Implantable cardiac systems with baseline correction in response to noise detection

• US 8,831,711 B2
• Filed: 06/04/2013
• Issued: 09/09/2014
• Est. Priority Date: 06/04/2012
• Status: Active Grant

• Current Assignee: Cameron Incorporated (Schlumberger NV)
• Original Assignee: Cameron Incorporated (Schlumberger NV)
• Inventors: Freer, Paul, Sanghera, Rick, Allavatam, Venugopal
• Primary Examiner(s): Wieland, Robert N
• Application Number:
  US13/909,657
• Publication Number:
  US 20130324867A1
• Time in Patent Office: 462 Days
• Field of Search: 600/509, 600/483, 600/510, 600/515, 600/516
• US Class Current: 600/509
• CPC Class Codes: A61B 5/316 Modalities, i.e. specific diagnostic methods
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61B 5/361 Detecting fibrillation
• CPC Class Codes: A61B 5/686 Permanently implanted devices, e.g. pacemakers, other stimulators, biochips A61B5/6861 takes precedence
• CPC Class Codes: A61B 5/7203 for noise prevention, reduction or removal
• CPC Class Codes: A61B 5/7217 of noise originating from a therapeutic or surgical apparatus, e.g. from a pacemaker
• CPC Class Codes: A61N 1/36 for stimulation
• CPC Class Codes: A61N 1/362 Heart stimulators heart defibrillators A61N1/39
• CPC Class Codes: A61N 1/37 Monitoring; Protecting

Abstract

Implantable cardiac devices and methods of their use. A method of operation in an implantable cardiac device may include steps for characterizing detected events as noise or not noise, identifying a set of consecutive noise events or a threshold quantity of noise events in a set period of time and declaring a noisy series to have occurred. In response to the declaration of a noisy series, the method initiates a baseline correction algorithm. Devices for performing such methods are also disclosed.

Claims

1. An implantable cardiac device comprising electrodes for receiving cardiac signals and operational circuitry for processing the cardiac signals received by the electrodes;

in which the operational circuitry is configured to;

receive signals via the electrodes;

detect events in the received signals by comparing the received signals to one or more thresholds and identifying threshold crossings;

determine which, if any, of the detected events are noisy;

determine whether a noise condition has been detected; and

if a noise condition has been detected, enable a baseline correction method to ensure that the noise that caused the noise condition does not induce a baseline offset and thereby impair sensing.

2. The implantable cardiac device of claim 1 wherein the operational circuitry is configured to determine whether each detected event is noisy by:

determining how many turning points occur in a window associated with a detected event; and

comparing the quantity of such turning points to a threshold;

wherein the operational circuitry is configured to determine that a given detected event is noisy if the quantity of turning points in the window for the given detected event exceeds the threshold.

3. The implantable cardiac device of claim 1 wherein the baseline correction method comprises operation of a dynamic heuristic filter.

4. The implantable cardiac device of claim 1 wherein the operational circuitry is configured to enable the baseline correction method for a set period of time.

5. The implantable cardiac device of claim 1 wherein the operational circuitry is configured to perform the baseline correction method by setting an initial dynamic adjustment period and performing each of the following steps several times:

a) repeatedly performing a sensing baseline adjustment protocol at intervals defined by the dynamic adjustment period; and

b) observing a distance between the sensing baseline and a desired quiescent point and modifying the dynamic adjustment period in response to the observed distance between the sensing baseline and desired quiescent point.

6. The implantable cardiac device of claim 1 wherein the operational circuitry is configured to determine whether a noise condition has been detected by observing whether a predefined quantity of consecutive noisy events has occurred.

7. The implantable cardiac device of claim 1 wherein the operational circuitry is configured to determine whether a noise condition has been detected by observing whether a predefined number of noisy events have occurred in a set period of time.

8. The implantable cardiac device of claim 1 wherein the operational circuitry is configured to determine whether a noise condition has been detected by observing whether a predefined number of noisy events have occurred in a predefined quantity of detected events.

9. A method of operation in an implantable cardiac device that includes electrodes for receiving cardiac signals and operational circuitry for processing the cardiac signals received by the electrodes;

the method comprising;

the operational circuitry receiving signals via the electrodes;

the operational circuitry detecting events in the received signals by comparing the received signals to one or more thresholds and identifying threshold crossings;

the operational circuitry determining which, if any, of the detected events are noisy;

the operational circuitry determining whether a noise condition has been detected; and

if a noise condition has been detected, the operational circuitry enabling a baseline correction method to ensure that the noise that caused the noise condition does not induce a baseline offset and thereby impair sensing.

10. The method of claim 9 wherein the step of determining whether each detected event is noisy is performed by:

determining how many turning points occur in a window associated with a detected event; and

comparing the quantity of such turning points to a threshold;

wherein a given detected event is determined to be noisy if the quantity of turning points in the window for the given detected event exceeds the threshold.

11. The method of claim 9 wherein the baseline correction method includes operation of a dynamic heuristic filter.

12. The method of claim 9 wherein the operational circuitry is configured to enable the baseline correction method for a set period of time.

13. The method of claim 9 wherein the baseline correction method includes setting an initial dynamic adjustment period and performing each of the following steps several times:

a) repeatedly performing a sensing baseline adjustment protocol at intervals defined by the dynamic adjustment period; and

b) observing a distance between the sensing baseline and a desired quiescent point and modifying the dynamic adjustment period in response to the observed distance between the sensing baseline and desired quiescent point.

14. The method of claim 9 wherein the step of determining whether a noise condition has been detected is performed by observing whether a predefined quantity of consecutive noisy events has occurred.

15. The method of claim 9 wherein determining whether a noise condition has been detected is performed by observing whether a predefined number of noisy events have occurred in a set period of time.

16. The method of claim 9 wherein determining whether a noise condition has been detected is performed by observing whether a predefined number of noisy events have occurred in a predefined quantity of detected events.

17. An implantable cardiac device comprising electrodes for receiving cardiac signals and operational circuitry for processing the cardiac signals received by the electrodes;

in which the operational circuitry is configured to;

receive signals via the electrodes;

detect events in the received signals by comparing the received signals to one or more detection thresholds and identifying detection threshold crossings;

identify an average magnitude for the received signals wherein average magnitude is determined by sampling the received signals across a period of time that exceeds a single cardiac cycle;

determine whether the average magnitude deviates from a quiescent point;

adjust the detection threshold using a correction factor related to the deviation of the average magnitude from the quiescent point; and

detect at least one cardiac event using the detection threshold as adjusted by the correction factor.

18. The implantable cardiac device as in claim 17 wherein the average magnitude is determined by sampling at least one second of cardiac signal.

19. The implantable cardiac device as in claim 17 wherein the operational circuitry is configured to determine that the average magnitude deviates from the quiescent point by determining if the average magnitude is different from the quiescent point by at least a predetermined amount.