CPC A61M 5/1723 (2013.01) [G16H 10/40 (2018.01); G16H 20/17 (2018.01); G16H 40/67 (2018.01); A61M 2205/18 (2013.01); A61M 2205/3584 (2013.01); A61M 2205/50 (2013.01); A61M 2205/502 (2013.01); A61M 2205/505 (2013.01); A61M 2205/52 (2013.01); A61M 2205/581 (2013.01); A61M 2205/582 (2013.01); A61M 2205/583 (2013.01); A61M 2205/702 (2013.01); A61M 2230/201 (2013.01)] | 20 Claims |
1. A processor-implemented method comprising:
obtaining a current sensor-generated value that is indicative of a physiological characteristic of a user of a medical device, the current sensor-generated value produced in response to operation of a continuous analyte sensor device;
obtaining a sensor quality metric that indicates accuracy of the current sensor-generated value;
causing, in response to obtaining the sensor quality metric, configuration of a quality-specific operating mode of the medical device, the quality-specific operating mode comprising separate regulation of basal and bolus deliveries of a fluid medication based on the obtained sensor quality metric; and
causing regulation of fluid medication delivery from the medical device, in accordance with the current sensor-generated value and the quality-specific operating mode of the medical device.
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