Chest
Volume 119, Issue 1, Supplement, January 2001, Pages 122S-131S
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Use of Antithrombotic Agents During Pregnancy

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Epidemiology of VTE During Pregnancy

The true incidence of VTE associated with pregnancy is unknown, but there is a strong clinical impression that the risk is increasedcompared to the incidence in nonpregnant individuals.1 Available evidence suggests that the risk of VTE is higher aftercesarean section (particularly emergency cesarean section) than aftervaginal delivery.2 There does not appear to be apreponderance of VTE in any trimester, although there is a strikingpredisposition for DVT to occur in the left leg

Anticoagulant Therapy During Pregnancy

The anticoagulants currently available for the prevention andtreatment of VTE and arterial thromboembolism include heparin andheparin-like compounds (UFH, LMWH, and heparinoids), coumarinderivatives, as well as aspirin. The “direct” thrombin inhibitors, such as hirudin, cross the placenta and have not yet been evaluatedduring pregnancy and therefore will not be further discussed.

Summary and Conclusions

Anticoagulant therapy is indicated during pregnancy for theprevention and treatment of VTE; for the prevention and treatment ofsystemic embolism in patients with mechanical heart valves; and, oftenin combination with aspirin, for the prevention of pregnancy loss inwomen with APLAs or thrombophilia and previous pregnancy losses.Several questions concerning anticoagulant therapy remain unanswered.It appears that LMWH will largely replace UFH. Oral anticoagulants arefetopathic, but the true risks

Recommendations

When describing the various regimens of UFH and LMWH, we will usethe following terminology:

  • 1.

    mini-dose UFH (UFH, 5,000 U s/c q12h);

  • 2.

    moderate-dose UFH (UFH s/c every 12 h in dosesadjusted to target an anti-Xa level of 0.1 to 0.3 U/mL);

  • 3.

    adjusted-dose UFH (UFH s/c every 12 h in dosesadjusted to target a mid-interval APTT into the therapeutic range);

  • 4.

    prophylactic LMWH (either dalteparin, 5,000 U s/c q24h, or enoxaparin, 40 mg s/c q24h, or any once-daily LMWH adjusted totarget a peak anti-Xa level of 0.2

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