Our 2015 approach to invasive pulmonary aspergillosis

被引:26
作者
Liss, B. [1 ,2 ]
Vehreschild, J. J. [1 ,2 ,3 ]
Bangard, C. [4 ]
Maintz, D. [4 ]
Frank, K. [5 ]
Groenke, S. [5 ]
Michels, G. [5 ]
Hamprecht, A. [6 ]
Wisplinghoff, H. [6 ]
Markiefka, B. [7 ]
Hekmat, K. [8 ]
Vehreschild, M. J. G. T. [1 ,2 ,3 ]
Cornely, O. A. [1 ,2 ,3 ,9 ,10 ]
机构
[1] Univ Hosp Cologne, Dept Internal Med 1, D-50937 Cologne, Germany
[2] Univ Cologne, Ctr Integrated Oncol CIO KolnBonn, D-50931 Cologne, Germany
[3] Partner Site Bonn Cologne, German Ctr Infect Res DZIF, Cologne, Germany
[4] Univ Hosp Cologne, Dept Radiol, D-50937 Cologne, Germany
[5] Univ Cologne, Ctr Heart, Dept Internal Med 3, D-50931 Cologne, Germany
[6] Univ Hosp Cologne, Inst Med Microbiol Immunol & Hyg, D-50937 Cologne, Germany
[7] Univ Hosp Cologne, Inst Pathol, D-50937 Cologne, Germany
[8] Univ Hosp Cologne, Dept Cardiothorac Surg, D-50937 Cologne, Germany
[9] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
[10] Univ Cologne, Clin Trials Ctr Cologne, ZKS Koln, D-50931 Cologne, Germany
关键词
Aspergillosis; mould pneumonia; neutropaenia; voriconazole; liposomal amphotericin B; caspofungin; DISEASES-WORKING-PARTY; LIPOSOMAL AMPHOTERICIN-B; STEM-CELL TRANSPLANTATION; EXPOSURE-RESPONSE RELATIONSHIP; BRONCHOALVEOLAR LAVAGE FLUID; EMPIRICAL ANTIFUNGAL THERAPY; ACUTE MYELOID-LEUKEMIA; LATERAL-FLOW DEVICE; HIGH-RISK PATIENTS; FUNGAL-INFECTIONS;
D O I
10.1111/myc.12319
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
At the University Hospital of Cologne, in general two patient groups at high risk for invasive aspergillosis receive posaconazole prophylaxis: Acute myelogenous leukaemia patients during remission induction chemotherapy and allogeneic haematopoietic stem cell transplant recipients. Other patients at risk undergo serum galactomannan testing three times weekly. At 72-96h of persisting fever despite broad-spectrum antibiotics, or at onset of lower respiratory tract symptoms a thoracic computed tomography (CT) scan is performed. Without lung infiltrates on CT, IPA is ruled out. In lung infiltrates not suggestive for IPA mycological confirmation is pursued. In patients without posaconazole prophylaxis empiric caspofungin will be considered. CT findings typical for IPA prompt targeted treatment, and mycological confirmation. Bronchoalveolar lavage (BAL) is most important for cultural identification and susceptibility testing, and facilitates diagnosing other pathogens. BAL performance is virtually independent of platelet counts. If despite suggestive infiltrates BAL does not yield the diagnosis, CT-guided biopsy follows as soon as platelet counts allow. Surgery can also be beneficial in diagnosis and treatment of IPA. If the diagnosis of IPA is not established, mucormycosis is a valid concern. In patients with breakthrough IPA during posaconazole prophylaxis liposomal amphotericin B is the drug of choice. If no posaconazole prophylaxis was given, voriconazole is the treatment of choice for IPA.
引用
收藏
页码:375 / 382
页数:8
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