Abstract 4348488: Multivalvular Disease in TAVR: The Impact of Non-Rheumatic Mitral Stenosis on Procedural Outcomes from the National Inpatient Sample 2020-2022

Introduction: Concomitant mitral stenosis (MS) is prevalent in ~10-15% of patients undergoing transcatheter aortic valve replacement (TAVR). There has been conflicting literature on the effect of multivalvular heart disease on TAVR outcomes. TAVR can induce geometric changes in the mitral apparatus, such as annular narrowing and anterior mitral leaflet restriction, which may aggravate MS or unmask previously subclinical disease. Our study aims to investigate the impact of coexisting MS on patients who undergo TAVR. Methods: Using the National Inpatient Sample (NIS) from 2020 to 2022, we retrospectively identified patients who had undergone TAVR as a primary procedure. We excluded those with concomitant valvular procedures, prior PPM, urgent procedures, and prior surgical valve repair. Co-existing non-rheumatic MS was identified, and two cohorts were created. Baseline characteristics were compared using t-tests. A multivariable logistic regression model with a 2-sided significance level of 0.05 was used. All baseline characteristics were included in the multivariate adjustment. Results: A total of 253,409 weighted hospitalizations for TAVR were identified. 1.05% (2,668) had non-rheumatic MS. The baseline characteristics are given in image-1. Patients with TAVR and concomitant MS were more likely to be female (64.8% vs 42.1%), have underlying HF (80.7% vs 70.6%), and have ESRD (7.3% vs 3.6%). On multivariate analysis, the concomitant MS were more likely to have acute respiratory failure (aOR 1.76, p < 0.001), heart block (aOR 1.81, p < 0.001), and PPM implantation (aOR 1.4, p = 0.005). This cohort was less likely to have a post-procedure systolic/diastolic heart failure exacerbation (aOR 0.58, 95% CI 0.42 to 0.82, p = 0.001). There were no differences in in-hospital mortality. Device embolization was not reported due to the low event rate. The results of the multivariate regression are shown in image-2. Conclusion: TAVR is associated with adverse clinical outcomes in patients with MS. However, there is no difference in in-hospital mortality. While the MS + TAVR cohort may have some hemodynamic improvement, as evident by a lower incidence of acute HF, there is an increased risk of PPM placement due to the TAVR valve frame and severe annular calcification affecting the conduction bundles. These findings underscore the importance of preprocedural assessment and risk stratification for patients with combined aortic and mitral valve disease.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4348488
Primary Topic
Cardiac Valve Diseases and Treatments
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article
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article

Abstract 4348488: Multivalvular Disease in TAVR: The Impact of Non-Rheumatic Mitral Stenosis on Procedural Outcomes from the National Inpatient Sample 2020-2022

Muhammad Zahid Anwar, Mahmoud Alsaiqali, Waleed Ahmed, Muhammad Faisal Riaz et al.
Circulation
Cardiac Valve Diseases and Treatments
article

Abstract 4348488: Multivalvular Disease in TAVR: The Impact of Non-Rheumatic Mitral Stenosis on Procedural Outcomes from the National Inpatient Sample 2020-2022

Muhammad Zahid Anwar, Mahmoud Alsaiqali, Waleed Ahmed, Muhammad Faisal Riaz, Tehreem Fatima, Dawood Shehzad, Michael Roberts, Humna Younis, I. Munshi Younis, Wahid Abdul, Sunia Chaudhary, Aiman Zia, Holly Gerberding
article en

Abstract

Introduction: Concomitant mitral stenosis (MS) is prevalent in ~10-15% of patients undergoing transcatheter aortic valve replacement (TAVR). There has been conflicting literature on the effect of multivalvular heart disease on TAVR outcomes. TAVR can induce geometric changes in the mitral apparatus, such as annular narrowing and anterior mitral leaflet restriction, which may aggravate MS or unmask previously subclinical disease. Our study aims to investigate the impact of coexisting MS on patients who undergo TAVR. Methods: Using the National Inpatient Sample (NIS) from 2020 to 2022, we retrospectively identified patients who had undergone TAVR as a primary procedure. We excluded those with concomitant valvular procedures, prior PPM, urgent procedures, and prior surgical valve repair. Co-existing non-rheumatic MS was identified, and two cohorts were created. Baseline characteristics were compared using t-tests. A multivariable logistic regression model with a 2-sided significance level of 0.05 was used. All baseline characteristics were included in the multivariate adjustment. Results: A total of 253,409 weighted hospitalizations for TAVR were identified. 1.05% (2,668) had non-rheumatic MS. The baseline characteristics are given in image-1. Patients with TAVR and concomitant MS were more likely to be female (64.8% vs 42.1%), have underlying HF (80.7% vs 70.6%), and have ESRD (7.3% vs 3.6%). On multivariate analysis, the concomitant MS were more likely to have acute respiratory failure (aOR 1.76, p < 0.001), heart block (aOR 1.81, p < 0.001), and PPM implantation (aOR 1.4, p = 0.005). This cohort was less likely to have a post-procedure systolic/diastolic heart failure exacerbation (aOR 0.58, 95% CI 0.42 to 0.82, p = 0.001). There were no differences in in-hospital mortality. Device embolization was not reported due to the low event rate. The results of the multivariate regression are shown in image-2. Conclusion: TAVR is associated with adverse clinical outcomes in patients with MS. However, there is no difference in in-hospital mortality. While the MS + TAVR cohort may have some hemodynamic improvement, as evident by a lower incidence of acute HF, there is an increased risk of PPM placement due to the TAVR valve frame and severe annular calcification affecting the conduction bundles. These findings underscore the importance of preprocedural assessment and risk stratification for patients with combined aortic and mitral valve disease.

CirculationVol. 152(Suppl_3)
Rawalpindi Medical University (PK), University of South Dakota (US), University of Sioux Falls (US)
Openalex Percentile: Top 51%
Cardiac Valve Diseases and Treatments
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