Abstract 4335849: Improvements in Diagnostic and Therapeutic Cardiovascular Risk Assessment Through Total Plaque Volume Burden: An Analysis of the Fish&Chips Study
Abstract
Background: Quantitative coronary plaque analysis from coronary computed tomographic angiography (CCTA) is a promising strategy for individualized cardiovascular disease (CVD) prevention. More population-level data is needed on how plaque burden can inform lipid lowering strategies to reduce CVD risk reduction. Objectives: To evaluate the prognostic utility of a total plaque volume (TPV)-based risk staging system and model its use in guiding lipid-lowering therapy in real-world patients undergoing clinically indicated CCTAs for evaluation of chest pain. Methods: We analyzed adult patients across a single-center NHS site who underwent clinically indicated CCTA with available AI-based quantitative plaque analysis. TPV was categorized into four risk stages (DECIDE 1–4) using predefined thresholds ( Table 1 ). The primary outcome was cardiac death or non-fatal MI. Secondary analyses reclassified prior myocardial infarction (MI) or early revascularization into DECIDE Stage 4. We modeled lipid-lowering strategies using both fixed-intensity treatment by DECIDE stage and stage-specific LDL-C goals to estimate risk reduction and number needed to treat (NNT) over 3-to-10-year durations. Results: Among the 2,827 patients, mean (SD) age was 58 (13) years, and 51.1% were female. Higher TPV stages were associated with progressively increased risk of CV death or MI (1.7%, 4.9%, 7.4%, 11.1% for stages 1–4, respectively) ( Figure 1 ). The fixed intensity strategy yielded a 10-year NNT of 52, which improved to 42 when using a stage-specific LDL-C goal strategy guided by plaque burden. Conclusions: Quantitative plaque burden measured by AI-enabled CCTA identifies patients at elevated long-term cardiovascular risk and may inform a personalized lipid-lowering strategy to mitigate risk.
Article Details
Authors (9)
Shyon Parsa
Stanford University Hospital, Mountain View, California, United States
Allison Peng
Johns Hopkins School of Medicine, Baltimore, Maryland, United States
Timothy Fairbairn
Liverpool Heart and Chest Hospital, Liverpool, United Kingdom
Jack Bell
Liverpool Heart and Chest Hospital, Liverpool, United Kingdom
Souma Sengupta
Heartflow Inc, Mountain View, California, United States
Sarah Mullen
Heartflow, San Carlos, California, United States
Campbell Rogers
Heartflow, San Carlos, California, United States
Seth Martin
Johns Hopkins School of Medicine, Baltimore, Maryland, United States
Fatima Rodriguez