PRE-EJECTION INTERVAL (PEI) MONITORING DEVICES, SYSTEMS AND METHODS

• US 20120065528A1
• Filed: 09/14/2010
• Published: 03/15/2012
• Est. Priority Date: 09/14/2010
• Status: Active Grant

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Inventors: Gill, Jong, Wenzel, Brian Jeffrey, Keel, Allen, Hou, Wenbo, Karst, Edward, Farazi, Taraneh G.
• Granted Patent: US 8,571,642 B2
• Time in Patent Office: Days
• US Class Current: 600/509
• CPC Class Codes: A61B 5/02028 Determining haemodynamic parameters not otherwise provided for, e.g. cardiac contractility or left ventricular ejection fraction
• CPC Class Codes: A61B 5/0295 using plethysmography, i.e. measuring the variations in the volume of a body part as modified by the circulation of blood therethrough, e.g. impedance plethysmography
• CPC Class Codes: A61B 5/287 Holders for multiple electrodes, e.g. electrode catheters for electrophysiological study [EPS]
• CPC Class Codes: A61B 5/352 Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
• CPC Class Codes: A61B 5/686 Permanently implanted devices, e.g. pacemakers, other stimulators, biochips A61B5/6861 takes precedence
• CPC Class Codes: A61B 5/7239 using differentiation including higher order derivatives
• CPC Class Codes: A61N 1/3684 for stimulating the heart at multiple sites of the ventricle or the atrium
• CPC Class Codes: A61N 1/36843 Bi-ventricular stimulation

Abstract

Provided herein are implantable systems, and methods for use therewith, for monitoring a patient'"'"'s pre-ejection interval (PEI). A signal indicative of cardiac electrical activity and a signal indicative of changes in arterial blood volume are obtained. One or more predetermined features of the signal indicative of cardiac electrical activity and the signal indicative of changes in arterial blood volume are detected. The patient'"'"'s PEI is determined by determining an interval between the predetermined feature of the signal indicative of cardiac electrical activity and the predetermined feature of the signal indicative of changes in arterial blood volume.

Claims

1. For use with an implantable system, a method for monitoring a patient'"'"'s pre-ejection interval (PEI), the method comprising:

(a) using one or more electrodes implanted within and/or on the patient'"'"'s heart to obtain a signal indicative of cardiac electrical activity;

(b) using an implanted sensor to obtain a signal indicative of changes in arterial blood volume;

(c) detecting a predetermined feature of the signal indicative of cardiac electrical activity;

(d) detecting a predetermined feature of the signal indicative of changes in arterial blood volume;

(e) determining an interval between the predetermined feature of the signal indicative of cardiac electrical activity and the predetermined feature of the signal indicative of changes in arterial blood volume; and

(f) monitoring the patient'"'"'s PEI based on the interval.

2. The method of claim 1, further comprising:

(g) triggering an alert, triggering therapy and/or adjusting therapy based on the monitored PEI.

3. The method of claim 1, further comprising:

(g) storing, within the implantable system, information indicative of the monitored PEI so that the stored information is available for transfer to a non-implanted system.

4. The method of claim 1, wherein:

steps (a), (b), (c), (d) and (e) are performed for each of a plurality of periods of time to thereby determine, for each of the plurality of periods of time, the interval between the predetermined feature of the signal indicative of cardiac electrical activity and the predetermined feature of the signal indicative of changes in arterial blood volume; and

step (f) comprises monitoring changes in the patient'"'"'s PEI based on changes in the interval over time.

5. The method of claim 4, further comprising:

(g) triggering an alert, triggering therapy and/or adjusting therapy based on the monitored changes in PEI.

6. The method of claim 4, wherein:

during a first one of the periods of time that steps (a), (b), (c), (d) and (e) are performed, a first measure of systolic blood pressure is obtained;

during a second one of the periods of time that steps (a), (b), (c), (d) and (e) are performed, a second measure of systolic blood pressure is obtained; and

at step (f), when monitoring changes in the patient'"'"'s PEI from the first period of time to the second period of time, calibrating the interval corresponding to the second period of time based on the change in the measure of systolic blood pressure from the first period of time to the second period of time, if any change.

7. The method of claim 4, further comprising:

(g) monitoring for an indication of disease and/or disease progression based on the monitored changes in the patient'"'"'s PEI.

8. The method of claim 1, wherein:

step (c) comprises detecting a predetermined feature indicative of ventricular depolarization of the signal indicative of cardiac electrical activity;

step (d) comprises detecting a predetermined feature corresponding to a systolic portion of the signal indicative of changes in arterial blood volume;

step (e) comprises detecting an interval between the predetermined feature indicative of ventricular depolarization of the signal indicative of cardiac electrical activity and the predetermined feature corresponding to a systolic portion of the signal indicative of changes in arterial blood volume; and

step (f) comprises monitoring the patient'"'"'s PEI based on the interval between the predetermined feature indicative of ventricular depolarization of the signal indicative of cardiac electrical activity and the predetermined feature corresponding to a systolic portion of the signal indicative of changes in arterial blood volume.

9. The method of claim 1, wherein:

step (a) comprises using one or more electrodes implanted within and/or on the patient'"'"'s heart to obtain an intracardiac electrogram (IEGM) signal or an electrocardiogram (ECG) signal indicative of cardiac electrical activity; and

step (b) comprises using an implanted photoplethysmography (PPG) sensor to obtain a photoplethysmography (PPG) signal indicative of changes in arterial blood volume, or using or an impedance plethysmography (IPG) sensor to obtain an impedance plethysmography (IPG) signal indicative of changes in arterial blood volume.

10. The method of claim 1, further comprising:

performing a calibration including

determining an echo-based measure of PEI at a point in time,

at about the same point in time that the echo-based measure of PEI is determined, performing steps (a), (b), (c), (d) and (e) to determine an interval between the predetermined feature of the signal indicative of cardiac electrical activity and the predetermined feature of the signal indicative of changes in arterial blood volume, and

determining a difference between the determined echo-based measure of PEI and the determined interval;

wherein when step (f) is performed after the calibration is performed, the patient'"'"'s PEI is estimated based on the interval determined at step (e) and the difference determined during calibration.

11. The method of claim 10, wherein:

when step (f) is performed after the calibration is performed, the patient'"'"'s PEI is estimated as being equal to the interval determined at step (e) minus the difference determined during calibration.

12. An implantable system capable of monitoring a patient'"'"'s pre-ejection interval (PEI), comprising

one or more electrodes configured to obtain a signal indicative of cardiac electrical activity;

an implantable sensor configured to obtain a signal that is indicative of changes in arterial volume;

a PEI monitor configured to

detect a predetermined feature of the signal indicative of cardiac electrical activity,

detect a predetermined feature of the signal indicative of changes in arterial blood volume,

determine an interval between the predetermined feature of the signal indicative of cardiac electrical activity and the predetermined feature of the signal indicative of changes in arterial blood volume, and

monitor the patient'"'"'s PEI based on the interval.

13. The implantable system of claim 12, wherein the PEI monitor is configured to trigger an alert, therapy and/or adjusting therapy based on the monitored PEI.

14. The implantable system of claim 12, further comprising memory, wherein the PEI monitor is also configured to store, within memory, information indicative of the monitored PEI so that the stored information is available for transfer to a non-implanted system.

15. The implantable system of claim 12, wherein the PEI monitor is configured to monitor changes in the patient'"'"'s PEI by monitoring changes in the interval over time.

16. The implantable system of claim 12, wherein the predetermined feature indicative of cardiac electrical activity is selected from the group consisting of:

a Q-wave;

a R-wave; and

a QRS complex.

17. The implantable system of claim 12, wherein the predetermined feature indicative of changes in arterial blood volume is selected from the group consisting of:

a foot of the signal indicative of changes in arterial blood volume;

a peak of the signal indicative of changes in arterial blood volume; and

a maximum positive slope of the signal indicative of changes in arterial blood volume.

18. For use with an implantable system, a method for monitoring a patient'"'"'s pre-ejection interval (PEI), the method comprising:

(a) obtaining a signal indicative of changes in arterial blood volume; and

(b) monitoring the patient'"'"'s PEI based on the signal indicative of changes in arterial blood volume.