Comparison of postpartum anti-Xa levels following enoxaparin administration to prevent venous thromboembolism using 2 weight-based protocols: a randomized controlled trial

被引:0
|
作者
Haj, Rozan [1 ]
Massalha, Manal [1 ,2 ]
Eitam, Harel [3 ]
Kassabri, Rula [3 ]
Yefet, Enav [4 ,5 ]
Nachum, Zohar [1 ,2 ]
机构
[1] Emek Med Ctr, Dept Obstet & Gynecol, Afula, Israel
[2] Technion, Rappaport Fac Med, Haifa, Israel
[3] Emek Med Ctr, Hematol Lab, Afula, Israel
[4] Baruch Padeh Med Ctr, Dept Obstet & Gynecol, Poriya, Israel
[5] Bar Ilan Univ, Azrieli Fac Med, Safed, Israel
关键词
enoxaparin; postpartum; prophylaxis; venous thromboem-bolism; weight; PREGNANCY; RISK; THROMBOPROPHYLAXIS; HEPARIN; BUNDLE; WOMEN;
D O I
10.1016/j.ajogmf.2023.100988
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: During the postpartum period, enoxaparin is given to high-risk women to prevent venous thromboembolism, a leading cause of maternal mortality. Enoxaparin activity is measured by peak plasma anti-Xa levels. The prophylactic range of anti-Xa is 0.2 to 0.6 IU/mL. Values above and below this range represent subprophylactic and supraprophy-lactic levels, respectively. Weight-based enoxaparin administration was superior to fixed-dose enoxaparin administration in achieving an anti-Xa prophylactic range. However, it is unknown which weight-based enoxa-parin administration is superior (once daily weight categories vs 1 mg/kg body weight).OBJECTIVE: This study aimed to compare the efficacy in reaching pro-phylactic anti-Xa levels and adverse effects profile of the 2 weight-based enoxaparin dosing protocols.STUDY DESIGN: A randomized open-label controlled trial was con-ducted. Women after delivery, who were intended to receive enoxaparin, were randomized to receive either enoxaparin treatment according to 1 mg/kg (up to 100 mg) or weight categories (& LE;90 kg, 40 mg; 91 -130 kg, 60 mg; 131-170 kg, 80 mg; >170 kg, 100 mg). Plasma anti-Xa levels were obtained 4 hours after the second enoxaparin administration (day 2 of enoxaparin treatment). If the woman was still hospitalized, anti-Xa levels were also obtained on day 4. The primary endpoint was the proportion of women with anti-Xa levels within the prophylactic range at day 2. In addi-tion, data regarding anti-Xa levels in different weight groups and rates of venous thromboembolism and adverse effects were evaluated.RESULTS: Of note, 60 and 64 women received enoxaparin according to 1 mg/kg and weight categories, respectively; moreover, 55 (92%) and 27 (42%) women reached the prophylactic range of anti-Xa at day 2, respec-tively (P<.0001). The mean anti-Xa levels on day 2 were 0.34+0.09 and 0.19+0.06 IU/mL, respectively (P<.0001). The anti-Xa levels were higher in the 1 mg/kg group than in the weight categories group in the subanaly-sis of different weight categories (51-70, 71-90, and 91-130 kg). There was no difference in anti-Xa levels on day 4 compared with day 2 in both cohorts (n=25). There was no case of supraprophylactic anti-Xa levels, venous thromboembolism events, or serious hemorrhage.CONCLUSION: Postpartum enoxaparin administration at 1 mg/kg was superior to weight categories in reaching anti-Xa prophylactic levels with-out leading to serious adverse effects. Given the high efficacy and safety profile, enoxaparin at 1 mg/kg once daily should be considered the pre-ferred protocol for postpartum venous thromboembolism prophylaxis.
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页数:8
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