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. 2015 Apr 14;180(2):218–226. doi: 10.1111/cei.12573

Table 1.

Patient characteristics and classification based on disease groups and anti-phospholipid syndrome (APS) clinical manifestations

Patients Characteristics
Number (n) of patients 104
Mean age in years 40 (range 18–79)
Gender Females (n) 78 (75%)
Males (n) 26 (25%)
Race Caucasian (n) 90 (79%)
Other* (n) 14 (21%)
APS clinical manifestations
Disease groups (number, n) VT (n = 19) AT (n = 24) Any TE (n = 40) Toxaemia (n = 5) Fetal demise (n = 5) RPL (n = 8) Any PRM (n = 14)
Primary APS (n = 8) 5 4 8 1 1 0 1
Secondary APS (n = 3) 1 1 2 0 0 1 1
SLE (n = 5) 1 0 1 0 0 0 0
Non-SLE autoimmune diseases (n = 11) 1 1 2 0 0 0 0
Inherited thrombophilia (n = 2) 0 2 2 0 0 0 0
Idiopathic thrombosis (n = 15) 5 10 15 0 0 0 0
Equivocal LAC with APS manifestations (n = 8) 2 3 5 0 1 3 3
Any PRM with negative criteria laboratory tests for APS (n = 8) 0 0 0 4 2 4 8
Other clinical conditions (n = 44) 4 3 6 0 1 0 1
*

Other included patients from diverse racial background or ethnicities with no definite majority. These include individuals of African American, Asian, Middle Eastern, non-Hispanic Latin American, Hawaiian/Pacific Island or undefined descent. VT = venous thrombosis; AT = arterial thrombosis; TE = any thrombotic event; RPL = recurrent pregnancy loss; any PRM = any pregnancy-related morbidity; SLE= systemic lupus erythematosus; LAC = lupus anti-coagulant.