Prevalence of genetically defined thrombophilia and the relative risk for venous thromboembolism in the normal population and in pregnancy
. | Factor V Leiden hetero-/homozygous . | Prothrombin G20210A mutation hetero-/homozygous . | Compound factor V Leiden and prothrombin G2021 mutation . | Antithrombin deficiency . | Protein C deficiency . | Protein S deficiency . | Hyperhomo cysteinemia . |
---|---|---|---|---|---|---|---|
Prevalence in the normal population | 2–7%/0.06–0.25% | 0.7–4%/rare | 0.1% | 0.02% | 0.2% | 0.03–0.13% | 5–10% |
Relative risk of first VTE | 5–7/6.8–19.3 | 2–3/2.2–20.7 | 1.1–5 | 15–20 | 15–20 | 15–20 | 1.5–2.5 |
After termination of anticoagulation | 1.4/1.8 | 1.4/not enough data | 2.7 | 1.9–2.6 | 1.4–1.8 | 1–1.4 | 2.5 |
Relative risk of pregnancy complication | 1–2.6 | 0.9–1.3 | — | 1.3–3.6 | 1.3–3.6 | 1.3–3.6 | — |
. | Factor V Leiden hetero-/homozygous . | Prothrombin G20210A mutation hetero-/homozygous . | Compound factor V Leiden and prothrombin G2021 mutation . | Antithrombin deficiency . | Protein C deficiency . | Protein S deficiency . | Hyperhomo cysteinemia . |
---|---|---|---|---|---|---|---|
Prevalence in the normal population | 2–7%/0.06–0.25% | 0.7–4%/rare | 0.1% | 0.02% | 0.2% | 0.03–0.13% | 5–10% |
Relative risk of first VTE | 5–7/6.8–19.3 | 2–3/2.2–20.7 | 1.1–5 | 15–20 | 15–20 | 15–20 | 1.5–2.5 |
After termination of anticoagulation | 1.4/1.8 | 1.4/not enough data | 2.7 | 1.9–2.6 | 1.4–1.8 | 1–1.4 | 2.5 |
Relative risk of pregnancy complication | 1–2.6 | 0.9–1.3 | — | 1.3–3.6 | 1.3–3.6 | 1.3–3.6 | — |
Adapted from ref.8–11
VTE, venous thromboembolism.
Prevalence of genetically defined thrombophilia and the relative risk for venous thromboembolism in the normal population and in pregnancy
. | Factor V Leiden hetero-/homozygous . | Prothrombin G20210A mutation hetero-/homozygous . | Compound factor V Leiden and prothrombin G2021 mutation . | Antithrombin deficiency . | Protein C deficiency . | Protein S deficiency . | Hyperhomo cysteinemia . |
---|---|---|---|---|---|---|---|
Prevalence in the normal population | 2–7%/0.06–0.25% | 0.7–4%/rare | 0.1% | 0.02% | 0.2% | 0.03–0.13% | 5–10% |
Relative risk of first VTE | 5–7/6.8–19.3 | 2–3/2.2–20.7 | 1.1–5 | 15–20 | 15–20 | 15–20 | 1.5–2.5 |
After termination of anticoagulation | 1.4/1.8 | 1.4/not enough data | 2.7 | 1.9–2.6 | 1.4–1.8 | 1–1.4 | 2.5 |
Relative risk of pregnancy complication | 1–2.6 | 0.9–1.3 | — | 1.3–3.6 | 1.3–3.6 | 1.3–3.6 | — |
. | Factor V Leiden hetero-/homozygous . | Prothrombin G20210A mutation hetero-/homozygous . | Compound factor V Leiden and prothrombin G2021 mutation . | Antithrombin deficiency . | Protein C deficiency . | Protein S deficiency . | Hyperhomo cysteinemia . |
---|---|---|---|---|---|---|---|
Prevalence in the normal population | 2–7%/0.06–0.25% | 0.7–4%/rare | 0.1% | 0.02% | 0.2% | 0.03–0.13% | 5–10% |
Relative risk of first VTE | 5–7/6.8–19.3 | 2–3/2.2–20.7 | 1.1–5 | 15–20 | 15–20 | 15–20 | 1.5–2.5 |
After termination of anticoagulation | 1.4/1.8 | 1.4/not enough data | 2.7 | 1.9–2.6 | 1.4–1.8 | 1–1.4 | 2.5 |
Relative risk of pregnancy complication | 1–2.6 | 0.9–1.3 | — | 1.3–3.6 | 1.3–3.6 | 1.3–3.6 | — |
Adapted from ref.8–11
VTE, venous thromboembolism.
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