Distinguishing exercise intolerance in early-stage pulmonary hypertension with invasive exercise hemodynamics: Rest V

ETCO2 VE/VCO2 cardiopulmonary exercise test invasive exercise hemodynamics pulmonary hypertension pulmonary vascular disease

Journal

Clinical cardiology
ISSN: 1932-8737
Titre abrégé: Clin Cardiol
Pays: United States
ID NLM: 7903272

Informations de publication

Date de publication:
Jul 2022
Historique:
revised: 29 03 2022
received: 21 01 2022
accepted: 05 04 2022
pubmed: 15 4 2022
medline: 20 7 2022
entrez: 14 4 2022
Statut: ppublish

Résumé

Among subjects with exercise intolerance and suspected early-stage pulmonary hypertension (PH), early identification of pulmonary vascular disease (PVD) with noninvasive methods is essential for prompt PH management. Rest gas exchange parameters (minute ventilation to carbon dioxide production ratio: V We conducted a retrospective review of 55 subjects with early-stage PH (per echocardiogram), undergoing invasive exercise hemodynamics with cardiopulmonary exercise test to distinguish exercise intolerance mechanisms. Based on the rest and exercise hemodynamics, three distinct phenotypes were defined: (1) PVD, (2) pulmonary venous hypertension, and (3) noncardiac dyspnea (no rest or exercise PH). For all tests, *p < .05 was considered statistically significant. The mean age was 63.3 ± 13.4 years (53% female). In the overall cohort, higher rest V In a broad cohort of subjects with suspected early-stage PH, referred for invasive exercise testing to distinguish mechanisms of exercise intolerance, rest gas exchange parameters (V

Sections du résumé

BACKGROUND BACKGROUND
Among subjects with exercise intolerance and suspected early-stage pulmonary hypertension (PH), early identification of pulmonary vascular disease (PVD) with noninvasive methods is essential for prompt PH management.
HYPOTHESIS OBJECTIVE
Rest gas exchange parameters (minute ventilation to carbon dioxide production ratio: V
METHODS METHODS
We conducted a retrospective review of 55 subjects with early-stage PH (per echocardiogram), undergoing invasive exercise hemodynamics with cardiopulmonary exercise test to distinguish exercise intolerance mechanisms. Based on the rest and exercise hemodynamics, three distinct phenotypes were defined: (1) PVD, (2) pulmonary venous hypertension, and (3) noncardiac dyspnea (no rest or exercise PH). For all tests, *p < .05 was considered statistically significant.
RESULTS RESULTS
The mean age was 63.3 ± 13.4 years (53% female). In the overall cohort, higher rest V
CONCLUSIONS CONCLUSIONS
In a broad cohort of subjects with suspected early-stage PH, referred for invasive exercise testing to distinguish mechanisms of exercise intolerance, rest gas exchange parameters (V

Identifiants

pubmed: 35419844
doi: 10.1002/clc.23831
pmc: PMC9286332
doi:

Substances chimiques

Carbon Dioxide 142M471B3J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

742-751

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL147590
Pays : United States
Organisme : University of Wisconsin-Madison Department of Medicine Pilot Grant
ID : 233-AAH9756

Informations de copyright

© 2022 The Authors. Clinical Cardiology published by Wiley Periodicals, LLC.

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Auteurs

Farhan Raza (F)

Department of Medicine-Division of Cardiology, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Naga Dharmavaram (N)

Department of Medicine-Division of Cardiology, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Timothy Hess (T)

Department of Medicine-Division of Cardiology, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Ravi Dhingra (R)

Department of Medicine-Division of Cardiology, University of Wisconsin-Madison, Madison, Wisconsin, USA.

James Runo (J)

Department of Medicine-Division of Pulmonary and Critical Care, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Amy Chybowski (A)

Department of Medicine-Division of Pulmonary and Critical Care, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Callyn Kozitza (C)

Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Supria Batra (S)

Department of Medicine-Division of Cardiology Weill Cornell Medicine, New York, New York, USA.

Evelyn M Horn (EM)

Department of Medicine-Division of Cardiology Weill Cornell Medicine, New York, New York, USA.

Naomi Chesler (N)

University of California-Irvine Edwards Lifesciences Foundation Cardiovascular Innovation and Research Center and Department of Biomedical Engineering, Irvine, California, USA.

Marlowe Eldridge (M)

Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, USA.

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