Coagulation Cascade
PT / aPTT INTERPRETATION
PLATELET DISORDERS
FACTOR DEFICIENCIES
LABORATORY TESTING
100

This pathway is initiated by tissue factor and monitored by PT.

What is the extrinsic pathway?

100

This coagulation test monitors Warfarin therapy.

What is PT/INR?

100

This disease is the most common inherited bleeding disorder.

What is von Willebrand disease?

100

Hemophilia A is caused by deficiency of this factor.

What is Factor VIII?

100

This test evaluates platelet plug formation under shear stress.

What is the PFA?

200

This pathway functions primarily as an amplifier of coagulation after clotting has begun.

What is the intrinsic pathway?

200

This coagulation test monitors heparin therapy.

What is aPTT?

200

A platelet count below this value is generally considered thrombocytopenic.

What is 150,000/µL?

200

Hemophilia B is caused by deficiency of this factor.

What is Factor IX?

200

This coagulation test measures conversion of fibrinogen to fibrin.

What is thrombin time?

300

This enzyme converts fibrinogen into fibrin.

What is thrombin?

300

An isolated prolonged aPTT with normal PT suggests this inherited disorder.

What is Hemophilia?

300

Petechiae, purpura, epistaxis, and menorrhagia are classic manifestations of disorders involving this phase of hemostasis.

What is primary hemostasis?

300

This factor deficiency prolongs aPTT but usually does NOT cause bleeding.

What is Factor XII deficiency?

300

This laboratory marker specifically indicates breakdown of cross-linked fibrin.

What is D-dimer?

400

A deficiency of this factor will prolong BOTH PT and aPTT because it is part of the common pathway.

What is Factor X?

400

Both PT and aPTT are prolonged, fibrinogen is low, and D-dimer is elevated. This disorder is likely present.

What is DIC?

400

This medication irreversibly inhibits cyclooxygenase and decreases thromboxane A2 production.

What is aspirin?

400

These factors are vitamin K dependent. (There are 4.)

What are II, VII, IX, and X?

400

This study is used to differentiate factor deficiencies from inhibitors.

What is a mixing study?

500

This factor stabilizes fibrin by cross-linking strands together.

What is Factor XIII?

500

A patient has prolonged aPTT that corrects with a mixing study. This suggests this type of problem.

What is a factor deficiency?

500

A patient has:

  • Giant platelets
  • Mild thrombocytopenia
  • Abnormal ristocetin aggregation

The diagnosis is:


What is Bernard-Soulier syndrome?

500

This factor helps distinguish liver disease from vitamin K deficiency because it is not vitamin K dependent.

What is Factor V?

500

This is the MOST common preanalytic error that falsely prolongs coagulation tests.

What is a short draw citrate tube?

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