Prognostic value of Murray law-based quantitative flow ratio after percutaneous coronary intervention.

EuroInterventionNov 2, 2026 (epub)
Clinical ResearchCardiologyOpen access

Rui Zhang, Jingjing Xu, Changdong Guan et al.

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In 30 seconds

This prespecified subgroup analysis of the randomised FAVOR III China trial assessed whether post-PCI Murray law-based quantitative flow ratio (μQFR) was associated with long-term outcomes. Offline μQFR was analysed in 4,196 vessels from 3,455 patients, and the primary outcome was 5-year major adverse cardiovascular events (MACE). MACE incidence was higher across descending μQFR tertiles: 23.1% vs 19.0% vs 17.2% (p=0.001). Compared with μQFR>0.95, the lowest tertile (μQFR ≤0.91) was associated with higher adjusted risk (aHR 1.30, 95% CI: 1.06-1.60).

Key findings

  • Five-year MACE incidence was 23.1% vs 19.0% vs 17.2% across low, intermediate, and high post-PCI μQFR tertiles (p=0.001).
  • Compared with μQFR>0.95, the lowest tertile (μQFR ≤0.91) had higher adjusted MACE risk: aHR 1.30 (95% CI: 1.06-1.60).
  • MACE occurred in 22.3% with μQFR <0.94 versus 17.4% with μQFR ≥0.94 (aHR 1.23, 95% CI: 1.04-1.47; p=0.02).
  • There was no significant interaction between treatment strategy and post-PCI μQFR (p for interaction=0.23).

Why it matters

The findings support an association between lower post-PCI μQFR and greater long-term cardiovascular risk, suggesting that physiological assessment after PCI may help stratify prognosis. The authors note that binary discrimination is limited and favour interpreting μQFR as a continuous risk measure rather than relying solely on a cutoff.

What to keep in mind

This was a prespecified subgroup analysis with offline μQFR assessment in eligible PCI-treated vessels; the reported associations do not establish that μQFR-guided management improves outcomes.

Source

Published in EuroIntervention. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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