Spatial orientation determination in portable clinical analysis systems

• US 9,915,643 B2
• Filed: 10/12/2016
• Issued: 03/13/2018
• Est. Priority Date: 12/17/2012
• Status: Active Grant

• Current Assignee: Abbott Point Of Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Point Of Care Incorporated (Abbott Laboratories Incorporated)
• Inventors: Vandersleen, Gary, Emeric, Pierre, Wasserman, Paul, Soman, Narendra, Davis, Graham
• Primary Examiner(s): Siefke, Samuel P
• Application Number:
  US15/291,454
• Publication Number:
  US 20170030888A1
• Time in Patent Office: 517 Days
• CPC Class Codes: G01N 33/48785 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 Class Codes: G01N 33/5091 for testing the pathological state of an organism

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.

Claims

1. A method of performing an analytical test on a test sample, the method comprising:

initiating, by an analyzer, a test cycle of a test device, the test cycle comprising a plurality of steps for performing on the test sample the analytical test for at least one target analyte;

determining spatial orientation of the analyzer during the test cycle;

comparing the determined spatial orientation to a threshold operating spatial plane for the test device, wherein the threshold operating special plane is a predetermined threshold plane for operating the test device during the test cycle; and

providing an alert that at least one of instructs and illustrates corrective action including required movement of the analyzer to bring the spatial orientation of the analyzer during the test cycle within the threshold operating spatial plane in order to prompt a user to take the corrective action for the test device during the test cycle, when the determined spatial orientation exceeds the threshold operating spatial plane,

wherein the analyzer comprises a processor, a computer readable memory, a non-transitory computer readable storage medium and program instructions, stored on the non-transitory computer readable storage medium for execution by the processor via the computer readable memory, to provide the alert and to receive the corrective action prior to the test cycle ending with a determination of a result of the analytical test.

2. The method of claim 1, further comprising receiving the corrective action for the test device prior to the test cycle ending.

3. The method of claim 1, further comprising correcting the result of the analytical test, when the determined spatial orientation during the test cycle exceeds the threshold operating spatial plane.

4. The method of claim 1, wherein the at least one target analyte is selected from the group consisting of:

hematocrit, troponin, creatine kinase myocardial band (CKMB), brain natriuretic peptide (BNP), beta human chorionic gonadotropin (bHCG), carbon dioxide partial pressure (pCO₂), partial pressure oxygen (pO₂), pH, prothrombin time (PT), activated clotting time (ACT), activated partial thromboplastin time (APTT), sodium, potassium, chloride, calcium, urea, glucose, creatinine, lactate, oxygen, and carbon dioxide.

5. The method of claim 1, further comprising:

determining motion of the analyzer during the test cycle;

comparing the determined motion to a predetermined threshold rate of motion for operating the test device during the test cycle; and

at least one of;

(i) providing a different alert prompting the user to take different corrective action for the test device during the test cycle, and (ii) suppressing the result of the analytical test, when the determined motion during the test cycle exceeds the predetermined threshold rate of motion.

6. The method of claim 1, further comprising receiving the test sample into the test device.

7. The method of claim 1, 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;

comparing the determined yaw of the analyzer to a threshold yaw; and

the providing the alert is performed, when at least one of;

(i) the determined roll of the analyzer exceeds the threshold roll, (ii) the determined pitch of the analyzer exceeds the threshold pitch, and (iii) the determined yaw of the analyzer exceeds the threshold yaw.

12. The method of claim 1, further comprising detecting the at least one target analyte during the test cycle.

13. The method of claim 1, wherein the test sample comprises whole blood.

14. The method of claim 1, wherein the test device is a cartridge comprising a sensor for the at least one target analyte.

15. The method of claim 1, further comprising, prior to the initiating step, inserting the test device into the analyzer.

8. A method of performing an analytical test on a test sample, the method comprising:

initiating, by an analyzer, a test cycle of a test device, the test cycle of the test device comprising a plurality of steps for performing on the test sample the analytical test for at least one target analyte;

determining motion of the analyzer during the test cycle;

comparing during the test cycle the determined motion to a predetermined threshold for operating the test device during the test cycle; and

providing an alert that at least one of instructs and illustrates corrective action including cessation or deceleration of movement of the analyzer to bring the motion of the analyzer during the test cycle within the predetermined threshold for the test device in order to prompt a user to take the corrective action for the test device during the test cycle, when the determined motion exceeds the predetermined threshold,

wherein the analyzer comprises a processor, a computer readable memory, a non-transitory computer readable storage medium and program instructions, stored on the non-transitory computer readable storage medium for execution by the processor via the computer readable memory, to provide the alert and to receive the corrective action prior to the test cycle ending with a determination of a result of the analytical test.

9. The method of claim 8, further comprising receiving the corrective action for the test device prior to the test cycle ending.

10. The method of claim 8, further comprising correcting the result of the analytical test, when the determined motion during the test cycle exceeds the predetermined threshold.

11. The method of claim 8, wherein the at least one target analyte is selected from the group consisting of:

hematocrit, troponin, creatine kinase myocardial band (CKMB), brain natriuretic peptide (BNP), beta human chorionic gonadotropin (bHCG), carbon dioxide partial pressure (pCO₂), partial pressure oxygen (pO₂), pH, prothrombin time (PT), activated clotting time (ACT), activated partial thromboplastin time (APTT), sodium, potassium, chloride, calcium, urea, glucose, creatinine, lactate, oxygen, and carbon dioxide.

16. The method of claim 8, further comprising detecting the at least one target analyte during the test cycle.

17. The method of claim 8, wherein the test sample comprises whole blood.

18. The method of claim 8, wherein the test device is a cartridge comprising a sensor for the at least one target analyte.

19. The method of claim 8, further comprising, prior to the initiating step, inserting the test device into the analyzer.

20. The method of claim 8, further comprising receiving the test sample into the test device.