Sökning: WFRF:(Yazdanbakhsh Maria) > (2010) > Vitamin A supplemen...
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000 | 04146naa a2200433 4500 | |
001 | oai:lup.lub.lu.se:4753be4d-e39e-4c9d-950d-115291cf19ae | |
003 | SwePub | |
008 | 160401s2010 | |||||||||||000 ||eng| | |
024 | 7 | a https://lup.lub.lu.se/record/15891402 URI |
024 | 7 | a https://doi.org/10.1136/bmj.c11012 DOI |
040 | a (SwePub)lu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a art2 swepub-publicationtype |
072 | 7 | a ref2 swepub-contenttype |
100 | 1 | a Benn, Christine Stabell4 aut |
245 | 1 0 | a Vitamin A supplementation and BCG vaccination at birth in low birthweight neonates: two by two factorial randomised controlled trial |
264 | c 2010-03-09 | |
264 | 1 | b BMJ,c 2010 |
520 | a Objective To investigate the effect of vitamin A supplementation and BCG vaccination at birth in low birthweight neonates. Design Randomised, placebo controlled, two by two factorial trial. Setting Bissau, Guinea-Bissau. Participants 1717 low birthweight neonates born at the national hospital. Intervention Neonates who weighed less than 2.5 kg were randomly assigned to 25 000 IU vitamin A or placebo, as well as to early BCG vaccine or the usual late BCG vaccine, and were followed until age 12 months. Main outcome measure Mortality, calculated as mortality rate ratios (MRRs), after follow-up to 12 months of age for infants who received vitamin A supplementation compared with those who received placebo. Results No interaction was observed between vitamin A supplementation and BCG vaccine allocation (P=0.73). Vitamin A supplementation at birth was not significantly associated with mortality: the MRR of vitamin A supplementation compared with placebo, controlled for randomisation to "early BCG" versus "no early BCG" was 1.08 (95% CI 0.79 to 1.47). Stratification by sex revealed a significant interaction between vitamin A supplementation and sex (P=0.046), the MRR of vitamin A supplementation being 0.74 ( 95% CI 0.45 to 1.22) in boys and 1.42 (95% CI 0.94 to 2.15) in girls. When these data were combined with data from a complementary trial among normal birthweight neonates in Guinea-Bissau, the combined estimate of the effect of neonatal vitamin A supplementation on mortality was 1.08 ( 95% CI 0.87 to 1.33); 0.80 ( 95% CI 0.58 to 1.10) in boys and 1.41 ( 95% CI 1.04 to 1.90) in girls (P=0.01 for interaction between neonatal vitamin A and sex). Conclusions The combined results of this trial and the complementary trial among normal birthweight neonates have now shown that, overall, it would not be beneficial to implement a neonatal vitamin A supplementation policy in Guinea-Bissau. Worryingly, the trials show that vitamin A supplementation at birth can be harmful in girls. Previous studies and future trials should investigate the possibility that vitamin A supplementation has sex differential effects. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Mikrobiologi inom det medicinska området0 (SwePub)301092 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Microbiology in the medical area0 (SwePub)301092 hsv//eng |
700 | 1 | a Fisker, Ane Baerent4 aut |
700 | 1 | a Napirna, Bitiguida Mutna4 aut |
700 | 1 | a Roth, Adamu Lund University,Lunds universitet,Klinisk mikrobiologi, Malmö,Forskargrupper vid Lunds universitet,Clinical Microbiology, Malmö,Lund University Research Groups4 aut0 (Swepub:lu)med-amr |
700 | 1 | a Diness, Birgitte Rode4 aut |
700 | 1 | a Lausch, Karen Rokkedal4 aut |
700 | 1 | a Ravn, Henrik4 aut |
700 | 1 | a Yazdanbakhsh, Maria4 aut |
700 | 1 | a Rodrigues, Amabelia4 aut |
700 | 1 | a Whittle, Hilton4 aut |
700 | 1 | a Aaby, Peter4 aut |
710 | 2 | a Klinisk mikrobiologi, Malmöb Forskargrupper vid Lunds universitet4 org |
773 | 0 | t BMJ: British Medical Journald : BMJg 340q 340x 1756-1833 |
773 | 0 | t BMJd : BMJg 340q 340x 0959-8138x 1468-5833 |
856 | 4 | u http://dx.doi.org/10.1136/bmj.c1101x freey FULLTEXT |
856 | 4 | u https://www.bmj.com/content/340/bmj.c1101.full.pdf |
856 | 4 8 | u https://lup.lub.lu.se/record/1589140 |
856 | 4 8 | u https://doi.org/10.1136/bmj.c1101 |
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