IP Library › Granted Patent US 9,421,061
Granted Patent B2
US 9,421,061 · App. 14/574,578 · Granted Aug 23, 2016

Ventricular far field reduction

Inventors: Yaniv Ben Zriham (Binyamina, IL); Roy Urman (Karkur, IL); Meir Bar-Tal (Haifa, IL); Richard P. M. Houben (Lanaken, BE)
Assignee: Biosense Webster (Israel) Ltd.
A61B18/1206A61B5/04012A61B5/0456A61B5/0472A61B2018/00023A61B2018/00351A61B2018/00577A61B2018/00642A61B2018/00702A61B2018/00839
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Quick Facts
Patent No.
US 9,421,061
App. No.
14/574,578
Granted
Aug 23, 2016
Kind
B2
Abstract

Far field reduction is carried out in a cardiac electrogram by extracting unipolar beats of an intracardiac electrogram that occur within a predetermined time interval that includes QRS peaks, constructing a first mean unipolar beat by averaging the extracted unipolar beats, and accepting unipolar beats that cross-correlate with the first mean unipolar beat. A second mean unipolar beat is constructed from the accepted unipolar beats. A ventricular far field component is determined from the extracted unipolar beats and subtracted from the intracardiac electrogram to distinguish a local component of the intracardiac electrogram.

Claims (45)

1. A method of far field reduction, comprising the steps of detecting peaks of a QRS complex of a cardiac electrogram;

extracting unipolar beats of an intracardiac electrogram that occur within a predetermined time interval that includes respective detected peaks;

constructing a first mean unipolar beat by averaging the extracted unipolar beats;

cross correlating the extracted unipolar beats with the first mean unipolar beat by determining respective time-lags therebetween;

accepting ones of the extracted unipolar beats wherein a cross correlation thereof exceeds a predetermined correlation threshold;

constructing a second mean unipolar beat from the accepted unipolar beats;

determining a ventricular far field component by subtracting the second mean unipolar beat from the extracted unipolar beats;

subtracting the ventricular far field component from the intracardiac electrogram to distinguish a local component of the intracardiac electrogram; and

controlling a medical procedure responsively to the local component.

2. The method according to claim 1 , wherein the predetermined correlation threshold comprises a time lag that does not exceed 10 ms.

3. The method according to claim 1 , wherein the predetermined correlation threshold comprises a difference between peak amplitudes of the extracted unipolar beats and the first mean unipolar beat that does not exceed 10 percent.

4. The method according to claim 1 , wherein constructing a first mean unipolar beat further comprises computing a median derivative beat by differentiating the extracted unipolar beats, and cross correlating is performed between the extracted unipolar beats and the median derivative beat.

5. The method according to claim 1 , wherein constructing a second mean unipolar beat comprises aligning the extracted unipolar beats.

6. The method according to claim 1 , wherein constructing a second mean unipolar beat comprises:

dividing the accepted unipolar beats into a plurality of clusters; and

constructing respective cluster-specific mean unipolar beats for each of the clusters.

7. The method according to claim 6 , wherein dividing the accepted unipolar beats is performed by k-means clustering according to Euclidean distances between the accepted unipolar beats.

8. The method according to claim 6 , wherein determining a ventricular far field component comprises:

selecting an optimum one of the cluster-specific mean unipolar beats for respective accepted unipolar beats; and

subtracting the selected cluster-specific mean unipolar beats from the extracted unipolar beats.

9. An apparatus, comprising:

an intra-body probe having an electrode, the probe being configured to contact tissue in a heart;

one or more body surface electrodes adapted to placed on an outer surface of a subject's body;

a display; and

a processor, which is configured to receive a cardiac electrogram signal from the one or more body surface electrodes and which is configured to receive an electrical signal from the electrode, to distinguish a local component, due to the tissue with which the electrode is in contact, in the electrical signal from a remote-field contribution to the signal by performing the steps of:

detecting peaks of a QRS complex of the cardiac electrogram;

extracting unipolar beats of an intracardiac electrogram received via the electrode, wherein the extracted unipolar beats occur within a predetermined time interval that includes respective detected peaks;

constructing a first mean unipolar beat by averaging the extracted unipolar beats;

cross correlating the extracted unipolar beats with the first mean unipolar beat by determining respective time-lags therebetween;

accepting ones of the extracted unipolar beats wherein a cross correlation thereof exceeds a predetermined correlation threshold;

constructing a second mean unipolar beat from the accepted unipolar beats;

determining a ventricular far field component by subtracting the second mean unipolar beat from the extracted unipolar beats;

subtracting the ventricular far field component from the intracardiac electrogram to distinguish the local component of the intracardiac electrogram; and

outputting the local component to the display.

10. The apparatus according to claim 9 , wherein the predetermined correlation threshold comprises a time lag that does not exceed 10 ms.

11. The apparatus according to claim 9 , wherein the predetermined correlation threshold comprises a difference between peak amplitudes of the extracted unipolar beats and the first mean unipolar beat that does not exceed 10 percent.

12. The apparatus according to claim 9 , wherein constructing a first mean unipolar beat further comprises computing a median derivative beat by differentiating the extracted unipolar beats, and cross correlating is performed between the extracted unipolar beats and the median derivative beat.

13. The apparatus according to claim 9 , wherein constructing a second mean unipolar beat comprises aligning the extracted unipolar beats.

14. The apparatus according to claim 9 , wherein constructing a second mean unipolar beat comprises:

dividing the accepted unipolar beats into a plurality of clusters; and

constructing respective cluster-specific mean unipolar beats for each of the clusters.

15. The apparatus according to claim 14 , wherein dividing the accepted unipolar beats is performed by k-means clustering according to Euclidean distances between the accepted unipolar beats.

16. The apparatus according to claim 14 , wherein determining a ventricular far field component comprises:

selecting an optimum one of the cluster-specific mean unipolar beats for respective accepted unipolar beats; and

subtracting the selected cluster-specific mean unipolar beats from the extracted unipolar beats, respectively.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2015
From: BEN ZRIHAM, YANIV; URMAN, ROY; BAR-TAL, MEIR; HOUBEN, RICHARD P.M.
To: BIOSENSE WEBSTER (ISRAEL) LTD.
Reel/Frame 035176/0880 →
Continuity (1)
Related Publication 20160175023A1 · Jun 23, 2016