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Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital

BACKGROUND: Chronic hepatitis C (CHC) is a global infection. In Saudi Arabia, the prevalence of CHC is declining due to the implementation of a blood screening program. However, CHC still remains a leading cause of liver cirrhosis and hepatocellular carcinoma. OBJECTIVES: This is a retrospective stu...

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Autores principales: Akbar, Hisham O, Al Ghamdi, Ahmad, Qattan, Faten, Fallatah, Hind I, Al Rumani, Maha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475025/
https://www.ncbi.nlm.nih.gov/pubmed/23087760
http://dx.doi.org/10.5812/hepatmon.6178
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author Akbar, Hisham O
Al Ghamdi, Ahmad
Qattan, Faten
Fallatah, Hind I
Al Rumani, Maha
author_facet Akbar, Hisham O
Al Ghamdi, Ahmad
Qattan, Faten
Fallatah, Hind I
Al Rumani, Maha
author_sort Akbar, Hisham O
collection PubMed
description BACKGROUND: Chronic hepatitis C (CHC) is a global infection. In Saudi Arabia, the prevalence of CHC is declining due to the implementation of a blood screening program. However, CHC still remains a leading cause of liver cirrhosis and hepatocellular carcinoma. OBJECTIVES: This is a retrospective study of CHC patients at the King Abdul Aziz University Hospital, Jeddah, Saudi Arabia. PATIENTS AND METHODS: Out of a total of 291 CHC patients from the hepatology clinic at King Abdul Aziz University hospital, Jeddah, 279 patients were included in the present study. They were primarily male (152, 54.5%), with a mean age of 50.41 ± 1.72 years. The majority of patients were either Saudi (108, 38.7%) or Egyptian (60, 21.5%). A total of 61 patients received combination treatment with pegylated interferon and ribavirin, and one patient with sickle-cell anemia received pegylated INF monotherapy. Demographic, clinical and laboratory features of the CHC patients, and their responses to treatment were studied. RESULTS: Decompensated cirrhosis was documented in 60 patients (21.5%), and hepatocellular carcinoma in 14 (5%). The mean level of serum alanine aminotransferase was 83.6 ± 231 u/L. The predominant genotype among the 70 patients tested, was genotype 4, followed by genotype 1 (39 and 18 patients, respectively). The sustained viral response (SVR) rate was 82.99%. The main predictive factors for SVR were baseline HCV viral load and rapid virologic response (RVR). The mean duration of follow-up was 4.2 ± .85 years. There were 24 patients who had liver disease-related mortality. CONCLUSIONS: our data showed that 22% of CHC patients progress to cirrhosis and another 22% had treatment. Liver related mortality was more common in patients with advanced cirrhosis.
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spelling pubmed-34750252012-10-21 Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital Akbar, Hisham O Al Ghamdi, Ahmad Qattan, Faten Fallatah, Hind I Al Rumani, Maha Hepat Mon Original Article BACKGROUND: Chronic hepatitis C (CHC) is a global infection. In Saudi Arabia, the prevalence of CHC is declining due to the implementation of a blood screening program. However, CHC still remains a leading cause of liver cirrhosis and hepatocellular carcinoma. OBJECTIVES: This is a retrospective study of CHC patients at the King Abdul Aziz University Hospital, Jeddah, Saudi Arabia. PATIENTS AND METHODS: Out of a total of 291 CHC patients from the hepatology clinic at King Abdul Aziz University hospital, Jeddah, 279 patients were included in the present study. They were primarily male (152, 54.5%), with a mean age of 50.41 ± 1.72 years. The majority of patients were either Saudi (108, 38.7%) or Egyptian (60, 21.5%). A total of 61 patients received combination treatment with pegylated interferon and ribavirin, and one patient with sickle-cell anemia received pegylated INF monotherapy. Demographic, clinical and laboratory features of the CHC patients, and their responses to treatment were studied. RESULTS: Decompensated cirrhosis was documented in 60 patients (21.5%), and hepatocellular carcinoma in 14 (5%). The mean level of serum alanine aminotransferase was 83.6 ± 231 u/L. The predominant genotype among the 70 patients tested, was genotype 4, followed by genotype 1 (39 and 18 patients, respectively). The sustained viral response (SVR) rate was 82.99%. The main predictive factors for SVR were baseline HCV viral load and rapid virologic response (RVR). The mean duration of follow-up was 4.2 ± .85 years. There were 24 patients who had liver disease-related mortality. CONCLUSIONS: our data showed that 22% of CHC patients progress to cirrhosis and another 22% had treatment. Liver related mortality was more common in patients with advanced cirrhosis. Kowsar 2012-09-30 /pmc/articles/PMC3475025/ /pubmed/23087760 http://dx.doi.org/10.5812/hepatmon.6178 Text en Copyright © 2012, Baqiyatallah Research Center for Gastroenterology and Liver Diseases http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Akbar, Hisham O
Al Ghamdi, Ahmad
Qattan, Faten
Fallatah, Hind I
Al Rumani, Maha
Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital
title Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital
title_full Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital
title_fullStr Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital
title_full_unstemmed Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital
title_short Chronic Hepatitis C in Saudi Arabia: Three Years Local Experience in a University Hospital
title_sort chronic hepatitis c in saudi arabia: three years local experience in a university hospital
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475025/
https://www.ncbi.nlm.nih.gov/pubmed/23087760
http://dx.doi.org/10.5812/hepatmon.6178
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