Why the study?
Impaired flow following PCI predicts adverse outcomes, but whether a pullback pressure gradient model can accurately predict post-PCI FFR and associated adverse events was unknown.
Does predicted suboptimal post-PCI physiology using a PPG model predict target vessel failure in patients with hemodynamically significant coronary artery disease undergoing PCI?
Cohort (n=855)
Yes
Does predicted suboptimal post-PCI physiology using a PPG model predict target vessel failure in patients with hemodynamically significant coronary artery disease undergoing PCI?
PPG-predicted post-PCI physiology effectively stratifies risk, with predicted suboptimal physiology associated with a nearly twofold increased risk of target vessel failure at 1 year.
BACKGROUND: Impaired flow following percutaneous coronary intervention (PCI) is a known predictor of adverse outcomes. The pullback pressure gradient (PPG) is a novel physiological metric that differentiates focal from diffuse disease and enables prediction of post-PCI fractional flow reserve (FFR). This post hoc analysis of the PPG Global (NCT04789317) study aimed to evaluate the prognostic performance of a PPG model for predicting post-PCI FFR and to determine whether the predicted physiological outcome is associated with adverse events following PCI. METHODS: Prospective and multicenter study including patients with hemodynamically significant coronary artery disease undergoing PCI. A prediction model based on FFR and PPG was used to estimate post-PCI FFR. Based on the predicted values, vessels were classified as having either optimal or suboptimal post-PCI physiology. The primary end point was target vessel failure at 1 year. Target vessel failure was defined as a composite of cardiac death, target-vessel myocardial infarction, and ischemia-driven target vessel revascularization. RESULTS: A total of 855 patients (890 vessels) were analyzed. The mean difference between predicted and measured post-PCI FFR was 0.001 (limits of agreement, –0.10 to 0.10). There was a strong correlation between predicted and measured delta FFR ( r =0.92 [95% CI, 0.91–0.93]; P <0.001). Vessels with predicted suboptimal post-PCI physiology had a significantly higher incidence of target vessel failure (adjusted hazard ratio, 1.97 [95% CI, 1.24–3.15]; P =0.004). Predicted suboptimal physiology was independently associated with adverse clinical outcomes. CONCLUSIONS: PPG-predicted post-PCI physiology was associated with target vessel failure at 1 year. These findings extend the role of coronary physiology beyond diagnostic assessment to include risk stratification and outcome prediction following PCI.
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Ikeda et al. (2025) conducted a cohort in Hemodynamically significant coronary artery disease (n=855). Predicted suboptimal post-PCI physiology vs. Predicted optimal post-PCI physiology was evaluated on Target vessel failure at 1 year (composite of cardiac death, target-vessel myocardial infarction, and ischemia-driven target vessel revascularization) (HR 1.97, 95% CI 1.24-3.15, p=0.004).
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