Post Pulmonary Embolism Phenotypes Described by Invasive Cardiopulmonary Exercise Testing.

CTEPH Dyspnea Pulmonary Embolism Pulmonary Vascular Disease iCPET

Journal

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

Informations de publication

Date de publication:
03 Sep 2024
Historique:
received: 04 02 2024
revised: 30 07 2024
accepted: 09 08 2024
medline: 6 9 2024
pubmed: 6 9 2024
entrez: 5 9 2024
Statut: aheadofprint

Résumé

Post pulmonary embolism (PE) dyspnea is common. Existing non-invasive studies have demonstrated that post PE dyspnea is associated with elevations in right ventricular afterload, dead space ventilation, and deconditioning. We aimed to use invasive cardiopulmonary exercise testing (iCPET) parameters in patients with post PE dyspnea to identify unique physiologic phenotypes. Are there distinct post pulmonary embolism dyspnea physiologic phenotypes described with iCPET? Patients were enrolled at the time of acute PE and through our pulmonary hypertension and dyspnea clinic. ICPET was performed if there was high suspicion for pulmonary hypertension or if there was unexplained dyspnea. A hierarchical cluster analysis was performed to identify dyspnea phenotypes. ICPET parameters assessing pulmonary hemodynamics, ventilation, and peripheral oxygen utilization were then compared within and across each cluster and with iCPET controls against peak oxygen consumption (Peak VO2). 173 patients were enrolled. Sixty-seven patients underwent iCPET. All patients had reductions in Peak VO2 and peak cardiac index relative to controls. Three clusters were identified. Cluster one was defined by having elevated RV afterload and impaired ventilatory efficiency. Cluster two had elevated RV afterload with reductions in respiratory mechanics. Cluster three had mild derangement in RV afterload with mild reductions in peak cardiac output. iCPET reveals significant heterogeneity in post PE dyspnea. Three phenotypes are characterized by differences in RV afterload, ventilatory efficiency, respiratory mechanics, and peripheral oxygen utilization.

Sections du résumé

BACKGROUND BACKGROUND
Post pulmonary embolism (PE) dyspnea is common. Existing non-invasive studies have demonstrated that post PE dyspnea is associated with elevations in right ventricular afterload, dead space ventilation, and deconditioning. We aimed to use invasive cardiopulmonary exercise testing (iCPET) parameters in patients with post PE dyspnea to identify unique physiologic phenotypes.
RESEARCH QUESTION OBJECTIVE
Are there distinct post pulmonary embolism dyspnea physiologic phenotypes described with iCPET?
STUDY DESIGN AND METHODS METHODS
Patients were enrolled at the time of acute PE and through our pulmonary hypertension and dyspnea clinic. ICPET was performed if there was high suspicion for pulmonary hypertension or if there was unexplained dyspnea. A hierarchical cluster analysis was performed to identify dyspnea phenotypes. ICPET parameters assessing pulmonary hemodynamics, ventilation, and peripheral oxygen utilization were then compared within and across each cluster and with iCPET controls against peak oxygen consumption (Peak VO2).
RESULTS RESULTS
173 patients were enrolled. Sixty-seven patients underwent iCPET. All patients had reductions in Peak VO2 and peak cardiac index relative to controls. Three clusters were identified. Cluster one was defined by having elevated RV afterload and impaired ventilatory efficiency. Cluster two had elevated RV afterload with reductions in respiratory mechanics. Cluster three had mild derangement in RV afterload with mild reductions in peak cardiac output.
INTERPRETATION CONCLUSIONS
iCPET reveals significant heterogeneity in post PE dyspnea. Three phenotypes are characterized by differences in RV afterload, ventilatory efficiency, respiratory mechanics, and peripheral oxygen utilization.

Identifiants

pubmed: 39236998
pii: S0012-3692(24)05134-1
doi: 10.1016/j.chest.2024.08.040
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Michael Insel (M)

Division of Pulmonary Allergy Sleep and Critical Care, Department of Medicine, University of Arizona, Tucson, AZ, USA. Electronic address: minsel@arizona.edu.

Tammer El Aini (T)

Division of Pulmonary Allergy Sleep and Critical Care, Department of Medicine, University of Arizona, Tucson, AZ, USA.

Gregory Woodhead (G)

Department of Radiology, University of Arizona, Tucson, AZ, USA.

Rebecca Wig (R)

Department of Medicine, University of Arizona, Tucson, AZ, USA.

Saad Kubba (S)

Division of Cardiology, Department of Medicine, University of Arizona, Tucson, AZ, USA.

Guido Claessen (G)

Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium; University Hospitals Leuven, Leuven, Belgium.

Erin Howden (E)

Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.

Franz Rischard (F)

Division of Pulmonary Allergy Sleep and Critical Care, Department of Medicine, University of Arizona, Tucson, AZ, USA.

Classifications MeSH