Implantable stimulus system having stimulus generator with pressure sensor and common lead for transmitting stimulus pulses to a body location and pressure signals from the body location to the stimulus generator

• US 6,223,081 B1
• Filed: 03/28/1996
• Issued: 04/24/2001
• Est. Priority Date: 03/28/1996
• Status: Expired due to Fees

• Current Assignee: Vitatron Medical BV
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Kerver, Harry B. A.
• Primary Examiner(s): LAYNO, CARL HERNANDZ
• Application Number:
  US08/625,714
• Time in Patent Office: 1,853 Days
• Field of Search: 607/17-19, 607/23, 607/36, 607/37
• US Class Current: 607/17
• CPC Class Codes: A61N 1/36564 controlled by blood pressure

Abstract

A medical device system such as a pacemaker system is provided wherein pressure signals representative of a patient'"'"'s cardiac movements are transmitted through a pacing lead to the pacemaker, where they are sensed and utilized for control of pacemaker operation. In a preferred embodiment, the invention utilizes a standard pacing lead, which may already be in place within the patient, the lead having a lumen through which relative pressure signals are transmitted from the patient'"'"'s heart to the proximal end of the lead. The proximal end of the lead is connected to a pressure sensor, mounted either in the pacemaker header portion or within the hermetically sealed pacemaker can. The sensor signals are coupled to appropriate processing circuitry and are used for control of one or more pacing parameters, such as pacing rate. In a first embodiment, the pressure sensor is mounted within the pacemaker header portion, and the electrical sensor signals are connected through an electrical feed-through to the interior of the pacemaker can. In a second embodiment, the sensor signals are passed through a capillary feed-through from the proximal end of the lead which is secured in the header portion, to the interior of the pacemaker can where the pressure sensor is mounted; the capillary feed-through may also conduct sensed heart signals from the proximal end of the lead to within the pacemaker.

Claims

1. A pacemaker system having a pacemaker for delivering pacing pulses and a standard pacing lead for transmitting electrical signals between said pacemaker and a patient'"'"'s heart, said lead having a distal end adapted to be placed in the patient'"'"'s heart, a proximal end, and a lumen throughout its length suitable for transmitting pressure variations caused by heart activity, said lumen having a proximal opening at its proximal end, whereby pressure variations caused by said heart activity arise within said lumen and are transmitted to said proximal opening, said pacemaker comprising:

a connector portion for receiving the proximal end of said lead;

a pressure sensor which produces signals corresponding to said transmitted pressure variations;

coupling means for coupling pressure variations between said lumen proximal opening and said pressure sensor, said coupling means having a cavity positioned to receive said pressure variations directly from said opening,

mounting means for mounting said sensor in said cavity, and

control means operatively connected to said pressure sensor for controlling pacemaker operation as a function of said transmitted pressure variations.

2. The pacemaker system as described in claim 1, wherein said pacemaker comprises a first portion containing a pulse generator and said control means, and wherein said pressure sensor is mounted in said first portion.

3. The pacemaker system as described in claim 2, comprising sealing means for sealing said first portion from entry of body fluids, and wherein sail coupling means comprises feed-through means for feeding said pressure variations from said proximal opening to said sensor.

4. The pacemaker system as described in claim 1, wherein said cavity has a size that provides an efficient match to receive said transmitted pressure variations.

5. The pacemaker system as described in claim 4, wherein said lumen has a first volume and said cavity has a second volume, and said second volume is about 10% of said first volume.

6. The pacemaker system as described in claim 1, wherein said pacemaker comprises a first sealed portion containing a pulse generator and said control means, first feed-through means for connecting electrical signals between said first portion and said connector portion, and second feed-through means for connecting said sensor signals to said control means.

7. The pacemaker as described in claim 6, comprising a cavity in said first portion, and wherein said mounting means and said sensor are placed in said cavity.

8. The pacemaker as described in claim 7, comprising second sealing means for sealing said cavity from the remainder of said first portion.

9. The pacemaker as described in claim 7, wherein said feed-through means has an opening into said cavity, and wherein said sensor is positioned proximal to said opening.

10. A pacemaker system having a pacemaker and a pacing lead connected with said pacemaker, said lead having a distal end for insertion into a patient'"'"'s heart and a proximal end for connection to said pacemaker, said lead having a lumen substantially throughout its length suitable for transmitting pressure variations caused by heart movements, said lumen having a proximal opening to which said pressure variations are transmitted, said pacemaker having:

a connector portion for connectedly receiving the proximal end of said lead,

a pressure sensor which produces signals corresponding to pressure variations delivered thereto,

coupling means matched to said lumen for coupling pressure variations received at said lumen proximal opening to said pressure sensor, and

control means connected to receive signals from said pressure sensor for controlling pacemaker operation as a function of said relative pressure variations; and

said lead comprising a portion at its distal end which is sensitive to pressure changes.

11. The pacemaker system as described in claim 10, wherein said coupling means comprises a cavity in said pacemaker having a volume which is small compared to the volume of said lumen, and wherein said sensor is mounted in said cavity.

12. The pacemaker system as described in claim 11, wherein said lead has a distal electrode for sensing patient heart signals and a conductor for conducting said heart signals to said lead proximal end, and wherein said coupling means further comprises means for coupling said heart signals from said lead proximal end to within said pacemaker.

13. An implantable medical system which obtains data representative of at least one body area or body function, said system comprising:

a catheter having a distal end for placement so as to be impacted by activity of said body area or by said body function, a proximal end and a lumen extending between said ends, said lumen having a lumen volume, and

a medical device having a connector portion which connectedly receives said proximal end;

at least one sensor;

a coupling portion which is at least partially in said connector portion for coupling signals from said lumen to said sensor, said coupling portion having a cavity having a volume no greater than about ten percent of said lumen volume, mounting means for mounting said at least one sensor in said cavity; and

signal means for obtaining from said at least one sensor signals representative of said body area or body function.

14. The system as described in claim 13, wherein said medical device is a pacemaker, said signal means further comprising means to obtain signals representative of both atrial and ventricular contractions.

15. The system as described in claim 13, wherein said pacemaker has control means for operating in a VDD mode.