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Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport

BACKGROUND: Nebulised drugs, including osmotic agents and saline, are increasingly used during noninvasive respiratory support, including nasal high-flow therapy. The authors conducted an in vitro study to compare the hydration effect of nebulised isotonic 0.9% and hypertonic 7.0% saline on mucocili...

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Autores principales: Kelly, Susyn, Valentine, Matthew, Chua, Wei Hang, Tatkov, Stanislav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258716/
https://www.ncbi.nlm.nih.gov/pubmed/37313398
http://dx.doi.org/10.1183/23120541.00724-2022
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author Kelly, Susyn
Valentine, Matthew
Chua, Wei Hang
Tatkov, Stanislav
author_facet Kelly, Susyn
Valentine, Matthew
Chua, Wei Hang
Tatkov, Stanislav
author_sort Kelly, Susyn
collection PubMed
description BACKGROUND: Nebulised drugs, including osmotic agents and saline, are increasingly used during noninvasive respiratory support, including nasal high-flow therapy. The authors conducted an in vitro study to compare the hydration effect of nebulised isotonic 0.9% and hypertonic 7.0% saline on mucociliary transport. METHODS: In a perfused organ bath, 10 sheep tracheas were exposed to 7.5 mL nebulised 0.9% and 7.0% saline entrained into heated (38°C) and humidified air delivered at high and low flow (20 and 7 L·min(−1), respectively). Simultaneous measurements of the airway surface liquid height, mucus transport velocity, cilia beat frequency and surface temperature were made over time. The data are presented as mean±sd. RESULTS: The airway surface liquid height increased significantly with both 0.9% and 7.0% saline: at low-flow by 37.2±10.0 µm and 152.7±10.9 µm, respectively, and at high-flow by 62.3±5.6 µm and 163.4±25.4 µm, respectively (p<0.001). Mucus velocity was increased by both 0.9% and 7.0% saline from a baseline of 8.2±0.8 mm·min(−1) to 8.8±0.7 mm·min(−1) and 17.1±0.5 mm·min(−1), respectively, with low-flow and at high-flow to 9.8±0.02 mm·min(−1) (p=0.04) and 16.9±0.5 mm·min(−1) (p<0.05), respectively. Ciliary beating did not change with 0.9% saline, but declined from 13.1±0.6 Hz to 10.2±0.6 Hz and 11.1±0.6 Hz (p<0.05) with 7.0% saline at low- and high-flow, respectively. CONCLUSIONS: The findings demonstrate that nebulised isotonic 0.9% saline, like hypertonic 7.0% saline, significantly stimulates basal mucociliary transport, and the use of high-flow delivery had no significantly different hydration effects compared with low-flow delivery. Hypertonic 7.0% saline suppressed ciliary beating, indicating an increase in airway surface liquid osmolarity, which may have negative effects on the airway surface with frequent use.
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spelling pubmed-102587162023-06-13 Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport Kelly, Susyn Valentine, Matthew Chua, Wei Hang Tatkov, Stanislav ERJ Open Res Original Research Articles BACKGROUND: Nebulised drugs, including osmotic agents and saline, are increasingly used during noninvasive respiratory support, including nasal high-flow therapy. The authors conducted an in vitro study to compare the hydration effect of nebulised isotonic 0.9% and hypertonic 7.0% saline on mucociliary transport. METHODS: In a perfused organ bath, 10 sheep tracheas were exposed to 7.5 mL nebulised 0.9% and 7.0% saline entrained into heated (38°C) and humidified air delivered at high and low flow (20 and 7 L·min(−1), respectively). Simultaneous measurements of the airway surface liquid height, mucus transport velocity, cilia beat frequency and surface temperature were made over time. The data are presented as mean±sd. RESULTS: The airway surface liquid height increased significantly with both 0.9% and 7.0% saline: at low-flow by 37.2±10.0 µm and 152.7±10.9 µm, respectively, and at high-flow by 62.3±5.6 µm and 163.4±25.4 µm, respectively (p<0.001). Mucus velocity was increased by both 0.9% and 7.0% saline from a baseline of 8.2±0.8 mm·min(−1) to 8.8±0.7 mm·min(−1) and 17.1±0.5 mm·min(−1), respectively, with low-flow and at high-flow to 9.8±0.02 mm·min(−1) (p=0.04) and 16.9±0.5 mm·min(−1) (p<0.05), respectively. Ciliary beating did not change with 0.9% saline, but declined from 13.1±0.6 Hz to 10.2±0.6 Hz and 11.1±0.6 Hz (p<0.05) with 7.0% saline at low- and high-flow, respectively. CONCLUSIONS: The findings demonstrate that nebulised isotonic 0.9% saline, like hypertonic 7.0% saline, significantly stimulates basal mucociliary transport, and the use of high-flow delivery had no significantly different hydration effects compared with low-flow delivery. Hypertonic 7.0% saline suppressed ciliary beating, indicating an increase in airway surface liquid osmolarity, which may have negative effects on the airway surface with frequent use. European Respiratory Society 2023-06-12 /pmc/articles/PMC10258716/ /pubmed/37313398 http://dx.doi.org/10.1183/23120541.00724-2022 Text en Copyright ©The authors 2023 https://creativecommons.org/licenses/by/4.0/This version is distributed under the terms of the Creative Commons Attribution Licence 4.0.
spellingShingle Original Research Articles
Kelly, Susyn
Valentine, Matthew
Chua, Wei Hang
Tatkov, Stanislav
Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
title Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
title_full Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
title_fullStr Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
title_full_unstemmed Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
title_short Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
title_sort impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258716/
https://www.ncbi.nlm.nih.gov/pubmed/37313398
http://dx.doi.org/10.1183/23120541.00724-2022
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