Key result
Severe TR linked to ~83% higher 5-year mortality risk in newly diagnosed PAH.
Why the study?
Does severe tricuspid valve regurgitation predict mortality or lung transplantation in patients with newly diagnosed pulmonary arterial hypertension?
Cohort (n=727)
Does severe tricuspid valve regurgitation predict mortality or lung transplantation in patients with newly diagnosed pulmonary arterial hypertension?
Effect estimate: adjusted HR 1.83 (95% CI 1.38-2.41)
p-value: p=<.001
Severe tricuspid regurgitation is a significant independent predictor of long-term mortality and correlates with disease severity in patients with newly diagnosed pulmonary arterial hypertension.
May refine PAH risk stratification; hypothesis-generating for targeted TR interventions.
INTRODUCTION: Tricuspid valve regurgitation (TR) is a frequent finding in patients with pulmonary arterial hypertension (PAH). However, its prognostic significance and relation to PAH, while suspected, are poorly understood. We assessed 727 consecutive patients with newly diagnosed PAH who underwent transthoracic echocardiographic evaluation of tricuspid valve function. OBJECTIVES: The study objective was to determine the association of TR presence and severity with patient characteristics, pulmonary artery hemodynamics and outcome. METHODS: Consecutive patients with newly diagnosed PAH (N = 727 with group 1 pulmonary hypertension) underwent transthoracic echocardiographic evaluation of tricuspid valve function at diagnosis. The primary study end point was all-cause mortality or lung transplantation. RESULTS: In this population, 702 patients (96.5%) had TR; in 165 patients (23%), TR was severe. Compared with those with no or mild TR by echocardiography criteria, patients with severe TR had shorter mean (SD) 6-minute walk distances (285 [125] m vs 360 [121] m; P = .02) and higher levels of B-type natriuretic peptide (695 [672] pg/dL vs 328 [300] pg/dL; P < .05). Severe TR was associated with greater right atrial dilatation (91% vs 47%; P = .004) and right ventricular (RV) dilatation (92% vs 51%; P = .008), greater right atrial pressure (mean [SD] 15 [7] mm Hg vs 10 [6] mm Hg; P < .001) and lower cardiac index (mean [SD], 2.2 [0.7] L/min/m2 vs 2.8 [0.9] L/min/m2; P < .001). Severe TR was strongly predictive of greater 5-year mortality risk after adjustment for age, sex, functional class, 6-minute walk distance, diffusing capacity, RV size and pulmonary vascular resistance index (adjusted hazard ratio, 1.83; 95% CI, 1.38-2.41; P < .001). CONCLUSIONS: Severe TR was a significant predictor of long-term mortality rate in PAH, and TR severity correlated with PAH severity.
No takes yet. Share an insight, caveat, or question.
Chen et al. (2017) conducted a cohort in pulmonary arterial hypertension (n=727). Severe tricuspid valve regurgitation vs. No or mild tricuspid valve regurgitation was evaluated on all-cause mortality or lung transplantation (adjusted HR 1.83, 95% CI 1.38-2.41, p=<.001). Severe tricuspid regurgitation was strongly predictive of greater 5-year mortality risk in newly diagnosed pulmonary arterial hypertension (adjusted HR 1.83; 95% CI 1.38-2.41; P<.001).
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: