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Vendor Independent Coronary Calcium Scoring Improves Individual Risk Assessment: The Multi-Ethnic Study of Atherosclerosis (MESA).
Vendor Independent Coronary Calcium Scoring Improves Individual Risk Assessment: The Multi-Ethnic Study of Atherosclerosis (MESA). JACC. Cardiovascular imaging van der Werf, N. R., Dobrolinska, M. M., Greuter, M. J., Willemink, M. J., Fleischmann, D., Bos, D., Slart, R. H., Budoff, M., Leiner, T. 2023Abstract
Substantial variation in Agatston scores (AS) acquired with different computed tomography (CT) scanners may influence patient risk classification.This study sought to develop a calibration tool for state-of-the-art CT systems resulting in vendor-neutral AS (vnAS), and to assess the impact of vnAS on coronary heart disease (CHD) event prediction.The vnAS calibration tool was derived by imaging 2 anthropomorphic calcium containing phantoms on 7 different CT and 1 electron beam tomography system, which was used as the reference system. The effect of vnAS on CHD event prediction was analyzed with data from 3,181 participants from MESA (Multi-Ethnic Study on Atherosclerosis). Chi-square analysis was used to compare CHD event rates between low (vnAS <100) and high calcium groups (vnAS =100). Multivariable Cox proportional hazard regression models were used to assess the incremental value of vnAS.For all CT systems, a strong correlation with electron beam tomography-AS was found (R2 >0.932). Of the MESA participants originally in the low calcium group (n = 781), 85 (11%) participants were reclassified to a higher risk category based on the recalculated vnAS. For reclassified participants, the CHD event rate of 15% was significantly higher compared with participants in the low calcium group (7%; P = 0.008) with a CHD HR of 3.39 (95% CI: 1.82-6.35; P = 0.001).The authors developed a calibration tool that enables calculation of a vnAS. MESA participants who were reclassified to a higher calcium category by means of the vnAS experienced more CHD events, indicating improved risk categorization.
View details for DOI 10.1016/j.jcmg.2023.05.005
View details for PubMedID 37318394