METHOD AND APPARATUS FOR ANALYTE MEASUREMENTS IN THE PRESENCE OF INTERFERENTS

• US 20080112853A1
• Filed: 08/15/2007
• Published: 05/15/2008
• Est. Priority Date: 08/15/2006
• Status: Abandoned Application

• Current Assignee: OptiScan Biomedical Corporation
• Original Assignee: OptiScan Biomedical Corporation
• Inventors: Hall, W. Dale
• Application Number:
  US11/839,447
• Publication Number:
  US 20080112853A1
• Time in Patent Office: Days
• US Class Current: 422/82.05
• CPC Class Codes: A61B 2560/0223 of calibration, e.g. protocols for calibrating sensors
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1495 Calibrating or testing of in-vivo probes
• CPC Class Codes: G01N 21/3577 for analysing liquids, e.g. polluted water

Abstract

Method and apparatus are described that permit an analyte concentration to be estimated from a measurement in the presence of compounds that interfere with the measurement. The method reduces the error in the analyte concentration in the presence of interferents. The method includes the use of a set of measurements obtained for a large population having a range of known analyte and interfering compound concentrations. From a sample measurement, which may or may not be one of the population, interferents likely to be present are identified, and a calibration coefficient is calculated. The calibration coefficient may be applied to the measurement to estimate the analyte concentration. In some implementations, the calibration coefficient may be determined as a weighted average of single interferent calibration coefficients. In some embodiments, the sample measurement includes a spectroscopic measurement.

Claims

1. A method for estimating a concentration of an analyte in a sample from a measurement of the sample, the method comprising:

determining, based on the measurement, a list of one or more possible interferents to the measurement of the analyte in the sample;

calculating, for each one of the possible interferents on the list, a single interferent analyte concentration based on the presumed presence in the sample of the one interferent and no other interferents from the list; and

determining an estimated analyte concentration based at least in part on the single interferent analyte concentrations.

2. The method of claim 1, wherein the list includes all the interferents in a library of interferents.

3. The method of claim 1, wherein the list includes a single interferent.

4. The method of claim 3, wherein the single interferent is the most probable interferent.

5. The method of claim 1, wherein determining the list of one or more possible interferents comprises performing a statistical test for the presence of the one or more possible interferents.

6. The method of claim 5, wherein the statistical test comprises determining information related to a Mahalanobis distance.

7. The method of claim 5, wherein the statistical test comprises comparing an estimated concentration of a possible interferent to a threshold concentration.

8. The method of claim 1, wherein determining a list of possible interferents comprises analyzing combinations of sample spectra and interferent spectra corresponding to varying combinations of a selected interferent and identifying the selected interferent as a possible interferent if any of the combinations are within predetermined bounds.

9. The method of claim 1, wherein calculating a single interferent analyte concentration comprises:

determining a calibration which reduces error attributable to the presumed presence in the sample of the one interferent;

applying the calibration to the measurement; and

estimating, based on the calibrated measurement, the single interferent analyte concentration.

10. The method of claim 9, wherein calculating a single-interferent analyte concentration further comprises determining, for each one of the interferents on the list, a weighting function, and wherein determining an estimated analyte concentration comprises combining the single interferent analyte concentrations and the weighting functions.

11. The method of claim 10, wherein the weighting function for an interferent is based at least in part on a probability of the presence of the interferent in the sample.

12. The method of claim 1, wherein the measurement comprises a spectrum.

13. The method of claim 1, wherein the measurement comprises an infrared spectrum.

14. The method of claim 1, wherein the sample includes at least one component of blood, and wherein the analyte comprises glucose.

15. The method of claim 1, wherein the sample comprises a bodily fluid and the list includes at least one exogenous interferent.

16. A carrier medium carrying one or more computer readable code segments to instruct a processor to implement a method for estimating the amount of an analyte in a sample from a measurement of the sample, the method comprising the method of claim 1.

17. An apparatus for estimating a concentration of an analyte in a sample from a measurement of the sample, the apparatus comprising:

means for determining, based on the measurement, a list of one or more possible interferents to the measurement of the analyte in the sample;

means for calculating, for each one of the interferents on the list, a single interferent analyte concentration based on the presumed presence in the sample of the one interferent and no other interferents from the list; and

means for determining an estimated analyte concentration based at least in part on the single interferent analyte concentrations.

18. The apparatus of claim 17, wherein the means for determining a list of possible interferents comprises:

means for analyzing combinations of sample spectra and interferent spectra corresponding to varying combinations of a selected interferent; and

means for identifying the selected interferent as a possible interferent if any of the combinations are within predetermined bounds.

19. The apparatus of claim 17, wherein the means for calculating a single interferent analyte concentration comprises:

means for determining a calibration which reduces error attributable to the presumed presence in the sample of the one interferent;

means for applying the calibration to the measurement; and

means for estimating, based on the calibrated measurement, the single interferent analyte concentration.

20. The apparatus of claim 17, further comprising means for outputting information related to the estimated analyte concentration.

21. The apparatus of claim 17, wherein the sample includes at least one component of blood, and wherein the analyte comprises glucose.

22. An analyte detection system comprising:

a sensor system configured to provide information relating to a measurement of an analyte in a sample; and

a processor system configured to execute stored program instructions such that the analyte detection system;

determines, based on the measurement, a list of one or more possible interferents to the measurement of the analyte in the sample;

calculates, for each one of the interferents on the list, a single interferent analyte concentration based on the presumed presence in the sample of the one interferent and no other interferents from the list; and

determines an estimated analyte concentration based at least in part on the single interferent analyte concentrations.

23. The analyte detection system of claim 22, wherein the sensor system comprises a spectroscope and the measurement comprises a spectrum.

24. The analyte detection system of claim 23, wherein the sample comprises at least one component of blood and the analyte comprises glucose.

25. The analyte detection system of claim 22, wherein the sample comprises a bodily fluid, and wherein the list includes at least one exogenous interferent.

26. The analyte detection system of claim 22, further comprising a source of electromagnetic radiation, wherein the sensor system comprises a detector configured to detect radiation emitted by the source that interacts with the sample.

27. The analyte detection system of claim 26, wherein at least a portion of the radiation emitted by the source is transmitted through the sample and detected by the detector.

28. The analyte detection system of claim 22, wherein the sensor system is physically remote from the processor system.

29. The analyte detection system of claim 28, wherein the sensor system is configured to communicate with the processor system via a network.

30. The analyte detection system of claim 29, wherein the network comprises a hospital information network.

31. The analyte detection system of claim 22, further comprising a user interface configured to output information related to the estimated analyte concentration.

32. The analyte detection system of claim 22, wherein the processor system is configured to execute stored program instructions such that the analyte detection system determines a list of possible interferents by analyzing combinations of sample spectra and interferent spectra corresponding to varying combinations of a selected interferent and identifying the selected interferent as a possible interferent if any of the combinations are within predetermined bounds.

33. The analyte detection system of claim 22, wherein the processor system is configured to execute stored program instructions such that the analyte detection system determines a list of possible interferents by performing a statistical test for the presence of the one or more possible interferents.

34. The analyte detection system of claim 33, wherein the list comprises a single most probable interferent.

35. The analyte detection system of claim 22, further comprising a sampling system configured to draw the sample from a patient periodically and to transport the sample into operative engagement with the sensor system.