Elitech UK Limited   Prothrombin Time (PT) Cuvette - Correlation
Protocol for HEMOCHRON® Jr. II and Signature
PT Correlation Protocol
- Fresh Blood
 
The HEMOCHRON Range
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PT Correlation Protocol - Fresh Blood
PT Citrated Protocol
Sample Collection
INR Calculation and reproducibility
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HEMOCHRON Signature
 
The HEMOCHRON Jr. offers a simple, one-step procedure using fresh whole blood samples to evaluate essential coagulation parameters: the ACT+, ACT-LR, APTT and PT. Test results are reported in plasma equivalent values and INR for PT, plasma equivalent values for APTT and in celite ACT equivalent values when performing the ACT+ or ACT-LR. By converting whole blood results into traditional, laboratory test value form, the HEMOCHRON Jr. delivers results in familiar clinical parameters facilitating accurate clinical data interpretation. In this way, near-patient testing can truly become an extension of the clinical laboratory.

Because of the varying sensitivities of different brands and lots of plasma based APTT and PT reagents, and because of different methodologies used on coagulation instrumentation, results obtained using various combinations of instrument/reagent systems will differ. Studies have shown that in the majority of instances clinical interpretation of test results is similar even if the actual results are not identical. The inherent value of point-of-care hemostasis monitoring, namely timeliness of test results, must be supplemented by determination of correlation with your current method.

While no two coagulation instrument/reagent systems produce results that match exactly, systems can be correlated to provide statistically acceptable results so as not to alter the overall clinical interpretation of the test results. To perform a correlation between two systems, ideally, samples would be tested simultaneously on each system using the same blood sample. Logistically, this becomes difficult when one system performs tests using a whole blood sample at the bedside, and the other system uses a plasma based sample and is performed in the laboratory.

ITC suggests the attached recommended correlation protocol and data collection form to minimize the data collection variables (such as time elapsed between blood sample collection and test performance) when performing a correlation between whole blood and plasma-based coagulation systems. The protocol is segmented into parts to allow the user to become familiar with the HEMOCHRON Jr. test procedures prior to
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