Morgan J, Wannemuehler K A, Marr K A, Hadley S, Kontoyiannis D P, Walsh T J, Fridkin S K, Pappas P G, Warnock D W
Mycotic Diseases Branch, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Atlanta, GA 30333, USA.
Med Mycol. 2005 May;43 Suppl 1:S49-58. doi: 10.1080/13693780400020113.
The incidence of invasive aspergillosis was estimated among 4621 hematopoietic stem cell transplants (HSCT) and 4110 solid organ transplants (SOT) at 19 sites dispersed throughout the United States, during a 22 month period from 1 March 2001 through 31 December 2002. Cases were identified using the consensus definitions for proven and probable infection developed by the Invasive Fungal Infections Cooperative Group of the European Organization for Research and Treatment of Cancer and the Mycoses Study Group of the National Institute of Allergy and Infectious Diseases. The cumulative incidence (CI) of aspergillosis was calculated for the first episode of the infection that occurred within the specified time period after transplantation. To obtain an aggregate CI for each type of transplant, data from participating sites were weighted according to the proportion of transplants followed-up for specified time periods (four and 12 months for HSCT; six and 12 months for SOT). The aggregate CI of aspergillosis at 12 months was 0.5% after autologous HSCT, 2.3% after allogeneic HSCT from an HLA-matched related donor, 3.2% after transplantation from an HLA-mismatched related donor, and 3.9% after transplantation from an unrelated donor. The aggregate CI at 12 months was similar following myeloablative or non-myeloablative conditioning before allogeneic HSCT (3.1 vs. 3.3%). After HSCT, mortality at 3 months following diagnosis of aspergillosis ranged from 53.8% of autologous transplants to 84.6% of unrelated-donor transplants. The aggregate CI of aspergillosis at 12 months was 2.4% after lung transplantation, 0.8% after heart transplantation, 0.3% after liver transplantation, and 0.1% after kidney transplantation. After SOT, mortality at three months after diagnosis of aspergillosis ranged from 20% for lung transplants to 66.7% for heart and kidney transplants. The Aspergillus spp. associated with infections after HSCT included A. fumigatus (56%), A. flavus (18.7%), A. terreus (16%), A. niger (8%), and A. versicolor (1.3%). Those associated with infections after SOT included A. fumigatus (76.4%), A. flavus (11.8%), and A. terreus (11.8%). In conclusion, we found that invasive aspergillosis is an uncommon complication of HSCT and SOT, but one that continues to be associated with poor outcomes. Our CI figures are lower compared to those of previous reports. The reasons for this are unclear, but may be related to changes in transplantation practices, diagnostic methods, and supportive care.
在2001年3月1日至2002年12月31日的22个月期间,在美国各地分散的19个地点对4621例造血干细胞移植(HSCT)和4110例实体器官移植(SOT)患者的侵袭性曲霉病发病率进行了评估。病例是根据欧洲癌症研究与治疗组织侵袭性真菌感染合作组和美国国立过敏与传染病研究所真菌病研究组制定的确诊和疑似感染的共识定义来确定的。计算移植后特定时间段内首次发生感染的曲霉病累积发病率(CI)。为了获得每种移植类型的汇总CI,根据在特定时间段(HSCT为4个月和12个月;SOT为6个月和12个月)进行随访的移植比例对参与研究地点的数据进行加权。自体HSCT后12个月曲霉病的汇总CI为0.5%,来自HLA匹配相关供体的异基因HSCT后为2.3%,来自HLA不匹配相关供体的移植后为3.2%,来自无关供体的移植后为3.9%。异基因HSCT前采用清髓或非清髓预处理后12个月的汇总CI相似(分别为3.1%和3.3%)。HSCT后,曲霉病诊断后3个月的死亡率从自体移植的53.8%到无关供体移植的84.6%不等。肺移植后12个月曲霉病的汇总CI为2.4%,心脏移植后为