Table 2: Inherited and acquired thrombophilia final diagnosis

Diagnosis Documented Diagnosis (%*), N=173 Lab confirmed Diagnosis
Inherited Thrombophilia Protein C Deficiency 1 (0.6%) 0
Protein S Deficiency 1 (0.6%) 0
Antithrombin Deficiency 0 1 (0.6%)
Factor V Leiden 1 (0.6%) 0
Thrombophilia, not specified 2 (1.2%) 0
Acquired Thrombophilia SLE (Systemic Lupus Erythematosus) 17 (9.8%) 9 (5.2%)
APL (Antiphospholipid antibodies) 3 (1.7%) 3 (1.7%)
Autoimmune, not specified 22 (12.7%)
Thrombosis secondary to infection 1 (0.6%)
Malignancy related thrombosis 2 (1.2%)
Hypervescosity syndromes 1 (0.6%)
Post-surgical thrombosis 1 (0.6%)
Thrombosis secondary to asphyxia 1 (0.6%)
No diagnosis made 119 (68.8%)


*Percentages may not add to 100 due to rounding to the closer decimal point.