Systems and methods for hematocrit correction in analyte test strips
A system for determining a level of a lipid analyte corrected for hematocrit includes a test strip configured to receive a sample and a meter configured to receive the test strip. The system further includes circuitry and a microprocessor, the circuitry and microprocessor configured to read the test strip and the sample and determine a level of a lipid analyte and correct the level of the lipid analyte based on a hematocrit level of the sample.
1. A system for determining a level of a lipid analyte corrected for hematocrit, comprising:
a test strip configured to receive a sample;
a meter configured to receive the test strip; and
further including circuitry and a microprocessor located in the meter, the circuitry and microprocessor configured to read the test strip and the sample when the test strip interfaces with the meter and determine a level of a lipid analyte, determine a hematocrit level of the sample, and correct the level of the lipid analyte based on the hematocrit level of the sample, wherein the correction of the level of the lipid analyte is based on correcting the level of the lipid analyte according to an angle of deflection of a line formed by a range of lipid analyte concentrations provided by the hematocrit level compared to said line provided by a normal hematocrit level.
2. The system of claim 1 , wherein the test strip is a hybrid strip.
3. The system of claim 2 , wherein the test strip has a first sample window and a second sample window configured to receive the sample, the first sample window is configured to enable a measurement of the level of lipid analyte, and the second sample window is configured to enable a measurement of hematocrit level.
4. The system of claim 3 , wherein the first sample window is an optical sample window.
5. The system of claim 4 , wherein the second sample window is an electrochemical sample window.
6. The system of claim 5 , wherein the first sample window includes a spreading layer and is configured to allow for testing of multiple analytes.
7. The system of claim 4 , wherein the lipid analyte is selected from the group consisting of HDL, LDL, triglycerides, and total cholesterol.
8. The system of claim 1 , wherein the meter is configured to receive the test strip and an additional test strip.
9. The system of claim 8 , wherein the additional test strip is configured to test for hematocrit.
10. The system of claim 1 , wherein the Law of Sines is used to determine an amount of correction.
11. A method for determining a level of a lipid analyte corrected for hematocrit, comprising:
providing a system, the system including:
a test strip configured to receive a sample;
a meter configured to receive the test strip; and
further including circuitry and a microprocessor located in the meter, the circuitry and microprocessor configured to read the test strip and the sample when the test strip interfaces with the meter, determine a hematocrit level of the sample, and determine a level of a lipid analyte and correct the level of the lipid analyte based on the hematocrit level of the sample;
receiving a sample at the test strip and inserting the test strip into the meter;
determining the level of the lipid analyte and the hematocrit level using the circuitry and microprocessor;
calculating a corrected level of the lipid analyte by correcting for the hematocrit level; and
providing an output of corrected level of the lipid analyte to a user, wherein the calculating is based on correcting the level of the lipid analyte according to an angle of deflection of a line formed by a range of lipid analyte concentrations provided by the hematocrit level compared to said line provided by a normal hematocrit level.
12. The method of claim 11 , wherein the level of hematocrit is based on an electrochemical test.
13. The method of claim 12 , wherein the test strip is a hybrid strip.
14. The method of claim 13 , wherein the test strip has a first sample window and a second sample window configured to receive the sample, the first sample window is configured to enable a measurement of the level of lipid analyte, and the second sample window is configured to enable a measurement of hematocrit level.
15. The method of claim 14 , wherein the first sample window is an optical sample window.
16. The method of claim 11 , wherein the level of the lipid analyte is based on an optical test.
17. The method of claim 11 , wherein the Law of Sines is used to determine an amount of correction.