Implantable cardiac monitoring and/or control devices having automatic sensitivity control, apparatus and methods therefor

Claim 3

The method of claim 1 characterized in that the decreasing in stages of said sensitivity threshold further comprises decreasing the sensitivity by decrements (DecS).

Claim 4

The method of claim 2 characterized in that decreasing in stages further comprises providing a first time interval and a uniform decrement, lowering the sensitivity threshold by said uniform decrement following each occurrence of said first time interval during which no cardiac event is detected, and wherein measuring the amplitude in stage (b) further comprises rectifying the ventricular complex and measuring the maximum amplitude of the rectified ventricular complex, wherein said uniform decrement is on the order of 0.8 mV and said first time interval is on the order of 47 ms.

Claim 5

The method as claimed in claim 1 characterized by counting from the detection of a ventricular complex a selected maximum period (Tmax) and, at the end of the selected maximum period (Tmax), returning the sensitivity threshold (S) to the low value (Smax) corresponding to maximum sensitivity.

Claim 6

The method of claim 1 characterized by providing a time window and measuring the amplitude (Amp) of said detected ventricular complex during said time window, the time window being selected from between 16 and 110 ms counted from the detection of a ventricular complex.

Claim 7

The method of claim 5 wherein the selected time window is on the order of 64 ms.

Claim 8

The method of claim 1 wherein the cardiac signal monitoring device is a cardiac pacemaker.

Claim 9

The method of claim 1 wherein the cardiac signal monitoring device is one of a cardioversion device and a defibrillation device.

Claim 10

A cardiac control device selected from among the group consisting of pacemaker, a cardioversion device and a defibrillation device, characterized in that it comprises a ventricular complex detection sensitivity threshold that can be automatically adjusted by the method of claim 1.

Claim 11

A cardiac monitoring device for sensing cardiac electrical signals and detecting cardiac events characterized by: means for providing an initial sensitivity threshold having a low value corresponding to maximum sensitivity; means for providing a time window following a sensed cardiac event and a time interval; means for providing an absolute refractory period in response to a sensed cardiac event; means for detecting the maximum amplitude of the sensed cardiac electrical signals occurring during said time window following said sensed cardiac event; means for adjusting the sensitivity threshold to a value that is a function of the detected amplitude, said adjustment occurring at the end of the absolute refractory period; and means for subsequently decreasing the sensitivity threshold following each occurrence of said time interval in the absence of said detecting means detecting a subsequent cardiac event, said decreasing means not decreasing the sensitivity level below the provided low value.

Claim 12

A cardiac monitoring device for sensing cardiac electrical signals and detecting cardiac events characterized by: means for providing an initial sensitivity threshold having a low value corresponding to maximum sensitivity; means for providing a time window following a sensed cardiac event and a time interval; means for providing an absolute refractory period in response to a sensed cardiac event; means for detecting the maximum amplitude of the sensed cardiac electrical signals occurring during said time window following said sensed cardiac event; means for adjusting the sensitivity threshold to a value that is a function of the detected amplitude, said adjustment occurring at the end of the absolute refractory period; and means for subsequently decreasing the sensitivity threshold following each occurrence of said time interval in the absence of said detecting means detecting a subsequent cardiac event, said decreasing means not decreasing the sensitivity level below the provided low value.

Claim 13

The device of claim 10 wherein the adjusting means comprises means for adjusting the sensitivity threshold to be a percent of the maximum amplitude of the sensed cardiac signals detected during said time window.

Claim 14

The device of claim 11 wherein the percent is on the order of 75%.

Claim 15

The device of claim 10 wherein the cardiac monitoring device further comprises a pacemaker including a cardiac stimulation pulse generator.

Claim 16

The device of claim 13 wherein the adjusting means is further characterized by: means for providing a sensitivity threshold that is a high value corresponding to a minimum sensitivity; and second means for adjusting the sensitivity threshold in response to a cardiac stimulation pulse to be a value less than the high value.

Claim 17

The device of claim 14 wherein the selected value of the second adjusting means is the minimum sensitivity threshold less a selected amount, the selected amount corresponding to the amount by which the sensitivity threshold is decreased following each time interval.

Claim 18

The device of claim 10 further comprising means for providing a decrement and characterized in that the decreasing means decreases the sensitivity threshold by said decrement after the occurrence of each selected time interval.

Claim 19

The device of claim 16 wherein the detecting means further comprises rectifying the cardiac electrical signal, the selected decrement is on the order of 0.8 mV, the time interval is on the order of 47 ms, and the maximum amplitude of the cardiac electrical signal is the maximum of the rectified cardiac electrical signal.

Claim 20

The device of claim 10 characterized in that the adjusting means further comprises means for counting a maximum period (Tmax) from the detection of a cardiac event and means for returning the sensitivity threshold to the low value corresponding to maximum sensitivity at the end of the maximum period (Tmax).

Claim 21

The device of claim 10 characterized in that the time window is selected from between 16 and 110 ms counted from the detection of the cardiac event.

Claim 22

The device of claim 19 wherein the selected time window is on the order of 64 ms.

Claim 23

The device of claim 10 in which the cardiac monitoring device is selected from among the group consisting of a cardiac pacemaker, a cardioversion device, and a cardiac defibrillation device.

Claim 26

The method of claim 22 wherein adjusting the sensitivity threshold further comprises selecting a value that is a percent of the maximum amplitude of the sensed cardiac signals detected during the window.

Claim 27

The method of claim 23 wherein the percent is on the order of 75%.

Claim 28

The method of claim 22 further comprising providing a selected minimum sensitivity threshold, providing a pacemaker and a generator for outputting cardiac stimulation pulses, wherein the adjusting step is further characterized by adjusting the sensitivity threshold in response to a cardiac stimulation to be a threshold value that is less than the selected minimum sensitivity threshold value.

Claim 29

The method of claim 25 wherein decreasing the sensitivity threshold further comprises decreasing the threshold by a uniform decrement after each time interval and the selected value is the minimum sensitivity threshold value less said decrement.

Claim 30

The method of claim 22 characterized in that decreasing the sensitivity threshold is characterized by decreasing the sensitivity threshold by a decrement after the occurrence of each selected time interval.

Claim 31

The method of claim 27 wherein the selected decrement is on the order of 0.8 mV, the time interval is on the order of 47 ms, and the detecting step further comprises rectifying the cardiac electrical signals and detecting the maximum amplitude of the rectified cardiac electrical signal.

Claim 32

The method of claim 22 characterized in that the adjusting step further comprises providing a selected maximum period (Tmax), counting the maximum period (Tmax) from the detection of a cardiac event, and at the end of the maximum period (Tmax), setting the sensitivity threshold to the low value corresponding to maximum sensitivity.

Claim 33

The method of claim 22 characterized in that the detecting step is characterized by detecting the maximum amplitude during a time window selected from between 16 and 110 ms counted from the detection of the cardiac event.

Claim 34

The method of claim 30 wherein the selected time window is on the order of 64 ms.

Claim 35

The method of claim 22 wherein the circuit providing step further comprises providing said circuit to a cardiac control device selected from among the group consisting of a cardiac pacemaker, a cardioversion device, and a cardiac defibrillation device.