Systems and methods for testing a medical device

1. An ambulatory medical device configured to perform self-testing during continuous patient monitoring, the ambulatory medical device comprising:

sensing circuitry configured to be coupled to a patient for detecting an electrocardiogram (ECG) signal of the patient continuously over an extended period of time; and

at least one processor operably coupled to the sensing circuitry, the at least one processor configured to:

receive the ECG signal of the patient from the sensing circuitry,

analyze the ECG signal throughout a patient monitoring period to determine one or more cardiac events experienced by the patient,

monitor for one or more self-test triggering events during the patient monitoring period,

detect at least one of the one or more self-test triggering events during the patient monitoring period, and

initiate one or more self-tests based upon detection of the at least one of the one or more self-test triggering events.

2. The ambulatory medical device of claim 1 , wherein the detected at least one of the one or more self-test triggering events comprises a detected change in ECG signal quality.

3. The ambulatory medical device of claim 2 , wherein the at least one processor is configured to initiate the one or more self-tests by being further configured to determine if the detected change in ECG signal quality is a result of one or more of noise caused by electrode movement or electrode falloff.

4. The ambulatory medical device of claim 1 , further comprising a response button operably coupled to the at least one processor and configured to receive an input from the patient in response to one or more alerts issued by the ambulatory medical device.

5. The ambulatory medical device of claim 4 , wherein the detected at least one of the one or more self-test triggering events comprises a detected number of inputs from the patient received by the at least one processor from the response button.

6. The ambulatory medical device of claim 5 , wherein the at least one processor is configured to initiate the one or more self-tests by being further configured to initiate a test of one or more parameters associated with cardiac arrythmia monitoring and detection.

7. The ambulatory medical device of claim 1 , wherein the at least one processor is further configured to:

identify at least one component of the ambulatory medical device to self-test based upon the detected at least one of the one or more self-test triggering events;

initiate a self-test of the at least one identified component; and

generate a set of test results based upon the self-test of the at least one identified component.

8. The ambulatory medical device of claim 7 , wherein the at least one processor is further configured to:

determine, based on the set of test results, whether the at least one identified component of the ambulatory medical device has experienced a critical error, and at least one of provide a notification of the critical error to the patient and transmit the set of test results to a remote server for storage and analysis.

9. The ambulatory medical device of claim 1 , further comprising self-test circuitry operably coupled to the at least one processor and configured to perform at least one of the one or more self-tests.

10. The ambulatory medical device of claim 9 , wherein the at least one processor is at least one first processor and the self-test circuitry comprises at least one second processor separate from the at least one first processor.

11. The ambulatory medical device of claim 1 , wherein the extended period of time is between two and three months.

12. A method for performing self-testing of an ambulatory medical device during continuous patient monitoring, the ambulatory medical device comprising:

receiving, by at least one processor, an electrocardiogram (ECG) signal of a patient from sensing circuitry operably coupled to the at least one processor and configured to be coupled to the patient for detecting the ECG signal of the patient continuously over an extended period of time;

analyzing, by the at least one processor, the ECG signal throughout a patient monitoring period to determine one or more cardiac events experienced by the patient;

monitoring, by the at least one processor, for one or more self-test triggering events during the patient monitoring period;

detecting, by the at least one processor, at least one of the one or more self-test triggering events during the patient monitoring period; and

initiating, by the at least one processor, one or more self-tests based upon detection of the at least one of the one or more self-test triggering events.

13. The method of claim 12 , wherein detecting at least one of the one or more self-test triggering events comprises detecting, by the at least one processor, a change in ECG signal quality.

14. The method of claim 13 , wherein the one or more self-tests are initiated by determining if the detected change in ECG signal quality is a result of one or more of noise caused by electrode movement or electrode falloff.

15. The method of claim 12 , further comprising receiving, by the at least one processor via a response button operably coupled to the at least one processor, an input from the patient in response to one or more alerts issued by the ambulatory medical device.

16. The method of claim 15 , wherein detecting at least one of the one or more self-test triggering events comprises detecting, by the at least one processor, a number of inputs from the patient received by the at least one processor from the response button.

17. The method of claim 16 , wherein initiating one or more self-tests comprises initiating, by the at least one processor, a test of one or more parameters associated with cardiac arrythmia monitoring and detection.

18. The method of claim 12 , further comprising:

identifying, by the at least one processor, at least one component of the ambulatory medical device to self-test based upon the detected at least one of the one or more self-test triggering events;

initiating, by the at least one processor, a self-test of the at least one identified component; and

generating, by the at least one processor, a set of test results based upon the self-test of the at least one identified component.

19. The method of claim 18 , further comprising:

determining, by the at least one processor, whether the at least one identified component of the ambulatory medical device has experienced a critical error based on the set of test results, and

at least one of providing, by the at least one processor, a notification of the critical error to the patient and transmitting, by the at least one processor, the set of test results to a remote server for storage and analysis.

20. The method of claim 12 , wherein the extended period of time is between two and three months.