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Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies

BACKGROUND: Aspiration of subglottic secretions past the endotracheal tube (ETT) cuff is a prerequisite for developing ventilator-associated pneumonia (VAP). Subglottic secretion drainage (SSD) ETTs reduce aspiration of subglottic secretions and have demonstrated lower VAP rates. We compared the per...

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Autores principales: Mariyaselvam, Maryanne Z., Marsh, Lucy L., Bamford, Sarah, Smith, Ann, Wise, Matt P., Williams, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336650/
https://www.ncbi.nlm.nih.gov/pubmed/28257624
http://dx.doi.org/10.1186/s12871-017-0328-0
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author Mariyaselvam, Maryanne Z.
Marsh, Lucy L.
Bamford, Sarah
Smith, Ann
Wise, Matt P.
Williams, David W.
author_facet Mariyaselvam, Maryanne Z.
Marsh, Lucy L.
Bamford, Sarah
Smith, Ann
Wise, Matt P.
Williams, David W.
author_sort Mariyaselvam, Maryanne Z.
collection PubMed
description BACKGROUND: Aspiration of subglottic secretions past the endotracheal tube (ETT) cuff is a prerequisite for developing ventilator-associated pneumonia (VAP). Subglottic secretion drainage (SSD) ETTs reduce aspiration of subglottic secretions and have demonstrated lower VAP rates. We compared the performance of seven SSD ETTs against a non-SSD ETT in preventing aspiration below inflated cuffs. METHODS: ETTs were positioned vertically in 2 cm diameter cylinders. Four ml of a standard microbial suspension was added above inflated cuffs. After 1 h, aspiration was measured and ETTs demonstrating no leakage were subjected to rotational movement and evaluation over 24 h. Collected aspirated fluid was used to inoculate agar media and incubated aerobically at 37 °C for 24 h. The aspiration rate, volume and number of microorganisms that leaked past the cuff was measured. Experiments were repeated (×10) for each type of ETT, with new ETTs used for each repeat. Best performing ETTs were then tested in five different cylinder diameters (1.6, 1.8, 2.0, 2.2 and 2.4 cm). Experiments were repeated as above using sterile water. Volume and time taken for aspiration past the cuff was measured. Experiments were repeated (×10) for each type of ETT. Results were analysed using non-parametric tests for repeated measures. RESULTS: The PneuX ETT prevented aspiration past the cuff in all experiments. All other ETTs allowed aspiration, with considerable variability in performance. The PneuX ETT was statistically superior in reducing aspiration compared to the SealGuard (p < 0.009), KimVent (p < 0.002), TaperGuard (p < 0.004), Lanz (p < 0.001), ISIS (p < 0.001), SACETT (p < 0.001) and Soft Seal (p < 0.001) ETTs. Of the 4 ETTs tested in differing cylinder sizes, the PneuX significantly reduced aspiration across the range of diameters compared to the SealGuard (p < 0.0001), TaperGuard (p < 0.0001) and KimVent (p < 0.0001) ETTs. CONCLUSIONS: ETTs showed substantial variation in fluid aspiration, relating to cuff material and design. Variability in performance was likely due to the random manner in which involutional folds form in the inflated ETT cuff. The PneuX ETT was the only ETT able to consistently prevent aspiration past the cuff in all experiments.
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spelling pubmed-53366502017-03-07 Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies Mariyaselvam, Maryanne Z. Marsh, Lucy L. Bamford, Sarah Smith, Ann Wise, Matt P. Williams, David W. BMC Anesthesiol Research Article BACKGROUND: Aspiration of subglottic secretions past the endotracheal tube (ETT) cuff is a prerequisite for developing ventilator-associated pneumonia (VAP). Subglottic secretion drainage (SSD) ETTs reduce aspiration of subglottic secretions and have demonstrated lower VAP rates. We compared the performance of seven SSD ETTs against a non-SSD ETT in preventing aspiration below inflated cuffs. METHODS: ETTs were positioned vertically in 2 cm diameter cylinders. Four ml of a standard microbial suspension was added above inflated cuffs. After 1 h, aspiration was measured and ETTs demonstrating no leakage were subjected to rotational movement and evaluation over 24 h. Collected aspirated fluid was used to inoculate agar media and incubated aerobically at 37 °C for 24 h. The aspiration rate, volume and number of microorganisms that leaked past the cuff was measured. Experiments were repeated (×10) for each type of ETT, with new ETTs used for each repeat. Best performing ETTs were then tested in five different cylinder diameters (1.6, 1.8, 2.0, 2.2 and 2.4 cm). Experiments were repeated as above using sterile water. Volume and time taken for aspiration past the cuff was measured. Experiments were repeated (×10) for each type of ETT. Results were analysed using non-parametric tests for repeated measures. RESULTS: The PneuX ETT prevented aspiration past the cuff in all experiments. All other ETTs allowed aspiration, with considerable variability in performance. The PneuX ETT was statistically superior in reducing aspiration compared to the SealGuard (p < 0.009), KimVent (p < 0.002), TaperGuard (p < 0.004), Lanz (p < 0.001), ISIS (p < 0.001), SACETT (p < 0.001) and Soft Seal (p < 0.001) ETTs. Of the 4 ETTs tested in differing cylinder sizes, the PneuX significantly reduced aspiration across the range of diameters compared to the SealGuard (p < 0.0001), TaperGuard (p < 0.0001) and KimVent (p < 0.0001) ETTs. CONCLUSIONS: ETTs showed substantial variation in fluid aspiration, relating to cuff material and design. Variability in performance was likely due to the random manner in which involutional folds form in the inflated ETT cuff. The PneuX ETT was the only ETT able to consistently prevent aspiration past the cuff in all experiments. BioMed Central 2017-03-04 /pmc/articles/PMC5336650/ /pubmed/28257624 http://dx.doi.org/10.1186/s12871-017-0328-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Mariyaselvam, Maryanne Z.
Marsh, Lucy L.
Bamford, Sarah
Smith, Ann
Wise, Matt P.
Williams, David W.
Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
title Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
title_full Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
title_fullStr Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
title_full_unstemmed Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
title_short Endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
title_sort endotracheal tubes and fluid aspiration: an in vitro evaluation of new cuff technologies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336650/
https://www.ncbi.nlm.nih.gov/pubmed/28257624
http://dx.doi.org/10.1186/s12871-017-0328-0
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