QFR-Based Functional SYNTAX Score System in Optimizing Revascularization Strategy for Multivessel Disease

Harbin Medical University

Status

Not yet enrolling

Conditions

Cardiovascular Diseases

Treatments

Procedure: Traditional SYNTAX scoring

Procedure: QFR-Based Functional SYNTAX Score System

Study type

Interventional

Funder types

Other

Identifiers

NCT07020195

QFR-FSS

Details and patient eligibility

About

The revascularization treatment of multi vessel coronary artery disease (MVD) has always been a complex and important field in the treatment of coronary heart disease. The relative benefits of PCI and CABG vascular reconstruction strategies have always been a controversial topic in the field of MVD treatment. At present, SYNTAX score is the most commonly used imaging scoring system in clinical practice for quantitatively evaluating the complexity of coronary artery MVD, preliminary selection of revascularization strategies, and risk stratification. However, the SYNTAX score is entirely based on anatomical information of the lesion, and the assessment of the degree of coronary artery ischemia caused by the lesion is not accurate enough. Relying solely on anatomical structures for scoring may overestimate the harm of non ischemic lesions. The functional SYNTAX score (FSS) combines functional assessment of coronary artery lesions with anatomical structure scoring, only including lesions with hemodynamic significance, effectively optimizing the traditional SYNTAX scoring system. Compared with traditional SYNTAX scoring, FSS can reduce the number of high-risk patients, objectively evaluate the functional significance of lesions, and guide PCI treatment, significantly improving clinical prognosis.

Quantitative flow ratio (QFR) is a novel method for evaluating the functional significance of coronary artery stenosis. However, it is currently unclear whether FSS based on QFR can achieve objective and accurate risk stratification, guide the selection of revascularization strategies, and improve the long-term prognosis of patients with coronary artery MVD. Higher quality prospective clinical trials need to be designed for verification.

Therefore, this study will use a functional SYNTAX scoring system based on QFR (QFR-FSS) to conduct a prospective, multicenter, randomized controlled clinical trial to evaluate the guiding value of QFR-FSS in selecting revascularization strategies for patients with coronary artery MVD and its impact on long-term cardiovascular prognosis.

Enrollment

1,200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥ 18 years old;
Diagnosed as MVD patient by coronary angiography (≥ 50% stenosis in ≥ 2 major vessels);
Plan to undergo PCI or CABG treatment, and ensure that the contrast images meet the imaging quality requirements for QFR analysis;
Voluntarily sign the informed consent form, be able to participate in randomization and cooperate in completing all follow-up visits.

Exclusion criteria

Acute myocardial infarction requires emergency PCI;
Severe left ventricular dysfunction (LVEF<30%) or cardiogenic shock;
The quality of coronary angiography images is poor, such as vascular overlap, respiratory artifacts, projection angles less than 25 °, or frame rates less than 15 frames per second;
Failure of QFR analysis due to severe calcified lesions (determined by the central laboratory);
eGFR<30 mL/min/1.73m ² or contrast agent allergy;
Patients using intravenous pressors, intra aortic balloon counterpulsation, or other mechanical circulatory support devices;
Patients undergoing tracheal intubation treatment;
Patients who have received thrombolytic therapy before admission;
Pregnant women;
Expected survival time<1 year due to non cardiac reasons;
Patients who are not expected to receive antiplatelet therapy for at least 6 months;
Patients who have received CABG treatment in the past or plan to receive CABG treatment;
Patients who plan to undergo any surgical procedure within 6 months;
There are other conditions that may interfere with follow-up, such as dementia, drug abuse including drug use and drug dependence for other reasons.