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Characterizing Real-World Use Of Tiotropium In Asthma In The USA

BACKGROUND: Tiotropium bromide (TIO) is a long-acting muscarinic antagonist recommended as an add-on therapy option for patients with uncontrolled asthma on inhaled corticosteroids (ICS) and long-acting β(2)-agonists (LABA). However, real-world data on TIO use in asthma remains limited. To identify...

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Autores principales: Averell, Carlyne M, Laliberté, François, Duh, Mei Sheng, Wu, Jennifer W, Germain, Guillaume, Faison, Sarai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789414/
https://www.ncbi.nlm.nih.gov/pubmed/31632091
http://dx.doi.org/10.2147/JAA.S216932
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author Averell, Carlyne M
Laliberté, François
Duh, Mei Sheng
Wu, Jennifer W
Germain, Guillaume
Faison, Sarai
author_facet Averell, Carlyne M
Laliberté, François
Duh, Mei Sheng
Wu, Jennifer W
Germain, Guillaume
Faison, Sarai
author_sort Averell, Carlyne M
collection PubMed
description BACKGROUND: Tiotropium bromide (TIO) is a long-acting muscarinic antagonist recommended as an add-on therapy option for patients with uncontrolled asthma on inhaled corticosteroids (ICS) and long-acting β(2)-agonists (LABA). However, real-world data on TIO use in asthma remains limited. To identify unmet needs, this study explored the use of TIO in US patients with asthma. METHODS: This retrospective cohort study used IQVIA(TM) Health Plan Claims Data (October 1, 2014─December 31, 2016). Patients with asthma diagnoses initiating TIO 1.25 or 2.5 mcg after September 16, 2015 (first dispensing on index date) with ≥6 and ≥3 months continuous enrollment pre- and post-index, respectively, were identified. Patients with COPD diagnoses were excluded. Baseline characteristics, healthcare resource utilization and costs, and treatment patterns before and following TIO initiation were described for TIO cohorts and subgroups classified by concomitant medications received during the 30-day period after initiation. RESULTS: The study included 766 TIO 1.25 mcg and 1055 TIO 2.5 mcg users. In the TIO 1.25 mcg cohort, 16% (126/766) used TIO monotherapy while 61% (465/766) used TIO+ICS/LABA± leukotriene receptor antagonists (triple therapy). In TIO 1.25 mcg monotherapy and triple therapy subgroups, 39% and 49% were treated by allergists/pulmonologists, 27% and 48% experienced a moderate/severe asthma exacerbation, and 50% and 68% used rescue oral corticosteroids during the baseline period, respectively. Following triple therapy initiation, 44% of patients discontinued ICS within 6 months. The TIO 2.5 mcg cohort demonstrated similar trends. CONCLUSION: This study provided insights into real-world US use of TIO in asthma. Overall, 16–19% of patients received TIO monotherapy and had high baseline exacerbation rates, suggesting that additional ICS-containing medication may be beneficial. Patients initiating triple therapy were among the most severe, with high baseline exacerbation rates and rescue medication use, and had high post-treatment ICS discontinuation rates, suggesting unmet needs in this population.
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spelling pubmed-67894142019-10-18 Characterizing Real-World Use Of Tiotropium In Asthma In The USA Averell, Carlyne M Laliberté, François Duh, Mei Sheng Wu, Jennifer W Germain, Guillaume Faison, Sarai J Asthma Allergy Original Research BACKGROUND: Tiotropium bromide (TIO) is a long-acting muscarinic antagonist recommended as an add-on therapy option for patients with uncontrolled asthma on inhaled corticosteroids (ICS) and long-acting β(2)-agonists (LABA). However, real-world data on TIO use in asthma remains limited. To identify unmet needs, this study explored the use of TIO in US patients with asthma. METHODS: This retrospective cohort study used IQVIA(TM) Health Plan Claims Data (October 1, 2014─December 31, 2016). Patients with asthma diagnoses initiating TIO 1.25 or 2.5 mcg after September 16, 2015 (first dispensing on index date) with ≥6 and ≥3 months continuous enrollment pre- and post-index, respectively, were identified. Patients with COPD diagnoses were excluded. Baseline characteristics, healthcare resource utilization and costs, and treatment patterns before and following TIO initiation were described for TIO cohorts and subgroups classified by concomitant medications received during the 30-day period after initiation. RESULTS: The study included 766 TIO 1.25 mcg and 1055 TIO 2.5 mcg users. In the TIO 1.25 mcg cohort, 16% (126/766) used TIO monotherapy while 61% (465/766) used TIO+ICS/LABA± leukotriene receptor antagonists (triple therapy). In TIO 1.25 mcg monotherapy and triple therapy subgroups, 39% and 49% were treated by allergists/pulmonologists, 27% and 48% experienced a moderate/severe asthma exacerbation, and 50% and 68% used rescue oral corticosteroids during the baseline period, respectively. Following triple therapy initiation, 44% of patients discontinued ICS within 6 months. The TIO 2.5 mcg cohort demonstrated similar trends. CONCLUSION: This study provided insights into real-world US use of TIO in asthma. Overall, 16–19% of patients received TIO monotherapy and had high baseline exacerbation rates, suggesting that additional ICS-containing medication may be beneficial. Patients initiating triple therapy were among the most severe, with high baseline exacerbation rates and rescue medication use, and had high post-treatment ICS discontinuation rates, suggesting unmet needs in this population. Dove 2019-10-07 /pmc/articles/PMC6789414/ /pubmed/31632091 http://dx.doi.org/10.2147/JAA.S216932 Text en © 2019 Averell et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Averell, Carlyne M
Laliberté, François
Duh, Mei Sheng
Wu, Jennifer W
Germain, Guillaume
Faison, Sarai
Characterizing Real-World Use Of Tiotropium In Asthma In The USA
title Characterizing Real-World Use Of Tiotropium In Asthma In The USA
title_full Characterizing Real-World Use Of Tiotropium In Asthma In The USA
title_fullStr Characterizing Real-World Use Of Tiotropium In Asthma In The USA
title_full_unstemmed Characterizing Real-World Use Of Tiotropium In Asthma In The USA
title_short Characterizing Real-World Use Of Tiotropium In Asthma In The USA
title_sort characterizing real-world use of tiotropium in asthma in the usa
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789414/
https://www.ncbi.nlm.nih.gov/pubmed/31632091
http://dx.doi.org/10.2147/JAA.S216932
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