Laboratory Tests for Blood Clots
The standard laboratory tests for diagnosing blood clots include prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen, and platelet count, which should be measured early and repeatedly to detect coagulopathy. 1
First-Line Laboratory Tests
Basic Coagulation Panel
- Prothrombin Time (PT): Evaluates the extrinsic pathway and common pathway of coagulation
- Activated Partial Thromboplastin Time (APTT): Assesses the intrinsic pathway and common pathway
- Fibrinogen: Measures the amount of fibrinogen in blood (using Clauss method)
- Platelet Count: Quantifies platelets in circulation
These tests form the cornerstone of coagulation assessment and should be performed early and repeatedly in patients with suspected coagulopathy 1, 2.
Additional First-Line Tests
- Complete Blood Count (CBC): To evaluate for anemia or other blood disorders
- D-dimer: A fibrin degradation product that can help exclude venous thromboembolism when negative in low-risk patients 1
- Ferritin/Iron Studies: To identify iron deficiency which may suggest chronic blood loss 1
Second-Line Laboratory Tests
When first-line tests are abnormal or clinical suspicion remains high despite normal initial tests, the following should be considered:
Advanced Coagulation Tests
- Viscoelastic Testing: Thromboelastometry or thromboelastography to assess clot formation and stability in real-time 1
- Platelet Function Testing: Light transmission aggregometry with multiple agonists 1, 2
- Von Willebrand Factor (VWF) Testing: Including VWF antigen (VWF:Ag) and VWF activity (VWF:RCo) 2
- Factor Assays: For specific factor deficiencies (Factors II, V, VII, VIII, IX, X, XI, XIII) 1
Specialized Tests
- Fibrinolysis Assays: To assess the breakdown of blood clots
- Thrombin Generation Assay: Measures overall coagulation potential
- Platelet Flow Cytometry: For platelet disorders 1
- Genetic Testing: For hereditary thrombophilias when clinically indicated 1
Interpretation of Results
Prolonged PT
- Indicates deficiency or inhibition of factors in the extrinsic pathway (VII) or common pathway (X, V, II, fibrinogen)
- Common causes: Liver disease, vitamin K deficiency, warfarin therapy 1
Prolonged APTT
- Indicates deficiency or inhibition of factors in the intrinsic pathway (XII, XI, IX, VIII) or common pathway
- Common causes: Heparin therapy, hemophilia, lupus anticoagulant 1
Low Fibrinogen
- Critical values (<100 mg/dL) are associated with bleeding in 90% of patients 3
- Seen in disseminated intravascular coagulation (DIC), severe liver disease, or consumption coagulopathy
Abnormal Platelet Count
- Thrombocytopenia (<150,000/μL) increases bleeding risk, especially when <50,000/μL 1
- A higher target level of 100,000/μL is recommended for patients with multiple trauma or CNS injury 1
Clinical Pitfalls to Avoid
Relying solely on PT/APTT: These tests only monitor the initiation phase of coagulation (first 4% of thrombin production) 1
Overlooking preanalytical variables: Sample collection, processing, and storage can affect results
Misinterpreting D-dimer: While sensitive, D-dimer has poor specificity and can be elevated in many conditions besides thrombosis 1
Failing to consider timing: D-dimer levels decline with time from symptom onset, potentially leading to false negatives 1
Not accounting for medications: Anticoagulants and antiplatelet drugs will affect test results 4
Overlooking hypermobility: Should be assessed as it's associated with bleeding symptoms 1
Missing iron deficiency: Persistent or recurrent iron deficiency may suggest a bleeding phenotype 1
By systematically applying these laboratory tests and understanding their limitations, clinicians can effectively diagnose and manage patients with suspected blood clots, ultimately reducing morbidity and mortality associated with these conditions.