by dermatophytes. The use of itraconazole in the standard dose and duration is commonly resulting in treatment failure. Aims and Objectives: To compare the efficacy and safety of three different dosage regimens of itraconazole in the treatment of dermatophytosis. Materials and Methods: Patients were enrolled and randomly assigned to three different groups A, B, and C after obtaining the proper consent. For four weeks, patients in Groups A, B, and C received itraconazole 100 mg once daily, 200 mg once daily, and 5 mg/kg or 400 mg daily, whichever was lesser, in two divided doses, respectively. All patients were advised to use topical eberconazole cream twice daily and levocetirizine 5 mg daily. Potassium hydroxide (KOH), culture for fungus, complete blood count (CBC), and liver function test (LFT) were done at the baseline visit and repeated in 4 weeks. A clinical assessment was done at both visits. Result: KOH was negative for fungal elements in 21.4%, 19%, and 17% of patients in groups A, B, and C respectively, after the completion of therapy. The culture was negative for fungal elements in 19%, 17.5%, and 19.5% of patients in groups A, B, and C respectively, post-therapy. At the end of four weeks, there was a statistically significant decrease in lesion count, body surface area involvement, erythema, and itching within all three groups. However, after 4 weeks of therapy, there was no significant difference in clinical outcome or mycological status among the three groups. Conclusion: Our study concludes that the higher dose of itraconazole does not prove to be more efficacious and has no added advantage over the conventional dose in the treatment of dermatophytosis at the end of four weeks. Therefore, we suggest for long-term (more than 4 weeks) itraconazole therapy with the conventional dose to achieve an adequate cure.
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CiteScore
0.50
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