Do Anti-Factor Xa Levels have any Impact on Pregnancy Outcome in Women with Previous Adverse Outcomes?

被引:2
作者
Oskovi-Kaplan, Z. Asli [1 ]
Erkenekli, Kudret [1 ]
Oztas, Efser [1 ]
Esmer, Seda Bilir [1 ]
Danisman, Nuri [1 ]
Uygur, Dilek [1 ]
Ozgu-Erdinc, A. Seval [1 ]
机构
[1] Univ Hlth Sci, Zekai Tahir Burak Hlth Practice Res Ctr, Perinatol, Talatpasa Bulvari, TR-06230 Ankara, Turkey
来源
ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE | 2020年 / 224卷 / 06期
关键词
Anti-FXa level; low molecular weight heparin; recurrent pregnancy loss; pregnancy; MOLECULAR-WEIGHT HEPARIN; ADJUSTMENT; ENOXAPARIN; LMWH;
D O I
10.1055/a-1130-2017
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective Low-molecular-weight heparin (LMWH) is used during pregnancy in women diagnosed with thrombophilia for prevention of thromboembolic events and prevention of recurrent pregnancy loss. Prophylactic dosing does not always achieve target anti-FXa levels of 0.2-0.6 IU/ml. We aimed to determine if anti-FXa levels, measured in the first trimester, have an influence on pregnancy outcome. Material and Methods Eighty-one first-trimester women with a history of adverse pregnancy outcomes under LMWH therapy during pregnancy were enrolled in this study. Anti-FXa levels were measured in the first trimester, and fetal and maternal outcomes were recorded. Results The mean age of women was 28 +/- 4 (19-40) and mean anti-FXa level 0.44 +/- 0.93 IU/ml. No bleeding or clotting complications were associated with LMWH administration. Anti-FXa levels did not have a relationship with gestational age at birth, fetal weight, type of delivery, cesarean indications, postpartum bleeding, APGAR scores, or admission to the neonatal intensive care unit (p > 0.005). Anti-FXa levels were not correlated with live birth rates. Conclusion Anti-FXa levels did not have an influence on pregnancy and fetal outcomes. The effect of LMWH on pregnancy outcomes may not be due to anticoagulant activity but other mechanisms.
引用
收藏
页码:355 / 359
页数:5
相关论文
共 28 条
  • [1] A case series of LMWH use in pregnancy: Should trough anti-Xa levels guide dosing?
    Berresheim, Michelle
    Wilkie, Jodi
    Nerenberg, Kara A.
    Ibrahim, Quazi
    Bungard, Tammy J.
    [J]. THROMBOSIS RESEARCH, 2014, 134 (06) : 1234 - 1240
  • [2] The value and impact of anti-Xa activity monitoring for prophylactic dose adjustment of low-molecular-weight heparin during pregnancy: a retrospective study
    Boban, Ana
    Paulus, Samuel
    Lambert, Catherine
    Hermans, Cedric
    [J]. BLOOD COAGULATION & FIBRINOLYSIS, 2017, 28 (03) : 199 - 204
  • [3] Analysis of unfractionated heparin dose requirements to target therapeutic anti-Xa intensity during pregnancy
    Clark, Nathan P.
    Delate, Thomas
    Cleary, Steven J.
    Witt, Daniel M.
    [J]. THROMBOSIS RESEARCH, 2010, 125 (05) : 402 - 405
  • [4] Aspirin and/or heparin for women with unexplained recurrent miscarriage with or without inherited thrombophilia
    de Jong, Paulien G.
    Kaandorp, Stef
    Di Nisio, Marcello
    Goddijn, Mariette
    Middeldorp, Saskia
    [J]. COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2014, (07):
  • [5] Planned elective repeat caesarean section versus planned vaginal birth for women with a previous caesarean birth
    Dodd, Jodie M.
    Crowther, Caroline A.
    Huertas, Erasmo
    Guise, Jeanne-Marie
    Horey, Dell
    [J]. COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2013, (12):
  • [6] Anti-factor Xa plasma levels in pregnant women receiving low molecular weight heparin thromboprophylaxis
    Fox, Nathan S.
    Laughon, S. Katherine
    Bender, Samuel D.
    Saltzman, Daniel H.
    Rebarber, Andrei
    [J]. OBSTETRICS AND GYNECOLOGY, 2008, 112 (04) : 884 - 889
  • [7] Fluctuations in anti-factor Xa levels with therapeutic enoxaparin anticoagulation in pregnancy
    Friedrich, E.
    Hameed, A. B.
    [J]. JOURNAL OF PERINATOLOGY, 2010, 30 (04) : 253 - 257
  • [8] Prophylactic dosing adjustment in pregnancy based upon measurements of anti-factor Xa levels
    Gyamfi, C
    Cohen, R
    Desancho, MT
    Gaddipati, S
    [J]. JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2005, 18 (05) : 329 - 331
  • [9] Tinzaparin for the treatment of foetal growth retardation: An open-labelled randomized clinical trial
    Hansen, Anette Tarp
    Sandager, Puk
    Ramsing, Mette
    Petersen, Olav B.
    Salvig, Jannie D.
    Juul, Svend
    Uldbjerg, Niels
    Hvas, Anne-Mette
    [J]. THROMBOSIS RESEARCH, 2018, 170 : 38 - 44
  • [10] HEIFETZ S A, 1988, Pediatric Pathology, V8, P37