William Krüger

William Krüger

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 May 2005 in Annals of Oncology
Verified
Journal Article
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WKWilliam Krüger
William Krüger
JBJulia Bohlius
Julia Bohlius
OCOliver A. Cornely
Oliver A. Cornely
HEH. Einsele
H. Einsele
HHH. Hebart
H. Hebart
HWH.-H. Wolf
H.-H. Wolf
Patients undergoing allogeneic stem cell transplantation are at high risk for infection with a variety of pathogens during different phases of the procedure. Bacteria and fungi predominate the first phase until engraftment. During the second phase, from engraftment to about day 100, major infectious problems are caused by fungi and cytomegalovirus. Both pathogens remain important under continued immunosuppression, however, in the late post-transplantation period infections with encapsulated bacteria may become a problem. In this review the Infectious Diseases Working Party of the DGHO gives recommendations for prophylaxis of infections under allogeneic stem cell transplantation with drugs and other measures. The aim of the group was to do this on an evidence-based-medicine rating, if possible.

30 April 2014 in Annals of Hematology
Verified
Journal Article
Closed access
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WKWilliam Krüger
William Krüger
CHCarsten Hirt
Carsten Hirt
NBNadezda Basara
Nadezda Basara
HSHerbert G. Sayer
Herbert G. Sayer
GBGerhard Behre
Gerhard Behre
GDGottfried Dölken
Gottfried Dölken

17 January 2012 in Annals of Hematology
Verified
Journal Article
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CBChristoph Busemann
Christoph Busemann
SRSilvia Ribback
Silvia Ribback
KZKathrin Zimmermann
Kathrin Zimmermann
VSVerena Sailer
Verena Sailer
TKThomas Kiefer
Thomas Kiefer
WKWilliam Krüger
William Krüger

1 June 2003 in Journal of Hematotherapy & Stem Cell Research
Verified
Journal Article
Closed access
WKWilliam Krüger
William Krüger
BZBernhard Zöllner
Bernhard Zöllner
PKPaul-Michael Kaulfers
Paul-Michael Kaulfers
AZAxel R. Zander
Axel R. Zander
High incidence of aspergillosis on transplant units or hematological wards without HEPA air conditioning during periods of demolishing or construction has been reported by several investigators. Here we report monitoring of fungal air contamination during a period of construction on a stem cell transplantation ward using the gravity air-setting plate (GASP) method. Fungal air contamination in HEPA-conditioned patient rooms was constantly low, independent from construction activity. Outside of the patient rooms at the ward's corridor, the fungal load was significantly higher with some peak values. Outside the transplant unit measures of construction led to a significant increase of fungal spore concentration in air. Transplant activity was not reduced during construction and patients were nursed strictly under HEPA conditions. Patients were monitored prospectively for incidence of infections since 1990 and data of patients grafted during construction (n = 28) were compared to those grafted outside building activity (n = 652). An increase of aspergillosis during construction could be clearly excluded. It can be concluded: Nursing of patients undergoing stem cell transplantation in HEPA-conditioned rooms is an effective protection against acquisition of aspergillus-infection, even under environmental conditions with increased air contamination by conidia. The gravity air-setting plate (GASP) method is not expensive and easy to use and allows reliable and quantitative aerobiological spore monitoring.

23 May 2007 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
GDGeorg Daeschlein
Georg Daeschlein
WKWilliam Krüger
William Krüger
CSChristian Selepko
Christian Selepko
MRMarkus Rochow
Markus Rochow
GDGottfried Dölken
Gottfried Dölken
AKAxel Kramer
Axel Kramer
Background: Microbial safe tap water is crucial for the safety of immunosuppressed patients. Methods: To evaluate the suitability of new, reusable point-of-use filters (Germlyser®, Aquafree GmbH, Hamburg, Germany), three variations of a reusable filter with the same filter principle but with different outlets (with and without silver) and inner surface coating of the filter encasements (with and without nano-crystalline silver) were tested. The filter efficacy was monitored over 1, 4 and 8 weeks operating time in a haematological oncology transplantation unit equipped with 18 water outlets (12 taps, 6 showers). Results: The filtered water fulfilled the requirements of absence of pathogens over time. From 348 samples, 8 samples (2.3%) exceeded 100 cfu/ml (no sample ≥ 500 cfu/ml). As no reprocessed filter exhibited 100% filter efficacy in the final quality control after each reprocessing, these contaminations could be explained by retrograde contamination during use. Conclusion: As a consequence of the study, the manufacturer recommends changing filters after 4 weeks in high risk areas and after 8 weeks in moderate infectious risk areas, together with routine weekly alcohol-based surface disinfection and additionally in case of visible contamination. The filter efficacy of the 3 filters types did not differ significantly regarding total bacterial counts. Manual reprocessing proved to be insufficient. Using a validated reprocessing in a washer/disinfector with alkaline, acid treatment and thermic disinfection, the filters were effectively reprocessable and now provide tap water meeting the German drinking water regulations as well as the WHO guidelines, including absence of pathogens.

1 November 1995 in British Journal of Haematology
Verified
Journal Article
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WKWilliam Krüger
William Krüger
MSMarcus Stockschläder
Marcus Stockschläder
BRBettina Rüssmann
Bettina Rüssmann
CBCarolina Berger
Carolina Berger
MHMatthias Hoffknecht
Matthias Hoffknecht
AZAxel R. Zander
Axel R. Zander