Monitoring and tracking bipolar ablation

• US 10,456,196 B2
• Filed: 12/15/2011
• Issued: 10/29/2019
• Est. Priority Date: 12/15/2011
• Status: Active Grant

• Current Assignee: Biosense Webster Incorporated (Johnson & Johnson)
• Original Assignee: Biosense Webster Incorporated (Johnson & Johnson)
• Inventors: Govari, Assaf, Altmann, Andres Claudio, Ephrath, Yaron
• Primary Examiner(s): Layno, Carl H
• Assistant Examiner(s): Plateski, Erin M
• Application Number:
  US13/326,456
• Publication Number:
  US 20130158545A1
• Time in Patent Office: 2,875 Days
• Field of Search: 606 41
• CPC Class Codes: A61B 18/1492 having a flexible, catheter-like structure, e.g. for heart ablation A61B18/1477 takes precedence
• CPC Class Codes: A61B 2018/00357 Endocardium
• CPC Class Codes: A61B 2018/00577 Ablation
• CPC Class Codes: A61B 5/0538 invasively, e.g. using a catheter
• CPC Class Codes: A61B 5/062 using magnetic field
• CPC Class Codes: A61B 5/287 Holders for multiple electrodes, e.g. electrode catheters for electrophysiological study [EPS]

Abstract

Methods and systems treat abnormal cardiac electrical activity employing a probe having first and second ablation electrodes disposed on a distal portion of the probe and a sensing electrode disposed between the first and second ablation electrodes, bringing the probe into contact with cardiac tissue, and applying energy through the first and second ablation electrodes to ablate target tissue along an ablation path, monitoring cardiac electrical activity using the sensing electrode to detect the cardiac electrical activity. After making an observation that the cardiac electrical activity is no longer detectable by the sensing electrode, energy application is terminated.

Claims

1. A medical apparatus, comprising:

a probe defining a longitudinal axis and having a bipolar ablation element disposed on a distal portion of the probe, the bipolar ablation element consisting of first and second ablation electrodes concentrically disposed on the distal portion of the probe relative to the longitudinal axis and a dedicated sensing electrode concentrically disposed on the distal portion of the probe relative to the longitudinal axis and between the first and second ablation electrodes, the first and second ablation electrodes being configured to operate as a bipolar pair in a bipolar mode to deliver RF energy to ablate tissue and form a lesion that extends between the first and second ablation electrodes, the dedicated sensing electrode being separate and distinct from the first and second ablation electrode and configured to sense local electrical activity in the heart when the ablation electrodes are delivering RF energy;

an ablation energy generator connected to the first and second ablation electrodes; and

a monitor connected to the sensing electrode and operative to detect cardiac electrical activity via the sensing electrode when the probe is brought into contact with a target tissue in a heart of a subject, the monitor comprising monitoring circuitry configured to track the progress of lesion formation by detecting a drop in the electrical amplitude of the electrical activity and a graphical display operative for displaying a map of a portion of the heart that includes the target tissue and a progression of energy application along an ablation path.

2. The apparatus according to claim 1, wherein the cardiac electrical activity is near-field activity.

3. The apparatus according to claim 1, wherein there is a phase shift of 90°

between an E field and an H field of the cardiac electrical activity.

4. The apparatus according to claim 1, further comprising configuration circuitry for configuring the first and second ablation electrodes to function in a bipolar mode of operation wherein the first and second ablation electrodes function as bipolar electrodes and in a unipolar mode of operation wherein at least one of the first and second ablation electrodes functions as a unipolar electrode.

5. The apparatus according to claim 4, wherein the monitor is operative for tagging the map to indicate first and second portions of the ablation path associated with the bipolar mode of operation and the unipolar mode of operation, respectively.

6. The apparatus according to claim 1, wherein the sensing electrode comprises at least two dedicated sensing electrodes disposed between the first and second ablation electrodes, the at least two dedicated sensing electrodes being configured to enable bipolar measurement of near-field electrical signals so that no energy is transported to the tissue.

7. The apparatus according to claim 1 wherein each of the ablation electrodes have a larger area than the sensing electrode.

8. The apparatus according to claim 7 wherein the ablation electrodes and sensing electrode are ring electrodes.

9. The apparatus according to claim 8 wherein each of the ablation electrodes are wider than the sensing electrode.