Investigação da trombose venosa na gravidez

BACKGROUND: Deep venous thrombosis (DVT) during pregnancy is a determining factor that contributes to increased maternal-fetal morbidity and mortality. It may occur when there is thrombophilia, due to compression of the inferior vena cava, venous stasis or hormonal changes. OBJECTIVES: To assess patients who are pregnant or have just given birth and who have a DVT condition in the lower limbs, to search for possible causes of thrombophilia and to perform a review of the literature. METHODS: Pregnant and puerperal patients were assessed by gynecologists and obstetricians when there was suspicion of DVT, from January 2004 through November 2006, during which time there were 24,437 childbirths at Hospital e Maternidade Sao Luiz; of these, 89% were cesarean, 7.5% were normal births and 3.5% were forceps deliveries. Of the total number of patients referred with a clinical status suggesting DVT, 42 cases were clinically diagnosed as DVT, in pregnant women aged between 21-39 years, confirmed by venous duplex scan. Right before the introduction of anticoagulant therapy, samples were collected to investigate thrombophilia, which were repeated after the treatment. RESULTS: Of the 42 patients with DVT, 32 were primigravid (three twin pregnancies with no thrombophilic changes, two resulting from in vitro fecundation), eight were mothers at second birth and two were at third birth. In four patients, DVT occurred in the first trimester of pregnancy (9.5%), in 11 patients DVT was present in the second trimester (26.2%) and in 27 patients the disease developed in the third trimester of pregnancy (64.3%). Of the 42 patients diagnosed with DVT, 18 (42.8%) occurred in infrapatellar veins. There was a case of pulmonary thromboembolism in a 37-year-old patient, who had been submitted to in vitro fecundation, with twin pregnancy and a diagnostic of DVT (no thrombophilia) after a cesarean section. Of the 42 patients, 16 (38.1%) had the cause of their DVT determined, with a prevalence of heterozygous mutation of factor V Leiden in six patients (14.2%), followed by phospholipid syndrome and other causes. Most patients were treated with low-molecular-weight heparin. CONCLUSION: DVT during pregnancy, despite having low frequency, is a major cause of increased maternal-fetal morbidity. Investigation of thrombophilia should be conducted in selected cases, such as personal or family history of thrombotic phenomena and/or thrombophilia. Twin pregnancy, cesarean birth and artificial insemination were also found as factors leading to DVT.

[1]  A. James Venous thromboembolism in pregnancy. , 2009, Arteriosclerosis, thrombosis, and vascular biology.

[2]  D. Arend J Vasc Bras , 2006 .

[3]  S. Bewley,et al.  The management and outcome of 18 pregnancies in women with polycythemia vera. , 2005, Haematologica.

[4]  I. Gouin-Thibault,et al.  Safety Profile of Different Low-Molecular Weight Heparins Used at Therapeutic Dose , 2005, Drug safety.

[5]  I. Greer,et al.  Low-molecular-weight heparin for the prevention and treatment of venous thromboembolism in pregnancy , 2004, Current opinion in pulmonary medicine.

[6]  M. Mára,et al.  [Thromboembolic complications in patients undergoing in vitro fertilization: retrospective clinical study]. , 2004, Ceska gynekologie.

[7]  R. Langan,et al.  Factor V Leiden mutation and pregnancy. , 2004, The Journal of the American Board of Family Practice.

[8]  P. D. de Groot,et al.  Antiphospholipid antibodies: update on detection, pathophysiology, and treatment , 2004, Current opinion in hematology.

[9]  Susan Cohen Factor V Leiden mutation in pregnancy. , 2004, Journal of obstetric, gynecologic, and neonatal nursing : JOGNN.

[10]  I. Greer Prevention of venous thromboembolism in pregnancy. , 2003, European journal of medical research.

[11]  L. Marsili,et al.  Venous thromboembolism in pregnancy. A case report of deep venous thrombosis (DVT) in puerperium. , 2004, Clinical and experimental obstetrics & gynecology.

[12]  D. L. Economides,et al.  Travel in pregnancy: pregnant women's experiences and knowledge of health issues. , 2006, Journal of travel medicine.

[13]  H. Morio [Economy class syndrome]. , 2003, Nihon rinsho. Japanese journal of clinical medicine.

[14]  A. Tosetto,et al.  Prevalence and risk factors of non‐fatal venous thromboembolism in the active population of the VITA Project , 2003, Journal of thrombosis and haemostasis : JTH.

[15]  V. Hach-Wunderle [Venous thrombosis in pregnancy]. , 2003, VASA. Zeitschrift fur Gefasskrankheiten.

[16]  I. Walker Venous and Arterial Thrombosis during Pregnancy: Epidemiology , 2003, Seminars in vascular medicine.

[17]  Jeffrey S. Ginsberg,et al.  How we manage venous thromboembolism during pregnancy. , 2002, Blood.

[18]  B. Jude,et al.  Preclinical Phase of Polycythemia Vera in Pregnancy , 2001, Obstetrics and gynecology.

[19]  C. Kearon Epidemiology of Venous Thromboembolism , 2001, Seminars in vascular medicine.

[20]  M. Martínez-González,et al.  Do the low molecular weight heparins improve efficacy and safety of the treatment of deep venous thrombosis? A meta-analysis. , 2000, Haematologica.

[21]  L. Eriksen,et al.  Venous Thrombectomy in Pregnancy: A Follow-up Study , 1997, Ugeskrift for laeger.

[22]  R. Tait,et al.  Superficial Vein Thrombosis: Incidence in Association with Pregnancy and Prevalence of Thrombophilic Defects , 1998, Thrombosis and Haemostasis.

[23]  J. Olsen,et al.  The cumulative incidence of venous thromboembolism during pregnancy and puerperium , 1998, Acta obstetricia et gynecologica Scandinavica.

[24]  Fiessinger Jn Treatment of venous thrombosis with low molecular weight heparin. Progress and outlook , 1997 .

[25]  Vazhenin Av,et al.  [Use of cava-filter in the treatment of acute venous thrombosis in the end of pregnancy]. , 1995 .

[26]  A. Eldor,et al.  Use of low molecular weight heparin for prophylaxis and treatment of thromboembolism in pregnancy , 1992, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

[27]  Richard L. Abbott,et al.  A Follow-up Study , 1990 .