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1.
Gynecol Endocrinol ; 38(5): 411-415, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-35277105

RESUMEN

BACKGROUND: Following the adoption of the International Association of Diabetes and Pregnancy Study Group (IADPSG) criteria for gestational diabetes mellitus (GDM) diagnosis by the World Health Organization (WHO) in 2014, many investigators have tried to identify independent risk factors for antenatal insulin therapy (AIT). The purpose of the current study is to build and validate a score that stratifies patients according to their need for AIT. METHODS: All pregnant women diagnosed with GDM according to the IADPSG definition were included. Group 1 comprised patients of 2018, and group 2 comprised patients of 2019. Each group was divided into two subgroups: subgroup A comprised patients diagnosed according to the 75-g oral glucose tolerance test (OGTT), and subgroup B comprised patients diagnosed according to fasting plasma glucose (FPG). RESULTS: A total of 1298 patients were included; 19.3% of those diagnosed by OGTT and 40.9% by FPG required AIT. The risk for AIT was stratified as low, moderate, and high. Brugmann FPG score comprised six risk factors and Brugmann OGTT score 12. Higher scores were associated with higher risk for AIT. The use of these scores in the two subgroups of group 2 showed no statistical differences compared to group 1. CONCLUSIONS: Both Brugmann FPG and OGTT scores may be useful to stratify patients with GDM according to their need for AIT. Future studies should be conducted to prospectively validate these scores, and to examine whether or not using oral anti-hyperglycemic agents in a high-risk group may decrease the need for AIT.


Asunto(s)
Diabetes Gestacional , Embarazo en Diabéticas , Glucemia , Diabetes Gestacional/diagnóstico , Diabetes Gestacional/tratamiento farmacológico , Ayuno , Femenino , Prueba de Tolerancia a la Glucosa , Humanos , Insulina/uso terapéutico , Embarazo
2.
Prenat Diagn ; 36(1): 81-7, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26518248

RESUMEN

OBJECTIVE: The aim of this study was to describe whether the prophylactic use of a cervical pessary decreases the rate of premature birth in congenital diaphragmatic hernia (CDH) fetuses treated with fetoscopic tracheal occlusion (FETO). METHODS: The study concerns a consecutive series of cases with CDH and FETO and a group of CDH without FETO. In a subgroup of the FETO group, a prophylactic cervical pessary was inserted the day following the procedure. Gestational age (GA) at birth was the primary outcome. RESULTS: Fifty-nine fetuses with FETO and 47 expectantly managed were included. The last 15 FETO had a cervical pessary inserted. The median GA at delivery in the FETO group with pessary was 35.1 weeks and was not different from that in the FETO group without a pessary (34.3 weeks; p = 0.28) but was below that in the expectantly managed group (38.3 weeks; p < 0.001). CONCLUSION: Early results suggest that prophylactic use of an Arabin cervical pessary does not prolong gestation of CDH fetuses treated with FETO. © 2015 John Wiley & Sons, Ltd.


Asunto(s)
Fetoscopía/efectos adversos , Hernias Diafragmáticas Congénitas/terapia , Pesarios , Nacimiento Prematuro/prevención & control , Adolescente , Adulto , Femenino , Fetoscopía/métodos , Estudios de Seguimiento , Humanos , Embarazo , Nacimiento Prematuro/etiología , Estudios Prospectivos , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Tráquea , Resultado del Tratamiento , Adulto Joven
3.
Radiology ; 267(3): 902-10, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23329652

RESUMEN

PURPOSE: To prospectively define fetal density in the second half of pregnancy by using magnetic resonance (MR) imaging and to compare estimates of fetal weight based on ultrasonography (US) and MR imaging with actual birth weight. MATERIALS AND METHODS: Written informed consent was obtained for this ethics committee-approved study. In this cross-sectional study between March 2011 and May 2012, fetal density was calculated as actual birth weight at delivery divided by fetal body volume at MR imaging in 188 fetuses between 20 weeks and 2 days and 42 weeks and 1 day of gestational age. Regression analysis was used to investigate the effect of variables, including sex, on fetal density. The US estimate of fetal weight was performed according to Hadlock et al, and the MR estimate of fetal weight was calculated based on the equation developed by Baker et al. US and MR estimates of fetal weight were compared with actual birth weights by using regression analysis. RESULTS: Median fetal density was equal to 1.04 (range, 0.95-1.18). Fetal density was significantly associated with gestational age at delivery but not with fetal sex. In 26.6% of fetuses, the US estimate of fetal weight had a relative error of more than 10%, while a similar relative error for the MR estimate of fetal weight occurred in only 1.1% of fetuses. The limits of agreement were narrower with the MR estimate of fetal weight compared with the US estimate of fetal weight. CONCLUSION: In the second half of pregnancy, fetal density varies with gestational age. Fetal weight estimates by using fetal MR imaging are better than those by using prenatal US.


Asunto(s)
Peso Fetal , Imagen por Resonancia Magnética/métodos , Ultrasonografía Prenatal/métodos , Peso al Nacer , Estudios Transversales , Femenino , Humanos , Recién Nacido , Masculino , Embarazo , Estudios Prospectivos , Análisis de Regresión , Factores Sexuales
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