Valved apical conduit with trocar for beating-heart ventricular assist device placement

• US 20020045846A1
• Filed: 08/14/2001
• Published: 04/18/2002
• Est. Priority Date: 08/14/2000
• Status: Active Grant

• Current Assignee: Miami University
• Original Assignee: Miami University
• Inventors: Margules, Gary S., Kaplon, Richard J.
• Granted Patent: US 6,726,648 B2
• Time in Patent Office: Days
• US Class Current: 604/9
• CPC Class Codes: A61B 17/3468 for implanting or removing devices, e.g. prostheses, implants, seeds, wires devices for implanting seeds A61M37/0069
• CPC Class Codes: A61B 2017/00243 cardiac
• CPC Class Codes: A61B 2017/00252 for by-pass connections, i.e. connections from heart chamber to blood vessel or from blood vessel to blood vessel
• CPC Class Codes: A61B 2017/3425 for internal organs, e.g. heart ports
• CPC Class Codes: A61M 1/3653 Interfaces between patient blood circulation and extra-corporal blood circuit
• CPC Class Codes: A61M 1/3659 Cannulae pertaining to extracorporeal circulation
• CPC Class Codes: A61M 60/148 in line with a blood vessel using resection or like techniques, e.g. permanent endovascular heart assist devices
• CPC Class Codes: A61M 60/178 drawing blood from a ventricle and returning the blood to the arterial system via a cannula external to the ventricle, e.g. left or right ventricular assist devices
• CPC Class Codes: A61M 60/268 the displacement member being flexible, e.g. membranes, diaphragms or bladders
• CPC Class Codes: A61M 60/427 the force acting on the blood contacting member being hydraulic or pneumatic
• CPC Class Codes: A61M 60/896 having flexible or resilient parts, e.g. flap valves

Abstract

An inflow cuff with trocar for apical cannulation of the heart. The inflow cuff has an omni-directional or unidirectional valve that prevents blood from flowing out of the heart, thus facilitating apical cannulation in beating-heart situations. The inflow cuff is particularly suited for use in ventricular assist device (VAD) implantation procedures, in which the trocar would be used to punch a hole in the apex, followed by immediate insertion of the inflow cuff. If used in a VAD implantation procedure, the valve of the inflow cuff prevents blood loss until an inflow conduit from the VAD is inserted.

Claims

1. An inflow cuff for beating-heart apical cannulation of a heart, comprising:

a tube having a first end and a second end, said first end constructed and adapted to be inserted into the heart;

a sewing ring disposed on an exterior surface of said tube proximate to said first end, said sewing ring constructed and adapted to be sutured to an exterior wall of the heart and to retain the first end of said tube at a selected position in the heart; and

a valve disposed on and integral with the interior of said tube, said valve having two or more compliant leaves constructed and adapted to form a releasable seal with one another, said valve (1) preventing blood flow out of the heart when closed and (2) opening in response to pressure directed towards the heart, said valve being disposed further from the first end of said tube than said sewing ring;

wherein said inflow cuff is constructed and arranged to allow the passage of a trocar through its lumen, the trocar constructed and arranged to form a hole in the heart of sufficient size to admit the first end of said inflow cuff, and wherein said inflow cuff is constructed and arranged to permit withdrawal of the trocar and the insertion of a conduit through the lumen of said inflow cuff to establish a route for blood flow out of the heart.

2. The inflow cuff of claim 1, wherein the valve has three compliant leaves, and wherein said tube optionally includes a bulged portion of the walls thereof, said bulged portion disposed at a location between said sewing ring and said valve such that said three compliant leaves fit into said bulged portion upon the insertion of the conduit.

3. The inflow cuff of claim 1, wherein the selected position is the apex of the heart.

4. The inflow cuff of claim 1, wherein the sewing ring is comprised of synthetic, biocompatible felt.

5. The inflow cuff of claim 1, wherein the inflow cuff is manufactured of a biocompatible, silicone rubber, wherein the silicone rubber is selectively reinforced by a woven mesh.

17. The medical device of claim 1, wherein the trocar further comprises a flange, said flange preventing the longitudinal insertion of the trocar beyond a selected point.

18. A method of providing a passageway for blood flow out of a patient'"'"'s heart, comprising:

inserting the device of claim 3 into the heart retracting said trocar and removing it from said inflow cuff; and

inserting the conduit through the lumen of said inflow cuff to open said valve.

6. A medical device which may be inserted into the heart of a patient to provide a passageway for blood flow, comprising:

an inflow cuff having a lumen and a valve, wherein said valve (1) prevents blood from flowing out of the heart when closed and (2) opens in response to pressure in the lumen of said conduit directed inward toward the heart;

a trocar which is inserted longitudinally through the lumen of said inflow cuff and protrudes beyond an insertion end of said inflow cuff, said trocar being retractable and removable from the lumen of said inflow cuff;

wherein the lumen of said inflow cuff is sized to allow the insertion of a conduit into the heart.

7. The medical device of claim 6, wherein said valve is comprised of at least two leaves, each of said at least two leaves integrally formed with an interior wall of said inflow cuff and having free ends, said free ends abutting and forming a releasable seal with one another.

8. The medical device of claim 7, further comprising a sewing ring disposed on an outer surface of said inflow cuff, said sewing ring allowing said inflow cuff to be secured to an exterior portion of the heart.

9. The medical device of claim 8, wherein said sewing ring comprises a synthetic, biocompatible felt composed of woven tetrafluoroethylene strands.

10. The medical device of claim 9, wherein said sewing ring comprises a synthetic, biocompatible felt composed of woven polyester strands.

11. The medical device of claim 10, wherein the conduit is the inflow conduit of a ventricular assist device.

12. The medical device of claim 11, wherein said inflow cuff is molded from a biocompatible, silicone rubber.

13. The medical device of claim 12, wherein the biocompatible, silicone rubber is reinforced with a woven mesh of synthetic strands.

14. The medical device of claim 13, wherein said inflow cuff and the conduit are sized such that there is substantially no clearance between the interior of said inflow cuff and the conduit when the conduit is inserted therein.

15. The medical device of claim 14, wherein the conduit is retained in said inflow cuff by an external tie secured around an exterior portion of said cuff.

16. The medical device of claim 15, wherein said sewing ring is located closer to the insertion end of said inflow cuff than said valve.

19. The method of claim 18, further comprising:

securing said sewing ring to the heart; and

applying an external tie to an exterior surface of said inflow cuff to retain the conduit within said inflow cuff.