CLINICAL EVIDENCE FOR
INTERMEDIATE-RISK PATIENTS

definitive outcomes chart
Thourani, V., et al. Transcatheter aortic valve replacement versus surgical valve replacement in intermediate-risk patients: A propensity score analysis. Lancet. 2016; 2218-25.
*The PARTNER II trial intermediate-risk cohort 30-day unadjusted clinical event rates for TAVI with the SAPIEN 3 valve, AT population (n=1,077).
 
Thourani V., et al. Transcatheter aortic valve replacement versus surgical valve replacement in intermediate-risk patients: A propensity score analysis. Lancet. 2016;387: 2218-25.
The PARTNER II trial intermediate-risk cohort unadjusted clinical event rates, AT population.
Edwards Lifesciences data on file.
promo

The PARTNER trials represent the largest, most rigorous comparative body of evidence in the history of aortic valve replacement

Transformational
Valve Design
  1. Outer Sealing Skirt
  2. Low Profile Access
  3. Frame Design
  4. Proven Valve Tissue
  5. Commander Delivery System
  6. Certitude Delivery System

Transformational
Valve Design
  • Outer Sealing Skirt
  • Low Profile Access
  • Frame Design
  • Proven Valve Tissue
  • Commander Delivery System
  • Certitude Delivery System
Complete Range of Valve Sizes
Complete Range of Valve Sizes
Video Library

Edwards SAPIEN 3 transcatheter heart valve

Transfemoral procedure with the Edwards Commander delivery system

Transapical procedure with the Edwards Certitude delivery system

Transaortic procedure with the Edwards Certitude delivery system

Edwards SAPIEN 3 transcatheter heart valve

Transfemoral procedure with the Edwards Commander delivery system

Transapical procedure with the Edwards Certitude delivery system

Transaortic procedure with the Edwards Certitude delivery system

For Professional Use

For Professional Use

See instructions for use for full prescribing information, including indications, contraindications, warnings, precautions and adverse event.

Edwards Lifesciences devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.

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