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.