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Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants

INTRODUCTION: Continuous positive airway pressure (CPAP) may induce nasal inflammation because of mucosal compression or dryness. This study examined the impact of humidified versus nonhumidified CPAP on nasal inflammation and upper airway symptoms. METHODS: Seventeen healthy male subjects with no p...

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Autores principales: Al-Otaibi, Hajed M., Alahmari, Mohammed D., Al-Maqati, Thekra N., Ghazwani, Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Canadian Society of Respiratory Therapists 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428007/
https://www.ncbi.nlm.nih.gov/pubmed/32844111
http://dx.doi.org/10.29390/cjrt-2020-005
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author Al-Otaibi, Hajed M.
Alahmari, Mohammed D.
Al-Maqati, Thekra N.
Ghazwani, Abdullah
author_facet Al-Otaibi, Hajed M.
Alahmari, Mohammed D.
Al-Maqati, Thekra N.
Ghazwani, Abdullah
author_sort Al-Otaibi, Hajed M.
collection PubMed
description INTRODUCTION: Continuous positive airway pressure (CPAP) may induce nasal inflammation because of mucosal compression or dryness. This study examined the impact of humidified versus nonhumidified CPAP on nasal inflammation and upper airway symptoms. METHODS: Seventeen healthy male subjects with no previous or current history of nasal symptoms were recruited. All subjects underwent 3 hours of nonhumidified CPAP at 12.5 cmH(2)O via nasal mask. Among the 17 studied subjects, seven returned to receive a humidified CPAP at 12.5 cmH(2)O via nasal mask. The nasal wash leukocyte count was assessed at baseline and after each CPAP setting. The white blood cell (WBC) count and levels of WBCs that are mononuclear cells (including lymphocytes and monocytes) were monitored. A six-point nasal score was also assessed before and after the CPAP intervention. RESULTS: The nasal wash WBC count (10(3)/µL) and mononuclear cell level (10(3)/µL) at baseline, on 12.5 cmH(2)O humidified CPAP, and on 12.5 cmH(2)O nonhumidified CPAP were significantly different (p = 0.016; p = 0.003). Changes in nasopharyngeal symptoms occurred in 12 of 17 subjects (70.5%) in the nonhumidified group. Participants experienced at least one nasal symptom after application of nonhumidified CPAP at 12.5 cmH(2)O. CONCLUSION: The present investigation suggests that humidified CPAP was not associated with early nasal inflammation and there were fewer nasopharyngeal symptoms. Further study is required to confirm the results and evaluate the impact of adding heat to the humidified CPAP system.
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spelling pubmed-74280072020-08-24 Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants Al-Otaibi, Hajed M. Alahmari, Mohammed D. Al-Maqati, Thekra N. Ghazwani, Abdullah Can J Respir Ther Research Article INTRODUCTION: Continuous positive airway pressure (CPAP) may induce nasal inflammation because of mucosal compression or dryness. This study examined the impact of humidified versus nonhumidified CPAP on nasal inflammation and upper airway symptoms. METHODS: Seventeen healthy male subjects with no previous or current history of nasal symptoms were recruited. All subjects underwent 3 hours of nonhumidified CPAP at 12.5 cmH(2)O via nasal mask. Among the 17 studied subjects, seven returned to receive a humidified CPAP at 12.5 cmH(2)O via nasal mask. The nasal wash leukocyte count was assessed at baseline and after each CPAP setting. The white blood cell (WBC) count and levels of WBCs that are mononuclear cells (including lymphocytes and monocytes) were monitored. A six-point nasal score was also assessed before and after the CPAP intervention. RESULTS: The nasal wash WBC count (10(3)/µL) and mononuclear cell level (10(3)/µL) at baseline, on 12.5 cmH(2)O humidified CPAP, and on 12.5 cmH(2)O nonhumidified CPAP were significantly different (p = 0.016; p = 0.003). Changes in nasopharyngeal symptoms occurred in 12 of 17 subjects (70.5%) in the nonhumidified group. Participants experienced at least one nasal symptom after application of nonhumidified CPAP at 12.5 cmH(2)O. CONCLUSION: The present investigation suggests that humidified CPAP was not associated with early nasal inflammation and there were fewer nasopharyngeal symptoms. Further study is required to confirm the results and evaluate the impact of adding heat to the humidified CPAP system. Canadian Society of Respiratory Therapists 2020-07-23 /pmc/articles/PMC7428007/ /pubmed/32844111 http://dx.doi.org/10.29390/cjrt-2020-005 Text en http://creativecommons.org/licenses/by-nc/4.0/ This open-access article is distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC) (http://creativecommons.org/licenses/by-nc/4.0/), which permits reuse, distribution and reproduction of the article, provided that the original work is properly cited and the reuse is restricted to noncommercial purposes. For commercial reuse, contact editor@csrt.com
spellingShingle Research Article
Al-Otaibi, Hajed M.
Alahmari, Mohammed D.
Al-Maqati, Thekra N.
Ghazwani, Abdullah
Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants
title Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants
title_full Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants
title_fullStr Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants
title_full_unstemmed Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants
title_short Effect of humidified versus nonhumidified CPAP on inflammatory response and nasopharyngeal symptoms in healthy participants
title_sort effect of humidified versus nonhumidified cpap on inflammatory response and nasopharyngeal symptoms in healthy participants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428007/
https://www.ncbi.nlm.nih.gov/pubmed/32844111
http://dx.doi.org/10.29390/cjrt-2020-005
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