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Continuing or discontinuing BCG revaccination in adolescents

Abstracts

BCG revaccination was introduced in Brazil in the mid-90's but no study has evaluated vaccine coverage through direct assessment of the scar. BCG scars were assessed in 2,785 public school adolescents, aged 13 to 14 years, in Southeastern Brazil, between September 2001 and May 2002. The prevalence rate of revaccination was 64.3% (95% CI: 62.5-66.0). Despite the efforts to implement and sustain revaccination, continuing this practice should be reevaluated by public health authorities due to the lack of evidence on its effectiveness.

BCG vaccine; Vaccination; Vaccinal coverage; Effectiveness; Adolescent


A revacinação com BCG foi introduzida no Brasil em meados dos anos 90 e desde então não foram conduzidos estudos que avaliassem a cobertura vacinal alcançada por meio de investigação da cicatriz do BCG. Nesse sentido, foram estudados 2.785 adolescentes de 13-14 anos matriculados em escolas públicas da cidade de Belo Horizonte, Estado de Minas Gerais, entre setembro de 2001 e maio de 2002. A prevalência da revacinação foi de 64,3% (IC 95%: 62,5-66,0). Os esforços empreendidos para obter tais níveis de cobertura conflitam com a falta de evidências sobre sua efetividade e recomendam a reavaliação da continuidade da revacinação nos serviços de saúde brasileiros.

Vacina BCG; Vacinação; Cobertura vacinal; Efetividade; Adolescente


BRIEF COMMUNICATIONS

Continuing or discontinuing BCG revaccination in adolescents

Paulo A M CamargosI; Maurício L BarretoII; Cristina AlvimI; Renata BedranI

IDepartamento de Pediatria. Faculdade de Medicina. Universidade Federal de Minas Gerais. Belo Horizonte, MG, Brasil

IIInstituto de Saúde Coletiva. Universidade Federal da Bahia. Salvador, BA, Brasil

Correspondence Correspondence: Paulo Camargos Departamento de Pediatria da Faculdade de Medicina - UFMG Av. Alfredo Balena, 190 sala 4061 30130-100 Belo Horizonte, MG, Brasil E-mail: pcamargs@medicina.ufmg.br

ABSTRACT

BCG revaccination was introduced in Brazil in the mid-90's but no study has evaluated vaccine coverage through direct assessment of the scar. BCG scars were assessed in 2,785 public school adolescents, aged 13 to 14 years, in Southeastern Brazil, between September 2001 and May 2002. The prevalence rate of revaccination was 64.3% (95% CI: 62.5-66.0). Despite the efforts to implement and sustain revaccination, continuing this practice should be reevaluated by public health authorities due to the lack of evidence on its effectiveness.

Keywords: BCG vaccine. Vaccination. Vaccinal coverage. Effectiveness. Adolescent.

INTRODUCTION

The administration of the second dose of BCG vaccine in Brazilian school students has started in the mid 1990s assuming that, among other rationale, neonatal BCG vaccination would become less effective over the years. Besides, revaccination was assumed to yield a booster effect and thus would prevent increasing tuberculosis rates in teenage years. Given high school dropout rates seen in Brazil, revaccination would preferably take place at school admission. The Brazilian Ministry of Health has left up to State Health Departments to set the best time for revaccinating this population. But estimating vaccine coverage based on the number of vaccine doses administered and population information is quite a complex undertaking by health services, as the target population has a wide range of age groups, i.e., it includes first to eighth grade school children aged between 6–7 years and 15–17 years.

Moreover, no Brazilian studies have assessed BCG vaccine coverage through direct assessment of the scar, which has proved to be a highly sensitive and specific marker of first BCG vaccination in the first 14 years of life.4

The present study was conducted aiming at assessing the prevalence of vaccine scar associated to the first BCG vaccination and revaccination among public school students.

METHODS

A cross-sectional study was carried out in the city of Belo Horizonte, Southeastern Brazil. BCG revaccination basically comprised children and adolescents aged 10 or more. First, a census of local public elementary and middle schools was conducted. Of 182 schools identified, for operating matters those with less than 200 students were excluded. Then, of 43 remaining schools, 14 (32.5%) were randomly selected using Epi Info 6.04 software package.

Between September 2001 and May 2002, data were collected only from those students aged 13 and 14. To minimize loss due to absenteeism, each school was visited two or three times.

BCG scar was defined as a flat or slightly hollowed out oval atrophic scar, 3–10 mm diameter, at the level of the lower insertion of the right deltoid muscle. No questions were asked to the students regarding their previous BCG vaccination and they were also blinded to the purpose of the study. Identification and counting of vaccine scars were conducted by specially trained people.

Given the difficulty of clinically differentiating first BCG vaccination from revaccination scars, students were classified as first vaccinated when there was one scar only and as revaccinated when there were two scars.

RESULTS

The Table shows the characteristics of the study population.

There is a slight preponderance of female students (53.1%) and those aged 14 years (54.6%). The prevalence of first BCG vaccination was 98.3% (95% CI: 97.8–98.7), estimated by summing up those students who had one scar only (34.0%) with those who had two scars (64.3%, 95% CI: 62.5–66.0). About two-thirds of first vaccinated students were revaccinated.

DISCUSSION

The finding of two scars does not necessarily mean that the subject was first BCG vaccinated in the first years of life and then revaccinated after turning 10 years old. However, the study results show similar coverage of first BCG vaccination to that reported in official estimates for the city of Belo Horizonte. One can thus reasonably assume as valid the BCG revaccination rate found in this study. Based on the study sampling process, it is most likely that the proportion of revaccinated students reflects revaccination rate in the study population.

A BCG revaccination coverage reaching about two-thirds of the target population can only be achieved by allocating and mobilizing economic, human and other resources. Yet, such logistic effort has been made with no definite evidence on the efficacy of BCG revaccination1,3 and despite the World Health Organization's recommendations against this practice.2

A recent randomized study conducted in Brazil,5 published in 2005, found that the efficacy of BCG revaccination in preventing tuberculosis among school children was only 9% (95% CI: –16% to 29%), which was not significant. Based on this evidence, it seems advisable to take actions aimed at discontinuing BCG revaccination in Brazil.

This result shows that adolescents who were revaccinated during school years are not protected against tuberculosis. Besides, BCG vaccination coverage in Belo Horizonte and other Brazilian cities favors further observational case-control studies. It is suggested to study different age groups from that of the study mentioned above,5 with different time point for either revaccination or outcome assessment (pulmonary or extra-pulmonary tuberculosis or not). The present study indicates that, in Belo Horizonte, students were on average older at the time of BCG revaccination than those included in the randomized study.5 But if outcomes are assessed at a later age, let's say, at the age of 25-30, these new observations could provide additional clinical and epidemiological information, which are undoubtedly important for understanding the impact of BCG revaccination as well as the particular epidemiology of tuberculosis disease.

ACKNOWLEDGEMENTS

To Maria Jussara Fontes MD, Cláudia Andrade MD, medical students Lucas Andrade, Marcelo Freire, Marina Fonseca, Marina Azevedo and Raquel Santos, from the Faculdade de Medicina, of Universidade Federal de Minas Gerais, for their help with data collection.

REFERENCES

Received: 11/3/2005. Approved: 1/11/2006.

  • 1. Fine PEM, Rodrigues LC. Vaccination against mycobacterial diseases. Lancet 1990;335(8696):1016-20.
  • 2. Global programme on tuberculosis and global programme on vaccines: statement on BCG revaccination for the prevention of tuberculosis. Wkly Epidemiol Rec 1995;70(32):229-31.
  • 3. Karonga Prevention Trial. Randomised controlled trial of single BCG, repeated BCG, or combined BCG and killed mycobacterium leprae vaccine for prevention of leprosy and tuberculosis in Malawi. Lancet 1996;348(9019):17-24.
  • 4. Pereira SM, Bierrenbach AL, Dourado I, Barreto ML, Ichihara MY, Hijjar MA, et al. Sensibilidade e especificidade da leitura da cicatriz vacinal do BCG. Rev Saúde Pública 2003;37(2):254-9.
  • 5. Rodrigues LC, Pereira SM, Cunha SS, Genser B, Ichihara MY, Brito SC, et al. Effect of BCG revaccination on incidence of tuberculosis in school-aged children in Brazil: the BCG-REVAC cluster-randomised trial. Lancet 2005;366(9493):1290-5.
  • Correspondence:
    Paulo Camargos
    Departamento de Pediatria da Faculdade de Medicina - UFMG
    Av. Alfredo Balena, 190 sala 4061
    30130-100 Belo Horizonte, MG, Brasil
    E-mail:
  • Publication Dates

    • Publication in this collection
      16 Aug 2006
    • Date of issue
      Apr 2006

    History

    • Accepted
      11 Jan 2006
    • Received
      03 Nov 2005
    Faculdade de Saúde Pública da Universidade de São Paulo Avenida Dr. Arnaldo, 715, 01246-904 São Paulo SP Brazil, Tel./Fax: +55 11 3061-7985 - São Paulo - SP - Brazil
    E-mail: revsp@usp.br