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. 2020 Mar 18;27(2):215–223. doi: 10.1093/ibd/izaa053

TABLE 2.

Thrombophilia Testing

Test Percentage Testing Positive
Factor V Leiden mutation 7% (2/27)*
Prothrombin gene mutation 4% (1/27)
APLS testing 4% (1/27)
Protein C deficiency§ 0% (0/24)
Protein S deficiency§ 0% (0/24)
Antithrombin III deficiency§ 0% (0/20)
JAK2V617F mutation 0% (0/16)
Paroxysmal nocturnal hemoglobinuria 0% (0/6)

The results of thrombophilia testing among our cohort are described above.

*One patient was heterozygous and 1 patient was homozygous.

This patient was heterozygous.

Testing included assessment for anticardiolipin antibodies, beta-2 glycoprotein I antibodies, and lupus anticoagulant. The 1 positive patient was subsequently found to be negative on repeat testing.

§Tests were excluded if sent in the context of acute thrombosis or while a patient was on warfarin (for proteins C and S).