Mem Inst Oswaldo Cruz, Rio de Janeiro, 112(8) August 2017
Full paper

Risk factors for hepatitis B transmission in South Brazil

Vagner Reinaldo Zingalli Bueno Pereira1,2, Jonas Michel Wolf1,2,+, Camila Albani da Silva Luz3, Gláucia Zuleide Stumm3, Thais da Rocha Boeira1,2, Josiane Galvan4, Daniel Simon1, Vagner Ricardo Lunge1,2

1Programa de Pós-Graduação em Biologia Celular e Molecular Aplicada à Saúde, Universidade Luterana do Brasil, Canoas, RS, Brasil
2Laboratório de Diagnóstico Molecular, Universidade Luterana do Brasil, Canoas, RS, Brasil
3Universidade de Caxias do Sul, Caxias do Sul, RS, Brasil
4Prefeitura Municipal de Caxias do Sul, Serviço Municipal de Infectologia, Caxias do Sul, RS, Brasil

Page: 544-550 DOI: 10.1590/0074-02760170043
459 views 214 downloads

BACKGROUND Hepatitis B virus (HBV) infection is a major public health problem in Brazil. Several risk factors are involved in HBV infection and their identification by a rational and essential approach is required to prevent the transmission of this infection in Brazil.

OBJECTIVES To evaluate risk factors associated with HBV infection in South Brazil.

METHODS A total of 260 patients with HBV and 260 controls from Caxias do Sul (state of Rio Grande do Sul, Brazil) participated in this study. All participants were given a standard questionnaire to yield the sociodemographic information and to identify HBV risk factors. HBV infection was detected by HBsAg test in all participants.

FINDINGS HBV infection in these cases was strongly associated with history of a family member HBV-infected, mainly mother odds ratio (OR) = 4.86; 95% confidence intervals (CI): 1.69u201313.91, father (OR = 5.28; 95% CI: 1.58u201317.71), and/or siblings (OR = 22.16; 95% CI: 9.39u201352.25); sharing personal objects (OR = 1.40; 95% CI: 1.37u20132.38); and having history of blood transfusion (OR = 2.05; 95% CI: 1.10u20132.84).

CONCLUSIONS HBV infection was strongly associated with having a family member infected with hepatitis B, sharing personal objects, and having history of blood transfusion.

Financial support: ULBRA
+ Corresponding author:
Received 2 February 2017
Accepted 26 March 2017

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