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氟康唑用于侵袭性念珠菌病的治疗:15年后我们处于什么位置?

Fluconazole for the management of invasive candidiasis: where do we stand after 15 years?

作者信息

Charlier C, Hart E, Lefort A, Ribaud P, Dromer F, Denning D W, Lortholary O

机构信息

Université Paris V, Service des Maladies Infectieuses et Tropicales, Hôpital Necker Enfants Malades, Paris, France.

出版信息

J Antimicrob Chemother. 2006 Mar;57(3):384-410. doi: 10.1093/jac/dki473. Epub 2006 Jan 31.

Abstract

Candida spp. are responsible for most of the fungal infections in humans. Available since 1990, fluconazole is well established as a leading drug in the setting of prevention and treatment of mucosal and invasive candidiasis. Fluconazole displays predictable pharmacokinetics and an excellent tolerance profile in all groups, including the elderly and children. Fluconazole is a fungistatic drug against yeasts and lacks activity against moulds. Candida krusei is intrinsically resistant to fluconazole, and other species, notably Candida glabrata, often manifest reduced susceptibility. Emergence of azole-resistant strains as well as discovery of new antifungal drugs (new triazoles and echinocandins) have raised important questions about its use as a first line drug. The aim of this review is to summarize the main available data on the position of fluconazole in the prophylaxis or curative treatment of invasive Candida spp. infections. Fluconazole is still a major drug for antifungal prophylaxis in the setting of transplantation (solid organ and bone marrow), intensive care unit, and in neutropenic patients. Prophylactic fluconazole still has a place in HIV-positive patients in viro-immunological failure with recurrent mucosal candidiasis. Fluconazole can be used in adult neutropenic patients with systemic candidiasis, as long as the species identified is a priori susceptible. Among non-neutropenic patients with candidaemia fluconazole is one of the first line drugs for susceptible species. Cases reports and uncontrolled studies have also reported its efficacy in the setting of osteoarthritis, endophthalmitis, meningitis, endocarditis and peritonitis caused by Candida spp. among immunocompetent adults. In paediatrics, fluconazole is a well tolerated and major prophylactic drug for high-risk neonates, as well as an alternative treatment for neonatal candidiasis. Importantly 15 years after its introduction in the antifungal armamentarium, fluconazole is still a first line treatment option in several cases of invasive candidiasis. Its prophylactic use should however be limited to selected high-risk patients to limit the risk of emergence of azole-resistant strains.

摘要

念珠菌属是人类大多数真菌感染的病原体。氟康唑自1990年上市以来,已被公认为预防和治疗黏膜及侵袭性念珠菌病的主要药物。氟康唑在包括老年人和儿童在内的所有人群中都表现出可预测的药代动力学和良好的耐受性。氟康唑是一种对酵母菌有抑菌作用的药物,对霉菌无活性。克柔念珠菌对氟康唑天然耐药,其他菌种,尤其是光滑念珠菌,通常表现出敏感性降低。唑类耐药菌株的出现以及新抗真菌药物(新三唑类和棘白菌素类)的发现,引发了关于其作为一线药物使用的重要问题。本综述的目的是总结关于氟康唑在侵袭性念珠菌属感染的预防或治疗中的地位的主要现有数据。在移植(实体器官和骨髓)、重症监护病房以及中性粒细胞减少患者中,氟康唑仍然是抗真菌预防的主要药物。预防性使用氟康唑在免疫病毒学失败且反复发生黏膜念珠菌病的HIV阳性患者中仍有一席之地。氟康唑可用于患有系统性念珠菌病的成年中性粒细胞减少患者,前提是预先确定所鉴定的菌种敏感。在念珠菌血症的非中性粒细胞减少患者中,氟康唑是敏感菌种的一线药物之一。病例报告和非对照研究也报道了其在免疫功能正常的成年人中由念珠菌属引起的骨关节炎、眼内炎、脑膜炎、心内膜炎和腹膜炎中的疗效。在儿科,氟康唑是高危新生儿耐受性良好的主要预防药物,也是新生儿念珠菌病的替代治疗药物。重要的是,在其被纳入抗真菌药物库15年后,氟康唑在几例侵袭性念珠菌病中仍然是一线治疗选择。然而,其预防性使用应限于选定的高危患者,以限制唑类耐药菌株出现的风险。

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