Granted Patent B2

US 12,350,505 · App. 17/559,925 · Granted Jul 8, 2025

Inventors: Fred W. Chapman (Newcastle, WA); Ryan William Apperson (Bothell, WA); Dale R. Beuning (Seattle, WA); Steven Barry Duke (Bothell, WA); Thangeswaran Natarajan (Bothell, WA); Daniel W Piraino (Seattle, WA); Mark Rutzer (Seattle, WA); David B. Stewart (Carnation, WA); Tyson G. Taylor (Bothell, WA)

Assignee: Stryker Corporation

A61N1/39044A61N1/3925

Abstract

Claims (86)

1. An external defibrillator, comprising:

a detection circuit configured to detect an electrocardiogram (ECG) of an individual;

a capacitor;

a battery configured to charge the capacitor;

a discharge circuit configured to discharge the capacitor;

a processor; and

memory storing instructions that, when executed by the processor, cause the processor to perform operations comprising:

identifying an end time of a cardiopulmonary resuscitation (CPR) period, wherein the individual is receiving chest compressions during the CPR period;

predicting a duration of a charging period of the capacitor based on a charge level of the battery, a capacitance of the capacitor, a temperature of the external defibrillator, and a dosage level of a defibrillation shock;

determining, based on the end time of the CPR period and the duration of the charging time of the capacitor, a start time of an analysis period;

identifying a segment of the ECG obtained during the analysis period, the analysis period occurring between the start time and an intermediate time;

generating a filtered ECG by removing a chest compression artifact from the segment of the ECG;

determining that the filtered ECG exhibits ventricular fibrillation (VF);

in response to determining that the filtered ECG exhibits the VF, causing the battery to charge the capacitor during the charging period such that the capacitor is charged at the end time of the CPR period; and

causing the discharge circuit to discharge energy stored in the capacitor to the individual as the defibrillation shock at the end of the CPR period.

2. The external defibrillator of claim 1 , further comprising:

a display configured to visually output a recommendation;

an input device configured to receive an input signal from a user,

wherein the operations further comprise:

generating the recommendation based on determining that the filtered ECG exhibits the shockable rhythm, and

wherein causing the discharge circuit to discharge the energy stored in the capacitor to the individual is in response to the input device receiving the input signal.

3. The external defibrillator of claim 1 , wherein a time period between the start time of the analysis period and the end time of the CPR period is greater than or equal to a sum of the charging period and the analysis period.

4. A medical device, comprising:

a detection circuit configured to detect an electrocardiogram (ECG) of an individual;

a capacitor;

a battery configured to charge the capacitor;

a processor; and

memory storing instructions that, when executed by the processor, cause the processor to perform operations comprising:

identifying an end time of a cardiopulmonary resuscitation (CPR) period, the individual receiving chest compressions during the CPR period;

determining a length of a charging period of the capacitor based on a charge level of the battery;

determining, based on the length of the charging period of the capacitor, a start time of an analysis period;

identifying, during the analysis period and the CPR period, a segment of the ECG;

determining that the segment of the ECG comprises a shockable rhythm; and

in response to determining that the segment of the ECG comprises the shockable rhythm, causing the battery to charge the capacitor such that the capacitor is charged at the end time of the CPR period.

5. The medical device of claim 4 , further comprising:

a temperature sensor configured to detect a temperature of the medical device,

wherein determining the length of the charging period of the capacitor is based on a capacitance of the capacitor, an internal resistance of the battery, the temperature of the medical device, a dosage level of a defibrillation shock, an impedance of the individual, or a combination thereof.

6. The medical device of claim 4 , wherein the operations further comprise:

predicting a length of the analysis period,

wherein determining the start time of the analysis period is further based on the length of the analysis period.

7. The medical device of claim 4 , wherein determining that the segment of the ECG comprises the shockable rhythm comprises:

generating a filtered ECG by removing a chest compression artifact from the segment of the ECG;

generating a shock index based on the filtered ECG; and

comparing the shock index to a threshold.

8. The medical device of claim 4 , wherein the capacitor is charged within ten seconds before the end time of the CPR period.

9. The medical device of claim 4 , wherein a time period between the start time of the analysis period and the end time of the CPR period is greater than or equal to a sum of the length of the charging period and a length of the analysis period.

10. The medical device of claim 4 , further comprising:

a discharge circuit configured to discharge the capacitor; and

electrodes connected to the skin of the individual,

wherein the operations further comprise:

causing the discharge circuit to discharge energy stored in the charged capacitor to the electrodes.

11. The medical device of claim 10 , further comprising:

an output device configured to output a recommendation to administer a defibrillation shock; and

an input device configured to receive an input signal,

wherein the operations further comprise:

determining that the capacitor is charged;

based on determining that the capacitor is charged, causing the output device to output the recommendation to administer the defibrillation shock; and

receiving an input signal based on the recommendation, and

wherein causing the discharge circuit to discharge the energy stored in the charged capacitor to the electrodes is in response to receiving the input signal.

12. The medical device of claim 10 , wherein the discharge circuit comprises first switches, and

wherein causing the discharge circuit to discharge the energy stored in the charged capacitor to the electrodes comprises:

disconnecting the battery from the capacitor by opening a second switch; and

connecting the capacitor to the electrodes by closing the first switches in the discharge circuit.

13. A method performed by a medical device, the method comprising:

identifying an end time of a cardiopulmonary resuscitation (CPR) period, wherein an individual is receiving chest compressions during the CPR period;

determining, based on a charge level of a battery, a length of a charging period of a capacitor of the medical device;

determining, based on the end time of the CPR period and the length of the charging period of the capacitor, a start time of an analysis period that overlaps the CPR period;

identifying, during the analysis period, a segment of an electrocardiogram (ECG) of the individual;

determining that the segment of the ECG comprises a shockable rhythm; and

based on determining that the segment of the ECG comprises the shockable rhythm, charging the capacitor during the charging period by connecting the battery to the capacitor, the capacitor being charged at the end time of the CPR period.

14. The method of claim 13 , wherein determining the charging period of the capacitor comprises determining a capacitance of the capacitor, determining an internal resistance of the battery, determining a temperature of the medical device, determining a dosage level of a defibrillation shock, determining an impedance of the individual, or a combination thereof.

15. The method of claim 13 , further comprising:

determining a length of the analysis period,

wherein determining the start time of the analysis period is further based on the length of the analysis period.

16. The method of claim 13 , wherein determining that the segment of the ECG comprises the shockable rhythm comprises:

generating a filtered ECG by removing a chest compression artifact from the segment of the ECG;

generating a shock index based on the filtered ECG; and

comparing the shock index to a threshold.

17. The method of claim 13 , wherein the capacitor is charged within ten seconds before the end time of the CPR period.

18. The method of claim 13 , wherein a time period between the start time of the analysis period and the end time of the CPR period is greater than or equal to a sum of the length of the charging period and a length of the analysis period.

19. The method of claim 13 , further comprising:

administering a defibrillation shock to the individual by discharging the charged capacitor.

20. The method of claim 19 , further comprising:

outputting a recommendation to administer the defibrillation shock; and

receiving an input signal based on the recommendation,

wherein administering the defibrillation shock to the individual by discharging the capacitor is in response to receiving the input signal.

Assignments (2)

Continuity (2)

References Cited (106)