Prognostic value of Murray law-based quantitative flow ratio after percutaneous coronary intervention.
Zhang R, Xu J, et al. • EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology • 2026
Post-PCI μQFR distributions were similar between treatment groups, but lower values were associated with higher 5-year adverse event risk without significant treatment interaction, and limited binary discrimination supports use as a continuous metric for post-PCI physiological risk stratification.
Key Findings
Results
Post-PCI μQFR was successfully analysed in most of the study population, with similar distributions between randomised treatment groups.
This was a prespecified subgroup analysis of the FAVOR III China trial including 3,825 patients.
Post-PCI μQFR was successfully analysed in 4,196 vessels from 3,455 patients.
Vessels analysed were PCI-treated with reference diameter ≥2.5 mm and 50-90% diameter stenosis, using offline analysis.
Results
Lower post-PCI μQFR tertiles were associated with a higher 5-year incidence of MACE.
5-year MACE (death, MI, or ischaemia-driven revascularisation) was 23.1% in the low tertile vs 19.0% intermediate vs 17.2% high (p=0.001).
After adjustment, the lowest μQFR tertile had significantly higher MACE risk than the highest tertile, while the intermediate tertile did not.
Using the highest tertile (μQFR >0.95) as reference, aHR for the intermediate tertile was 1.08 (95% CI: 0.87-1.34).
aHR for the lowest tertile (μQFR ≤0.91) was 1.30 (95% CI: 1.06-1.60).
Results
A ROC-derived cutoff of post-PCI μQFR <0.94 identified patients with higher MACE rates.
MACE occurred in 22.3% of patients with μQFR <0.94 vs 17.4% with μQFR ≥0.94.
Adjusted HR was 1.23 (95% CI: 1.04-1.47; p=0.02).
Results
No significant interaction was found between treatment strategy and post-PCI μQFR in relation to outcomes.
The p for interaction was 0.23.
The association of lower μQFR with higher risk was therefore not significantly modified by the randomised treatment strategy.
Conclusions
The authors conclude that limited binary discrimination supports using post-PCI μQFR as a continuous metric for risk stratification.
Association with outcomes was modest (aHR 1.23 for the ROC-derived binary cutoff; 1.30 for the lowest tertile).
This supports μQFR as a continuous measure of post-PCI physiological risk rather than a binary threshold.
What This Means
This study looked at whether a measurement of blood flow in heart arteries taken right after a stent procedure (PCI) can predict later heart problems. The measurement, called μQFR, is calculated by computer from a single angiogram image, without inserting a pressure wire. The researchers analysed 4,196 treated vessels from 3,455 patients in the FAVOR III China trial and followed them for five years.
Patients whose post-procedure μQFR was lowest had more major adverse events (death, heart attack, or repeat revascularisation for ischaemia) over five years: 23.1% in the lowest group versus 17.2% in the highest. After adjusting for other factors, the lowest group had about a 30% higher relative risk. A single cutoff of 0.94 also separated higher-risk from lower-risk patients (22.3% vs 17.4%), but the separation was modest. The relationship did not differ significantly by which treatment strategy patients had been randomised to.
This research suggests that μQFR after stenting may help gauge a patient's later risk, with lower values signalling higher risk. Because a single cutoff did not discriminate strongly, the authors suggest the value is better viewed as a continuous scale than a pass/fail test. This was a subgroup analysis of a trial, so it shows association rather than proving that acting on the value would improve outcomes.
Zhang R, Xu J, Guan C, Jiang Y, Shi Y, Tu S, et al.. (2026). Prognostic value of Murray law-based quantitative flow ratio after percutaneous coronary intervention.. EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology. https://doi.org/10.4244/EIJ-D-26-00457