a Department of Anaesthesia and Critical Care Medicine , St. James's Hospital , Dublin , Ireland.
b Polyvalent Intensive Care Unit , Hospital de São Francisco Xavier, Centro Hospital de Lisboa Ocidental , Lisboa , Portugal.
Expert Rev Anti Infect Ther. 2018 Nov;16(11):839-847. doi: 10.1080/14787210.2018.1528872. Epub 2018 Oct 4.
Invasive candidiasis is the most common fungal infection affecting critically ill adults. International guidelines provide differing recommendations for first-line antifungal therapy, with echinocandins considered first-line in the majority. Amphotericin B has broad activity and low minimum inhibitory concentration resistance patterns across most Candida species and guidance away from its use should be supported by the available evidence. Areas Covered: A systematic literature review was conducted from August to September 2017 to determine whether treatment with echinocandins or other available drugs, namely voriconazole, confers a therapeutic or survival benefit over amphotericin B in critically ill adults with invasive candidiasis. Inclusion criteria were: (1) studies describing critically ill adults with invasive candidiasis, (2) studies describing therapeutic benefit or survival as an outcome, and (3) studies comparing amphotericin B, deoxycholate or lipid preparations, with any newer antifungal agent. Eight studies were included in the final review, incorporating 2352 unique patients. No difference in treatment efficacy or mortality outcomes in critically ill patients with invasive candidiasis receiving an amphotericin B formulation compared with those receiving an echinocandin or voriconazole was shown. Expert Commentary: We conclude that in the existing literature, there is no evidence that choice between echinocandins, voriconazole, or amphotericin B formulations as first-line therapy for critically ill adults with invasive candidiasis is associated with a therapeutic or survival benefit. Clinicians must therefore consider other factors in the selection of first-line therapy.
侵袭性念珠菌病是影响危重病成人最常见的真菌感染。国际指南对一线抗真菌治疗提供了不同的建议,大多数指南将棘白菌素类药物作为一线治疗药物。两性霉素 B 在大多数念珠菌属中具有广泛的活性和低最小抑菌浓度耐药模式,并且应该根据现有证据支持避免使用该药物。
2017 年 8 月至 9 月进行了系统文献回顾,以确定在患有侵袭性念珠菌病的危重病成人中,使用棘白菌素类药物或其他可用药物(即伏立康唑)与两性霉素 B 相比是否具有治疗或生存获益。纳入标准为:(1)描述患有侵袭性念珠菌病的危重病成人的研究;(2)描述治疗效果或生存作为结局的研究;(3)比较两性霉素 B、去氧胆酸盐或脂质制剂与任何新型抗真菌药物的研究。最终综述纳入了 8 项研究,共纳入了 2352 名独特患者。与接受棘白菌素类药物或伏立康唑治疗的患者相比,接受两性霉素 B 制剂治疗的侵袭性念珠菌病危重病患者在治疗效果或死亡率方面没有差异。
我们的结论是,在现有文献中,没有证据表明在选择棘白菌素类药物、伏立康唑或两性霉素 B 制剂作为侵袭性念珠菌病危重病成人的一线治疗药物时,与治疗或生存获益相关。因此,临床医生在选择一线治疗药物时必须考虑其他因素。