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Biosafety of Non-Return Valves for Infusion Systems in Radiology
Cross-infection in contrast injectors is still a subject under discussion with little understanding. This study evaluated the biosafety of non-return valves (NRVs). Initially, the maximum pressure during backflow of intact and disrupted flexible diaphragms (FDs) from NRVs, as well as the functionali...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293231/ https://www.ncbi.nlm.nih.gov/pubmed/32533091 http://dx.doi.org/10.1038/s41598-020-66491-y |
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author | Azevedo, Marcela Padilha Facetto Monteiro, Rachel Maciel Castelani, Carla Bim, Felipe Lazarini Bim, Lucas Lazarini Macedo, Ana Paula Oliveira, Viviane de Cássia Watanabe, Evandro |
author_facet | Azevedo, Marcela Padilha Facetto Monteiro, Rachel Maciel Castelani, Carla Bim, Felipe Lazarini Bim, Lucas Lazarini Macedo, Ana Paula Oliveira, Viviane de Cássia Watanabe, Evandro |
author_sort | Azevedo, Marcela Padilha Facetto |
collection | PubMed |
description | Cross-infection in contrast injectors is still a subject under discussion with little understanding. This study evaluated the biosafety of non-return valves (NRVs). Initially, the maximum pressure during backflow of intact and disrupted flexible diaphragms (FDs) from NRVs, as well as the functionality of connectors with NRVs were verified. The performance of air columns interposed by water in connectors with NRVs was analyzed, and the diffusion distance of crystal violet through connectors with NRVs was measured. The efficacy of NRVs as a barrier to bacterial contamination from backflow was evaluated. Finally, a clinical study of bacteriological contamination from syringes was conducted. There were differences among the maximum tolerated pressure by intact and disrupted FDs. Disrupted FDs showed no failures in the functionality of connectors with NRVs based on the lack of air bubbles released. Air columns could move through connectors with NRVs with intact and disrupted FDs. The longest diffusion distance of crystal violet was 6 cm of connector length, and NRVs showed efficacy as a barrier to bacterial contamination. In the clinical study, there was no bacterial growth in any of the evaluated samples. In conclusion, biosafety depends on the functionality of NRVs as well as proper practical clinical performance. |
format | Online Article Text |
id | pubmed-7293231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72932312020-06-15 Biosafety of Non-Return Valves for Infusion Systems in Radiology Azevedo, Marcela Padilha Facetto Monteiro, Rachel Maciel Castelani, Carla Bim, Felipe Lazarini Bim, Lucas Lazarini Macedo, Ana Paula Oliveira, Viviane de Cássia Watanabe, Evandro Sci Rep Article Cross-infection in contrast injectors is still a subject under discussion with little understanding. This study evaluated the biosafety of non-return valves (NRVs). Initially, the maximum pressure during backflow of intact and disrupted flexible diaphragms (FDs) from NRVs, as well as the functionality of connectors with NRVs were verified. The performance of air columns interposed by water in connectors with NRVs was analyzed, and the diffusion distance of crystal violet through connectors with NRVs was measured. The efficacy of NRVs as a barrier to bacterial contamination from backflow was evaluated. Finally, a clinical study of bacteriological contamination from syringes was conducted. There were differences among the maximum tolerated pressure by intact and disrupted FDs. Disrupted FDs showed no failures in the functionality of connectors with NRVs based on the lack of air bubbles released. Air columns could move through connectors with NRVs with intact and disrupted FDs. The longest diffusion distance of crystal violet was 6 cm of connector length, and NRVs showed efficacy as a barrier to bacterial contamination. In the clinical study, there was no bacterial growth in any of the evaluated samples. In conclusion, biosafety depends on the functionality of NRVs as well as proper practical clinical performance. Nature Publishing Group UK 2020-06-12 /pmc/articles/PMC7293231/ /pubmed/32533091 http://dx.doi.org/10.1038/s41598-020-66491-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Azevedo, Marcela Padilha Facetto Monteiro, Rachel Maciel Castelani, Carla Bim, Felipe Lazarini Bim, Lucas Lazarini Macedo, Ana Paula Oliveira, Viviane de Cássia Watanabe, Evandro Biosafety of Non-Return Valves for Infusion Systems in Radiology |
title | Biosafety of Non-Return Valves for Infusion Systems in Radiology |
title_full | Biosafety of Non-Return Valves for Infusion Systems in Radiology |
title_fullStr | Biosafety of Non-Return Valves for Infusion Systems in Radiology |
title_full_unstemmed | Biosafety of Non-Return Valves for Infusion Systems in Radiology |
title_short | Biosafety of Non-Return Valves for Infusion Systems in Radiology |
title_sort | biosafety of non-return valves for infusion systems in radiology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293231/ https://www.ncbi.nlm.nih.gov/pubmed/32533091 http://dx.doi.org/10.1038/s41598-020-66491-y |
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