4.3 Article

Echocardiographic assessment and clinical implication of functional tricuspid regurgitation in heart failure with reduced or preserved ejection fraction (ECLIPSE-HF)

Journal

INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING
Volume 38, Issue 12, Pages 2581-2591

Publisher

SPRINGER
DOI: 10.1007/s10554-022-02599-8

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The study aims to characterize the echocardiographic morphology of the tricuspid valve apparatus and the pathophysiology of FTR in heart failure patients, as well as to correlate the severity of FTR with clinical outcomes. With a prospective, multicenter design, the study will provide insights into the pathophysiological mechanisms of FTR across different heart failure phenotypes, potentially guiding future tricuspid valve interventions for patients.
Purpose Functional tricuspid regurgitation (FTR) has been shown to be associated with increased morbidity and mortality in several clinical conditions, including heart failure (HF) with reduced left ventricular ejection fraction as well as pulmonary arterial hypertension (PAH). We have designed a study aiming at: characterizing the echocardiographic morphology of the tricuspid valve apparatus and the pathophysiology of FTR in heart failure with reduced, mid-range or preserved left ventricular ejection fraction (HFrEF, HFmrEF, HFpEF) and in PAH patients; correlating the morphologic characteristics of tricuspid valve apparatus with hemodynamic severity of FTR; correlating the severity of FTR with the clinical condition and outcome. Methods The study will be a non-interventional, prospective, international, multicenter, longitudinal study (ClinicalTrials.gov Identifier NCT05209919). The minimum number of patients which are expected to be enrolled is 300 HF patients, including HFrEF, HFmrEF and HFpEF patients, whereas 100 PAH patients will serve as control. The patients will be enrolled in 20 centers in Europe, North America and Saudi Arabia Standard echocardiographic parameters will be analyzed by local investigators; strain measurements will be performed in a single central core-lab. Conclusions This study has been designed to improve our understanding of pathophysiological mechanisms and clinical relevance of FTR across all HF phenotypes. The results could potentially allow a more appropriate selection of heart failure patients with FTR for tricuspid valve intervention by percutaneous or surgical repair or replacement.

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