Methods and systems for improved arrhythmia discrimination

• US 8,249,707 B2
• Filed: 05/14/2008
• Issued: 08/21/2012
• Est. Priority Date: 05/14/2008
• Status: Active Grant

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Inventors: Nabutovsky, Yelena, Donnay, Rafael, Xi, Cecilia Qin
• Primary Examiner(s): Layno, Carl H
• Assistant Examiner(s): PORTER, JR, GARY A
• Application Number:
  US12/120,471
• Publication Number:
  US 20090287268A1
• Time in Patent Office: 1,560 Days
• Field of Search: 600508-510, 600/515, 600/518, 607 2- 15, 607 59- 63
• US Class Current: 607/27
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/3624 occurring in the atrium, i.e. atrial tachycardia

Abstract

A non-implanted system receives, from an implantable cardiac device implanted within a patient, data corresponding to detected potential episodes of tachycardia. A representation of the data corresponding to the detected potential episodes of tachycardia is displayed to a user, and the user that observes the displayed representation of the data is allowed to enter a user diagnosis for each of the detected potential episodes of tachycardia. The non-implanted system simulates how the implantable cardiac device can use its discriminators to produce device diagnoses, based on the data for the detected potential episodes of tachycardia, including how adjustments to the discriminators affect how the device diagnoses match the user diagnoses. Thereafter, the non-implanted system can reprogram the implantable cardiac device to increase a likelihood that future device diagnoses produced by the implantable cardiac device would more closely match future user diagnoses produced by the user.

Claims

1. A method for use by a non-implanted system configured to communicate with an implantable cardiac device implanted within a patient, wherein the implantable cardiac device is configured to detect potential episodes of tachycardia and to store data corresponding to the detected potential episodes of tachycardia, and wherein the implantable cardiac device has programmable arrhythmia discriminators and corresponding discriminator settings that the device uses to discriminate between different types of tachycardia, the method comprising:

(a) receiving, from the implantable cardiac device implanted within the patient, data corresponding to detected potential episodes of tachycardia;

(b) displaying a representation of the data corresponding to the detected potential episodes of tachycardia;

(c) accepting a user diagnosis for each of the detected potential episodes of tachycardia;

(d) simulating the implantable cardiac device'"'"'s use of the discriminator settings to produce device diagnoses based on the data for the detected potential episodes of tachycardia, and

repeating step (d) a plurality of times, wherein between each successive iteration of step (d) one or more of the discriminator settings is automatically adjusted, and wherein a result of each iteration of step (d) comprises a simulated device diagnosis for each of the detected potential episodes of tachycardia;

(e) comparing the simulated device diagnoses produced during multiple iterations of step (d) to the user diagnoses accepted at step (c) to thereby identify discriminator settings, and/or adjustments to currently programmed discriminator settings, that cause the device diagnoses to more closely match the user diagnoses; and

(f) displaying information about the identified discriminator settings, and/or adjustments to currently programmed discriminator settings, that cause the device diagnoses to more closely match the user diagnoses;

wherein each of steps (a), (b) and (c) occur prior to each of steps (d), (e) and (f); and

wherein at step (e), if a plurality of different settings for a specific one of the discriminators results in the same match between the simulated device diagnoses and the user diagnoses, then selecting one of the plurality of different settings for the specific one of the discriminators based on;

which one of the different settings for the specific one of the discriminators provides the greatest allowance for error;

which one of the different settings for the specific one of the discriminators is the same as or closest to a corresponding default setting of the implantable cardiac device; and

/or

which one of the different settings for the specific one of the discriminators is the same as or closest to a corresponding currently programmed setting of the implantable cardiac device.

2. The method of claim 1, wherein step (d) includes automatically adjusting one or more of the discriminator settings until results of the comparing at step (e) indicate that the simulated device diagnoses match the user diagnoses to within a specified tolerance.

3. The method of claim 1, further comprising:

(g) sending instructions to the implantable cardiac device, the instructions specifying the identified discriminator settings and/or adjustments to currently programmed discriminator settings that cause the device diagnoses to more closely match the user diagnoses.

4. The method of claim 1, wherein step (d) includes automatically adjusting one or more of the following settings:

which discriminators are used;

when discriminators are used;

how discriminators are used;

an order in which discriminators are used;

how many discriminators must be satisfied for a rhythm to be characterized as a specific type of tachycardia; and

a value of a parameter of at least one of the discriminators.

5. The method of claim 1, wherein at step (e), if more than one setting for one of the discriminators results in the same match between the simulated device diagnoses and the user diagnoses, then selecting the setting that provides the greatest allowance for error.

6. The method of claim 5, wherein at step (e), if more than one setting for one of the discriminators results in the same match between the simulated device diagnoses and the user diagnoses, and results in the same allowance for error, then selecting the setting that is the same as or closest to a corresponding default setting of the implantable cardiac device.

7. The method of claim 1, wherein at step (e), if more than one setting for one of the discriminators results in the same match between the simulated device diagnoses and the user diagnoses, then selecting the setting that is the same as or closest to a corresponding default setting of the implantable cardiac device.

8. The method of claim 1, wherein at step (e), if more than one setting for one of the discriminators results in the same match between the simulated device diagnoses and the user diagnoses, then selecting the setting that is the same as or closest to a corresponding currently programmed setting of the implantable cardiac device.

9. The method of claim 1, wherein step (b) includes displaying EGM and/or ECG waveforms corresponding to the detected potential episodes of tachycardia.

10. The method of claim 9, step (b) includes displaying attribute information about the displayed EGM and/or ECG waveforms corresponding to the detected potential episodes of tachycardia.

11. The method of claim 9, wherein:

step (a) includes receiving, from the implantable cardiac device implanted within the patient, physiologic data corresponding to detected potential episodes of tachycardia, the physiologic data obtained using one or more physiologic sensor;

step (b) includes displaying, along with the EGM and/or ECG waveforms, a representation of the physiologic data that corresponds to the detected potential episodes of tachycardia.

12. The method of claim 1, wherein:

step (c) includes allowing the user to select from among at least VT and SVT user diagnosis options for each of the detected episodes of tachycardia.

13. The method of claim 1, wherein step (d) includes automatically adjusting one or more of the following settings:

an order in which discriminators are used; and

how many discriminators must be satisfied for a rhythm to be characterized as a specific type of tachycardia.

14. A non-implanted system configured to communicate with an implantable cardiac device implanted within a patient, wherein the implantable cardiac device is configured to detect potential episodes of tachycardia and to store data corresponding to the detected potential episodes of tachycardia, and wherein the implantable cardiac device has programmable arrhythmia discriminators and corresponding discriminator settings that the device uses to discriminate between different types of tachycardia, the non-implanted system comprising:

a telemetry subsystem to receive, from the implantable cardiac device implanted within the patient, data corresponding to detected potential episodes of tachycardia;

a display to display a representation of the data corresponding to the detected potential episodes of tachycardia;

an input device to accept, from a user that observes the displayed representation of the data, a user diagnosis for each of the detected potential episodes of tachycardia;

one or more processor to

perform a simulation to simulate the implantable cardiac device'"'"'s use of the discriminator settings to produce device diagnoses based on the data for the detected potential episodes of tachycardia,

repeat the simulation a plurality of times, wherein between each successive iteration of the simulations one or more of the discriminator settings is automatically adjusted, and wherein a result of each iteration of the simulations comprises a simulated device diagnosis for each of the detected potential episodes of tachycardia, and

compare the simulated device diagnoses produced during multiple iterations of the simulations to the accepted user diagnoses to thereby identify discriminator settings, and/or adjustments to currently programmed discriminator settings, that cause the device diagnoses to more closely match the user diagnoses;

wherein the display also displays information about the identified discriminator settings, and/or adjustments to currently programmed discriminator settings, that cause the device diagnoses to more closely match the user diagnoses; and

wherein if a plurality of different settings for a specific one of the discriminators results in the same match between the simulated device diagnoses and the user diagnoses, then the one or more processor selects one of the plurality of different settings for the specific one of the discriminators based on;

which one of the different settings for the specific one of the discriminators provides the greatest allowance for error;

which one of the different settings for the specific one of the discriminators is the same as or closest to a corresponding default setting of the implantable cardiac device; and

/or

which one of the different settings for the specific one of the discriminators is the same as or closest to a corresponding currently programmed setting of the implantable cardiac device.

15. The system of claim 14, wherein the one or more processor automatically adjusts one or more of the discriminator settings until results of the comparison indicate that the simulated device diagnoses match the user diagnoses to within a specified tolerance.

16. The system of claim 14, wherein:

the telemetry subsystem also sends instructions to the implantable cardiac device, the instructions specifying the identified discriminator settings and/or adjustments to currently programmed discriminator settings that cause the device diagnoses to more closely match the user diagnoses.

17. The system of claim 14, wherein the one or more processors automatically adjust one or more of the following settings between at least some of the iterations of the simulations:

an order in which discriminators are used; and

how many discriminators must be satisfied for a rhythm to be characterized as a specific type of tachycardia.