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Hepatitis B in pregnancy.
Dyson, Jessica Katharine; Waller, Julia; Turley, Andrena; Michael, Enid; Moses, Samuel; Valappil, Manoj; Hudson, Mark; Bassendine, Margaret; McPherson, Stuart.
Afiliação
  • Dyson JK; Liver Unit , Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust , Newcastle upon Tyne , UK.
  • Waller J; Health Protection Agency , Newcastle upon Tyne , UK.
  • Turley A; Department of Obstetrics , Royal Victoria Infirmary, Newcastle Upon Tyne Hospitals NHS Trust , Newcastle upon Tyne , UK.
  • Michael E; Department of Obstetrics , Royal Victoria Infirmary, Newcastle Upon Tyne Hospitals NHS Trust , Newcastle upon Tyne , UK.
  • Moses S; Health Protection Agency , Newcastle upon Tyne , UK ; Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
  • Valappil M; Health Protection Agency , Newcastle upon Tyne , UK ; Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
  • Hudson M; Liver Unit , Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust , Newcastle upon Tyne , UK ; Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
  • Bassendine M; Liver Unit , Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust , Newcastle upon Tyne , UK ; Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
  • McPherson S; Liver Unit , Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust , Newcastle upon Tyne , UK ; Institute of Cellular Medicine, Newcastle University , Newcastle upon Tyne , UK.
Frontline Gastroenterol ; 5(2): 111-117, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24683447
OBJECTIVE: Vertical transmission of the hepatitis B virus (HBV) is the commonest mode of infection and can be prevented with immunoprophylaxis of the infant and antiviral therapy in the mother. Our aim was to review a cohort of subjects with HBV in pregnancy to determine the prevalence of active disease or high HBV-DNA levels that required treatment to prevent transmission, and to review the management of mothers and infants. METHODS: A retrospective case-note review was conducted of all the HBV-infected pregnant women and their infants who attended the Newcastle obstetric services from 2007 to 2011. RESULTS: There were 113 pregnancies in 81 women (median age 28 years; 15% hepatitis B e antigen (HBeAg) positive) during 2007-11. 71% of mothers were first diagnosed with HBV during pregnancy. The mothers were born in 28 different countries. 69% of mothers had an HBV-DNA level less than 2000 IU/mL and 13% had HBV-DNA levels greater than 1.0×107 IU/mL so would be eligible for antiviral therapy to prevent transmission to the infant. 9% had active eAg-positive HBV and 3% had active eAg-negative HBV requiring treatment. All infants born to HBeAg-positive mothers received hepatitis B immunoglobulin (HBIG) appropriately and 76% of infants received a full HBV vaccination course. One infant born to an HBeAg-negative mother was hepatitis B surface antigen positive 1 year post-delivery. CONCLUSIONS: One in six women had active HBV requiring treatment or high HBV-DNA levels that would benefit from antiviral treatment to reduce the transmission risk. HBIG was administered appropriately but completion of the vaccination course was suboptimal.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article