Valve-in-Valve TAVI Recommendations
Valve-in-valve Transcatheter Aortic Valve Implantation (ViV-TAVI) is recommended for patients with degenerated aortic bioprostheses who are at high risk for conventional redo surgery, with decision-making performed by a multidisciplinary heart team. 1
Patient Selection Criteria
The selection of candidates for ViV-TAVI should follow a structured approach:
- ViV-TAVI is indicated specifically for patients with calcified pure or predominant aortic stenosis in a previously implanted bioprosthetic valve 1
- Patient selection must involve multidisciplinary consultation between cardiologists, surgeons, imaging specialists, and anesthesiologists 1
- High surgical risk is defined by a logistic EuroSCORE of ≥15-20% or an STS mortality risk score of ≥10% 1
- Patient characteristics favoring ViV-TAVI over surgical reoperation include:
Contraindications
ViV-TAVI should not be performed in patients with:
- Life expectancy less than 1 year 1
- Unlikely improvement in quality of life due to comorbidities 1
- Severe primary disease of other valves that can only be treated surgically 1
- Thrombus in the left ventricle 1
- Active endocarditis 1
- Elevated risk of coronary ostium obstruction 1
- Inadequate vascular access for the chosen approach 1
Procedural Considerations and Challenges
ViV-TAVI presents specific challenges compared to primary TAVI:
- Higher rates of malposition due to lack of anatomic markers in stentless valves 2
- Increased risk of prosthesis-patient mismatch 3, 4
- Higher potential for coronary obstruction 5, 3
- Optimal procedural planning is crucial to minimize complications 5
Outcomes
The evidence on ViV-TAVI outcomes shows:
- High procedural success rates of approximately 93.8% 1
- Low 30-day mortality rates (0-6.3% for transfemoral approach) 1, 2
- One-year mortality of approximately 14.3% in high-risk patients 2
- Potential for device migration (reported in about 14% of cases with stentless valves) 2
- Need for permanent pacemaker implantation in 14-24% of cases, which is lower than with redo surgery 2, 4
Hemodynamic Outcomes
- ViV-TAVI generally results in good short and mid-term hemodynamic outcomes up to 2 years 1
- However, surgical redo AVR offers superior echocardiographic outcomes compared to ViV-TAVI:
Decision Algorithm
- Confirm the severity of bioprosthetic valve degeneration through echocardiography 1
- Evaluate symptoms and their attribution to valve dysfunction 1
- Assess surgical risk using validated scores (EuroSCORE, STS) 1
- Evaluate life expectancy (must be >1 year) and potential for quality of life improvement 1
- Assess feasibility and exclude contraindications for ViV-TAVI 1
- For patients at low surgical risk, conventional redo surgery should remain the standard of care due to superior hemodynamic outcomes 4
- For high-risk or inoperable patients, ViV-TAVI offers a less invasive alternative with acceptable mortality and morbidity 4
Imaging Requirements
- Comprehensive echocardiographic assessment is essential for evaluating valve degeneration 1
- Coronary angiography should be performed to assess coronary anatomy 1
- Accurate measurement of the aortic annulus is critical to minimize paravalvular leakage and avoid prosthesis migration 1
- Multiple imaging modalities (angiography, MSCT, MRI) should be used to evaluate vascular access routes 1