Publication:
Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis

dc.contributor.authorDikici, Bünyamin
dc.contributor.buuauthorMıstık, Reşit
dc.contributor.buuauthorÖzkan, Tanju Başarır
dc.contributor.buuauthorNazlıoğlu, Hülya Öztürk
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentİnfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Ana Bilim Dalı Başkanlığı
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
dc.contributor.departmentPatoloji Ana Bilim Dalı
dc.contributor.orcid0000-0001-7572-6525
dc.contributor.scopusid7004474005
dc.contributor.scopusid6602564624
dc.contributor.scopusid57197115377
dc.date.accessioned2022-10-06T08:13:57Z
dc.date.available2022-10-06T08:13:57Z
dc.date.issued2007-03-13
dc.description.abstractBackground: 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.
dc.identifier.citationÖzkan, T. B. vd. (2007). "Antiviral therapy in neonatal cholestatic cytomegalovirus hepatitis". BMC Gastroenterology, 7(9).
dc.identifier.issn1471-230X
dc.identifier.issue3
dc.identifier.pubmed17355631
dc.identifier.scopus2-s2.0-34147105041
dc.identifier.urihttps://doi.org/10.1186/1471-230X-7-9
dc.identifier.urihttps://bmcgastroenterol.biomedcentral.com/articles/10.1186/1471-230X-7-9
dc.identifier.urihttp://hdl.handle.net/11452/28996
dc.identifier.volume7
dc.identifier.wos000245455600001
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherBMC
dc.relation.collaborationYurt içi
dc.relation.journalBMC Gastroenterology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGanciclovir therapy
dc.subjectInfection
dc.subjectDisease
dc.subject.emtreeBilirubin
dc.subject.emtreeAlanine aminotransferase
dc.subject.emtreeAlkaline phosphatase
dc.subject.emtreeAntivirus agent
dc.subject.emtreeAspartate aminotransferase
dc.subject.emtreeGamma glutamyltransferase
dc.subject.emtreeAminotransferase
dc.subject.emtreeIntrahepatic cholestasis
dc.subject.emtreeGanciclovir
dc.subject.emtreeImmunoglobulin G
dc.subject.emtreeImmunoglobulin M
dc.subject.emtreeAlkaline phosphatase
dc.subject.emtreeClinical article
dc.subject.emtreeAntivirus agent
dc.subject.emtreeBilirubin
dc.subject.emtreeGamma glutamyltransferase
dc.subject.emtreeVirus DNA
dc.subject.emtreeArticle
dc.subject.emtreeBiochemistry
dc.subject.emtreeCholestatic hepatitis
dc.subject.emtreeCytomegalovirus
dc.subject.emtreeCytomegalic inclusion body disease
dc.subject.emtreeControlled study
dc.subject.emtreeEnzyme linked immunosorbent assay
dc.subject.emtreeControlled clinical trial
dc.subject.emtreeDisease severity
dc.subject.emtreeDrug efficacy
dc.subject.emtreeDrug safety
dc.subject.emtreeHuman
dc.subject.emtreeVirus identification
dc.subject.emtreeFemale
dc.subject.emtreeInfant
dc.subject.emtreeVirus hepatitis
dc.subject.emtreeMale
dc.subject.emtreeTreatment outcome
dc.subject.emtreeLiver biopsy
dc.subject.emtreePolymerase chain reaction
dc.subject.emtreeTreatment duration
dc.subject.emtreeNewborn hepatitis
dc.subject.emtreePhysical examination
dc.subject.emtreeSerology
dc.subject.emtreeSymptom
dc.subject.emtreeVirology
dc.subject.emtreeClinical trial
dc.subject.emtreeHepatomegaly
dc.subject.emtreeNewborn
dc.subject.emtreeNewborn jaundice
dc.subject.meshAntiviral agents
dc.subject.meshAlkaline phosphatase
dc.subject.meshDNA, viral
dc.subject.meshHepatomegaly
dc.subject.meshBilirubin
dc.subject.meshCholestasis, intrahepatic
dc.subject.meshCytomegalovirus infections
dc.subject.meshFemale
dc.subject.meshHepatitis, hiral, human
dc.subject.meshGamma-glutamyltransferase
dc.subject.meshGanciclovir
dc.subject.meshHumans
dc.subject.meshInfant
dc.subject.meshInfant, newborn
dc.subject.meshJaundice, neonatal
dc.subject.meshMale
dc.subject.meshTransaminases
dc.subject.scopusCytomegalovirus Infections; Cytomegalovirus-Specific Hyperimmune Globulin; Valganciclovir Prominence percentile
dc.subject.wosGastroenterology & hepatology
dc.titleAntiviral therapy in neonatal cholestatic cytomegalovirus hepatitis
dc.typeArticle
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Patoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/İnfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Ana Bilim Dalı Başkanlığı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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