Abstract 4143986: Non-ischemic septal fibrosis on delayed enhancement CMR provides incremental prognostic value in functional tricuspid regurgitation

Introduction: CMR enables assessment of cardiac chamber remodeling and associated alterations in myocardial tissue substrate. Primary aim of this study was to examine the relative prognostic utility of chamber remodeling and myocardial tissue alterations in patients with functional tricuspid regurgitation. Methods: The population comprised patients with advanced functional TR (≥moderate) undergoing CMR. LGE-CMR was used to identify myocardial scar/infarction inclusive of non-ischemic septal fibrosis (NIsF) which was defined as hyperenhancement in the mid-myocardial or epicardial aspect of the interventricular septum. Clinical characteristics including follow-up and all-cause mortality were obtained blinded to imaging analyses. Results: 894 pts (71±15yo; 52% male) with advanced functional TR undergoing CMR were studied; LV dysfunction was present in 44% and RV dysfunction in 57%. Paralleling ventricular dysfunction, adverse LV and RV chamber remodeling was also common, occuring in 25% and 43% of the population, respectively. Regarding tissue substrate, over half (50.4%) had LV scar/infarction (9.2±10.8 %LV), 50.8% of which represented NIsF. Prevalence of NIsF was 3-fold higher in patients with concomitant RV dysfunction versus those without (36.1% vs 11.5%, p<0.001). Regarding outcomes, 215 patients died during a median follow-up of 4.6 years. As shown in Table 1 , LV and RV dysfunction, LV and RV dilation, advanced mitral regurgitation and NIsF were each linked to increased mortality risk (all p<0.001). A combined model incorporating indices known to impact TR prognosis demonstrates NIsF to be independently linked to increased mortality risk even after controlling for RV dysfunction (HR 1.78 [CI 1.31-2.43]; p<0.001). Kaplan-Meier analysis demonstrates significantly increased risk of death in patients with NIsF (p<0.001) ( Figure 1 ). Conclusions: Among patients with advanced TR, NIsF provides incremental prognostic risk stratification beyond conventional risk markers.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4143986
Primary Topic
Cardiac Valve Diseases and Treatments
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article
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article

Abstract 4143986: Non-ischemic septal fibrosis on delayed enhancement CMR provides incremental prognostic value in functional tricuspid regurgitation

Pablo Villar Calle, Omar Khalique, Caitlin Chiu, Giorgia Falco et al.
Circulation
Cardiac Valve Diseases and Treatments
article

Abstract 4143986: Non-ischemic septal fibrosis on delayed enhancement CMR provides incremental prognostic value in functional tricuspid regurgitation

Pablo Villar Calle, Omar Khalique, Caitlin Chiu, Giorgia Falco, Jonathan W. Weinsaft, Vasudev Baburaya Pai, Jonathan Kochav, Aditya Sahai, Rachel Axman, Letizia Ruoli, Jiwon Kim, Josep Mayol, Mahniz Reza
article en

Abstract

Introduction: CMR enables assessment of cardiac chamber remodeling and associated alterations in myocardial tissue substrate. Primary aim of this study was to examine the relative prognostic utility of chamber remodeling and myocardial tissue alterations in patients with functional tricuspid regurgitation. Methods: The population comprised patients with advanced functional TR (≥moderate) undergoing CMR. LGE-CMR was used to identify myocardial scar/infarction inclusive of non-ischemic septal fibrosis (NIsF) which was defined as hyperenhancement in the mid-myocardial or epicardial aspect of the interventricular septum. Clinical characteristics including follow-up and all-cause mortality were obtained blinded to imaging analyses. Results: 894 pts (71±15yo; 52% male) with advanced functional TR undergoing CMR were studied; LV dysfunction was present in 44% and RV dysfunction in 57%. Paralleling ventricular dysfunction, adverse LV and RV chamber remodeling was also common, occuring in 25% and 43% of the population, respectively. Regarding tissue substrate, over half (50.4%) had LV scar/infarction (9.2±10.8 %LV), 50.8% of which represented NIsF. Prevalence of NIsF was 3-fold higher in patients with concomitant RV dysfunction versus those without (36.1% vs 11.5%, p<0.001). Regarding outcomes, 215 patients died during a median follow-up of 4.6 years. As shown in Table 1 , LV and RV dysfunction, LV and RV dilation, advanced mitral regurgitation and NIsF were each linked to increased mortality risk (all p<0.001). A combined model incorporating indices known to impact TR prognosis demonstrates NIsF to be independently linked to increased mortality risk even after controlling for RV dysfunction (HR 1.78 [CI 1.31-2.43]; p<0.001). Kaplan-Meier analysis demonstrates significantly increased risk of death in patients with NIsF (p<0.001) ( Figure 1 ). Conclusions: Among patients with advanced TR, NIsF provides incremental prognostic risk stratification beyond conventional risk markers.

CirculationVol. 150(Suppl_1)
Cornell University (US), Presbyterian Hospital (US), Weill Cornell Medicine (US), Columbia University (US)
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Openalex Percentile: Top 62%
Cardiac Valve Diseases and Treatments
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