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异基因干细胞移植后延迟性侵袭性曲霉病的预防

Delayed ABLC prophylaxis after allogeneic stem-cell transplantation.

作者信息

Jansen Jan, Akard Luke P, Wack Matthew F, Thompson James M, Dugan Michael J, Leslie Jill K, Mattison Reid

机构信息

Indiana Blood and Marrow Transplantation, 1500 Albany #911, Beech Grove, IN 46107, USA.

出版信息

Mycoses. 2006 Sep;49(5):397-404. doi: 10.1111/j.1439-0507.2006.01264.x.

Abstract

Invasive fungal infections (IFI) are frequent causes of mortality after allogeneic stem-cell transplantation (SCT). A very important risk factor for IFI is the use of steroids. We used a risk-based chemoprevention in an open-labelled pilot study. All patients received oral fluconazole or itraconazole (200-400 mg day(-1)) during their neutropenic episode. Starting on day +30, patients receiving prednisone > or =30 mg day(-1) were switched to twice weekly Amphotericin-B-lipid-complex (ABLC) in a dose of 4 mg kg(-1). Patients receiving lower steroid doses continued on the fluconazole/itraconazole prophylaxis. Between 1999 and 2002, 100 patients were enrolled and followed for IFI for 1 year. Seven patients were started on therapeutic daily ABLC treatment before day +30 because of documented or suspected IFI; four had definite or probable aspergillosis, and two had candidaemia. Thirty patients did not need prophylactic ABLC; only one developed candidaemia. Sixty-three patients received ABLC prophylaxis for a median of 52 days (range: 1-289). Seven of these patients developed IFI; one definite and two probable cases of aspergillosis, one case of probable Trichosporon beigelii infection, and three cases of candidaemia. The twice weekly ABLC was well tolerated. This risk-based chemoprevention appears to be effective and might diminish the role of steroids as risk factor for IFI after allogeneic SCT. The relatively high incidence of early IFI suggests that additional prophylaxis for IFI may be indicated for poor-risk patients prior to day +30.

摘要

侵袭性真菌感染(IFI)是异基因干细胞移植(SCT)后常见的死亡原因。使用类固醇是IFI的一个非常重要的危险因素。在一项开放标签的试点研究中,我们采用了基于风险的化学预防措施。所有患者在中性粒细胞减少期均接受口服氟康唑或伊曲康唑(200 - 400 mg/天)。从第30天开始,接受泼尼松≥30 mg/天的患者改为每周两次使用两性霉素B脂质复合物(ABLC),剂量为4 mg/kg。接受较低类固醇剂量的患者继续接受氟康唑/伊曲康唑预防。1999年至2002年期间,纳入了100例患者,并对IFI进行了1年的随访。7例患者因记录在案或疑似IFI在第30天前开始每日接受ABLC治疗;4例患有确诊或可能的曲霉病,2例患有念珠菌血症。30例患者不需要预防性使用ABLC;只有1例发生念珠菌血症。63例患者接受了ABLC预防,中位时间为52天(范围:1 - 289天)。其中7例患者发生了IFI;1例确诊和2例可能的曲霉病病例,1例可能的白吉利丝孢酵母感染病例,以及3例念珠菌血症病例。每周两次的ABLC耐受性良好。这种基于风险的化学预防似乎是有效的,并且可能会降低类固醇作为异基因SCT后IFI危险因素的作用。早期IFI的相对高发病率表明,对于高危患者,在第30天之前可能需要额外的IFI预防措施。

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