Publication: Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
dc.contributor.author | Dikici, Bünyamin | |
dc.contributor.buuauthor | Mıstık, Reşit | |
dc.contributor.buuauthor | Özkan, Tanju Başarır | |
dc.contributor.buuauthor | Nazlıoğlu, Hülya Öztürk | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | İnfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Ana Bilim Dalı Başkanlığı | |
dc.contributor.orcid | 0000-0001-7572-6525 | tr_TR |
dc.contributor.scopusid | 7004474005 | tr_TR |
dc.contributor.scopusid | 6602564624 | tr_TR |
dc.contributor.scopusid | 57197115377 | tr_TR |
dc.date.accessioned | 2022-10-06T08:13:57Z | |
dc.date.available | 2022-10-06T08:13:57Z | |
dc.date.issued | 2007-03-13 | |
dc.description.abstract | 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. | en_US |
dc.identifier.citation | Özkan, T. B. vd. (2007). "Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis". BMC Gastroenterology, 7(9). | tr_TR |
dc.identifier.issn | 1471-230X | |
dc.identifier.issue | 3 | tr_TR |
dc.identifier.pubmed | 17355631 | tr_TR |
dc.identifier.scopus | 2-s2.0-34147105041 | tr_TR |
dc.identifier.uri | https://doi.org/10.1186/1471-230X-7-9 | |
dc.identifier.uri | https://bmcgastroenterol.biomedcentral.com/articles/10.1186/1471-230X-7-9 | |
dc.identifier.uri | http://hdl.handle.net/11452/28996 | |
dc.identifier.volume | 7 | tr_TR |
dc.identifier.wos | 000245455600001 | |
dc.indexed.pubmed | PubMed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | BMC | en_US |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.journal | BMC Gastroenterology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Ganciclovir therapy | en_US |
dc.subject | Infection | en_US |
dc.subject | Disease | en_US |
dc.subject.emtree | Bilirubin | en_US |
dc.subject.emtree | Alanine aminotransferase | en_US |
dc.subject.emtree | Alkaline phosphatase | en_US |
dc.subject.emtree | Antivirus agent | en_US |
dc.subject.emtree | Aspartate aminotransferase | en_US |
dc.subject.emtree | Gamma glutamyltransferase | en_US |
dc.subject.emtree | Aminotransferase | en_US |
dc.subject.emtree | Intrahepatic cholestasis | en_US |
dc.subject.emtree | Ganciclovir | en_US |
dc.subject.emtree | Immunoglobulin G | en_US |
dc.subject.emtree | Immunoglobulin M | en_US |
dc.subject.emtree | Alkaline phosphatase | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | Antivirus agent | en_US |
dc.subject.emtree | Bilirubin | en_US |
dc.subject.emtree | Gamma glutamyltransferase | en_US |
dc.subject.emtree | Virus DNA | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Biochemistry | en_US |
dc.subject.emtree | Cholestatic hepatitis | en_US |
dc.subject.emtree | Cytomegalovirus | en_US |
dc.subject.emtree | Cytomegalic inclusion body disease | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Enzyme linked immunosorbent assay | en_US |
dc.subject.emtree | Controlled clinical trial | en_US |
dc.subject.emtree | Disease severity | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Drug safety | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Virus identification | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Infant | en_US |
dc.subject.emtree | Virus hepatitis | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Treatment outcome | en_US |
dc.subject.emtree | Liver biopsy | en_US |
dc.subject.emtree | Polymerase chain reaction | en_US |
dc.subject.emtree | Treatment duration | en_US |
dc.subject.emtree | Newborn hepatitis | en_US |
dc.subject.emtree | Physical examination | en_US |
dc.subject.emtree | Serology | en_US |
dc.subject.emtree | Symptom | en_US |
dc.subject.emtree | Virology | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Hepatomegaly | en_US |
dc.subject.emtree | Newborn | en_US |
dc.subject.emtree | Newborn jaundice | en_US |
dc.subject.mesh | Antiviral agents | tr_TR |
dc.subject.mesh | Alkaline phosphatase | tr_TR |
dc.subject.mesh | DNA, viral | tr_TR |
dc.subject.mesh | Hepatomegaly | tr_TR |
dc.subject.mesh | Bilirubin | tr_TR |
dc.subject.mesh | Cholestasis, intrahepatic | tr_TR |
dc.subject.mesh | Cytomegalovirus infections | tr_TR |
dc.subject.mesh | Female | tr_TR |
dc.subject.mesh | Hepatitis, hiral, human | tr_TR |
dc.subject.mesh | Gamma-glutamyltransferase | tr_TR |
dc.subject.mesh | Ganciclovir | tr_TR |
dc.subject.mesh | Humans | tr_TR |
dc.subject.mesh | Infant | tr_TR |
dc.subject.mesh | Infant, newborn | tr_TR |
dc.subject.mesh | Jaundice, neonatal | tr_TR |
dc.subject.mesh | Male | tr_TR |
dc.subject.mesh | Transaminases | tr_TR |
dc.subject.scopus | Cytomegalovirus Infections; Cytomegalovirus-Specific Hyperimmune Globulin; Valganciclovir Prominence percentile | tr_TR |
dc.subject.wos | Gastroenterology & hepatology | tr_TR |
dc.title | Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis | tr_TR |
dc.type | Article | |
dc.wos.quartile | Q3 | tr_TR |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Patoloji Ana Bilim Dalı | tr_TR |
local.contributor.department | Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı | tr_TR |
local.contributor.department | Tıp Fakültesi/İnfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Ana Bilim Dalı Başkanlığı | tr_TR |