Method and apparatus for identifying cardiac and non-cardiac oversensing using intracardiac electrograms

• US 7,283,863 B2
• Filed: 04/29/2002
• Issued: 10/16/2007
• Est. Priority Date: 04/29/2002
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Gunderson, Bruce D., Patel, Amisha S., Bounds, Chad A.
• Primary Examiner(s): Bockelman; Mark
• Application Number:
  US10/135,080
• Publication Number:
  US 20030204215A1
• Time in Patent Office: 1,996 Days
• Field of Search: 600/509, 600/510, 600/515, 607/27
• US Class Current: 600/509
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61B 5/352 Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/3925 Monitoring; Protecting

Abstract

A method and apparatus for automatically identifying various types of cardiac and non-cardiac oversensing is provided. EGM data, including time intervals between sensed and paced events and signal morphologies, are analyzed for patterns indicative of various types of oversensing, including oversensing of far-field R-waves, R-waves, T-waves, or noise associated with electromagnetic interference, non-cardiac myopotentials, a lead fracture, or a poor lead connection. Identification of oversensing and its suspected cause are reported so that corrective action may be taken.

Claims

1. An implantable medical device system for identifying cardiac and non-cardiac oversensing using intracardiac electrograms, the system comprising:

an implantable medical device (IMD) containing EGM data;

means for accessing said EGM data;

means for evaluating interval differences;

means for evaluating interval patterns;

means for determining the presence of short and long intervals;

means for identifying oversensing based on the evaluated interval differences, the evaluated interval patterns, and the determined presence of short and long intervals; and

means for recommending a corrective action based on at least one characteristic of an identified oversensing to implement said corrective action in said IMD.

2. The system of claim 1 wherein said EGM data relates to data collected by an arrhythmia detection means.

3. The system of claim 1 wherein said EGM data relates to data collected by monitoring means.

4. The system of claim 1 wherein said means for accessing includes one of a programmer, a personal computer and an external device in data communication with the said IMD.

5. The system of claim 1 wherein said EGM includes EGM signal, sensed and/or paced interval data, and annotations of sensed and/or paced events.

6. The system of claim 4 wherein one of said programmer, said personal computer and said external device is implemented to perform said analysis of said EGM data.

7. The system of claim 1 wherein said means for accessing is implemented in said IMD.

8. The system of claim 1 wherein said means for performing analysis is implemented in said IMD.

9. The system of claim 1 wherein said means for recommending a corrective action is implemented in said IMD.

10. The system of claim 9 wherein said corrective action includes warning a patient via a notification means.

11. The system of claim 10 wherein said corrective action includes one of reprogramming a sensitivity setting, reprogramming a sensing electrode configuration, tightening set screws in the connector block, investigating for a likely lead fracture to thereby repair or replace, and implement investigation to eliminate oversensing.