Insulin pump based expert system

US2019388015A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2019388015-A1
Application numberUS-201916560555-A
CountryUS
Kind codeA1
Filing dateSep 4, 2019
Priority dateMay 30, 2007
Publication dateDec 26, 2019
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

An apparatus including a controller can determine a rate of change of a blood glucose level of a subject from blood glucose data and determine if there is a risk of the blood glucose level going high or low.

First claim

Opening claim text (preview).

1 - 20 . (canceled) 21 . A system comprising: a pump configured to deliver insulin; an input configured to receive sensor glucose data representative of a blood glucose level of a user from a continuous glucose monitor via a wireless connection; and a controller communicatively coupled to the pump and the input, the controller configured to: monitor the sensor glucose data from the continuous glucose monitor; determine a rate of change of the blood glucose level and a current glucose level of the user from the sensor glucose data; compare the current glucose level of the user and the rate of change of the blood glucose level to a predetermined high glucose level; determine that a correction bolus should be delivered when the current glucose level of the user is not over the predetermined high glucose level but the rate of change indicates that there is a risk of the user going over the predetermined high glucose level in the future; automatically calculate the correction bolus; and cause the pump to deliver the correction bolus to the user. 22 . The system of claim 21 , wherein the controller is configured to automatically deliver the correction bolus. 23 . The system of claim 21 , wherein the controller is further configured to present a recommendation to deliver the correction bolus on a user interface and to deliver the correction bolus only after receiving a confirmation in response to the recommendation. 24 . The system of claim 21 , wherein the controller is configured to determine, based on a current blood glucose level of the user and the rate of change of the blood glucose level, that a correction bolus should be delivered if the blood glucose level is high and increasing at a certain rate. 25 . The system of claim 21 , wherein the controller is further configured to provide a notification to the user regarding the correction bolus. 26 . The system of claim 21 , wherein the controller, the input and the pump are part of a common device. 27 . The system of claim 21 , wherein the controller and the input are part of a handheld device that is separate from the pump. 28 . A system comprising: a pump configured to deliver insulin; an input configured to receive sensor glucose data representative of a blood glucose level of a user from a continuous glucose monitor via a wireless connection; and a controller communicatively coupled to the pump and the input, the controller configured to: monitor the sensor glucose data from the continuous glucose monitor; determine a rate of change of the blood glucose level of the user and a current glucose level from the sensor glucose data; compare the current glucose level of the user and the rate of change of the blood glucose level to a target glucose level; determine that a current insulin delivery pattern should be modified based on the current glucose level of the user and the rate of change of the blood glucose level; automatically calculate a modification to the insulin delivery pattern; and cause the pump to employ the modified insulin delivery pattern. 29 . The system of claim 28 , wherein the target glucose level is a predetermined high glucose level, and the controller is configured to determine that the current insulin delivery pattern should be modified when the current glucose level of the user is not over the predetermined high glucose level but the rate of change indicates that there is a risk of the user going over the predetermined high glucose level in the future. 30 . The system of claim 29 , wherein when the controller determines that the current insulin delivery pattern should be modified, the controller is configured to calculate the modification to the insulin delivery pattern by calculating an insulin correction bolus. 31 . The system of claim 28 , wherein the target glucose level is a predetermined low glucose level, and the controller is configured to determine that the current insulin delivery pattern should be modified when the current glucose level of the user is not below the predetermined high glucose level but the rate of change indicates that there is a risk of the user going below the predetermined high glucose level in the future. 32 . The system of claim 31 , wherein when the controller determines that the current insulin delivery pattern should be modified, the controller is configured to calculate the modification to the insulin delivery pattern by reducing an amount of insulin delivered. 33 . The system of claim 28 , wherein the controller comparing the current glucose level to a target glucose level includes comparing the current glucose level to a target range of glucose levels. 34 . The system of claim 28 , wherein the controller is configured to automatically deliver the modified insulin delivery pattern. 35 . The system of claim 28 , wherein the controller is further configured to present a recommendation to modify the insulin delivery pattern on a user interface and to deliver the modified insulin delivery pattern only after receiving a confirmation in response to the recommendation. 36 . The system of claim 28 , wherein the controller is further configured to provide a notification to the user regarding the modification to the insulin delivery pattern. 37 . The system of claim 28 , wherein the controller, the input and the pump are part of a common device. 38 . The system of claim 28 , wherein the controller and the input are part of a handheld device that is separate from the pump.

Assignees

Inventors

Classifications

  • with a programmable infusion control system, characterised by the infusion program · CPC title

  • User input or interface means, e.g. keyboard, pointing device, joystick · CPC title

  • combined with drug delivery · CPC title

  • Determining trends in physiological measurement data; Predicting development of a medical condition based on physiological measurements, e.g. determining a risk factor · CPC title

  • for local operation · CPC title

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Frequently asked questions

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What does patent US2019388015A1 cover?
An apparatus including a controller can determine a rate of change of a blood glucose level of a subject from blood glucose data and determine if there is a risk of the blood glucose level going high or low.
Who is the assignee on this patent?
Tandem Diabetes Care Inc
What technology area does this patent fall under?
Primary CPC classification A61B5/14532. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Dec 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).