Connector for use in an implantable stimulator device

• US 20060167522A1
• Filed: 01/25/2005
• Published: 07/27/2006
• Est. Priority Date: 01/25/2005
• Status: Abandoned Application

• Current Assignee: Boston Scientific Neuromodulation Corporation (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Neuromodulation Corporation (Boston Scientific Corporation)
• Inventors: Malinowski, Zdzislaw B.
• Application Number:
  US11/043,640
• Publication Number:
  US 20060167522A1
• Time in Patent Office: Days
• US Class Current: 607/37
• CPC Class Codes: A61N 1/3752 Details of casing-lead connections

Abstract

A connector is configured to couple an implantable pulse generator (IPG) to an electrical stimulation lead or electrical leads while allowing the implantable pulse generator to be hermetically sealed within a case assembly. The connector includes a resilient body having a lead insertion lumen defined therein. Connector contacts for connecting to multiple contacts at the proximal end of the stimulation may be disposed along the length of the insertion lumen as an array. The connector contacts are configured to be coupled to lead extensions or leads, which direct electrical stimuli to a desired body location.

Claims

1. A connector block for use in an implantable stimulator device, comprising:

a resilient, substantially compressible body having at least one lead insertion lumen defined in said resilient body; and

a plurality of connector contacts disposed within said lumen, said contacts being configured to yield to compressive forces in response to external compressive forces applied to the resilient, substantially compressible body and thereby exert a clamping force on the connector end of a lead or a lead extension.

2. The connector block of claim 1, wherein said at least one insertion lumen is dimensioned to be larger than the connector end of a lead or a lead extension for zero insertion force.

3. The connector block of claim 1, wherein said resilient body comprises silicone.

4. The connector block of claim 1, wherein said resilient body comprises a substantially transparent material.

5. The connector block of claim 1, wherein said connector block is configured to permit selective attachment and detachment from a case frame of the implantable stimulator.

6. The connector block of claim 5, further comprising:

a plurality of feedthru receptacles coupled to said connector contacts, said feedthru receptacles being configured to be electrically coupled to a feedthru member.

7. The connector block of claim 1, wherein said connector contacts comprise a substantially ring-shaped body with a gap formed in said ring-shaped body.

8. The connector block of claim 7, wherein said connector contacts comprise a biocompatible metallic material.

9. The connector block of claim 8, wherein said biocompatible metallic material comprises one of platinum or platinum/iridium alloy.

10. An implantable stimulator device, comprising:

a circuit board;

a case assembly having a case frame; and

a removable, lead connector block having at least one lead insertion lumen defined in said connector block and a plurality of connector contacts disposed within said lumen, wherein the lead connector block is configured to be attachable to the case frame.

11. The implantable stimulator device of claim 10, wherein the removable lead connector block and case frame are each configured to permit selective attachment and detachment of the lead connector block to the case frame.

12. The implantable stimulator device of claim 10, further comprising:

a connector block cover that is dimensioned to fit over the lead connector block, wherein the connector block cover is pivotably attached to the case frame, the connecter block cover having a locked and unlocked position, wherein in the locked position, the lead connector block is secured to the case frame.

13. The device of claim 12, wherein said case frame comprises:

a locking protrusion; and

a connector block cover having a lock receiving orifice for accepting the locking protrusion, wherein said connector block cover, lead connector block, and case frame are configured such that, when said connector block cover is secured in the locked position, and said lock receiving orifice engages with said locking protrusion, a compressive force is applied to said lead connector block causing the lead insertion lumen to decrease in size.

14. An implantable stimulator system comprising:

a medical device, having a case;

a removable connector block having a lead insertion lumen, which lumen is dimensioned to a size larger than a connector end of a stimulation lead or a lead extension;

a pivotable connector block cover, attached on end of the case to the implantable medical device, the connector block cover having an open, unlocked position and a locked, closed position, wherein in the locked position, the removable connector block is securely attached to the medical device case; and

an opening tool, configured to open the connector block cover and release the connector block from the medical device case.

15. The stimulator system of claim 14, wherein the medical device case has a locking protrusion and the connector block cover has a complementary lock receiving orifice for accepting the locking protrusion into the lock receiving orifice in the locked position;

and

wherein the opening tool is a prying tool configured to separate the connector block cover from the medical device case to permit the connector block cover to be placed into the unlocked position.

16. The stimulator system of claim 15, wherein the opening tool has at least one prong, which prong is used to pry apart the connector block cover from the medical device case.

17. The stimulator system of claim 15, further comprising:

a plurality of removable connector blocks, each connector block having an insertion lumen dimensioned to a size for accepting a different sized connector end of a lead or lead extension.

18. A method of using a stimulator system comprising:

providing a stimulator device case configured to accept a removable lead connector block;

selecting a stimulation lead or extension lead with a proximal connector end having a predetermined size;

selecting a removable lead connector block with a lead insertion lumen sized to accept the proximal connector end of the stimulation lead or extension lead;

securely inserting the proximal connector end of the stimulation lead or extension lead into the insertion lumen;

securing the lead connector block to the stimulator;

if an extension lead has been inserted into the insertion lumen, attaching the, proximal connector end of the selected stimulation lead to the distal female of the extension lead; and

implanting the stimulator and connected stimulation lead into a patient.

19. The method of using a stimulator system of claim 18, further comprising:

releasing the removable lead connector block from the stimulator.

20. The method of using a stimulator system of claim 19, further comprising:

releasing the connected proximal end of the lead or lead extension from the removable lead connector block.

21. The method of using a stimulator system of claim 18, wherein securing the lead connector block to the stimulator comprises compressing the lead connector block and compressing the lead insertion lumen over the inserted proximal connector end of the stimulation lead or extension lead.

22. The method of using a stimulator system of claim 21, wherein compressing the lead connector block and compressing the lead insertion lumen comprises placing a pivotable connector block cover into a locked position, wherein the connector block cover has a locked position and unlocked position.