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

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health care, is feasible <strong>and</strong> achieves satisfactory coverage rates. Intensive follow up is needed toimprove adherence to the immunisation schedule.Hipgrave DB, Maynard JE, Biggs B-A. Improv<strong>in</strong>g birth dose coverage <strong>of</strong> <strong>hepatitis</strong> B vacc<strong>in</strong>e.Bull WHO 2006; 84:65-70.UNICEF Indonesia, Wisma Metropolitan 11, Jalan Sudirman 31, Jakarta 12920, Indonesia.dhipgrave@unicef.orgAdm<strong>in</strong>istration <strong>of</strong> a birth dose <strong>of</strong> <strong>hepatitis</strong> B vacc<strong>in</strong>e (HepB vacc<strong>in</strong>e) to neonates is recommendedto prevent mother-to-<strong>in</strong>fant <strong>transmission</strong> <strong>and</strong> chronic <strong>in</strong>fection with the <strong>hepatitis</strong> B <strong>virus</strong> (HBV).Although manufacturers recommend HepB vacc<strong>in</strong>e distribution <strong>and</strong> storage at 2-8 degrees C,recognition <strong>of</strong> the heat stability <strong>of</strong> <strong>hepatitis</strong> B surface antigen stimulated research <strong>in</strong>to its use afterstorage at, or exposure to, ambient or high temperatures. Storage <strong>of</strong> HepB vacc<strong>in</strong>e at ambienttemperatures would enable birth dos<strong>in</strong>g for neonates delivered at home <strong>in</strong> remote areas or at healthposts lack<strong>in</strong>g refrigeration. This article reviews the current evidence on the thermostability <strong>of</strong>HepB vacc<strong>in</strong>e when stored outside the cold cha<strong>in</strong> (OCC). The reports reviewed show that thevacc<strong>in</strong>es studied were safe <strong>and</strong> effective whether stored cold or OCC. Field <strong>and</strong> laboratory dataalso verifies the reta<strong>in</strong>ed potency <strong>of</strong> the vacc<strong>in</strong>e after exposure to heat. The attachment <strong>of</strong> a highlystable variety <strong>of</strong> a vacc<strong>in</strong>e vial monitor (measur<strong>in</strong>g cumulative exposure to heat) on many HepBvacc<strong>in</strong>es strongly supports policies allow<strong>in</strong>g their storage OCC, when this will benefit birth dosecoverage. We recommend that this strategy be <strong>in</strong>troduced to improve birth dose coverage,especially <strong>in</strong> rural <strong>and</strong> remote areas. Concurrent monitor<strong>in</strong>g <strong>and</strong> evaluation should be undertakento affirm the safe implementation <strong>of</strong> this strategy, <strong>and</strong> assess its cost, feasibility <strong>and</strong> effect onreduc<strong>in</strong>g HBV <strong>in</strong>fection rates. Meanwhile, release <strong>of</strong> manufacturer data verify<strong>in</strong>g the potency <strong>of</strong>currently available HepB vacc<strong>in</strong>es after exposure to heat will <strong>in</strong>crease confidence <strong>in</strong> the use <strong>of</strong>vacc<strong>in</strong>e vial monitors as a managerial tool dur<strong>in</strong>g storage <strong>of</strong> HepB vacc<strong>in</strong>e OCC.Hipgrave DB, Nguyen TV, Vu MH, Hoang TL, Do TD, Tran NT, Jolley D, Maynard JE,Biggs BA. Hepatitis B <strong>in</strong>fection <strong>in</strong> rural Vietnam <strong>and</strong> the implications for a national program <strong>of</strong><strong>in</strong>fant immunization. Am J Trop Med Hyg 2003; 69:288-294.International Health Unit, The Burnet Institute, Alfred Medical Research & Education Prec<strong>in</strong>ct,Melbourne, Australia.To ascerta<strong>in</strong> <strong>hepatitis</strong> B <strong>virus</strong> (HBV) <strong>in</strong>fection rates for Vietnam, we surveyed HBV markers <strong>in</strong>two districts <strong>of</strong> Thanh Hoa prov<strong>in</strong>ce. We r<strong>and</strong>omly selected 536 <strong>in</strong>fants (9- < or = 18 months old),228 children (4 to < or = 6 years old), 219 adolescents (14 to < or = 16 years old), <strong>and</strong> 596 adults(25 to < or = 40 years old). On question<strong>in</strong>g, none <strong>of</strong> those surveyed had received vacc<strong>in</strong>e aga<strong>in</strong>stHBV. Hepatitis B <strong>virus</strong> surface antigen (HBsAg) <strong>and</strong> total HBV core antibody (anti-HBc) weremeasured <strong>in</strong> all specimens, <strong>and</strong> HBV e antigen (HBeAg) <strong>in</strong> those positive for HBsAg, <strong>and</strong> HBVsurface antibody (anti-HBs) were measured <strong>in</strong> all others. Current <strong>in</strong>fection (HBsAg+) rates were<strong>in</strong>fants = 12.5%, children = 18.4%, adolescents = 20.5%, <strong>and</strong> adults = 18.8%. Current or previous<strong>in</strong>fection (HBsAg+, anti-HBc+, or anti-HBs+) <strong>in</strong>creased with age (<strong>in</strong>fants = 19.6%, children =36.4%, adolescents = 55.3%, adults = 79.2%). Rates <strong>of</strong> HBeAg among those HBsAg+ were <strong>in</strong>fants= 85.1%, children = 88.1%, adolescents = 71.1%, <strong>and</strong> adults = 30.4%. The epidemiology <strong>of</strong> HBV<strong>in</strong> Vietnam resembles that <strong>of</strong> many southeast Asian nations before <strong>in</strong>troduction <strong>of</strong> vacc<strong>in</strong>e.Immunization <strong>of</strong> newborns will have enormous impact on HBV-related morbidity <strong>and</strong> mortalitythere.19

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