Techniques for identifying and analyzing events-of-interest indicated by physiological parameters

Patent metadata

Field	Value
Publication number	US-12446818-B2
Application number	US-202217949080-A
Country	US
Kind code	B2
Filing date	Sep 20, 2022
Priority date	Sep 21, 2021
Publication date	Oct 21, 2025
Grant date	Oct 21, 2025

Abstract

Various techniques related to post-treatment parameters of patients are described. An example method includes identifying a segment of an electrocardiogram (ECG) of an individual, wherein the segment is detected during a time interval that begins when an electrical shock is output to the individual's heart. The method further includes identifying a parameter of the electrical shock and generating a report including the segment of the ECG and indicating the parameter of the electrical shock. The report is output or transmitted to an external device.

First claim

What is claimed is:

1. A monitor-defibrillator, comprising:
a detection circuit configured to detect an electrocardiogram (ECG) of an individual;
a discharge circuit configured to output a first electrical shock to the individual at a first time and to output a second electrical shock to the individual at a second time, the second time being after the first time;
a display configured to output a report summarizing the first electrical shock, the first time, the second electrical shock, and the second time; and
a processor configured to:
identify a pre-shock segment of the ECG, the pre-shock segment being before the first time;
determine that the pre-shock segment of the ECG is indicative of a shockable arrhythmia, the shockable arrhythmia comprising ventricular fibrillation (VF) or ventricular tachycardia (VT);
based on determining that the pre-shock segment of the ECG is indicative of the shockable arrhythmia, cause the discharge circuit to output the first electrical shock;
identify a post-shock segment of the ECG, the post-shock segment beginning within ten seconds of the first time and ending before the second time;
determine that the post-shock segment of the ECG is indicative of the shockable arrhythmia temporarily resolving; and
in response to determining that the post-shock segment of the ECG is indicative of the shockable arrhythmia temporarily resolving, cause the discharge circuit to output the second electrical shock at the same vector as the first electrical shock.

2. The monitor-defibrillator of claim 1 , wherein the report further summarizes the same vector, the pre-shock segment of the ECG, the post-shock segment of the ECG, the pre-shock segment of the ECG being indicative of the shockable arrhythmia, and the post-shock segment of the ECG being indicative of the shockable arrhythmia temporarily resolving.

3. The monitor-defibrillator of claim 1 , the post-shock segment being a first post-shock segment, the same vector being a first vector, wherein the discharge circuit is configured to output a third electrical shock to the individual at a third time; and
wherein the processor is further configured to:
identify a second post-shock segment of the ECG, the second post-shock segment beginning within ten seconds of the second time and ending before the third time;
determine that the second post-shock segment of the ECG is indicative of the shockable arrhythmia failing to resolve; and
in response to determining that the second post-shock segment of the ECG is indicative of the shockable arrhythmia failing to resolve, cause the discharge circuit to output the third electrical shock at a second vector that is different than the first vector.

4. A medical device, comprising:
a detection circuit configured to detect an electrocardiogram (ECG) of an individual; and
a processor configured to:
identify a post-shock segment of the ECG, the post-shock segment beginning within a threshold time period of a first electrical shock being administered to the individual;
determine that the post-shock segment of the ECG is indicative of a non-shockable heart rhythm;
identify a pre-shock segment of the ECG, the pre-shock segment being detected after the post-shock segment and before a second electrical shock is administered to the individual;
determine that the pre-shock segment of the ECG is indicative of a shockable arrhythmia, the shockable arrhythmia comprising ventricular fibrillation (VF) or ventricular tachycardia (VT); and
in response to determining that the post-shock segment of the ECG is indicative of the non-shockable heart rhythm and that the pre-shock segment is indicative of the shockable arrhythmia:
output a report indicating that the arrhythmia has temporarily resolved; or
output a recommendation to administer the second electrical shock at a same shock parameter as the first electrical shock.

5. The medical device of claim 4 , wherein the shock parameter comprises an energy level, a voltage amplitude, a vector, a duration, a shape, or an electrode placement.

6. The medical device of claim 4 , wherein the threshold time period is between one second and one minute.

7. The medical device of claim 4 , wherein the processor is further configured to:
remove a chest compression artifact from the post-shock segment.

8. The medical device of claim 4 , wherein the processor is further configured to:
output an instruction to pause administration of chest compressions to the individual between a first time and a second time, and
wherein the post-shock segment of the ECG begins at the first time and ends at the second time.

9. The medical device of claim 4 , the post-shock segment being a first post-shock segment, wherein the processor is further configured to:
identify a second post-shock segment of the ECG, the second post-shock segment beginning within one second of the second electrical shock being administered to the individual;
determine that the second post-shock segment of the ECG is indicative of the arrhythmia failing to resolve; and
in response to determining that the second post-shock segment of the ECG is indicative of the arrhythmia failing to resolve:
modify the report to indicate that the arrhythmia has failed to resolve; or
output a recommendation to administer a third electrical shock at a different shock parameter than the same shock parameter of the first electrical shock and the second electrical shock.

10. The medical device of claim 4 , wherein the processor is further configured to:
identify a pre-shock segment of the ECG;
determine whether the pre-shock segment of the ECG is indicative of the arrhythmia; and
in response to determining whether the pre-shock segment of the ECG is indicative of the arrhythmia, output a report indicating whether the pre-shock segment of the ECG is indicative of the arrhythmia.

11. The medical device of claim 4 , further comprising:
a screen configured to visually present the report or the recommendation; or
a transceiver configured to transmit a signal comprising the report or the recommendation to an external device.

12. The medical device of claim 4 , further comprising:
a discharge circuit, wherein the processor further configured to cause the discharge circuit to output the second electrical shock in response to determining that the post-shock segment of the ECG is indicative of the non-shockable arrhythmia.

13. A method, comprising:
identifying a post-shock segment of an ECG of an individual, the post-shock segment beginning within a threshold time period of a first electrical shock being administered to the individual;
determining that the post-shock segment of the ECG is indicative of a non-shockable heart rhythm;
identify a pre-shock segment of the ECG, the pre-shock segment being detected after the post-shock segment and before a second electrical shock is administered to the individual;

determine that the pre-shock segment of the ECG is indicative of a shockable arrhythmia, the shockable arrhythmia comprising ventricular fibrillation (VF) or ventricular tachycardia (VT); and
in response to determining that the post-shock segment of the ECG is indicative of the non-shockable heart rhythm and determining that the pre-shock segment is indicative of the shockable arrhythmia:
outputting a report indicating that the arrhythmia has temporarily resolved; or
outputting a recommendation to administer the second electrical shock at a same shock parameter as the first electrical shock.

14. The method of claim 13 , wherein the shock parameter comprises an energy level, a voltage amplitude, a vector, a duration, a sh

Assignees

• Stryker Corp

Inventors

• Chapman Fred W
• Walker Robert G

Classifications

• A61B5/361 Primary

  Detecting fibrillation · CPC title

• A61N1/39044

  in combination with cardiopulmonary resuscitation [CPR] therapy · CPC title

• A61B5/363

  Detecting tachycardia or bradycardia · CPC title

• A61B5/742

  using visual displays (displays for heart-related electrical signals, e.g. ECG, A61B5/339) · CPC title

• A61N1/395

  for treating atrial fibrillation · CPC title