Abstract
Objective:
To compare two enoxaparin dosing strategies at achieving prophylactic anti-Xa levels in women with a body mass index (BMI) ⩾35 (kg m−2) postcesarean delivery.
Study Design:
Women with BMI ⩾35 were randomized to receive prophylactic enoxaparin at a fixed dose of 40 mg daily or weight-based dosing of 0.5 mg kg−1 twice daily. The primary outcome was the proportion of subjects with peak anti-Xa levels in the prophylactic range of 0.2 to 0.6 IU ml−1.
Result:
From August 2013 through February 2014, 84 demographically similar women completed the protocol. In the weight-based group, 88% (37/42) of the women reached prophylactic anti-Xa levels versus 14% (6/42) in the fixed dose group (odds ratio 44.4, 95% confidence interval 12.44, 158.48, P<0.001). No anti-Xa level exceeded 0.48 IU ml−1. There were no venous thromboembolic or bleeding events requiring reoperation or transfusion in either group.
Conclusion:
Compared with fixed dosing daily, weight-based dosing twice daily more effectively achieved prophylactic anti-Xa levels without reaching the therapeutic range.
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Acknowledgements
This study was conducted at the Memorial Care Center for Women at Miller Children’s Hospital, Long Beach Memorial Medical Center, Long Beach, CA 90806, USA and funded by a grant from the Long Beach Memorial Medical Center Foundation.
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Presented at the 35th Annual Meeting of the Society for Maternal Fetal Medicine, San Diego, CA, USA, 2–7 February 2015, Abstract number 26.
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Stephenson, M., Serra, A., Neeper, J. et al. A randomized controlled trial of differing doses of postcesarean enoxaparin thromboprophylaxis in obese women. J Perinatol 36, 95–99 (2016). https://doi.org/10.1038/jp.2015.130
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DOI: https://doi.org/10.1038/jp.2015.130
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