Multipolar in-line proximal connector assembly for an implantable stimulation device

• US 5,304,219 A
• Filed: 06/05/1992
• Issued: 04/19/1994
• Est. Priority Date: 06/14/1991
• Status: Expired due to Term

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Siemens Pacesetter, Inc. (Abbott Laboratories)
• Inventors: Fletcher, Harry W., Chernoff, Edward, Walter, Jeryle L., Barcel, James E.
• Primary Examiner(s): Cohen, Lee S.
• Assistant Examiner(s): Casler, Brian L.
• Application Number:
  US07/894,395
• Time in Patent Office: 683 Days
• Field of Search: 607/116, 607/122, 607/126, 607/37, 607/38, 439/909, 439/669, 439/675, 439/668
• US Class Current: 607/122
• CPC Class Codes: A61N 1/056 Transvascular endocardial electrode systems
• CPC Class Codes: A61N 1/36557 controlled by chemical substances in blood
• CPC Class Codes: A61N 1/3702 Physiological parameters A61N1/365 takes precedence; evoked response A61N1/371
• CPC Class Codes: Y10T 29/49117 Conductor or circuit manufacturing

Abstract

An in-line, multipolar proximal connector assembly for an implantable stimulation lead is provided which incorporates at least one sensor. Advantageously, the present invention uses straight conductive rods, or wires, to electrically connect the proximal terminals to a multilumen lead body. The straight conductive rods enable the diameter of the lead assembly to remain small. Additional terminals can easily be added by simply decreasing the spacing between terminals and adding additional conductive rods. In one embodiment, insulating spacers are premolded to include protruding portions which interlock with the ring terminals. Recesses within the insulating spacers are dimensioned to self-position the ring terminals a precise distance from the pin terminal according to precise dimensions defined by the VS-1 (or other) standards. In another embodiment, the terminals are injection molded. While the present invention is directed towards a quadrapolar (four conductors) design, it may be easily adapted to a bipolar, tripolar or multipolar (five conductors or more) design.

Claims

1. An implantable stimulation lead having a proximal end and a distal end having at least tip and ring electrodes and a sensor for sensing a physiological parameter of the body, the sensor having a first and second sensor terminal, the tip and ring electrodes and the first and second sensor terminals being coupled to at least a first, a second, a third and a fourth conductor, respectively, the implantable stimulation lead further comprising:

a pin terminal at the proximal end;

at least a first, second and third ring terminal at its proximal end;

at least a first, second and third conductive rod, each rod having a proximal end in electrical contact with only one of the ring terminals without touching the other of the ring terminals, each rod having a distal end electrically connected to a respective one of the second, third and fourth conductors;

a conductive tube electrically connected to the pin terminal, the conductive tube being shaped to avoid electrical contact with the ring terminals and their respective rods, the conductive tube being electrically connected to the first conductor; and

a plurality of prefabricated insulating spacers, each spacer having mechanical joining means for slidably joining, while electrically insulating, one pair of adjacent proximal terminals;

whereby the sensor is electrically connected between the second and third ring terminals and electrically isolated from the tip and ring electrodes.

2. The implantable stimulation lead, as recited in claim 1, wherein:

the plurality of prefabricated insulating spacers have a predetermined width for axially positioning each of the respective pairs of adjacent proximal terminals a prescribed distance.

3. The implantable stimulation lead, as recited in claim 2, wherein the plurality of prefabricated insulating spacers comprise:

a first prefabricated insulating spacer axially positioning the pin terminal a first prescribed distance from the first ring terminal;

a second prefabricated insulating spacer axially positioning the first ring terminal a prescribed distance from the second ring terminal; and

a third prefabricated insulating spacer axially positioning the second ring terminal a prescribed distance from the third ring terminal.

4. The implantable stimulation lead, as recited in claim 1, wherein the plurality of insulating spacers further comprise:

a plurality of inner insulating spacers, slidable over the conductive tube, insulating each of the ring terminals and their respective rods from the conductive tube.

5. The implantable stimulation lead, as recited in claim 1, further comprising:

a liquified biocompatible material placed around the conductive tube and within a channel formed by the ring terminals and the plurality of prefabricated insulating spacers so that the ring terminals and their respective rods are insulated from the conductive tube.

6. An implantable stimulation lead having at least distal tip and ring electrodes and a sensor for sensing a physiological parameter of the body, the sensor having a first and second sensor terminal, the tip and ring electrodes and the first and second sensor terminals being coupled to at least a first, a second, a third and a fourth conductor, respectively, the implantable stimulation lead further comprising:

a pin terminal;

at least a first, second and third ring terminal;

at least a first, second and third conductive rod, each rod having a proximal end in electrical contact with only one of the ring terminals without touching the other of the ring terminals, each rod having a distal end electrically connected to a respective one of the second, third and fourth conductors;

a conductive tube electrically connected to the pin terminal, the conductive tube being shaped to avoid electrical contact with the ring terminals and their respective rods, the conductive tube being electrically connected to the first conductor; and

insulating means for providing electrical isolation between each of the pin, the first, the second and the third ring terminals;

whereby the sensor is electrically connected between the second and third ring terminals and electrically isolated from the tip and ring electrodes.

7. The implantable stimulation lead, as recited in claim 6, wherein:

the insulating means comprises injection molded biocompatible material.