# US 8,831,705 B2 · Devices and method for accelerometer-based characterization of cardiac synchrony and dyssynchrony

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- Number: US 8,831,705 B2
- Document ID: US8831705B2
- Status: Granted
- Kind: B2
- Application number: 13/230,084
- Filed: 2011-09-12
- Published: 2012-01-05
- Granted: 2014-09-09
- Earliest claimed: 2005-02-07
- Assignees: Cardiosync, Inc.
- Applicants: John Daniel Dobak
- Inventors: John Daniel Dobak
- Web page: https://patentgrep.com/patent/US8831705B2

## CPC

- A61B 5/11: Measuring movement of the entire body or parts thereof, e.g. head or hand tremor or mobility of a limb {(A61B5/1038 takes precedence; motion detection to correct for motion artifacts in physiological signals A61B5/721)}
- A61B 5/021: Measuring pressure in heart or blood vessels
- A61B 5/1102: {Ballistocardiography}
- A61B 5/287: Holders for multiple electrodes, e.g. electrode catheters for electrophysiological study [EPS]
- A61B 5/352: Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
- A61B 5/355: Detecting T-waves
- A61B 5/0031: {Implanted circuitry}
- A61B 5/6851: {Guide wires}
- A61B 5/6852: {Catheters}
- A61B 5/6862: {Stents}
- A61B 5/6869: {Heart}
- A61B 5/6876: {Blood vessel}
- A61B 5/726: {using Wavelet transforms}
- A61B 7/00: Instruments for auscultation
- A61B 2562/028: Microscale sensors, e.g. electromechanical sensors [MEMS]
- A61N 1/3627: {for treating a mechanical deficiency of the heart, e.g. congestive heart failure or cardiomyopathy}
- A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D)
- A61N: ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY (measurement of bioelectric currents A61B; surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body A61B18/00; anaesthetic apparatus in general A61M; incandescent lamps H01K; infrared radiators for heating H05B)

## Abstract

Systems and methods according to the invention employ an acceleration sensor to characterize the synchrony or dyssynchrony of the left ventricle. Patterns of acceleration related to myocardial contraction can be used to assess synchrony or dyssynchrony. Time-frequency transforms and coherence are derived from the acceleration. Information and numerical indices determined from the acceleration time frequency transforms and coherence can be used to find the optimal pacing location for cardiac resynchronization therapy. Similarly, the information can be used to optimize timing intervals including V to V and A to V timing.

## Claims

### Claim 1

A method for identifying an optimal pacing location, comprising:
a. introducing an acceleration-measuring catheter into a coronary sinus of a patient;
b. measuring a baseline pattern of left ventricular myocardial acceleration;
c. placing a right ventricular pacing device in a right ventricle of the patient;
d. placing a left ventricular pacing device in or on the left ventricle of the patient;
e. moving the left ventricular pacing device to a plurality of locations in or on the left ventricle;
f. performing biventricular or left ventricular pacing at each of the plurality of locations with the left ventricular pacing device;
g. measuring an acceleration pattern at each of the plurality of locations caused by the biventricular or left ventricular pacing; and
h. determining a location within the left ventricle having a least dyssynchronous acceleration pattern; and
i. selecting the location with the least dyssynchronous acceleration pattern to implant a CRT pacing lead.

### Claim 2 (depends on 1)

The method of claim 1, further comprising converting said acceleration pattern into one or more dyssynchrony indices.

### Claim 3 (depends on 2)

The method of claim 2, further comprising moving said right ventricular pacing device to a plurality of locations in the right ventricle and measuring and acceleration pattern at each of the plurality of locations in the right ventricle, and determining a location within the right ventricle having a least dvssynchronous acceleration pattern.

### Claim 4 (depends on 3)

The method of claim 3, further comprising implanting a right ventricular pacing lead in a location with a least dyssynchronous acceleration pattern.

### Claim 5 (depends on 1)

A non-transitory computer-readable medium, containing instructions for causing a computing device to perform the method of claim 1.

### Claim 6 (depends on 4)

The method of claim 4, further comprising converting said acceleration patterns from said right ventricle into one or more dyssynchrony indices.

### Claim 7 (depends on 1)

The method of claim 1, wherein the acceleration measuring catheter includes a single 3-axis acceleration sensor.

### Claim 8 (depends on 1)

The method of claim 1, wherein the measuring a baseline pattern of left ventricular myocardial acceleration includes measuring a global acceleration of a left ventricle of a patient.

### Claim 9 (depends on 2)

The method of claim 2, wherein said numerical or dyssynchrony index includes at least one of the following:
a time delay from onset of ventricular electrical activity to onset of LV motion during systole;
a time delay from onset of ventricular electrical activity to peak LV motion during systole;
a time delay from onset of ventricular electrical activity to onset of LV motion during diastole;
a time delay from onset of ventricular electrical activity to peak LV motion during diastole;
a ratio of a peak motion during systole and diastole;
a time interval between a peak motion of systole and diastole;
a number of motion peaks during systole greater than a threshold;
a time delay between two highest peaks of motion during systole;
a variability of time delay from onset of ventricular electrical activity to peak motion in each acceleration axis (X, Y, or Z);
a variability of peak motion in each independent axis Y, or Z);
a reduction in a peak acceleration of delayed motion;
a frequency of peak amplitude of power spectrum; or
an acceleration axis with a dominant frequency in power spectrum cross correlations of time-frequency transforms between ECG signal and acceleration signals or between different acceleration signal axes.

### Claim 10 (depends on 1)

The method of claim 1, wherein the left ventricular pacing device is a pacing guide wire, and further comprising delivering an implantable pacing lead over the pacing guide wire following the determining a location step.

### Claim 11 (depends on 3)

The method of claim 3, wherein the right ventricular pacing device is a pacing guide wire, and further comprising delivering an implantable pacing lead over the pacing guide wire following the determining a location step.

### Claim 12 (depends on 1)

The method of claim 1, wherein the location within the left ventricle having a least dyssynchronous acceleration pattern is identified by finding a region that produces a left ventricular contraction pattern resembling a synchronous LV contraction.