Prognostic Role of TAPSE-to-PASP ratio for the identification of early clinical deterioration in intermediate-high risk pulmonary embolism patients.

Echocardiography Pulmonary embolism TAPSE intermediate high-risk pulmonary arterial pressure

Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
11 Jan 2024
Historique:
received: 07 12 2023
accepted: 22 12 2023
medline: 14 1 2024
pubmed: 14 1 2024
entrez: 13 1 2024
Statut: aheadofprint

Résumé

The ratio of tricuspid annular plane systolic excursion (TAPSE) to echocardiographically measured systolic pulmonary artery pressure (PASP) has been proposed as a surrogate of RV-arterial coupling. In this analysis, we assess the prognostic role of TAPSE/PASP for early clinical deterioration and short-term mortality in an often clinically challenging population of intermediate high-risk PE patients. A post-hoc analysis of intermediate-high risk PE patients enrolled in the Italian Pulmonary Embolism Registry (IPER) (ClinicalTrials.gov: NCT01604538) was performed. All patients underwent a transthoracic echocardiography (TTE) at admission. The primary and secondary outcomes were clinical deterioration within 48 hours from admission and 30-day all-cause mortality, respectively. Among 422 intermediate high-risk PE patients (mean age 71.2±5.3 years, 238 males), 37 (8.7%) experienced clinical deterioration within 48 hours of admission. The 30-day mortality rate was 6.6% (n=28). Receiver operating characteristic analysis established 0.33 as the optimal cut-off value for the TAPSE/PASP in predicting 48-h clinical deterioration (AUC of 0.79 ± 0.1). Sensitivity, specificity, PPV and NPV were 81%, 88.5%, 40.5% and 97.9%, respectively. Multivariate Cox regression analysis showed that a TAPSE/PASP≤0.33 was an independent predictor of 48-h clinical deterioration (HR: 2.06, 95% CI 1.98-2.11, p<0.0001) and 30-day mortality (HR: 2.28, 95% CI: 2.25-2.33, p<0.001). TAPSE/PASP shows promise as a non-invasive prognostic predictor to identify intermediate-high risk PE patients at higher risk of early clinical deterioration and short-term mortality.

Identifiants

pubmed: 38218392
pii: S0002-9149(24)00006-7
doi: 10.1016/j.amjcard.2023.12.053
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT01604538']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Gregory Piazza reports a relationship with Bristol Myers Squibb Co that includes: consulting or advisory and funding grants. Gregory Piazza reports a relationship with Bayer Corporation that includes: funding grants. Gregory Piazza reports a relationship with Janssen Pharmaceuticals Inc that includes: consulting or advisory and funding grants. Gregory Piazza reports a relationship with Alexion that includes: funding grants. Gregory Piazza reports a relationship with Amgen that includes: consulting or advisory and non-financial support. Gregory Piazza reports a relationship with Boston Scientific Corp that includes: consulting or advisory and funding grants. Gregory Piazza reports a relationship with NAMSA that includes: consulting or advisory. Gregory Piazza reports a relationship with Prairie Educatin and Research Cooperative that includes: consulting or advisory. Gregory Piazza reports a relationship with Boston Clinical research Institute that includes: consulting or advisory. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Marco Zuin (M)

Department of Translational Medicine, University of Ferrara, Ferrara, Italy. Electronic address: zuinml@yahoo.it.

Gregory Piazza (G)

Cardiovascular Medicine Division and Thrombosis Research Group, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Gianluca Rigatelli (G)

Department of Cardiology, Madre Teresa Hospital, Schiavonia, Italy.

Claudio Bilato (C)

Department of Cardiology, West Vicenza Hospital, Arzignano, Italy.

Amedeo Bongarzoni (A)

Department of Cardiology, ASST Santi Paolo e Carlo, University of Milan, Milano, Italy.

Stanislav Henkin (S)

Gonda Vascular Center, Mayo Clinic, Rochester, MN, USA.

Pietro Zonzin (P)

Department of Cardiology, Santa Maria della Misericordia Hospital, Rovigo, Italy.

Franco Casazza (F)

Department of Cardiology, San Carlo Borromeo Hospital, Milano, Italy.

Loris Roncon (L)

Department of Cardiology, Santa Maria della Misericordia Hospital, Rovigo, Italy; Cardiology Clinic, Casa di Cura Città di Rovigo, Rovigo.

Classifications MeSH