Table 5 Characteristics of the performed tests.

From: Reference intervals for coagulation parameters in non-pregnant and pregnant women

Test (units)

MRI

Method

Reagent

Batch numbers

Stability (h)

AT (%)

83–128

Chromogenic assay

HemosIL Liquid Antithrombin kit

Cat.No.0020300400

Cat.No.0020030100

48

PC (%)

70–140

Chromogenic assay

HemosIL Protein C kit

Cat.No.0020300500

120

fPS (%)

63.5–149.0

Clotting time method (by turbidimetry)

HemosIL Protein S kit

Cat.No.0020302000

8

LA normalized ratio

 < 1.2

Clotting time method (by turbidimetry)

HemosILdRVVT Screen and dRVVT Confirm kit

Cat.No.0020301500

Cat.No.0020301600

72

D-dimer (μg/ml)

 < 0.24

Latex enhanced immunoassay

HemosIL D-Dimer HS kit

Cat.No.0020007700

96

FDP (μg/ml)

 < 2.01

Latex enhanced immunoassay

HemosIL FDP kit

Cat.No.0020009900

72

FVII (%)

50–129

Clotting time method (by turbidimetry)

HemosIL Factor VII Deficient Plasma

Cat.No.0020011700

24

FVIII (%)

50–150

Clotting time method (by turbidimetry)

HemosIL Factor VIII Deficient Plasma

Cat.No.0020011800

4

  1. AT antithrombin, PC protein C, fPS free protein S, LA normalized ratio lupus anticoagulant normalized ratio, FDP fibrin/fibrinogen degradation products, FVII factor VII, FVIII factor VIII, MRI manufacturer's reference interval, the test method and the batch number of each test are indicated. Stability time is presented when opened or reconstitution reagents stored at 2–8 °C.