초록 ▼

An electronic device may be configured to prompt a user via an on-board display to measure user glucose via an on-board glucose meter, to compute a first drug bolus value based on the measured user glucose, to display the first drug bolus value on the display and prompt the user via the display to e

An electronic device may be configured to prompt a user via an on-board display to measure user glucose via an on-board glucose meter, to compute a first drug bolus value based on the measured user glucose, to display the first drug bolus value on the display and prompt the user via the display to enter carbohydrate information into the device, to compute a second drug bolus value based on the entered carbohydrate information, to display the second drug bolus value on the display and prompt the user via the display to enter user health information into the device, to compute a third drug bolus value based on the entered health information and a total drug bolus value as a sum of the first, second and third drug bolus values, and to display the third and total drug bolus values on the display.

대표청구항 ▼

1. A method reconciling bolus records between an electronic device including a blood glucose meter and a liquid infusion pump for more accurate records to improve therapy advice, comprising: transferring commanded pump event records not previously transmitted to an electronic device including a bloo

1. A method reconciling bolus records between an electronic device including a blood glucose meter and a liquid infusion pump for more accurate records to improve therapy advice, comprising: transferring commanded pump event records not previously transmitted to an electronic device including a blood glucose meter, each commanded pump event record having delivered bolus information;associating the delivered bolus information with electronic device diary records having programmed bolus information that is not confirmed;if the delivered bolus information is associated with the programmed bolus information, updating the programmed bolus information with delivered bolus information and confirming the delivered bolus information is associated with the programmed bolus information to prevent other associations;if the delivered bolus information is not associated with the programmed bolus information, creating a new electronic device diary record having programmed bolus information including the delivered bolus information and confirming the delivered bolus information is associated with the programmed bolus information to prevent other associations; andimproving accuracy of programmed bolus information by modifying the programmed bolus information with delivered bolus information for more accurate records to improve therapy advice. 2. The method as in claim 1, further comprising transferring non-commanded pump event records, created by manually initiated directly delivered boluses from a pump, insulin pen, or syringe, not previously transmitted to the electronic device, each non-commanded pump event record having a delivered bolus type, delivered bolus amount, and a delivered time stamp;updating the electronic device diary records with non-commanded pump event records; andimproving accuracy of electronic device diary records with non-commanded pump event records for improved therapy advice. 3. The method as in claim 1, wherein associating the commanded pump event record bolus information with electronic device non-confirmed diary records programmed bolus information is performed within a predetermined variation between a delivered bolus time stamp and a programmed bolus time stamp. 4. The method as in claim 1, wherein the predetermined variation of the delivered bolus time stamp and programmed bolus time stamp is less than six minutes. 5. The method as in claim 1, wherein delivered bolus information comprises a delivered bolus type, delivered bolus amount, and delivered bolus time stamp. 6. The method as in claim 1, wherein programmed bolus information comprises a programmed bolus type, programmed bolus amount, and programmed bolus time stamp. 7. A method reconciling bolus records between an electronic device including a blood glucose meter and a liquid infusion pump for more accurate records to improve therapy advice, comprising: means for transferring commanded pump event records not previously transmitted to an electronic device including a blood glucose meter, each commanded pump event record having delivered bolus information;means for associating the delivered bolus information with electronic device diary records having programmed bolus information that is not confirmed;if the delivered bolus information is associated with the programmed bolus information, means for updating the programmed bolus information with delivered bolus information and confirming the delivered bolus information is associated with the programmed bolus information to prevent other associations;if the delivered bolus information is not associated with the programmed bolus information, means for creating a new non-confirmed diary record have programmed bolus information including the delivered bolus information and confirming the delivered bolus information is associated with the programmed bolus information to prevent other associations; andimproving accuracy of programmed bolus information by modifying the programmed bolus information with delivered bolus information for more accurate records to improve therapy advice. 8. The method as in claim 7, further comprising means for transferring non-commanded pump event records, created by manually initiated directly delivered boluses from a pump, insulin pen, or syringe, not previously transmitted to the electronic device, each non-commanded pump event record having a delivered bolus type, delivered bolus amount, and a delivered time stamp;means for updating the electronic device diary records with non-commanded pump event; andimproving accuracy of electronic device diary records with non-commanded pump event records for improved therapy advice.