Epidemiology and outcomes of patients with invasive mould infections: a retrospective observational study from a single centre (2005-2009)

被引:35
作者
Klingspor, Lena [1 ]
Saaedi, Baharak [1 ]
Ljungman, Per [2 ]
Szakos, Attila [3 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp, Div Clin Microbiol, SE-14186 Stockholm, Sweden
[2] Karolinska Inst, Karolinska Univ Hosp, Div Haematol, SE-14186 Stockholm, Sweden
[3] Karolinska Inst, Karolinska Univ Hosp, Div Pathol, SE-14186 Stockholm, Sweden
关键词
Invasive mould infection; epidemiology; outcome; aspergillosis; mucormycosis; fusariosis; TRANSPLANT RECIPIENTS; FUNGAL-INFECTIONS; ASPERGILLOSIS; MUCORMYCOSIS; SURVEILLANCE; FUSARIOSIS;
D O I
10.1111/myc.12344
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Invasive mould infection (IMI) is an important cause of morbidity and mortality in immunocompromised patients. However, Swedish epidemiology data are lacking. The aim of this study was to investigate the epidemiology and outcome of IMI. Cases of proven/probable IMI at Karolinska University Hospital, Stockholm, from 2005 to 2009, were included. A total of 100 patients with 104 episodes of IMI were enrolled. Identified isolates included 101 mould isolates. The majority of the isolates were Aspergillus spp. (74.3%), followed by Mucorales spp. (13.9%), Fusarium spp. (4.9%) and other mould spp. (6.9%). In 13% of the episodes, more than one mould caused the IMI. The lung was most often affected (88.5%). The most frequent underlying disease was haematological malignancies (70%). Following diagnosis, 83.7% initially received antifungal monotherapy, 9.6% received combination therapy and 6.7% no treatment. The overall 90-day and 1-year overall survival was 49% and 46% respectively. Survival at 90days post diagnosis was 71.4% in the solid tumour cohort, 62.5% in patients with solid organ transplants, 43.5% in haematological malignancy (HMs) and 37% in those undergoing allogeneic haematopoietic stem cell transplantation (HSCT). Overall survival was poor in the studied cohort, but is variable among different host categories, with particular opportunities for improvement in patients with underlying HMs and allogeneic HSCT.
引用
收藏
页码:470 / 477
页数:8
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