Blood testing system and method

1. A system comprising:

a cartridge body comprising multiple fluid channels, a fluid channel among the multiple fluid channels comprising:

a measuring chamber for receiving a test sample;

a mixing chamber for holding at least one reagent and for receiving the test sample from the measuring chamber, the mixing chamber being in fluid communication with the measuring chamber;

a testing chamber for receiving a liquid that is based on a mixture of the test sample and the at least one reagent, the testing chamber being in fluid communication with the mixing chamber;

a first pressure port in fluid communication with the measuring chamber and configured to provide first pressure along a fluidic path to the measuring chamber to enable the measuring chamber to receive the test sample;

a second pressure port in fluid communication with the mixing chamber and configured to provide second pressure along a fluidic path to the mixing chamber to enable mixing of the test sample and the at least one reagent, the first pressure being in an opposite direction to the second pressure;

a vent port; and

conduits fluidically connecting the measuring chamber, the mixing chamber, and the testing chamber, each of the measuring chamber, the mixing chamber, and the testing chamber having a three-dimensional structure that is expanded relative to each of the conduits;

a heating element to apply heat to at least part of the cartridge body;

wherein the testing chamber is arranged to enable a test on the liquid received in the testing chamber, the test for measuring a viscoelastic characteristic of the liquid; and

wherein one fluid flow to the measuring chamber is based also on a state of the vent port.

2. The system of claim 1 , wherein the cartridge body comprises:

an input port in fluid communication with a sample tube holding a test liquid, the test sample being from the test liquid.

3. The system of claim 2 , wherein the at least one reagent comprises lyophilized beads; and

wherein the heating element is separate from the cartridge body.

4. The system of claim 2 , wherein the at least one reagent comprises liquid; and

wherein the heating element is separate from the cartridge body.

5. The system of claim 2 , wherein the input port is a part of a needle assembly configured to establish fluidic communication with, and evacuate content of, the sample tube.

6. The system of claim 2 , wherein the conduits comprise a non-linear conduit between the mixing chamber and the testing chamber.

7. The system of claim 1 , wherein the fluid channel is configured so that mixing of reagent and the test sample occurs within the mixing chamber and outside of the mixing chamber.

8. The system of claim 2 , wherein the at least one reagent comprises a coagulation activator.

9. The system of claim 1 , wherein the cartridge body comprises N (N>1) measuring chambers including the measuring chamber, N mixing chambers including the mixing chamber, and N testing chambers including the testing chamber;

wherein each N th testing chamber is for receiving a liquid that is based on a mixture of a test sample from an N th measuring chamber and a reagent from an N th mixing chamber; and

wherein each N th testing chamber is arranged to enable a test on the liquid received in the N th testing chamber.

10. The system of claim 9 , wherein at least two of the N mixing chambers contain reagents that are different.

11. The system of claim 1 , wherein the test sample comprises blood; and

wherein the test sample is received into the cartridge body via a needle.

12. The system of claim 1 , wherein the vent port is configured to be closed to enable fluid flow of the test sample into the measuring chamber based on negative pressure applied to the first pressure port, where closed is the state of the vent port.

13. The system of claim 1 , wherein the first pressure comprises negative pressure.

14. The system of claim 1 , wherein the second pressure comprises a positive pressure.

15. The system of claim 1 , wherein the fluid channel is configured so that mixing of reagent and the test sample occurs, in part, in the mixing chamber.

16. The system of claim 1 , wherein the fluid channel is configured so that changes in pressure within the fluid channel cause the test sample to flow to the mixing chamber and cause the liquid that is based on the mixture of the test sample and the at least one reagent to flow to the testing chamber.

17. The system of claim 1 , wherein the cartridge body comprises four fluid channels comprising four measuring chambers including the measuring chamber, four mixing chambers including the mixing chamber, and four testing chambers including the testing chamber;

wherein each testing chamber is for receiving a liquid that is based on a mixture of a test sample from a measuring chamber in a same fluid channel and a reagent from a mixing chamber in the same fluid channel; and

wherein each testing chamber is arranged to enable a test on the liquid received in the testing chamber.

18. The system of claim 1 , wherein the conduits each have a different three-dimensional structure than each of the measuring chamber, the mixing chamber, and the testing chamber.

19. The system of claim 18 , wherein the measuring chamber is devoid of reagent prior to receiving the test sample.

20. The system of claim 1 , wherein the conduits comprise a non-linear conduit between the mixing chamber and the testing chamber.

21. The system of claim 20 , wherein the measuring chamber is devoid of reagent prior to receiving the test sample.

22. A method of using the system of claim 1 , the method comprising:

attaching the cartridge body to an analyzer console for measuring a blood hemostasis characteristic;

causing opening or closing of the least vent port and controlling pressure applied to at least one of the first pressure port or the second pressure port to control fluid flow through the fluid channel;

wherein controlling flow of the test sample into the measuring chamber comprises causing the vent port to be closed.

23. The method of claim 22 , further comprising:

applying heat to at least part of the cartridge body after attaching the cartridge body to the analyzer console and before testing the liquid in the testing chamber.

24. The method of claim 23 , further comprising controlling the heating element to apply the heat to heat the at least part of the cartridge body to a predetermined temperature.

25. The method of claim 22 , wherein controlling flow of the test sample into the measuring chamber comprises applying negative pressure to the first pressure port.

26. The method of claim 22 , wherein controlling flow of the test sample from the measuring chamber into the mixing chamber comprises causing the vent port to be opened.

27. The method of claim 22 , wherein movement of the liquid between the mixing chamber and the test chamber is based, at least in part, on to positive pressure at the second pressure port.

28. The method of claim 22 , wherein the multiple fluid channels comprise a first mixing chamber that is the mixing chamber and a second mixing chamber, the first mixing chamber and the second mixing chamber containing different reagents.

29. The cartridge method of claim 28 , wherein the first mixing chamber contains a first reagent and the second mixing chamber contain a second reagent; and

wherein at least one of the first reagent or the second reagent comprises an activator of coagulation.

30. The method of claim 29 , wherein the first mixing chamber and the second mixing chamber each contain reagent beads configured to dissolve in respective first and second portions of a test sample.

31. The method of claim 22 , further comprising, after attaching the cartridge body to the analyzer console, adding the blood test sample into the cartridge.

32. The method of claim 22 , wherein attaching the cartridge body to the analyzer console comprises releasably mating the cartridge body with an interface element housed in the analyzer console.