Lead stabilizer with retention features

• US 8,249,719 B2
• Filed: 11/05/2008
• Issued: 08/21/2012
• Est. Priority Date: 11/09/2007
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Bodner, Jeffrey P., Koop, Brendan E., Aschenbeck, Kurt S.
• Primary Examiner(s): Manuel, George
• Assistant Examiner(s): Alter, Alyssa M
• Application Number:
  US12/265,273
• Publication Number:
  US 20090125058A1
• Time in Patent Office: 1,385 Days
• Field of Search: 607/116, 607/126, 295/57
• US Class Current: 607/116
• CPC Class Codes: A61N 1/057 Anchoring means; Means for fixing the head inside the heart
• CPC Class Codes: A61N 2001/0582 Suture sleeves
• CPC Class Codes: Y10T 29/49995 Shaping one-piece blank by removing material

Abstract

An anchoring device for anchoring a medical lead implanted in a patient includes a substantially elongate, hollow, tubular, and elastically compressible body. The body has a longitudinal axis, a groove formed circumferentially about the body for receiving a suture and an inner bore forming a recessed portion. The anchoring device also has a surrounding portion adjacent the recessed portion, where the recessed portion has increased retention characteristics on a medical lead relative to the surrounding portion of the inner bore.

Claims

1. An anchoring device for anchoring a medical lead implanted in a patient, the anchoring device comprising:

a substantially elongate, hollow, tubular, and elastically compressible body, the body having a longitudinal axis;

a suture groove formed circumferentially about the tubular body for receiving a suture; and

an inner bore extending through the tubular body and configured to accommodate a medical lead extending through the inner bore, the inner bore forming a recessed portion having an inner bore diameter, and a surrounding portion having an inner bore diameter adjacent the recessed portion, the recessed portion having an inner surface area having a friction enhancing characteristic relative to the surrounding portion;

wherein the recessed portion has a relaxed configuration in which the inner bore diameter of the recessed portion is greater than the inner bore diameter of the surrounding portion and that permits the anchoring device to be slid onto the medical lead and a contact configuration in which the inner surface area of the recessed portion is configured to frictionally engage the medical lead so as to secure the medical lead relative to the anchoring device, the recessed portion moving from the relaxed configuration to the contact configuration in response to a compressive force applied via a suture disposed within the suture groove.

2. The device of claim 1, wherein the recessed portion is adapted to have increased retention characteristics on a polyurethane sheath of a medical lead.

3. The device of claim 1, wherein the recessed portion includes an uncoated silicone surface for interacting with the medical lead.

4. The device of claim 1, wherein the recessed portion is substantially smoother than the surrounding portion of the inner bore.

5. The device of claim 1, wherein the recessed portion defines a surface roughness of about 15 micro inches Ra or less.

6. The device of claim 1, wherein the recessed portion defines a surface area of at least about 10 square mm.

7. The device of claim 1, wherein the recessed portion has an arcuate shape when viewed in side profile perpendicular to the longitudinal axis of the body.

8. The device of claim 1, wherein the recessed portion includes a friction-enhancing coating.

9. The device of claim 1, wherein the recessed portion is located at least partially under the suture groove.

10. The device of claim 1, wherein the recessed portion has a greater stiction characteristic than the surrounding portion.

11. The device of claim 1, further comprising an additional suture groove.

12. The device of claim 11, wherein the inner bore further comprises an additional recessed portion.

13. The device of claim 12, wherein the additional recessed portion is located at least partially under the additional suture groove.

14. The device of claim 1, wherein the recessed portion has a surface roughness that is substantially less than the surrounding portion.

15. The device of claim 1, wherein the compressible body is formed of silicone.

16. The device of claim 1, wherein the recessed portion is substantially circular in transverse cross-section and substantially arcuate in longitudinal cross section.

17. An implantable lead system comprising:

an implantable lead; and

an anchoring device disposed on the implantable lead, the anchoring device comprising;

a substantially elongate, hollow, tubular, and elastically compressible body, the body having a longitudinal axis;

a suture groove formed circumferentially about the tubular body for receiving a suture; and

an inner bore extending through the tubular body and configured to accommodate the implantable lead extending through the inner bore, the inner bore forming a recessed portion having an inner diameter, and a surrounding portion having an inner bore diameter adjacent the recessed portion, the recessed portion having an inner surface area having a friction enhancing characteristic relative to the surrounding portion;

wherein the recessed portion has a relaxed configuration in which the inner diameter of the recessed portion is greater than the inner diameter of the surrounding portion and that permits the anchoring device to be slid onto the implantable lead and a contact configuration in which the inner surface area of the recessed portion is configured to frictionally engage the implantable lead so as to secure the implantable lead relative to the anchoring device, the recessed portion moving from the relaxed configuration to the contact configuration in response to a compressive force applied via a suture disposed within the suture groove.

18. The implantable lead system of claim 17, further comprising a fastener received in the suture groove of the anchoring device and compression the recessed portion against the implantable lead.

19. The implantable lead system of claim 18, wherein a portion of the implantable lead at a location where the recessed portion is compressed against the implantable lead is formed of at least one of polyurethane and silicone and a portion of the anchoring device at the same location is formed of at least one of polyurethane and silicone.