System and method for electrocardiogram analysis and optimization of cardiopulmonary resuscitation and therapy delivery

Patent metadata

Field	Value
Publication number	US-12414721-B2
Application number	US-202418646184-A
Country	US
Kind code	B2
Filing date	Apr 25, 2024
Priority date	Mar 27, 2012
Publication date	Sep 16, 2025
Grant date	Sep 16, 2025

Abstract

The system and method provide for electrocardiogram analysis and optimization of patient-customized cardiopulmonary resuscitation and therapy delivery. An external medical device includes a housing and a processor within the housing. The processor can be configured to receive an input signal for a patient receiving chest compressions and to select at least one filter mechanism and to apply the filter mechanism to the signal to at least substantially remove chest compression artifacts from the signal. A real time dynamic analysis of a cardiac rhythm is applied to adjust and integrate CPR prompting of a medical device. Real-time cardiac rhythm quality is facilitated using a rhythm assessment meter.

First claim

The invention claimed is:

1. A defibrillator, comprising:
a measurement circuit configured to generate electrocardiogram (ECG) data by detecting an ECG signal of a patient receiving chest compressions from a mechanical chest compression device between a first time and a second time;
a capacitor configured to store energy;
a power source configured to charge the capacitor;
a discharge circuit configured to output a defibrillation shock by discharging the energy stored in the capacitor;
a processor connected to the measurement circuit and to the power source; and
memory storing instructions that, when executed by the processor, cause the processor to perform operations comprising:
generating filtered ECG data by removing, from the ECG data, an artifact associated with the chest compressions using a comb filter;
determining, by analyzing the filtered ECG data, that a heart rhythm of the patient is indicative of ventricular fibrillation (VF); and
in response to determining that the heart rhythm is indicative of VF, causing the power source to charge the capacitor before the second time.

2. The defibrillator of claim 1 , wherein determining, by analyzing the filtered ECG data, that the heart rhythm of the patient is shockable comprises:
determining a shock index by determining a median frequency of the filtered ECG data; and
comparing the shock index to a threshold.

3. The defibrillator of claim 1 , wherein the operations further comprise:
in response to causing the power source to charge the capacitor before the second time, causing the discharge circuit to output the defibrillation shock by discharging the energy stored in the capacitor before the second time.

4. A medical device, comprising:
a measurement circuit configured to generate physiological parameter data by detecting a physiological parameter of a patient; and
a processor configured to:
generate filtered physiological parameter data by removing, from the physiological parameter data, an artifact associated with chest compressions applied to the patient;
determine, by analyzing the filtered physiological parameter data, that a heart rhythm of the patient is treatable by an electric shock; and
in response to determining that the heart rhythm is treatable by the electric shock, cause a power source to charge a capacitor.

5. The medical device of claim 4 , wherein the physiological parameter comprises an electrocardiogram (ECG) or an electrical impedance.

6. The medical device of claim 4 , wherein removing, from the physiological parameter data, the artifact associated with the chest compressions applied to the patient comprises:
applying a comb filter to the physiological parameter data.

7. The medical device of claim 4 , wherein the processor is configured to determine, by analyzing the filtered physiological parameter data, that the heart rhythm of the patient is treatable by the electric shock by:
determining a shock index by determining a median frequency of the filtered physiological parameter data; and
comparing the shock index to a threshold.

8. The medical device of claim 7 , wherein the processor is further configured to:
determine whether a previous shock has been administered to the patient; and
determine the threshold by analyzing whether the previous shock has been administered to the patient.

9. The medical device of claim 4 , wherein the processor is configured to determine, by analyzing the filtered physiological parameter data, that the heart rhythm of the patient is treatable by the electric shock by:
determining a first shock index by analyzing a first portion of the filtered physiological parameter data;
determining that the heart rhythm indicated by the first portion of the filtered physiological parameter data is indeterminate by determining that the first shock index is greater than a first threshold and less than a second threshold;
in response to determining that the heart rhythm indicated by the first portion of the filtered physiological parameter data is indeterminate, determining a second shock index by analyzing a second portion of the filtered physiological parameter data; and
determining that the heart rhythm of the patient is treatable by an electric shock by determining that the second shock index is greater than the first threshold and greater than the second threshold.

10. The medical device of claim 9 , wherein the processor is further configured to:
determine that greater than a threshold amount of the chest compressions have been performed on the patient,
wherein the first portion of the filtered physiological parameter data corresponds to a portion of the physiological parameter data generated by the measurement circuit after the processor determines that greater than the threshold amount of the chest compressions have been performed on the patient.

11. The medical device of claim 4 , wherein determining, by analyzing the filtered physiological parameter data, that the heart rhythm of the patient is treatable by an electric shock comprises determining that the filtered physiological parameter data is indicative of ventricular fibrillation (VF).

12. The medical device of claim 4 , wherein the chest compressions are applied to the patient continuously between a first time and a second time, and
wherein causing the power source to charge the capacitor occurs before the second time.

13. The medical device of claim 12 , wherein the processor is further configured to:
in response to causing the power source to charge the capacitor before the second time, causing a discharge circuit to output an electrical shock to the patient by discharging energy stored in the capacitor before the second time.

14. The medical device of claim 13 , wherein causing the discharge circuit to output the electrical shock to the patient by discharging the energy stored in the capacitor before the second time is further in response to receiving an input from a user.

15. A system, comprising:
a mechanical chest compression device configured to administer chest compressions to a patient during a time period extending from a first time to a second time; and
a medical device comprising:
a measurement circuit configured to generate physiological parameter data by detecting a physiological parameter of a patient; and
a processor configured to:
generate filtered physiological parameter data by removing, from the physiological parameter data, an artifact associated with the chest compressions applied to the patient;
determine, by analyzing the filtered physiological parameter data, that a heart rhythm of the patient is treatable by an electric shock; and
in response to determining that the heart rhythm is treatable by the electric shock, cause a power source to charge a capacitor.

16. The system of claim 15 , wherein the mechanical chest compression device is further configured to output an indication of a frequency of the chest compressions to the medical device,
wherein the processor is configured to generate a filter defined by the frequency of the chest compressions, and
wherein the processor is configured to generate the filtered physiological parameter data by applying the filter to the physiological parameter data.

17. The system of claim 15 , wherein the filter comprises a comb filter.

18. The system of claim 15 , wherein the processor is configured to determine, by analyzing the filtered physiological parameter data, that the heart rhythm of the patient is treatable by the electric shock by:
determining a shock index by determi

Assignees

• Physio Control Inc

Inventors

• Sullivan Joseph L
• Stickney Ronald Eugene
• Walker Robert G
• Piraino Daniel W
• Banville Isabelle
• Chapman Fred

Classifications

• A61B5/347

  Detecting the frequency distribution of signals · CPC title

• A61B5/339 Primary

  Displays specially adapted therefor · CPC title

• A61B5/7217 Primary

  of noise originating from a therapeutic or surgical apparatus, e.g. from a pacemaker · CPC title

• A61N1/3993

  User interfaces for automatic external defibrillators · CPC title

• A61N1/3987

  characterised by the timing or triggering of the shock · CPC title