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1.
Clin Exp Obstet Gynecol ; 39(3): 288-92, 2012.
Article in English | MEDLINE | ID: mdl-23157026

ABSTRACT

AIM: The aim of the study was to compare maternal and perinatal mortality and short-term outcomes of maternal and perinatal health between a cesarean group with relative indications and a vaginal delivery group. METHODS: A total of 1,119 patients were included; 582 were delivered by spontaneous vaginal birth and 537 delivered by cesarean section without labor. The indication for cesarean section was tocophobia and fear of childbirth for all patients. Maternal and perinatal morbidity and mortality were compared between the groups. RESULTS: No maternal mortality was recorded. Maternal morbidity was significantly lower in the vaginal birth group than the cesarean group (7 vs 30, p<0.05). Perinatal mortality (2 vs 0) and perinatal morbidity were not significantly different between the two groups (33 vs 17). The vaginallly delivered group had significantly higher newborn hospitalization rates than the cesarean group (p<0.05), but hospitalization time did not differ. Newborns with the first minute Apgar score below 7 were higher in the cesarean group (p<0.05). Fifth minute Apgar scores and umblical cord pH values were similiar. Cesarean neonates weighed more than vaginally delivered ones (p<0.05). CONCLUSION: Short-term maternal complications were more frequently seen in cesarean deliveries with relative indications than spontanous vaginal deliveries but no difference was found in perinatal mortality and morbidity. There is a clear need for research on health outcomes for mothers and infants associated with cesarean delivery without any medical indication.


Subject(s)
Cesarean Section/adverse effects , Delivery, Obstetric/adverse effects , Pregnancy Outcome , Adult , Apgar Score , Female , Gestational Age , Hospitalization , Humans , Infant, Newborn , Maternal Mortality , Morbidity , Perinatal Mortality , Pregnancy
2.
Gynecol Obstet Invest ; 72(4): 269-73, 2011.
Article in English | MEDLINE | ID: mdl-22086108

ABSTRACT

AIMS: To assess the efficacy of vaginal micronized natural progesterone as a tocolytic and in maintenance therapy during threatened preterm birth. METHODS: Eighty-three women with symptoms of threatened preterm birth were either randomized to study groups receiving tocolytic treatment combined with intravaginal micronized natural progesterone (200 mg daily) or to a control group receiving only tocolysis. RESULTS: Micronized natural progesterone treatment resulted in a prolonged latency period of 32.1 ± 17.8 versus 21.2 ± 16.3 days in the control group and heavier birth weights of 2,982.8 ± 697.8 g versus 2,585.3 ± 746.6 g. No significant differences were found between the groups in admission to the neonatal intensive care unit, stay at the neonatal intensive care unit, need for a mechanical ventilator, respiratory distress syndrome or neonatal sepsis. CONCLUSION: The treatment of threatened preterm birth with tocolytics combined with intravaginal micronized natural progesterone significantly prolonged pregnancy and increased birth weight. However, an improvement in adverse perinatal outcomes was not observed.


Subject(s)
Obstetric Labor, Premature/drug therapy , Progesterone/administration & dosage , Progestins/administration & dosage , Ritodrine/administration & dosage , Tocolytic Agents/administration & dosage , Administration, Intravaginal , Birth Weight , Capsules , Drug Therapy, Combination , Female , Gestational Age , Humans , Pregnancy , Treatment Outcome
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