Key result
Inherited thrombophilia increased primary upper-extremity DVT risk and was associated with a recurrence rate of 4.4% vs 1.6% patient-years compared to no thrombophilia (HR 2.7; 95% CI 0.7-9.8).
Why the study?
Does inherited thrombophilia increase the risk of occurrence and recurrence of primary upper-extremity DVT?
Case-Control (n=912)
Does inherited thrombophilia increase the risk of occurrence and recurrence of primary upper-extremity DVT?
Inherited thrombophilia is a strong risk factor for primary upper-extremity DVT, and its combination with oral contraceptives further amplifies this risk, though overall recurrence rates remain relatively low.
BACKGROUND: One third of cases of upper-extremity deep vein thrombosis (DVT) are primary, ie, they occur in the absence of central venous catheters or cancer. Risk factors for primary upper-extremity DVT are not well established, and the recurrence rate is unknown. METHODS AND RESULTS: We studied 115 primary upper-extremity DVT patients and 797 healthy controls for the presence of thrombophilia due to factor V Leiden, prothrombin G20210A, antithrombin, protein C, protein S deficiency, and hyperhomocysteinemia. Transient risk factors for venous thromboembolism were recorded. Recurrent upper-extremity DVT was evaluated prospectively over a median of 5.1 years of follow-up. The adjusted odds ratio for upper-extremity DVT was 6.2 (95% CI 2.5 to 15.7) for factor V Leiden, 5.0 (95% CI 2.0 to 12.2) for prothrombin G20210A, and 4.9 (95% CI 1.1 to 22.0) for the anticoagulant protein deficiencies. Hyperhomocysteinemia and oral contraceptives were not associated with upper-extremity DVT. However, in women with factor V Leiden or prothrombin G20210A who were taking oral contraceptives, the odds ratio for upper-extremity DVT was increased up to 13.6 (95% CI 2.7 to 67.3). The recurrence rate was 4.4% patient-years in patients with thrombophilia and 1.6% patient-years in those without thrombophilia. The hazard ratio for recurrent upper-extremity DVT in patients with thrombophilia compared with those without was 2.7 (95% CI 0.7 to 9.8). CONCLUSIONS: Inherited thrombophilia is associated with an increased risk of upper-extremity DVT. Oral contraceptives increase the risk only when combined with inherited thrombophilia. The recurrence rate of primary upper-extremity DVT is low but tends to be higher in patients with thrombophilia than in those without.
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Martinelli et al. (2004) conducted a case-control in Primary upper-extremity deep vein thrombosis (n=912). Inherited thrombophilia vs. Patients without thrombophilia was evaluated on Recurrent upper-extremity DVT (HR 2.7, 95% CI 0.7 to 9.8). Inherited thrombophilia increased primary upper-extremity DVT risk and was associated with a recurrence rate of 4.4% vs 1.6% patient-years compared to no thrombophilia (HR 2.7; 95% CI 0.7-9.8).
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