Blood pump blood compatibility device

A system, comprising:

• a pump control module configured to control an intravascular blood pump;
• and
• one or more processors operably communicating with the pump control module, the one or more processors being within a patient console and/or a blood monitoring console, and the one or more processors configured with instructions that, when executed by the one or more processors, cause the system to:
• receive information about a blood sample from a sensor;
• determine a value of a blood parameter based on the information about the blood sample;
• and
• display the value of the blood parameter on the first display screen and/or on a second display screen,
• wherein the one or more processors comprises a plurality of processors, including a first processor and a second processor, the pump control module comprising the first processor and the blood monitoring module comprising the second processor;
• and/or
• wherein the blood monitoring module is within a first housing of the patient console;
• and/or
• wherein the blood monitoring console comprises a second housing with a second display screen, wherein a blood monitoring module is disposed in the second housing;
• and/or
• wherein the system further comprises a first port configured to receive the blood sample;
• and/or
• wherein the blood parameter comprises a prothrombin time (PT), an activated clotting time (ACT), a clot propagation rate, a clot strength, a rate of clot breakdown, a platelet mapping, a functional fibrinogen, and/or a fibrin polymerization;
• and/or
• wherein the value related to the blood parameter comprises an international normalized ratio (INR).

A method comprising:

• receiving information about a blood sample from a blood monitoring sensor;
• determining a value of a blood parameter based on the received blood sample information, wherein the blood parameter is or relates to blood coagulation;
• displaying the value of the blood parameter on a display screen of a patient console and/or a blood monitoring console;
• and
• operating a blood pump via a pump control module that is at least partially disposed in the patient console,
• wherein the pump control module comprises a first processor and a blood monitoring module comprises a second processor;
• and/or
• wherein the blood monitoring module is within a first housing of the patient console;
• and/or
• wherein the blood monitoring console comprises a second housing with a second display screen, wherein a blood monitoring module is disposed in the second housing;
• and/or
• wherein the method further comprises receiving the blood sample at a port of the patient console or blood monitoring console;
• and/or
• wherein the blood parameter comprises a prothrombin time (PT), an activated clotting time (ACT), a clot propagation rate, a clot strength, a rate of clot breakdown, a platelet mapping, a functional fibrinogen, and/or a fibrin polymerization;
• and/or
• wherein the value related to the blood parameter comprises an international normalized ratio (INR).