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1.
J Matern Fetal Neonatal Med ; 32(20): 3367-3378, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29635952

RESUMO

Background/objective: The purpose of this study is to investigate the use of a more biologic parameter for evaluation of the effect of nuchal cord tightness; the study of blood flow in the umbilical arteries of nuchal cord using Doppler ultrasonography. Methods: This prospective cohort study was conducted at Ain Shams University Maternity Hospital, Cairo, Egypt in the period between August 2015 and August 2017. Hundred primigravidas were recruited with nuchal cord diagnosed by Doppler ultrasonography; whereas the rest of the study population was included in the "Control group". Doppler velocimetry study was then performed on a free-floating loop of the umbilical cord and Doppler indices were calculated. Both groups were followed up during labor: intrapartum events, mode of delivery, and neonatal outcome were recorded. Results: Intrapartum fetal heart rate abnormalities were significantly more common in the nuchal cord group compared to the control group. The overall cardiotocography category was significantly more commonly reflecting abnormal fetal heart rate patterns in the nuchal cord group compared to the control group with 46.74% of the nuchal group patients falling within the "suspicious - pathological - need urgent intervention" categories. Intervention rate was significantly higher in the nuchal cord group than the control group (33.69 versus 21.84%). Moreover, incidence of intrapartum fetal heart rate abnormalities and intervention rate were significantly higher in the nuchal cord with abnormal Doppler subgroup compared to both nuchal cord with normal Doppler subgroup and the control group; with a calculated number needed to harm of 2.11. Conclusions: In view of these results, it might be concluded that umbilical cord tightness affecting fetal hemodynamics (expressed by changes in umbilical artery Doppler) might be a determinate factor affecting the intrapartum course.


Assuntos
Indicadores Básicos de Saúde , Cordão Nucal/diagnóstico , Parto/fisiologia , Resultado da Gravidez , Ultrassonografia Pré-Natal/métodos , Artérias Umbilicais/diagnóstico por imagem , Adolescente , Adulto , Velocidade do Fluxo Sanguíneo , Cardiotocografia , Estudos de Coortes , Egito , Feminino , Humanos , Recém-Nascido , Gravidez , Ultrassonografia Doppler em Cores , Cordão Umbilical/diagnóstico por imagem , Adulto Jovem
2.
J Matern Fetal Neonatal Med ; 32(3): 483-487, 2019 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-29219012

RESUMO

BACKGROUND: Approximately 8-15% of all infants are born with evidence of meconium-stained amniotic fluid (MSAF). MSAF is a potentially serious sign of fetal compromise and may indicate fetal hypoxia Objectives and aim of the work: The present study was designed to evaluate the relationship between meconium stained amniotic fluid and fetal nucleated red blood cell counts. As well, we aim to evaluate the relationship between the presence of meconium in amniotic fluid and Apgar scores in neonates. SUBJECTS AND METHODS: A prospectively case-controlled study was performed on 40 women with clear amniotic fluid as control and 40 women with meconium-stained amniotic fluid as the study group. At delivery, 2 ml of umbilical cord blood was collected and analyzed for nucleated red blood cell (NRBC). RESULTS: The mean NRBC counts in meconium-stained amniotic fluid was significantly higher than the control group (18.35 ± 7.7 and 9.6 ± 4.96), respectively (p < .001). There were statistically significant differences concerning 1- and 5-min Apgar scores with lower values in the MSAF group (p < .001 and .001, respectively). CONCLUSION: Our results support previous studies which indicate the presence of meconium can be associated with chronic fetal hypoxia as demonstrated by elevated fetal NRBC levels.


Assuntos
Líquido Amniótico/metabolismo , Eritroblastos/citologia , Sangue Fetal/citologia , Mecônio/metabolismo , Adolescente , Adulto , Índice de Apgar , Contagem de Células Sanguíneas , Estudos de Casos e Controles , Feminino , Hipóxia Fetal/sangue , Hipóxia Fetal/etiologia , Humanos , Recém-Nascido , Doenças do Recém-Nascido/sangue , Doenças do Recém-Nascido/etiologia , Masculino , Gravidez , Adulto Jovem
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