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Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma
BACKGROUND: The aim of this study was to compare the efficacy of ciclesonide (80 mg/day) and fluticasone propionate (200 mg/day) for mild to moderate persistent asthma. MATERIALS AND METHODS: Female and male patients older than 12 years with a history of persistent bronchial asthma for at least 6 mo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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National Research Institute of Tuberculosis and Lung Disease
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515324/ https://www.ncbi.nlm.nih.gov/pubmed/26221146 |
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author | Jamaati, Hamidreza Malekmohammad, Majid Fahimi, Fanak Najafi, Arvin Hashemian, Seyed Mohammadreza |
author_facet | Jamaati, Hamidreza Malekmohammad, Majid Fahimi, Fanak Najafi, Arvin Hashemian, Seyed Mohammadreza |
author_sort | Jamaati, Hamidreza |
collection | PubMed |
description | BACKGROUND: The aim of this study was to compare the efficacy of ciclesonide (80 mg/day) and fluticasone propionate (200 mg/day) for mild to moderate persistent asthma. MATERIALS AND METHODS: Female and male patients older than 12 years with a history of persistent bronchial asthma for at least 6 months were enrolled. Patients were eligible to enter into a 2-week run-in period before randomization (baseline) if they had received inhaled corticosteroids (fluticasone propionate 250 μg/day or equivalent) at a constant dose during the last 4 weeks before the run-in period. In order to enter into the double blind 18-week treatment period, patients had to have a forced expiratory volume in 1s (FEV(1)) of 61–90% of predicted and a decrease in FEV(1) throughout the run-in period of more than 10%. Patients (n =230) were assigned to ciclesonide 80 mg once daily or fluticasone propionate 100 mg twice daily group. The primary outcome variable was change in FEV(1) compared to its baseline value. Secondary outcome variables were asthma-specific quality of life and asthma control. RESULTS: Both drugs significantly increased FEV(1) and other lung function parameters compared to baseline (P< 0.0001, both groups, all variables). Progress in the percentage of days with no asthma symptoms and no use of rescue medication and asthma-specific quality of life were similar in the two treatment groups. CONCLUSION: Ciclesonide at a dose of 80 μg once daily can provide efficient maintenance therapy for mild to moderate persistent asthma. |
format | Online Article Text |
id | pubmed-4515324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | National Research Institute of Tuberculosis and Lung Disease |
record_format | MEDLINE/PubMed |
spelling | pubmed-45153242015-07-28 Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma Jamaati, Hamidreza Malekmohammad, Majid Fahimi, Fanak Najafi, Arvin Hashemian, Seyed Mohammadreza Tanaffos Original Article BACKGROUND: The aim of this study was to compare the efficacy of ciclesonide (80 mg/day) and fluticasone propionate (200 mg/day) for mild to moderate persistent asthma. MATERIALS AND METHODS: Female and male patients older than 12 years with a history of persistent bronchial asthma for at least 6 months were enrolled. Patients were eligible to enter into a 2-week run-in period before randomization (baseline) if they had received inhaled corticosteroids (fluticasone propionate 250 μg/day or equivalent) at a constant dose during the last 4 weeks before the run-in period. In order to enter into the double blind 18-week treatment period, patients had to have a forced expiratory volume in 1s (FEV(1)) of 61–90% of predicted and a decrease in FEV(1) throughout the run-in period of more than 10%. Patients (n =230) were assigned to ciclesonide 80 mg once daily or fluticasone propionate 100 mg twice daily group. The primary outcome variable was change in FEV(1) compared to its baseline value. Secondary outcome variables were asthma-specific quality of life and asthma control. RESULTS: Both drugs significantly increased FEV(1) and other lung function parameters compared to baseline (P< 0.0001, both groups, all variables). Progress in the percentage of days with no asthma symptoms and no use of rescue medication and asthma-specific quality of life were similar in the two treatment groups. CONCLUSION: Ciclesonide at a dose of 80 μg once daily can provide efficient maintenance therapy for mild to moderate persistent asthma. National Research Institute of Tuberculosis and Lung Disease 2015 /pmc/articles/PMC4515324/ /pubmed/26221146 Text en Copyright© 2015 National Research Institute of Tuberculosis and Lung Disease This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Jamaati, Hamidreza Malekmohammad, Majid Fahimi, Fanak Najafi, Arvin Hashemian, Seyed Mohammadreza Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma |
title | Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma |
title_full | Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma |
title_fullStr | Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma |
title_full_unstemmed | Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma |
title_short | Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma |
title_sort | efficacy of low-dose ciclesonide and fluticasone propionate for mild to moderate persistent asthma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4515324/ https://www.ncbi.nlm.nih.gov/pubmed/26221146 |
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