AI Article Synopsis

  • The study focuses on pregnancy outcomes in women with the obstetric form of antiphospholipid syndrome (APS) treated with low-molecular-weight heparin (LMWH) and low-dose aspirin (LDA), highlighting a lack of current documentation on this topic.
  • APS women with a history of fetal loss were found to have increased risks of complications like preeclampsia (PE), premature birth, and other placenta-related issues compared to women without APS.
  • The research suggests that while the LMWH + LDA treatment may lower overall pregnancy loss in APS women, these patients still face higher rates of PE, indicating a need for improved therapies targeting late pregnancy complications based on the type of previous pregnancy loss.

Article Abstract

The incidence of pregnancy outcomes for women with the purely obstetric form of antiphospholipid syndrome (APS) treated with prophylactic low-molecular-weight heparin (LMWH) plus low-dose aspirin (LDA) has not been documented. We observed women without a history of thrombosis who had experienced 3 consecutive spontaneous abortions before the 10th week of gestation or 1 fetal loss at or beyond the 10th week. We compared the frequencies of complications during new pregnancies between treated women with APS (n = 513; LMWH + LDA) and women negative for antiphospholipid antibodies as controls (n = 791; no treatment). Among APS women, prior fetal loss was a risk factor for fetal loss, preeclampsia (PE), premature birth, and the occurrence of any placenta-mediated complication. Being positive for anticardiolipin immunoglobulin M antibodies was a risk factor for any placenta-mediated complication. Among women with a history of recurrent abortion, APS women were at a higher risk than other women of PE, placenta-mediated complications, and neonatal mortality. Among women with prior fetal loss, LMWH + LDA-treated APS women had lower pregnancy loss rates but higher PE rates than other women. Improved therapies, in particular better prophylaxis of late pregnancy complications, are urgently needed for obstetric APS and should be evaluated according to the type of pregnancy loss.

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Source
http://dx.doi.org/10.1182/blood-2013-08-522623DOI Listing

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