TY - JOUR
T1 - Long-Term Follow-Up of Thalassemia Major Patients with Hepatitis C Virus Treated with Sofosbuvir and Daclatasvir
T2 - A Cohort Study
AU - Safarnezhad Tameshkel, Fahimeh
AU - Karbalaie Niya, Mohammad Hadi
AU - Amirkalali, Bahare
AU - Motamed, Nima
AU - Vafaeimanesh, Jamshid
AU - Maadi, Mansooreh
AU - Sohrabi, Masodreza
AU - Faraji, Amir Hossein
AU - Khoonsari, Mahmoodreza
AU - Ajdarkosh, Hossein
AU - Nikkhah, Mehdi
AU - Sobrakhshankhah, Elham
AU - Zamani, Farhad
N1 - Copyright © 2022 Instituto Mexicano del Seguro Social (IMSS). Published by Elsevier Inc. All rights reserved.
PY - 2022/11
Y1 - 2022/11
N2 - BACKGROUND: Treatment of Chronic Hepatitis C virus (HCV) infection in patients suffering from hereditary β-thalassemia major is a concern due to drug complications and liver malfunction. The aim of the present study was to evaluate treatment outcome of Direct-Acting Antiviral (DAA) therapy in thalassemia major patients infected with HCV in a three year follow-up.METHODS: In a cohort study, long-term safety and efficacy of DAA therapy were evaluated in a group of thalassemia major patients suffering from chronic HCV infection. Hematologic and biochemical parameters as well as liver Fibroscan monitoring were assessed at the onset and three years after the treatment.RESULTS: From among 84 patients enrolled in the study, 53.6% were males, 36.9% had cirrhosis, 96.4% had a history of Desferal usage, and 78.6% had a history of splenectomy. Unfortunately, 7 participants (8.3%) died prior to the end of follow-up with nearly half of them having Iron overload and heart failure complications. Fibroscan score, ALT, AST, and ferritin were significantly lower compared with baseline evaluation, while Hb, creatinine, and direct bilirubin increased significantly in the third year after the treatment.CONCLUSION: Safety and efficacy of Sofosbuvir and Daclatasvir in thalassemia patients assessed previously but our three year follow-up showed their mild complications and death into a long-term period after DAAs treatment and 91.7% three year survival rate, which may affected by other confounding factors, such as liver malfunction and Iron overload.
AB - BACKGROUND: Treatment of Chronic Hepatitis C virus (HCV) infection in patients suffering from hereditary β-thalassemia major is a concern due to drug complications and liver malfunction. The aim of the present study was to evaluate treatment outcome of Direct-Acting Antiviral (DAA) therapy in thalassemia major patients infected with HCV in a three year follow-up.METHODS: In a cohort study, long-term safety and efficacy of DAA therapy were evaluated in a group of thalassemia major patients suffering from chronic HCV infection. Hematologic and biochemical parameters as well as liver Fibroscan monitoring were assessed at the onset and three years after the treatment.RESULTS: From among 84 patients enrolled in the study, 53.6% were males, 36.9% had cirrhosis, 96.4% had a history of Desferal usage, and 78.6% had a history of splenectomy. Unfortunately, 7 participants (8.3%) died prior to the end of follow-up with nearly half of them having Iron overload and heart failure complications. Fibroscan score, ALT, AST, and ferritin were significantly lower compared with baseline evaluation, while Hb, creatinine, and direct bilirubin increased significantly in the third year after the treatment.CONCLUSION: Safety and efficacy of Sofosbuvir and Daclatasvir in thalassemia patients assessed previously but our three year follow-up showed their mild complications and death into a long-term period after DAAs treatment and 91.7% three year survival rate, which may affected by other confounding factors, such as liver malfunction and Iron overload.
KW - Humans
KW - Male
KW - Female
KW - Sofosbuvir/therapeutic use
KW - Hepacivirus/genetics
KW - Antiviral Agents/therapeutic use
KW - Hepatitis C, Chronic/complications
KW - Follow-Up Studies
KW - Cohort Studies
KW - beta-Thalassemia/complications
KW - Hepatitis C/complications
KW - Pyrrolidines/therapeutic use
KW - Treatment Outcome
KW - Iron Overload
KW - Drug Therapy, Combination
U2 - 10.1016/j.arcmed.2022.09.004
DO - 10.1016/j.arcmed.2022.09.004
M3 - Article
C2 - 36216685
SN - 0188-4409
VL - 53
SP - 666
EP - 672
JO - Archives of Medical Research
JF - Archives of Medical Research
IS - 7
ER -