Analyte monitoring device and methods of use
An analyte monitor includes a sensor, a sensor control unit, and a display unit. The sensor has, for example, a substrate, a recessed channel formed in the substrate, and conductive material disposed in the recessed channel to form a working electrode. The sensor control unit typically has a housing adapted for placement on skin and is adapted to receive a portion of an electrochemical sensor. The sensor control unit also includes two or more conductive contacts disposed on the housing and configured for coupling to two or more contact pads on the sensor. A transmitter is disposed in the housing and coupled to the plurality of conductive contacts for transmitting data obtained using the sensor. The display unit has a receiver for receiving data transmitted by the transmitter of the sensor control unit and a display coupled to the receiver for displaying an indication of a level of an analyte. The analyte monitor may also be part of a drug delivery system to alter the level of the analyte based on the data obtained using the sensor.
1. A receiver unit in an analyte monitoring system, comprising:
a housing;
a receiver coupled to the housing, the receiver configured to receive one or more signals related to an analyte level;
an input device operatively coupled to the housing, the input device configured to initiate one or more functions of the receiver; and
a display unit coupled to the housing, the display unit configured to display an indicator substantially corresponding to the received one or more signals related to the analyte level, where the indicator includes a directional arrow, and further, wherein a position of the displayed directional arrow substantially corresponds to the received one or more signals related to the analyte level;
wherein the receiver is configured to activate the directional arrow indicator upon detection of a predetermined condition associated with the received one or more signals related to the analyte level, the predetermined condition resulting from a comparison of the received one or more signals related to the analyte level to a threshold value and a determination that the comparison results in the received one or more signals related to the analyte level reaching the threshold value; and further
wherein the receiver unit enters a sleep mode if the input device has not been activated for a predetermined period of time, and the sleep mode allows the receiver to receive information associated with the one or more signals related to the analyte level but not output the information on the display unit.
2. The receiver unit of claim 1 , wherein the displayed directional arrow is indicative of a trend of the received one or more signals related to the analyte level.
3. The receiver unit of claim 1 , wherein a radial position of the directional arrow displayed on the display unit substantially corresponds to a rate of change of the received one or more signals related to the analyte level.
4. The receiver unit of claim 3 , wherein the radial position of the directional arrow substantially corresponds to the rate of change of the analyte level over a predetermined period of time.
5. The receiver unit of claim 1 , wherein a gradient of the directional arrow substantially corresponds to a rate of change of the received one or more signals related to the analyte level.
6. The receiver unit of claim 1 , wherein the one or more signals related to the analyte level includes one or more glucose levels.
7. The receiver unit of claim 1 , wherein the predetermined condition includes one of an impending hypoglycemic condition, a hypoglycemic condition, an impending hyperglycemic condition, or a hyperglycemic condition.
8. The receiver unit of claim 7 , wherein the threshold value associated with the impending hypoglycemic condition includes one of about 70 mg/dL, about 80 mg/dL or about 90 mg/dL of glucose concentration.
9. The receiver unit of claim 7 , wherein the threshold value associated with the hypoglycemic condition includes one of about 60 mg/dL, about 70 mg/dL, or about 80 mg/dL of glucose concentration.
10. The receiver unit of claim 7 , wherein the threshold value associated with the impending hyperglycemic condition or the hyperglycemic condition includes one of about 130 mg/dL, about 150 mg/dL, about 175 mg/dL, about 200 mg/dL, about 225 mg/dL, about 250 mg/dL, or about 275 mg/dL of glucose concentration.
11. The receiver unit of claim 1 , wherein the receiver activates the indicator when a predetermined number of the received one or more signals related to the analyte level meets the threshold value over a predetermined time period.
12. The receiver unit of claim 1 , wherein the receiver is configured to activate the indicator when an average value of a predetermined number of the received one or more signals related to the analyte level meets the threshold value over a predetermined time period.
13. The receiver unit of claim 1 , wherein the receiver is configured to deactivate the indicator when the received one or more signals related to the analyte level indicate that the predetermined condition is no longer present.
14. The receiver unit of claim 1 , wherein the indicator further includes one or more of an auditory indicator, a visual indicator, a vibratory indicator, a temperature dependent sensory indicator, or an electrical sensory indicator.
15. The receiver unit of claim 1 , wherein the indicator is color coded.
16. The receiver unit of claim 1 , wherein the receiver is configured to automatically deactivate the indicator when the predetermined condition is associated with a first predefined condition, and further, wherein the receiver deactivates the indicator in response to a manual input when the predetermined condition is associated with a second predefined condition.
17. The receiver unit of claim 16 , wherein the first predefined condition includes an impending condition, and further, wherein the second predefined condition includes a current condition.
18. The receiver unit of claim 17 , wherein the impending condition includes one of an impending hyperglycemic condition, or an impending hypoglycemic condition, and further, wherein the current condition includes one of a hyperglycemic condition or a hypoglycemic condition.
19. The receiver unit of claim 16 , wherein the receiver is configured to automatically deactivate the indicator after a predetermined time period has elapsed since the first predefined condition is detected.
20. The receiver unit of claim 16 , wherein the receiver is configured to deactivate the indicator only in response to the manual input when the predetermined condition is associated with the second predefined condition.
21. The receiver unit of claim 1 , wherein the received one or more signals related to the analyte level is associated with a monitored glucose level.
22. The receiver unit of claim 1 , wherein the one or more signals related to the analyte level are received wirelessly.
23. The receiver unit of claim 1 , wherein the one or more signals related to the analyte level are received from an analyte sensor.
24. The receiver unit of claim 23 , wherein the analyte sensor includes a glucose sensor.
25. The receiver unit of claim 1 , including a strip port coupled to the housing to receive an in vitro glucose test strip.
26. The receiver unit of claim 25 , wherein the test strip includes a sample, wherein the receiver is configured to process the sample to determine a corresponding blood glucose level.
27. The receiver unit of claim 26 , wherein the receiver is configured to calibrate the received one or more signals related to the analyte level based on the processed sample.
28. The receiver unit of claim 27 , wherein the display unit outputs the calibrated received one or more signals related to the analyte level.
29. The receiver unit of claim 1 , wherein the preset time period is provided to the receiver by the input device.
30. The receiver unit of claim 23 , wherein the analyte sensor comprises a plurality of electrodes including a working electrode, wherein the working electrode comprises an analyte-responsive enzyme and a mediator, wherein at least one of the analyte-responsive enzyme and the mediator is chemically bonded to a polymer disposed on the working electrode, and wherein at least one of the analyte-responsive enzyme and the mediator is crosslinked with the polymer.
31. The receiver unit of claim 1 , wherein the received one or more signals related to the analyte level includes a temperature signal.