Change in Coronary Microcirculation and FFR After TAVI in Patients With Cardiovascular Comorbidities

This monocentric and prospective observational study aims to include patients with stable coronary artery disease and undergoing TAVI for severe aortic stenosis via transfemoral access, from November 2020 at Nantes University Hospital, France.

All patients have severe symptomatic aortic stenosis, secondary to degenerative disease confirmed by transthoracic echocardiography (mean gradient >40 mmHg and/or valve area <1 cm2) and significant epicardial coronary stenosis (> or = 50%) assessed by coronarography performed in systematic preoperative work-up. These patients are deemed for TAVI and a first-line medical treatment for CAD, after heart team decision.

The collegially chosen strategy to manage CAD in this population consists in assessing hemodynamic parameters from a coronary stenosis during the TAVI procedure, using functionals tests for ischemia (FFR, IMR, CFR) from a concomitant coronarography. Patients will be routinely admitted in hospital 6 months after TAVI, for clinical and echocardiographic reassessment, and coronarography control. Functional tests will be repeated and according to results, continuation of medical therapy or PCI is proposed, at operator's discretion.

All procedures are performed within the same site by 1 medical team including 4 interventional cardiologists.

Before the TAVI procedure, a computerized multi-sliced tomography is systematically performed to validate the percutaneous approach by femoral access and to choose which prothesis model will be used.

In most cases, TAVI procedure are performed under local anesthesia and mild sedation, under anesthetist supervision.

The common femoral artery is punctured by percutaneous approach, above the femoral bifurcation and a 16-French sheath is inserted.

Three available models of aortic bioprothesis are implanted in our center, the Sapien 3 (EDWARDS Lifescience) the Corevalve Evolute R (Metdtronik) and the Accurate Neo 2 (Boston Scientific) Two Perclose ProGlide devices (Abbott Vascular) are used to perform the perpendicular preclosing. After the deployment of the prosthesis, the TAVI sheath is removed and the nodes from the two previously placed ProGlide devices are tightened. Final femoral angiographic control is not systematic.

Concomitant coronarography is performed by radial artery access site, using a 6-French sheath.

Hemodynamics measures are recorded by PressureWire X Guidewire (Abott Vascular) wireless devices to a computer and processed by the CoroFlow Coroventis software (Abbott Vascular) to carry out multimodal physiological evaluation. FFR, CFR, and IMR measures will be repeated before and immediately after valve implantation. These parameters will be reassessed 6 months after TAVI.

Inclusion criteria

• Adults older than 18 years. For female of childbearing age, active contraceptive method is recommended.
• patients with severe symptomatic aortic stenosis secondary to degenerative disease confirmed by transthoracic echocardiography (mean gradient >40 mmHg and/or valve area <1 cm2) and with significant coronary artery disease (epicardial coronary stenosis angiography > or = to 50%)

Exclusion criteria

• Severe CAD with tritroncular lesions or severe stenosis (>90 %) of left main artery or proximal left anterior descending artery

• Lack of viability in myocardial territory of interest
• History of bypass coronary surgery or heart transplantation
• Severe left ventricular systolic dysfunction, characterized by an ejection fraction < 35 %
• Severe renal impairment (Creatinine clearance <30 ml/min/1.73 m2)
• Absolute contraindication to intravenous adenosin
• Pregnant or nursing women Patients under guardianship, curatorship, or protection of justice