Riley Treavor T, Muzny Christina A, Swiatlo Edwin, Legendre Davey P
Wingate University, Hendersonville, NC, USA
University of Alabama at Birmingham, AL, USA.
Ann Pharmacother. 2016 Sep;50(9):747-57. doi: 10.1177/1060028016655425. Epub 2016 Jun 15.
To review the current literature for the pathogenesis of mucormycosis, discuss diagnostic strategies, and evaluate the efficacy of polyenes, triazoles, and echinocandins as pharmacological treatment options.
An electronic literature search was conducted in PubMed using the MESH terms Rhizopus, zygomycetes, zygomycosis, Mucorales and mucormycosis, with search terms amphotericin B, micafungin, anidulafungin, caspofungin, extended infusion amphotericin B, liposomal amphotericin B, combination therapy, triazole, posaconazole, isavuconazole, diagnosis, and clinical manifestations.
Studies written in the English language from January 1960 to March 2016 were considered for this review article. All search results were reviewed, and the relevance of each article was determined by the authors independently.
Mucormycosis is a rare invasive fungal infection with an exceedingly high mortality and few therapeutic options. It has a distinct predilection for invasion of endothelial cells in the vascular system, which is likely important in dissemination of disease from a primary focus of infection. Six distinct clinical syndromes can occur in susceptible hosts, including rhino-orbital-cerebral, pulmonary, gastrointestinal, cutaneous, widely disseminated, and miscellaneous infection.
Diagnosis of mucormycosis is typically difficult to make based on imaging studies, sputum culture, bronchoalveolar lavage culture, or needle aspirate. Surgical debridement prior to dissemination of infection improves clinical outcomes. Surgery combined with early, high-dose systemic antifungal therapy yields greater than a 1.5-fold increase in survival rates. The Mucorales are inherently resistant to most widely used antifungal agents. Amphotericin B is appropriate for empirical therapy, whereas posaconazole and isavuconazole are best reserved for de-escalation, refractory cases, or patients intolerant to amphotericin B.
回顾当前关于毛霉病发病机制的文献,讨论诊断策略,并评估多烯类、三唑类和棘白菌素类作为药物治疗选择的疗效。
在PubMed中使用医学主题词“根霉属”“接合菌纲”“接合菌病”“毛霉目”和“毛霉病”进行电子文献检索,并使用检索词“两性霉素B”“米卡芬净”“阿尼芬净”“卡泊芬净”“延长输注两性霉素B”“脂质体两性霉素B”“联合治疗”“三唑类”“泊沙康唑”“艾沙康唑”“诊断”和“临床表现”。
本综述文章纳入1960年1月至2016年3月以英文撰写的研究。对所有检索结果进行了回顾,每篇文章的相关性由作者独立确定。
毛霉病是一种罕见的侵袭性真菌感染,死亡率极高且治疗选择有限。它对血管系统中的内皮细胞具有明显的侵袭倾向,这可能在疾病从原发性感染灶传播中起重要作用。易感宿主可出现六种不同的临床综合征,包括鼻眶脑型、肺型、胃肠型、皮肤型、广泛播散型和其他感染。
基于影像学检查、痰培养支气管肺泡灌洗培养或针吸活检通常难以诊断毛霉病。在感染播散前进行手术清创可改善临床结局。手术联合早期、大剂量全身抗真菌治疗可使生存率提高超过1.5倍。毛霉目对大多数广泛使用的抗真菌药物具有固有耐药性。两性霉素B适用于经验性治疗,而泊沙康唑和艾沙康唑最好用于降阶梯治疗、难治性病例或不耐受两性霉素B的患者。