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TRIFORMIS RESILIA tricuspid valve

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The first and only surgical valve designed specifically for the tricuspid position

Triformis overview product
  • Unique sewing ring shape and profile tailored to native tricuspid anatomy
  • Features designed to ease orientation and implantation, and avoid suture looping
  • RESILIA tissue preservation technology, designed to enhance durability*1
  • Built on the trusted PERIMOUNT valve platform

*Clinical data on valves with RESILIA tissue up to 7-year follow-up have been published, with additional follow-up of up to 10 years in process.

Pre-clinical study performance of the TRIFORMIS RESILIA valve in the tricuspid position demonstrated: 

  • Good leaflet mobility
  • Good hemodynamic performance
  • No significant conduction abnormalities
  • Optimal seating

The TRIFORMIS RESILIA tricuspid valve is a timely innovation

Historically, surgery for isolated tricuspid regurgitation is rarely performed because of perceptions of high mortality.



A new analysis of STS outcomes shows that the risk is lower than previously observed2, providing a new benchmark for current and future isolated tricuspid valve interventions.

5.6%

overall predicted risk of operative mortality

References

  1. Beaver T, Bavaria J, Griffith B, et al. Seven-year outcomes following aortic valve replacement with a novel tissue bioprosthesis. J Thorac Cardiovasc Surg.  2023;x:1-11. doi: 10.1016/j.jtcvs.2023.09.047  
  2. Thourani VH, Bonnell L, Wyler von Ballmoos MC, et al. Outcomes of isolated tricuspid valve surgery: a Society of Thoracic Surgeons analysis and risk model. Ann Thorac Surg. 2024;118:873-881. doi: 10.1016/j.athoracsur.2024.04.014
Important Safety Information

Important Safety Information

TRIFORMIS RESILIA Tricuspid Valve

Indications: For use in replacement of native or prosthetic tricuspid heart valves.

Contraindications: The TRIFORMIS RESILIA tricuspid valve is contraindicated in patients who have untreatable hypersensitivity to nitinol alloys (nickel and titanium).

Complications and Side Effects: Thromboembolism, valve thrombosis, hemorrhage, hemolysis, regurgitation, endocarditis, structural valve deterioration, nonstructural dysfunction, stenosis, arrhythmia, transient ischemic attack/stroke, congestive heart failure, myocardial infarction, ventricular perforation by stent posts, any of which could lead to reoperation, explantation, permanent disability, and death.

CAUTION: US law restricts this device to sale by or on the order of a physician. See Instructions for Use for full prescribing information.