Devices, systems, and methods for supplementing, repairing, or replacing a native heart valve leaflet

• US 7,381,220 B2
• Filed: 10/01/2003
• Issued: 06/03/2008
• Est. Priority Date: 09/20/2000
• Status: Expired due to Term

• Current Assignee: MVRx, Inc.
• Original Assignee: Ample Medical, Inc. (MVRx, Inc.)
• Inventors: Machold, Timothy R., Rahdert, David A., Chang, Robert T., Macoviak, John A., Soss, Rick A.
• Primary Examiner(s): Stewart; Alvin J.
• Application Number:
  US10/676,815
• Publication Number:
  US 20050010287A1
• Time in Patent Office: 1,707 Days
• Field of Search: 623/1.24, 623/1.26, 623/2.14, 623/2.18, 623/2.12, 623/2.36, 623/2.37, 623/2.38
• US Class Current: 623/2.12
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2445 Annuloplasty rings in direct contact with the valve annulus
• CPC Class Codes: A61F 2/2454 Means for preventing inversion of the valve leaflets, e.g. chordae tendineae prostheses

Abstract

Devices, systems and methods supplement, repair, or replace a native heart valve. The devices, systems, and methods employ an implant that, in use, extends adjacent a valve annulus. The implant includes a mobile neoleaflet element that occupies the space of at least a portion of one native valve leaflet. The implant mimics the one-way valve function of a native leaflet, to resist or prevent retrograde flow. The implant restores normal coaptation of the leaflets to resist retrograde flow, thereby resisting eversion and/or prolapse, which, in turn, reduces regurgitation.

Claims

1. A method for supplementing, repairing, or replacing a native heart valve leaflet or leaflets comprising

selecting a native heart valve having an annulus, native heart valve leaflets, and generally opposite leaflet commissures spaced apart by a maximum cross-annulus distance defining a major axis of the annulus,

providing an implant comprising an elastic scaffold, at least a portion of the elastic scaffold defining a pseudo-annulus, the elastic scaffold comprising a normal, unloaded condition including a spring constant to undergo compression in response to applied external compression forces into an elastically loaded condition, the implant further comprising at least two struts coupled to the elastic scaffold in generally oppositely spaced apart positions defining, when the elastic scaffold is in the normal, unloaded condition, a normal cross-strut distance that is greater than the maximum cross-annulus distance, the implant further comprising a neoleaflet element coupled to the elastic scaffold within pseudo-annulus and being sized and shaped to occupy the space of at least a portion of one native heart valve leaflet to provide a one-way valve function that, in response to a first pressure condition, assumes a valve opened condition within the pseudo-annulus and, in response to a second pressure condition, assumes a valve closed condition within the pseudo-annulus,

introducing the implant into a heart with the elastic scaffold in the normal, unloaded condition,

applying external compression forces at the at least two struts to reduce the normal cross-strut distance to place the elastic scaffold into the elastically loaded condition,

while the elastic scaffold is in the elastically loaded condition, placing the struts into engagement with tissue at or near the leaflet commissures to apply tension and outwardly displace and separate tissue along the major axis of the annulus to reshape the annulus for leaflet coaptation, and

while the struts are placed in engagement with tissue at or near the leaftlet commissures, providing a one-way valve function with the neoleaflet element that, in response to a first pressure condition, assumes the valve opened condition and, in response to second pressure condition, assumes the valve closed condition, the at least two struts engaging tissue at or near the leaflet commissures to brace the elastic scaffold while in the elastically loaded condition against migration within the annulus during the one-way valve function.

2. A method according to claim 1

wherein the introducing comprises using an open heart surgical procedure.

3. A method according to claim 1

wherein the introducing comprises using a surgical procedure in which the implant is carried within a catheter.

4. A method according to claim 1

wherein the introducing comprises using an intravascular surgical procedure.