Kimura Muneyoshi, Araoka Hideki, Yamamoto Hisashi, Asano-Mori Yuki, Nakamura Shigeki, Yamagoe Satoshi, Ohno Hideaki, Miyazaki Yoshitsugu, Abe Masahiro, Yuasa Mitsuhiro, Kaji Daisuke, Kageyama Kosei, Nishida Aya, Ishiwata Kazuya, Takagi Shinsuke, Yamamoto Go, Uchida Naoyuki, Izutsu Koji, Wake Atsushi, Taniguchi Shuichi, Yoneyama Akiko
Department of Infectious Diseases, Toranomon Hospital, Tokyo, Japan.
Department of Infectious Diseases, Toranomon Hospital, Tokyo, Japan
Antimicrob Agents Chemother. 2017 Mar 24;61(4). doi: 10.1128/AAC.01791-16. Print 2017 Apr.
Few data on breakthrough candidemia (BC), defined as candidemia that develops on administration of antifungal agents (AFAs), in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients are available. The medical and microbiological records of recipients of an allo-HSCT obtained between December 2008 and December 2014 were reviewed. Of 768 allo-HSCT cases, 26 developed BC. Among the 26 causative strains, 22 strains were stored and identified by sequencing. The following species were isolated: (9 strains), (4 strains), (3 strains), and other species (6 strains). The AFAs being used when BC developed were micafungin (17 cases), liposomal amphotericin B (5 cases), itraconazole (2 cases), and voriconazole (2 cases). All 17 cases who developed BC during micafungin administration were administered 150 mg/day of micafungin. The susceptibilities of the causative species to the administered AFAs when breakthrough occurred ranged from susceptible to resistant. Especially, 85% of the species that caused BC during micafungin administration were susceptible to micafungin. Additionally, 75% of the strains were wild type for susceptibility to the administered AFAs when breakthrough occurred. Systemic steroid administration and a longer severe neutropenic phase (≥5 days) were independent risk factors for BC ( = 0.016 and = 0.015, respectively). BC developed in allo-HSCT recipients even when they received a sufficient dose of AFA, including micafungin, to which the causative species were susceptible and/or had wild-type susceptibility Systemic steroid administration and a longer severe neutropenic phase were host-based factors associated with BC.
关于突破性念珠菌血症(BC)的数据较少,BC定义为在接受抗真菌药物(AFA)治疗期间发生的念珠菌血症,目前尚无关于异基因造血干细胞移植(allo-HSCT)受者的相关数据。我们回顾了2008年12月至2014年12月期间接受allo-HSCT的受者的医学和微生物学记录。在768例allo-HSCT病例中,有26例发生了BC。在26株致病菌株中,保存了22株并通过测序进行鉴定。分离出的菌种如下:(9株)、(4株)、(3株)和其他菌种(6株)。发生BC时使用的AFA有米卡芬净(17例)、脂质体两性霉素B(5例)、伊曲康唑(2例)和伏立康唑(2例)。在使用米卡芬净期间发生BC的17例患者均接受了每日150mg的米卡芬净治疗。突破性感染发生时,致病菌种对所使用的AFA的敏感性范围从敏感到耐药。特别是,在使用米卡芬净期间引起BC的菌种中,85%对米卡芬净敏感。此外,75%的菌株在突破性感染发生时对所使用的AFA的敏感性为野生型。全身使用类固醇和较长的严重中性粒细胞减少期(≥5天)是BC的独立危险因素(分别为=0.016和=0.015)。即使allo-HSCT受者接受了足够剂量的AFA,包括致病菌种敏感和/或具有野生型敏感性的米卡芬净,仍会发生BC。全身使用类固醇和较长的严重中性粒细胞减少期是与BC相关的基于宿主的因素。