Key result
Inherited thrombophilia linked to ~6-fold higher venous thrombosis risk after liver transplantation for HCC.
Why the study?
Does the presence of inherited thrombophilia abnormalities increase the risk of thrombosis in patients undergoing liver transplantation for hepatocellular carcinoma?
Cohort (n=430)
Yes
Does the presence of inherited thrombophilia abnormalities increase the risk of thrombosis in patients undergoing liver transplantation for hepatocellular carcinoma?
Effect estimate: OR 6.26 (95% CI 1.19-32.85)
Inherited thrombophilia abnormalities in recipients significantly increase the risk of venous thrombosis after liver transplantation for hepatocellular carcinoma, though thrombosis does not impact overall mortality.
Recipient thrombophilia may raise post-LT thrombosis risk in HCC; leaves open whether screening or prophylaxis alters outcomes.
The influence of thrombosis on the prognosis of patients with hepatocellular carcinoma (HCC) after liver transplantation (LT) and the role of the commonest inherited thrombophilia abnormalities factor V Leiden and prothrombin G20210A in the development of thrombosis are unknown. We investigated a cohort of patients who underwent LT for HCC with the aim to estimate the incidence rate (IR) of thrombosis, its influence on mortality and re-transplantation rates and, in the frame of a nested case-control study, the role of thrombophilia in donors and recipients for the development of thrombosis. Four-hundred and thirty patients underwent LT and were followed for a median of 7.2 years. Twenty-six recipients (6%) developed thrombosis (IR 1.06 [95%CI: 0.71-1.53] per 100 pts-yr). Mortality rate after LT was 3.95 (95%CI: 3.22-4.79) per 100 pts-yr and was not influenced by thrombosis. Re-transplantation was planned for 33 patients and was more common in patients with thrombosis than in those without (HR 2.50 [95%CI: 0.87-7.17]). The risk of thrombosis was 4 times higher in recipients with thrombophilia than in those without (OR 4.23 [95%CI: 0.99-18.04]) and 6 times higher when the analysis was restricted to venous thrombosis (OR 6.26 [95%CI: 1.19-32.85]). The presence of inherited thrombophilia in the donors did not increase the risk of thrombosis of the recipient. In conclusion, thrombosis is a complication of 6% of patients transplanted for HCC and increases the risk of re-transplantation but not of mortality. The risk of thrombosis, particularly venous, is increased in the presence of thrombophilia abnormalities in the recipients.
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Martinelli et al. (2017) conducted a cohort in Hepatocellular carcinoma (n=430). Inherited thrombophilia (factor V Leiden or prothrombin G20210A mutation) vs. No thrombophilia was evaluated on Venous thrombosis (OR 6.26, 95% CI 1.19-32.85). Inherited thrombophilia abnormalities in recipients increased the risk of venous thrombosis by 6-fold (OR 6.26) after liver transplantation for hepatocellular carcinoma.
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