CPC A61F 2/2427 (2013.01) [A61B 17/0401 (2013.01); A61F 2/2412 (2013.01); A61F 2/2418 (2013.01); A61F 2/2454 (2013.01); A61F 2/2457 (2013.01); A61B 2017/0409 (2013.01); A61B 2017/0414 (2013.01); A61B 2017/0417 (2013.01); A61B 2017/044 (2013.01); A61B 2017/0464 (2013.01); A61F 2210/0057 (2013.01); A61F 2220/0016 (2013.01); A61F 2220/0041 (2013.01); A61F 2220/0075 (2013.01); A61F 2230/0013 (2013.01); A61F 2230/005 (2013.01); A61F 2230/008 (2013.01); A61F 2250/0004 (2013.01); A61F 2250/0012 (2013.01); A61F 2250/0039 (2013.01)] | 20 Claims |
1. A method of treating a disorder of a native mitral valve in a heart, comprising:
inserting a delivery device with a mitral valve prosthesis into a left ventricle of the heart;
advancing the delivery device into the left ventricle to position the mitral valve prosthesis within the native mitral valve, wherein the mitral valve prosthesis comprises a prosthetic valve and a frame having an expandable inflow region, with a cross-sectional diameter larger than an annulus of the native mitral valve, and an expandable outflow region; and
releasing the mitral valve prosthesis from the delivery device to permit the inflow region to expand into apposition with a wall of a left atrium of the heart, and to permit the outflow region to expand into apposition with the annulus of the native mitral valve;
positioning at least one anchor between the outflow region of the mitral valve prosthesis and the heart to tether the mitral valve prosthesis to the heart; and
adjusting tension on the at least one anchor to provide stability to the mitral valve prosthesis
wherein the at least one anchor includes an anchoring element at a first end thereof, the anchoring element being configured in an open state to permit adjustment of the tension on the at least one anchor and in a closed state to attach the at least one anchor to the heart by gripping and holding the heart.
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