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Assessing Proportionate and Disproportionate Functional Mitral Regurgitation with individualized thresholds outperforms the risk stratification proposed by current guidelines
Session:
CO 06 - Valvulopatias
Speaker:
Pedro M. Lopes
Congress:
CPC 2021
Topic:
B. Imaging
Theme:
03. Imaging
Subtheme:
03.1 Echocardiography
Session Type:
Comunicações Orais
FP Number:
---
Authors:
Pedro M. Lopes; Francisco Albuquerque; Pedro Freitas; Francisco Gama; Eduarda Horta; Carla Reis; João Abecasis; Marisa Trabulo; António m. Ferreira; Carlos Aguiar; Manuel Canada; Regina Ribeiras; Miguel Mendes; Maria j. Andrade
Abstract
<p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">Background:</span></span></span></strong> </span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">The clinical application of the concept of Proportionate and Disproportionate Functional Mitral Regurgitation (FMR) has been limited by the lack of a simple way to assess it.<strong> </strong>The aim of our study was<strong> </strong>to evaluate the prognostic value of an individualized method of assessing FMR Proportionality and to compare it with current established guidelines.</span></span></span></span></span></p> <p style="text-align:justify"> </p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">Methods: </span></span></span></strong></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">Patients with at least mild FMR and reduced left ventricular ejection fraction (LVEF <50%) under </span></span></span><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif">guideline-directed medical therapy were <span style="color:black">retrospectively identified at a single-center. Considering regurgitant fraction ≥50% as the threshold for hemodynamically significant FMR, an individualized theoretical regurgitant volume (RegVol) </span>cut-off can be derived by a simple equation that accounts for <span style="color:black">LV dilation and dysfunction (Figure panel A). Accordingly, the difference between the measured RegVol and the individual theoretical RegVol cut-off can be used to categorize FMR proportionality as non-severe, proportionate or disproportionate (Figure panel B). The discriminative ability (area under the ROC curve – AUC) of FMR proportionality status was compared against the European and American guidelines. </span>Integrated discrimination improvement (IDI) was used to ascertain if FMR disproportionality improves individual risk stratification provided by both guidelines. <span style="color:black">The primary endpoint was all-cause mortality.</span></span></span></span></span></p> <p style="text-align:justify"> </p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">Results: </span></span></span></strong></span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">A total of 572 patients (median age 70 years; 76% male) were included. </span></span></span><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif">Median LVEF <span style="color:black">was 35% (IQR 28-40) </span>and <span style="color:black">LVEDV was 169 ml (IQR 132-215). </span>Disproportionate FMR was present <span style="color:black">in 109 patients (19%), Proportionate FMR </span>in <span style="color:black">148 patients (26%) and Non-Severe FMR in 315 patients (55%).</span> <span style="color:black">During a median follow-up of 3.8 years (IQR 1.8-6.2), 254 patients died. The unadjusted mortality incidence per 100 persons-year (black line, Figure panel C) and the survival probability (Figure panel D) worsened as the degree of FMR disproportionality increased. On multivariable analysis, disproportionate FMR remained independently associated with all-cause mortality (adjusted HR: 1.79; 95%CI: 1.25-2.55; <em>P</em>=0.001). The FMR proportionality concept showed greater discriminative power (AUC 0.64; 95%CI: 0.60-0.68) than the American (</span>AUC 0.58; 95%CI: 0.55-0.62; <em>P</em> for comparison <0.001<span style="color:black">) and European guidelines (AUC</span> 0.58; 95%CI: 0.55-0.62; <em>P</em> for comparison <0.001<span style="color:black">). When added to any of these guidelines, FMR proportionality also improved risk stratification by reclassifying patients into lower and higher risk subsets </span>(IDI = 0.037 [<em>P</em><0.001] and 0.034 [<em>P</em><0.001], respectively).</span></span></span></span></p> <p style="text-align:justify"> </p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><strong><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif"><span style="color:black">Conclusions:</span></span></span></strong> </span></span></p> <p style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:12.0pt"><span style="font-family:"Times New Roman",serif">Disproportionate FMR assessed by an individualized method was independently associated with an increased risk of all-cause mortality. <span style="color:black">When added to the American and European guidelines, FMR proportionality also improved risk stratification by reclassifying patients into lower and higher risk subsets.</span></span></span></span></span></p>
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