Iwen P C, Reed E C, Armitage J O, Bierman P J, Kessinger A, Vose J M, Arneson M A, Winfield B A, Woods G L
Department of Pathology, University of Nebraska Medical Center, Omaha 68198-6495.
Infect Control Hosp Epidemiol. 1993 Mar;14(3):131-9. doi: 10.1086/646698.
To determine the prevalence of aspergillosis in lymphoma patients housed in a protective environment while undergoing a bone marrow transplant or peripheral stem cell transplant and its relation to lymphoma type, type of transplant, period of neutropenia, method of diagnosis, species of Aspergillus, and the use of empiric amphotericin B.
Clinical, autopsy, and microbiology records were reviewed retrospectively to determine the presence or absence of invasive aspergillosis. All positive specimens underwent further review to determine parameters outlined above.
The review took place at the University of Nebraska Medical Center with lymphoma patients housed in the oncology/hematology special care unit, which consists of 30 single-patient rooms under positive pressure with high-efficiency particulate air filtration.
417 lymphoma patients admitted to the oncology/hematology special care unit who underwent 427 courses of high-dose chemotherapy with or without total body irradiation followed by a stem cell rescue.
Twenty-two cases (5.2%) of nosocomial invasive aspergillosis (14 caused by Aspergillus flavus, 2 by Aspergillus terreus, 2 by Aspergillus fumigatus, and 4 by characteristic histology) were diagnosed. The prevalence of disease according to transplant was 8.7% for allogeneic bone marrow transplant (2/23 treatments), 5.6% for autologous peripheral stem cell transplant (9/161), and 4.5% for autologous bone marrow transplant (11/243). Fifteen patients were presumptively diagnosed prior to death (68.2%) most commonly by histologic examination of skin biopsies. All 22 patients received amphotericin B therapy, 17 prior to aspergillosis diagnosis, and 7 (31.8%) survived. No patient with disseminated disease survived.
Even when housing lymphoma patients undergoing myeloablative therapy in a protective environment containing high-efficiency particulate air filtration, there was a risk of developing aspergillosis. These data also showed that antemortem diagnosis with aggressive amphotericin B therapy was most effective in the management of infected lymphoma patients when engraftment occurred and the disease did not become disseminated.
确定在接受骨髓移植或外周干细胞移植且处于保护环境中的淋巴瘤患者曲霉病的患病率,以及其与淋巴瘤类型、移植类型、中性粒细胞减少期、诊断方法、曲霉菌种和经验性使用两性霉素B的关系。
回顾性审查临床、尸检和微生物学记录,以确定是否存在侵袭性曲霉病。对所有阳性标本进行进一步审查,以确定上述参数。
审查在内布拉斯加大学医学中心进行,淋巴瘤患者安置在肿瘤/血液学特别护理单元,该单元由30间配备高效微粒空气过滤的正压单人病房组成。
417名入住肿瘤/血液学特别护理单元的淋巴瘤患者,接受了427个疗程的大剂量化疗,伴或不伴全身照射,随后进行干细胞救援。
诊断出22例(5.2%)医院获得性侵袭性曲霉病(14例由黄曲霉引起,2例由土曲霉引起,2例由烟曲霉引起,4例由特征性组织学确诊)。根据移植类型,异基因骨髓移植的疾病患病率为8.7%(2/23次治疗),自体外周干细胞移植为5.6%(9/161),自体骨髓移植为4.5%(11/243)。15名患者在死亡前被初步诊断(68.2%),最常见的诊断方法是皮肤活检组织学检查。所有22例患者均接受了两性霉素B治疗,17例在曲霉病诊断前接受治疗,7例(31.8%)存活。没有播散性疾病患者存活。
即使将接受清髓性治疗的淋巴瘤患者安置在配备高效微粒空气过滤的保护环境中,仍有发生曲霉病的风险。这些数据还表明,在植入成功且疾病未播散时,积极的两性霉素B治疗进行生前诊断对感染淋巴瘤患者的管理最为有效。