Dialab GmbH
Operator's Manual DIAcheck series Rev-4 Page 13
1.4.4 PRINCIPLE OF MEASURMENT
The detection of plasma clotting is based on a photometric principle. No mechanical aids
like mixing bars are required. Blood plasma is filled into a cuvette. Special reagents are
added, which initiate the blood coagulation. The cuvette is transmitted by ultra violet light
during the coagulation process. When the sample starts to clot a change of light absorbance
is measured. The time from measurement start to change of light (turning point) is called
clotting time and expressed in seconds [s].
The conversion of coagulation time into a specific test unit is one using a linear, hyperbolic,
semi-logarithmic or double-logarithmic interpolation of the stored calibration points. The
current mathematical model is printed out in "TEST SETUP." Values outside the calibration
range are calculated by extrapolation and flagged as " * ".
places
value
R = clotting time / normal time
NR = 100 *(normal time/clotting time)
INR = Ratio
ISI
(International Normal Ratio)
IU/mL = IE/mL = International Units (1.00 IU/mL = 100 % activity)