Table 1.
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.