Angiographic Quantitative Flow Ratio-Guided Treatment of Patients With Physiologically Intermediate Coronary Lesions

Jiannan Dai1, Changdong Guan2,3, Xueming Xu1

  • 1Department of Cardiology The Second Affiliated Hospital of Harbin Medical University Harbin Heilongjiang Province China.

Insights

Quantitative Flow Ratio (QFR) guidance did not significantly improve 2-year outcomes for intermediate coronary lesions compared to angiography. This analysis of the FAVOR III China trial found no major benefit in major adverse cardiac events for QFR-guided interventions.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Medical Imaging

Background:

  • The FAVOR III China trial showed benefits of quantitative flow ratio (QFR) guided percutaneous coronary intervention (PCI) over angiography.
  • Uncertainty exists regarding QFR's efficacy in intermediate lesions ('uncertainty zone').
  • This study investigates QFR vs. angiography guidance in these specific lesions.

Purpose of the Study:

  • To evaluate the impact of QFR-guided PCI versus angiography-guided PCI on patient management and outcomes.
  • To specifically analyze outcomes in patients with "uncertainty-zone" coronary lesions.

Main Methods:

  • A prespecified subgroup analysis of the FAVOR III China trial.
  • Identified 873 patients (22.9%) with uncertainty-zone lesions (offline QFR 0.75-0.85).
  • Compared major adverse cardiac events (MACE) at 2 years between QFR-guided and angiography-guided PCI groups.

Main Results:

  • At 2 years, MACE occurred in 7.0% of the QFR group and 8.3% of the angiography group (HR 0.85).
  • Landmark analysis showed differing treatment effects before and after 1 year (P_interaction=0.03).
  • QFR guidance showed benefit after 1 year, driven by reduced myocardial infarctions and revascularizations.

Conclusions:

  • QFR-guided revascularization did not significantly improve 2-year clinical outcomes in this subgroup of patients with intermediate coronary lesions.
  • The findings suggest that the benefits observed in the overall FAVOR III China trial may not extend to this specific patient subgroup.
Abstract