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Bronchodilator response after two methods of salbutamol nebulization in asthmatic children

INTRODUCTION: Salbutamol is used in bronchodilator response testing (BDRT), which is an important diagnostic tool in bronchial obstructive diseases. Most available studies compare the bronchodilator response of salbutamol administered with a pressurized metered-dose inhaler and salbutamol in a nebul...

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Autores principales: Emeryk, Andrzej, Janeczek, Kamil, Markut-Miotła, Ewa, Pirożyński, Michał, Florkiewicz, Emil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837600/
https://www.ncbi.nlm.nih.gov/pubmed/36685998
http://dx.doi.org/10.5114/ada.2022.117038
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author Emeryk, Andrzej
Janeczek, Kamil
Markut-Miotła, Ewa
Pirożyński, Michał
Florkiewicz, Emil
author_facet Emeryk, Andrzej
Janeczek, Kamil
Markut-Miotła, Ewa
Pirożyński, Michał
Florkiewicz, Emil
author_sort Emeryk, Andrzej
collection PubMed
description INTRODUCTION: Salbutamol is used in bronchodilator response testing (BDRT), which is an important diagnostic tool in bronchial obstructive diseases. Most available studies compare the bronchodilator response of salbutamol administered with a pressurized metered-dose inhaler and salbutamol in a nebulization solution. AIM: The spirometric evaluation of the bronchodilator response of two methods of salbutamol nebulization in asthmatic children. MATERIAL AND METHODS: A randomized, open, comparative study was conducted in which 132 children with partially controlled asthma and current bronchial obstruction determined by spirometry were enrolled. BDRT was conducted using salbutamol solution administered with either a continuous jet nebulizer (CON) or a breath-actuated jet nebulizer (BAN). The BAN group received half the dose of the drug compared to the CON group, i.e. 2.5 mg. Changes in FEV(1) and FEF25–75 after drug administration were calculated in relation to the baseline values. RESULTS: The change in FEV(1) after salbutamol administration was 16.9 ±9.7% in the BAN group and was statistically significantly higher than in the CON group (12.6 ±8.8%) (p = 0.026). The change in FEF25-75 was 37.7 ±23.2% in the BAN group and 32.7 ±25.5% in the CON group (p = 0.061). There were no statistically significant differences in the frequency of adverse events between the compared groups. CONCLUSIONS: Salbutamol inhaled from BAN results in a better bronchodilator response than twice the nominal dose of this drug inhaled from CON, which is due to the absence of drug loss during the expiratory phase and therefore greater pulmonary deposition.
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spelling pubmed-98376002023-01-20 Bronchodilator response after two methods of salbutamol nebulization in asthmatic children Emeryk, Andrzej Janeczek, Kamil Markut-Miotła, Ewa Pirożyński, Michał Florkiewicz, Emil Postepy Dermatol Alergol Original Paper INTRODUCTION: Salbutamol is used in bronchodilator response testing (BDRT), which is an important diagnostic tool in bronchial obstructive diseases. Most available studies compare the bronchodilator response of salbutamol administered with a pressurized metered-dose inhaler and salbutamol in a nebulization solution. AIM: The spirometric evaluation of the bronchodilator response of two methods of salbutamol nebulization in asthmatic children. MATERIAL AND METHODS: A randomized, open, comparative study was conducted in which 132 children with partially controlled asthma and current bronchial obstruction determined by spirometry were enrolled. BDRT was conducted using salbutamol solution administered with either a continuous jet nebulizer (CON) or a breath-actuated jet nebulizer (BAN). The BAN group received half the dose of the drug compared to the CON group, i.e. 2.5 mg. Changes in FEV(1) and FEF25–75 after drug administration were calculated in relation to the baseline values. RESULTS: The change in FEV(1) after salbutamol administration was 16.9 ±9.7% in the BAN group and was statistically significantly higher than in the CON group (12.6 ±8.8%) (p = 0.026). The change in FEF25-75 was 37.7 ±23.2% in the BAN group and 32.7 ±25.5% in the CON group (p = 0.061). There were no statistically significant differences in the frequency of adverse events between the compared groups. CONCLUSIONS: Salbutamol inhaled from BAN results in a better bronchodilator response than twice the nominal dose of this drug inhaled from CON, which is due to the absence of drug loss during the expiratory phase and therefore greater pulmonary deposition. Termedia Publishing House 2022-06-07 2022-12 /pmc/articles/PMC9837600/ /pubmed/36685998 http://dx.doi.org/10.5114/ada.2022.117038 Text en Copyright: © 2022 Termedia Sp. z o. o. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Emeryk, Andrzej
Janeczek, Kamil
Markut-Miotła, Ewa
Pirożyński, Michał
Florkiewicz, Emil
Bronchodilator response after two methods of salbutamol nebulization in asthmatic children
title Bronchodilator response after two methods of salbutamol nebulization in asthmatic children
title_full Bronchodilator response after two methods of salbutamol nebulization in asthmatic children
title_fullStr Bronchodilator response after two methods of salbutamol nebulization in asthmatic children
title_full_unstemmed Bronchodilator response after two methods of salbutamol nebulization in asthmatic children
title_short Bronchodilator response after two methods of salbutamol nebulization in asthmatic children
title_sort bronchodilator response after two methods of salbutamol nebulization in asthmatic children
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837600/
https://www.ncbi.nlm.nih.gov/pubmed/36685998
http://dx.doi.org/10.5114/ada.2022.117038
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