초록 ▼

In general, the disclosure is directed to techniques for identification and remediation of oversensed cardiac events using far-field electrograms (FFEGMs). Identification of oversensed cardiac events can be used in an ICD to prevent ventricular fibrillation (VF) detection, and thereby avoid delivery

In general, the disclosure is directed to techniques for identification and remediation of oversensed cardiac events using far-field electrograms (FFEGMs). Identification of oversensed cardiac events can be used in an ICD to prevent ventricular fibrillation (VF) detection, and thereby avoid delivery of an unnecessary defibrillation shock. Alternatively, or additionally, identification of oversensed cardiac events can be used in an ICD to support delivery of bradycardia pacing during an oversensing condition. In some cases, bradycardia pacing delivered in response to detection of oversensed cardiac events may include pacing pulses from multiple vectors to provide redundancy in the event the oversensing may be due to a lead-related condition.

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1. A method comprising: acquiring a first cardiac signal via a first sense electrode configuration;acquiring a second cardiac signal via a second sense electrode configuration;detecting a plurality of cardiac events in the first cardiac signal;measuring a plurality of intervals between the cardiac e

1. A method comprising: acquiring a first cardiac signal via a first sense electrode configuration;acquiring a second cardiac signal via a second sense electrode configuration;detecting a plurality of cardiac events in the first cardiac signal;measuring a plurality of intervals between the cardiac events detected in the first cardiac signal;analyzing one or more characteristics of the second cardiac signal to determine whether at least one of the plurality of cardiac events detected in the first cardiac signal comprises an oversensed event;identifying at least one oversensed event of the plurality of cardiac events in the first cardiac signal based on the analysis of the one or more characteristics of the second cardiac signal; andcontrolling delivery of a cardiac electrical stimulation therapy to a patient based on the identification of at least one oversensed event by: withholding a first interval of the plurality of intervals from a therapy delivery control module in response to identifying the at least one oversensed event causing the first interval to have been measured;obtaining a summed interval by summing the first interval with one or more next intervals of the plurality of intervals until a last of the next intervals that is not between oversensed events; andproviding the summed interval to the therapy delivery control module for use in controlling delivery of the cardiac electrical stimulation therapy. 2. The method of claim 1, wherein controlling delivery of the cardiac electrical stimulation therapy further comprises: detecting that the summed interval is greater than a threshold time interval; anddelivering pacing therapy to the patient in response to the detection that the summed interval is greater than the threshold time interval. 3. The method of claim 2, wherein delivering pacing therapy comprises: delivering first pacing therapy via a first stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval; anddelivering second pacing therapy via a second stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval. 4. The method of claim 3, wherein the first stimulation electrode configuration comprises electrodes carried by a first lead implanted to deliver the first pacing therapy to a first chamber of the heart, and the second stimulation electrode configuration comprises electrodes carried by a second lead implanted to deliver the second pacing therapy to a second chamber of the heart. 5. The method of claim 3, further comprising measuring impedance values of at least one of the first and second stimulation electrode configurations. 6. The method of claim 1, wherein controlling delivery of the cardiac electrical stimulation therapy further comprises: determining time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;determining a count of a number of the time intervals that are shorter than a threshold time interval;detecting that the count is greater than a threshold count; anddelivering at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 7. The method of claim 1, wherein controlling delivery of the cardiac electrical stimulation therapy further comprises: determining time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;detecting that at least one of the time intervals is greater than a first threshold time interval;delivering pacing therapy to the patient in response to the detection that at least one of the time intervals is greater than the first threshold time interval;determining a count of a number of the time intervals that are shorter than a second threshold time interval;detecting that the count is greater than a threshold count; anddelivering at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 8. The method of claim 1, wherein the first cardiac signal is a near-field electrogram signal, the second cardiac signal is a far-field electrogram signal, the first sense electrode configuration comprises a tip electrode and a ring electrode carried by a ventricular lead, and the second sense electrode configuration comprises a coil electrode carried by the ventricular lead and a can electrode carried by a housing of an implantable medical device. 9. The method of claim 1, wherein identifying at least one oversensed event of the plurality of cardiac events in the first cardiac signal comprises identifying each of the cardiac events as an oversensed event if an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 10. The method of claim 1, wherein analyzing one or more characteristics of the second cardiac signal comprises determining whether an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 11. An implantable medical device comprising: an electrical sensing module configured to acquire a first cardiac signal via a first sense electrode configuration, and to acquire a second cardiac signal via a second sense electrode configuration;a stimulation module configured to deliver a cardiac electrical stimulation therapy to a patient via a plurality of stimulation electrodes;a therapy delivery control module configured to control the stimulation module configured to deliver the cardiac electrical stimulation therapy; anda processor configured to: detect a plurality of cardiac events in the first cardiac signal;measure a plurality of intervals between the plurality of cardiac events detected in the first cardiac signal;analyze one or more characteristics of the second cardiac signal to determine whether at least one of the plurality of cardiac events detected in the first cardiac signal comprises an oversensed event; andidentify at least one oversensed event of the plurality of cardiac events in the first cardiac signal based on the analysis of the one or more characteristics of the second cardiac signal, andcontrol the stimulation module to deliver the cardiac electrical stimulation therapy to the patient based on the identification of at least one oversensed event by: withholding a first interval of the plurality of intervals from the therapy delivery control module in response to identifying the at least one oversensed event causing the first interval to have been measured;obtaining a summed interval by summing the first interval with one or more next intervals of the plurality of intervals until a last of the next intervals that is not between oversensed events; andproviding the summed interval to the therapy delivery control module for use in controlling delivery of the cardiac electrical stimulation therapy by the stimulation module. 12. The device of claim 11, wherein the therapy delivery control module is further configured to detect that the summed interval is greater than a threshold time interval, and to control the stimulation module to deliver pacing therapy to the patient in response to the detection that the summed interval is greater than the threshold time interval. 13. The device of claim 12, wherein the therapy delivery control module is further configured to control the stimulation module to deliver first pacing therapy via a first stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval, and deliver second pacing therapy via a second stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval. 14. The device of claim 13, further comprising the first stimulation electrode configuration and the second stimulation electrode configuration, wherein the first stimulation electrode configuration comprises electrodes carried by a first implantable lead to deliver the first pacing therapy to a first chamber of the heart, and the second stimulation electrode configuration comprises electrodes carried by a second lead implantable to deliver the second pacing therapy to a second chamber of the heart. 15. The device of claim 13, further comprising an impedance measurement module configured to measure impedance values of at least one of the first and second stimulation electrode configurations. 16. The device of claim 11, wherein the therapy delivery control module is further configured to: determine time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;determine a count of a number of the time intervals that are shorter than a threshold time interval;detect that the count is greater than a threshold count; andcontrol the stimulation module to deliver at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 17. The device of claim 11, wherein the therapy delivery control module is further configured to: determine time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;detect that at least one of the time intervals is greater than a first threshold time interval;deliver pacing therapy to the patient in response to the detection that one of the time intervals is greater than the first threshold time interval;determine a count of a number of the time intervals that are shorter than a second threshold time interval;detect that the count is greater than a threshold count; anddeliver at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 18. The device of claim 11, wherein the first cardiac signal is a near-field electrogram signal, the second cardiac signal is a far-field electrogram signal, and the device further comprises a ventricular lead, the first sense electrode configuration, and the second sense electrode configuration, wherein the first sense electrode configuration comprises a tip electrode and a ring electrode carried by the ventricular lead, and the second sense electrode configuration comprises a coil electrode carried by the ventricular lead and a can electrode carried by a housing of the implantable medical device. 19. The device of claim 11, wherein the processor is configured to identify each of the cardiac events as an oversensed event if an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 20. The device of claim 11, wherein the processor is further configured to determine whether an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 21. An implantable medical device comprising: means for acquiring a first cardiac signal via a first sense electrode configuration;means for acquiring a second cardiac signal via a second sense electrode configuration;means for detecting a plurality of cardiac events in the first cardiac signal;means for measuring a plurality of intervals between the plurality of cardiac events detected in the first cardiac signal;means for analyzing one or more characteristics of the second cardiac signal to determine whether at least one of the plurality of cardiac events detected in the first cardiac signal comprises an oversensed event;means for identifying at least one oversensed event of the plurality of cardiac events in the first cardiac signal based on the analysis of the whether one or more characteristics of the second cardiac; andmeans for controlling delivery of a cardiac electrical stimulation therapy to a patient based on the identification of at least one oversensed event by: withholding a first interval of the plurality of intervals from a therapy control module in response to identifying the at least one oversensed event causing the first interval to have been measured;obtaining a summed interval by summing the first interval with one or more next intervals of the plurality of intervals until a last of the next intervals that is not between oversensed events; andproviding the summed interval to the therapy delivery control module for use in controlling delivery of the cardiac electrical stimulation therapy. 22. The device of claim 21, wherein the means for controlling delivery comprises: means for detecting that the summed interval is greater than a threshold time interval; andmeans for delivering pacing therapy to the patient in response to the detection that the summed interval is greater than the threshold time interval. 23. The device of claim 22, wherein the means for delivering pacing therapy comprises: means for delivering first pacing therapy via a first stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval; andmeans for delivering second pacing therapy via a second stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval. 24. The device of claim 23, wherein the first stimulation electrode configuration comprises electrodes carried by a first lead implantable to deliver the first pacing therapy to a first chamber of the heart, and the second stimulation electrode configuration comprises electrodes carried by a second lead implantable to deliver the second pacing therapy to a second chamber of the heart. 25. The device of claim 23, further comprising means for measuring impedance values of at least one of the first and second stimulation electrode configurations. 26. The device of claim 21, wherein the means for controlling delivery of the cardiac electrical stimulation therapy further comprises: means for determining time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;means for determining a count of a number of the time intervals that are shorter than a threshold time interval;means for detecting that the count is greater than a threshold count; andmeans for delivering at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 27. The device of claim 21, wherein the means for controlling delivery of the cardiac electrical stimulation therapy further comprises: means for determining time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;means for detecting that at least one of the time intervals is greater than a first threshold time interval;means for delivering pacing therapy to the patient in response to the detection that at least one of the time intervals is greater than the first threshold time interval;means for determining a count of a number of the time intervals that are shorter than a second threshold time interval;means for detecting that the count is greater than a threshold count; andmeans for delivering at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 28. The device of claim 21, wherein the first cardiac signal is a near-field electrogram signal, the second cardiac signal is a far-field electrogram signal, the first sense electrode configuration comprises a tip electrode and a ring electrode carried by a ventricular lead, and the second sense electrode configuration comprises a coil electrode carried by the ventricular lead and a can electrode carried by a housing of the implantable medical device. 29. The device of claim 21, wherein the means for identifying at least one oversensed event of the plurality of cardiac events in the first cardiac signal comprises means for identifying each of the cardiac events as an oversensed event if an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 30. The device of claim 21, wherein the means for analyzing one or more characteristics of the second cardiac signal comprises means for determining whether an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 31. A non-transitory computer-readable storage medium comprising instructions that, when executed by a processor in an implantable medical device, cause the processor to: detect a plurality of cardiac events in a first cardiac signal acquired via a first sense electrode configuration;measure a plurality of intervals between the plurality of cardiac events detected in the first cardiac signal;analyze one or more characteristics of a second cardiac signal acquired via a second sense electrode configuration to determine whether at least one of the plurality of cardiac events detected in the first cardiac signal comprises an oversensed event;identify at least one oversensed event of the plurality of cardiac events in the first cardiac signal based on the analysis of the one or more characteristics of the second cardiac signal; andcontrol a stimulation module to deliver a cardiac electrical stimulation therapy to a patient based on the identification of at least one oversensed event by: withholding a first interval of the plurality of intervals from a therapy delivery control module in response to identifying at least one oversensed event causing the first interval to have been measured;obtaining a summed interval by summing the first interval with one or more next intervals of the plurality of intervals until a last of the next intervals that is not between oversensed events; andproviding the summed interval to the therapy delivery control module for use in controlling delivery of the cardiac electrical stimulation therapy. 32. The computer-readable storage medium of claim 31, wherein the instructions cause the processor to: detect that the summed interval is greater than a threshold time interval; andcontrol the stimulation module to deliver pacing therapy to the patient in response to the detection that the summed interval is greater than the threshold time interval. 33. The computer-readable storage medium of claim 32, wherein the instructions cause the processor to: control the stimulation module to deliver first pacing therapy via a first stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval; andcontrol the stimulation module to deliver second pacing therapy via a second stimulation electrode configuration in response to the detection that the summed interval is greater than the threshold time interval. 34. The computer-readable storage medium of claim 33, wherein the instructions cause the processor to obtain measured impedance values of at least one of the first and second stimulation electrode configurations. 35. The computer-readable storage medium of claim 31, wherein the instructions cause the processor to: determine time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;determine a count of a number of the time intervals that are shorter than a threshold time interval;detect that the count is greater than a threshold count; andcontrol the stimulation module to deliver at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 36. The computer-readable storage medium of claim 31, wherein the instructions cause the processor to: determine time intervals between the detected cardiac events that are not identified as oversensed events, wherein at least one of the time intervals includes the summed interval;detect that at least one of the time intervals is greater than a first threshold time interval;control the stimulation module to deliver pacing therapy to the patient in response to the detection that one of the time intervals is greater than the first threshold time interval;determine a count of a number of the time intervals that are shorter than a second threshold time interval;detect that the count is greater than a threshold count; andcontrol the stimulation module to deliver at least one of cardioversion or defibrillation therapy to the patient in response to the detection that the count is greater than the threshold count. 37. The computer-readable storage medium of claim 31, wherein the first cardiac signal is a near-field electrogram signal, the second cardiac signal is a far-field electrogram signal, the first sense electrode configuration comprises a tip electrode and a ring electrode carried by a ventricular lead, and the second sense electrode configuration comprises a coil electrode carried by the ventricular lead and a can electrode carried by a housing of the implantable medical device. 38. The computer-readable storage medium of claim 31, wherein the instructions cause the processor to identify each of the cardiac events as an oversensed event if an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude. 39. The computer-readable storage medium of claim 31, wherein the instructions cause the processor to determine whether an amplitude of the second cardiac signal at a time substantially coincident with the respective cardiac event detected in the first cardiac signal is below a threshold amplitude.