Vacinação rápida contra a infecção por VHB é uma estratégia importante para o controle da infecção pelo VHB em presídios
Seyed Moayed Alavian 1 Dear Editor:I read with interest the article by Stief et al. published in your journal recently 1 . It showed us that hepatitis B virus (HBV) infection remains a significant problem in prisons, and it was related with other published studies 2,3 . The finding on higher prevalence of HBV infection in the male gender and in prisoners with positive history of intravenous drug use and STD demonstrated a new strategy for the control of HBV infection in prisons. Low vaccination coverage and the high number of injecting drug users (IDUs) suggest that most of them are susceptible to this infection.Prisoners and IDUs are at constant risk of HBV infection, and the classic 6-month HBV vaccination might not provide immunization rapidly enough 4,5 . Compared with classic HBV vaccination regimen, an accelerated 0, 1, 4, and 8 weeks vaccination schedule can achieve early seroprotection more rapidly, provides clinically sufficient seroprotection with higher compliance in prisoners, and can be suggested in situations that rapid immunization against HBV infection is warranted 4 . I suggest the selection of higher-risk groups in prisons, including males with history of IDUs and STD, to start the accelerated vaccination against HBV infection early. This will be extremely useful to ensure immunity against HBV infection soon.I would like to inform those identified by Stief et al. as having high risk of contracting HBV infection, particularly those in prisons and of old age, that being infected would be related to more duration of staying in high-risk place (prison) and more exposure with the risk factors. And finally, I would like to ask about hepatitis C virus (HCV) and HIV infections, which are more common in IDU groups 6 as stated in the literature; the authors did not present this in their study. A total of 408 individuals were interviewed regarding sociodemographic characteristics, associated factors and HBV vaccination using a standardized questionnaire. Blood samples were collected from all participants and serological markers for HBV were detected by enzyme-linked immunosorbent assay. Hepatitis B surface antigen (HBsAg) and/or antibodies against hepatitis B core antigen (anti-HBc) positive samples were tested for HBV-DNA by polymerase chain reaction. Results: