Comparative Effectiveness of Umeclidinium/Vilanterol versus Inhaled Corticosteroid/Long-Acting β

adherence chronic obstructive pulmonary disease (COPD) treatment comparative effectiveness inhaled corticosteroid/long-actingβ2-agonist (ICS/LABA) dual therapy long-acting muscarinic antagonist (LAMA)/LABA dual therapy

Journal

International journal of chronic obstructive pulmonary disease
ISSN: 1178-2005
Titre abrégé: Int J Chron Obstruct Pulmon Dis
Pays: New Zealand
ID NLM: 101273481

Informations de publication

Date de publication:
2023
Historique:
received: 20 01 2023
accepted: 06 04 2023
medline: 10 5 2023
pubmed: 8 5 2023
entrez: 8 5 2023
Statut: epublish

Résumé

To compare adherence to once-daily umeclidinium/vilanterol (UMEC/VI), a long-acting muscarinic antagonist/long-acting β Active comparator, new-user, retrospective cohort study using CPRD-Aurum primary care data and linked Hospital Episode Statistics secondary care administrative data. Patients without exacerbations in the previous year were indexed on first/earliest prescription date of once-daily UMEC/VI or twice-daily ICS/LABA as initial maintenance therapy between July 2014-September 2019. Primary outcome: medication adherence at 12 months post-index, defined as proportion of days covered (PDC) ≥80%. PDC represented proportion of time over the treatment duration that the patient was theoretically in possession of the medication. Secondary outcomes: adherence at 6, 18, and 24 months post-index, time-to-triple therapy, time-to-first on-treatment COPD exacerbation, COPD-related and all-cause healthcare resource utilization (HCRU), and direct health-care costs. A propensity score was generated and inverse probability of treatment weighting (IPTW) was used to balance potential confounders. Superiority was defined as >0% difference between treatment groups. In total, 6815 eligible patients were included (UMEC/VI:1623; ICS/LABA:5192). At 12 months post-index, weighted odds of a patient being adherent were significantly greater with UMEC/VI versus ICS/LABA (odds ratio [95% CI]: 1.71 [1.09, 2.66]; p=0.0185), demonstrating superiority of UMEC/VI. Patients taking UMEC/VI were statistically significantly more adherent than those taking ICS/LABA at 6, 18, and 24 months post-index (p<0.05). Differences in time-to-triple therapy, time-to-moderate COPD exacerbations, HCRU, and direct medical costs were not statistically significant between treatments after IPTW was applied. At 12 months post-treatment initiation, once-daily UMEC/VI was superior to twice-daily ICS/LABA in medication adherence among patients with COPD without exacerbations in the previous year, newly initiating dual maintenance therapy in England. The finding was consistent at 6, 18, and 24 months.

Identifiants

pubmed: 37155496
doi: 10.2147/COPD.S405498
pii: 405498
pmc: PMC10122847
doi:

Substances chimiques

vilanterol 028LZY775B
GSK573719 0
Adrenergic beta-2 Receptor Agonists 0
Chlorobenzenes 0
Adrenal Cortex Hormones 0
Quinuclidines 0
Muscarinic Antagonists 0
Bronchodilator Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

643-659

Informations de copyright

© 2023 Czira et al.

Déclaration de conflit d'intérêts

AC, GR, CC, KJR, and ASI are employees of GSK and hold stock and shares at GSK. ASI also holds an unpaid faculty position at McMaster University in Canada. FH is an employee of the Translational Lung Research Center Heidelberg, part of the Germany lung research Foundation (DZL) and he also reports lecturing and adboard activities for GSK. JKQ holds a position at Imperial College London. CMC, TT, RWo, and RWi are employees of Adelphi Real World. VB is currently an employee of Bayer AG UK and holds stock and shares there. VB and JY were employees of Adelphi Real World at the time of the study. Adelphi Real World is a business that provides consulting and other research services to pharmaceutical, device, government, and non-government organizations, which received funding from GSK to conduct the study. Adelphi Real World employees work with a variety of companies and organizations and are expressly prohibited from receiving any payment or honoraria directly from these organizations for services rendered. The authors report no other conflicts of interest in this work.

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Auteurs

Alexandrosz Czira (A)

R&D Global Medical, GSK, Brentford, Middlesex, UK.

Gema Requena (G)

R&D Global Medical, GSK, Brentford, Middlesex, UK.

Victoria Banks (V)

Real-World Evidence, Adelphi Real World, Bollington, Cheshire, UK.

Robert Wood (R)

Real-World Evidence, Adelphi Real World, Bollington, Cheshire, UK.

Theo Tritton (T)

Real-World Evidence, Adelphi Real World, Bollington, Cheshire, UK.

Catherine M Castillo (CM)

Real-World Evidence, Adelphi Real World, Bollington, Cheshire, UK.

Jie Yeap (J)

Real-World Evidence, Adelphi Real World, Bollington, Cheshire, UK.

Rosie Wild (R)

Real-World Evidence, Adelphi Real World, Bollington, Cheshire, UK.

Chris Compton (C)

R&D Global Medical, GSK, Brentford, Middlesex, UK.

Kieran J Rothnie (KJ)

R&D Global Medical, GSK, Brentford, Middlesex, UK.

Felix Herth (F)

Department of Pulmonology and Respiratory Care Medicine, Thoraxklinik at the University of Heidelberg, Heidelberg, Germany.
Translational Lung Research Center Heidelberg, Member of the German Center for Lung Research DZL, Heidelberg, Germany.

Jennifer K Quint (JK)

National Heart and Lung Institute, Imperial College London, London, UK.

Afisi S Ismaila (AS)

Value Evidence and Outcomes, GSK, Collegeville, PA, USA.
Department of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, ON, Canada.

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Classifications MeSH