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Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial
BACKGROUND: Antibiotics are frequently used to treat wheezing children. Macrolides may be effective in treating bronchiolitis and asthma. METHOD: We completed a prospective, double-blinded, randomized placebo-control trial of azithromycin among pre-school children (12 to 60 months of age) presenting...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542589/ https://www.ncbi.nlm.nih.gov/pubmed/28771627 http://dx.doi.org/10.1371/journal.pone.0182411 |
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author | Mandhane, Piush J. Paredes Zambrano de Silbernagel, Patricia Aung, Yin Nwe Williamson, Janie Lee, Bonita E. Spier, Sheldon Noseworthy, Mary Craig, William R. Johnson, David W. |
author_facet | Mandhane, Piush J. Paredes Zambrano de Silbernagel, Patricia Aung, Yin Nwe Williamson, Janie Lee, Bonita E. Spier, Sheldon Noseworthy, Mary Craig, William R. Johnson, David W. |
author_sort | Mandhane, Piush J. |
collection | PubMed |
description | BACKGROUND: Antibiotics are frequently used to treat wheezing children. Macrolides may be effective in treating bronchiolitis and asthma. METHOD: We completed a prospective, double-blinded, randomized placebo-control trial of azithromycin among pre-school children (12 to 60 months of age) presenting to the emergency department with wheeze. Patients were randomized to receive either five days of azithromycin or placebo. Primary outcome was time to resolution of respiratory symptoms after treatment initiation. Secondary outcomes included the number of days children used a Short-Acting Beta-Agonists during the 21 day follow-up and time to disease exacerbation during the following six months (unscheduled health care visit or treatment with an oral corticosteroid for acute respiratory symptoms). RESULTS: Of the 300 wheezing children recruited, 222 and 169 were analyzed for the primary and secondary outcomes, respectively. The treatment groups had similar demographics and clinical parameters at baseline. Median time to resolution of respiratory symptoms was four days for both treatment arms (interquartile range (IQR) 3,6; p = 0.28). Median number of days of Short-Acting Beta-Agonist use among those who received azithromycin was four and a half days (IQR 2, 7) and five days (IQR 2, 9; p = 0.22) among those who received placebo. Participants who received azithromycin had a 0.91 hazard ratio for time to six-month exacerbation compared to placebo (95% CI 0.61, 1.36, p = 0.65). A pre-determined subgroup analysis showed no differences in outcomes for children with their first or repeat episode of wheezing. There was no significant difference in the proportion of participants experiencing an adverse event. CONCLUSION: Azithromycin neither reduced duration of respiratory symptoms nor time to respiratory exacerbation in the following six months after treatment among wheezing preschool children presenting to an emergency department. There was no significant effect among children with either first-time or prior wheezing. |
format | Online Article Text |
id | pubmed-5542589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55425892017-08-12 Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial Mandhane, Piush J. Paredes Zambrano de Silbernagel, Patricia Aung, Yin Nwe Williamson, Janie Lee, Bonita E. Spier, Sheldon Noseworthy, Mary Craig, William R. Johnson, David W. PLoS One Research Article BACKGROUND: Antibiotics are frequently used to treat wheezing children. Macrolides may be effective in treating bronchiolitis and asthma. METHOD: We completed a prospective, double-blinded, randomized placebo-control trial of azithromycin among pre-school children (12 to 60 months of age) presenting to the emergency department with wheeze. Patients were randomized to receive either five days of azithromycin or placebo. Primary outcome was time to resolution of respiratory symptoms after treatment initiation. Secondary outcomes included the number of days children used a Short-Acting Beta-Agonists during the 21 day follow-up and time to disease exacerbation during the following six months (unscheduled health care visit or treatment with an oral corticosteroid for acute respiratory symptoms). RESULTS: Of the 300 wheezing children recruited, 222 and 169 were analyzed for the primary and secondary outcomes, respectively. The treatment groups had similar demographics and clinical parameters at baseline. Median time to resolution of respiratory symptoms was four days for both treatment arms (interquartile range (IQR) 3,6; p = 0.28). Median number of days of Short-Acting Beta-Agonist use among those who received azithromycin was four and a half days (IQR 2, 7) and five days (IQR 2, 9; p = 0.22) among those who received placebo. Participants who received azithromycin had a 0.91 hazard ratio for time to six-month exacerbation compared to placebo (95% CI 0.61, 1.36, p = 0.65). A pre-determined subgroup analysis showed no differences in outcomes for children with their first or repeat episode of wheezing. There was no significant difference in the proportion of participants experiencing an adverse event. CONCLUSION: Azithromycin neither reduced duration of respiratory symptoms nor time to respiratory exacerbation in the following six months after treatment among wheezing preschool children presenting to an emergency department. There was no significant effect among children with either first-time or prior wheezing. Public Library of Science 2017-08-03 /pmc/articles/PMC5542589/ /pubmed/28771627 http://dx.doi.org/10.1371/journal.pone.0182411 Text en © 2017 Mandhane et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mandhane, Piush J. Paredes Zambrano de Silbernagel, Patricia Aung, Yin Nwe Williamson, Janie Lee, Bonita E. Spier, Sheldon Noseworthy, Mary Craig, William R. Johnson, David W. Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial |
title | Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial |
title_full | Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial |
title_fullStr | Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial |
title_full_unstemmed | Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial |
title_short | Treatment of preschool children presenting to the emergency department with wheeze with azithromycin: A placebo-controlled randomized trial |
title_sort | treatment of preschool children presenting to the emergency department with wheeze with azithromycin: a placebo-controlled randomized trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542589/ https://www.ncbi.nlm.nih.gov/pubmed/28771627 http://dx.doi.org/10.1371/journal.pone.0182411 |
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