What is a TAVI (Transcatheter Aortic Valve Implantation) and in which patients is it indicated?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 23, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

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

References

Guideline

TAVR Guidelines for High-Risk Patients with Severe Aortic Stenosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Transcatheter aortic valve implantation: the procedure.

Heart (British Cardiac Society), 2012

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Transcatheter aortic valve replacement (TAVR): access planning and strategies.

Methodist DeBakey cardiovascular journal, 2012

Guideline

Aortic Stenosis Diagnosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.