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公开(公告)号:US20190336684A1
公开(公告)日:2019-11-07
申请号:US16404456
申请日:2019-05-06
Applicant: Insulet Corporation
Inventor: Jason O'CONNOR , Joon Bok LEE , Trang LY , Yibin ZHENG , Thomas Arnold PEYSER , Jennifer Lena SCHNEIDER
Abstract: Disclosed are a system, methods and computer-readable medium products that provide safety constraints for an insulin-delivery management program. Various examples provide safety constraints for a control algorithm-based drug delivery system that provides automatic delivery of a drug based on sensor input. Glucose measurement values may be received at regular time intervals from a sensor. A processor may predict future glucose values based on prior glucose measurement values. The safety constraints assist in safe operation of the drug delivery system during various operational scenarios. In some examples, predicted future glucose values may be used to implement safety constraints that mitigate under-delivery or over-delivery of the drug while not overly burdening the user of the drug delivery system and without sacrificing performance of the drug delivery system. Other safety constraints are also disclosed.
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公开(公告)号:US20190038835A1
公开(公告)日:2019-02-07
申请号:US16049388
申请日:2018-07-30
Applicant: Insulet Corporation
Inventor: David NAZZARO , Ian MCLAUGHLIN , Daniel ALLIS , Jason O'CONNOR
Abstract: A fluid flow regulator of a fluid delivery system that can adjust a flow rate of a liquid drug dispensed from a liquid drug container to a user is provided. The fluid flow regulator can be coupled to an end of the liquid drug container. The fluid flow regulator can include a compliance plate and a flow channel selector plate having a fluid flow channel. The flow channel selector plate can be rotated relative to the compliance plate and the liquid drug container to expose a selected portion of the fluid flow channel to openings in the compliance plate that are in fluid communication with the liquid drug stored in the liquid drug container. The selected portion of the fluid flow channel can correspond to a corresponding flow resistance of the liquid drug through the fluid flow channel, thereby regulating the flow of the liquid drug to the user.
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公开(公告)号:US20240293617A1
公开(公告)日:2024-09-05
申请号:US18436410
申请日:2024-02-08
Applicant: INSULET CORPORATION
Inventor: Joon Bok LEE , Mengdi LI , Jason O'CONNOR , Yibin ZHENG
IPC: A61M5/172 , G16H10/40 , G16H10/60 , G16H20/17 , G16H40/60 , G16H40/67 , G16H50/20 , G16H50/30 , G16H50/50 , G16H50/70 , H04L67/141
CPC classification number: A61M5/1723 , G16H10/40 , G16H10/60 , G16H20/17 , G16H40/60 , G16H40/67 , G16H50/20 , G16H50/30 , G16H50/50 , G16H50/70 , A61M2202/07 , A61M2205/3584 , A61M2205/50 , A61M2205/502 , A61M2230/20 , A61M2230/201 , H04L67/141
Abstract: Disclosed are techniques to establish initial settings for an automatic insulin delivery device. An adjusted total daily insulin (TDI) factor usable to calculate a TDI dosage may be determined. The adjusted TDI factor may be a TDI per unit of a physical characteristic of the user (e.g., weight) times a reduction factor. The adjusted TDI factor may be compared to a maximum algorithm delivery threshold. Based on the comparison result, the application or algorithm may set a TDI dosage and output a control signal. Blood glucose measurement values may be collected from a sensor over a period of time. A level of glycated hemoglobin of the blood may be determined based on the obtained blood glucose measurement values. In response to the level of glycated hemoglobin, the set TDI dosage may be modified. A subsequent control signal including the modified TDI dosage may be output to actuate delivery of insulin.
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公开(公告)号:US20240148971A1
公开(公告)日:2024-05-09
申请号:US18386647
申请日:2023-11-03
Applicant: INSULET CORPORATION
Inventor: Matthew ALLES , Yibin ZHENG , Joon Bok LEE , James CAUSEY , Jason O'CONNOR
CPC classification number: A61M5/1723 , A61M5/14248 , A61M2202/0486
Abstract: Exemplary embodiments may provide an on-body medicament delivery system that provides basal delivery of a medicament to a type 2 diabetes patient and that automatically performs medicament titration for the patient. The medicament delivery system performs medicament titration based on glucose level readings for the patient. These glucose levels may be provided wirelessly from a glucose sensor, such as a continuous glucose monitor, or may be entered manually by the patient into a management device, such as a smartphone running an application that provides a user interface for the patient to enter the glucose level readings. The medicament delivery system adjusts the basal medicament delivery rate/dose based on the glucose level readings for the patient. The adjustments may be performed by a programmatic mechanism, such as by computer programming instructions executing on a processor.
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公开(公告)号:US20240000347A1
公开(公告)日:2024-01-04
申请号:US18345371
申请日:2023-06-30
Applicant: INSULET CORPORATION
Inventor: Jason O'CONNOR , Joon Bok LEE , Graeme NELSON
CPC classification number: A61B5/14532 , A61B5/7267 , A61B5/7275 , A61B5/746 , A61B5/743 , A61M2005/1726
Abstract: Disclosed herein is a method, implemented in an automated drug delivery system for determining a risk of a hypoglycemic or hyperglycemic condition based on risk factors calculated each time a new blood glucose reading is received and providing an alert to the user should a risk be determined. The risk factors may include the current CGM reading, the trend of CGM readings, the amount of insulin-on-board of the user and the accuracy of previous alerts provided to the user. The method may be modified to provide the risk of hypoglycemia if the user were to engage in exercise or other physical activities.
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公开(公告)号:US20230355874A1
公开(公告)日:2023-11-09
申请号:US18353523
申请日:2023-07-17
Applicant: INSULET CORPORATION
Inventor: Joon Bok LEE , Bonnie DUMAIS , Jason O'CONNOR , Yibin ZHENG
CPC classification number: A61M5/1723 , A61M5/14244 , A61M2230/201
Abstract: Disclosed are techniques and devices that are operable to receive one or a number of generalized parameters of an automated insulin delivery algorithm. An input of at least one generalized parameter corresponding to a user may be used to set one or more of the number of specific parameters of the automated insulin delivery algorithm based on the inputted at least one generalized parameter. Physiological condition data related to the user may be collected. The automated insulin delivery algorithm may determine a dosage of insulin to be delivered based on the collected physiological condition. Signals may be output to cause a liquid drug to be delivered to the user based on an output of the automated insulin delivery algorithm related to the determined dosage of insulin.
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公开(公告)号:US20230310741A1
公开(公告)日:2023-10-05
申请号:US18192380
申请日:2023-03-29
Applicant: INSULET CORPORATION
Inventor: Joon Bok LEE , Yibin ZHENG , Jason O'CONNOR , Ashutosh ZADE , James CAUSEY
IPC: A61M5/172
CPC classification number: A61M5/172 , A61M2205/50
Abstract: Disclosed herein is a drug delivery system wherein wearable components of the system are provided with Wi-Fi and/or cellular capabilities such as to allow different modalities for inter-component communications and, further, to allow access to a plethora of cloud-based services to enhance the functionality of the system.
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公开(公告)号:US20230248909A1
公开(公告)日:2023-08-10
申请号:US18164669
申请日:2023-02-06
Applicant: INSULET CORPORATION
Inventor: Joon Bok LEE , James GRAHAM , Jason O'CONNOR , Yibin ZHENG
CPC classification number: A61M5/1723 , G16H20/17 , A61M2202/0486 , A61M2205/52
Abstract: Disclosed are processes and techniques for a correction factor determination process for determining a correction factor for delivering a drug to a patient via a drug delivery device. For example, for an insulin delivery device, the disclosed techniques enable adjustment of the patient’s correction factor in real time based on the deviation of the patient’s glucose concentrations against clinically recommended targets. For example, a method for determining a correction factor may include determining an insulin action (Iaction) for a patient over a duration, the insulin action representing a total insulin metabolized, determining glucose information for the patient over the duration, the glucose information representing glucose activity, and determining an estimated correction factor (CFest) based on (glucose information) / (insulin action) for the duration. Other embodiments are described.
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公开(公告)号:US20230233762A1
公开(公告)日:2023-07-27
申请号:US18156497
申请日:2023-01-19
Applicant: INSULET CORPORATION
Inventor: Joon Bok LEE , Yibin ZHENG , Jason O'CONNOR , Kerrie GALLAGHER , Lindsay PHILBRICK , Alex NGUYEN , Joshua WILLIAMS
CPC classification number: A61M5/172 , A61B5/14532 , A61M2230/201
Abstract: Exemplary embodiments may provide a user interface and logic for assisting a user in calculating a proper medicament bolus dosage. The user interface may be simple and easy to understand. The user interface may clearly specify needed inputs, such as a carbohydrates amount for a meal that is about to be ingested and the current glucose level reading for the user. Entered inputs may be displayed on the user interface. The user interface may depict key calculated values resulting from calculations that involve the inputs, including the total bolus dosage calculation. The user interface also may depict the values that contribute to the total bolus dosage calculation. Some of the input values, such as carbohydrates amount, may be prepopulated by the management device or medicament delivery device. The user interface may permit overriding of prepopulated input values.
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公开(公告)号:US20230166034A1
公开(公告)日:2023-06-01
申请号:US17752236
申请日:2022-05-24
Applicant: Insulet Corporation
Inventor: Joon Bok LEE , Yibin ZHENG , Jason O'CONNOR , Ashutosh ZADE
CPC classification number: A61M5/1723 , A61M5/14244 , G16H20/17 , A61M2230/201 , A61M2005/14208
Abstract: Disclosed herein is a method for execution by a drug delivery device for determining an optimal dose of a liquid drug for current cycle of a medication delivery algorithm, the method utilizing a stepwise evaluation of a model and a cost function across a coarse search space consisting of coarse discrete quantities of the drug and a refined search space consisting of refined discrete quantities of the drug.
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