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ABSTRACT: Background
The EVOQUE transcatheter tricuspid heart valve (Edwards Lifesciences) is approved for high-risk patients with severe tricuspid regurgitation (TR). This report describes the first EVOQUE implantation after failed percutaneous tricuspid annuloplasty and edge-to-edge repair.Case summary
An 80-year-old man with atrial fibrillation underwent percutaneous annuloplasty with a Cardioband (Edwards Lifesciences) for torrential TR. Initially improved, TR recurred within a year, accompanied by severe mitral regurgitation. The patient underwent mitral and tricuspid edge-to-edge repairs, improving symptoms to NYHA functional class II, but TR persisted because of a large coaptation gap. Three years later, TR worsened as a result of single-leaflet device attachment. After multid
SUBMITTER: Toggweiler S
PROVIDER: S-EPMC12441407 | biostudies-literature | 2025 Jul
REPOSITORIES: biostudies-literature