Hume A L, Kerkering T M
Drug Intell Clin Pharm. 1983 Mar;17(3):169-74. doi: 10.1177/106002808301700301.
The treatment of most fungal infections is difficult, at best. Antifungal therapy is complicated by the development of resistant organisms and by the toxicity of many agents. Ketoconazole, an orally active imidazole derivative, has been approved by the Food and Drug Administration for the treatment of candidiasis, chronic mucocutaneous candidiasis, oral thrush, candiduria, coccidioidomycosis, histoplasmosis, chromomycosis, and paracoccidioidomycosis. At present, there is very little peer review literature on ketoconazole's effectiveness for several of its approved indications. Gastrointestinal side effects account for the majority of reported adverse reactions; however, preliminary evidence suggests that higher dosages of ketoconazole may decrease adrenal steroidogenesis. Currently, ketoconazole 200-400 mg/d is recommended; the duration of therapy remains to be firmly established. Until well-designed clinical trials are completed and ketoconazole's effectiveness is compared to that of established antifungal agents, its use should be limited.
大多数真菌感染的治疗即便往好里说也很困难。抗真菌治疗因耐药菌的出现以及许多药物的毒性而变得复杂。酮康唑是一种口服活性咪唑衍生物,已获美国食品药品监督管理局批准用于治疗念珠菌病、慢性黏膜皮肤念珠菌病、鹅口疮、念珠菌尿症、球孢子菌病、组织胞浆菌病、着色芽生菌病和副球孢子菌病。目前,关于酮康唑在其多个获批适应症方面疗效的同行评议文献非常少。胃肠道副作用是报告的不良反应的主要原因;然而,初步证据表明,较高剂量的酮康唑可能会降低肾上腺类固醇生成。目前,推荐使用酮康唑200 - 400毫克/天;治疗持续时间仍有待确定。在精心设计的临床试验完成并将酮康唑的疗效与已有的抗真菌药物进行比较之前,其使用应受到限制。