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Comprehensive Myocardial Assessment by Computed Tomography: Impact on Short-Term Outcomes After Transcatheter
Hideki Koike1, Miho Fukui1, Thomas Treibel2
1Cardiovascular Imaging Research Center and Core Lab at Minneapolis Heart Institute Foundation, Minneapolis, Minnesota, USA.
Insights
Computed tomography extracellular volume (CT-ECV) and global longitudinal strain (CT-GLS) measured via CTA predict outcomes after transcatheter aortic valve replacement (TAVR). These myocardial assessments can guide treatment decisions for severe aortic stenosis (AS).
Area of Science:
- Cardiology
- Radiology
- Medical Imaging
Background:
- Quantifying myocardial changes in severe aortic stenosis (AS) is crucial for prognosis.
- The utility of computed tomography angiography (CTA) for comprehensive pre-transcatheter aortic valve replacement (TAVR) myocardial assessment remains unclear.
Purpose of the Study:
- To assess if left ventricular (LV) extracellular volume (CT-ECV) and global longitudinal strain (CT-GLS) quantified by baseline CTA correlate with post-TAVR outcomes.
- Investigate the prognostic value of myocardial fibrosis and deformation markers derived from CTA.
Main Methods:
- Included 300 patients with severe AS undergoing pre-TAVR CTA.
- Quantified CT-ECV from 3D CT-ECV maps and CT-GLS using semi-automated feature tracking.
- Clinical endpoint: composite of all-cause mortality and heart failure hospitalization.
Main Results:
- Median CT-ECV was 28.5% and median CT-GLS was -20.1%.
- Both CT-ECV (HR: 1.09) and CT-GLS (HR: 1.07) independently predicted the composite outcome.
- Combined elevated CT-ECV and CT-GLS significantly increased risk (HR: 7.14).
Conclusions:
- CT-ECV and CT-GLS derived from CTA are associated with post-TAVR outcomes in patients with severe AS.
- These imaging biomarkers may aid in clinical decision-making for AS intervention timing and TAVR follow-up.
- Further integration into clinical trials is needed to validate their use.
Background:
Quantification of myocardial changes in severe aortic stenosis (AS) is prognostically important. The potential for comprehensive myocardial assessment pre-transcatheter aortic valve replacement (TAVR) by computed tomography angiography (CTA) is unknown.
Objectives:
This study sought to evaluate whether quantification of left ventricular (LV) extracellular volume-a marker of myocardial fibrosis-and global longitudinal strain-a marker of myocardial deformation-at baseline CTA associate with post-TAVR outcomes.
Methods:
Consecutive patients with symptomatic severe AS between January 2021 and June 2022 who underwent pre-TAVR CTA were included. Computed tomography extracellular volume (CT-ECV) was derived from septum tracing after generating the 3-dimensional CT-ECV map. Computed tomography global longitudinal strain (CT-GLS) used semi-automated feature tracking analysis. The clinical endpoint was the composite outcome of all-cause mortality and heart failure hospitalization.
Results:
Among the 300 patients (80.0 ± 9.4 years of age, 45% female, median Society of Thoracic Surgeons Predicted Risk of Mortality score 2.80%), the left ventricular ejection fraction (LVEF) was 58% ± 12%, the median CT-ECV was 28.5% (IQR: 26.2%-32.1%), and the median CT-GLS was -20.1% (IQR: -23.8% to -16.3%). Over a median follow-up of 16 months (IQR: 12-22 months), 38 deaths and 70 composite outcomes occurred. Multivariable Cox proportional hazards model, accounting for clinical and echocardiographic variables, demonstrated that CT-ECV (HR: 1.09 [95% CI: 1.02-1.16]; P = 0.008) and CT-GLS (HR: 1.07 [95% CI: 1.01-1.13]; P = 0.017) associated with the composite outcome. In combination, elevated CT-ECV and CT-GLS (above median for each) showed a stronger association with the outcome (HR: 7.14 [95% CI: 2.63-19.36]; P < 0.001).
Conclusions:
Comprehensive myocardial quantification of CT-ECV and CT-GLS associated with post-TAVR outcomes in a contemporary low-risk cohort with mostly preserved LVEF. Whether these imaging biomarkers can be potentially used for the decision making including timing of AS intervention and post-TAVR follow-up will require integration into future clinical trials.
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