Fixation and strain relief element for temporary therapy delivery device

• US 9,486,622 B2
• Filed: 09/18/2013
• Issued: 11/08/2016
• Est. Priority Date: 11/08/2012
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Clark, Bryan A., Jackson, Timothy R., Liu, Lili, Foster, Arthur J.
• Primary Examiner(s): Stice, Paula J
• Application Number:
  US14/030,741
• Publication Number:
  US 20140128948A1
• Time in Patent Office: 1,147 Days
• Field of Search: 607/116
• US Class Current: 1/1
• CPC Class Codes: A61N 1/0558 Anchoring or fixation means therefor

Abstract

A temporary neurostimulation lead may be secured relative to patient using a fixation device. The fixation device may include an attachment portion that is configured to be releasably fixated to the patient and a lead fixation portion that is configured to secure the temporary neurostimulation lead. The fixation device can be adhesively fixated to the patient via the attachment portion and the temporary neurostimulation lead can be fixated to the lead fixation portion of the fixation device.

Claims

1. A method of securing a temporary neurostimulation lead relative to an entry point on a patient, the method comprising:

implanting the temporary neurostimulation lead within the patient such that the temporary neurostimulation lead extends through the entry point and is disposed proximate a desired nerve within the patient;

advancing a fixation device over the temporary neurostimulation lead to a position proximate the entry point, the fixation device including an attachment portion configured to be releasably fixated to the patient and a lead fixation portion configured to secure the temporary neurostimulation lead, the lead fixation portion comprising one or more raised portions that are configured to frictionally engage a spiral-cut strain relief element having a groove around a circumference and continuous along a length of the strain-relief element;

adhesively fixating the attachment portion of the fixation device to the patient; and

fixating the temporary neurostimulation lead to the lead fixation portion of the fixation device by wrapping the temporary neurostimulation lead within the groove of the spiral-cut strain relief snapping the spiral-cut strain relief into the one or more raised portions.

2. The method of claim 1, wherein the lead fixation portion comprises a curved channel formed in an upper surface of the lead fixation portion, and fixating the temporary neurostimulation lead to the lead fixation portion of the fixation device comprises fitting the temporary neurostimulation lead into the curved channel.

3. The method of claim 1, wherein the lead fixation portion comprises an upper surface and one or more resilient fingers extending from the upper surface and biased into contact with the upper surface, and fixating the temporary neurostimulation lead to the lead fixation portion of the fixation device comprises:

lifting each of the one or more resilient fingers;

placing the temporary neurostimulation lead under each of the one or more resilient fingers; and

allowing each of the one or more resilient fingers to return to their biased position in contact with the upper surface.

4. The method of claim 1, wherein the lead fixation portion comprises a resilient polymeric body including a lumen therethrough to accommodate the temporary neurostimulation lead, and advancing the fixation device over the temporary neurostimulation lead to a position proximate the entry point comprises advancing the fixation device over the temporary neurostimulation lead with the temporary neurostimulation lead extending through the lumen.

5. The method of claim 4, wherein fixating the temporary neurostimulation lead to the lead fixation portion of the fixation device comprises disposing an external clamp over the resilient polymeric body to compress the resilient polymeric body into frictional contact with the temporary neurostimulation lead.

6. The method of claim 4, wherein the resilient fixation portion comprises an upper portion that is rotatable relative to a lower portion, and the lumen is defined at least in part by polymeric bands extending between the upper portion and the lower portion, and fixating the temporary neurostimulation lead to the lead fixation portion of the fixation device comprises:

rotating the upper portion relative to the lower portion in order to tighten the polymeric bands around the temporary neurostimulation lead; and

securing the upper portion relative to the lower portion to maintain the polymeric bands in their tightened configuration.

7. The method of claim 4, wherein the lead fixation portion comprises an under skin fixation feature and an activation portion that is operably connected to the under skin fixation feature, and adhesively fixating the attachment portion of the fixation device to the patient further comprises:

squeezing the activation portion to move the under skin fixation feature into a configuration that permits the under skin fixation feature to be inserted under the skin;

inserting the under skin fixation feature under the skin; and

releasing the activation portion to permit the under skin fixation feature to return to a biased position that anchors the under skin fixation feature under the skin.

8. A fixation device configured to releasably secure a temporary neurostimulation lead relative to an entry point on a patient, the device comprising:

a polymeric device body having a lower surface and a upper surface;

a dermatologically safe adhesive disposed on the lower surface for releasably securing the fixation device to the patient proximate the entry point;

a strain relief member arranged on the upper surface of the polymeric device body and having a groove configured to engage the temporary neurostimulation lead within the groove, the groove being spirally arranged around a circumference and continuous along a length of the strain relief member; and

a lead fixation structure formed on the upper surface having a curved channel configured to frictionally engage with the strain relief member to releasably secure the temporary neurostimulation lead.

9. The fixation device of claim 8, wherein the groove has a width approximately equal to a diameter of the temporary neurostimulation thereby allowing the temporary neurostimulation to wind into the groove and provide at least some resistance to removal of the temporary neurostimulation.

10. The fixation device of claim 8, wherein the lead fixation structure comprises one or more raised portions that are configured to frictionally engage the temporary neurostimulation lead.

11. The fixation device of claim 10, wherein the groove has a depth from approximately 10 percent to approximately 40 percent of a diameter of the strain relief member.

12. The fixation device of claim 8, wherein the lead fixation structure comprises one or more resilient fingers that extend from the upper surface and are biased into contact with the upper surface.

13. The fixation device of claim 8, further comprising an external clamp that is configured to clamp onto the lead fixation structure to releasably secure the temporary neurostimulation lead.

14. The device of claim 8, wherein the polymeric device body comprises an upper portion that is rotatable relative to a lower portion, with polymeric bands extending between the upper portion and the lower portion, and wherein rotating the upper portion relative to the lower portion enables the polymeric bands to tighten around the temporary neurostimulation lead.

15. The device of claim 8, further comprising an under skin fixation element and an activation portion that is operably connected to the under skin fixation element, and wherein squeezing the activation portion moves the under skin fixation element into a configuration that permits the under skin fixation element to be inserted under the skin and releasing the activation portion permits the under skin fixation element to return to a biased position that anchors the under skin fixation element under the skin.

16. A fixation device configured to releasably secure a temporary neurostimulation lead relative to an entry point on a patient, the device comprising:

a polymeric device body having a lower surface and an upper surface;

a dermatologically safe adhesive disposed on the lower surface for releasably securing the fixation device to the patient proximate the entry point;

a spiral-cut strain relief element including an elongate body and a spiral groove formed within the elongate body, the spiral groove arranged around a circumference and continuous along a length of the strain-relief element and configured to accommodate the temporary neurostimulation lead therein; and

a pair of raised portions molded into the upper surface, the pair of raised portions being configured to frictionally engage the spiral-cut strain relief element.

17. The fixation device of claim 16, further comprising a peel away layer disposed on the dermatologically safe adhesive in order to protect the adhesive.

18. The fixation device of claim 16, wherein the pair of raised portions are integrally molded as part of the polymeric device body.

19. The fixation device of claim 16, wherein the polymeric device body includes an elongate slot formed within the polymeric device body such that the elongate slot permits the fixation device to be slid laterally onto the temporary neurostimulation lead.