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. 2025 Jan 8.
doi: 10.1007/s10354-024-01068-2. Online ahead of print.

Vaginal versus caesarean delivery in fetal macrosomia-a retrospective cohort study

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Vaginal versus caesarean delivery in fetal macrosomia-a retrospective cohort study

Gordana Grgić et al. Wien Med Wochenschr. .

Abstract

Objective: The aims of this study were to determine the incidence of macrosomic births over a 5-year period and to examine the childbirth complications for both mother and newborn.

Patients and methods: During the study period there were a total of 16,126 deliveries, of which 1905 were macrosomic fetuses (defined as those with a birthweight of 4000 g or more). Data on the course of pregnancy and childbirth were collected from existing maternal and peripartum medical records. Patients were divided into two groups: those who delivered vaginally and those who delivered by caesarean section. The groups were compared in terms of obstetric, fetal, and neonatal data as well as perinatal outcomes.

Results: We included 1905 women in the study, 1286 (67.5%) with vaginal delivery and 619 (32.4%) with caesarean section. Primiparous women more frequently delivered by caesarean section, whereas multiparous women more commonly delivered vaginally (p < 0.00001). Male fetuses were significantly more prevalent in both examined groups. Risk factors for fetal macrosomia, such as gestational diabetes, maternal obesity, pregnancy-induced hypertension, polyhydramnios, and multiparity, were significantly more prevalent in the group with caesarean section (p < 0.00001). Delivery complications such as dorsoposterior presentation of the fetal head; fetal asphyxia, dystocia, and cephalopelvic disproportion; and uterine rupture were statistically significantly more frequent with caesarean section CONCLUSION: Our data show that caesarean deliveries for fetal macrosomia were associated with more maternal and neonatal complications than vaginal deliveries.

Keywords: Diabetes gestational; Labor; Perinatal outcome; Uterine hemorrhage; Uterine rupture.

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Conflict of interest statement

Declarations. Conflict of interest: G. Grgić, A. Cerovac, A. Hadžimehmedović, and D. Habek declare that they have no competing interests. Ethical standards: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. For this type of study, formal consent is not required. This article does not contain any studies with animals performed by any of the authors. The University Clinical Center Tuzla institutional ethical board approved the study (registration no. 1912-21), with waiver of informed consent due to the retrospective observational design of the study.

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