Portable clinical analysis system for immunometric measurement

Patent metadata

Field	Value
Publication number	US-9885706-B2
Application number	US-201314099398-A
Country	US
Kind code	B2
Filing date	Dec 6, 2013
Priority date	Dec 17, 2012
Publication date	Feb 6, 2018
Grant date	Feb 6, 2018

Abstract

The present invention covers the integration and utility of accelerometer features into a clinical analysis system. For example, measurement of dynamic acceleration and orientation of a blood-testing instrument with respect to Earth's gravitational field may be used to determine reliability of a test procedure and optionally to provide corrective elements thereof.

First claim

We claim:

1. A portable clinical system for performing an immunoassay on a biological sample, the system comprising:
a test device comprising a sample entry port and a sensing region comprising an immunosensor for performing the immunoassay on the biological sample, which generates an electric signal based on a concentration of an analyte in the biological sample determined by the immunoassay; and
an analyzer to initiate a test cycle of the test device, including performance of the immunoassay, comprising:
a processor, a computer readable memory, and a non-transitory computer readable storage medium;
a port to receive the test device;
an accelerometer to collect data during the test cycle;
program instructions stored on the non-transitory computer readable storage medium for execution by the processor via the computer readable memory, the program instructions comprising:
program instructions to determine motion of the analyzer during a test cycle of the test device based on the data collected by the accelerometer during the test cycle;
program instructions to compare the determined motion to a threshold rate of motion for the test device; and
program instructions to at least one of: (i) provide an alert prompting a user to take corrective action during the test cycle, (ii) correct a result of the immunoassay, and/or (iii) suppress the result of the immunoassay, when the determined motion exceeds the threshold rate of motion.

2. The system of claim 1 , wherein the analyzer further comprises program instructions to provide the alert prompting the user to take the corrective action during the test cycle, when the determined motion exceeds the threshold rate of motion.

3. The system of claim 1 , wherein the analyzer further comprises program instructions to suppress the result of the immunoassay, when the determined motion exceeds the threshold rate of motion.

4. The system of claim 1 , wherein the analyzer further comprises program instructions to correct the result of the immunoassay, when the determined motion exceeds the threshold rate of motion.

5. The system of claim 1 , wherein the analyzer further comprises program instructions to provide the alert prompting the user to take the corrective action during the test cycle, and suppress the result of the immunoassay, when the determined motion exceeds the threshold rate of motion.

6. The system of claim 1 , the analyzer further comprises program instructions to provide the alert prompting the user to take the corrective action during the test cycle, and correct the result of the immunoassay, when the determined motion exceeds the threshold rate of motion.

7. The system of claim 1 , wherein the threshold rate of motion is no more than about 50 meters/second.

8. The system of claim 1 , wherein the analyzer further comprises program instructions to measure dynamic acceleration based on the data collected by the accelerometer during the test cycle to determine the motion of the analyzer.

9. The system of claim 1 , wherein the analyzer further comprises:
program instructions to determine spatial orientation of the analyzer during the test cycle of the test device based on the data collected by the accelerometer during the test cycle;
program instructions to compare the determined spatial orientation to a threshold operating spatial plane for the test device; and
program instructions to at least one of: (i) provide a different alert prompting the user to take different corrective action during the test cycle, (ii) correct the result of the immunoassay, and/or (iii) suppress the result of the immunoassay, when the determined spatial orientation exceeds the threshold operating spatial plane.

10. The system of claim 9 , wherein the providing the different alert prompting the user to take the different corrective action comprises displaying the different alert on the analyzer and the different alert instructs the user to move the spatial orientation of the analyzer below the threshold operating spatial plane.

11. The system of claim 9 , wherein:
the providing the different alert prompting the user to take the different corrective action comprises displaying the different alert on the analyzer and the different alert instructs the user to move the spatial orientation of the analyzer below the threshold operating spatial plane; and
the analyzer further comprises:
program instructions to detect a change in the spatial orientation of the analyzer during the test cycle;
program instructions to determine a new spatial orientation of the analyzer;
program instructions to compare the determined new spatial orientation to the threshold operating spatial plane; and
program instructions to complete the test cycle and provide the result of the immunoassay when the determined new spatial orientation is below the threshold operating spatial plane.

12. The system of claim 9 , wherein:
the analyzer further comprises a base having a horizontal plane; and
the threshold operating spatial plane is no more than about 15° from the horizontal plane of the base.

13. The system of claim 12 , wherein the threshold operating spatial plane is no more than about 10° from the horizontal plane of the base.

14. The system of claim 9 , wherein:
the analyzer further comprises a base having a horizontal plane;
the port is substantially aligned to a first plane parallel to the horizontal plane of the base; and
the immunosensor is substantially aligned to a second plane parallel to the horizontal plane of the base.

15. The system of claim 14 , wherein the threshold operating spatial plane is no more than about 15° from the horizontal plane of the base.

16. The system of claim 15 , wherein:
the providing the different alert prompting the user to take the different corrective action comprises displaying the different alert on the analyzer and the different alert instructs the user to move the spatial orientation of the analyzer below the threshold operating spatial plane; and
the analyzer further comprises:
program instructions to detect a change in the spatial orientation of the analyzer during the test cycle based on the data collected by the accelerometer during the test cycle;
program instructions to determine a new spatial orientation of the analyzer;
program instructions to compare the determined new spatial orientation to the threshold operating spatial plane; and
program instructions to complete the test cycle and provide the result of the immunoassay when the determined new spatial orientation is below the threshold operating spatial plane.

17. The system of claim 9 , wherein the analyzer further comprises program instructions to measure static acceleration on at least three axes of the analyzer based on the data collected by the accelerometer during the test cycle to determine the spatial orientation of the analyzer, and the determining the spatial orientation comprises determining at least one of roll, pitch, and yaw of the analyzer based on the measured static acceleration on the at least three axes of the analyzer.

18. The system of claim 17 , wherein:
the comparing the determined spatial orientation to the threshold operating spatial plane comprises at least one of:
comparing the determined roll of the analyzer to a threshold roll;
comparing the determined pitch of the analyzer to a threshold pitch; and
comparing the determined yaw of the analyzer to a threshold yaw; and

the at least one of: (i) the providing the different alert prompting the user to take the different corrective action during

Assignees

• Abbott Point Of Care Inc

Inventors

• Vandersleen Gary
• Emeric Pierre
• Wasserman Paul
• Soman Narendra
• Davis Graham
• Miller Cary

Classifications

• G01N33/5306 Primary

  Improving reaction conditions, e.g. reduction of non-specific binding, promotion of specific binding · CPC title

• G01N33/49

  Blood {(chemical methods for determining blood cell populations G01N33/5094; chemical analysis of blood groups or blood types G01N33/80)} · CPC title

• G01N35/00712

  Automatic status testing, e.g. at start-up or periodic · CPC title

• G01N35/00693

  Calibration · CPC title

• G01N33/48785

  Electrical and electronic details of measuring devices for physical analysis of liquid biological material not specific to a particular test method, e.g. user interface or power supply · CPC title