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Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose

OBJECTIVE: Antenatal multiple micronutrient supplements (MMS) are a cost-effective intervention to reduce adverse pregnancy and birth outcomes. However, the current WHO recommendation on the use of antenatal MMS is conditional, partly due to concerns about the effect on neonatal mortality in a subgr...

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Autores principales: Gomes, Filomena, Agustina, Rina, Black, Robert E, Christian, Parul, Dewey, Kathryn G, Kraemer, Klaus, Shankar, Anuraj H, Smith, Emily, Tumilowicz, Alison, Bourassa, Megan W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991737/
https://www.ncbi.nlm.nih.gov/pubmed/35466910
http://dx.doi.org/10.1017/S1368980022001008
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author Gomes, Filomena
Agustina, Rina
Black, Robert E
Christian, Parul
Dewey, Kathryn G
Kraemer, Klaus
Shankar, Anuraj H
Smith, Emily
Tumilowicz, Alison
Bourassa, Megan W
author_facet Gomes, Filomena
Agustina, Rina
Black, Robert E
Christian, Parul
Dewey, Kathryn G
Kraemer, Klaus
Shankar, Anuraj H
Smith, Emily
Tumilowicz, Alison
Bourassa, Megan W
author_sort Gomes, Filomena
collection PubMed
description OBJECTIVE: Antenatal multiple micronutrient supplements (MMS) are a cost-effective intervention to reduce adverse pregnancy and birth outcomes. However, the current WHO recommendation on the use of antenatal MMS is conditional, partly due to concerns about the effect on neonatal mortality in a subgroup of studies comparing MMS with iron and folic acid (IFA) supplements containing 60 mg of Fe. We aimed to assess the effect of MMS v. IFA on neonatal mortality stratified by Fe dose in each supplement. METHODS: We updated the neonatal mortality analysis of the 2020 WHO guidelines using the generic inverse variance method and applied the random effects model to calculate the effect estimates of MMS v. IFA on neonatal mortality in subgroups of trials (n 13) providing the same or different amounts of Fe, that is, MMS with 60 mg of Fe v. IFA with 60 mg of Fe; MMS with 30 mg of Fe v. IFA with 30 mg of Fe; MMS with 30 mg of Fe v. IFA with 60 mg of Fe; and MMS with 20 mg of Fe v. IFA with 60 mg of Fe. RESULTS: There were no statistically significant differences in neonatal mortality between MMS and IFA within any of the subgroups of trials. Analysis of MMS with 30 mg v. IFA with 60 mg of Fe (7 trials, 14 114 participants), yielded a non-significant risk ratio of 1·12 (95 % CI 0·83 to 1·50). CONCLUSION: Neonatal mortality did not differ between MMS and IFA regardless of Fe dose in either supplement.
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spelling pubmed-99917372023-03-08 Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose Gomes, Filomena Agustina, Rina Black, Robert E Christian, Parul Dewey, Kathryn G Kraemer, Klaus Shankar, Anuraj H Smith, Emily Tumilowicz, Alison Bourassa, Megan W Public Health Nutr Commentary OBJECTIVE: Antenatal multiple micronutrient supplements (MMS) are a cost-effective intervention to reduce adverse pregnancy and birth outcomes. However, the current WHO recommendation on the use of antenatal MMS is conditional, partly due to concerns about the effect on neonatal mortality in a subgroup of studies comparing MMS with iron and folic acid (IFA) supplements containing 60 mg of Fe. We aimed to assess the effect of MMS v. IFA on neonatal mortality stratified by Fe dose in each supplement. METHODS: We updated the neonatal mortality analysis of the 2020 WHO guidelines using the generic inverse variance method and applied the random effects model to calculate the effect estimates of MMS v. IFA on neonatal mortality in subgroups of trials (n 13) providing the same or different amounts of Fe, that is, MMS with 60 mg of Fe v. IFA with 60 mg of Fe; MMS with 30 mg of Fe v. IFA with 30 mg of Fe; MMS with 30 mg of Fe v. IFA with 60 mg of Fe; and MMS with 20 mg of Fe v. IFA with 60 mg of Fe. RESULTS: There were no statistically significant differences in neonatal mortality between MMS and IFA within any of the subgroups of trials. Analysis of MMS with 30 mg v. IFA with 60 mg of Fe (7 trials, 14 114 participants), yielded a non-significant risk ratio of 1·12 (95 % CI 0·83 to 1·50). CONCLUSION: Neonatal mortality did not differ between MMS and IFA regardless of Fe dose in either supplement. Cambridge University Press 2022-08 2022-04-25 /pmc/articles/PMC9991737/ /pubmed/35466910 http://dx.doi.org/10.1017/S1368980022001008 Text en © The Authors 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Gomes, Filomena
Agustina, Rina
Black, Robert E
Christian, Parul
Dewey, Kathryn G
Kraemer, Klaus
Shankar, Anuraj H
Smith, Emily
Tumilowicz, Alison
Bourassa, Megan W
Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
title Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
title_full Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
title_fullStr Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
title_full_unstemmed Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
title_short Effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
title_sort effect of multiple micronutrient supplements v. iron and folic acid supplements on neonatal mortality: a reanalysis by iron dose
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991737/
https://www.ncbi.nlm.nih.gov/pubmed/35466910
http://dx.doi.org/10.1017/S1368980022001008
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