Clinical and Prognostic Impact of Low Diffusing Capacity for Carbon Monoxide Values in Patients With Global Initiative for Obstructive Lung Disease I COPD.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
09 2021
Historique:
received: 20 01 2021
revised: 01 03 2021
accepted: 12 04 2021
pubmed: 27 4 2021
medline: 7 1 2022
entrez: 26 4 2021
Statut: ppublish

Résumé

The Global Initiative for Obstructive Lung Disease (GOLD) does not promote diffusing capacity for carbon monoxide (Dlco) values in the evaluation of COPD. In GOLD spirometric stage I COPD patients, the clinical and prognostic impact of a low Dlco has not been explored. Could a Dlco threshold help define an increased risk of death and a different clinical presentation in these patients? GOLD stage I COPD patients (n = 360) were enrolled and followed over 109 ± 50 months. Age, sex, pack-years' history, BMI, dyspnea, lung function measurements, exercise capacity, BODE index, and history of exacerbations were recorded. A cutoff value for Dlco was identified for all-cause mortality and the clinical and physiological characteristics of patients above and below the threshold compared. Cox regression analysis explored the predictive power of that cutoff value for all-cause mortality. A Dlco cutoff value of <60% predicted was associated with all-cause mortality (Dlco ≥ 60%: 9% vs Dlco < 60%: 23%, P = .01). At a same FEV

Sections du résumé

BACKGROUND
The Global Initiative for Obstructive Lung Disease (GOLD) does not promote diffusing capacity for carbon monoxide (Dlco) values in the evaluation of COPD. In GOLD spirometric stage I COPD patients, the clinical and prognostic impact of a low Dlco has not been explored.
RESEARCH QUESTION
Could a Dlco threshold help define an increased risk of death and a different clinical presentation in these patients?
STUDY DESIGN AND METHODS
GOLD stage I COPD patients (n = 360) were enrolled and followed over 109 ± 50 months. Age, sex, pack-years' history, BMI, dyspnea, lung function measurements, exercise capacity, BODE index, and history of exacerbations were recorded. A cutoff value for Dlco was identified for all-cause mortality and the clinical and physiological characteristics of patients above and below the threshold compared. Cox regression analysis explored the predictive power of that cutoff value for all-cause mortality.
RESULTS
A Dlco cutoff value of <60% predicted was associated with all-cause mortality (Dlco ≥ 60%: 9% vs Dlco < 60%: 23%, P = .01). At a same FEV

Identifiants

pubmed: 33901498
pii: S0012-3692(21)00757-1
doi: 10.1016/j.chest.2021.04.033
pmc: PMC8448999
pii:
doi:

Substances chimiques

Carbon Monoxide 7U1EE4V452

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

872-878

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

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Auteurs

Juan P de-Torres (JP)

Respirology and Sleep Medicine Division, Queen's University, Kingston, Canada. Electronic address: jupa65@hotmail.com.

Denis E O'Donnell (DE)

Respirology and Sleep Medicine Division, Queen's University, Kingston, Canada.

Jose M Marín (JM)

Pulmonary Department, Hospital Universitario Miguel Servet, Instituto Aragonés Ciencias Salud & CIBERES, Zaragoza, Spain.

Carlos Cabrera (C)

Pulmonary Department, Hospital Universitario Doctor Negrín, Las Palmas, Spain.

Ciro Casanova (C)

Pulmonary Department, Hospital Ntra Sra de Candelaria, Tenerife, Spain and Respiratory Research Unit, Hospital Ntra Sra de Candelaria, Tenerife, Spain.

Marta Marín (M)

Pulmonary Department, Clínica Universidad de Navarra, Pamplona, Spain.

Ana Ezponda (A)

Radiology Department, Clínica Universidad de Navarra, Pamplona, Spain.

Borja G Cosio (BG)

Hospital Universitario Son Espases, Instituto de Investigación Sanitaria de Baleares (IdISBa), Palma, Mallorca, Spain, and Centro de Investigación en Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III (ISCIII), Madrid, España.

Cristina Martinez (C)

Department of Respiratory Medicine, Hospital Central de Asturias, Oviedo, Spain.

Ingrid Solanes (I)

Pulmonary Department, Hospital Santa Creu i Sant Pau, Universidad Autónoma de Barcelona, Barcelona, Spain.

Antonia Fuster (A)

Pulmonary Department, Hospital Universitario Son Llatzer, Palma de Mallorca, Spain.

J Alberto Neder (JA)

Respirology and Sleep Medicine Division, Queen's University, Kingston, Canada.

Jessica Gonzalez-Gutierrez (J)

Pulmonary Department, Hospital Universitari Arnau de Villanova, Lleida, Spain.

Bartolome R Celli (BR)

Pulmonary Department, Brigham and Women's Hospital, Boston, MA.

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Classifications MeSH