The laboratory plays a central role in evaluation of a bleeding patient. Every patients with bleeding needs to be screened with a prothrombin time, activated partial thromboplastin time, thrombin time, platelet count and assessment of factor XIII. These tests help to classify the patients into one of the following groups of defects – thrombocytopenia, defects of the intrinsic coagulation system or defects of the extrinsic coagulation system. The patterns of bleeding in disease of platelets and coagulation are sufficiently distinct to allow a clinical distinction between the two groups of bleeding disorders.
The table below gives the differences between bleeding due to a platelet/vascular disease and a coagulopathy.
Clinical Feature | Platelet/Vascular Defects | Coagulopathy |
Gender Predilection | Slight female preponderance as immunotrhrombocytopenia is more common in women | Domanantly male because the commonest coagulation factor deficiencies are X linked inherited disorders |
Family/Personal History of bleeding | Uncommon | Common |
Mucosal Bleeding | Common | Less common |
Muscle and Joint Bleeding | Uncommon | Typical. Dissecting haematomas seen. |
Skin Bleeding | Typically petechiae. Ecchymosis when present tend to few in number | Typically bruising. Ecchymosis when present tend to be large and multiple |
Delayed Bleeding | Unusual | May be present |
Bleeding from superficial wounds | Persistant | Minimal |