CT-Derived Features as Predictors of Clot Burden and Resolution

<b>Objectives</b>: To evaluate the prognostic utility of CT-imaging-derived biomarkers in distinguishing acute pulmonary embolism (PE) resolution and its progression to chronic PE, as well as their association with clot burden. <b>Materials and Methods</b>: We utilized a cohort of 45 patients (19 male (42.2%)) and 96 corresponding CT scans with exertional dyspnea following an acute PE. These patients were referred for invasive cardiopulmonary exercise testing (CPET) at the University of Pittsburgh Medical Center from 2018 to 2022, for whom we have ground truth classification of chronic PE, as well as CT-derived features related to body composition, cardiopulmonary vasculature, and PE clot burden using artificial intelligence (AI) algorithms. We applied Lasso regularization to select parameters, followed by (1) Ordinary Least Squares (OLS) regressions to analyze the relationship between clot burden and the selected parameters and (2) logistic regressions to differentiate between chronic and resolved patients. <b>Results</b>: Several body composition and cardiopulmonary factors showed statistically significant association with clot burden. A multivariate model based on cardiopulmonary features demonstrated superior performance in predicting PE resolution (AUC: 0.83, 95% CI: 0.71-0.95), indicating significant associations between airway ratio (negative correlation), aorta diameter, and heart volume (positive correlation) with PE resolution. Other multivariate models integrating demographic features showed comparable performance, while models solely based on body composition and baseline clot burden demonstrated inferior performance. <b>Conclusions</b>: Our analysis suggests that cardiopulmonary and demographic features hold prognostic value for predicting PE resolution, whereas body composition and baseline clot burden do not. <b>Clinical Relevance</b>: Our identified prognostic factors may facilitate the follow-up procedures for patients diagnosed with acute PE.