Herbrecht R, Neuville S, Letscher-Bru V, Natarajan-Amé S, Lortholary O
Departement d'Hématologie et d'Oncologie, H pitaux Universitaires de Strasbourg, France.
Drugs Aging. 2000 Nov;17(5):339-51. doi: 10.2165/00002512-200017050-00002.
Fungal infections are a leading cause of mortality in patients with neutropenia. Candidiasis and aspergillosis account for most invasive fungal infections. General prophylactic measures include strict hygiene and environmental measures. Haemopoietic growth factors shorten the duration of neutropenia and thus may reduce the incidence of fungal infections. Fluconazole is appropriate for antifungal prophylaxis and should be offered to patients with prolonged neutropenia, such as high-risk patients with leukaemia undergoing remission induction or consolidation therapy and high-risk stem cell transplant recipients. Empirical antifungal therapy is mandatory in patients with persistent febrile neutropenia who fail to respond to broad-spectrum antibacterials. Intravenous amphotericin B at a daily dose of 0.6 to 1 mg/kg is preferred whenever aspergillosis cannot be ruled out. Lipid formulations of amphotericin B have demonstrated similar efficacy and are much better tolerated. Fluconazole is the best choice for acute candidiasis in stable patients; amphotericin B should be used in patients with unstable disease. Use of fluconazole is restricted by the existence of resistant strains (Candida krusei and, to a lesser extent, C. glabrata). Amphotericin B still remains the gold standard for invasive aspergillosis. Lipid formulations of amphotericin B are effective in aspergillosis and because they are less nephrotoxic are indicated in patients with poor renal function. Itraconazole is an alternative in patients who have good intestinal function and are able to eat. Mucormycosis, trichosporonosis, fusariosis and cryptococcosis are less common but require specific management. New antifungal agents, especially new azoles, are under development. Their broad in vitro spectrum and preliminary clinical results are promising.
真菌感染是中性粒细胞减少患者死亡的主要原因。念珠菌病和曲霉病占大多数侵袭性真菌感染。一般预防措施包括严格的卫生和环境措施。造血生长因子可缩短中性粒细胞减少的持续时间,从而可能降低真菌感染的发生率。氟康唑适用于抗真菌预防,应给予长期中性粒细胞减少的患者,如正在接受缓解诱导或巩固治疗的高危白血病患者以及高危干细胞移植受者。对于对广谱抗菌药物无反应的持续性发热性中性粒细胞减少患者,必须进行经验性抗真菌治疗。只要不能排除曲霉病,每日剂量为0.6至1mg/kg的静脉注射两性霉素B是首选。两性霉素B的脂质制剂已显示出相似的疗效,且耐受性要好得多。氟康唑是稳定患者急性念珠菌病的最佳选择;病情不稳定的患者应使用两性霉素B。氟康唑的使用受到耐药菌株(克柔念珠菌,光滑念珠菌程度较轻)存在的限制。两性霉素B仍然是侵袭性曲霉病的金标准。两性霉素B的脂质制剂对曲霉病有效,并且由于它们的肾毒性较小,适用于肾功能差的患者。伊曲康唑是肠道功能良好且能够进食的患者的替代选择。毛霉病、毛孢子菌病、镰刀菌病和隐球菌病较少见,但需要特殊处理。新型抗真菌药物,尤其是新型唑类药物正在研发中。它们广泛的体外活性谱和初步临床结果很有前景。