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Prevention and control of perinatal hepatitis B virus transmission in ...

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Papaevangelou G. Hepatitis B immunization programme: lessons learnt <strong>in</strong> Greece. Vacc<strong>in</strong>e 1998;16(Suppl):S45-S47.Faculty <strong>of</strong> Nurs<strong>in</strong>g, University <strong>of</strong> Athens, Greece.Historically, Greece has had the highest burden <strong>of</strong> <strong>hepatitis</strong> B <strong>virus</strong> (HBV) <strong>in</strong>fection <strong>in</strong> theEuropean Union (EU). Heterosexual contact is the primary means <strong>of</strong> HBV <strong>transmission</strong> <strong>in</strong> Greece,account<strong>in</strong>g for approximately 30% <strong>of</strong> acute cases <strong>in</strong> adult males <strong>and</strong> 50% <strong>of</strong> acute cases <strong>in</strong> women<strong>of</strong> reproductive age [Kattamis C, Papevangelou G. Workshop Group: Greece. Vacc<strong>in</strong>e 1995;13:S97-S98.]. In 1982, Greece implemented a <strong>hepatitis</strong> B prevention programme aimed at highriskgroups; unfortunately, this approach had little impact on disease <strong>in</strong>cidence or prevalence. Atthe recommendation <strong>of</strong> the WHO <strong>and</strong> the World Health Assembly <strong>and</strong> after susta<strong>in</strong>ed lobby<strong>in</strong>g byseveral scientific <strong>and</strong> medical associations <strong>in</strong> Greece, the Greek government decided to implementa national prevention programme for <strong>hepatitis</strong> B. The programme, <strong>in</strong> effect from early 1998,<strong>in</strong>cludes the screen<strong>in</strong>g <strong>of</strong> pregnant women, universal <strong>in</strong>fant <strong>and</strong> adolescent immunization <strong>and</strong>immunization <strong>of</strong> high-risk groups.Poovorawan Y, Chongsrisawat V, Theamboonlers A, Vimolkej L, Yano M. Is there evidencefor <strong>in</strong>trauter<strong>in</strong>e HBV <strong>in</strong>fection <strong>in</strong> newborns <strong>of</strong> <strong>hepatitis</strong> B carrier mothers? Southeast Asian J TropMed Public Health 1997; 28:365-369.Viral Hepatitis Research Unit, Faculty <strong>of</strong> Medic<strong>in</strong>e, Chulalongkorn University <strong>and</strong> Hospital,Bangkok, Thail<strong>and</strong>.It has been proposed that some neonates <strong>in</strong>fected with <strong>hepatitis</strong> B <strong>virus</strong> (HBV), acquire their<strong>in</strong>fections <strong>in</strong> utero as demonstrated by HBV seromarkers <strong>in</strong> venous blood samples at birth. In thisstudy, paired blood samples from 13 HBsAg-positive, 19 HBsAg- <strong>and</strong> HBeAg-positive, 2 HBsAgnegativemothers <strong>and</strong> 34 <strong>of</strong> their neonates, were drawn 24-72 hours after birth <strong>and</strong> tested for HBV-DNA <strong>in</strong> their peripheral blood mononuclear cells (PBMC). The presence <strong>of</strong> HBV-DNA <strong>in</strong> PBMCwas detected <strong>in</strong> 69.2% (9/13) <strong>of</strong> HBsAg-positive mothers, 94.7% (18/19) <strong>of</strong> HBsAg- <strong>and</strong> HBeAgpositivemothers, <strong>and</strong> <strong>in</strong> none <strong>of</strong> their neonates. The conclusion from these results is that theevidence for <strong>hepatitis</strong> B <strong>in</strong>fections occurr<strong>in</strong>g <strong>in</strong> neonates <strong>of</strong> <strong>hepatitis</strong> B carrier mothers <strong>in</strong> utero isuncommon.Poovorawan Y, Theamboonlers A, Vimolket T, S<strong>in</strong>laparatsamee S, Chaiear K, SiraprapasiriT, Khwanjaipanich S, Owatanapanich S, Hirsch P, Chunsuttiwat S. Impact <strong>of</strong> <strong>hepatitis</strong> Bimmunisation as part <strong>of</strong> the EPI. Vacc<strong>in</strong>e 2000; 19:943-949.Viral Hepatitis Research Unit, Department <strong>of</strong> Pediatrics, Faculty <strong>of</strong> Medic<strong>in</strong>e, ChulalongkornUniversity <strong>and</strong> Hospital, 10330, Bangkok, Thail<strong>and</strong>. yong.p@chula.ac.thS<strong>in</strong>ce 1992, <strong>hepatitis</strong> B vacc<strong>in</strong>e has been an <strong>in</strong>tegrated part <strong>of</strong> Thail<strong>and</strong>'s exp<strong>and</strong>ed programme onimmunisation (EPI). Based on the data from five representative prov<strong>in</strong>ces, we have evaluated itsimpact on the countrywide prevalence <strong>of</strong> HBV <strong>in</strong>fection <strong>and</strong> carrier rate. The population studiedcomprised 400-488 healthy <strong>and</strong> immuno-competent, subjects per area. The subjects' ages rangedfrom 6 months to 18 years. We exam<strong>in</strong>ed their sera for viral <strong>hepatitis</strong> markers us<strong>in</strong>g commerciallyavailable test kits <strong>and</strong> established the coverage rate <strong>of</strong> <strong>hepatitis</strong> B vacc<strong>in</strong>ation after its <strong>in</strong>clusion<strong>in</strong>to the EPI to be 71.2-94.3%. The number <strong>of</strong> <strong>in</strong>dividuals undergo<strong>in</strong>g the complete course <strong>of</strong>vacc<strong>in</strong>ations had <strong>in</strong>creased four-fold. Consequently, only 0.7% <strong>of</strong> the children born after theimplementation <strong>of</strong> this the novel EPI strategy were HBV carriers.34

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