Characteristics of Patients with Chronic Obstructive Pulmonary Disease Treated with Long-Acting Bronchodilators in a Real-World Setting in Singapore: A Single-Center Observational Study.


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:
2022
Historique:
received: 10 01 2022
accepted: 19 05 2022
entrez: 17 6 2022
pubmed: 18 6 2022
medline: 22 6 2022
Statut: epublish

Résumé

There is limited real-world evidence regarding clinical practice for chronic obstructive pulmonary disease (COPD) in Singapore. We compared baseline clinical characteristics and evaluated outcomes in patients with COPD who initiated treatment with either a long-acting muscarinic antagonist (LAMA) or a LAMA and a long-acting β This was a single-center observational study at Changi General Hospital, Singapore. Routine clinical data (hospital visits, case management, lung function, laboratory/imaging results, medication orders) were collected and compiled into a data warehouse. Eligible patients with COPD were ≥40 years old and newly prescribed LAMA or LAMA+LABA during the enrollment period. Patient characteristics in the baseline period (6 months) were compared between treatments. Clinical worsening was measured as a composite endpoint, defined as the first of a change in maintenance treatment class or a moderate-to-severe exacerbation during follow-up (12 months). In total, 261 patients were included in the baseline period (LAMA: 73; LAMA+LABA: 188). In the baseline period, patients receiving LAMA+LABA versus LAMA had significantly lower body mass index, higher COPD Assessment Test score and worse lung function, and numerically higher exacerbation history. Prevalence of comorbidities was similar between treatment groups. In follow-up, high rates of clinical worsening were observed regardless of treatment regimen (LAMA: 38/73 [52%]; LAMA+LABA: 86/188 [46%]). Median time-to-clinical worsening was 340 days for the LAMA cohort and the raw median 154 days (interquartile range: 44-225) for the LAMA+LABA cohort. Median medication dispensation rate (0.86; interquartile range: 0.56-1.00) was similar between treatments. Patients initiating treatment with LAMA+LABA had more severe COPD than patients prescribed LAMA. The proportion of patients experiencing clinical worsening was similarly high in both cohorts, suggesting that early identification and treatment optimization are necessary.

Identifiants

pubmed: 35711173
doi: 10.2147/COPD.S357820
pii: 357820
pmc: PMC9192350
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Adrenergic beta-2 Receptor Agonists 0
Bronchodilator Agents 0
Muscarinic Antagonists 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1349-1363

Informations de copyright

© 2022 Sim et al.

Déclaration de conflit d'intérêts

MS reports non-financial support from GSK for manuscript writing support, during the conduct of the study. AY reports grants, non-financial support from GSK, during the conduct of the study. AT reports grants from GSK for supporting the systems integration of the COPD database, during the conduct of the study. XX and PB are employees of GSK. AANR and DM are employees of GSK and hold stock and shares at GSK. The authors report no other conflicts of interest in this work.

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Auteurs

Marcus Sim (M)

Department of Respiratory and Critical Care Medicine, Changi General Hospital, Singapore, Singapore.

Anthony Yii (A)

Department of Respiratory and Critical Care Medicine, Changi General Hospital, Singapore, Singapore.

Xiaomeng Xu (X)

Value Evidence & Outcomes, Greater China and Intercontinental, GSK, Singapore, Singapore.

Priti Bahety (P)

Medical Affairs, GSK, Singapore, Singapore.

Chee Hong Loh (CH)

Department of Respiratory and Critical Care Medicine, Changi General Hospital, Singapore, Singapore.

Aldo Amador Navarro Rojas (AA)

Respiratory & Specialty Medical Lead, Greater China and Intercontinental, GSK, Singapore, Singapore.

Dominique Milea (D)

Value Evidence & Outcomes, Greater China and Intercontinental, GSK, Singapore, Singapore.

Augustine Tee (A)

Department of Respiratory and Critical Care Medicine, Changi General Hospital, Singapore, Singapore.

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Classifications MeSH