Clinical importance of respiratory muscle fatigue in patients with cardiovascular disease.
Journal
Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R
Informations de publication
Date de publication:
21 Aug 2020
21 Aug 2020
Historique:
entrez:
28
8
2020
pubmed:
28
8
2020
medline:
9
9
2020
Statut:
ppublish
Résumé
Patients with cardiovascular diseases frequently experience exertional dyspnea. However, the relationship between respiratory muscle strength including its fatigue and cardiovascular dysfunctions remains to be clarified.The maximal inspiratory pressure/maximal expiratory pressure (MIP/MEP) before and after cardiopulmonary exercise testing (CPX) in 44 patients with heart failure and ischemic heart disease were measured. Respiratory muscle fatigue was evaluated by calculating MIP (MIPpost/MIPpre) and MEP (MEPpost/MEPpre) changes.The mean MIPpre and MEPpre values were 67.5 ± 29.0 and 61.6 ± 23.8 cm H2O, respectively. After CPX, MIP decreased in 25 patients, and MEP decreased in 22 patients. We evaluated the correlation relationship between respiratory muscle function including respiratory muscle fatigue and exercise capacity evaluated by CPX such as peak VO2 and VE/VCO2 slope. Among MIP, MEP, change in MIP, and change in MEP, only the value of change in MIP had an association with the value of VE/VCO2 slope (R = -0.36, P = .017). In addition, multivariate analysis for determining factor of change in MIP revealed that the association between the change in MIP and eGFR was independent from other confounding parameters (beta, 0.40, P = .017). The patients were divided into 2 groups, with (MIP change < 0.9) and without respiratory muscle fatigue (MIP change > 0.9), and a significant difference in peak VO2 (14.2 ± 3.4 [with fatigue] vs 17.4 ± 4.7 [without fatigue] mL/kg/min; P = .020) was observed between the groups.Respiratory muscle fatigue demonstrated by the change of MIP before and after CPX significantly correlated with exercise capacity and renal function in patients with cardiovascular disease.
Identifiants
pubmed: 32846812
doi: 10.1097/MD.0000000000021794
pii: 00005792-202008210-00066
pmc: PMC7447364
doi:
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
e21794Références
Circulation. 2009 Jun 30;119(25):3189-97
pubmed: 19528334
J Intern Med. 2004 Jan;255(1):115-24
pubmed: 14687247
Eur Respir Rev. 2016 Sep;25(141):317-32
pubmed: 27581831
Am J Respir Crit Care Med. 2011 May 15;183(10):1302-10
pubmed: 21257789
Respir Physiol Neurobiol. 2006 Apr 28;151(2-3):242-50
pubmed: 16616716
Am Rev Respir Dis. 1990 Aug;142(2):474-80
pubmed: 2382912
Respir Care. 2009 Oct;54(10):1321-8
pubmed: 19796411
Nutr Metab (Lond). 2015 Nov 25;12:49
pubmed: 26612997
Heart Vessels. 2018 Jul;33(7):752-759
pubmed: 29335797
PLoS One. 2013;8(3):e60119
pubmed: 23533671
J Appl Physiol (1985). 2018 Jan 1;124(1):208-224
pubmed: 29051336
J Card Fail. 2017 Nov;23(11):777-782
pubmed: 28736291
J Appl Physiol (1985). 2008 Mar;104(3):879-88
pubmed: 18096752
Exp Physiol. 2013 Dec;98(12):1705-17
pubmed: 24014807
Am J Physiol Heart Circ Physiol. 2015 Nov;309(9):H1419-39
pubmed: 26320036
PLoS One. 2013 Dec 06;8(12):e83432
pubmed: 24324843
Br Heart J. 1995 Jul;74(1):27-33
pubmed: 7662449
Curr Heart Fail Rep. 2009 Jun;6(2):95-101
pubmed: 19486593
Int J Cardiol Heart Vasc. 2019 Jan 08;22:84-91
pubmed: 30671533
Kidney Int. 2000 Aug;58(2):867-72
pubmed: 10916112
PLoS One. 2015 Feb 11;10(2):e0118218
pubmed: 25671566
ESC Heart Fail. 2018 Dec;5(6):1074-1082
pubmed: 30570227
Circulation. 1999 Aug 3;100(5):503-8
pubmed: 10430764
Prog Cardiovasc Dis. 1995 May-Jun;37(6):347-70
pubmed: 7777667
BBA Clin. 2014 Jun 1;1:12-23
pubmed: 25147756