Implantable sensor devices, systems, and methods
Disclosed herein are devices, systems, and methods for a continuous analyte sensor, such as a continuous glucose sensor. In certain embodiments disclosed herein, various in vivo properties of the sensor's surroundings can be measured. In some embodiments, the measured properties can be used to identify a physiological response or condition in the body. This information can then be used by a patient, doctor, or system to respond appropriately to the identified condition.
1. A method for processing data from a continuous glucose sensor, the method comprising:
receiving sensor data generated by the continuous glucose sensor, wherein the sensor data is indicative of a concentration of glucose in a host;
identifying, using a processor, a post-implantation transient loss of sensitivity of the continuous glucose sensor; and
automatically releasing a bin-active agent configured to minimize reduction or cessation of blood flow to a site surrounding sensor implantation, the releasing being responsive to an occurrence of identifying of the post-implantation transient loss of sensitivity.
2. The method of claim 1 , wherein the sensor data comprises data indicative of a signal response to at least one event selected from the group consisting of a signal response to cessation of blood flow to a site surrounding sensor implantation, a signal response to reduction of blood flow to a site surrounding sensor implantation, and a signal response to a vasospastic event.
3. The method of claim 1 , wherein identifying the post-implantation transient loss of sensitivity comprises determining a severity of the loss of sensitivity.
4. The method of claim 3 , wherein processing the sensor data is performed based on the severity of the post-implantation transient loss of sensitivity.
5. The method of claim 1 , wherein identifying the post-implantation transient loss of sensitivity comprises:
deactivating the continuous glucose sensor for a time period, whereby a product from a catalyzed reaction of glucose and oxygen accumulates over the time period;
subsequently activating the continuous glucose sensor and measuring a signal value of the continuous glucose sensor immediately after the time period; and
determining an occurrence of a post-implantation transient loss of sensitivity event if the signal value is greater than a predetermined value.
6. The method of claim 1 , wherein the continuous glucose sensor comprises a first electrode and a second electrode, and wherein identifying the post-implantation transient loss of sensitivity comprises:
measuring a stimulus signal passed across the first electrode and the second electrode; and
determining an occurrence of a post-implantation transient loss of sensitivity event if the measured stimulus signal is greater or less than a predetermined value.
7. The method of claim 6 , wherein the stimulus signal measured is impedance.
8. The method of claim 1 , wherein identifying the post-implantation transient loss of sensitivity comprises determining a pH of a biological fluid surrounding the continuous glucose sensor.
9. The method of claim 1 , wherein identifying the post-implantation transient loss of sensitivity comprises:
measuring a concentration value of a non-glucose analyte; and
determining an occurrence of a post-implantation transient loss of sensitivity event if the concentration value of the non-glucose analyte changes more than a predetermined amount.
10. The method of claim 1 , wherein the continuous glucose sensor comprises a first electrode and a second electrode.
11. The method of claim 10 , wherein the first electrode and second electrode have different dimensions.
12. The method of claim 11 , wherein the second electrode is configured to have a dimension that positions the second electrode post-implantation outside of a site affected by cessation or reduction of blood flow.
13. The method of claim 10 , wherein at least one of the first electrode and the second electrode is configured to minimize tissue trauma from implantation.
14. The method of claim 10 , further comprising:
determining that the second electrode is positioned outside of a site affected by cessation or reduction of blood flow; and
wherein processing the sensor data responsive to the identification of the transient loss of sensitivity comprises according more weight to sensor data generated by the second electrode than sensor data generated by the first electrode.
15. The method of claim 1 , wherein the continuous glucose sensor comprises a first electrode configured to generate a first signal and a second electrode configured to generate a second signal, and wherein identifying the post-implantation transient loss of sensitivity of the continuous glucose sensor comprises:
evaluating a difference between the first signal with the second signal; and
recognizing a similarity between the difference and a pattern indicative of post-implantation transient loss of sensitivity.
16. The method of claim 15 , wherein the first electrode and the second electrode are substantially collocated.
17. The method of claim 15 , wherein the first electrode and the second electrode are separated by a distance greater than 1 mm.