Methods and devices to detect analyte in body fluid are provided. Embodiments include positioning an analyte sensor in fluid contact with an analyte, detecting an attenuation in a signal from an analyte sensor after positioning during a predetermined time period, categorizing the detected attenuatio
Methods and devices to detect analyte in body fluid are provided. Embodiments include positioning an analyte sensor in fluid contact with an analyte, detecting an attenuation in a signal from an analyte sensor after positioning during a predetermined time period, categorizing the detected attenuation in the analyte sensor signal based, at least in part, on one or more characteristics of the signal, performing signal processing to generate a reportable data associated with the detected analyte sensor signal during the predetermined time period, managing if and when to request additional reference signal measurements, and managing if and when to temporarily not display results.
대표청구항▼
1. A method, comprising: positioning an analyte sensor in fluid contact with interstitial fluid;detecting an attenuation in a signal from the analyte sensor after positioning the analyte sensor during a predetermined time period;categorizing, using one or more processors, the detected attenuation in
1. A method, comprising: positioning an analyte sensor in fluid contact with interstitial fluid;detecting an attenuation in a signal from the analyte sensor after positioning the analyte sensor during a predetermined time period;categorizing, using one or more processors, the detected attenuation in the analyte sensor signal based, at least in part, on one or more characteristics of the signal; andperforming, using the one or more processors, signal processing to generate a reportable data associated with the detected attenuation in the analyte sensor signal during the predetermined time period; wherein the detected attenuation in the signal from the analyte sensor is associated with an early signal attenuation condition. 2. The method of claim 1 wherein the signal from the analyte sensor is associated with a monitored analyte level. 3. The method of claim 1 wherein the predetermined time period does not exceed approximately 24 hours. 4. The method of claim 1 wherein categorizing the detected analyte sensor signal attenuation is based at least in part on a predetermined plurality of signal attenuation conditions. 5. The method of claim 4 wherein the plurality of signal attenuation conditions includes a reportable signal condition, a conditional reportable signal condition, and an unreportable signal condition. 6. The method of claim 5 including outputting data associated with the monitored analyte level based on the detected analyte sensor signal when the detected analyte sensor signal attenuation includes a reportable signal condition or a conditional reportable signal condition. 7. The method of claim 6 wherein outputting data associated with the monitored analyte level includes outputting data for a preset time period when the detected analyte sensor signal attenuation includes the conditional reportable signal condition. 8. The method of claim 7 wherein the preset time period does not exceed approximately two hours. 9. The method of claim 7 including requesting a reference blood glucose measurement during the preset time period. 10. The method of claim 9 including calibrating the analyte sensor signal based at least in part on the reference blood glucose measurement received during the preset time period. 11. The method of claim 7 including disabling outputting of the data associated with the monitored analyte level after the preset time period has elapsed. 12. The method of claim 1 wherein performing signal processing includes: requesting a reference data; anddetermining a sensitivity value associated with the analyte sensor based on the reference data. 13. The method of claim 12 wherein the reference data includes an in vitro blood glucose measurement data. 14. The method of claim 12 including calibrating the analyte sensor based at least in part on the determined sensitivity value. 15. An apparatus, comprising: a data communication interface;one or more processors operatively coupled to the data communication interface; anda memory storing instructions which, when executed by the one or more processors, causes the one or more processors to detect positioning of an analyte sensor in fluid contact with interstitial fluid, detect an attenuation in a signal from the analyte sensor after detecting the positioning of the analyte sensor during a predetermined time period, categorize the detected attenuation in the analyte sensor signal based, at least in part, on one or more characteristics of the signal, and perform signal processing to generate a reportable data associated with the detected attenuation in the analyte sensor signal during the predetermined time period, wherein the detected attenuation in the signal from the analyte sensor is associated with an early signal attenuation condition. 16. The apparatus of claim 15 wherein the signal from the analyte sensor is associated with a monitored analyte level. 17. The apparatus of claim 15 wherein the predetermined time period does not exceed approximately 24 hours. 18. The apparatus of claim 15 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to categorize the detected analyte sensor signal attenuation based at least in part on a predetermined plurality of signal attenuation conditions. 19. The apparatus of claim 18 wherein the plurality of signal attenuation conditions includes a reportable signal condition, a conditional reportable signal condition, and an unreportable signal condition. 20. The apparatus of claim 19 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to output data associated with the monitored analyte level based on the detected analyte sensor signal when the detected analyte sensor signal attenuation includes a reportable signal condition or a conditional reportable signal condition. 21. The apparatus of claim 20 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to output data for a preset time period when the detected analyte sensor signal attenuation includes the conditional reportable signal condition. 22. The apparatus of claim 21 wherein the preset time period does not exceed approximately two hours. 23. The apparatus of claim 21 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to request a reference blood glucose measurement during the preset time period. 24. The apparatus of claim 23 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to calibrate the analyte sensor signal based at least in part on the reference blood glucose measurement received during the preset time period. 25. The apparatus of claim 21 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to disable the outputting of the data associated with the monitored analyte level after the preset time period has elapsed. 26. The apparatus of claim 15 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to request a reference data, and determine a sensitivity value associated with the analyte sensor based on the reference data. 27. The apparatus of claim 26 wherein the reference data includes an in vitro blood glucose measurement data. 28. The apparatus of claim 26 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to calibrate the analyte sensor based at least in part on the determined sensitivity value. 29. A method, comprising: positioning an analyte sensor in fluid contact with interstitial fluid;detecting an attenuation in a signal from the analyte sensor after positioning the analyte sensor during a predetermined time period;categorizing, using one or more processors, the detected attenuation in the analyte sensor signal based, at least in part, on one or more characteristics of the signal; andperforming, using the one or more processors, signal processing to generate a reportable data associated with the detected attenuation in the analyte sensor signal during the predetermined time period; wherein categorizing the detected analyte sensor signal attenuation is based at least in part on a predetermined plurality of signal attenuation conditions. 30. The method of claim 29 wherein the signal from the analyte sensor is associated with a monitored analyte level. 31. The method of claim 29 wherein the predetermined time period does not exceed approximately 24 hours. 32. The method of claim 29 wherein the plurality of signal attenuation conditions includes a reportable signal condition, a conditional reportable signal condition, and an unreportable signal condition. 33. The method of claim 32 including outputting data associated with the monitored analyte level based on the detected analyte sensor signal when the detected analyte sensor signal attenuation includes a reportable signal condition or a conditional reportable signal condition. 34. The method of claim 33 wherein outputting data associated with the monitored analyte level includes outputting data for a preset time period when the detected analyte sensor signal attenuation includes the conditional reportable signal condition. 35. The method of claim 34 wherein the preset time period does not exceed approximately two hours. 36. The method of claim 34 including requesting a reference blood glucose measurement during the preset time period. 37. The method of claim 36 including calibrating the analyte sensor signal based at least in part on the reference blood glucose measurement received during the preset time period. 38. The method of claim 34 including disabling outputting of the data associated with the monitored analyte level after the preset time period has elapsed. 39. The method of claim 29 wherein performing signal processing includes: requesting a reference data; anddetermining a sensitivity value associated with the analyte sensor based on the reference data. 40. The method of claim 39 wherein the reference data includes an in vitro blood glucose measurement data. 41. The method of claim 39 including calibrating the analyte sensor based at least in part on the determined sensitivity value. 42. An apparatus, comprising: a data communication interface;one or more processors operatively coupled to the data communication interface; anda memory storing instructions which, when executed by the one or more processors, causes the one or more processors to detect positioning of an analyte sensor in fluid contact with interstitial fluid, detect an attenuation in a signal from the analyte sensor after detecting the positioning of the analyte sensor during a predetermined time period, categorize the detected attenuation in the analyte sensor signal based, at least in part, on one or more characteristics of the signal, categorize the detected analyte sensor signal attenuation based, at least in part, on a predetermined plurality of signal attenuation conditions, and perform signal processing to generate a reportable data associated with the detected attenuation in the analyte sensor signal during the predetermined time period. 43. The apparatus of claim 42 wherein the signal from the analyte sensor is associated with a monitored analyte level. 44. The apparatus of claim 42 wherein the predetermined time period does not exceed approximately 24 hours. 45. The apparatus of claim 42 wherein the plurality of signal attenuation conditions includes a reportable signal condition, a conditional reportable signal condition, and an unreportable signal condition. 46. The apparatus of claim 45 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to output data associated with the monitored analyte level based on the detected analyte sensor signal when the detected analyte sensor signal attenuation includes a reportable signal condition or a conditional reportable signal condition. 47. The apparatus of claim 46 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to output data for a preset time period when the detected analyte sensor signal attenuation includes the conditional reportable signal condition. 48. The apparatus of claim 47 wherein the preset time period does not exceed approximately two hours. 49. The apparatus of claim 47 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to request a reference blood glucose measurement during the preset time period. 50. The apparatus of claim 49 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to calibrate the analyte sensor signal based at least in part on the reference blood glucose measurement received during the preset time period. 51. The apparatus of claim 47 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to disable the outputting of the data associated with the monitored analyte level after the preset time period has elapsed. 52. The apparatus of claim 42 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to request a reference data, and determine a sensitivity value associated with the analyte sensor based on the reference data. 53. The apparatus of claim 52 wherein the reference data includes an in vitro blood glucose measurement data. 54. The apparatus of claim 52 wherein the memory storing instructions which, when executed by the one or more processors, causes the one or more processors to calibrate the analyte sensor based at least in part on the determined sensitivity value.
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이 특허에 인용된 특허 (261)
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