Implantable medical device with connector blocks

• US 9,427,572 B2
• Filed: 04/10/2015
• Issued: 08/30/2016
• Est. Priority Date: 10/26/2007
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Kast, John E., Witt, William
• Primary Examiner(s): Bertram, Eric D.
• Application Number:
  US14/683,725
• Publication Number:
  US 20150209578A1
• Time in Patent Office: 508 Days
• US Class Current: 1/1
• CPC Class Codes: A61N 1/0553 Paddle shaped electrodes, e.g. for laminotomy
• CPC Class Codes: A61N 1/0558 Anchoring or fixation means therefor
• CPC Class Codes: A61N 1/36071 Pain
• CPC Class Codes: A61N 1/375 Constructional arrangements, e.g. casings
• CPC Class Codes: A61N 1/3752 Details of casing-lead connections
• CPC Class Codes: A61N 1/3758 Packaging of the components within the casing

Abstract

An implantable medical device comprises one or more electrical stimulation generators, and a housing that contains the one or more electrical stimulation generators. The implantable medical device includes a first connector block that electrically connects the first medical lead to at least one of the one or more electrical stimulation generators, and a second connector block that electrically connects the second medical lead to at least one of the one or more electrical stimulation generators.

Claims

1. An implantable medical device comprising:

one or more electrical stimulation generators;

a housing that contains the one or more electrical stimulation generators;

a first connector block forming a first connection port with a first terminal configured to electrically connect a first medical lead to at least one of the one or more electrical stimulation generators; and

a second connector block forming a second connection port with a second terminal configured to electrically connect a second medical lead to at least one of the one or more electrical stimulation generators,

wherein the first connector block is not in direct contact with the second connector block, and

wherein the one or more electrical stimulation generators are configured to deliver electrical stimulation to a patient via each of the first medical lead electrically connected to the first terminal and the second medical lead electrically connected to the second terminal.

2. The device of claim 1,

wherein the housing has a width and a length that are each greater than a thickness of the housing, and

wherein the first connector block and the second connector block are located at least a third of the length of the housing apart from one another.

3. The device of claim 1, wherein a major surface of the housing is curved to accommodate implantation inferior to the external occipital protuberance.

4. The device of claim 1, wherein the housing has a volume between about 0.5 cubic centimeters (cc) and 5 cc.

5. The device of claim 1,

wherein the housing has a width and a length that are each greater than a thickness of the housing, and

wherein an aspect ratio of the length of the housing to the width of the housing is between about 1.5:

1 and 2;

1.

6. The device of claim 1,

wherein the housing has a width and a length that are each greater than a thickness of the housing, and

wherein the first connector block and the second connector block are located on at least one surface of the housing defined by the thickness.

7. The device of claim 6, wherein the first connector block and the second connector block are oriented in about the same direction.

8. The device of claim 6, wherein the first connector block and the second connector block are oriented in about opposite directions.

9. The device of claim 1, wherein the first connector block and the second connector block are separated by between about 0.5 inches and about 1.3 inches.

10. The device of claim 1, wherein the one or more electrical stimulation generators are configured to deliver electrical stimulation selected to alleviate occipital neuralgia when applied to at least one of an occipital nerve and a branch of the occipital nerve.

11. The device of claim 1, further comprising:

the first medical lead electrically connected to the first terminal; and

the second medical lead electrically connected to the second terminal.

12. The device of claim 11, wherein at least one of the first medical lead or the second medical lead includes a paddle lead.

13. The device of claim 11, wherein at least one of the first medical lead or the second medical lead includes an axial lead.

14. An electrical stimulation system comprising:

an electrical stimulator comprising;

a housing having a width and a length that are each greater than a thickness of the housing,

one or more stimulation generators within the housing, and

at least two connector blocks, wherein each connector block includes a connection port with a terminal that accepts a medical lead; and

at least two implantable medical leads extending from the housing and electrically coupled to the one or more stimulation generators via the connection ports and terminals of the at least two connector blocks, wherein the at least two implantable medical leads exit the housing at separate locations, wherein the separate locations are separated by at least a third of the length of the housing, and

wherein the one or more stimulation generators are configured to deliver electrical stimulation to a patient via each of the at least two implantable medical leads.

15. The system of claim 14, wherein the at least two implantable medical leads connect to the housing on opposing external surfaces of the housing.

16. The system of claim 14, wherein the one or more stimulation generators are configured to deliver electrical stimulation selected to alleviate occipital neuralgia when applied to at least one of a trigeminal nerve, a greater occipital nerve, a lesser occipital nerve, a third occipital nerve, or a suboccipital nerve.

17. The system of claim 14, wherein the at least two implantable medical leads are permanently coupled to the housing and the one or more stimulation generators.

18. The system of claim 14, wherein the at least two implantable medical leads include a paddle lead.

19. The system of claim 14, wherein the at least two implantable medical leads include an axial lead.

20. The system of claim 14, wherein the separate locations are separated by between about 0.5 inches and about 1.3 inches.