Thromb Haemost 2006; 96(03): 285-289
DOI: 10.1160/TH06-03-0165
Theme Issue Article
Schattauer GmbH

Preeclampsia and pregnancy loss in women with a history of venous thromboembolism and prophylactic low-molecular-weight heparin (LMWH) during pregnancy

Guelay Alguel
1   Department of Internal Medicine I, Vienna, Austria
,
Rainer Vormittag
1   Department of Internal Medicine I, Vienna, Austria
,
Ralph Simanek
1   Department of Internal Medicine I, Vienna, Austria
,
Paul A. Kyrle
1   Department of Internal Medicine I, Vienna, Austria
,
Peter Quehenberger
2   Clinical Institute of Medical and Chemical Laboratory Diagnostics, Vienna, Austria
,
Christine Mannhalter
2   Clinical Institute of Medical and Chemical Laboratory Diagnostics, Vienna, Austria
,
Peter Husslein
3   Department of Obstetrics and Gynecology, Medical University Vienna; Vienna, Austria
,
Ingrid Pabinger
1   Department of Internal Medicine I, Vienna, Austria
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received 21. März 2006

Accepted after resubmission 02. August 2006

Publikationsdatum:
30. November 2017 (online)

Summary

Limited data are available regarding complications of pregnancy and pregnancy outcome under prophylaxis with low-molecular-weight heparin (LMWH) in women with a history of thromboembolism (TE).We retrospectively evaluated pregnancy complications ina cohort of 80 women. All hada history of TE (76 venous, two arterial and two venous and arterial) and received prophylactic LMWH during 86 pregnancies. The rate of preeclampsia and stillbirth in these women was compared to that of a control group of 313 women without a history of TE and LMWH. Prophylaxis was started at a median of 10 weeks of gestation and usually continued until six weeks post partum. In 94% of the cases the outcome of pregnancy was favourable with a live birth. Four pregnancies (4.7%) ended in miscarriage. Two (2.3%) pregnancies were complicated bya thromboembolic event (one deep leg vein thrombosis and PRIND, respectively). One patient developed HELLP-syndrome. Severe preeclampsia occurred in three (3.8%) and stillbirth in one (1.3%) of the patients (n=80), whereas this was the case in four (1.3%, odds ratio 3.01; 95% confidence interval (CI) 0.66–13.73, p=0.15) and 10 (3.2%, OR=0.38; 95% CI 0.05–3.04, p=0.72) control women. Mean birth weight and standard deviation of infants was 3,160± 930 g in patients and 3,300 ± 540 g in controls (p=0.11).We conclude that a favourable pregnancy outcome in women with a history of thromboembolism who use prophylactic LMWH during pregnancy can be expected. There was a trend towardsa higher risk of preeclampsia, and these women should be carefully monitored for this complication.

 
  • References

  • 1 Redman CW. Current topic: pre-eclampsia and the placenta. Placenta 1991; 12: 301-8.
  • 2 Kupferminc MJ, Eldor A, Steinman N. et al. Increased frequency of genetic thrombophilia in women with complications of pregnancy. N Engl J Med 1999; 340: 9-13.
  • 3 Kosmas IP, Tatsioni A, Ioannidis JP. Association of Leiden mutation in factor V gene with hypertension in pregnancy and pre-eclampsia: a meta-analysis. J Hypertens 2003; 21: 1221-8.
  • 4 Robertson L, Wu O, Langhorne P. et al. Thrombophilia in pregnancy: a systematic review. Br J Haematol 2006; 132: 171-96.
  • 5 Triplett DA. Antiphospholipid antibodies and recurrent pregnancy loss. Am J Reprod Immunol 1989; 20: 52-67.
  • 6 Rai RS, Clifford K, Cohen H. et al. High prospective fetal loss rate in untreated pregnancies of women with recurrent miscarriage and antiphospholipid antibodies. Hum Reprod 1995; 10: 3301-4.
  • 7 Pabinger I, Vormittag R. Thrombophilia and pregnancy outcomes. J Thromb Haemost 2005; 03: 1603-10.
  • 8 Sibai B, Dekker G, Kupferminc M. Pre-eclampsia. Lancet 2005; 365: 785-99.
  • 9 Pabinger I, Grafenhofer H, Kaider A. et al. Preeclampsia and fetal loss in women with a history of venous thromboembolism. Arterioscler Thromb Vasc Biol 2001; 21: 874-9.
  • 10 Greer IA, Nelson-Piercy C. Low-molecular-weight heparins for thromboprophylaxis and treatment of venous thromboembolism in pregnancy: a systematic review of safety and efficacy. Blood 2005; 106: 401-7.
  • 11 Sanson BJ, Lensing AW, Prins MH, Ginsberg JS, Barkagan ZS, Lavenne-Pardonge E. et al. Safety of low-molecular-weight heparin in pregnancy: a systematic review. Thromb Haemost 1999; 81: 668-72.
  • 12 Davey DA, MacGillivray I. The classification and definition of the hypertensive disorders of pregnancy. Am J Obstet Gynecol 1988; 158: 892-8.
  • 13 Brandt JT, Triplett DA, Alving B. et al. Criteria for the diagnosis of lupus anticoagulants: an update. On behalf of the Subcommittee on Lupus Anticoagulant/ Antiphospholipid Antibody of the Scientific and Standardisation Committee of the ISTH. Thromb Haemost 1995; 74: 1185-90.
  • 14 Male C, Lechner K, Eichinger S. et al. Clinical significance of lupus anticoagulants in children. J Pediatr 1999; 134: 199-205.
  • 15 Endler G, Kyrle PA, Eichinger S. et al. Multiplexed mutagenically separated PCR: simultaneous singletube detection of the factor V R506Q (G1691A), the prothrombin G20210A, and the methylenetetrahydrofolate reductase A223V (C677T) variants. Clin Chem 2001; 47: 333-5.
  • 16 Bakketeig LS. Current growth standards, definitions, diagnosis and classification of fetal growth retardation. Eur J Clin Nutr 1998; 52 (Suppl. 01) S1-4.
  • 17 Hadlock FP, Harrist RB, Martinez-Poyer J. In utero analysis of fetal growth: a sonographic weight standard. Radiology 1991; 181: 129-33.
  • 18 Mello G, Parretti E, Marozio L. et al. Thrombophilia is significantly associated with severe preeclampsia: results of a large-scale, case-controlled study. Hypertension 2005; 46: 1270-4.
  • 19 Dekker GA, de Vries JI, Doelitzsch PM. et al. Underlying disorders associated with severe early-onset preeclampsia. Am J Obstet Gynecol 1995; 173: 1042-8.
  • 20 Kupferminc MJ, Fait G, Many A. et al. Severe preeclampsia and high frequency of genetic thrombophilic mutations. Obstet Gynecol 2000; 96: 45-9.
  • 21 Sottilotta G, Oriana V, Latella C. et al. Genetic prothrombotic risk factors in women with unexplained pregnancy loss. Thromb Res 2006; 117: 681-4.
  • 22 Martinelli I, Taioli E, Cetin I. et al. Mutations in coagulation factors in women with unexplained late fetal loss. N Engl J Med 2000; 343: 1015-8.
  • 23 van Pampus MG, Dekker GA, Wolf H. et al. High prevalence of hemostatic abnormalities in women with a history of severe preeclampsia. Am J Obstet Gynecol 1999; 180: 1146-50.
  • 24 Preston FE, Rosendaal FR, Walker ID. et al. Increased fetal loss in women with heritable thrombophilia. Lancet 1996; 348: 913-6.
  • 25 Vossen CY, Preston FE, Conard J. et al. Hereditary thrombophilia and fetal loss: a prospective follow-up study. J Thromb Haemost 2004; 02: 592-6.
  • 26 Gris JC, Mercier E, Quere I. et al. Low-molecular-weight heparin versus low-dose aspirin in women with one fetal loss and a constitutional thrombophilic disorder. Blood 2004; 103: 3695-9.
  • 27 Brenner B, Bar J, Ellis M. et al. Effects of enoxaparin on late pregnancy complications and neonatal outcome in women with recurrent pregnancy loss and thrombophilia: results from the Live-Enox study. Fertil Steril 2005; 84: 770-3.
  • 28 Brill-Edwards P, Ginsberg JS, Gent M. et al. Safety of withholding heparin in pregnant women with a history of venous thromboembolism. Recurrence of Clot in This Pregnancy Study Group. N Engl J Med 2000; 343: 1439-44.
  • 29 Pabinger I, Grafenhofer H, Kaider A. et al. Risk of pregnancy-associated recurrent venous thromboembolism in women with a history of venous thrombosis. J Thromb Haemost 2005; 03: 949-54.
  • 30 Bates SM, Greer IA, Hirsh J. et al. Use of antithrombotic agents during pregnancy: the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy. Chest 2004; 126 (Suppl. 03) 627S-644S.