Accurex Cardiac Troponin 1 Fast

Overview Accurex Cardiac Troponin 1 Fast

Accurex Cardiac Troponin I Rapid Assay is a quantitative in vitro diagnostic tool measuring cTnI in serum, plasma, or whole blood. Its primary application is assisting in the diagnosis of acute myocardial infarction (AMI), unstable angina, acute myocarditis, and acute coronary syndrome (ACS). Post-AMI, cTnI is released into the bloodstream within hours, typically detectable 4–6 hours after chest pain onset, peaking at 8–28 hours, and remaining elevated for 3–10 days. cTnI serves as a crucial marker for diagnosing and assessing suspected AMI patients. Intended Use: Quantifying cardiac troponin I levels to diagnose myocardial injury. Technical Specifications: The assay employs fluorescence-labeled anti-human cTnI monoclonal antibodies and a capture antibody on the test line. Following sample application, labeled antibodies bind cTnI, forming a complex that migrates via capillary action to the detection zone. The captured complex’s fluorescence intensity is directly proportional to cTnI concentration. The AccuDx CQ Immunofluorescence Analyzer measures and displays the concentration, storing results and transmitting them to the hospital information system. Instructions: Collect samples using aseptic phlebotomy techniques. Bring reagents and samples to room temperature. Verify the test kit and SD card lot numbers match; calibrate the SD card with lot number changes. Access the testing interface on the AccuDx CQ Analyzer. Label the test card. Safety Precautions: For in vitro diagnostic use by trained professionals only. Do not use beyond the expiry date. Discard damaged test cards and do not reuse components. Handle all samples as biohazards. Store test cards at 4–30°C and use within one hour of opening. Store blood buffer at 0–30°C (2–8°C preferred for whole blood buffer).

How to Use Accurex Cardiac Troponin 1 Fast:

Employ approved phlebotomy techniques for sample collection. Equilibrate the test card, reagent, and specimen to ambient temperature prior to analysis. Verify congruency between the SD card and test kit lot numbers. Calibrate the SD card upon any lot number change or as needed. Access the ACCUDx CQ Analyzer's testing module via the main menu's ENT key. Aseptically retrieve the test card from its packaging before use. Clearly identify each test card with the patient's unique identifier.

Safety Instruction of Accurex Cardiac Troponin 1 Fast:

• Intended solely for laboratory diagnostic applications.
• Exclusive to healthcare practitioners.
• Discard the kit after the expiration date.
• Dispose of the test device if its protective pouch or the internal component shows any signs of damage.
• Begin the test only after opening the pouch or cartridge.
• Discard the test strip after use.
• Discard each pipette tip after a single use.
• Treat all samples as if they are capable of transmitting infection.
• Keep the test card refrigerated between 4 and 30 degrees Celsius.
• The test card must be used within 60 minutes of its package being opened.
• Maintain the blood buffer within a temperature range of 0-30°C.
• Optimal storage of the whole blood buffer is achieved at temperatures between 2 and 8 degrees Celsius.