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Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital
BACKGROUND: To determine the incidence and risk factors of fetal macrosomia and maternal and perinatal outcome. PATIENTS AND METHODS: This was a 1-year prospective case–control study of singleton pregnancies in a Nigerian tertiary hospital. Only women who gave consent were recruited for the study. T...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743291/ https://www.ncbi.nlm.nih.gov/pubmed/26903699 http://dx.doi.org/10.4103/0300-1652.171622 |
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author | Olokor, Oghenefegor Edwin Onakewhor, Joseph Ubini Aderoba, Adeniyi Kolade |
author_facet | Olokor, Oghenefegor Edwin Onakewhor, Joseph Ubini Aderoba, Adeniyi Kolade |
author_sort | Olokor, Oghenefegor Edwin |
collection | PubMed |
description | BACKGROUND: To determine the incidence and risk factors of fetal macrosomia and maternal and perinatal outcome. PATIENTS AND METHODS: This was a 1-year prospective case–control study of singleton pregnancies in a Nigerian tertiary hospital. Only women who gave consent were recruited for the study. The maternal and perinatal outcomes in women who delivered macrosomic infants (birth weight ≥ 4000 g) were compared with the next consecutive delivery of normal birth weight (2500–3999 g) infants. RESULTS: The total deliveries for the study period were 2437, of which 135 were macrosomic babies. The incidence of fetal macrosomia was 5.5%. The mean birth weights of macrosomic and nonmacrosomic babies were 4.26 ± 0.29 kg and 3.20 ± 0.38 kg, respectively, P = 0.000. Mothers with macrosomic babies were more likely to be older (P = 0.047), of higher parity (0.001), taller (P = 0.007), and weighed more at delivery (P = 0.000). Previous history of fetal macrosomia (P = 0.000) and maternal diabetes (P = 0.007) were factors strongly associated with the delivery of macrosomic infants. Pregnancies associated with fetal macrosomia had increased duration of labor (P = 0.007), interventional deliveries (P = 0.000), shoulder dystocia, and genital laceration (P = 0.000). There was no significant difference in the incidence of primary postpartum hemorrhage (P = 0.790), birth asphyxia, and perinatal mortality (P = 0.197). CONCLUSION: Fetal macrosomia is associated with maternal and fetal morbidities. The presence of the observed risk factors should elicit the suspicion of a macrosomic fetus and the need for appropriate management to reduce maternal and fetal morbidities. |
format | Online Article Text |
id | pubmed-4743291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47432912016-02-22 Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital Olokor, Oghenefegor Edwin Onakewhor, Joseph Ubini Aderoba, Adeniyi Kolade Niger Med J Original Article BACKGROUND: To determine the incidence and risk factors of fetal macrosomia and maternal and perinatal outcome. PATIENTS AND METHODS: This was a 1-year prospective case–control study of singleton pregnancies in a Nigerian tertiary hospital. Only women who gave consent were recruited for the study. The maternal and perinatal outcomes in women who delivered macrosomic infants (birth weight ≥ 4000 g) were compared with the next consecutive delivery of normal birth weight (2500–3999 g) infants. RESULTS: The total deliveries for the study period were 2437, of which 135 were macrosomic babies. The incidence of fetal macrosomia was 5.5%. The mean birth weights of macrosomic and nonmacrosomic babies were 4.26 ± 0.29 kg and 3.20 ± 0.38 kg, respectively, P = 0.000. Mothers with macrosomic babies were more likely to be older (P = 0.047), of higher parity (0.001), taller (P = 0.007), and weighed more at delivery (P = 0.000). Previous history of fetal macrosomia (P = 0.000) and maternal diabetes (P = 0.007) were factors strongly associated with the delivery of macrosomic infants. Pregnancies associated with fetal macrosomia had increased duration of labor (P = 0.007), interventional deliveries (P = 0.000), shoulder dystocia, and genital laceration (P = 0.000). There was no significant difference in the incidence of primary postpartum hemorrhage (P = 0.790), birth asphyxia, and perinatal mortality (P = 0.197). CONCLUSION: Fetal macrosomia is associated with maternal and fetal morbidities. The presence of the observed risk factors should elicit the suspicion of a macrosomic fetus and the need for appropriate management to reduce maternal and fetal morbidities. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4743291/ /pubmed/26903699 http://dx.doi.org/10.4103/0300-1652.171622 Text en Copyright: © 2015 Nigerian Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Olokor, Oghenefegor Edwin Onakewhor, Joseph Ubini Aderoba, Adeniyi Kolade Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital |
title | Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital |
title_full | Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital |
title_fullStr | Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital |
title_full_unstemmed | Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital |
title_short | Determinants and outcome of fetal macrosomia in a Nigerian tertiary hospital |
title_sort | determinants and outcome of fetal macrosomia in a nigerian tertiary hospital |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743291/ https://www.ncbi.nlm.nih.gov/pubmed/26903699 http://dx.doi.org/10.4103/0300-1652.171622 |
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