2014, Number 6
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Ann Hepatol 2014; 13 (6)
Survival of hepatitis C-infected haemophilia patients is predicted by presence of cirrhosis but not by anti-viral treatment
Maor Y, Schapiro JM, Bashari D, Martinowitz U
Language: English
References: 26
Page: 753-761
PDF size: 103.62 Kb.
ABSTRACT
Background/Purpose. Hepatitis C (HCV) is a major cause of morbidity and mortality in haemophilia patients
who received clotting factor concentrates before the availability of virus-inactivated factors in the mid-
1980s. Recently, it has been suggested that anti-HCV treated patients, particularly those achieving a sustained
virological response (SVR) have an improved outcome. We sought to examine the survival of treated
and untreated HCV-infected haemophilia patients.
Material and methods. We studied overall and liver-related
survival of patients with haemophilia and other congenital bleeding disorders between 2000 and 2010.
The outcome was compared in 3 sub-groups: HCV mono-infected (N = 127), HCV/HIV co-infected (N = 28),
and patients with either HCV-antibodies negative or persistent HCV RNA-negative (referred to as non-infected)
(N = 45). Sixty-two (40%) (HCV and HCV/HIV) patients underwent anti-HCV treatment with an SVR
rate of 40.3%.
Results. Overall and liver-related 10-year survival were: 82.1 and 89.3%, 95.3 and 99.2 and
100% for HCV/HIV co-infected, HCV mono-infected and non-infected haemophilia patients, respectively (p =
0.015 and 0.023 for comparisons of HCV/HIV
vs. HCV; p = 0.003 for comparison of HCV/HIV and non-infected).
One HCV mono-infected and 3 co-infected patients died of end-stage liver disease (2 underwent liver
transplantation). There was no survival benefit from anti-HCV treatment or from attaining of an SVR. Only
clinically suspected cirrhosis remained as an independent predictor of survival.
Conclusion. The prognosis
of haemophilia patients who acquired HCV/HIV co-infection is worse than that of HCV mono-infected or
non-infected or haemophiliacs. This is mainly due to liver-related mortality. Anti-HCV treatment or SVR had
no observable impact on survival rate.
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