by caryn » Fri Nov 18, 2011 07:40 pm
Just having these polymorphisms doesn't always count as having a medical need for a blood thinner in pregnancy. I suspect women with prior early losses, with pregnancy bloodwork that looks ominous for systemic clotting, are given anticoagulants routinely (and screened for SLE/APS) but at this point hardly anyone else is going to get them *routinely*.
From what the docs said at the CME last week, there is really no good data supporting Lovenox/heparin in other cases. Some of the MFMs were questioning why we screened women for these things in the first place just because they had rough pregnancies, absent symptoms that suggest clotting issues - because a history of PE isn't considered a symptom. (Despite my case of severe PE at 34 weeks I have no underlying thrombophilias!)