Can Lovenox (enoxaparin) be used during pregnancy?

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Last updated: February 11, 2025View editorial policy

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From the Guidelines

Lovenox (enoxaparin) can be used during pregnancy, but with caution and careful monitoring.

Important Considerations

  • Lovenox is a low-molecular-weight heparin (LMWH) that does not cross the placenta and is likely safe for the fetus 1.
  • However, the use of LMWH during pregnancy remains controversial due to reports of treatment failures and safety concerns 1.
  • In a clinical study, 2 of 8 women with prosthetic heart valves developed prosthetic valve thromboses while taking subcutaneous enoxaparin, leading to maternal and fetal death 1.

Monitoring and Dosing

  • Plasma anti-Xa levels should be measured 4 to 6 hours after the morning dose and the dose of LMWH adjusted to achieve an anti-Xa level of approximately 0.7 to 1.2 units per ml 1.
  • The dose of LMWH should be weight-adjusted, and adaptation according to anti-Xa monitoring may be considered in women at extremes of body weight or with renal disease 1.

Alternatives and Risks

  • Unfractionated heparin (UFH) is an alternative to LMWH, but it has a higher risk of heparin-induced thrombocytopenia, osteoporosis, and bleeding complications 1.
  • Warfarin crosses the placenta and is associated with a well-defined embryopathy during the first trimester, as well as fetal and neonatal hemorrhage in the third trimester 1.

From the Research

Use of Lovenox (Enoxaparin) During Pregnancy

  • Enoxaparin is a low molecular weight heparin that can be used during pregnancy for the treatment and prevention of thromboembolism 2, 3, 4, 5, 6.
  • International guidelines support the use of low molecular weight heparins, such as enoxaparin, for the treatment of thromboembolism and thromboprophylaxis during pregnancy 2.
  • Studies have shown that enoxaparin is safe and effective for preventing thromboembolism and adverse obstetrical complications in pregnant women, including those with multiple gestations 3, 5, 6.
  • The use of enoxaparin during pregnancy has been associated with a low incidence of complications, including bleeding events, thrombocytopenia, and osteoporotic fractures 3, 4, 5, 6.
  • Enoxaparin does not cross the placenta and is safe for the fetus, with no reported cases of teratogenicity or congenital malformations 4.

Indications for Enoxaparin Use During Pregnancy

  • Prophylaxis of venous thromboembolism 2, 3, 4, 5, 6.
  • Prevention of pregnancy loss in thrombophilic women 2, 3, 4.
  • Treatment of venous thromboembolism 5, 6.
  • Prophylaxis of arterial thrombosis in pregnant women with mechanical heart valves 4.
  • Prevention of late gestational complications, such as pre-eclampsia and intrauterine growth restriction 4.

Dosage and Administration

  • The recommended dose of enoxaparin during pregnancy is 40 mg once daily, although some studies have used doses of 1 mg/kg twice daily or 1.5 mg/kg once daily 3, 5, 6.
  • Enoxaparin should be discontinued 12-24 hours before delivery and restarted within 8-12 hours after delivery 6.
  • Warfarin can be given as adjuvant therapy along with enoxaparin in the post-partum period 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

A protocol for the use of enoxaparin during pregnancy: results from 85 pregnancies including 13 multiple gestation pregnancies.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2005

Research

Enoxaparin use in pregnancy: state of the art.

Women's health (London, England), 2007

Research

Antenatal use of enoxaparin for prevention and treatment of thromboembolism in pregnancy.

BJOG : an international journal of obstetrics and gynaecology, 2000

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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