US4640285A
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US
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Sense margin evaluation system and method for use same
Assignee: Pacesetter Inc
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Filing: 1985-01-22
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Granted: 1987-02-03
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Expires: 2005-01-22
Abstract
Abstract The sense margin evaluation system and method for use of same is based upon (1) the interposition of a variable broad-band attenuator between an implanted cardiac pacer lead set and a pacer which is about to be implanted and (2) the inclusion of a pacer pulse detector at the pacer port. In use, the pacer is first programmed to a standby mode and a condition of 100% inhibition with the attenuator set to 0 dB. This affirms that the pacer's sense amplifier can sense the cardiac signal. Then, attenuation is incrementally added until the pacer just begins to output. The attenuation ratio (input/output) at this point is a direct measure of the ratio effective between the patient's cardiac signal and the pacer's sensing threshold, i.e., the sense margin. The advantage of this technique is that by using a broad-band attenuator, measurement inaccuracies due to the convolution of the cardiac signal's spectral content with a pacer system analyzer and a pacer sense amplifier's disparate narrow-band frequency response are avoided. The patient's cardiac signal serves as the test waveform generator for the pacer that is about to be implanted in his body and the sense amplifier'frequency response is identically that of the pacer about to be implanted.
Inventors
- 👤 Robert DeCote, Jr.
- 👤 Peter P. Tarjan
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-30 02:18
CPC Classifications
A; A61; A61N; A61N1/00; A61N1/18; A61N1/32; A61N1/36; A61N1/372; A61N1/37211
Claims Analysis
Total Claims: 50
Claim 1
Independent Claim
193 words
An apparatus for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a cardiac signal (R-wave or P-wave) from a patient's heart and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a pacer to be implanted in the patient's heart where: ##EQU5## said apparatus comprising: a bandpass adjustable attentuator circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the cardiac signal; first means for coupling said attenuator circuit input to at least one cardiac signal sensing probe connected to the patient's heart; second means for coupling said attenuator circuit output to the sense amplifier in the pacer; means coupled to the pacer for detecting a pacing pulse generated by the pacer; means coupled to said attenuator circuit for controlling cardiac signal attenuation and for ascertaining the amount of attenuation at the time a pacing pulse is detected to enable a numerical determination of the sense margin ratio to be made by expression of the maximum attenuation value as a ratio of: signal input/signal output.
Claim 2
Independent Claim
193 words
An apparatus for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a cardiac signal (R-wave or P-wave) from a patient's heart and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a pacer to be implanted in the patient's heart where: ##EQU5## said apparatus comprising: a bandpass adjustable attentuator circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the cardiac signal; first means for coupling said attenuator circuit input to at least one cardiac signal sensing probe connected to the patient's heart; second means for coupling said attenuator circuit output to the sense amplifier in the pacer; means coupled to the pacer for detecting a pacing pulse generated by the pacer; means coupled to said attenuator circuit for controlling cardiac signal attenuation and for ascertaining the amount of attenuation at the time a pacing pulse is detected to enable a numerical determination of the sense margin ratio to be made by expression of the maximum attenuation value as a ratio of: signal input/signal output.
Claim 3
Dependent Claim
71 words
The apparatus of claim 1 wherein said first input coupling means comprise an amplifier with a broader bandpass than the spectrum of the signals of interest to enhance the signal-to-noise ratio while continuing to provide a net passband which is considerably greater than that of the sense amplifier so that operation of said apparatus is independent of the passbands of the sense amplifier and the frequency spectrum of the cardiac signal.
Claim 4
Dependent Claim
22 words
The apparatus of claim 1 wherein said attenuator circuit includes a programmable attentuator and an oscillator circuit coupled to said programmable attenuator.
Claim 5
Dependent Claim
22 words
The apparatus of claim 1 including a regulated power supply circuit for providing regulated voltage to said attenuator circuit and associated circuits.
Claim 6
Dependent Claim
29 words
The apparatus of claim 1 wherein said means for detecting a pacer pulse includes a visual display device for providing a visual indication of when a pulse is detected.
Claim 7
Dependent Claim
15 words
The apparatus of claim 5 wherein said visual display device is a light emitting diode.
Claim 8
Dependent Claim
22 words
The apparatus of claim 1 wherein said means for detecting a pacer pulse includes non-visual means for generating a "pulse detected" signal.
Claim 9
Dependent Claim
54 words
The apparatus of claim 1 wherein said means for detecting a pacing pulse includes a comparator having one input coupled to a pacer output, a threshold reference voltage coupled to the other input of said comparator and a univibrator (one shot) coupled to the output of said comparator for providing a pulse detected signal.
Claim 10
Dependent Claim
34 words
The apparatus of claim 8 wherein said means for detecting a pacing pulse further includes a light emitting diode coupled to the output of said univibrator for providing a visual indication of "pulse detected".
Claim 11
Dependent Claim
33 words
The apparatus of claim 1 wherein said attenuator circuit includes manually controlled means including an encoded set of switches for adjusting the attenuation and including means for displaying the signal attenuation in decibels.
Claim 12
Dependent Claim
17 words
The apparatus of claim 1 wherein said attenuator circuit includes a digitally controlled, incremental step-type attenuator circuit.
Claim 13
Dependent Claim
35 words
The apparatus of claim 1 wherein said means for controlling attenuation and for ascertaining when a pacer pulse is detected includes a microprocessor coupled to said attenuator circuit for providing automatic control of the attenuation.
Claim 14
Dependent Claim
21 words
The apparatus of claim 12 including a digital-to-analog converter coupled between said microprocessor and said attenuator circuit for controlling signal attenuation.
Claim 15
Dependent Claim
19 words
The apparatus of claim 1 including an analog signal divider coupled to said attenuator circuit for adjusting the attenuation.
Claim 16
Dependent Claim
19 words
The apparatus of claim 1 wherein said bandpass adjustable attenuator circuit has a bandpass between 10 and 200 Hz.
Claim 17
Dependent Claim
19 words
The apparatus of claim 1 wherein said bypass adjustable attenuator circuit has a bandpass between 0.1 and 480 Hz.
Claim 18
Dependent Claim
28 words
The apparatus of claim 1 including a microprocessor and means coupled to said means for detecting a pacing pulse for routing a "pulse detected" signal to said microprocessor.
Claim 19
Dependent Claim
30 words
The apparatus of claim 1 wherein said first coupling means includes buffer circuit means so that the operation of said apparatus is substantially independent of the pacing lead's output impedance.
Claim 20
Dependent Claim
31 words
The apparatus of claim 1 wherein said second coupling means includes buffer circuit means so that the operation of said apparatus is substantially independent of the pacer sense amplifier's input impedance.
Claim 21
Dependent Claim
44 words
The apparatus of claim 1 wherein said first coupling means includes buffer circuit means and said second coupling means includes buffer circuit means whereby opration of said apparatus is substantially independent of the pacing lead's output impedance and the pacer sense amplifier's input impedance.
Claim 22
Independent Claim
331 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a cardiac signal (R-wave or P-wave) from a patient's heart and the mininum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a pacer to be implanted in the patient where: ##EQU6## said method comprising the steps of: coupling a sensing/pacing electrode to the patient's heart; coupling a lead from the sensing/pacing electrode to the input of a sense margin determining apparatus including a bandpass attenuator circuit, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the cardiac signal; coupling the output from said bandpass attenuator circuit to a pacer sense amplifier in a pacer; coupling a pacing pulse detecting circut to the output of the pacer; setting the attenuator circuit to zero attenuation; placing the pacer in a standby/sense mode of operation; attenuating the cardiac signals received in an iterative process, continuously or in steps; simultaneously monitoring the output of the pulse detecting circuit to see if a pacer pulse has been detected; detecting when a pacer pulse is generated by the pacer and noting the amount of attenuation of the attenuated signal received by the pacer sense amplifier when an pacer pulse is generated; converting the attenuated value of effective cardiac signal when a pulse is generated, relative to the value of the cardiac signal sensed to a ratio; and determining if the ratio or sense margin is at least 1.1:1 (effective cardiac signal value to attenuated cardiac signal value which is below the sense amplifier threshold such that a pacer pulse is generated by the pacer), and if so, proceeding with the inplanting of the pacer, and if not, taking corrective action such as: checking the electrode connection to the heart and the pacer circuitry and/or adjusting the gain of the sense amplifier, or repeating the above steps with a new electrode coupled to the heart and/or a new pacer.
Claim 23
Independent Claim
331 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a cardiac signal (R-wave or P-wave) from a patient's heart and the mininum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a pacer to be implanted in the patient where: ##EQU6## said method comprising the steps of: coupling a sensing/pacing electrode to the patient's heart; coupling a lead from the sensing/pacing electrode to the input of a sense margin determining apparatus including a bandpass attenuator circuit, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the cardiac signal; coupling the output from said bandpass attenuator circuit to a pacer sense amplifier in a pacer; coupling a pacing pulse detecting circut to the output of the pacer; setting the attenuator circuit to zero attenuation; placing the pacer in a standby/sense mode of operation; attenuating the cardiac signals received in an iterative process, continuously or in steps; simultaneously monitoring the output of the pulse detecting circuit to see if a pacer pulse has been detected; detecting when a pacer pulse is generated by the pacer and noting the amount of attenuation of the attenuated signal received by the pacer sense amplifier when an pacer pulse is generated; converting the attenuated value of effective cardiac signal when a pulse is generated, relative to the value of the cardiac signal sensed to a ratio; and determining if the ratio or sense margin is at least 1.1:1 (effective cardiac signal value to attenuated cardiac signal value which is below the sense amplifier threshold such that a pacer pulse is generated by the pacer), and if so, proceeding with the inplanting of the pacer, and if not, taking corrective action such as: checking the electrode connection to the heart and the pacer circuitry and/or adjusting the gain of the sense amplifier, or repeating the above steps with a new electrode coupled to the heart and/or a new pacer.
Claim 24
Dependent Claim
25 words
The method of claim 21 including the step of monitoring a visual display device included in said pulse circuit whereby pulse detection is visually monitored.
Claim 25
Dependent Claim
23 words
The method of claim 21 wherein the step of monitoring the pulse detecting circuit comprises visually monitoring a visual display of detected pulses.
Claim 26
Dependent Claim
22 words
The method of claim 21 wherein the cardiac input signal is attenuated in an analog manner, i.e., continuously, as opposed to incrementally.
Claim 27
Independent Claim
17 words
The method of claimed 21 wherein the cardiac input signal is attenuated in increments of 0.1 dB.
Claim 28
Dependent Claim
30 words
The method of claim 21 wherein said step of determining if the ratio or sense margin is above 1.1:1 includes determining if the ratio or sense margin is above 2:1.
Claim 29
Dependent Claim
46 words
The method of claim 21 including the additional steps of: amplifying the incoming cardiac signal a set amount to obtain a higher signal-to-noise ratio; and attenuating the output signal from the attenuator circuit by said set amount prior to supplying same to the pacer sense amplifer.
Claim 30
Dependent Claim
39 words
The method of claim 21 including the step of electronically buffering the coupling of the pacing lead to the input of the sense margin determining apparatus so that said determination is substantially independent of the pacing lead output impedance.
Claim 31
Dependent Claim
35 words
The method of claim 21 including the step of electronically buffering the coupling to the input to the pacer sense amplifier so that said determination is substantially independent of the pacer sense amplifier's input impedance.
Claim 32
Dependent Claim
66 words
The method of claim 21 including the steps of electronically buffereing the coupling of the pacing lead to the input of the sense margin determining apparatus so that said determination is substantially independent of the pacing lead output impedance; and electronically buffering the coupling to the input to the pacer sense amplifier so that said determination is substantially independent of the pacer sense amplifier's input impedance.
Claim 33
Independent Claim
121 words
A system for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a stimulator to be implanted in the living body where: ##EQU7## said system comprising: a bandpass adjustable attenuator circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the living body generated signal; first means for coupling said attenuator circuit input to a signal sensing probe; second means for coupling said attenuator circuit output to the sense amplifier;
Claim 34
Independent Claim
121 words
A system for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a stimulator to be implanted in the living body where: ##EQU7## said system comprising: a bandpass adjustable attenuator circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the living body generated signal; first means for coupling said attenuator circuit input to a signal sensing probe; second means for coupling said attenuator circuit output to the sense amplifier;
Claim 35
Dependent Claim
97 words
means coupled to the stimulator for detecting a stimulation signal generated by the stimulator when the sense amplifier cannot sense the attenuated living body generated signal; means coupled to said attenuator circuit for controlling the attenuation of the living body generated signal and for ascertaining the amount of attenuation when a stimulation signal is detected to enable a numerical determination of the sense margin ratio to be made by expression of the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 36
Dependent Claim
97 words
means coupled to the stimulator for detecting a stimulation signal generated by the stimulator when the sense amplifier cannot sense the attenuated living body generated signal; means coupled to said attenuator circuit for controlling the attenuation of the living body generated signal and for ascertaining the amount of attenuation when a stimulation signal is detected to enable a numerical determination of the sense margin ratio to be made by expression of the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 37
Independent Claim
64 words
A system for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a stimulator to be implanted in a living body where: ##EQU8## said system comprising:
Claim 38
Independent Claim
64 words
A system for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a stimulator to be implanted in a living body where: ##EQU8## said system comprising:
Claim 39
Dependent Claim
168 words
an adjustable attenuator circuit having an input and an output; first means for coupling said attenuator circuit input to a signal sensing probe, said first coupling means including buffer circuit means so that operation of said system is substantially independent of the sensing probe's output impedance; second means for coupling said attenuator circuit output to the sense amplifier; said second coupling means including buffer circuit means so that operation of said system is substantially independent of the sense amplifier's input impedance; means coupled to the stimulator for detecting a stimulation signal generated by the stimulator when the sense amplifier cannot sense the attenuated living body generated signal; means coupled to said attenuator circuit for controlling the attenuation of the living body generated signal and for ascertaining the amount of attenuation when a stimulation signal is detected to enable a numerical determination of the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 40
Dependent Claim
168 words
an adjustable attenuator circuit having an input and an output; first means for coupling said attenuator circuit input to a signal sensing probe, said first coupling means including buffer circuit means so that operation of said system is substantially independent of the sensing probe's output impedance; second means for coupling said attenuator circuit output to the sense amplifier; said second coupling means including buffer circuit means so that operation of said system is substantially independent of the sense amplifier's input impedance; means coupled to the stimulator for detecting a stimulation signal generated by the stimulator when the sense amplifier cannot sense the attenuated living body generated signal; means coupled to said attenuator circuit for controlling the attenuation of the living body generated signal and for ascertaining the amount of attenuation when a stimulation signal is detected to enable a numerical determination of the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 41
Independent Claim
263 words
A system for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a lving body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a stimulator to be implanted in the living body where: ##EQU9## said system comprising: a bandpass adjustable attenuator circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the living body generated signal; first means for coupling said attenuator circuit input to a signal sensing probe, said first coupling means including buffer circuit means so that operation of said system is substantially independent of the sensing probe's output impedance; second means for coupling said attenuator circuit output to the sense amplifier, said second coupling means including buffer circuit means so that operation of said system is substantially independent of the sense amplifier's input impedance; means coupled to the stimulator detecting a stimulation signal generated by the stimulator when the sense amplifier cannot sense the attenuated living body generated signal; means coupled to said attenuator circuit for controlling the attenuation of the living body generated signal and for ascertaining the amount of attenuation when a stimulation signal is detected to enable a numerical determination of the sense margin ratio to be made by expression of the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 42
Independent Claim
263 words
A system for enabling an in-vivo determination of the ratio or "sense margin" between the effective amplitude of a lving body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier in a stimulator to be implanted in the living body where: ##EQU9## said system comprising: a bandpass adjustable attenuator circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the living body generated signal; first means for coupling said attenuator circuit input to a signal sensing probe, said first coupling means including buffer circuit means so that operation of said system is substantially independent of the sensing probe's output impedance; second means for coupling said attenuator circuit output to the sense amplifier, said second coupling means including buffer circuit means so that operation of said system is substantially independent of the sense amplifier's input impedance; means coupled to the stimulator detecting a stimulation signal generated by the stimulator when the sense amplifier cannot sense the attenuated living body generated signal; means coupled to said attenuator circuit for controlling the attenuation of the living body generated signal and for ascertaining the amount of attenuation when a stimulation signal is detected to enable a numerical determination of the sense margin ratio to be made by expression of the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 43
Independent Claim
235 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense margin amplifier in a stimulator to be implanted in the living body where: ##EQU10## said method compring the steps of: coupling a sensing probe to a living body; coupling a lead from the sensing probe to the input of a sense margin determining apparatus including a bandpass adjustable attenuating circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spetrum of the living body generated signal; coupling the output from said attenuator circuit to the sense amplifier; coupling a detector for detecting a stimulation signal to the output of the stimulator; attenuating the living body generated signal in an iterative process, continuously or in steps; simultaneously monitoring the output of the stimulator to see if a stimulation signal has been generated; detecting when a stimulation signal is generated by the stimulator; noting the amount of attenuation of the attenuated signal received by the sense amplifier when a stimulation signal is generated; and expressing the maximum attenuation value at which a stimulation signal is generated by the stimular as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 44
Independent Claim
235 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense margin amplifier in a stimulator to be implanted in the living body where: ##EQU10## said method compring the steps of: coupling a sensing probe to a living body; coupling a lead from the sensing probe to the input of a sense margin determining apparatus including a bandpass adjustable attenuating circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spetrum of the living body generated signal; coupling the output from said attenuator circuit to the sense amplifier; coupling a detector for detecting a stimulation signal to the output of the stimulator; attenuating the living body generated signal in an iterative process, continuously or in steps; simultaneously monitoring the output of the stimulator to see if a stimulation signal has been generated; detecting when a stimulation signal is generated by the stimulator; noting the amount of attenuation of the attenuated signal received by the sense amplifier when a stimulation signal is generated; and expressing the maximum attenuation value at which a stimulation signal is generated by the stimular as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 45
Independent Claim
264 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier and a stimulator to be implanted in the living body, where: ##EQU11## said method comprising the steps of: coupling a sensing probe to a living body; coupling a lead from the sensing probe to the input of a sense margin determining apparatus including an adjustable attenuator circuit having an input and an output; electronically buffering the coupling of the lead to the input of the sense margin determining apparatus so that said determination is substantially independent of the lead output impedance; coupling the output from said attenuator circuit to the sense amplifier; electronically buffering the coupling to the input signal to the sense amplifier so that said determination is substantially independent of the sense amplifier's input impedance; coupling a detector for detecting a stimulation signal to the output of the stimulator; attenuating the living body generated signal in an iterative process, continuously or in steps; simultaneously monitoring the output of the stimulator to see if the stimulation signal has been generated; detecting when a stimulation signal is generated by the stimulator; noting the amount of attenuation of the attenuated signal received by the sense amplifier when a stimulation signal is generated; and, expressing the maximum value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 46
Independent Claim
264 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minimum attenuated amplitude of said signal which can be readily sensed by a sense amplifier and a stimulator to be implanted in the living body, where: ##EQU11## said method comprising the steps of: coupling a sensing probe to a living body; coupling a lead from the sensing probe to the input of a sense margin determining apparatus including an adjustable attenuator circuit having an input and an output; electronically buffering the coupling of the lead to the input of the sense margin determining apparatus so that said determination is substantially independent of the lead output impedance; coupling the output from said attenuator circuit to the sense amplifier; electronically buffering the coupling to the input signal to the sense amplifier so that said determination is substantially independent of the sense amplifier's input impedance; coupling a detector for detecting a stimulation signal to the output of the stimulator; attenuating the living body generated signal in an iterative process, continuously or in steps; simultaneously monitoring the output of the stimulator to see if the stimulation signal has been generated; detecting when a stimulation signal is generated by the stimulator; noting the amount of attenuation of the attenuated signal received by the sense amplifier when a stimulation signal is generated; and, expressing the maximum value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 47
Independent Claim
261 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minmum attenuated amplitude of said signal which can be readily sensed by a sense amplifier and a stimulator to be implanted in the living body, where: ##EQU12## said method comprising the steps of: coupling a sensing probe to a living body; coupling a lead from the sensing probe to the input of a sense margin determining apparatus including a band passage adjustable attenuating circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the living body generated signal; electronically buffering the coupling of the lead to the input of the sense margin determining apparatus so that said determination is substantially independent of the lead output impedance; coupling the output from said attenuator circuit to the sense amplifier; electronically buffering the coupling to the input signal to the sense amplifier so that said determination is substantially independent of the sense amplifier's input impedance; coupling a detector for detecting a stimulation signal to the output of the stimulator; attenuating the living body generated signal in an iterative process, continuously or in steps; simultaneously monitoring the output of the stimulator to see if the stimulation signal has been generated; detecting when a stimulation signal is generated by the stimulator; noting the amount of attenuation of the attenuated signal received by the sense amplifier when a stimulation signal is generated; and,
Claim 48
Independent Claim
261 words
A method for determining in-vivo the ratio or "sense margin" between the effective amplitude of a living body generated signal sensed by a sensing probe in a living body and the minmum attenuated amplitude of said signal which can be readily sensed by a sense amplifier and a stimulator to be implanted in the living body, where: ##EQU12## said method comprising the steps of: coupling a sensing probe to a living body; coupling a lead from the sensing probe to the input of a sense margin determining apparatus including a band passage adjustable attenuating circuit having an input and an output, said bandpass being greater than the bandpass of the sense amplifier and the frequency spectrum of the living body generated signal; electronically buffering the coupling of the lead to the input of the sense margin determining apparatus so that said determination is substantially independent of the lead output impedance; coupling the output from said attenuator circuit to the sense amplifier; electronically buffering the coupling to the input signal to the sense amplifier so that said determination is substantially independent of the sense amplifier's input impedance; coupling a detector for detecting a stimulation signal to the output of the stimulator; attenuating the living body generated signal in an iterative process, continuously or in steps; simultaneously monitoring the output of the stimulator to see if the stimulation signal has been generated; detecting when a stimulation signal is generated by the stimulator; noting the amount of attenuation of the attenuated signal received by the sense amplifier when a stimulation signal is generated; and,
Claim 49
Dependent Claim
27 words
expressing the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
Claim 50
Dependent Claim
27 words
expressing the maximum attenuation value at which a stimulation signal is generated by the stimulator as a ratio of: living body generated signal input/stimulator generated signal output.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1990-02-02 | 1990-08-04 | 1991-02-03 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1994-02-02 | 1994-08-04 | 1995-02-03 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1998-02-02 | 1998-08-04 | 1999-02-03 | $7700.00 | Window Closed / Lapsed |