[Modern approaches to treatment of thrombosis in pregnant women, carriers of hereditary anomalies--F-V-Leiden and G20210A mutation]

Georgian Med News. 2008 Sep:(162):46-50.
[Article in Russian]

Abstract

studying of efficiency low-molecular heparin for preventive maintenance and treatment of thromboembolic disorders in pregnant women, carriers of F-V- L and F-II-20210 G-A mutation. Under supervision, there were 27 women with thrombosis during pregnancy from 19 to 39 years old. The lower extremities veins thromboses was diagnosed by duplex sonography. F-V- Leiden, F-II-20210 G-A and MTHFR C 677T gene mutation was defined by PCR-PELP method. To all pregnant women Fraxiparin and vitamins of B group was appointed during pregnancy period; at presence of MTHFR a folic acid was appointed in addition. It is concluded that application of Fraxiparin is an effective method of treatment of thrombosis during pregnancy and women--carriers F-V- Leiden, F-II-20210 G-A and MTHFR C 677T gene mutation. High efficiency of Fraxiparin confirms with change of parameters of various parts of a hemostasis and return development of thrombosis evidence.

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • Factor V / genetics*
  • Female
  • Genetic Carrier Screening
  • Humans
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Point Mutation / genetics
  • Pregnancy
  • Risk Factors
  • Thrombosis / drug therapy*
  • Thrombosis / genetics*

Substances

  • Factor V
  • Methylenetetrahydrofolate Reductase (NADPH2)