Burden and Characteristics of Severe Chronic Hypoxemia in a Real-World Cohort of Subjects with COPD.
airflow limitation
chronic obstructive pulmonary disease
severe hypoxemia
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:
Historique:
received:
01
01
2021
accepted:
31
03
2021
entrez:
19
5
2021
pubmed:
20
5
2021
medline:
28
7
2021
Statut:
epublish
Résumé
Chronic respiratory failure may occur as a consequence of chronic obstructive pulmonary disease (COPD) and is associated with significant morbidity and mortality. Hypoxemia is determined by underlying disease characteristics and comorbidities. Severe hypoxemia is typically only found in subjects with severe airflow obstruction (FEV In the French Initiatives BPCO real-life cohort, arterial blood gases were routinely collected in most patients. Relationships between severe hypoxemia, defined by a Pa0 Arterial blood gases were available from 887 subjects, of which 146 (16%) exhibited severe hypoxemia. Compared to subjects with a PaO2≥60 mmHg, the severe hypoxemia group exhibited higher mMRC dyspnea score, lower FEV In this cohort of stable COPD subjects, severe hypoxemia was associated with worse prognosis and more severe symptoms, airflow limitation and hyperinflation. Compared to subjects with severe hypoxemia and severe airflow limitation, subjects with severe hypoxemia despite non-severe airflow limitation were older, had higher BMI and more diagnosed diabetes. 04-479.
Sections du résumé
BACKGROUND
BACKGROUND
Chronic respiratory failure may occur as a consequence of chronic obstructive pulmonary disease (COPD) and is associated with significant morbidity and mortality. Hypoxemia is determined by underlying disease characteristics and comorbidities. Severe hypoxemia is typically only found in subjects with severe airflow obstruction (FEV
METHODS
METHODS
In the French Initiatives BPCO real-life cohort, arterial blood gases were routinely collected in most patients. Relationships between severe hypoxemia, defined by a Pa0
RESULTS
RESULTS
Arterial blood gases were available from 887 subjects, of which 146 (16%) exhibited severe hypoxemia. Compared to subjects with a PaO2≥60 mmHg, the severe hypoxemia group exhibited higher mMRC dyspnea score, lower FEV
CONCLUSION
CONCLUSIONS
In this cohort of stable COPD subjects, severe hypoxemia was associated with worse prognosis and more severe symptoms, airflow limitation and hyperinflation. Compared to subjects with severe hypoxemia and severe airflow limitation, subjects with severe hypoxemia despite non-severe airflow limitation were older, had higher BMI and more diagnosed diabetes.
TRIAL REGISTRATION
BACKGROUND
04-479.
Identifiants
pubmed: 34007166
doi: 10.2147/COPD.S295381
pii: 295381
pmc: PMC8121159
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1275-1284Informations de copyright
© 2021 Zysman et al.
Déclaration de conflit d'intérêts
MZ reports grants and personal fees from Boehringer Ingelheim, grants and personal fees from Novartis, personal fees from Chiesi, personal fees from Astra Zeneca and personal fees from GSK outside the submitted work. PRB reports personal fees from Aptalis, personal fees from Astra-Zeneca, grants and personal fees from Boehringer Ingelheim, personal fees from Chiesi, personal fees from GSK, personal fees from Novartis, personal fees from Pfizer, personal fees from Vertex, personal fees from Zambon, personal fees from Insmed, outside the submitted work. ICF reports grants and personal fees from Boehringer Ingelheim, grants and personal fees from Novartis, and GSK outside the submitted work. GBR reports grants and personal fees from Boehringer Ingelheim, grants and personal fees from Novartis, grants and personal fees from Astra Zeneca, personal fees and non-financial support from Chiesi, outside the submitted work. PNM reports grants and personal fees from Boehringer Ingelheim, grants and personal fees from NOVARTIS, personal fees and non-financial support from Chiesi, outside the submitted work. PS reports grants and personal fees from Boehringer Ingelheim outside the submitted work. GD reports personal fees from Novartis, personal fees and grants from Astra Zeneca, personal fees from BTG/PneumRx, personal fees from Chiesi, personal fees from Boehringer Ingelheim, personal fees from GSK, outside the submitted work. TP reports personal fees from Boehringer Ingelheim, personal fees from Novartis, personal fees from GSK, personal fees from Chiesi, personal fees from Pierre Fabre, outside the submitted work. OLR reports grants and personal fees personal fees and non-financial support from Astra Zeneca, Boehringer Ingelheim, Chiesi, Lilly and Novartis; non-financial support from Glaxo Smith Kline, Correvio, Mayoli, Mylan, MSD, PulmonX, Zambon, Novartis, MundiPharma, Pfizer, Teva, Santelys Association, Vertex and Vitalaire, all outside the submitted work. GJ reports personal fees from Boehringer Ingelheim, personal fees from GSK, personal fees from Novartis, personal fees from Menarini, personal fees from Astra Zeneca, personal fees from Chiesi, outside the submitted work. PC reports personal fees from Boehringer Ingelheim, personal fees from GSK, personal fees and grants from ALK, personal fees and grants from Almirall, personal fees and grants from Boehringer-Ingelheim, personal fees from Novartis, personal fees from Teva, personal fees from Astra Zeneca, grants and personal fees from Chiesi, personal fees from Sanofi, personal fees and non-financial support from SNCF, personal fees from GlaxoSmithKline, grants and personal fees from Sanofi-Aventis, grants from Amu, outside the submitted work. JLP reports grants from iBPCO association, during the conduct of the study. DC has nothing to disclose. NR reports grants and personal fees from Boehringer Ingelheim, grants and personal fees from Novartis, grant and personal fees from Pfizer, grants and personal fees from GSK, personal fees from AstraZeneca, personal fees from Chiesi, personal fees from Sanofi, personal fees from Zambon, personal fees and grants from Boehringer Ingelheim, outside the submitted work.
Références
Ann Intern Med. 1980 Sep;93(3):391-8
pubmed: 6776858
Acta Diabetol. 2014 Dec;51(6):933-40
pubmed: 24728837
Eur Respir J. 1999 Nov;14(5):1002-8
pubmed: 10596681
Lancet. 1981 Mar 28;1(8222):681-6
pubmed: 6110912
Eur Respir J. 2005 Aug;26(2):319-38
pubmed: 16055882
Eur Respir J. 2017 Nov 2;50(5):
pubmed: 29097431
Eur Respir J. 2017 Aug 3;50(2):
pubmed: 28775046
Pediatr Res. 1997 Jun;41(6):852-6
pubmed: 9167198
BMC Pulm Med. 2016 Dec 1;16(1):169
pubmed: 27903260
N Engl J Med. 2016 Oct 27;375(17):1617-1627
pubmed: 27783918
Am J Respir Crit Care Med. 2018 Oct 15;198(8):1000-1011
pubmed: 29746142
Diabet Med. 2010 Sep;27(9):977-87
pubmed: 20722670
Ann Intern Med. 1981 Mar;94(3):410
pubmed: 7224394
Eur Respir J. 2010 Sep;36(3):531-9
pubmed: 20075045
Respir Med. 1998 Sep;92(9):1122-6
pubmed: 9926166
Respiration. 2010;80(2):112-9
pubmed: 20134148
Int J Chron Obstruct Pulmon Dis. 2017 Jul 20;12:2095-2100
pubmed: 28790812
Chest. 2005 May;127(5):1531-6
pubmed: 15888824
Endocrine. 1999 Aug;11(1):37-9
pubmed: 10668639
Thorax. 1997 Aug;52(8):674-9
pubmed: 9337824