Exploring the effects of BCG vaccination in patients diagnosed with tuberculosis: Observational study using the Enhanced Tuberculosis Surveillance system.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
14 08 2019
Historique:
received: 06 07 2018
revised: 28 05 2019
accepted: 18 06 2019
pubmed: 13 7 2019
medline: 7 10 2020
entrez: 13 7 2019
Statut: ppublish

Résumé

Bacillus Calmette-Guérin (BCG) is one of the most widely-used vaccines worldwide. BCG primarily reduces the progression from infection to disease, however there is evidence that BCG may provide additional benefits. We aimed to investigate whether there is evidence in routinely-collected surveillance data that BCG vaccination impacts outcomes for tuberculosis (TB) cases in England. We obtained all TB notifications for 2009-2015 in England from the Enhanced Tuberculosis surveillance system. We considered five outcomes: All-cause mortality, death due to TB (in those who died), recurrent TB, pulmonary disease, and sputum smear status. We used logistic regression, with complete case analysis, to investigate each outcome with BCG vaccination, years since vaccination and age at vaccination, adjusting for potential confounders. All analyses were repeated using multiply imputed data. We found evidence of an association between BCG vaccination and reduced all-cause mortality (aOR:0.76 (95%CI 0.64-0.89), P:0.001) and weak evidence of an association with reduced recurrent TB (aOR:0.90 (95%CI 0.81-1.00), P:0.056). Analyses using multiple imputation suggested that the benefits of vaccination for all-cause mortality were reduced after 10 years. We found that BCG vaccination was associated with reduced all-cause mortality in people with TB although this benefit was less pronounced more than 10 years after vaccination. There was weak evidence of an association with reduced recurrent TB.

Sections du résumé

BACKGROUND
Bacillus Calmette-Guérin (BCG) is one of the most widely-used vaccines worldwide. BCG primarily reduces the progression from infection to disease, however there is evidence that BCG may provide additional benefits. We aimed to investigate whether there is evidence in routinely-collected surveillance data that BCG vaccination impacts outcomes for tuberculosis (TB) cases in England.
METHODS
We obtained all TB notifications for 2009-2015 in England from the Enhanced Tuberculosis surveillance system. We considered five outcomes: All-cause mortality, death due to TB (in those who died), recurrent TB, pulmonary disease, and sputum smear status. We used logistic regression, with complete case analysis, to investigate each outcome with BCG vaccination, years since vaccination and age at vaccination, adjusting for potential confounders. All analyses were repeated using multiply imputed data.
RESULTS
We found evidence of an association between BCG vaccination and reduced all-cause mortality (aOR:0.76 (95%CI 0.64-0.89), P:0.001) and weak evidence of an association with reduced recurrent TB (aOR:0.90 (95%CI 0.81-1.00), P:0.056). Analyses using multiple imputation suggested that the benefits of vaccination for all-cause mortality were reduced after 10 years.
CONCLUSIONS
We found that BCG vaccination was associated with reduced all-cause mortality in people with TB although this benefit was less pronounced more than 10 years after vaccination. There was weak evidence of an association with reduced recurrent TB.

Identifiants

pubmed: 31296375
pii: S0264-410X(19)30818-7
doi: 10.1016/j.vaccine.2019.06.056
pii:
doi:

Substances chimiques

BCG Vaccine 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5067-5072

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Sam Abbott (S)

Bristol Medical School: Population Health Sciences, University of Bristol, Bristol, UK. Electronic address: sam.abbott@bristol.ac.uk.

Hannah Christensen (H)

Bristol Medical School: Population Health Sciences, University of Bristol, Bristol, UK.

Maeve K Lalor (MK)

TB Unit, T.A.R.G.E.T, National Infection Service (NIS), Public Health England, London, UK.

Dominik Zenner (D)

Institute for Global Health, University College London, London, UK.

Colin Campbell (C)

TB Unit, T.A.R.G.E.T, National Infection Service (NIS), Public Health England, London, UK.

Mary E Ramsay (ME)

Immunisation, Hepatitis and Blood Safety Department, Public Health England, London, UK.

Ellen Brooks-Pollock (E)

Bristol Medical School: Population Health Sciences, University of Bristol, Bristol, UK.

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