AM/PM dosing of LAMA for COPD: a randomized controlled trial protocol using digital recruitment and registries.

COPD exacerbation all-cause mortality chronic obstructive pulmonary disease intensive care admission long-acting muscarinic antagonists

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2024
Historique:
received: 09 05 2024
accepted: 15 07 2024
medline: 21 8 2024
pubmed: 21 8 2024
entrez: 21 8 2024
Statut: epublish

Résumé

Long-acting muscarinic antagonists (LAMAs) reduce the risk of acute exacerbations of chronic obstructive pulmonary disease (AECOPD), usually taken once daily in the morning. However, the circadian activity of autonomic regulation suggests that the highest need for anticholinergic therapy may be in the late night/early morning. This is supported by evidence that AECOPD most often begins in the morning. Furthermore, the trough spirometry effect of LAMA is lower than the peak effect, which further argues that evening dosing may be more optimal than morning dosing. This trial aims to determine whether evening administration of LAMA reduces hospitalization-requiring AECOPD or death from all causes within 1 year as compared to morning administration of the same LAMA. Randomized controlled open-label trial. Persons aged 30 years or older with a once-daily LAMA prescription and a confirmed COPD diagnosis were recruited. Participants were randomized in a 1:1 ratio to either morning or evening LAMA administration. Complete follow-up for the primary outcome, hospitalization-requiring AECOPD, or death from all causes within 1 year was captured from the Danish National Health Register, as were patient-reported outcome assessments at 6 and 12 months. A total of 10,013 participants were randomized, and the recruitment process started on 9 March 2023. Secondary outcomes include (i) moderate COPD exacerbations; (ii) all-cause hospitalization; (iii) ICU admission; (iv) need for non-invasive ventilation; and (v) all-cause mortality, among others. All outcomes will be evaluated 12 months after recruitment.

Identifiants

pubmed: 39165373
doi: 10.3389/fmed.2024.1430169
pmc: PMC11334606
doi:

Banques de données

ClinicalTrials.gov
['NCT05563675']

Types de publication

Journal Article

Langues

eng

Pagination

1430169

Informations de copyright

Copyright © 2024 Sivapalan, Rømer, Wirenfeldt Klausen, Dyrby Johansen, Pareek, Modin, Mathioudakis, Vestbo, Eklöf, Jordan, Hurst, Biering-Sørensen and Jensen.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Pradeesh Sivapalan (P)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Valdemar Rømer (V)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

Tobias Wirenfeldt Klausen (T)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

Niklas Dyrby Johansen (N)

Department of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

Manan Pareek (M)

Department of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

Daniel Modin (D)

Department of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

Alexander Mathioudakis (A)

Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, United Kingdom.
North West Lung Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Jørgen Vestbo (J)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.
Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, United Kingdom.
North West Lung Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Josefin Eklöf (J)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

Alexander Jordan (A)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.

John R Hurst (JR)

UCL Respiratory, University College London, London, United Kingdom.

Tor Biering-Sørensen (T)

Department of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.
Center for Translational Cardiology and Pragmatic Randomized Trials, Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Hellerup, Denmark.
Steno Diabetes Center Copenhagen, Herlev, Denmark.

Jens-Ulrik Jensen (JU)

Department of Medicine, Respiratory Medicine Section, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Classifications MeSH