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Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis

BACKGROUND: Neonatal hepatitis refers to a heterogeneous group of disorders, caused by many factors including cytomegalovirus infection, revealing similar morphologic changes in the liver of an infant less than 3 months of age. Approximately 40% of cholestasis in infants is due to neonatal hepatitis...

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Autores principales: Ozkan, Tanju Basarir, Mistik, Resit, Dikici, Bunyamin, Nazlioglu, Hülya Ozturk
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847446/
https://www.ncbi.nlm.nih.gov/pubmed/17355631
http://dx.doi.org/10.1186/1471-230X-7-9
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author Ozkan, Tanju Basarir
Mistik, Resit
Dikici, Bunyamin
Nazlioglu, Hülya Ozturk
author_facet Ozkan, Tanju Basarir
Mistik, Resit
Dikici, Bunyamin
Nazlioglu, Hülya Ozturk
author_sort Ozkan, Tanju Basarir
collection PubMed
description BACKGROUND: Neonatal hepatitis refers to a heterogeneous group of disorders, caused by many factors including cytomegalovirus infection, revealing similar morphologic changes in the liver of an infant less than 3 months of age. Approximately 40% of cholestasis in infants is due to neonatal hepatitis. It may cause latent or acute cholestatic or chronic hepatitis, including cirrhosis in immunocompetant infant. METHODS: Twelve infants diagnosed with neonatal cytomegalovirus hepatitis in the last one year were included in the study. Group 1 consisted of seven babies treated with ganciclovir for 21 days. Group 2 included five cases who did not receive antiviral treatment. Physical examination, biochemical, serologic and virologic tests were done for both groups at the time of diagnosis and in the third month. RESULTS: Initial levels of total bilirubin, aminotransferases, gamma glutamyl transpeptidase, and alkaline phosphatase revealed a significant decrease after the treatment in Group 1 (p < 0.05) when compared with Group 2. This study revealed that ganciclovir treatment is a safe and effective in cases with cholestatic hepatitis. Similarly, all the patients in the treatment group had evidence of improvement serologically and virologically, while the comparison group did not reveal any significant change(p < 0.01). CONCLUSION: The clinical spectrum of perinatal infection varies from an asymptomatic infection or a mild disease to a severe systemic involvement, including central nervous system. The treatment in the early period of infection improved serologic markers and cholestatic parameters significantly. Further studies will lead us to clarify the efficacy of ganciclovir treatment in the early period of cytomegalovirus hepatitis, and the preventive role of anti-viral therapy on progressive liver disease due to cholestasis and hepatitis in neonatal cytomegalovirus infection.
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spelling pubmed-18474462007-04-04 Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis Ozkan, Tanju Basarir Mistik, Resit Dikici, Bunyamin Nazlioglu, Hülya Ozturk BMC Gastroenterol Research Article BACKGROUND: Neonatal hepatitis refers to a heterogeneous group of disorders, caused by many factors including cytomegalovirus infection, revealing similar morphologic changes in the liver of an infant less than 3 months of age. Approximately 40% of cholestasis in infants is due to neonatal hepatitis. It may cause latent or acute cholestatic or chronic hepatitis, including cirrhosis in immunocompetant infant. METHODS: Twelve infants diagnosed with neonatal cytomegalovirus hepatitis in the last one year were included in the study. Group 1 consisted of seven babies treated with ganciclovir for 21 days. Group 2 included five cases who did not receive antiviral treatment. Physical examination, biochemical, serologic and virologic tests were done for both groups at the time of diagnosis and in the third month. RESULTS: Initial levels of total bilirubin, aminotransferases, gamma glutamyl transpeptidase, and alkaline phosphatase revealed a significant decrease after the treatment in Group 1 (p < 0.05) when compared with Group 2. This study revealed that ganciclovir treatment is a safe and effective in cases with cholestatic hepatitis. Similarly, all the patients in the treatment group had evidence of improvement serologically and virologically, while the comparison group did not reveal any significant change(p < 0.01). CONCLUSION: The clinical spectrum of perinatal infection varies from an asymptomatic infection or a mild disease to a severe systemic involvement, including central nervous system. The treatment in the early period of infection improved serologic markers and cholestatic parameters significantly. Further studies will lead us to clarify the efficacy of ganciclovir treatment in the early period of cytomegalovirus hepatitis, and the preventive role of anti-viral therapy on progressive liver disease due to cholestasis and hepatitis in neonatal cytomegalovirus infection. BioMed Central 2007-03-13 /pmc/articles/PMC1847446/ /pubmed/17355631 http://dx.doi.org/10.1186/1471-230X-7-9 Text en Copyright © 2007 Ozkan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ozkan, Tanju Basarir
Mistik, Resit
Dikici, Bunyamin
Nazlioglu, Hülya Ozturk
Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
title Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
title_full Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
title_fullStr Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
title_full_unstemmed Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
title_short Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
title_sort antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847446/
https://www.ncbi.nlm.nih.gov/pubmed/17355631
http://dx.doi.org/10.1186/1471-230X-7-9
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