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Patients with haemoglobinopathies and chronic hepatitis C: A real difficult to treat population in 2016?

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Συγγραφέας
Zachou K., Arvaniti P., Gatselis N.K., Azariadis K., Papadamou G., Rigopoulou E., Dalekos G.N.
Ημερομηνία
2017
Γλώσσα
en
DOI
10.4084/MJHID.2017.003
Λέξη-κλειδί
alanine aminotransferase
albumin
alkaline phosphatase
alpha interferon
antivirus agent
aspartate aminotransferase
bilirubin
daclatasvir
dasabuvir
deferasirox
deferiprone
deferoxamine
ferritin
gamma glutamyltransferase
interferon
ledipasvir
ombitasvir plus paritaprevir plus ritonavir
peginterferon
ribavirin
simeprevir
sofosbuvir
adolescent
adult
anxiety disorder
arthralgia
Article
beta thalassemia
chelation therapy
chronic hepatitis C
controlled study
disease duration
drug withdrawal
female
genotype
Greece
hemochromatosis
hemoglobinopathy
hepatitis C
human
iron overload
liver cirrhosis
liver disease
major clinical study
male
medical record review
monotherapy
myalgia
neutropenia
prevalence
quantitative analysis
real time polymerase chain reaction
relapse
retrospective study
sickle cell anemia
splenectomy
thalassemia major
treatment response
Universita Cattolica del Sacro Cuore
Εμφάνιση Μεταδεδομένων
Επιτομή
Background & objectives: In the past, patients with haemoglobinopathies were at high risk of acquiring hepatitis C virus (HCV) due to multiple transfusions before HCV screening. In these patients, the coexistence of haemochromatosis and chronic hepatitis C (CHC) often leads to more severe liver disease. We assessed the HCV prevalence, clinical characteristics and outcome in this setting with particular attention to the response to treatment including therapies with the new direct acting antivirals (DAAs). Methods: The medical records of 81 consecutive patients followed the last 15 years were reviewed retrospectively. Results: 43/81 (53%) patients were anti-HCV positive including 31/43 (72.1%) with CHC (HCV-RNA positive; age 25±7 years; 45.2% with genotype 1b; 19.4% cirrhotics; baseline ferritin 887 ng/ml; range: 81-10.820). Thirty patients received IFN-based therapy with or without ribavirin with sustained virological response (SVR) in 14/30 (46.7%). Eleven patients (9 non-responders to IFN-based therapies, one in relapse and one naïve) received treatment with DAAs (SVR: 100%). 3/11 patients increased their transfusion needs while 1/11 reported mild arthralgias. No drug-drug interactions between DAAs and chelation agents were observed as attested by the stability of ferritin levels during treatment. Conclusions: More than 1/3 of patients with haemoglobinopathies suffered from CHC. Response rates to IFN-based treatment seem to be similar to other patients with CHC, while most importantly, treatment with DAAs was excellent and safe even in difficult to treat patients (most null responders with severe fibrosis) suggesting that this group of HCV patients should no longer be regarded as a difficult to treat.
URI
http://hdl.handle.net/11615/80918
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