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1.
Reprod Sci ; 30(4): 1257-1265, 2023 04.
Article in English | MEDLINE | ID: mdl-36068375

ABSTRACT

The transfer of frozen-thawed embryos has been associated with an increased risk of large for gestational age at birth. Our objective is to assess its impact on the risk of large for gestational age (LGA) in order to improve the bias control in relation with the available studies. Retrospective cohort study on cumulative sample of 801 single live births of 32 weeks or longer of gestation, resulting from pregnancies obtained by cryopreserved or fresh embryo transfer which are not affected by disorders that could impair fetal growth and carried out at Hospital General Universitario Gregorio Marañón, in Madrid, during the period 2005-2017. The relative risk (RR) of LGA has been estimated with its confidence interval (CI) at 95%. Multivariate analysis using logistic regression was applied to adjust the crude effect. LGA was more frequent in babies born after cryotransfer in comparison with the reference group (20.9% vs. 6.0%; p < 0.001), as well as macrosomia (8.2% vs. 0.9%; p < 0.001). Frequencies of weight > 4500 g were similar (0.7% vs. 0.1%; p > 0.05). Nulliparity was associated to a higher risk of LGA (RR: 3.8; CI95%: 2.0-7.0; p < 0.005), as well as cleaving embryo transfer (RR: 2; CI95%: 1.07-3.8; p < 0.05). According to the multivariate analysis, the exposure variable was the only one independently associated with LGA (OR: 3.5; CI95%: 2.0-6.1; p < 0.001). Frozen-thawed embryo transfer significantly increases the risk of LGA, regardless of the influence of factors relating to the patient's condition, the embryos transferred, or the fetal sex.


Subject(s)
Embryo Transfer , Fertilization in Vitro , Infant, Newborn , Pregnancy , Infant , Female , Humans , Retrospective Studies , Gestational Age , Fertilization in Vitro/methods , Embryo Transfer/adverse effects , Embryo Transfer/methods , Cryopreservation/methods , Cohort Studies , Birth Weight
2.
J Perinat Med ; 47(7): 717-723, 2019 Sep 25.
Article in English | MEDLINE | ID: mdl-31369397

ABSTRACT

Background We aimed to analyze the success rate of external cephalic version (ECV) for breech presentations performed in our center between March 2011 and March 2016. We evaluated factors related to a successful ECV, delivery mode, complications and newborn status after ECV. Methods Analysis of assembled data of 327 consecutive ECVs in the third trimester was done. Results The total success rate was 56.6%. After a successful ECV, 85.9% of the fetuses were delivered vaginally. Logistic regression analysis of background factors leading to a successful ECV showed that tocolysis with ritodrine and anterior placenta were each significantly correlated with the rate of successful version. No severe complications were registered during the ECVs, and all babies had normal Apgar scores at delivery. Conclusion These findings suggest that attempting an ECV in breech presentations, once or even twice, seems to be an appropriate management given that a successful ECV decreases the rate of cesarean section in this group of patients and by doing so, it might also decrease the risk of cesarean sections in future pregnancies.


Subject(s)
Breech Presentation , Cesarean Section , Ritodrine/therapeutic use , Version, Fetal , Adult , Apgar Score , Breech Presentation/diagnosis , Breech Presentation/epidemiology , Breech Presentation/therapy , Cesarean Section/methods , Cesarean Section/statistics & numerical data , Female , Humans , Infant, Newborn , Pregnancy , Pregnancy Outcome/epidemiology , Prognosis , Spain/epidemiology , Tocolytic Agents/therapeutic use , Treatment Outcome , Version, Fetal/adverse effects , Version, Fetal/methods , Version, Fetal/statistics & numerical data
3.
J Ultrasound Med ; 34(11): 1921-7, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26446822

ABSTRACT

A double aortic arch is a relatively uncommon anomaly occasionally associated with congenital heart disease or the chromosome 22q11 deletion. We report a case of prenatal diagnosis of a double aortic arch in which the sonographic features in the 3-vessel and trachea view are highlighted. A PubMed-based search was made to retrieve all cases of prenatal diagnosis of double aortic arch. A total of 13 articles and 35 cases were found. The average gestational age at diagnosis was 29 weeks. Six cases had associated cardiac anomalies. Only 1 case had the 22q11 deletion, showing extracardiac anomalies without cardiac defect. The postnatal evolution was characterized by symptoms of tracheoesophageal compression in 72.4% of the cases. Detection of a double aortic arch should be followed by a thorough fetal scan and echocardiography, and a chromosomal study should be considered when the sonographic findings are consistent with the 22q11 deletion.


Subject(s)
Aorta, Thoracic/abnormalities , Aorta, Thoracic/diagnostic imaging , Heart Defects, Congenital/diagnostic imaging , Ultrasonography, Prenatal/methods , Adult , Aorta, Thoracic/embryology , Female , Heart Defects, Congenital/therapy , Humans , Male , Perinatal Care , Pregnancy , Treatment Outcome
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