Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium

Thrombophilias are a group of coagulation disorders associated with a predisposition to thrombotic events. They could be inherited (genetic) or acquired. The most encountered inherited thrombophilias are factor V Leiden (FVL), prothrombin gene mutation (G20210A) (PGM), protein S deficiency, protein...

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Main Authors: Ana SCUTELNICU, Corina GICA, Radu BOTEZATU, Nicolae GICA, Anca Marina CIOBANU, Brindusa CIMPOCA, Gheorghe PELTECU, Anca Maria PANAITESCU
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2020-12-01
Series:Romanian Journal of Medical Practice
Subjects:
Online Access:https://rjmp.com.ro/articles/2020.4/RJMP_2020_4_Art-06.pdf
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author Ana SCUTELNICU
Corina GICA
Radu BOTEZATU
Nicolae GICA
Anca Marina CIOBANU
Brindusa CIMPOCA
Gheorghe PELTECU
Anca Maria PANAITESCU
author_facet Ana SCUTELNICU
Corina GICA
Radu BOTEZATU
Nicolae GICA
Anca Marina CIOBANU
Brindusa CIMPOCA
Gheorghe PELTECU
Anca Maria PANAITESCU
author_sort Ana SCUTELNICU
collection DOAJ
description Thrombophilias are a group of coagulation disorders associated with a predisposition to thrombotic events. They could be inherited (genetic) or acquired. The most encountered inherited thrombophilias are factor V Leiden (FVL), prothrombin gene mutation (G20210A) (PGM), protein S deficiency, protein C deficiency and antithrombin (AT) deficiency. Based upon the risk of thrombosis, there are two types of inherited thrombophilias, high risk and low risk. The high risk inherited thrombophilia includes antithrombin III deficiency, factor V Leiden homozygotes, prothrombin gene mutation and compound heterozygotes FVL and PGM. The low risk thrombophilia includes factor V Leiden heterozygote, PGM heterozygote, protein C deficiency and protein S deficiency. The incidence of all thromboembolic events is estimated to approximately 1-2 per 1000 pregnancies and about an equal number are identified antepartum and in the puerperium. Screening for thrombophilia in pregnancy is not universally recommended because of the low incidence of the condition and because it is not cost-effective. Some adverse pregnancy outcomes could be associated with some types of thrombophilia, but this association is weak and there is no reason to initiate extensive investigations or therapeutic measures. Both obstetricians and hematologists and women need to be correctly informed and avoid emotional decisions and unnecessary invasive treatments.
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spelling doaj.art-8a8c2ca2bc25453883270a4419ec96a22022-12-21T20:05:51ZengAmaltea Medical Publishing HouseRomanian Journal of Medical Practice1842-82582069-61082020-12-0115440040410.37897/RJMP.2020.4.6Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperiumAna SCUTELNICU0Corina GICA1Radu BOTEZATU2Nicolae GICA3Anca Marina CIOBANU4Brindusa CIMPOCA5Gheorghe PELTECU6Anca Maria PANAITESCU7Filantropia Clinical Hospital, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, Romania; “Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, Romania; “Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, Romania; “Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaFilantropia Clinical Hospital, Bucharest, Romania; “Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaThrombophilias are a group of coagulation disorders associated with a predisposition to thrombotic events. They could be inherited (genetic) or acquired. The most encountered inherited thrombophilias are factor V Leiden (FVL), prothrombin gene mutation (G20210A) (PGM), protein S deficiency, protein C deficiency and antithrombin (AT) deficiency. Based upon the risk of thrombosis, there are two types of inherited thrombophilias, high risk and low risk. The high risk inherited thrombophilia includes antithrombin III deficiency, factor V Leiden homozygotes, prothrombin gene mutation and compound heterozygotes FVL and PGM. The low risk thrombophilia includes factor V Leiden heterozygote, PGM heterozygote, protein C deficiency and protein S deficiency. The incidence of all thromboembolic events is estimated to approximately 1-2 per 1000 pregnancies and about an equal number are identified antepartum and in the puerperium. Screening for thrombophilia in pregnancy is not universally recommended because of the low incidence of the condition and because it is not cost-effective. Some adverse pregnancy outcomes could be associated with some types of thrombophilia, but this association is weak and there is no reason to initiate extensive investigations or therapeutic measures. Both obstetricians and hematologists and women need to be correctly informed and avoid emotional decisions and unnecessary invasive treatments.https://rjmp.com.ro/articles/2020.4/RJMP_2020_4_Art-06.pdfpregnancypuerperiuminherited thrombophiliavenous thromboembolismprophylaxis
spellingShingle Ana SCUTELNICU
Corina GICA
Radu BOTEZATU
Nicolae GICA
Anca Marina CIOBANU
Brindusa CIMPOCA
Gheorghe PELTECU
Anca Maria PANAITESCU
Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
Romanian Journal of Medical Practice
pregnancy
puerperium
inherited thrombophilia
venous thromboembolism
prophylaxis
title Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
title_full Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
title_fullStr Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
title_full_unstemmed Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
title_short Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
title_sort screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium
topic pregnancy
puerperium
inherited thrombophilia
venous thromboembolism
prophylaxis
url https://rjmp.com.ro/articles/2020.4/RJMP_2020_4_Art-06.pdf
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