Table 1

Clinical characteristics of the women at baseline and the characteristics at follow-up

Control groupAPS groupP
796 517  
Age, y 30 (5) [17-44] 29 (4) [16-41] .19 
 >35 y, n (%) 43 (5.4%) 15 (2.9%) .031 
BMI, kg/m2 25.6 (4.5) [15.3-36.1] 26.0 (4.6) [15.3-37.0] .18 
 >30 kg/m2 78 (9.8%) 60 (11.6%) .30 
 <18.5 kg/m2 12 (1.5%) 5 (1%) .55 
Ethnicity   .92 
 White 753 (94.6%) 489 (94.6%)  
  From Europe 647 (81.3%) 420 (81.2%)  
  From North Africa 106 (13.3%) 69 (13.4%)  
 Black Africans 36 (4.5%) 22 (4.2%)  
 Asians 7 (0.9%) 6 (1.2%)  
PL subtypes    
 Embryonic PL <10 WG 483 (60.7%) 206 (39.8%) <.0001 
 Fetal PL >10 WG 313 (39.3%) 311 (60.2%) 
 Primary PL 549 (68.9%) 342 (66.1%) .29 
 Secondary PL 247 (31.1%) 175 (33.9%) 
Inflammatory disease 7 (0.9%) 32 (6.2%) <.0001 
Current tobacco users 83 (10.4%) 50 (9.7%) .66 
Hypertension 19 (2.4%) 17 (3.3%) .33 
Positive history in a first-degree relative    
 Venous thromboembolism 15 (1.9%) 12 (2.3%) .59 
 Atherothrombosis 96 (12.1%) 53 (10.3%) .31 
 Recurrent abortion 49 (6.2%) 14 (2.7%) .004 
 Fetal loss 33 (4.1%) 6 (1.2%) .003 
Hyperlipidemia    
 Hypercholesterolemia 42 (5.3%) 31 (6.0%) .58 
 Hypertriglyceridemia 34 (4.3%) 27 (5.2%) .42 
New pregnancy during the 18-mo observational period 791 (99.4%) 513 (99.2%) .98 
Interval between the inclusion and the new pregnancy, days 156 (29) [95-386] 143 (33) [91-378] .32 
Length of time between stopping LMWH/LDA treatment and pregnancy related procedures, number of complete hours NA 14 (3) [7-29]  
Control groupAPS groupP
796 517  
Age, y 30 (5) [17-44] 29 (4) [16-41] .19 
 >35 y, n (%) 43 (5.4%) 15 (2.9%) .031 
BMI, kg/m2 25.6 (4.5) [15.3-36.1] 26.0 (4.6) [15.3-37.0] .18 
 >30 kg/m2 78 (9.8%) 60 (11.6%) .30 
 <18.5 kg/m2 12 (1.5%) 5 (1%) .55 
Ethnicity   .92 
 White 753 (94.6%) 489 (94.6%)  
  From Europe 647 (81.3%) 420 (81.2%)  
  From North Africa 106 (13.3%) 69 (13.4%)  
 Black Africans 36 (4.5%) 22 (4.2%)  
 Asians 7 (0.9%) 6 (1.2%)  
PL subtypes    
 Embryonic PL <10 WG 483 (60.7%) 206 (39.8%) <.0001 
 Fetal PL >10 WG 313 (39.3%) 311 (60.2%) 
 Primary PL 549 (68.9%) 342 (66.1%) .29 
 Secondary PL 247 (31.1%) 175 (33.9%) 
Inflammatory disease 7 (0.9%) 32 (6.2%) <.0001 
Current tobacco users 83 (10.4%) 50 (9.7%) .66 
Hypertension 19 (2.4%) 17 (3.3%) .33 
Positive history in a first-degree relative    
 Venous thromboembolism 15 (1.9%) 12 (2.3%) .59 
 Atherothrombosis 96 (12.1%) 53 (10.3%) .31 
 Recurrent abortion 49 (6.2%) 14 (2.7%) .004 
 Fetal loss 33 (4.1%) 6 (1.2%) .003 
Hyperlipidemia    
 Hypercholesterolemia 42 (5.3%) 31 (6.0%) .58 
 Hypertriglyceridemia 34 (4.3%) 27 (5.2%) .42 
New pregnancy during the 18-mo observational period 791 (99.4%) 513 (99.2%) .98 
Interval between the inclusion and the new pregnancy, days 156 (29) [95-386] 143 (33) [91-378] .32 
Length of time between stopping LMWH/LDA treatment and pregnancy related procedures, number of complete hours NA 14 (3) [7-29]  

The control group comprised women with negative thrombophilia screening results. The APS group comprised women positive for antiphospholipid antibodies. Quantitative data are given as medians (interquartile range) [range] and qualitative data as numbers (percentages).

NA, not applicable; PL, pregnancy loss.

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