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Randomized Controlled Trial
. 2017 Mar;102(3):224-231.
doi: 10.1136/archdischild-2016-310760. Epub 2016 Jul 21.

BCG vaccination at birth and early childhood hospitalisation: a randomised clinical multicentre trial

Affiliations
Randomized Controlled Trial

BCG vaccination at birth and early childhood hospitalisation: a randomised clinical multicentre trial

Lone Graff Stensballe et al. Arch Dis Child. 2017 Mar.

Abstract

Background: The BCG vaccine is administered to protect against tuberculosis, but studies suggest there may also be non-specific beneficial effects upon the infant immune system, reducing early non-targeted infections and atopic diseases. The present randomised trial tested the hypothesis that BCG vaccination at birth would reduce early childhood hospitalisation in Denmark, a high-income setting.

Methods: Pregnant women planning to give birth at three Danish hospitals were invited to participate. After parental consent, newborn children were allocated to BCG or no intervention within 7 days of age. Randomisation was stratified by prematurity. The primary study outcome was number of all-cause hospitalisations analysed as repeated events. Hospitalisations were identified using The Danish National Patient Register. Data were analysed by Cox proportional hazards models in intention-to-treat and per-protocol analyses.

Results: 4184 pregnant women were randomised and their 4262 children allocated to BCG or no intervention. There was no difference in risk of hospitalisation up to 15 months of age; 2129 children randomised to BCG experienced 1047 hospitalisations with a mean of 0.49 hospitalisation per child compared with 1003 hospitalisations among 2133 control children (mean 0.47), resulting in a HR comparing BCG versus no BCG of 1.05 (95% CI 0.93 to 1.18) (intention-to-treat analysis). The effect of BCG was the same in children born at term (1.05 (0.92 to 1.18)) and prematurely (1.07 (0.63 to 1.81), p=0.94). The effect was also similar in the two sexes and across study sites. The results were essentially identical in the per-protocol analysis and after adjustment for baseline characteristics.

Conclusions: BCG vaccination at birth did not reduce the risk of hospitalisation for somatic acquired disease until 15 months of age in this Danish study population.

Trial registration number: NCT01694108, results.

Keywords: Bacillus Calmette-Guérin (BCG; hospitalisation; infant; non-specific effect; vaccine.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Flow chart. Data collection of The Danish Calmette Study, by telephone interviews, clinical examinations and health registers. Percentages in parentheses (): Percentage among the eligible children. Percentages in square brackets []: Percentage among all randomised children. *Interviews conducted between child age 2–4 months: BCG 98.1% (2089/2129), control 96.8% (2064/2133). #Interviews conducted between child age 10–14 months: BCG 97.9% (2084/2129), control 96.2% (2052/2133).
Figure 2
Figure 2
Estimated mean number of all-cause hospitalisations per child for children randomised to BCG or no BCG.

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