Functional tricuspid regurgitation of degenerative mitral valve disease: a crucial determinant of survival

Abstract Aims  To assess functional tricuspid regurgitation (FTR) determinants, consequences, and independent impact on outcome in degenerative mitral regurgitation (DMR). Methods and results  All patients diagnosed with isolated DMR 2003–2011, with structurally normal tricuspid leaflets, prospectiv...

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Veröffentlicht in:European heart journal 2020-05, Vol.41 (20), p.1918-1929
Hauptverfasser: Essayagh, Benjamin, Antoine, Clémence, Benfari, Giovanni, Maalouf, Joseph, Michelena, Hector I, Crestanello, Juan A, Thapa, Prabin, Avierinos, Jean-François, Enriquez-Sarano, Maurice
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Sprache:eng
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Zusammenfassung:Abstract Aims  To assess functional tricuspid regurgitation (FTR) determinants, consequences, and independent impact on outcome in degenerative mitral regurgitation (DMR). Methods and results  All patients diagnosed with isolated DMR 2003–2011, with structurally normal tricuspid leaflets, prospective FTR grading and systolic pulmonary artery pressure (sPAP) estimation by Doppler echocardiography at diagnosis were identified and long-term outcome analysed. The 5083 DMR eligible patients [63 ± 16 years, 47% female, ejection fraction (EF) 63 ± 7%, and sPAP 35 ± 13 mmHg] presented with FTR graded trivial in 45%, mild in 37%, moderate in 15%, and severe in 3%. While pulmonary hypertension (PHTN-sPAP ≥ 50 mmHg) was the most powerful FTR severity determinant, other strong FTR determinants were older age, female sex, lower left ventricle EF, DMR, and particularly atrial fibrillation (AFib) (all P ≤ 0.002). Functional tricuspid regurgitation moderate/severe was independently linked to more severe clinical presentation, more oedema, lower stroke volume, and impaired renal function (P ≤ 0.01). Survival (95% confidence interval) throughout follow-up [70% (69–72%) at 10 years] was strongly associated with FTR severity [82% (80–84%) for trivial, 69% (66–71%) for mild, 51% (47–57%) for moderate, and 26% (19–35%) for severe, P 
ISSN:0195-668X
1522-9645
DOI:10.1093/eurheartj/ehaa192