Case Study Flashcards
What is impacted if PT/INR and APTT Both Prolonged
-Intrinsic and extrinsic pathways
-single factor deficiency in common pathway (FX, V, II, or severe Fibrinogen deficiency)
What conditions are associated with PT/INR and APTT Both Prolonged
Congenital especially if PT and APTT are prolonged and TT/FIB are normal
Single factor deficiency FX, V, II (Prothrombin) or Fibrinogen
Acquired
Multiple factor deficiency in Intrinsic & Extrinsic pathways
Severe Liver Disease
Severe Vitamin K Deficiency
DIC
Specific inhibitor directed to common pathway factor
Hypofibrinogenemia/Dysfibrinogenemia
How would we assess both PT/INR and APTT Both Prolonged
TT/Fibrinogen assay
Mixing Studies
Factor Assays
Factor Inhibitor Assays
D-Dimer
Liver Enzymes
CBC + PBF Morphology
Liver Disease – Macrocytes & Targets
DIC – Thrombocytopenia (PLT estimate ↓ & Fragments)
Vitamin K levels
What will happen if PT/INR Prolonged and APTT Normal
What could be the conditions
Probable cause related to FVII
What are the conditions?
Congenital -
Single Factor deficiency of FVII
Acquired-
Early Liver Disease
Early Vitamin K Deficiency
Early Coumadin therapy (or initial dose)
Specific inhibitor to FVII (rare)
PT/INR Prolonged APTT Normal
How do we assess?
Mixing Studies
Factor Assays
Factor Inhibitor Assays
Liver Enzymes
CBC + PBF Morphology
Liver Disease – Macrocytes & Targets
Vitamin K levels
APTT Prolonged PT/INR Normal
cause
Probable cause related to intrinsic pathway FVIII, IX, XI, or the contact factors
What are the conditions?
Congenital -
APTT Prolonged PT/INR Normal
-Single factor Deficiency of FVIII, IX, and XI with accompanying bleeding - indicates Hemophilia A, B, or C
-VWD (can lead to FVIII deficiency)
-Deficiency of FXII, Pre-K, HMWK (contact factors)
- prolongs APTT but does not result in clinically significant bleeding
Acquired condition due to
APTT Prolonged PT/INR Normal
-Non-specific inhibitor - antiphospholipid antibodies (such as, Lupus anticoagulant in patients with SLE)
-Specific inhibitor directed against intrinsic -factors
-Hemophilic patients can develop anti-FVIII or IX due to treatment
-Acquired Hemophilia or Acquired VWD
Heparin therapy