Accumulation of low molecular mass heparin during prophylactic treatment in pregnancy

被引:6
作者
Bremme, K [1 ]
van Rooijen, M
Yu, A
Blombäck, M
机构
[1] Karolinska Hosp, Div Obstet & Gynecol, Dept Woman & Child Hlth, S-17176 Stockholm, Sweden
[2] Karolinska Hosp, Karolinska Inst, Dept Surg Sci, S-17176 Stockholm, Sweden
关键词
heparin; low molecular mass; accumulation; pregnancy; prophylactic treatment;
D O I
10.1097/00001721-200103000-00010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A history of thromboembolism is associated with an increased risk of new thromboembolic events during pregnancy. Prophylaxis with heparin during pregnancy implicates long-term treatment with daily injections with either unfractionated heparin (UFH) or low molecular mass heparin (LMMH). Prolonged treatment with heparin may result in endothelial absorption and drug accumulation. In order to test this hypothesis, anti-FXa activity during pregnancy was measured in four women allergic to conventional UFH, who were treated with LMMH (dalteparin; Pharmacia). It was found that, at the commencement of treatment, it took more than 8 days to reach a steady maximum peak value, located 3 h after the given dose. One daily dosage of 5000 IU anti-Xa resulted in a measurable level of FXa for 24 h in pregnancy week 40, compared with 17 h at pregnancy week 37. The implications of an elevated anti-FXa activity during pregnancy, especially during the third trimester and at partus, are discussed. We present a reduced dose regime near term and during delivery. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:149 / 155
页数:7
相关论文
共 28 条
[1]  
ANDERSON DR, 1991, THROMB HAEMOSTASIS, V65, P248
[2]   RECURRENCE OF VENOUS THROMBOEMBOLIC DISEASE AND USE OF ORAL-CONTRACEPTIVES [J].
BADARACC.MA ;
VESSEY, MP .
BRITISH MEDICAL JOURNAL, 1974, 1 (5901) :215-217
[3]  
BARZU T, 1984, NOUV REV FR HEMATOL, V26, P243
[4]   A pharmacokinetic study of dalteparin (Fragmin®) during late pregnancy [J].
Blombäck, M ;
Bremme, K ;
Hellgren, M ;
Lindberg, H .
BLOOD COAGULATION & FIBRINOLYSIS, 1998, 9 (04) :343-350
[5]  
Blombäck M, 1998, BLOOD COAGUL FIBRIN, V9, P1
[6]  
BRANCAZIO LR, 1995, AM J OBSTET GYNECOL, V173, P1204
[7]   Changes in the pharmacokinetics of the low-molecular-weight heparin enoxaparin sodium during pregnancy [J].
Casele, HL ;
Laifer, SA ;
Woelkers, DA ;
Venkataramanan, R .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1999, 181 (05) :1113-1117
[8]   Pharmacokinetic profile of a low-molecular weight heparin (reviparin) in pregnant patients: A prospective cohort study [J].
Crowther, MA ;
Spitzer, K ;
Julian, J ;
Ginsberg, J ;
Johnston, M ;
Crowther, R ;
Laskin, C .
THROMBOSIS RESEARCH, 2000, 98 (02) :133-138
[9]  
*DEP HLTH WELSH OF, 1998, CONF ENQ MAT DEATHS
[10]   Low-molecular-weight heparin during pregnancy and delivery: Preliminary experience with 41 pregnancies [J].
Dulitzki, M ;
Pauzner, R ;
Langevitz, P ;
Pras, M ;
Many, A ;
Schiff, E .
OBSTETRICS AND GYNECOLOGY, 1996, 87 (03) :380-383