Indications for TAVR
TAVR is recommended for patients with severe, symptomatic, calcific stenosis of a trileaflet aortic valve who have prohibitive surgical risk (≥50% mortality or irreversible morbidity at 30 days), and is a reasonable alternative to surgical AVR in high-risk patients (STS score ≥8%). 1
Primary Indications
Prohibitive Surgical Risk (Class I Recommendation)
TAVR is the preferred treatment when patients meet ALL of the following criteria 1:
Severe AS defined as:
- Aortic jet velocity ≥4.0 m/s, OR
- Aortic valve area (AVA) ≤1.0 cm², OR
- AV index ≤0.6 cm²/m², OR
- Mean gradient ≥40 mm Hg
- Severely reduced, calcified leaflet motion
Symptomatic disease (dyspnea, angina, syncope, or heart failure)
Prohibitive surgical risk defined as:
- Estimated ≥50% risk of mortality or irreversible morbidity at 30 days (assessed by one cardiologist and 2 cardiothoracic surgeons), OR
- Other prohibitive factors: frailty, prior radiation therapy, porcelain aorta, severe hepatic or pulmonary disease
Suitable anatomy:
- Aortic annulus size appropriate for available TAVR devices
- Valve plane to coronary ostium height adequate
- Adequate vascular access (femoral, iliac, subclavian, axillary) OR suitability for apical approach
Predicted survival >12 months
High Surgical Risk (Class IIa Recommendation)
TAVR is a reasonable alternative to surgical AVR when 1:
- All criteria above are met EXCEPT
- STS score ≥8% (originally ≥10% in PARTNER trial, modified to ≥8%)
- Documented by 2 surgeons that true predicted mortality is ≥15%
Expanded Indications (2020 Guidelines)
The 2021 ACC/AHA guidelines expanded TAVR indications to include 2:
- Age ≥70 years with suitable anatomy across all risk categories when transfemoral approach is feasible
- LVEF <50% with severe AS (same considerations as symptomatic patients)
- Preference for transfemoral TAVI over surgical AVR in patients >80 years due to valve durability likely exceeding life expectancy
Contraindications and Situations Where TAVR is NOT Currently Recommended
TAVR should NOT be performed in 1:
- Acceptable/low surgical risk in patients <70 years (insufficient data)
- Bicuspid aortic valve (limited data, though evolving)
- Failing bioprosthetic aortic valve (valve-in-valve procedures require specific consideration)
- Severe mitral annular calcification or severe MR
- Moderate AS (not severe)
- Severe aortic regurgitation without stenosis
- Subaortic stenosis
- Unsuitable anatomy (annulus too small/large, inadequate vascular access)
Critical Anatomical Requirements
Severe AS in Low-Flow States
In patients with LV systolic dysfunction, severe AS diagnosis requires 1:
- Calcified leaflets with reduced systolic motion, AND
- Dobutamine stress echo showing:
- Aortic velocity ≥4.0 m/s OR mean gradient ≥40 mm Hg
- Valve area ≤1.0 cm² OR AV index ≤0.6 cm²/m² at any flow rate
Essential Pre-TAVR Evaluation
Every patient requires 1:
- Risk stratification: STS score calculation
- Comorbidity assessment: Pulmonary function tests (if COPD), malignancy staging, cognitive assessment
- Imaging confirmation:
- Severity of AS and associated CAD
- LV function
- Associated valvular disease
- Cerebrovascular disease extent
- Procedural planning imaging:
- Annular sizing for device selection
- Detailed arterial anatomy (peripheral aortoiliac, aortic arch, ascending aorta)
Team-Based Approach Requirement
TAVR mandates a multidisciplinary heart team including 1:
- Primary cardiologist
- Cardiovascular surgeon
- Interventional cardiologist
- Cardiac anesthesiologist
- Heart failure specialist
- Imaging specialists
- Nursing care team
- Patient and family as active participants
Common Pitfalls to Avoid
Do not perform TAVR without surgical backup available onsite - this is a foundational requirement 1
Do not rely solely on STS score - prohibitive risk includes qualitative factors (frailty, porcelain aorta, radiation) that scores miss 1
Transfemoral access is critical - mortality is higher with non-femoral approaches; when transfemoral is not feasible, strongly reconsider surgical AVR or palliative care 2
Do not assume TAVR is appropriate for bicuspid valves - this remains investigational despite emerging data 1
Verify trileaflet anatomy - the current evidence base and FDA approval specifically applies to trileaflet valves 1
Key Complications to Discuss
TAVR carries specific risks that differ from surgical AVR 1:
- Mortality: 3-5%
- Stroke: 6-7% (higher than surgical AVR's 2%)
- Access complications: 17%
- Pacemaker insertion: 2-9% (Sapien) to 19-43% (CoreValve)
- Paravalvular aortic regurgitation
- Acute kidney injury
- Rare but catastrophic: coronary occlusion, valve embolization, aortic rupture