ELLIPTA Versus DISKUS plus HandiHaler in COPD: A Randomized, Open-Label, Crossover Study in a Clinical Trial Setting.

DISKUS ELLIPTA HandiHaler copd correct use patient preference

Journal

Chronic obstructive pulmonary diseases (Miami, Fla.)
ISSN: 2372-952X
Titre abrégé: Chronic Obstr Pulm Dis
Pays: United States
ID NLM: 101635411

Informations de publication

Date de publication:
Apr 2020
Historique:
entrez: 24 4 2020
pubmed: 24 4 2020
medline: 24 4 2020
Statut: ppublish

Résumé

Inhaler errors among patients with chronic obstructive pulmonary disease (COPD) can reduce treatment efficacy. This randomized, open-label, crossover study evaluated correct use of ELLIPTA versus DISKUS plus HandiHaler. Participants with COPD attended at least 3 study visits (Day 1 [Visit 1], Day 28 [Visit 2], and Day 56 [Visit 3]). Inhalers contained placebo; usual maintenance medication was continued. Participants were randomized to an inhaler sequence (ELLIPTA then DISKUS plus HandiHaler, or the reverse) and preference questionnaire at Visit 1. Participants read the instructions for use in the approved prescribing information for their inhaler(s) and correct use was assessed at Visit 1 (verbal guidance provided if required). Correct use was reassessed at Visit 2, and with the next inhaler(s) at Visit 3. Primary endpoint was the proportion of participants demonstrating correct use (0 errors) with the assigned inhaler(s) after 28 days. A greater proportion of study participants (n = 217) correctly used ELLIPTA (96%) versus DISKUS plus HandiHaler (87%) after 28 days. The odds of demonstrating correct use with ELLIPTA were 6.88 times that of DISKUS plus HandiHaler ( Delivery of COPD maintenance therapy via ELLIPTA demonstrates higher correct use rates and lower critical error rates compared with DISKUS plus HandiHaler.

Sections du résumé

BACKGROUND BACKGROUND
Inhaler errors among patients with chronic obstructive pulmonary disease (COPD) can reduce treatment efficacy.
METHODS METHODS
This randomized, open-label, crossover study evaluated correct use of ELLIPTA versus DISKUS plus HandiHaler. Participants with COPD attended at least 3 study visits (Day 1 [Visit 1], Day 28 [Visit 2], and Day 56 [Visit 3]). Inhalers contained placebo; usual maintenance medication was continued. Participants were randomized to an inhaler sequence (ELLIPTA then DISKUS plus HandiHaler, or the reverse) and preference questionnaire at Visit 1. Participants read the instructions for use in the approved prescribing information for their inhaler(s) and correct use was assessed at Visit 1 (verbal guidance provided if required). Correct use was reassessed at Visit 2, and with the next inhaler(s) at Visit 3. Primary endpoint was the proportion of participants demonstrating correct use (0 errors) with the assigned inhaler(s) after 28 days.
RESULTS RESULTS
A greater proportion of study participants (n = 217) correctly used ELLIPTA (96%) versus DISKUS plus HandiHaler (87%) after 28 days. The odds of demonstrating correct use with ELLIPTA were 6.88 times that of DISKUS plus HandiHaler (
CONCLUSIONS CONCLUSIONS
Delivery of COPD maintenance therapy via ELLIPTA demonstrates higher correct use rates and lower critical error rates compared with DISKUS plus HandiHaler.

Identifiants

pubmed: 32324983
doi: 10.15326/jcopdf.7.2.2019.0153
pmc: PMC7454022
doi:

Types de publication

Journal Article

Langues

eng

Pagination

118-129

Subventions

Organisme : GlaxoSmithKline plc.
Pays : United States
Organisme : GlaxoSmithKline plc.
Pays : United Kingdom

Informations de copyright

JCOPDF © 2020.

Déclaration de conflit d'intérêts

EMK has participated in consulting, advisory boards, speaker panels, or received travel reimbursement from Amphastar, AstraZeneca, Boehringer Ingelheim, Chiesi, Cipla, GlaxoSmithKline plc., Mylan, Novartis, Oriel, Pearl, Sunovion, Teva, and Theravance. He has conducted multicenter clinical research trials for approximately 40 pharmaceutical companies. SS has been a principal investigator for 20 years and has conducted clinical research trials for a large number of pharmaceutical companies. He has also participated as a consultant and on advisory boards and speaker panels for pharmaceutical companies including AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline plc., Mylan, Menlo, Novartis, Pearl, Sunovion, Teva, and Theravance. MZ, VM, RJ, KC, and RS are employees of, and own shares in, GlaxoSmithKline plc. Editorial support (in the form of writing assistance, collating author comments, assembling tables and/or figures, grammatical editing, fact checking, and referencing) was provided by Matthew Hallam, MSc(Res) and Joanna Wilson, PhD, of Gardine—Caldwell Communications (Macclesfield, UK) and was funded by GlaxoSmithKline plc. Trademarks are the property of their respective owners.

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Auteurs

Edward M Kerwin (EM)

Clinical Research Institute of Southern Oregon, Medford.

Selwyn Spangenthal (S)

American Health Research, Charlotte, North Carolina.

Michael Zvarich (M)

GlaxoSmithKline plc., Research Triangle Park, Durham, North Carolina.

Valerie Millar (V)

GlaxoSmithKline plc., Uxbridge, United Kingdom.

Renu Jain (R)

GlaxoSmithKline plc., Research Triangle Park, Durham, North Carolina.

Kathryn Collison (K)

GlaxoSmithKline plc., Research Triangle Park, Durham, North Carolina.

Raj Sharma (R)

Respiratory Medical Franchise, GlaxoSmithKline plc., Brentford, United Kingdom.

Classifications MeSH