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Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study
BACKGROUND: Fetal macrosomia defined as birth weight of 4000 g and above regardless of gestational age and associated with adverse maternal and fetal outcomes, especially among women in developing countries like Ethiopia. Despite the observed burden, there is limited evidence on determinants of feta...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161488/ https://www.ncbi.nlm.nih.gov/pubmed/35655197 http://dx.doi.org/10.1186/s12884-022-04734-8 |
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author | Woltamo, Deginesh Dawit Meskele, Mengistu Workie, Shimelash Bitew Badacho, Abebe Sorsa |
author_facet | Woltamo, Deginesh Dawit Meskele, Mengistu Workie, Shimelash Bitew Badacho, Abebe Sorsa |
author_sort | Woltamo, Deginesh Dawit |
collection | PubMed |
description | BACKGROUND: Fetal macrosomia defined as birth weight of 4000 g and above regardless of gestational age and associated with adverse maternal and fetal outcomes, especially among women in developing countries like Ethiopia. Despite the observed burden, there is limited evidence on determinants of fetal macrosomia. This study aimed to identify determinants of fetal macrosomia among live births at Wolaita Sodo town Southern Ethiopia. METHODS: A facility-based matched case–control study design involved 360 singletons deliveries attended at hospitals in Wolaita Sodo town, southern Ethiopia, with 120 cases and 240 controls included. Cases and control were matched by maternal age. Cases were neonates with a birth weight of ≥ 4000, while controls were neonates with a birthweight between 2500gm and less than 4000gm. Data were collected by interviews, measuring, and reviewing mothers' medical documents. Conditional logistic regression analysis was carried to identify the independent predictor variables. Statistical significance was set using a p-value < 0.05 and 95% CI for AOR. RESULTS: Male neonates were four times more likely to be macrosomia than female neonates MAOR = 4.0 [95%CI; 2.25–7.11, p < 0.001]. Neonates born at gestational age ≥ 40 weeks were 4.33 times more likely to be macrosomia with MAOR = 4.33 [95%CI; 2.37–7.91, p < 0.001]. Neonates born from physically inactive mothers were 7.76 times more likely to be macrosomia with MAOR = 7.76 [95CI; 3.33–18.08, p < 0.001]. Neonates born from mothers who consumed fruits and dairy products in their diet frequently were 2 and 4.9 times more likely to be macrosomia MAOR = 2.03 [95%CI; 1.11–3.69, p = 0.021] and AOR = 4.91[95%CI; 2.36–10.23, p < 0.001] respectively. CONCLUSION: Mothers' physical exercise and consumption of fruit and dairy products were significant predictor variables for fetal macrosomia. Hence, health care providers may use these factors as a screening tool for the prediction, early diagnosis, and timely intervention of fetal macrosomia and its complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-04734-8. |
format | Online Article Text |
id | pubmed-9161488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91614882022-06-03 Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study Woltamo, Deginesh Dawit Meskele, Mengistu Workie, Shimelash Bitew Badacho, Abebe Sorsa BMC Pregnancy Childbirth Research BACKGROUND: Fetal macrosomia defined as birth weight of 4000 g and above regardless of gestational age and associated with adverse maternal and fetal outcomes, especially among women in developing countries like Ethiopia. Despite the observed burden, there is limited evidence on determinants of fetal macrosomia. This study aimed to identify determinants of fetal macrosomia among live births at Wolaita Sodo town Southern Ethiopia. METHODS: A facility-based matched case–control study design involved 360 singletons deliveries attended at hospitals in Wolaita Sodo town, southern Ethiopia, with 120 cases and 240 controls included. Cases and control were matched by maternal age. Cases were neonates with a birth weight of ≥ 4000, while controls were neonates with a birthweight between 2500gm and less than 4000gm. Data were collected by interviews, measuring, and reviewing mothers' medical documents. Conditional logistic regression analysis was carried to identify the independent predictor variables. Statistical significance was set using a p-value < 0.05 and 95% CI for AOR. RESULTS: Male neonates were four times more likely to be macrosomia than female neonates MAOR = 4.0 [95%CI; 2.25–7.11, p < 0.001]. Neonates born at gestational age ≥ 40 weeks were 4.33 times more likely to be macrosomia with MAOR = 4.33 [95%CI; 2.37–7.91, p < 0.001]. Neonates born from physically inactive mothers were 7.76 times more likely to be macrosomia with MAOR = 7.76 [95CI; 3.33–18.08, p < 0.001]. Neonates born from mothers who consumed fruits and dairy products in their diet frequently were 2 and 4.9 times more likely to be macrosomia MAOR = 2.03 [95%CI; 1.11–3.69, p = 0.021] and AOR = 4.91[95%CI; 2.36–10.23, p < 0.001] respectively. CONCLUSION: Mothers' physical exercise and consumption of fruit and dairy products were significant predictor variables for fetal macrosomia. Hence, health care providers may use these factors as a screening tool for the prediction, early diagnosis, and timely intervention of fetal macrosomia and its complications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-04734-8. BioMed Central 2022-06-02 /pmc/articles/PMC9161488/ /pubmed/35655197 http://dx.doi.org/10.1186/s12884-022-04734-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Woltamo, Deginesh Dawit Meskele, Mengistu Workie, Shimelash Bitew Badacho, Abebe Sorsa Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study |
title | Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study |
title_full | Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study |
title_fullStr | Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study |
title_full_unstemmed | Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study |
title_short | Determinants of fetal macrosomia among live births in southern Ethiopia: a matched case–control study |
title_sort | determinants of fetal macrosomia among live births in southern ethiopia: a matched case–control study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161488/ https://www.ncbi.nlm.nih.gov/pubmed/35655197 http://dx.doi.org/10.1186/s12884-022-04734-8 |
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