US2015314062A1PendingUtilityA1
Pump with therapy coaching
Est. expiryJan 7, 2028(~1.5 yrs left)· nominal 20-yr term from priority
A61M 5/1723A61M 2205/3327A61M 2202/0007A61M 5/14244A61B 5/746A61M 2230/201A61M 2005/14208A61M 5/142A61B 5/4836G16Z 99/00G16H 70/20G16H 20/17A61B 5/14532
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Claims
Abstract
An apparatus comprising a pump, an input configured to receive information related to a user, a user interface, and a controller communicatively coupled to the pump, the input, and the user interface. The controller includes a timing module configured to initiate delivery of a drug in time and to adjust delivery according to the received information. Other devices, systems, and methods are disclosed.
Claims
exact text as granted — not AI-modified1 . An apparatus comprising:
a pump configured to deliver a drug from a cartridge; a user interface; a memory to store guideline parameters related to use of the apparatus; and a controller communicatively coupled to the pump, the memory, and the user interface, wherein the controller includes:
a comparison module configured to compare patient use parameters to the stored guideline parameters; and
a scoring module configured to calculate a score indicative of efficacy of patient pump use based on a comparison by the comparison module, and
wherein the controller is configured to communicate advice to the user on how to increase the efficacy of patient pump use.
2 . The apparatus of claim 1 , including:
an input communicatively coupled to the controller and configured to receive user information, including a level of user information, and wherein the comparison module is configured to monitor the level of the user information.
3 . The apparatus of claim 2 , including a communication port communicatively coupled to the input and configured to receive user information from a second separate device.
4 . The apparatus of claim 2 , wherein the user interface includes a display, and wherein the controller is configured to prompt the user, via the display, to begin a measurement using a separate device.
5 . The apparatus of claim 2 , wherein the user interface is configured to receive manual entry of the information from the user.
6 . The apparatus of claim 1 , wherein the comparison module is configured to compare a frequency of entering user information into the device to a stored frequency.
7 . The apparatus of claim 1 , wherein the comparison module is configured to compare at least one of:
a frequency of cartridge changes to a stored cartridge change frequency value, a frequency of infusion set changes to a stored set change frequency value, a difference in timing of cartridge changes to a stored threshold change time difference value, or a frequency that cartridges are allowed to empty to a stored empty cartridge frequency value.
8 . The apparatus of claim 1 , wherein the comparison module is configured to compare at least one of:
a frequency of using test features of the pump device to a stored test frequency value, a total time that the pump device is inoperative to a stored total time value, a frequency that a pump generated report is viewed to a stored report-view frequency value, or a time from when an alert is generated by the device to a time when a user responds to the alert to a stored response time value.
9 . The apparatus of claim 1 , wherein the user interface includes a display, wherein the scoring module is configured to trend the score, and wherein the controller is configured to display the score and score trend on the device.
10 . The apparatus of claim 1 , wherein calculating a score based on the monitored patient use includes assigning different weights to outcomes of comparisons of use parameters to guideline parameters when calculating the score.
11 . The apparatus of claim 1 , including a communication port communicatively coupled to the controller, and wherein the controller is configured to communicate the advice on how to increase pump efficacy to a second separate device.
12 . A method comprising:
monitoring patient use of a device that includes a pump, wherein the monitoring includes comparing patient use parameters to stored guideline parameters; calculating a score indicative of efficacy of patient pump use based on the monitoring; and communicating advice to the user on how to increase pump efficacy.
13 . The method of claim 12 , including receiving patient information into the device, and wherein monitoring patient use includes monitoring the patient information.
14 . The method of claim 12 , wherein comparing patient use parameters to stored guideline parameters includes comparing a frequency of entering readings into the device to a stored frequency.
15 . The method of claim 12 , wherein comparing patient use parameters to stored guideline parameters includes comparing at least one of:
a frequency of cartridge changes to a stored change frequency value, a difference in timing of cartridge changes to a stored threshold cartridge change time difference value, a difference in timing of infusion set changes to a stored threshold infusion set change time difference value, or a frequency that cartridges are allowed to empty to a stored empty cartridge frequency value.
16 . The method of claim 12 , wherein comparing patient use parameters to stored guideline parameters includes comparing at least one of:
a frequency of using test features of the pump device to a stored test frequency value, a total time that the pump device is inoperative to a stored total time value, a frequency that a pump generated report is viewed to a stored report-view frequency value, or a time from when an alert is generated by the device to a time when a user responds to the alert to a stored response time value.
17 . The method of claim 12 , wherein calculating a score based on the monitored patient use includes assigning different weights to outcomes of the comparing when calculating the score.
18 . The method of claim 12 , including:
trending the score; and displaying the score and a score trend on the device.
19 . The method of claim 12 , wherein communicating advice includes communicating advice on how to increase pump efficacy to a second separate device.
20 . An apparatus comprising:
a pump configured to deliver a drug therapy; a memory configured to store a delivery pattern of the drug therapy; a user interface configured to receive time change information; and a controller communicatively coupled to the pump, the memory, and the user interface, wherein the controller includes a timing module configured to shift the delivery pattern in time according to the received time change information.Join the waitlist — get patent alerts
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