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815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use

BACKGROUND: Flexible endoscopes are complex-design reusable devices, with long and narrow channels, making reprocessing difficult. Biofilm formation is a key factor for persistent contamination, as it protects microorganism against cleaning and disinfection agents. The aim of this study was to asses...

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Autores principales: Primo, Mariusa G, Costa, Dayane M, Guadagnin, Simone V, Azevedo, Adriana S, Alfa, Michelle J, Vickery, Karen, Leão-Vasconcelos, Lara Stefânia N, Tipple, Anaclara F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776197/
http://dx.doi.org/10.1093/ofid/ofaa439.1004
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author Primo, Mariusa G
Costa, Dayane M
Guadagnin, Simone V
Azevedo, Adriana S
Alfa, Michelle J
Vickery, Karen
Leão-Vasconcelos, Lara Stefânia N
Tipple, Anaclara F
author_facet Primo, Mariusa G
Costa, Dayane M
Guadagnin, Simone V
Azevedo, Adriana S
Alfa, Michelle J
Vickery, Karen
Leão-Vasconcelos, Lara Stefânia N
Tipple, Anaclara F
author_sort Primo, Mariusa G
collection PubMed
description BACKGROUND: Flexible endoscopes are complex-design reusable devices, with long and narrow channels, making reprocessing difficult. Biofilm formation is a key factor for persistent contamination, as it protects microorganism against cleaning and disinfection agents. The aim of this study was to assess the accumulation of biofilm on the inner surfaces of new flexible gastroscope channels after 30 days of patient-use and full reprocessing. METHODS: Three flexible gastroscopes (FG) (GIF–Q150, Olympus(TM)) with new internal channels (Teflon(TM)) were subjected to 30 days of clinical use and reprocessing by trained nursing personnel, using a revised reprocessing protocol, at the endoscopy service of a Brazilian teaching hospital (235 beds). The reprocessing protocol included: pre-cleaning; manual cleaning; automated cleaning and disinfection - 2% Glutaraldehyde; manual drying (forced-air drying) and alcohol rinsing, and storage in vertical position in exclusive cabinets. Then, internal channels were removed from the three patient-ready FG (three biopsy, three air, three water and three air/water junction channels), and the inner surface subjected to bacteriological culture (~30 cm) (n=9) and Scanning Electron Microscopy (SEM) (~1 cm) (n=12). Air/water junctions (~1 cm) were subjected to SEM only. RESULTS: The average of use/reprocessing of the FG was 60 times. Bacterial growth was detected in 6/9 channels (three from FG#1 showed residual moisture) and seven bacterial isolates were recovered, most from air or water channels (Fig 1). Inner surface structural damage was identified in 11/12 channels by SEM. Extensive biofilm was detected in air, water and air/water junction channels (7/12) (Fig 2). Residuals matter were detected in all channels (12/12). Fig 1. Distribution of bacterial growth and genera/species identified in new flexible gastroscope channels after 30 days of patient-use and reprocessing at the endoscopy service of a large Brazilian teaching hospital. *FG1: flexible gastroscope nº1 **FG2: flexible gastroscope nº2 ***FG3: flexible gastroscope nº3 ¥Moisture was visually detected inside the channels during longitudinal cutting for SEM. [Image: see text] Fig 2. Scanning Electron Micrographs showing extensive biofilm, containing bacilli/rods and/or cocci shape bacteria, on the inner surface of new flexible gastroscope channels after 30 days of patient-use and reprocessing at the endoscopy service of a large Brazilian teaching hospital. *FG1: flexible gastroscope nº1 **FG2: flexible gastroscope nº2 ***FG3: flexible gastroscope nº3 [Image: see text] CONCLUSION: The short timeframe before damage and biofilm accumulation in the channels were evident and suggests that improving endoscope design is necessary, while better reprocessing methods and channel maintenance needs to be investigated in detail. Improving design, maintenance and reprocessing of endoscopes will ensure safe use of these devices. DISCLOSURES: Michelle J. Alfa, B.Sc., M.Sc., Ph.D, Healthmark (Consultant, Other Financial or Material Support, Royalty monies from University of Manitoba that are provided through a License agreement with Healthmark)Kikkoman (Consultant)Olympus (Consultant, Advisor or Review Panel member, Speaker’s Bureau)STERIS (Consultant, Speaker’s Bureau)
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spelling pubmed-77761972021-01-07 815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use Primo, Mariusa G Costa, Dayane M Guadagnin, Simone V Azevedo, Adriana S Alfa, Michelle J Vickery, Karen Leão-Vasconcelos, Lara Stefânia N Tipple, Anaclara F Open Forum Infect Dis Poster Abstracts BACKGROUND: Flexible endoscopes are complex-design reusable devices, with long and narrow channels, making reprocessing difficult. Biofilm formation is a key factor for persistent contamination, as it protects microorganism against cleaning and disinfection agents. The aim of this study was to assess the accumulation of biofilm on the inner surfaces of new flexible gastroscope channels after 30 days of patient-use and full reprocessing. METHODS: Three flexible gastroscopes (FG) (GIF–Q150, Olympus(TM)) with new internal channels (Teflon(TM)) were subjected to 30 days of clinical use and reprocessing by trained nursing personnel, using a revised reprocessing protocol, at the endoscopy service of a Brazilian teaching hospital (235 beds). The reprocessing protocol included: pre-cleaning; manual cleaning; automated cleaning and disinfection - 2% Glutaraldehyde; manual drying (forced-air drying) and alcohol rinsing, and storage in vertical position in exclusive cabinets. Then, internal channels were removed from the three patient-ready FG (three biopsy, three air, three water and three air/water junction channels), and the inner surface subjected to bacteriological culture (~30 cm) (n=9) and Scanning Electron Microscopy (SEM) (~1 cm) (n=12). Air/water junctions (~1 cm) were subjected to SEM only. RESULTS: The average of use/reprocessing of the FG was 60 times. Bacterial growth was detected in 6/9 channels (three from FG#1 showed residual moisture) and seven bacterial isolates were recovered, most from air or water channels (Fig 1). Inner surface structural damage was identified in 11/12 channels by SEM. Extensive biofilm was detected in air, water and air/water junction channels (7/12) (Fig 2). Residuals matter were detected in all channels (12/12). Fig 1. Distribution of bacterial growth and genera/species identified in new flexible gastroscope channels after 30 days of patient-use and reprocessing at the endoscopy service of a large Brazilian teaching hospital. *FG1: flexible gastroscope nº1 **FG2: flexible gastroscope nº2 ***FG3: flexible gastroscope nº3 ¥Moisture was visually detected inside the channels during longitudinal cutting for SEM. [Image: see text] Fig 2. Scanning Electron Micrographs showing extensive biofilm, containing bacilli/rods and/or cocci shape bacteria, on the inner surface of new flexible gastroscope channels after 30 days of patient-use and reprocessing at the endoscopy service of a large Brazilian teaching hospital. *FG1: flexible gastroscope nº1 **FG2: flexible gastroscope nº2 ***FG3: flexible gastroscope nº3 [Image: see text] CONCLUSION: The short timeframe before damage and biofilm accumulation in the channels were evident and suggests that improving endoscope design is necessary, while better reprocessing methods and channel maintenance needs to be investigated in detail. Improving design, maintenance and reprocessing of endoscopes will ensure safe use of these devices. DISCLOSURES: Michelle J. Alfa, B.Sc., M.Sc., Ph.D, Healthmark (Consultant, Other Financial or Material Support, Royalty monies from University of Manitoba that are provided through a License agreement with Healthmark)Kikkoman (Consultant)Olympus (Consultant, Advisor or Review Panel member, Speaker’s Bureau)STERIS (Consultant, Speaker’s Bureau) Oxford University Press 2020-12-31 /pmc/articles/PMC7776197/ http://dx.doi.org/10.1093/ofid/ofaa439.1004 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Primo, Mariusa G
Costa, Dayane M
Guadagnin, Simone V
Azevedo, Adriana S
Alfa, Michelle J
Vickery, Karen
Leão-Vasconcelos, Lara Stefânia N
Tipple, Anaclara F
815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use
title 815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use
title_full 815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use
title_fullStr 815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use
title_full_unstemmed 815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use
title_short 815. Biofilm Accumulation in New Flexible Gastroscope Channels within 30 Days in Clinical Use
title_sort 815. biofilm accumulation in new flexible gastroscope channels within 30 days in clinical use
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776197/
http://dx.doi.org/10.1093/ofid/ofaa439.1004
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