What is TAVI (Transcatheter Aortic Valve Implantation)?
TAVI is a minimally invasive catheter-based procedure that replaces a severely stenotic aortic valve without open-heart surgery, primarily indicated for patients with severe symptomatic aortic stenosis who are at high or prohibitive surgical risk. 1, 2
Definition and Procedure Overview
TAVI involves delivering a bioprosthetic valve (bovine pericardial) through a catheter to replace the diseased native aortic valve, avoiding the need for sternotomy and cardiopulmonary bypass. 3, 2
The procedure was first performed in humans in 2002 by Alain Cribier, initially using an antegrade transseptal approach, which was subsequently replaced by more practical access routes. 3
Two main valve types are used: balloon-expandable and self-expandable prostheses, each with specific anatomic requirements and deployment characteristics. 4
Access Routes
The transfemoral (retrograde arterial) approach is the preferred and most common access route for TAVI when anatomy permits. 3, 5
Alternative Access Options:
Transapical access involves direct puncture of the left ventricular apex through a small thoracotomy, providing antegrade valve delivery when femoral access is unsuitable. 3, 5
Transsubclavian and direct transaortic approaches serve as additional alternatives for patients with prohibitive peripheral vascular disease. 3, 5
Patient Selection Criteria
Primary Indication:
TAVI is indicated for patients with severe symptomatic aortic stenosis (valve area ≤1.0 cm², mean gradient ≥40 mmHg, or peak velocity ≥4.0 m/sec) who are at high surgical risk (STS score ≥8%) or deemed inoperable. 1, 6
Patients must have predicted survival >12 months and an estimated ≥50% risk of mortality or irreversible morbidity at 30 days from surgical aortic valve replacement. 1
Multidisciplinary Assessment:
- A Heart Valve Team including interventional cardiologists, cardiac surgeons, imaging specialists, anesthesiologists, and heart failure specialists must evaluate all TAVI candidates. 1
Absolute Contraindications
General Contraindications:
Aortic annulus <18 mm or >25 mm for balloon-expandable devices, or <20 mm or >27 mm for self-expandable devices. 4
Bicuspid aortic valves due to risk of incomplete prosthesis deployment. 4
Asymmetric heavy valvular calcification that may compress coronary arteries during valve deployment. 4
Aortic root dimension <45 mm at the aorto-tubular junction for self-expandable prostheses. 4
Presence of left ventricular apical thrombus. 4
Transfemoral Approach Contraindications:
Iliac arteries with severe calcification, tortuosity, or diameter <6-9 mm (depending on device used). 4
Severe aortic angulation, severe atheroma of the arch, coarctation, or abdominal aortic aneurysm with protruding mural thrombus. 4
Bulky atherosclerosis of the ascending aorta and arch detected by transesophageal echocardiography. 4
Transapical Approach Contraindications:
Previous left ventricular surgery using a patch (e.g., Dor procedure). 4
Calcified pericardium. 4
Severe respiratory insufficiency or severe pulmonary hypertension (transapical route only; transfemoral remains permissible). 1
Non-reachable left ventricular apex. 4
Pre-Procedural Imaging Requirements
CT angiography of chest, abdomen, and pelvis with ECG-gated thoracic acquisition is required to assess iliofemoral vessel diameter, aortic annulus sizing, coronary ostia height, and calcification distribution. 1
Transthoracic echocardiography must confirm maximum aortic velocity, mean gradient, aortic valve area, left ventricular ejection fraction, and pulmonary artery pressure. 1
Transesophageal echocardiography should be performed if borderline annular measurements create doubt about procedural feasibility, as TEE shows larger values than transthoracic echo. 4
Clinical Outcomes
Mortality and Efficacy:
At 1 year, TAVI reduces all-cause mortality to 30.7% compared to 50.7% with standard therapy in inoperable patients (hazard ratio 0.55, P<0.001). 2
TAVI significantly reduces the composite endpoint of death or repeat hospitalization to 42.5% versus 71.6% with standard therapy (hazard ratio 0.46, P<0.001). 2
Among survivors at 1 year, cardiac symptoms (NYHA class III or IV) are reduced to 25.2% with TAVI versus 58.0% with standard therapy (P<0.001). 2
Procedural Complications:
30-day mortality ranges from 5-18% depending on patient risk profile and center experience. 4
Major stroke occurs in 3-9% of patients, with higher rates at 30 days (5.0%) compared to standard therapy (1.1%, P=0.06). 4, 2
Vascular complications occur in 10-17% and remain a significant cause of morbidity and mortality. 4, 2
Permanent pacemaker implantation is required in 4-24% of patients, with higher rates for self-expandable devices. 4
Paravalvular aortic regurgitation (mild-to-moderate) occurs in approximately 50%, though severe regurgitation has decreased to 5% with improved sizing techniques. 4
Special Populations
Severely Reduced LVEF:
LVEF <20% is a relative contraindication but not absolute, requiring careful individualized evaluation. 1
LVEF between 20-35% is acceptable for TAVI candidacy. 1
Pulmonary Hypertension:
Severe pulmonary hypertension is a relative contraindication only for the transapical approach, while transfemoral access remains permissible. 1
Right-heart catheterization should be considered in TAVI candidates with pulmonary hypertension to characterize severity and mechanism before proceeding. 1
Facility and Team Requirements
TAVI should be performed only in high-volume centers with both cardiology and cardiac surgery departments, with expertise in structural heart disease intervention and high-risk valvular surgery. 4
The optimal environment should be spacious, sterile, and feature high-quality imaging equipment with hemodynamic monitoring capabilities—ideally a hybrid suite combining operating room and catheterization laboratory features. 4
Close cooperation between clinical cardiologists, echocardiographists, interventional cardiologists, cardiac surgeons, and anesthesiologists is mandatory for procedural success. 4
Post-Procedural Follow-Up
Transthoracic echocardiography immediately post-TAVR must assess maximum aortic velocity, mean gradient, valve area, paravalvular regurgitation severity, and left ventricular function. 1
Serial echocardiography at specified intervals is required for long-term surveillance to monitor valve function and paravalvular regurgitation progression. 1
Valve function remains stable at 1-2 years with no deterioration in stenosis or regurgitation on echocardiographic assessment. 4, 2