Purpose of the Screening
- Detecting risks of venous thromboembolism
- Identifying causes of recurrent pregnancy loss
- Protecting the fetus from placental insufficiency
Book Thrombophilia Screening in Saudi Arabia | Lahalak Medical Platform
A specialized screening to detect genetic blood clotting disorders that may impact pregnancy and fetal safety, enabling a precise preventive plan to avoid complications and ensure a healthy pregnancy journey.
Scientific name: Screening for Hereditary Thrombophilia in Pregnancy
This screening analyzes genetic mutations like Factor V Leiden and Protein C/S levels to assess risks of venous thromboembolism or recurrent miscarriage, guiding necessary anticoagulation therapy.
Service type
Laboratory test
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Factor V Leiden Mutation test
- Prothrombin G20210A Mutation test
- Protein C and S activity levels
Medical Service Information
Who Should Get Tested
- Pregnant women with family history of thrombosis
- Women with unexplained recurrent miscarriages
- Women who experienced prior pregnancy complications like preeclampsia
Clinical Significance
- Guides the dosage of anticoagulant therapy
- Reduces the risk of pulmonary embolism during pregnancy
- Ensures optimal blood flow to the placenta and fetus
Conditions & Notices
- Preferably performed before starting anticoagulants
- Inform the doctor about family history of thrombosis
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