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Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units
A contaminated hospital environment has been identified as an important reservoir of pathogens causing healthcare-associated infections. This study is to evaluate the efficacy of bacteria killing nanotechnology Bio-Kil on reducing bacterial counts in an intensive care unit (ICU). Two single-bed room...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087826/ https://www.ncbi.nlm.nih.gov/pubmed/24136062 http://dx.doi.org/10.1007/s10096-013-1989-3 |
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author | Hsueh, P.-R. Huang, H.-C. Young, T.-G. Su, C.-Y. Liu, C.-S. Yen, M.-Y. |
author_facet | Hsueh, P.-R. Huang, H.-C. Young, T.-G. Su, C.-Y. Liu, C.-S. Yen, M.-Y. |
author_sort | Hsueh, P.-R. |
collection | PubMed |
description | A contaminated hospital environment has been identified as an important reservoir of pathogens causing healthcare-associated infections. This study is to evaluate the efficacy of bacteria killing nanotechnology Bio-Kil on reducing bacterial counts in an intensive care unit (ICU). Two single-bed rooms (S-19 and S-20) in the ICU were selected from 7 April to 27 May 2011. Ten sets of new textiles (pillow cases, bed sheets, duvet cover, and patient clothing) used by patients in the two single-bed rooms were provided by the sponsors. In the room S-20, the 10 sets of new textiles were washed with Bio-Kil; the room walls, ceiling, and air-conditioning filters were treated with Bio-Kil; and the surfaces of instruments (respirator, telephone, and computer) were covered with Bio-Kil-embedded silicon pads. Room S-19 served as the control. We compared the bacterial count on textiles and environment surfaces as well as air samples between the two rooms. A total of 1,364 samples from 22 different sites in each room were collected. The mean bacterial count on textiles and environmental surfaces in room S-20 was significantly lower than that in room S-19 (10.4 vs 49.6 colony-forming units [CFU]/100 cm(2); P < 0.001). Room S-20 had lower bacterial counts in air samples than room S-19 (33.4–37.6 vs 21.6–25.7 CFU/hour/plate; P < 0.001). The density of microbial isolations was significantly greater among patients admitted to room S-19 than those to room S-20 (9.15 vs 5.88 isolates per 100 patient-days, P < 0.05). Bio-Kil can significantly reduce bacterial burden in the environment of the ICU. |
format | Online Article Text |
id | pubmed-7087826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70878262020-03-23 Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units Hsueh, P.-R. Huang, H.-C. Young, T.-G. Su, C.-Y. Liu, C.-S. Yen, M.-Y. Eur J Clin Microbiol Infect Dis Article A contaminated hospital environment has been identified as an important reservoir of pathogens causing healthcare-associated infections. This study is to evaluate the efficacy of bacteria killing nanotechnology Bio-Kil on reducing bacterial counts in an intensive care unit (ICU). Two single-bed rooms (S-19 and S-20) in the ICU were selected from 7 April to 27 May 2011. Ten sets of new textiles (pillow cases, bed sheets, duvet cover, and patient clothing) used by patients in the two single-bed rooms were provided by the sponsors. In the room S-20, the 10 sets of new textiles were washed with Bio-Kil; the room walls, ceiling, and air-conditioning filters were treated with Bio-Kil; and the surfaces of instruments (respirator, telephone, and computer) were covered with Bio-Kil-embedded silicon pads. Room S-19 served as the control. We compared the bacterial count on textiles and environment surfaces as well as air samples between the two rooms. A total of 1,364 samples from 22 different sites in each room were collected. The mean bacterial count on textiles and environmental surfaces in room S-20 was significantly lower than that in room S-19 (10.4 vs 49.6 colony-forming units [CFU]/100 cm(2); P < 0.001). Room S-20 had lower bacterial counts in air samples than room S-19 (33.4–37.6 vs 21.6–25.7 CFU/hour/plate; P < 0.001). The density of microbial isolations was significantly greater among patients admitted to room S-19 than those to room S-20 (9.15 vs 5.88 isolates per 100 patient-days, P < 0.05). Bio-Kil can significantly reduce bacterial burden in the environment of the ICU. Springer Berlin Heidelberg 2013-10-18 2014 /pmc/articles/PMC7087826/ /pubmed/24136062 http://dx.doi.org/10.1007/s10096-013-1989-3 Text en © Springer-Verlag Berlin Heidelberg 2013 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Hsueh, P.-R. Huang, H.-C. Young, T.-G. Su, C.-Y. Liu, C.-S. Yen, M.-Y. Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units |
title | Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units |
title_full | Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units |
title_fullStr | Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units |
title_full_unstemmed | Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units |
title_short | Bacteria killing nanotechnology Bio-Kil effectively reduces bacterial burden in intensive care units |
title_sort | bacteria killing nanotechnology bio-kil effectively reduces bacterial burden in intensive care units |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087826/ https://www.ncbi.nlm.nih.gov/pubmed/24136062 http://dx.doi.org/10.1007/s10096-013-1989-3 |
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