Prediction of central venous catheter–related bloodstream infections (CRBSIs) in patients with haematologic malignancies using a modified Infection Probability Score (mIPS)
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  • 作者:Enrico Schalk ; Lynn Hanus ; Jacqueline F?rber ; Thomas Fischer…
  • 关键词:Central venous catheter ; Bloodstream infection ; Probability ; IPS ; Haematologic malignancies
  • 刊名:Annals of Hematology
  • 出版年:2015
  • 出版时间:September 2015
  • 年:2015
  • 卷:94
  • 期:9
  • 页码:1451-1456
  • 全文大小:148 KB
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  • 作者单位:Enrico Schalk (1)
    Lynn Hanus (1)
    Jacqueline F?rber (2)
    Thomas Fischer (1)
    Florian H. Heidel (1)

    1. Department of Haematology and Oncology, Medical Centre, Otto-von-Guericke University Magdeburg, Leipziger Str. 44, 39120, Magdeburg, Germany
    2. Department of Medical Microbiology, Infection Control and Prevention, Medical Centre, Otto-von-Guericke University Magdeburg, Magdeburg, Germany
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Hematology
    Oncology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-0584
文摘
The aim of this study was to predict the probability of central venous catheter–related bloodstream infections (CRBSIs) in patients with haematologic malignancies using a modified version of the Infection Probability Score (mIPS). In order to perform a prospective, mono-centric surveillance of complications in clinical routine due to short-term central venous catheters (CVCs) in consecutive patients receiving chemotherapy from March 2013 to September 2014, IPS was calculated at CVC insertion and removal (mIPSin and mIPSex, respectively). We used the 2012 Infectious Diseases Working Party of the German Society of Haematology and Medical Oncology (AGIHO/DGHO) criteria to define CRBSI. In total, 143 patients (mean 59.5?years, 61.4?% male) with 267 triple-lumen CVCs (4044 CVC days; mean 15.1?days, range 1-0?days) were analysed. CVCs were inserted for therapy of acute leukaemia (53.2?%), multiple myeloma (24.3?%) or lymphoma (11.2?%), and 93.6?% were inserted in the jugular vein. A total of 66 CRBSI cases (24.7?%) were documented (12 definite/13 probable/41 possible). The incidence was 16.3/1000 CVC days (2.9/3.1/10.1 per 1000 CVC days for definite/probable/possible CRBSI, respectively). In CRBSI cases, the mIPSex was higher as compared to cases without CRBSI (13.1 vs. 7.1; p-lt;-.001). The best mIPSex cutoff for CRBSI prediction was 8 points (area under the curve (AUC)--.77; sensitivity = 84.9?%, specificity = 60.7?%, negative predictive value = 92.4?%). For patients with an mIPSex ?, the risk for a CRBSI was high (odds ratio [OR]--.9; p-lt;-.001) and even increased if, additionally, CVC had been in use for about 10?days (OR--.8; p-lt;-.001). In case other causes of infection are excluded, a mIPSex ? and duration of CVC use of about 10?days predict a very high risk of CRBSI. Patients with a mIPSex <8 have a low risk of CRBSI of 8?%.

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