AUTOMATIC DISABLING OF ALERTS FOR DIABETIC CONDITIONS
In general, techniques are described for automatic disablement of alerts for diabetic conditions. A device including a memory and a processor may be configured to perform the techniques. The memory may store alert data. The processor may obtain projected levels of glucose in a patient over a time frame, and determine whether the projected levels of glucose leave a prescribed range. The processor may generate, when the projected levels of glucose in the patient leave the prescribed range during the time frame and based on the alert data, a graphical alert indicating that the projected levels of glucose will leave the prescribed range. The processor may further determine that a maintenance event alters the projected levels of glucose, and disable, without user input and based on the determination that the maintenance event alters the projected levels of glucose, the graphical alert for a temporary period of time.
1 . A device for assisting in therapy delivery, the device comprising:
a memory configured to store alert data, and
one or more processors configured to:
obtain projected levels of glucose in a patient over a time frame;
determine whether the projected levels of glucose leave a prescribed range;
generate, when the projected levels of glucose in the patient leave the prescribed range during the time frame and based on the alert data, a graphical alert indicating that the projected levels of glucose will leave the prescribed range;
determine that a maintenance event alters the projected levels of glucose such that the projected levels of glucose do not leave the prescribed range; and
disable, without user input and based on the determination that the maintenance event alters the projected levels of glucose such that the projected levels of glucose do not leave the prescribed range, the graphical alert for a temporary period of time.
2 . The device of claim 1 , wherein the one or more processors are configured to:
obtain, from a glucose sensor, a current level of glucose in the patient; and
obtain, based on the current level of glucose, the projected levels of glucose in the patient over the time frame.
3 . The device of claim 1 , wherein the one or more processors are, when determining that the maintenance event alters the projected levels of glucose, configured to:
automatically detect a meal event indicating that the patient is currently eating a meal,
obtain, based on the meal event, a revised version of the projected levels of glucose; and
determine that the revised version of the projected levels of glucose do not leave the prescribed range.
4 . The device of claim 3 , wherein the one or more processors are configured to:
interface with a wearable computing device worn by the patient to identify movements performed by the patient and
automatically detect, based on the move tints, the mal event indicating that the patient is currently eating a meal.
5 . The device of claim 1 , wherein the one or more processors are, when determining that the maintenance event alters the projected levels of glucose, configured to:
automatically detect an insulin delivery event indicating that the patient has injected insulin;
obtain, based on the insulin delivery event, a revised version of the projected levels of glucose; and
determine that the revised version of the projected levels of glucose do not leave the prescribed range.
6 . The device of claim 1 ,
wherein the maintenance event is a first maintenance event, and
wherein the one or more processors are further configured to:
detect initiation of a second maintenance event;
determine an amount associated with the second maintenance event; and
determine, based on the amount associated with the second maintenance event, that the projected levels of glucose will leave the prescribed range.
7 . The device of claim 6 , wherein the one or more processors are further configured to:
present the graphical alert along with an audible alert to the patient,
present, responsive to determining that the projected levels of glucose will leave the prescribed range, a haptic alert in place of the audible alert such that the audible alert is disabled for the temporary period of time.
8 . The device of claim 1 , wherein the one or more processors are further configured to:
determine a duration until the projected levels of glucose are projected to leave the prescribed range; and
determine, based on the duration, the temporary period of time by which to automatically disable the graphical alert.
9 . The device of claim 1 , wherein the graphical alert further includes a prompt for a user to disable the graphical alert for the temporary period of time via user input.
10 . The device of claim 9 , wherein the one or more processors are configured to:
determine a duration until the projected levels of glucose are projected to leave the prescribed range; and
determine, based on the duration, the temporary period of time by which to automatically disable the graphical alert.
11 . The device of claim 1 , wherein the prescribed range includes values between a lower threshold identifying a hypoglycemic condition for the patient and an upper threshold identifying a hyperglycemic condition for the patient.
12 . A method for assisting in therapy delivery, the method comprising:
obtaining, by one or more processors, projected levels of glucose in a patient over a time frame;
determining, by the one or more processors, whether the projected levels of glucose leave a prescribed range;
generating, by the one or more processors, when the projected levels of glucose in the patient leave the prescribed range, and based on alert data, a graphical alert indicating that the projected levels of glucose will leave the prescribed range;
determine, by the one or more processors, that a maintenance event alters the projected levels of glucose such that the projected levels of glucose do not leave the prescribed range; and
automatically disabling, by the one or more processors and based on the determination that the maintenance event alters the projected levels of glucose such that the projected levels of glucose do not leave the prescribed range, the graphical alert for a temporary period of time.
13 . The method of claim 12 , wherein obtaining the projected levels of glucose comprises:
obtaining, from a glucose sensor, a current level of glucose in the patient; and
obtaining, based on the current level of glucose, the projected levels of glucose in the patient over the time frame.
14 . The method of claim 12 , wherein determining that the maintenance event alters the projected levels of glucose comprises:
automatically detecting a meal event indicating that the patient is currently eating a meal;
obtaining, based on the meal event, a revised version of the projected levels of glucose; and
determining that the revised version of the projected levels of glucose do not leave the prescribed range.
15 . The method of claim 14 , wherein automatically detecting the meal event comprises:
interfacing with a wearable computing device worn by the patient to identify movements performed by the patient; and
automatically detecting, based on the movements, the meal event indicating that the patient is currently eating a meal.
16 . The method of claim 12 , wherein determining that the maintenance event alters the projected levels of glucose comprises:
automatically detecting an insulin delivery event indicating that the patient has injected insulin;
obtaining, based on the insulin delivery event, a revised version of the projected levels of glucose; and
determining that the revised version of the projected levels of glucose do not leave the prescribed range.
17 . The method of claim 12 ,
wherein the maintenance event is a first maintenance event, and
wherein the method further comprises:
detecting initiation of a second maintenance event:
determining; an amount associated with the second maintenance event; and
determining, based on the amount associated with the second maintenance event, that the projected levels of glucose will leave the prescribed range.
18 . The method of claim 17 , further comprising;
presenting the graphical alert along with an audible alert to the patient,
presenting, responsive to determining that the projected levels of glucose will leave the prescribed range, a haptic alert in place of the audible alert such that the audible alert is disabled for the temporary period of time.
19 . The method of claim 12 , further comprising:
determining a duration until the projected levels of glucose are projected to leave the prescribed range; and
determining, based on the duration, the temporary period of time by which to automatically disable the graphical alert.
20 . A non-transitory computer-readable storage medium having instructions stored thereon that, when executed, cause one or more processors to:
obtain projected levels of glucose in a patient over a time frame;
determine whether the projected levels of glucose leave a prescribed range;
generate, when the projected levels of glucose in the patient leave the prescribed range and based on an alert template, a graphical alert indicating that the projected levels of glucose will leave the prescribed range:
determine that a maintenance event alters the projected levels of glucose such that the projected levels of glucose do not leave the prescribed range; and
automatically disable, based on the determination that the maintenance event alters the projected levels of glucose such that the projected levels of glucose do not leave the prescribed range, the graphical alert for a temporary period of time.