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

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clusters (obstetrics wards/hospitals) selected from those 108 obstetrics wards/hospitals <strong>in</strong> the south<strong>of</strong> Romania. Overall, 31.8% (95% C.I. 27.3%-36.4%) <strong>of</strong> pregnant women admitted for birth <strong>in</strong>southern Romania had the evidence <strong>of</strong> past or current HBV <strong>in</strong>fection (anti-HBc, AgHBs). In astudy done <strong>in</strong> 1990, Bradley A. Woodruff et al. have reported a prevalence <strong>of</strong> past or current HBV<strong>in</strong>fection <strong>of</strong> 36.7% among pregnant women <strong>in</strong> northeastern Romania.Bart PA, Jacquier P, Zuber PL, Lavanchy D, Frei PC. Seroprevalence <strong>of</strong> HBV (anti-HBc,HBsAg <strong>and</strong> anti-HBs) <strong>and</strong> HDV <strong>in</strong>fections among 9006 women at delivery. Liver 1996; 16:110-116.Division <strong>of</strong> Immunology <strong>and</strong> Allergy, Centre Hospitalier Universitaire Vaudois, Lausanne,Switzerl<strong>and</strong>.Serum samples from 9006 women, who delivered <strong>in</strong> Switzerl<strong>and</strong> <strong>in</strong> 1990 <strong>and</strong> 1991, were collectedaround the country. Of these women, 62.7% were Swiss <strong>and</strong> 37.3% orig<strong>in</strong>ated from foreigncountries. Samples were first screened for anti-HBc <strong>and</strong> those found positive were further testedfor HBsAg, anti-HBs <strong>and</strong> anti-HDV. Anti-HBc was found <strong>in</strong> 640 <strong>of</strong> the 9006 women (overallprevalence, 7.1%; Swiss, 3.3%; foreigners, 13.5%). Of these 640 positive samples, 61 (9.5%) werepositive for HBsAg (without anti-HBs), 467 (73.0%) positive for anti-HBs (without HBsAg) <strong>and</strong> 8(1.3%) positive for both HBsAg <strong>and</strong> anti-HBs. The rema<strong>in</strong><strong>in</strong>g 104 were thus anti-HBc positivewithout HBsAg or anti-HBs. These 104 specimens with the so-called ‘isolated anti-HBc’ reactivityrepresented 1.2% <strong>of</strong> the whole population or 16.3% <strong>of</strong> the 640 anti-HBc positive mothers. Allwere HBV DNA negative (PCR). Anti-HDV antibody was found <strong>in</strong> only five women. HBsAg wasseen <strong>in</strong> 38 <strong>of</strong> the cord-blood samples from the anti-HBc positive mothers. In this large sampl<strong>in</strong>g,we observed a relatively high seroprevalence <strong>of</strong> HBV <strong>in</strong>fection. Cases with isolated anti-HBcreactivity, be<strong>in</strong>g HBV DNA negative by PCR, were probably non-<strong>in</strong>fectious at the time <strong>of</strong> bloodcollection.Belloni C, Chirico G, Pistorio A, Orsol<strong>in</strong>i P, T<strong>in</strong>elli C, Rond<strong>in</strong>i G. Immunogenicity <strong>of</strong> <strong>hepatitis</strong>B vacc<strong>in</strong>e <strong>in</strong> term <strong>and</strong> preterm <strong>in</strong>fants. Acta Paediatr 1998; 87:336-338.Division <strong>of</strong> Neonatal Intensive Care, IRCCS Policl<strong>in</strong>ico San Matteo, Pavia, Italy.Some studies have suggested that decreased seroconversion rates might be found <strong>in</strong> premature<strong>in</strong>fants with low birthweight (< 2000 g) follow<strong>in</strong>g adm<strong>in</strong>istration <strong>of</strong> <strong>hepatitis</strong> B vacc<strong>in</strong>e at birth.The aim <strong>of</strong> the present <strong>in</strong>vestigation was to evaluate possible differences <strong>in</strong> seropositive ratesbetween full-term <strong>and</strong> preterm <strong>in</strong>fants after primary vacc<strong>in</strong>ation, <strong>in</strong> particular when gestational ageor birthweight is very low. Two-thous<strong>and</strong> <strong>and</strong> n<strong>in</strong>e neonates born to HBsAg-negative motherswere vacc<strong>in</strong>ated with 10 microg <strong>of</strong> recomb<strong>in</strong>ant <strong>hepatitis</strong> B <strong>virus</strong> (HBV) vacc<strong>in</strong>e, from May 1991to October 1994. Children with <strong>in</strong>fections, congenital malformations or serious illnesses wereexcluded. HBV vacc<strong>in</strong>e was adm<strong>in</strong>istered <strong>in</strong>tramuscularly, on the fourth day <strong>of</strong> life <strong>and</strong> aga<strong>in</strong> at 1<strong>and</strong> 6 months <strong>of</strong> age. A 1-ml blood sample was drawn from each <strong>in</strong>fant 1 month after the thirdvacc<strong>in</strong>e dose for determ<strong>in</strong>ation <strong>of</strong> the level <strong>of</strong> anti-HBs antibody. The response to HBVvacc<strong>in</strong>ation was evaluated <strong>in</strong> 241 preterm (gestational age < 38 weeks) <strong>in</strong>fants <strong>and</strong> 1727 termneonates. No statistical difference was observed <strong>in</strong> the distribution <strong>of</strong> anti-HBs antibody level,either between preterm <strong>in</strong>fants (< 38 weeks) <strong>and</strong> newborns <strong>of</strong> normal gestational age, or betweenlow birthweight (< 2500 g) <strong>and</strong> normal weight <strong>in</strong>fants. The results suggest that preterm <strong>and</strong> lowbirthweight <strong>in</strong>fants (< 2500 g) respond to HBV vacc<strong>in</strong>e <strong>in</strong> the same measure as normal-term<strong>in</strong>fants.7

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