Pacemaker with automatic sensitivity adjustment

• US 5,913,880 A
• Filed: 04/07/1997
• Issued: 06/22/1999
• Est. Priority Date: 04/07/1997
• Status: Expired due to Term

• Current Assignee: Vitatron Medical BV (Medtronic Plc)
• Original Assignee: Vitatron Medical BV (Medtronic Plc)
• Inventors: Vonk, Bernardus F. M.
• Primary Examiner(s): Jastrzab, Jeffrey R.
• Application Number:
  US08/835,349
• Time in Patent Office: 806 Days
• Field of Search: 607/9, 607/27, 607/28, 607/5, 600/509, 600/517, 600/518, 600/521
• US Class Current: 607/27
• CPC Class Codes: A61N 1/3704 Circuits specially adapted therefor, e.g. for sensitivity control

Abstract

There is provided a pacemaker having automatic adjustment of the sensitivity for sensing cardiac signals such as QRS, T and P waves. The pacemaker has software for examining each inputted signal, obtaining a measure of the peak amplitude, e.g. one-half, comparing such measure with a stored software sensitivity level, and adjusting the software sensitivity level each beat so that it effectively tracks beat-to-beat changes in the signal amplitude. The adjusted software sensitivity level is used for determining when an input signal is to be accepted as a true signal, or rejected.

Claims

1. An implantable cardiac pacemaker for pacing a patient as a function of sensed cardiac signals from said patient'"'"'s heart, comprising:

stimulus means for delivering stimulus pulses to said patient'"'"'s heart;

sensing means for sensing said patient cardiac signals, said sensing means having measure means for determining a measure of the magnitude of sensed signals, comparing means for comparing each said determined measure to a variable reference and for recognizing a sense when said measure is greater than said reference, and means for adjusting said reference as a function of said comparing; and

control means for controlling said stimulus means as a function of said recognized senses.

2. The pacemaker as described in claim 1, comprising signal means for determining each occurrence when a said sensed signal has a magnitude at least as great as a first level and enabling means for enabling said measure means in response to each said occurrence.

3. The pacemaker as described in claim 2, wherein said adjusting means comprises peak means for determining a peak value of each cardiac signal and fraction means for generating said measure as a fraction of said peak value.

4. The pacemaker as described in claim 3, comprising a software routine for providing said adjusting means.

5. A system in an implantable pacemaker for sensing patient cardiac signals and automatically adjusting the sensitivity level for accepting a signal as a true cardiac signal, comprising:

sense means for sensing said cardiac signals having a peak magnitude above a predetermined level;

measure means for obtaining a measure of the peak value of each said sensed signal;

sensitivity means for providing a variable sensitivity level, said sensitivity means having a software routine for adjusting said variable sensitivity level as a function of each said sensed software means having means for comparing said peak value measure with said sensitivity level, and adjusting means for adjusting said sensitivity level as a function of said comparison signal.

6. The system as described in claim 5, wherein said measure means has means for measuring an absolute peak value of each said sensed signal.

7. The system as described in claim 5, wherein said software routine has fraction means for obtaining a fraction of said peak value, and second comparing means for comparing said fraction with said variable sensitivity level, and wherein said adjusting means has means for adjusting said variable sensitivity level as a function of the comparison of said fraction with said variable sensitivity level.

8. The system as described in claim 7, wherein said fraction means has means for obtaining one-half of said peak value.

9. The system as described in claim 5, wherein said software routine has limit means for limiting said sensitivity level to a lower limit of said predetermined level.

10. A method of automatically setting the sense sensitivity level of a pacemaker to a level related to the peak amplitude of periodic input signals being sensed, comprising:

comparing each said input signal to a predetermined minimum reference level and providing a trigger signal each time said input signal is greater than said reference level;

converting said input signal to a digital signal in response to a said trigger signal and determining the peak value of said digital signal;

maintaining by software a software sensitivity level;

comparing each said peak value with said sensitivity level, and indicating a sensed signal only when said peak value exceeds said sensitivity level; and

said maintaining including adjusting said sensitivity level following each said trigger signal so that said sensitivity level is varied as a function of said peak value and the prior maintained sensitivity level.

11. The method as described in claim 10, comprising carrying out said maintaining and comparing steps by a software routine.

12. The method as described in claim 11, wherein said adjusting comprises determining a predetermined fraction of said peak value, determining whether said fraction is greater or less than the value of said sensitivity level, and adjusting said sensitivity level as a function of said determining.

13. The method as described in claim 12, comprising setting said predetermined fraction to about one half.

14. The method as described in claim 12, wherein said adjusting step comprises adjusting said sensitivity level by a predetermined amount.

15. The method as described in claim 14, wherein said adjusting comprises incrementing said software sensitivity level by said amount when said fraction is greater than said software sensitivity level.

16. The method as described in claim 14, wherein said adjusting comprises decrementing said software sensitivity level by said amount when said fraction is lesser than said software sensitivity level.

17. The method as described in claim 15, comprising programming said fraction and said amount from an external programmer.

18. The method as described in claim 10, wherein said adjusting comprises decrementing said software sensitivity level when said comparing indicates that said peak value does not exceed said software sensitivity level.

19. The method as described in claim 10, comprising detecting depolarization signals from a patient'"'"'s ventricle, and providing said depolarization signals as said input signals.

20. The method as described in claim 10, comprising detecting depolarization signals from a patient'"'"'s atrium, and providing said depolarization signals as said input signals.