2012
DOI: 10.1097/inf.0b013e3182458289
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Small Randomized Trial Among Low–birth-weight Children Receiving Bacillus Calmette-Guérin Vaccination at First Health Center Contact

Abstract: A total of 105 low-birth-weight children presenting for first vaccination were randomized to receive bacillus Calmette-Guérin (BCG) immediately or later (current practice). The mortality rate ratio for BCG was 0.17 (95% CI = 0.02-1.35) within 3 days of enrollment, 0.28 (0.06-1.37) in the first month, and 0.27 (0.07-0.98) after 2 months of age. The mortality rate ratio was 0.41 (0.14-1.18) (P = 0.098) in infancy. Administration of BCG vaccine at first contact may contribute to lower mortality.

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Cited by 220 publications
(229 citation statements)
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“…78 Whereas in low birth weight neonates it reduced the mortality by almost 50% as demonstrated by fewer cases of sepsis and respiratory infections. 79,80 This is similar to results in adult mouse models of heterologous immunity where it was demonstrated that BCG-immune mice were more resistant to vaccinia virus infection and that this resistance was mediated by IFNg-producing CD4 T cells. 81 Interestingly, Steenhuis and others showed that in children, by 18 months of age, immunization with BCG resulted in lowered numbers of children with eczema, a Th2-immune mediated disease.…”
Section: Measles Vaccinesupporting
confidence: 68%
“…78 Whereas in low birth weight neonates it reduced the mortality by almost 50% as demonstrated by fewer cases of sepsis and respiratory infections. 79,80 This is similar to results in adult mouse models of heterologous immunity where it was demonstrated that BCG-immune mice were more resistant to vaccinia virus infection and that this resistance was mediated by IFNg-producing CD4 T cells. 81 Interestingly, Steenhuis and others showed that in children, by 18 months of age, immunization with BCG resulted in lowered numbers of children with eczema, a Th2-immune mediated disease.…”
Section: Measles Vaccinesupporting
confidence: 68%
“…Previous studies have shown that BCG has beneficial non-specific or heterologous effects, providing protection also against many non-tuberculosis causes of death: in randomized trials of early BCG to low-birth-weight children, BCG at birth versus delayed BCG, as is normal practice, decreased neonatal mortality by 38% (17–54%) [3739]. With most infant deaths occurring during the neonatal period [40] and with less than half of children vaccinated during the first two weeks of life, most children do not benefit from BCG when they are most at risk.…”
Section: Discussionmentioning
confidence: 99%
“…Fifty-nine articles were found, 15 were eligible for detailed analysis, and nine were included in the final analysis (Figures 2 and 3; Table 1) [10][11][12][13][14][15][16][17][18]. The nine studies with a low to moderate risk of bias consisted of two randomized trials, six cohort studies and one case-control study.…”
Section: Resultsmentioning
confidence: 99%
“…Unfortunately, most investigators did not record the strain of BCG that was used in the studies reported here. We know that BCG-Denmark was used in the two randomized trials in lowbirth-weight babies in Guinea-Bissau [9,10], but it cannot be assumed that other strains of BCG will have the same effect. BCG-Denmark and BCG-Japan both contain at least two different genomes, which may explain the considerable variation in clinical effects between batches from individual manufacturers.…”
Section: Journal Of Infectitious Diseases and Treatment Issn 2472-1093mentioning
confidence: 99%
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