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Recurrent congenital cytomegalovirus infection in a sequential pregnancy with severe sequelae, and a possible association with prophylactic valacyclovir treatment: a case report.
Brosh-Nissimov, Tal; Benshalom-Tirosh, Neta; Bucris, Efrat; Morad, Hagar; Zuckerman, Neta S; Tepperberg Oikawa, Michal.
Affiliation
  • Brosh-Nissimov T; Infectious Diseases Unit, Samson Assuta Ashdod University Hospital, Ashdod, Israel; Faculty of Health Sciences, Ben Gurion University in the Negev, Beer Sheva, Israel. Electronic address: talbros@assuta.co.il.
  • Benshalom-Tirosh N; Faculty of Health Sciences, Ben Gurion University in the Negev, Beer Sheva, Israel; Department of Obstetrics and Gynecology, Samson Assuta Ashdod University Hospital, Ashdod, Israel. Electronic address: netabens@assuta.co.il.
  • Bucris E; Central Virology Laboratory, Ministry of Health, Tel Hashomer, Israel. Electronic address: efrat.bucris@moh.health.gov.il.
  • Morad H; Central Virology Laboratory, Ministry of Health, Tel Hashomer, Israel. Electronic address: hagar.morad@moh.health.gov.il.
  • Zuckerman NS; Central Virology Laboratory, Ministry of Health, Tel Hashomer, Israel. Electronic address: neta.zuckerman@sheba.health.gov.il.
  • Tepperberg Oikawa M; Central Virology Laboratory, Ministry of Health, Tel Hashomer, Israel. Electronic address: michal.teperberg@sheba.health.gov.il.
Int J Infect Dis ; 125: 93-95, 2022 Dec.
Article de En | MEDLINE | ID: mdl-36229004
Recurrent congenital cytomegalovirus infections in consecutive pregnancies are rarely reported. Due to the risk of fetal infection from preconception maternal infection, a 6-month interval after primary maternal infection is generally advised before a new conception. Recently, high-dose valacyclovir treatment was shown to prevent fetal infection in first trimester primary infections. We present a case of first trimester primary infection treated with high-dose valacyclovir but resulting in polymerase chain reaction-confirmed fetal infection. Cytomegalovirus-specific immunoglobulin G titers remained very low during treatment and rose only after cessation of antiviral treatment. Six months after primary seroconversion, in a sequential pregnancy, recurrent fetal infection was diagnosed and resulted in severe fetal sequella. Whole genome sequencing of both amniotic fluid isolates proved them to be identical. Both pregnancies were terminated. We hypothesize that valacyclovir treatment, although unsuccessful in preventing fetal infection, had delayed the adaptive maternal immune response and might have contributed to fetal infection during the sequential pregnancy. We suggest that a longer delay might be warranted after valacyclovir treatment and before a new conception.
Sujet(s)
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Complications infectieuses de la grossesse / Infections à cytomégalovirus / Maladies foetales Type d'étude: Risk_factors_studies Limites: Female / Humans / Pregnancy Langue: En Journal: Int J Infect Dis Sujet du journal: DOENCAS TRANSMISSIVEIS Année: 2022 Type de document: Article Pays de publication: Canada

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Complications infectieuses de la grossesse / Infections à cytomégalovirus / Maladies foetales Type d'étude: Risk_factors_studies Limites: Female / Humans / Pregnancy Langue: En Journal: Int J Infect Dis Sujet du journal: DOENCAS TRANSMISSIVEIS Année: 2022 Type de document: Article Pays de publication: Canada