Association between Increased Risk of Pneumonia with ICS in COPD: A Continuous Variable Analysis of Patient Factors from the IMPACT Study.

COPD ICS IMPACT Pneumonia risk Post hoc analysis

Journal

Pulmonary therapy
ISSN: 2364-1746
Titre abrégé: Pulm Ther
Pays: United States
ID NLM: 101687144

Informations de publication

Date de publication:
06 Mar 2024
Historique:
received: 11 01 2024
accepted: 08 02 2024
medline: 6 3 2024
pubmed: 6 3 2024
entrez: 6 3 2024
Statut: aheadofprint

Résumé

Despite the proven benefits of inhaled corticosteroid (ICS)-containing triple therapy for chronic obstructive pulmonary disease (COPD), clinicians limit patient exposure to ICS due to the risk of pneumonia. However, there are multiple factors associated with the risk of pneumonia in patients with COPD. This post hoc analysis of IMPACT trial data aims to set the risks associated with ICS into a context of specific patient-related factors that contribute to the risk of pneumonia. The 52-week, double-blind IMPACT trial randomized patients with symptomatic COPD and ≥1 exacerbation in the prior year 2:2:1 to once-daily fluticasone furoate (FF)/umeclidinium (UMEC)/vilanterol (VI), FF/VI or UMEC/VI. Annual rate of on-treatment pneumonias in the intent-to-treat population associated with age, body mass index (BMI), percent predicted forced expiratory volume in 1 s (FEV This analysis revealed that the annual rate of pneumonia showed the lowest risk at the age of 50 years. The 95% confidence intervals (CI) between ICS-containing and non-ICS containing treatments diverged in ages > 63 years, suggesting a significantly increased ICS-related risk in older patients. In contrast, the annual rate of pneumonia rose in both groups below BMI of 22.5 kg/m There was little evidence of a differential effect of older age, lower BMI, lower FEV IMPACT ClinicalTrials.gov number, NCT02164513.

Identifiants

pubmed: 38446336
doi: 10.1007/s41030-024-00255-1
pii: 10.1007/s41030-024-00255-1
doi:

Banques de données

ClinicalTrials.gov
['NCT02164513']

Types de publication

Journal Article

Langues

eng

Informations de copyright

© 2024. The Author(s).

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Auteurs

Bhumika Aggarwal (B)

Emerging Markets, GSK, 23 Rochester Park, Singapore, 139234, Singapore. bhumika.x.aggarwal@gsk.com.

Paul Jones (P)

Global Medical, Regulatory and Quality, GlaxoSmithKline Plc., Brentford, UK.

Alejandro Casas (A)

AIREPOC (Integrated Care and Rehabilitation Program of COPD), Pulmonary Colombian Foundation, and El Rosario University, Bogotá, Colombia.

Mauro Gomes (M)

Department of Pneumology at Santa Casa Medical School, São Paulo, Brazil.
Hospital Samaritano-Higienopolis, São Paulo, Brazil.

Siwasak Juthong (S)

Division of Respiratory and Respiratory Critical Care Medicine, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.

Diego Litewka (D)

Unidad Neumonologia, Hospital Juan A. Fernandez, Buenos Aires, Argentina.

Bernice Ong-Dela Cruz (B)

Division of Pulmonary and Critical Care Medicine, Philippine Heart Center, Quezon, Philippines.

Alejandra Ramirez-Venegas (A)

Department of Research in Tobacco and COPD, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.

Abdullah Sayiner (A)

Department of Chest Diseases, Ege University Faculty of Medicine, Izmir, Turkey.

James van Hasselt (J)

GSK, Regional Medical Affairs, Bryanston, Gauteng, South Africa.

Chris Compton (C)

GSK, Brentford, UK.

Lee Tombs (L)

Precise Approach Ltd, London, UK.

Stephen Weng (S)

GSK, Brentford, UK.

Gur Levy (G)

Emerging Markets, GSK, Panama City, Panama.

Classifications MeSH