Implantable heart assist system and method of applying same
View Patent ↗An extracardiac pumping for supplementing the circulation of blood, including the cardiac output, in a patient without any component thereof being connected to the patient's heart, and methods of using same. One embodiment provides a vascular graft that has a first end that is sized and configured to couple to a non-primary blood vessel and a second end that is fluidly coupled to a pump to conduct blood between the pump and the non-primary blood vessel. An outflow conduit is also provided that has a first end sized and configured to be positioned within the same or different blood vessel, whether primary or non-primary, through the vascular graft. The outflow conduit is fluidly coupled to the pump to conduct blood between the pump and the patient. The vascular graft may be connected to the blood vessel subcutaneously to permit application of the extracardiac pumping system in a minimally-invasive procedure.
1. A method for treating a patient, comprising:
providing a pump adapted to provide a flow rate of about 3 liters/minute or less, said pump having an inflow conduit and an outflow conduit;
providing fluid communication between a distal end of the inflow conduit and the patient's circulatory system to permit the flow of blood to the pump from the patient;
connecting via anastomosis a distal end of the outflow conduit with the patient's subclavian artery using a minimally invasive surgical procedure to permit the flow of blood away from the pump to the subclavian artery;
implanting said pump extrathoracically and minimally subdermally beneath the skin of the patient; and
operating said pump to perfuse blood through the patient's circulatory system at a flow rate of about 3 liters/minute or less.
2. The method of claim 1 , wherein at least one of the pump, inflow conduit and outflow conduit comprise a synthetic biocompatible material selected from the group consisting of polyethylene terephthalate (PET) and polytetrafluoroethylene (PTFE).
3. The method of claim 1 , wherein fluid communication is provided between the distal end of the inflow conduit and an iliac artery of the patient.
4. The method of claim 1 , wherein fluid communication is provided between the distal end of the inflow conduit and a femoral artery of the patient.
5. The method of claim 1 , wherein fluid communication is provided between the distal end of the inflow conduit and a vein of the patient.
6. The method of claim 1 , wherein fluid communication is provided between the distal end of the outflow conduit and an axillary artery of the patient.
7. The method of claim 1 , wherein an anastomosis connection is provided between the distal end of the outflow conduit and a subclavian artery of the patient.
8. The method of claim 1 , wherein providing fluid communication between the inflow conduit and the patient's circulatory system comprises providing an anastomosis connection between the distal end of the inflow conduit and the patient's circulatory system.
9. The method of claim 1 , further comprising coupling a connector with a blood vessel and coupling the distal end of the outflow conduit with the connector to provide fluid communication between the outflow conduit and the vasculature.
10. The method of claim 9 , wherein the connector comprises a T-shaped fitting.
11. The method of claim 9 , wherein the connector comprises a divergence configured to have a selected angle relative to the vessel to which the connector is connected.
12. A method for treating a patient, comprising:
providing a pump adapted to provide a flow rate of about 3 liters/minute or less, said pump having an inflow conduit and an outflow conduit;
providing fluid communication between a distal end of the inflow conduit and the patient's circulatory system to permit the flow of blood to the pump from the patient;
connecting via anastomosis a distal end of the outflow conduit with a non-primary blood vessel of the patient using a minimally invasive surgical procedure to permit the flow of blood away from the pump to the non-primary blood vessel;
implanting said pump subcutaneously; and
operating said pump to perfuse blood through the patient's circulatory system at a flow rate of about 3 liters/minute or less.
13. The method of claim 12 , wherein the distal end of the outflow conduit is connected via anastomosis to the patient's subclavian artery to direct blood flow into the aorta.
14. The method of claim 13 , further comprising providing an acute angle between the direction of flow from the outflow conduit toward the subclavian artery and the direction of flow within the subclavian artery such that blood flow from the outflow conduit is directed toward the aorta.
15. The method of claim 12 , further comprising percutaneously placing in fluid communication with the patient's circulatory system the distal end of at least one of said inflow conduit and said outflow conduit.
16. The method of claim 12 , wherein said minimally invasive surgical procedure comprises a percutaneous procedure.
17. A method for treating a patient, comprising:
providing a pump adapted to provide a subcardiac volumetric flow rate, said pump having an inflow conduit and an outflow conduit;
providing fluid communication between a distal end of the inflow conduit and the patient's circulatory system to permit the flow of blood to the pump from the patient;
connecting via anastomosis a distal end of the outflow conduit with the patient's subclavian artery using a minimally invasive surgical procedure to permit the flow of blood away from the pump to the subclavian artery;
implanting said pump extrathoracically and minimally subdermally beneath the skin of the patient; and
operating said pump to perfuse blood through the patient's circulatory system at a subcardiac volumetric flow rate.
18. The method of claim 17 , further comprising implanting the pump in the patient's groin area.
19. The method of claim 17 , further comprising powering the pump using an extracorporeal battery.
20. The method of claim 19 , further comprising attaching the extracorporeal battery to the outside of the patient.
21. The method of claim 17 , further comprising implanting a battery within the patient and powering the pump with the implanted battery.
22. The method of claim 21 , wherein the battery is transcutaneously rechargeable.