Apical Papillary Msucle Attachment for Left Ventricular Reduction

• US 20100185278A1
• Filed: 01/21/2010
• Published: 07/22/2010
• Est. Priority Date: 01/21/2009
• Status: Abandoned Application

• Current Assignee: Tendyne Medical, Inc. (Abbott Laboratories Incorporated)
• Original Assignee: Tendyne Medical, Inc. (Abbott Laboratories Incorporated)
• Inventors: Schankereli, Kemal
• Application Number:
  US12/691,591
• Publication Number:
  US 20100185278A1
• Time in Patent Office: Days
• US Class Current: 623/2.360
• CPC Class Codes: A61B 17/00234 for minimally invasive surgery A61B17/0218, A61B17/0469, A61B17/12013, A61B17/1285, A61B17/29, A61B17/320016 take precedence
• CPC Class Codes: A61B 17/0401 Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors A61B17/0642 takes precedence; fixation devices for tendons or ligaments A61F2/0811
• CPC Class Codes: A61B 17/0487 Suture clamps, clips or locks, e.g. for replacing suture knots; Instruments for applying or removing suture clamps, clips or locks suture anchors A61B17/0401; wound clamps or clips A61B17/08; ligaturing clamps or clips A61B17/122
• CPC Class Codes: A61B 17/064 Surgical staples, i.e. penetrating the tissue
• CPC Class Codes: A61B 17/0644 penetrating the tissue, deformable to closed position
• CPC Class Codes: A61B 17/1227 Spring clips
• CPC Class Codes: A61B 2017/00243 cardiac
• CPC Class Codes: A61B 2017/0409 Instruments for applying suture anchors for applying suture clamps, clips or locks A61B2017/0488
• CPC Class Codes: A61B 2017/0496 for tensioning sutures
• CPC Class Codes: A61F 2/2457 Chordae tendineae prostheses

Abstract

This invention relates to devices and methods for the therapeutic changing of the geometry of the left ventricle of the human heart. Specifically, the invention relates to the apical introduction of an anchoring device to align the papillary muscles.

Claims

1. A method for improving cardiac function, comprising the steps of:

inserting a tether device into a patient; and

inserting said tether device through the apex of the patient'"'"'s heart and into the left ventricle of the patient'"'"'s heart; and

attaching a first papillary muscle anchor of said tether device to a first papillary muscle within said left ventricle; and

attaching a second papillary muscle anchor of said tether device to a second papillary muscle of the patient'"'"'s heart; and

wherein said first papillary muscle anchor and said second papillary muscle anchor are joined by a tether member so as to reduce the volume of the left ventricle.

2. The method as claimed in claim 1, further comprising the step of adjusting the tether member to achieve a desired geometry of the left ventricle.

3. The method as claimed in claim 1, further comprising the steps of attaching at least one additional papillary muscle anchor joined by an additional tether member so as to achieve a desired geometry of the left ventricle.

4. The method as claimed in claim 1, further comprising the step of adjusting the tether member to achieve coaptation of the mitral valve. (Original)

5. The method as claimed in claim 1, further comprising wherein the inserting of said tether device includes passing said tether device through a trocar sleeve or cannula.

11. The method of claim 1 or 6, further comprising where inserting the tether device into a patient is performed by inserting a catheter into the patient through the vascular system of the patient.

12. The method of claim 1 or 6, further comprising implanting a valve at the apex insertion site on the heart of the patient, wherein said valve is a blood leakage control valve/sleeve.

6. A method for reducing ventricular volume, comprising the steps of:

inserting a tether device into a patient; and

inserting said tether device through the apex of the patient'"'"'s heart and into the left ventricle of the patient'"'"'s heart; and

attaching a first papillary muscle anchor of said tether device to a first papillary muscle within said left ventricle; and

attaching a second papillary muscle anchor of said tether device to a second papillary muscle of the patient'"'"'s heart; and

wherein said first papillary muscle anchor and said second papillary muscle anchor are joined by a tether member so as to reduce the volume of the left ventricle.

7. The method as claimed in claim 6, further comprising the step of adjusting the tether member to achieve a desired geometry of the left ventricle.

8. The method as claimed in claim 6, further comprising the steps of attaching at least one additional papillary muscle anchor joined by an additional tether member so as to achieve a desired geometry of the left ventricle.

9. The method as claimed in claim 6, further comprising the step of adjusting the tether member to achieve coaptation of the mitral valve.

10. The method as claimed in claim 6, further comprising wherein the inserting of said tether device includes passing said tether device through a trocar sleeve or cannula.

13. A medical device for improving cardiac function or reducing ventricular volume, comprising:

a cannula having a tethering device disposed therein;

said cannula having a trocar for piercing the apex of the patient'"'"'s heart and a leakage control valve/sleeve;

said tethering device comprising at least one first papillary muscle anchor for attaching to a first papillary muscle within said left ventricle and at least one second papillary muscle anchor for attaching to a second papillary muscle of the patient'"'"'s heart;

said tethering device further comprising a tether member for joining said first papillary muscle anchor to said second papillary muscle anchor so as to reduce the left ventricular volume of the patient.

14. The device of claim 13, wherein said tether member has an adjustable mechanism for adjusting the length of said tether.

15. The device of claim 14, further comprising at least one additional papillary muscle anchor joined by an additional tether member so as to achieve a desired geometry of the left ventricle.

16. The device of claim 13, wherein the tether member is comprised of nitinol (nickel-titanium shape memory alloy) or austinetic stainless steel.