Why ROTEM instead of traditional tests
ROTEM assays
ROTEM Assays
* INTEM: Activates coagulation via intrinsic pathway (contact activation).
* EXTEM: Activates coagulation via tissue factor (extrinsic).
* HEPTEM: Same as INTEM but with heparinase – neutralizes heparin.
* FIBTEM: Assesses fibrinogen contribution (platelets inhibited).
* APTEM: Modified EXTEM with antifibrinolytic (e.g., aprotinin) – detects hyperfibrinolysis.
ROTEM graph parameters
***ROTEM Graph Parameters
* CT (Clotting Time): Time until initial clot formation – reflects thrombin generation.
* CFT (Clot Formation Time): Time from CT to 20 mm amplitude – reflects clot propagation. * A10/A20/MCF (Amplitude at 10/20 mins, Max Clot Firmness): - Measures clot strength. - Reflects platelets, fibrinogen, and factor XIII(Fibrin stabilizing factor) * ML (Maximum Lysis): Degree of clot breakdown – indicates fibrinolysis. * ALPHA Angle- -It is the tangent to clotting curve from 2mm -Normal alpha in EXTEM- 60-80 degrees - Normal alpha in INTEM_ 70-80 degrees - low alpha angle indicates slow clot formation- clotting factor def/fibrin def - High alpha angle- hypercoagulability -Reflects speed of fibrinogen accumulation -Provides indication of hyper/hypo coagulable state _Dependent mainly upon Fibrinogen
LY 30**
- percentage amplitude reduction 30mins after the maximum amplitude
- A measure of fibrinolysis
ROTEM interpretation
Clinical use
refrence ranges were derived from healthy volunteers hence target range may be higher in acutely bleeding patients.