PREGNANCY OUTCOME AND ANTICARDIOLIPIN ANTIBODY IN WOMEN WITH SYSTEMICLUPUS-ERYTHEMATOSUS

Citation
R. Ramseygoldman et al., PREGNANCY OUTCOME AND ANTICARDIOLIPIN ANTIBODY IN WOMEN WITH SYSTEMICLUPUS-ERYTHEMATOSUS, American journal of epidemiology, 138(12), 1993, pp. 1057-1069
Citations number
62
Categorie Soggetti
Public, Environmental & Occupation Heath
ISSN journal
00029262
Volume
138
Issue
12
Year of publication
1993
Pages
1057 - 1069
Database
ISI
SICI code
0002-9262(1993)138:12<1057:POAAAI>2.0.ZU;2-2
Abstract
Pregnancies in women with systemic lupus erythematosus are recognized to result in excessive fetal morbidity and mortality. Maternal autoant ibody status may explain some of these problems. Anti-cardiolipin anti body has been associated with recurrent pregnancy losses in some women with lupus, but the risk of these losses has not been defined. At the University of Pittsburgh between January 1, 1979, and December 31, 19 89, an unmatched case-control study design was used to determine wheth er patients with lupus and anti-cardiolipin antibody (81 cases) were a t increased risk for adverse pregnancy outcomes in comparison with lup us patients without the antibody (174 controls). Cases had 98 of 192 ( 51%) pregnancies with an adverse outcome, while controls had 212 of 49 4 (43%). The odds ratio for having any adverse pregnancy outcome was 1 .40 (95% confidence interval (Cl) 0.98-1.98). When pregnancies were cl assified according to specific adverse outcome types, the frequency of late miscarriages (14-20 weeks gestation) in cases and controls was 8 % and 3%, respectively. The odds ratio for late miscarriage was 2.94 ( 95% Cl 1.31-6.60). When pregnancies were stratified by birth number an d by occurrence of pregnancy before or after diagnosis, the increased frequency of late miscarriages in cases was noted only in the first pr egnancy when the pregnancy occurred before recognized disease. Preterm births (before 38 weeks gestation) were increased in cases compared w ith controls in pregnancies that occurred after diagnosis for second a nd third pregnancies. If a case had one previous adverse outcome, the odds ratio for another adverse outcome was 3.00 (95% Cl 1.62-5.57). If a case had two previous adverse outcomes, the odds ratio for a third adverse pregnancy outcome was 4.14 (95% Cl 1.62-10.58). Thus, a previo us adverse pregnancy outcome was the most important risk factor for an adverse outcome in a subsequent pregnancy.