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DOI 10.1016/j.healun.2024.06.003

Медицинская библиотека · The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2024

Right ventricular phenotyping in incident patients with idiopathic pulmonary arterial hypertension.

Ghio Stefano, Badagliacca Roberto, D'Alto Michele, Scelsi Laura, Argiento Paola, Brunetti Natale D, Casu Gavino, Cedrone Nadia, Confalonieri Marco, Corda Marco, Correale Michele, D'Agostino Carlo, De Tommasi Elisabetta, Filomena Domenico, Galgano Giuseppe, Greco Alessandra, Grimaldi Massimo, Lombardi Carlo, Madonna Rosalinda, Manzi Giovanna, Mercurio Valentina, Mihai Alexandra, Mulè Massimiliano, Paciocco Giuseppe, Papa Silvia, Recchioni Tommaso, Romaniello Antonella, Romeo Emanuele, Stolfo Davide, Vitulo Patrizio, Benza Raymond L, Vizza Carmine D, Italian Pulmonary Hpertension NETwork (iPHNET)

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Аннотация

BACKGROUND

Right ventricular (RV) imaging has not a definite role in risk stratification of pulmonary arterial hypertension (PAH) patients. We tested the hypothesis that echocardiography-derived phenotypes, depicting different degrees of RV remodeling and dysfunction, may provide additional prognostic information to current risk stratification tools.

METHODS

Consecutive incident PAH patients aged ≥18 years, diagnosed between January 2005 and December 2021, underwent clinical assessment, right heart catheterization, standard echocardiography. Simple echocardiographic variables were combined in order to define a priori four phenotypes representing different degrees of RV dilatation and RV-pulmonary arterial (PA) coupling: Phenotype 1 with mildy dilated right ventricle and preserved RV-PA coupling (n = 152 patients); phenotype 2 with mildly dilated right ventricle and poor RV-PA coupling (n = 143 patients); phenotype 3 with severely dilated right ventricle and preserved RV-PA coupling (n = 201 patients); phenotype 4 with severely dilated right ventricle and poor RV-PA coupling, with or without severe tricuspid regurgitation (n = 519 patients). Risk stratification was based on the European Society of Cardiology/European Respiratory Society (ESC/ERS) 3-strata model and Registry to Evaluate Early and Long-Term PAH disease Management (REVEAL) 2.0 score.

RESULTS

These phenotypes were present in all risk groups. Notably, regardless of the ESC/ERS risk stratum assigned to the patient, phenotype 4 was associated with a 2-fold increase of the odds of death (HR 2.1, 95% CI 1.6-2.8, p < 0.001), while phenotype 1 was associated with a 71% reduction in the odds of dying (HR 0.29, 95% CI 0.18-0.47, p < 0.001).

CONCLUSIONS

Echocardiography-derived phenotypes describing RV remodeling and dysfunction may provide prognostic information which is independent of and additional to the clinically defined risk in incident PAH patients.

Для цитирования: Ghio Stefano, Badagliacca Roberto, D'Alto Michele, Scelsi Laura, Argiento Paola, Brunetti Natale D, Casu Gavino, Cedrone Nadia, Confalonieri Marco, Corda Marco, Correale Michele, D'Agostino Carlo, De Tommasi Elisabetta, Filomena Domenico, Galgano Giuseppe, Greco Alessandra, Grimaldi Massimo, Lombardi Carlo, Madonna Rosalinda, Manzi Giovanna, Mercurio Valentina, Mihai Alexandra, Mulè Massimiliano, Paciocco Giuseppe, Papa Silvia, Recchioni Tommaso, Romaniello Antonella, Romeo Emanuele, Stolfo Davide, Vitulo Patrizio, Benza Raymond L, Vizza Carmine D, Italian Pulmonary Hpertension NETwork (iPHNET). Right ventricular phenotyping in incident patients with idiopathic pulmonary arterial hypertension.. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 2024. DOI: 10.1016/j.healun.2024.06.003.

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