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The effects of respiratory inhaled drugs on the prevention of acute mountain sickness
BACKGROUND: Acute mountain sickness (AMS) is common in high-altitude travelers, and may lead to life-threatening high-altitude cerebral edema (HACE) or high-altitude pulmonary edema (HAPE). The inhaled drugs have a much lower peak serum concentrations and a shorter half-life period than oral drugs,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133459/ https://www.ncbi.nlm.nih.gov/pubmed/30095637 http://dx.doi.org/10.1097/MD.0000000000011788 |
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author | Wang, Xiaomei Chen, Hong Li, Rong Fu, Weiling Yao, Chunyan |
author_facet | Wang, Xiaomei Chen, Hong Li, Rong Fu, Weiling Yao, Chunyan |
author_sort | Wang, Xiaomei |
collection | PubMed |
description | BACKGROUND: Acute mountain sickness (AMS) is common in high-altitude travelers, and may lead to life-threatening high-altitude cerebral edema (HACE) or high-altitude pulmonary edema (HAPE). The inhaled drugs have a much lower peak serum concentrations and a shorter half-life period than oral drugs, which give them a special character, greater local effects in the lung. Meanwhile, short-term administration of inhaled drugs results in almost no adverse reactions. METHODS: We chose inhaled ipratropium bromide/salbutamol sulfate (combivent, COM), budesonide (pulmicortrespules, BUD), and salbutamol sulfate (ventolin, VEN) in our study to investigate their prophylactic efficacy against AMS. Since COM is a compound drug of ipratropium bromide and salbutamol sulfate, to verify which part of COM plays a role in the prevention of AMS, we also tested VEN in our experiment. RESULTS: In our study, Lake Louise scores (LLS) in the COM (1.14 ± 0.89 vs 1.91 ± 1.23, P < .05) and BUD (1.35 ± 0.94 vs 1.91 ± 1.23, P < .05) groups were both significantly lower than the placebo group at 72 hours. There were no significant differences in LLS scores among the 4 groups at 120 hours. The incidence of AMS in the COM group was significantly reduced at 72 hours (16.7% in COM group vs 43.4% in placebo group, P < .05) after exposure to high-altitude. There were no significant differences in AMS incidences at 120 hours among the 4 groups. CONCLUSION: The prophylactic use of COM could prevent AMS in young Chinese male at 72 hours after high-altitude exposure. BUD also could reduce LLS but not prevent AMS at 72 hours. Ipratropium bromide maybe the effective drug in COM work on the prevention of AMS alone. |
format | Online Article Text |
id | pubmed-6133459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-61334592018-09-19 The effects of respiratory inhaled drugs on the prevention of acute mountain sickness Wang, Xiaomei Chen, Hong Li, Rong Fu, Weiling Yao, Chunyan Medicine (Baltimore) Research Article BACKGROUND: Acute mountain sickness (AMS) is common in high-altitude travelers, and may lead to life-threatening high-altitude cerebral edema (HACE) or high-altitude pulmonary edema (HAPE). The inhaled drugs have a much lower peak serum concentrations and a shorter half-life period than oral drugs, which give them a special character, greater local effects in the lung. Meanwhile, short-term administration of inhaled drugs results in almost no adverse reactions. METHODS: We chose inhaled ipratropium bromide/salbutamol sulfate (combivent, COM), budesonide (pulmicortrespules, BUD), and salbutamol sulfate (ventolin, VEN) in our study to investigate their prophylactic efficacy against AMS. Since COM is a compound drug of ipratropium bromide and salbutamol sulfate, to verify which part of COM plays a role in the prevention of AMS, we also tested VEN in our experiment. RESULTS: In our study, Lake Louise scores (LLS) in the COM (1.14 ± 0.89 vs 1.91 ± 1.23, P < .05) and BUD (1.35 ± 0.94 vs 1.91 ± 1.23, P < .05) groups were both significantly lower than the placebo group at 72 hours. There were no significant differences in LLS scores among the 4 groups at 120 hours. The incidence of AMS in the COM group was significantly reduced at 72 hours (16.7% in COM group vs 43.4% in placebo group, P < .05) after exposure to high-altitude. There were no significant differences in AMS incidences at 120 hours among the 4 groups. CONCLUSION: The prophylactic use of COM could prevent AMS in young Chinese male at 72 hours after high-altitude exposure. BUD also could reduce LLS but not prevent AMS at 72 hours. Ipratropium bromide maybe the effective drug in COM work on the prevention of AMS alone. Wolters Kluwer Health 2018-08-10 /pmc/articles/PMC6133459/ /pubmed/30095637 http://dx.doi.org/10.1097/MD.0000000000011788 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | Research Article Wang, Xiaomei Chen, Hong Li, Rong Fu, Weiling Yao, Chunyan The effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
title | The effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
title_full | The effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
title_fullStr | The effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
title_full_unstemmed | The effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
title_short | The effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
title_sort | effects of respiratory inhaled drugs on the prevention of acute mountain sickness |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133459/ https://www.ncbi.nlm.nih.gov/pubmed/30095637 http://dx.doi.org/10.1097/MD.0000000000011788 |
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