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A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation

BACKGROUND: Leukotriene receptor antagonists (LTRAs) are well established in the management of outpatient asthma. However, there is very little information as to their role in acute asthma exacerbations. We hypothesized that LTRAs may accelerate lung function recovery when given in an acute exacerba...

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Autores principales: Zubairi, Ali Bin Sarwar, Salahuddin, Nawal, Khawaja, Ali, Awan, Safia, Shah, Adil Aijaz, Haque, Ahmed Suleman, Husain, Shahid Javed, Rao, Nisar, Khan, Javaid Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616955/
https://www.ncbi.nlm.nih.gov/pubmed/23537391
http://dx.doi.org/10.1186/1471-2466-13-20
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author Zubairi, Ali Bin Sarwar
Salahuddin, Nawal
Khawaja, Ali
Awan, Safia
Shah, Adil Aijaz
Haque, Ahmed Suleman
Husain, Shahid Javed
Rao, Nisar
Khan, Javaid Ahmad
author_facet Zubairi, Ali Bin Sarwar
Salahuddin, Nawal
Khawaja, Ali
Awan, Safia
Shah, Adil Aijaz
Haque, Ahmed Suleman
Husain, Shahid Javed
Rao, Nisar
Khan, Javaid Ahmad
author_sort Zubairi, Ali Bin Sarwar
collection PubMed
description BACKGROUND: Leukotriene receptor antagonists (LTRAs) are well established in the management of outpatient asthma. However, there is very little information as to their role in acute asthma exacerbations. We hypothesized that LTRAs may accelerate lung function recovery when given in an acute exacerbation. METHODS: A randomized, double blind, placebo-controlled trial was conducted at the Aga Khan University Hospital to assess the efficacy of oral montelukast on patients of 16 years of age and above who were hospitalized with acute asthma exacerbation. The patients were given either montelukast or placebo along with standard therapy throughout the hospital stay for acute asthma. Improvements in lung function and duration of hospital stay were monitored. RESULTS: 100 patients were randomized; their mean age was 52 years (SD +/− 18.50). The majority were females (79%) and non-smokers (89%). The mean hospital stay was 3.70 ± 1.93 days with 80% of patients discharged in 3 days. There was no significant difference in clinical symptoms, PEF over the course of hospital stay (p = 0.20 at day 2 and p = 0.47 at day 3) and discharge (p = 0.15), FEV(1) at discharge (p = 0.29) or length of hospital stay (p = 0.90) between the two groups. No serious adverse effects were noted during the course of the study. CONCLUSION: Our study suggests that there is no benefit of addition of oral montelukast over conventional treatment in the management of acute asthma attack. TRIAL REGISTRATION: Trial registration number: 375-Med/ERC-04
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spelling pubmed-36169552013-04-05 A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation Zubairi, Ali Bin Sarwar Salahuddin, Nawal Khawaja, Ali Awan, Safia Shah, Adil Aijaz Haque, Ahmed Suleman Husain, Shahid Javed Rao, Nisar Khan, Javaid Ahmad BMC Pulm Med Research Article BACKGROUND: Leukotriene receptor antagonists (LTRAs) are well established in the management of outpatient asthma. However, there is very little information as to their role in acute asthma exacerbations. We hypothesized that LTRAs may accelerate lung function recovery when given in an acute exacerbation. METHODS: A randomized, double blind, placebo-controlled trial was conducted at the Aga Khan University Hospital to assess the efficacy of oral montelukast on patients of 16 years of age and above who were hospitalized with acute asthma exacerbation. The patients were given either montelukast or placebo along with standard therapy throughout the hospital stay for acute asthma. Improvements in lung function and duration of hospital stay were monitored. RESULTS: 100 patients were randomized; their mean age was 52 years (SD +/− 18.50). The majority were females (79%) and non-smokers (89%). The mean hospital stay was 3.70 ± 1.93 days with 80% of patients discharged in 3 days. There was no significant difference in clinical symptoms, PEF over the course of hospital stay (p = 0.20 at day 2 and p = 0.47 at day 3) and discharge (p = 0.15), FEV(1) at discharge (p = 0.29) or length of hospital stay (p = 0.90) between the two groups. No serious adverse effects were noted during the course of the study. CONCLUSION: Our study suggests that there is no benefit of addition of oral montelukast over conventional treatment in the management of acute asthma attack. TRIAL REGISTRATION: Trial registration number: 375-Med/ERC-04 BioMed Central 2013-03-28 /pmc/articles/PMC3616955/ /pubmed/23537391 http://dx.doi.org/10.1186/1471-2466-13-20 Text en Copyright © 2013 Zubairi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zubairi, Ali Bin Sarwar
Salahuddin, Nawal
Khawaja, Ali
Awan, Safia
Shah, Adil Aijaz
Haque, Ahmed Suleman
Husain, Shahid Javed
Rao, Nisar
Khan, Javaid Ahmad
A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
title A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
title_full A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
title_fullStr A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
title_full_unstemmed A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
title_short A randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
title_sort randomized, double-blind, placebo-controlled trial of oral montelukast in acute asthma exacerbation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3616955/
https://www.ncbi.nlm.nih.gov/pubmed/23537391
http://dx.doi.org/10.1186/1471-2466-13-20
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