Diagnostic reasoning
Start with the bleeding phenotype and organize PT/aPTT before the differential.
Choose an objective, study one block at a time, and use search to quickly locate tests, concepts, and diagnostic traps.
The Clinical Bench guides you through hypothesis, test selection, interpretation, and targeted confirmation in six progressive cases.
6 modules found
Start with the bleeding phenotype and organize PT/aPTT before the differential.
Connect collection, citrate, processing, interference, and quality control to the result.
Compare the classic assay cascade with the cell-based model of in-vivo coagulation.
Review morphology, activation, and platelet participation in hemostasis.
Integrate clinical observation, safety, communication, and nursing care.
Look up technical terms and the role of each factor in the classic pathways.
Distinguish primary hemostasis, secondary hemostasis, global consumption, and inhibitors.
Start with the clinical bleeding pattern, then connect laboratory tests to the most likely pathway in the cascade.
Petechiae, purpura, epistaxis, gum bleeding, menorrhagia.
Suggests platelet, vascular, or von Willebrand-related problems.
Hemarthrosis, muscle hematomas, delayed post-trauma bleeding.
Suggests a coagulation factor deficiency.
Extrinsic pathway
Factor VII, early vitamin K deficiency, warfarin, or early liver disease.
Intrinsic pathway
Factors VIII, IX, XI, XII, heparin, or lupus anticoagulant.
Common pathway or global consumption
Factors X, V, II, I, DIC, liver disease, or severe vitamin K deficiency.
Think beyond global tests
Platelets, von Willebrand disease, Factor XIII, or vascular abnormalities.
A practical pathway from the clinical complaint to the most likely group of causes.
Petechiae, purpura, and mucosal bleeding suggest platelets/von Willebrand. Hemarthrosis, deep hematomas, and delayed bleeding suggest coagulation factors.
Bleeding since childhood, affected male relatives, or familial recurrence increase suspicion for hemophilia and inherited disorders.
Anticoagulants, antiplatelets, antibiotics, liver disease, sepsis, malnutrition, and recent surgery change test interpretation.
Start with platelets, PT/INR, PTT, fibrinogen, and D-dimer. The combined pattern often points to the likely pathway or systemic process.
Abnormal PT suggests the extrinsic pathway. Abnormal PTT suggests the intrinsic pathway. Both abnormal suggests common pathway, consumption, or liver disease.
Normal PT/PTT does not exclude bleeding: assess platelets, von Willebrand, vascular disorders, and Factor XIII deficiency.