Surveillance of nosocomial infections in adult recipients of allogeneic and autologous bone marrow and peripheral blood stem-cell transplantation

被引:0
作者
M Dettenkofer
W Ebner
H Bertz
R Babikir
J Finke
U Frank
H Rüden
F D Daschner
机构
[1] Institute of Environmental Medicine and Hospital Epidemiology,Department of Internal Medicine I (Haematology/Oncology)
[2] University Hospital of Freiburg,undefined
[3] University Hospital of Freiburg,undefined
[4] Institute of Hygiene Free University of Berlin,undefined
[5] German National Reference Centre for Hospital Hygiene*,undefined
来源
Bone Marrow Transplantation | 2003年 / 31卷
关键词
BMT; HSCT; neutropenia; nosocomial infection; PBSCT; surveillance;
D O I
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学科分类号
摘要
To identify overall and site-specific rates of nosocomial infections (NIs) during the neutropenic, as compared to the non-neutropenic stage of treatment in adult recipients of allogeneic and autologous bone marrow transplantation (BMT) and peripheral blood stem-cell transplantation (PBSCT), a prospective, 54-month study was started at the Haematological Stem Cell Transplantation Unit of the University Hospital of Freiburg, Germany. NI types were identified using modified CDC definitions. A total of 351 patients (14 256 in-patient days, 5026 neutropenic days) were investigated (316/90% allogeneic, 35/10% autologous; BMT: 119 patients, PBSCT: 234 patients). The mean length of neutropenia was 14.3 days (range: 0–66). Antimicrobial prophylaxis for allogeneic transplantation consisted of ciprofloxacin, trimethoprim/sulpha-methoxazole, fluconazole, and metronidazole. In total, 239 NIs were identified in 169 patients (48.1%), and of these 171 (71.5%) occurred during neutropenia (34.0 NIs per 1000 days at risk). The main pathogens were coagulase-negative staphylococci (36.3%), Clostridium difficile (20.4%), and enterococci (10.0%). Site-specific incidence densities during neutropenia vs non-neutropenia were: 13.9 vs 1.6 bloodstream infections (all central line-associated), 11.9 vs 1.8 pneumonias, 3.0 vs 2.9 gastroenteritis, and 1.6 vs 0.3 urinary tract infections. The greatest number of NI in BMT and PBSCT recipients is acquired during neutropenia, and multicentre surveillance programmes should focus on this.
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页码:795 / 801
页数:6
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