Devices and methods for treating heart failure

• US 9,005,155 B2
• Filed: 02/03/2013
• Issued: 04/14/2015
• Est. Priority Date: 02/03/2012
• Status: Active Grant

• Current Assignee: Corvia Medical, Inc.
• Original Assignee: DC Devices Inc.
• Inventors: Sugimoto, Hiroatsu
• Primary Examiner(s): Wiest, Philip R
• Assistant Examiner(s): KLEIN, BENJAMIN JACOB
• Application Number:
  US13/757,839
• Publication Number:
  US 20130204175A1
• Time in Patent Office: 800 Days
• Field of Search: 604 8- 9, 623/1.26, 606/213
• US Class Current: 604/8
• CPC Class Codes: A61F 2/2493 Transmyocardial revascularisation [TMR] devices
• CPC Class Codes: A61M 27/002 Implant devices for drainage of body fluids from one part of the body to another intraocular A61F9/00781; middle ear A61F11/202

Abstract

The present teachings provide a device and method of making and using thereof. Specifically, one aspect of the present teachings provides a device comprising a shunt having a distal end and a proximal end and the shunt positionable across the septum of a heart. Certain embodiments of the present teachings also include a distal anchoring portion connecting to the distal end of the shunt portion and a proximal anchoring portion connecting to the proximal end of the shunt portion. Another aspect of the present teachings provide methods of using thereof to modify the pressure difference in a heart chamber.

Claims

1. A device comprising:

a shunt portion comprising a distal end, a proximal end, and a central lumen,

a distal anchoring portion connecting to the distal end of the shunt portion, and

a proximal anchoring portion connecting to the proximal end of the shunt portion,

wherein the device has a first configuration where the shunt portion, the distal anchoring portion, and the proximal anchoring portion approximately align along a longitudinal axis, and

the device has a second configuration where the distal anchoring portion and the proximal anchoring portion turn radially away from the longitudinal axis and the device assumes a general “

U”

shape.

2. The device of claim 1, wherein the distal anchoring portion, the proximal anchoring portion, and the shunt portion form an elongated tube in the first configuration.

3. The device of claim 1, wherein the distal anchoring portion, the proximal anchoring portion, and the shunt portion form an U shaped tube in the second configuration.

4. The device of claim 3, wherein the distal anchoring portion, the proximal anchoring portion, and the shunt portion each comprises a tubular surface with a plurality of openings.

5. The device of claim 1, wherein the shunt portion further comprises a tubular surface with a plurality of openings.

6. The device of claim 1, wherein the shunt portion has a first cross-sectional size when the device is in the first configuration, and a second cross-sectional size when the device is in the second configuration, wherein the first cross-sectional size is smaller than the second cross-sectional size.

7. The device of claim 1, wherein the device is adapted to be positioned across an aperture in the heart in its second configuration with the distal anchoring portion contacting one side of the aperture, the proximal anchoring portion contacting the other side of the aperture, and the shunt portion positioned across the aperture.

8. The device of claim 7, wherein the device is adapted to allow blood to flow from one side of the aperture through the central lumen of the shunt portion to the other side of the aperture.

9. The device of claim 1 comprising at least one tissue anchor on at least one of the distal anchoring portion and the proximal anchoring portion.

10. The device of claim 1, wherein the distal and proximal anchoring portions each has a generally tubular profile.

11. The device of claim 1, wherein the distal and proximal anchoring portions each has a half cylindrical profile.

12. The device of claim 1, wherein at least one of the distal and proximal anchoring portions is more flexible than the shunt portion.

13. A delivery assembly comprising:

a delivery sheath comprising a distal portion and a lumen,

a delivery catheter comprising a distal end,

wherein the delivery catheter is disposed within the lumen of the distal portion of the delivery sheath, and

a device disposed within the lumen of the distal portion of the delivery sheath,

wherein the device comprises a shunt portion, a distal anchoring portion, and a proximal anchoring portion,

wherein the shunt portion comprising a distal end, a proximal end, and a central lumen;

the distal anchoring portion is connected to the distal end of the shunt portion;

the proximal anchoring portion is connected to the proximal end of the shunt portion;

the device has a first configuration where the shunt portion, the distal anchoring portion, and the proximal anchoring portion of the device approximately align with a longitudinal axis; and

the device has a second configuration where the distal anchoring portion and the proximal anchoring portion turn radially away from the longitudinal axis and the device assumes a general “

U”

shape; and

the distal end of the delivery catheter engages the proximal anchoring portion of the device.

14. The delivery assembly of claim 13, wherein the shunt portion further comprises to tubular surface with a plurality of openings.

15. The delivery assembly of claim 13, wherein the shunt portion has a first cross-sectional size when the device is in the first configuration and a second cross-sectional size when the device is in the second configuration, wherein the first cross-sectional size is smaller than the second cross-sectional size.

16. The delivery assembly of claim 13, wherein the device is adapted to be positioned across an aperture in the heart in its second configuration with the distal anchoring portion contacting one side of the aperture, the proximal anchoring portion contacting the other side of the aperture, and the shunt portion positioned across the aperture.

17. The delivery assembly of claim 13, wherein at least one of the distal and proximal anchoring portions of the device is more flexible than the shunt portion.

18. A method of implanting a device between the left and right atria of a heart comprising:

providing a delivery assembly comprising a delivery system comprising a lumen and a device disposed within the lumen of the delivery system,

wherein the device comprises a shunt portion, a distal anchoring portion, and to proximal anchoring portion,

wherein the shunt portion comprising a distal end, a proximal end, and a central lumen;

the distal anchoring portion is connected to the distal end of the shunt portion;

the proximal anchoring portion is connected to the proximal end of the shunt portion;

the device has a first configuration where the shunt portion, the distal anchoring portion, and the proximal anchoring portion of the device approximately align with a longitudinal axis; and

the device has a second configuration where the distal anchoring portion and the proximal anchoring portion turn radially away from the longitudinal axis and the device assumes a general “

U”

shape; and

advancing the delivery assembly through an aperture in the septum between the left and right atria of a heart, exposing the distal anchoring portion of the device so that the distal anchoring portion of the device turns radially away from the longitudinal axis,

retracting the delivery assembly proximally so that the distal anchoring portion of the device contacts the left atrial side of the septum,

exposing the proximal anchoring portion of the device so that the distal anchoring portion of the device turn radially away from the longitudinal axis,

retracting the delivery system from the body, leaving the device positioned across the aperture in its second configuration with the distal anchoring portion contacting the left atrial side of the septum, the proximal anchoring portion contacting the right atrial side of the septum, and the shunt portion positioned across the aperture.

19. The method of claim 18, wherein the delivery system comprises a delivery catheter engaging the proximal anchoring portion of the device.