Detection of reduced defibrillation pad contact

• US 9,427,597 B2
• Filed: 03/06/2014
• Issued: 08/30/2016
• Est. Priority Date: 03/07/2013
• Status: Active Grant

• Current Assignee: Zoll Medical Corporation (Asahi Kasei Corporation)
• Original Assignee: Zoll Medical Corporation (Asahi Kasei Corporation)
• Inventors: Herken, Ulrich
• Primary Examiner(s): Lee, Erica
• Application Number:
  US14/199,344
• Publication Number:
  US 20140257422A1
• Time in Patent Office: 908 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: A61N 1/046 Specially adapted for shock therapy, e.g. defibrillation
• CPC Class Codes: A61N 1/3925 Monitoring; Protecting
• CPC Class Codes: A61N 1/3931 Protecting, e.g. back-up systems
• CPC Class Codes: A61N 1/3993 User interfaces for automatic external defibrillators

Abstract

A system and method of detecting a loss of electrical contact between a pair of electrodes that are electrically coupled to skin of a subject. The method includes monitoring parameters of a transthoracic impedance between the pair of electrodes in at least one of a low frequency regime and a high frequency regime, detecting an occurrence of chest compressions based on a signal indicative of chest compressions, establishing baseline levels of the parameters in at least one of the low and high frequency regimes, detecting whether changes in at least one parameter exceeds the baseline level by a threshold, determining that at least one electrode of the pair of electrodes is losing electrical contact with the skin responsive to the at least one parameter exceeding the baseline level by the threshold, and issuing an alert in response to a determination that the at least one electrode is losing electrical contact.

Claims

1. A life support device, comprising:

a pair of electrodes configured to be attached to a skin of a subject;

a therapy interface electrically coupled to the pair of electrodes; and

a transthoracic impedance monitor electrically coupled to the therapy interface, the transthoracic impedance monitor being configured

to monitor transthoracic impedance parameters of a transthoracic impedance signal between the pair of electrodes over time, wherein the transthoracic impedance signal has a high frequency waveform component that varies with a frequency of CPR chest compressions, and wherein the transthoracic impedance parameters include at least one of a slope of the high frequency waveform component of the transthoracic impedance signal, a shape of the high frequency waveform component of the transthoracic impedance signal, and a relative energy content of the high frequency waveform component of the transthoracic impedance signal at a fundamental frequency of the transthoracic impedance signal and/or at a harmonic of the fundamental frequency of the transthoracic impedance signal,

to establish baseline levels of the transthoracic impedance parameters,

to detect whether changes over time in at least one transthoracic impedance parameter exceeds a corresponding baseline level by a threshold,

to determine that at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject in response to detecting that the changes in the at least one transthoracic impedance parameter exceeds the corresponding baseline level by the threshold, and

to issue an alert in response to a determination that the at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject.

2. The life support device of claim 1, further comprising:

a user interface including at least one of an audio output device and a video output device; and

at least one processor, electrically coupled to the therapy interface, the transthoracic impedance monitor, and user interface, the at least one processor being configured to present a message on the at least one of the audio output device and the video output device in response to receiving the alert.

3. The life support device of claim 2, wherein the message indicates that the at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject.

4. The life support device of claim 3, wherein the transthoracic impedance monitor is configured to identify the frequency of the CPR chest compressions based on a fundamental frequency of the transthoracic impedance signal.

5. The life support device of claim 1, wherein the transthoracic impedence monitor is further configured to detect CPR chest compressions based on a signal indicative of the CPR chest compressions.

6. The life support device of claim 5, wherein the transthoracic impedance monitor is configured to receive the signal indicative of the frequency of the CPR chest compressions from one of a compression sensor and a mechanical chest compression device and to identify the frequency of the CPR chest compressions based on the signal.

7. The life support device of claim 6, wherein the transthoracic impedance monitor is further configured to correlate at least one of the slope of the high frequency waveform component of the transthoracic impedance signal and the shape of the high frequency waveform component of the transthoracic impedance signal with the frequency of the CPR chest compressions.

8. The life support device of claim 7, further comprising a filter electrically coupled to the therapy interface, the filter being configured to filter out frequencies of the high frequency waveform component of the transthoracic impedance signal that do not correspond to the frequency of the CPR chest compressions and harmonics thereof.

9. The life support device of claim 8, wherein the transthoracic impedance parameters further include an amount of background noise at frequencies other than a frequency of the high frequency waveform component and harmonics of the high frequency waveform component.

10. The life support device of claim 9, wherein the transthoracic impedance parameters further include an amplitude of the transthoracic impedance signal.

11. A method of detecting a loss of electrical contact between at least one electrode of a pair of electrodes that are electrically coupled to a skin of a subject, comprising acts of:

monitoring transthoracic impedance parameters of a transthoracic impedance signal between the pair of electrodes, wherein the transthoracic impedance signal has a high frequency waveform component that varies with a frequency of CPR chest compressions, and wherein the transthoracic impedance parameters include at least one of a slope of the high frequency waveform component of the transthoracic impedance signal, a shape of the high frequency waveform component of the transthoracic impedance signal, and a relative energy content of the high frequency waveform component of the transthoracic impedance signal at a fundamental frequency of the transthoracic impedance signal and/or at a harmonic of the fundamental frequency of the transthoracic impedance signal;

establishing baseline levels of the transthoracic impedance parameters;

detecting whether changes in at least one transthoracic impedance parameter exceeds the a corresponding baseline level by a threshold;

determining, prior to loss of electrical contact between the at least one electrode of the pair of electrodes and the skin of the subject, that the at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject in response to the at least one transthoracic impedance parameter exceeding the corresponding baseline level by the threshold; and

issuing an alert in response to a determination that the at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject.

12. The method of claim 11, further comprising detecting an occurrence of CPR chest compressions based upon a signal indicative of the CPR chest compressions.

13. The method of claim 12, wherein the act of detecting an occurrence of CPR chest compressions includes one of analyzing the transthoracic impedance signal to identify the frequency of the CPR chest compressions based on a fundamental frequency of the transthoracic impedance signal and receiving the signal indicative of the CPR chest compressions from one of a compression sensor and a mechanical chest compression device and identifying the frequency of the CPR chest compressions based on the signal.

14. The method of claim 13, further comprising an act of correlating at least one of the slope of the high frequency waveform component of the transthoracic impedance signal and the shape of the waveform of the transthoracic impedance signal with the frequency of the CPR chest compressions.

15. The method of claim 14, further comprising an act of filtering frequencies of the high frequency waveform component of the transthoracic impedance signal that do not correspond to the frequency of the CPR chest compressions and harmonics thereof.

16. The method of claim 15, wherein the act of monitoring transthoracic impedance parameters further includes monitoring an amount of background noise at frequencies other than a frequency of the high frequency waveform component and harmonics of the high frequency component.

17. The method claim 12, further comprising acts of:

determining whether the signal indicative of the CPR compressions is from one of a compression sensor and a mechanical chest compression device; and

adjusting the threshold in response to a determination that the signal is from one of the compression sensor and the mechanical chest compression device.

18. A life support device, comprising:

a pair of electrodes configured to be attached to a skin of a subject;

a therapy interface electrically coupled to the pair of electrodes; and

a transthoracic impedance monitor electrically coupled to the therapy interface, the transthoracic impedance monitor being configured to

monitor transthoracic impedance parameters of a transthoracic impedance signal between the pair of electrodes, wherein the transthoracic impedance signal has a high frequency waveform component that varies with a frequency of CPR chest compressions, and wherein the transthoracic impedance parameters include at least one of a slope of the high frequency waveform component of the transthoracic impedance signal, a shape of the high frequency waveform component of the transthoracic impedance signal, and a relative energy content of the high frequency waveform component of the transthoracic impedance signal at a fundamental frequency of the transthoracic impedance signal and/or at a harmonic of the fundamental frequency of the transthoracic impedance signal,

to establish baseline levels of the transthoracic impedance parameters,

to detect whether changes in at least one transthoracic impedance parameter exceeds a corresponding baseline level by a threshold,

to determine that at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject in response to detecting that the changes in the at least one transthoracic impedance parameter exceeds the corresponding baseline level by the threshold, and

to issue an alert in response to a determination that the at least one electrode of the pair of electrodes is losing electrical contact with the skin of the subject.