NONCONTACT ELECTROPHYSIOLOGICAL MEASUREMENT AND IMAGING OF THE HEART

• US 20140371574A1
• Filed: 09/17/2012
• Published: 12/18/2014
• Est. Priority Date: 09/16/2011
• Status: Abandoned Application

• Current Assignee: University of Pittsburgh of The Commonwealth System of Higher Education
• Original Assignee: University of Pittsburgh of The Commonwealth System of Higher Education
• Inventors: Shusterman, Vladimir, London, Barry, Schelbert, Erik Branin
• Application Number:
  US14/345,204
• Publication Number:
  US 20140371574A1
• Time in Patent Office: Days
• US Class Current: 600/411
• 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 5/021 Measuring pressure in heart or blood vessels A61B5/0205 takes precedence
• CPC Class Codes: A61B 5/055 involving electronic [EMR] or nuclear [NMR] magnetic resonance, e.g. magnetic resonance imaging
• CPC Class Codes: A61B 5/24 Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
• CPC Class Codes: A61B 5/318 Heart-related electrical modalities, e.g. electrocardiography [ECG]
• CPC Class Codes: A61B 5/7285 for synchronising or triggering a physiological measurement or image acquisition with a physiological event or waveform, e.g. an ECG signal A61B6/5205, A61B6/541, A61B8/5207, A61B8/543 take precedence
• CPC Class Codes: A61B 8/02 Measuring pulse or heart rate

Abstract

Method and system for noncontact electrophysiologic imaging of the heart. The methods may employ the magnetization and its relaxation-based measurements, sensitive or specifically sensitized to the properties of cardiac electrical activity, to determine the spatio-temporal distribution of cardiac electromagnetic field and cardiac electrical potentials, and to display such spatio-temporal distribution (image) for assisting in the identification of the regions with abnormal cardiac electrical activity. In one embodiment, the system uses external magnets, gradient magnetic fields and radio-frequency waves, such as those commonly used for MRI, to generate the magnetic resonance. The system synchronizes scanning to the cardiac cycle using a measure of cardiac activity (e.g., electrocardiogram, ultrasound, ballistocardiogram, arterial pressure or cardiac sounds) and examines the difference between the cardiac electromagnetic properties (magnetization and relaxation) modulated by the oscillating radio-frequency fields and/or gradient fields of different orientations and magnitudes in the presence and absence of the cardiac electrical currents.

Claims

1. A method assessing cardiac electrophysiologic activity in a patient, comprising the steps of:

applying a first magnetic resonance pulse sequence to a heart of a subject at a point in a cardiac cycle where said heart is electrically active;

obtaining a first image of said heart at said point in said cardiac cycle where said heart is electrically active;

applying a second magnetic resonance pulse sequence to said heart of said patient at a point in said cardiac cycle where said heart is not electrically active, wherein said second magnetic resonance pulse sequence is the same as said first magnetic resonance pulse sequence;

obtaining a second image of said heart at said point in said cardiac cycle where said heart is not electrically active;

subtracting said second image from said first image to obtain a subtracted image of said heart; and

evaluating said subtracted image to ascertain said cardiac electrophysiological activity.

2. The method of claim 1, wherein said point in the cardiac cycle where said heart is electrically active is selected from the group consisting of atrial depolarization, atrial repolarization, ventricular depolarization, and ventricular repolarization.

3. The method of claim 1, wherein said first and second magnetic resonance pulse sequences are both a spin-lock pulse sequence.

4. The method of claim 3, wherein said spin-lock pulse sequence comprises a magnetic field matched to the frequency of oscillating electrical currents generated in the heart.

5. The method of claim 1, wherein said first and second magnetic resonance pulse sequences are both a gradient-switching pulse sequence.

6. The method of claim 5, wherein said gradient-switching pulse sequence is synchronized with said cardiac cycle.

7. The method of claim 1, wherein said first and second images of said heart are images of a region of said heart.

8. The method of claim 1, wherein said applying and obtaining steps are performed using at least one external magnet.

9. The method of claim 1, wherein said applying and obtaining steps are performed using at least one of the Earth'"'"'s magnetic field, an atomic magnetometer, and a gradient magnetic field.

10. The method of claim 1, in which said applying and obtaining steps are performed using at least one gradient magnetic field with at least one temporal change in the field being consistently synchronized with at least one time point of the cardiac cycle.

11. The method of claim 1, wherein said patient needs electrophysiological evaluation of the heart due to at least one indication selected from the group consisting of an arrhythmia, history of arrhythmia, risk of arrhythmias, electrical dyssynchrony, abnormal conduction, depolarization abnormalities, repolarization abnormalities, suspected electrophysiological abnormalities of the heart, the measurement of abnormal conduction in heart failure, and the measurement of abnormal conduction in cardiomyopathy.

12. The method of claim 1, further comprising the step of measuring said cardiac cycle.

13. The method of claim 12, wherein said measuring step is achieved through electrocardiogram, ultrasound, cardiac sounds, arterial pressure, or ballistocardiogram.

14. The method of claim 12, further comprising the step of gating said applying and obtaining steps based on said measuring step.

15. The method of claim 14, wherein said gating synchronizes said applying and obtaining steps to said cardiac cycle.

16. The method of claim 1, wherein said subject is selected from a human subject and an animal subject.

17. The method of claim 1, wherein said heart is selected from the entire heart, atria of the heart, ventricles of the heart, a segment of the heart, a wall of the heart and tissue of the heart.

18. The method of claim 1, in which said applying and obtaining steps are performed using at least one rotating magnetic field with at least one temporal change in the field being consistently synchronized with at least one time point of the cardiac cycle.

19. A system adapted for cardiac electrophysiologic imaging of a heart of a patient comprising:

a collection unit for collecting information related to magnetic properties of a heart using at least one programmable sequence of MRI-based electromagnetic events selected from the rotating-frame resonance, spin-locking, and synchronized gradient switching;

an analysis unit for analyzing spatio-temporal dynamics of said information within a cardiac cycle to obtain the spatio-temporal distribution of at least one of an electromagnetic field and electrical potentials generated by the heart; and

a display for displaying said spatio-temporal distribution of electrical potentials in the heart to enable direct tracking of at least one electrophysiological process selected from a path and speed of cardiac electrical activation and detection of regions of abnormal cardiac electrical activity.