a Division of Haematology , Saitama Medical Center, Jichi Medical University , Saitama , Japan.
Infect Dis (Lond). 2018 Apr;50(4):280-288. doi: 10.1080/23744235.2017.1396621. Epub 2017 Oct 31.
Consensus has yet to be reached regarding secondary prophylaxis in allogeneic hematopoietic stem cell transplantation (HSCT) with a complete resolution of invasive aspergillosis (IA) confirmed by chest computed tomography (CT).
We retrospectively evaluated the feasibility of antifungal prophylaxis with fluconazole in allogeneic HSCT recipients who had previously developed IA which showed complete resolution as confirmed by chest CT before HSCT. Consecutive adult patients who underwent allogeneic HSCT at our institution and who had received fluconazole as systemic antifungal prophylaxis from June 2007 to January 2015 were included. We compared the clinical outcomes between patients with a past history of IA who showed a complete resolution of chest CT abnormalities (n = 13) and those without a previous history of IA (n = 137).
The cumulative incidence of proven or probable IA was 8.8% in the group without a past history of IA and 0.0% in the group with a past history of IA (p = .268). The cumulative incidence of proven or probable invasive fungal disease (IFD) within 100 days after allogeneic HSCT was 10.9% in the group without a past history of IA and 15.4% in the group with a past history of IA (p = .647). Fluconazole was switched to anti-mould agents in two-thirds of the patients in each group by day 100 after HSCT.
Fluconazole was confirmed to be an acceptable prophylactic agent early after allogeneic HSCT in appropriately selected patients.
对于经胸部计算机断层扫描(CT)证实完全缓解的异基因造血干细胞移植(HSCT)中侵袭性曲霉菌病(IA),尚未达成关于二级预防的共识。
我们回顾性评估了氟康唑在异基因 HSCT 受者中的抗真菌预防的可行性,这些受者在 HSCT 前曾发生过经胸部 CT 证实完全缓解的 IA。本研究纳入了 2007 年 6 月至 2015 年 1 月期间在我院接受异基因 HSCT 且接受氟康唑全身抗真菌预防的连续成年患者。我们比较了胸部 CT 异常完全缓解(n=13)和无既往 IA 史(n=137)患者的临床结局。
无既往 IA 史组确诊或拟诊 IA 的累积发生率为 8.8%,而有既往 IA 史组为 0.0%(p=0.268)。无既往 IA 史组和有既往 IA 史组在异基因 HSCT 后 100 天内确诊或拟诊侵袭性真菌感染(IFD)的累积发生率分别为 10.9%和 15.4%(p=0.647)。在 HSCT 后 100 天内,两组中各有三分之二的患者将氟康唑转换为抗真菌药物。
氟康唑被证实是一种合适选择的患者在异基因 HSCT 后早期可接受的预防药物。