Method for discriminating between ventricular and supraventricular arrhythmias

• US 8,050,754 B2
• Filed: 10/28/2008
• Issued: 11/01/2011
• Est. Priority Date: 05/29/2003
• Status: Active Grant

• Current Assignee: Cameron Incorporated (Schlumberger NV)
• Original Assignee: Cameron Incorporated (Schlumberger NV)
• Inventors: Ostroff, Alan H., Bardy, Gust H., Warren, Jay A.
• Primary Examiner(s): Getzow; Scott
• Application Number:
  US12/259,926
• Publication Number:
  US 20090054938A1
• Time in Patent Office: 1,099 Days
• Field of Search: 607 4- 28, 600508-520
• US Class Current: 607/5
• CPC Class Codes: A61B 5/287 Holders for multiple electrodes, e.g. electrode catheters for electrophysiological study [EPS]
• CPC Class Codes: A61B 5/35 by template matching
• CPC Class Codes: A61B 5/363 Detecting tachycardia or bradycardia
• CPC Class Codes: A61B 5/686 Permanently implanted devices, e.g. pacemakers, other stimulators, biochips A61B5/6861 takes precedence
• CPC Class Codes: A61N 1/3925 Monitoring; Protecting
• CPC Class Codes: A61N 1/3956 Implantable devices for applying electric shocks to the heart, e.g. for cardioversion
• CPC Class Codes: A61N 1/3987 characterised by the timing or triggering of the shock

Abstract

The present invention is directed toward a detection architecture for use in implantable cardiac rhythm devices. The detection architecture of the present invention provides methods and devices for discriminating between arrhythmias. Moreover, by exploiting the enhanced specificity in the origin of the identified arrhythmia, the detection architecture can better discriminate between rhythms appropriate for device therapy and those that are not.

Claims

1. A method of cardiac signal analysis in an implantable medical device having at least a housing containing operational circuitry and a plurality of electrodes coupled to the operational circuitry for capturing cardiac signals comprising:

capturing a cardiac event using at least first and second vector views from the electrodes;

analyzing the captured cardiac event using a first method of analysis by comparing the captured cardiac event as seen from the first vector view to a stored sinus template of the first vector view;

analyzing the captured cardiac event using a second method of analysis including comparing the captured cardiac event as seen from the second vector view to a cardiac event just previous to the captured cardiac event, as seen from the second vector view;

identifying whether an arrhythmia is likely occurring and, if so, distinguishing a supraventricular arrhythmia from a ventricular originating arrhythmia using results from the first and second methods to determine whether a ventricular originating arrhythmia is occurring; and

if a ventricular originating arrhythmia is occurring, directing cardiac defibrillation therapy to the patient.

2. The method of claim 1 wherein the plurality of electrodes includes a first electrode disposed on the surface of the housing, and the implantable medical device comprises a lead attached to the housing, the lead including at least second and third electrodes, wherein the lead is disposed only subcutaneously in the patient.

3. The method of claim 1 wherein the plurality of electrodes includes a first electrode disposed on the surface of the housing, and the implantable medical device comprises a lead attached to the housing, the lead including at least second and third electrodes, wherein the lead is disposed transvenously in the patient such that at least one electrode is disposed internal to the patient'"'"'s heart.

4. The method of claim 1 wherein:

the first method of analysis further comprises comparing the captured cardiac events as seen from second first vector view to a stored sinus template of the second vector view; and

the second method of analysis further comprises comparing the captured cardiac event as seen from the first vector view to the cardiac event, as seen from the first vector view, just previous to the captured cardiac event.

5. The method of claim 4 wherein the step of identifying whether an arrhythmia is likely occurring includes estimating cardiac rate and comparing the rate to a threshold, wherein if the cardiac rate exceeds the threshold, an arrhythmia is likely occurring.

6. The method of claim 4 wherein:

the first method of analysis generates, for each detected event, correlation scores indicating similarity between the stored sinus template and the detected event in each vector view;

the second method of analysis further comprises repeatedly comparing a set of captured cardiac events to immediately previous captured cardiac events using both the first and second vector views to establish sets of results for each of the first and second vector views and calculating a variability for the sets of results, and

if an arrhythmia is likely occurring, then the step of distinguishing a supraventricular arrhythmia from a ventricular originating arrhythmia includes determining that a ventricular originating arrhythmia is occurring if, for either of the first or second vector views, both a low correlation score is found in the first method and a high variability is found in the second method.

7. The method of claim 1 wherein the step of identifying whether an arrhythmia is likely occurring includes estimating cardiac rate and comparing the rate to a threshold, wherein if the cardiac rate exceeds the threshold, an arrhythmia is likely occurring.

8. An implantable cardiac stimulus device system comprising:

a housing containing operational circuitry including at least a battery and a controller, the operational circuitry configured to observe electrical cardiac activity of the patient and, if determined necessary, to provide electrical cardiac stimulus to a patient if implanted in the patient; and

a lead electrode assembly comprising at least one electrode for use in at least one of observing electrical cardiac activity and/or delivering electrical cardiac stimulus to a patient;

wherein the operational circuitry is configured to observe electrical cardiac activity as follows in order to determine whether electrical cardiac stimulus is indicated;

capture a cardiac event using at least first and second vector views defined by electrodes included in the lead electrode assembly and/or located on the canister;

analyze the captured cardiac event using a first method of analysis which includes comparing the captured cardiac event as seen from the first vector view to a stored sinus template of the first vector view;

analyze the captured cardiac event using a second method of analysis including comparing the captured cardiac event as seen from the second vector view to a cardiac event just previous to the captured cardiac event as seen from the second vector view;

identify whether an arrhythmia is likely occurring and, if so, distinguish a supraventricular arrhythmia from a ventricular originating arrhythmia using results from the first and second methods to determine whether a ventricular originating arrhythmia is occurring; and

determine electrical cardiac stimulus is indicated if a ventricular originating arrhythmia is occurring.

9. The system of claim 8 wherein operational circuitry is configured such that:

the first method of analysis further comprises comparing the captured cardiac events as seen from second first vector view to a stored sinus template of the second vector view; and

the second method of analysis further comprises comparing the captured cardiac event as seen from the first vector view to the cardiac event, as seen from the first vector, view just previous to the captured cardiac event.

10. The system of claim 9 wherein the operational circuitry is configured such that, in order to identify whether an arrhythmia is likely occurring, the operational circuitry estimates cardiac rate and compares the rate to a threshold, wherein if the cardiac rate exceeds the threshold, the operational circuitry will identify that an arrhythmia is likely occurring.

11. The system of claim 9 wherein the operational circuitry is configured such that:

the first method of analysis generates, for each detected event, correlation scores indicating similarity between the stored sinus template and the detected event in each vector view;

the second method of analysis further comprises repeatedly comparing a set of captured cardiac events to immediately previous captured cardiac events using both the first and second vector views to establish sets of results for each of the first and second vector views and calculating a variability for the sets of results, and

if the operational circuitry determines an arrhythmia is likely occurring, then the operational circuitry determines whether a high variability is found in the second method and a low correlation score form the first method for either of the first or second vector views and, if so, the operational circuitry determines a ventricular arrhythmia is occurring.

12. The system of claim 8 wherein the operational circuitry is configured such that, in order to identify whether an arrhythmia is likely occurring, the operational circuitry estimates cardiac rate and compares the rate to a threshold, wherein if the cardiac rate exceeds the threshold, the operational circuitry will identify that an arrhythmia is likely occurring.