Fetal echocardiography indications and lack of association between abnormal exams and advanced maternal age: A cross-sectional study - Fetal abnormal echocardiography / Indicações para realização de ecocardiografia fetal e ausência de associação entre exames alterados e idade materna avançada: Um estudo transversal - Ecocardiografia fetal anormal

Abstract Objective To analyze the most frequent referrals for fetal echocardiography, including advanced maternal age and its association with abnormal results. Methods We included all pregnant women referred to perform fetal echocardiography (gestational age 22-32 weeks) in 2 health centers in Rio de Janeiro, from June 2015 to June 2016. Advanced maternal age was considered when age was > 35 years at the time of delivery). Referral reasons and results were recorded, according to the Brazilian Fetal Cardiology Statement. Crude and adjusted prevalence ratios were calculated (Poisson regression). We considered p < 0.05 as significant. Results A total of 1,221 tests were analyzed. Abnormal fetal echocardiography was observed in 14.82% of the cases. The most frequent abnormalities were interventricular septal defect (6.39%), septal hypertrophy (3.35%) and atrioventricular septal defect (1.14%). Routine exams were performed in 559 women, 289 were referred for advanced maternal age and 373 were referred according to the Brazilian FetalCardiology Statement criteria. An obstetric ultrasound suggesting fetal cardiacabnormality, maternal diabetes, increased nuchal translucency, and obstetric ultrasound suggesting a noncardiac abnormality were strongly associated with an abnormal fetal echocardiography. Abnormal results were not more frequent in women with advanced maternal age when compared with the rest of the study group. Conclusions It was observed that routine exams and advancedmaternal age referrals were very frequent. Those exams were not associated to fetal echocardiography abnormalities. In this scenario, when the obstetric ultrasound suggests a fetal cardiac

Resumo Objetivo Analisar as indicações mais frequentes para realização de ecocardiografia fetal, incluindo idade materna avançada, e a associação destas com exames alterados. Métodos Foram incluídas todas as gestantes que realizaram ecocardiografia fetal na idade gestacional entre 22 e 32 semanas, em 2 centros de referência no Rio de Janeiro, no período de junho de 2015 a junho de 2016. Foi considerada idadematerna avançada se no momento do parto a idade materna fosse> 35 anos. As indicações e os resultados dos exames foram registrados, segundo a Diretriz Brasileira de Cardiologia Fetal. Foramcalculadas as razões de prevalência brutas e ajustadas através da regressão de Poisson, considerando-se p < 0,05. Resultados Um total de 1.221 exames foram analisados. A frequência de exame ecocardiográfico alterado foi 14,82%. As alterações mais frequentes foram defeito do septo interventricular (6,39%), hipertrofia septal (3,35%) e defeito do septo atrioventricular (1,14%). Quinhentos e cinquenta e nove exames foram realizados com indicação de rotina, 289 por idade materna avançada e 373 preenchiam critério de acordo com a Diretriz Brasileira de Cardiologia Fetal. O exame ecocardiográfico alterado foi associado ao ultrassom obstétrico sugerindo cardiopatia fetal, ao diabetes materno, à translucência nucal aumentada e ao ultrassom obstétrico sugerindo alteração extracardíaca. Não foi observada maior frequência de exame ecocardiográfico alterado nas gestantes com idade materna avançada, comparado ao restante da amostra. Conclusão Constatou-se elevada frequência de indicações de rotina, e por idade materna avançada isoladamente, que não foram associados a alterações da ecocardiografia fetal. Em nosso meio, quando o ultrassom obstétrico sugere cardiopatia fetal, é muito provável que a ecocardiografia fetal tambémseja anormal. Portanto, o ultrassom obstétrico é um bom método de rastreio pré-natal.

Effect of Obesity on Gestational and Perinatal Outcomes / Efeito da obesidade sobre os resultados gestacionais e perinatais

Abstract Purpose To assess the impact of pre-pregnancy obesity (body mass index [BMI] ≥30 kg/m2) on the gestational and perinatal outcomes. Methods Retrospective cohort study of 731 pregnant women with a BMI ≥30 kg/m2 at the first prenatal care visit, comparing them with 3,161 women with a BMI between 18.5 kg/m2 and 24.9 kg/m2. Maternal and neonatal variables were assessed. Statistical analyses reporting the demographic features of the pregnant women (obese and normal) were performed with descriptive statistics followed by two-sided independent Student's t tests for the continuous variables, and the chi-squared (χ2) test, or Fisher's exact test, for the categorical variables. We performed a multiple linear regression analysis of newborn body weight based on the mother's BMI, adjusted by maternal age, hyperglycemic disorders, hypertensive disorders, and cesarean deliveries to analyze the relationships among these variables. All analyses were performed with the R (R Foundation for Statistical Computing, Vienna, Austria) for Windows software, version 3.1.0. A value of p < 0.05 was considered statistically significant. Results Obesity was associated with older age [OR 9.8 (7.8-12.2); p < 0.01], hyperglycemic disorders [OR 6.5 (4.8-8.9); p < 0.01], hypertensive disorders [OR 7.6 (6.1-9.5); p < 0.01], caesarean deliveries [OR 2.5 (2.1-3.0); p < 0.01], fetal macrosomia [OR 2.9 (2.3-3.6); p < 0.01] and umbilical cord pH [OR 2.1 (1.4-2.9); p < 0.01). Conversely, no association was observed with the duration of labor, bleeding during labor, Apgar scores at 1 and 5 minutes after birth, gestational age, stillbirth and early neonatal mortality, congenital malformations, and maternal and fetal injury. Conclusion We observed that pre-pregnancy obesity was associated with maternal age, hyperglycemic disorders, hypertension syndrome, cesarean deliveries, fetal macrosomia, and fetal acidosis.

Resumo Objetivo Avaliar o impacto da obesidade pré-gestacional (índice de massa corpórea [IMC] ≥30 kg/m2) sobre os resultados gestacionais e perinatais. Métodos Estudo transversal retrospectivo, com 731 gestantes que apresentaram IMC ≥ 30 kg/m2 na primeira consulta de pré-natal, comparando-as a 3.161 gestantes com IMC entre 18,5 kg/m2 e 24,9 kg/m2. Foram avaliadas variáveis maternas e neonatais. A análise estatística baseou-se nas características demográficas das gestantes (obesas e com peso normal), e foi realizada com estatísticas descritivas seguidas de testes t de Student independentes bicaudais para variáveis contínuas, e teste de qui-quadrado (χ2) ou exato de Fisher para as variáveis categóricas. Foi realizada uma regressão linear múltipla do peso do recém-nascido sobre o IMC materno, ajustado por idade materna, síndromes hiperglicêmicas, síndromes hipertensivas hipertensivas e operações cesarianas, a fim de analisar a relação entre essas variáveis. Todas as análises foram realizadas com o uso de R (R Foundation for Statistical Computing, Viena, Áustria) para Windows, versão 3.1.0. Um valor de p < 0,05 foi considerado estatisticamente significante. Resultados A obesidade associou-se à idade materna [OR 9,8 (7,8-12,2); p < 0,01], distúrbios hiperglicêmicos [OR 6.5 (4,8-8,9); p < 0,01], distúrbios hipertensivos (RP: 7,6 [6,1-9,5]; p < 0,01), maior taxa de operação cesariana [OR 2,5 (2,1-3,0); p < 0,01], macrossomia fetal [OR 2,9 (2,3-3,6); p < 0,01] e baixo pH na artéria umbilical [OR 2,1 (1,4-2,9); p < 0,01]. Não foi observada associação com tempo de trabalho de parto, sangramento durante o trabalho de parto, índice de Apgar no 1° e 5° minutos, idade gestacional, natimortalidade e mortalidade neonatal precoce, malformações congênitas e tocotraumatismo materno e fetal. Conclusões O estudo mostrou que a obesidade pré-gestacional associou-se com idade materna mais elevada, distúrbios hiperglicêmicos e hipertensivos, taxas mais altas de operação cesariana, macrossomia e acidose fetal.

Prevalence of Hypertrophic Cardiomyopathy in Fetuses of Mothers with Gestational Diabetes before Initiating Treatment / Prevalência de miocardiopatia hipertrófica em fetos de mães com diabetes gestacional antes do tratamento

ABSTRACT Objective: To evaluate the prevalence of hypertrophic cardiomyopathy (HCM) in fetuses of pregnant women with gestational diabetes mellitus (GDM) in the beginning of the treatment. Methods: A cross-sectional study was performed between July 1, 2013, and Decem-ber 20, 2013, in a public maternity clinic in southern Brazil. The subjects were 63 fetuses of mothers with gestational diabetes, with a single pregnancy and no other associated pathologies. We diagnosed HCM through a fetal echocardiography before treatment and evaluated the maternal and fetal characteristics. Results: The average age of the pregnant women was 32.32 (±6.2) years, and the average gestational age at the time of the evaluation was 30.59 (±2.27) weeks. The interventricular septum thickness showed a standard deviation of more than two in 50.8% of the fetuses (95% confidence interval [95%CI]: 38.1-63.5%). The left ventricular wall thickness showed a standard deviation of more than 2 in 13 (20.6%) fetuses (95%CI: 11.1-30.2%). The HCM was confirmed in 54% of the fetuses (95%CI: 41.3-65.1%). The fetal abdominal circumference was normal in 46 (73%) fetuses, and 50% of these fetuses had HCM. Conclusion: The prevalence of hypertrophic cardiomyopathy in fetuses of pregnant women with GDM before treatment was of 54% (95%CI: 41.3-65.1%).

RESUMO Objetivo: Avaliar a prevalência de miocardiopatia hipertrófica em fetos de gestantes com diabetes mellitus gestacional antes do início do tratamento. Métodos: Foi realizado um estudo de corte transversal, no período de 1o de julho de 2013 até 20 de dezembro de 2013, em uma maternidade pública. Foram objetos do estudo 63 fetos de gestantes portadoras de diabetes mellitus gestacional (DMG), em gestação única e sem outras patologias associadas. Foi realizada ecocardiografia fetal antes do início do tratamento do diabetes. O diagnóstico de miocardiopatia hipertrófica (MH) foi realizado quando a medida do septo interventricular ou da parede ventricular estava superior a dois desvios-padrão. O desfecho primário avaliado foi presença de MH. Resultados: As gestantes apresentavam idade média de 32,32 (±6,2) anos, e a idade gestacional média no momento da avaliação foi de 30,59 (±2,27) semanas. A medida do septo interventricular estava acima de 2 desvios-padrão em 50,8% (intervalo de confiança de 95% [IC95%]: 38,1-63,5%). A parede do ventrículo esquerdo estava acima de 2 desvios-padrão em 13 fetos, totalizando 20,6% (IC95%: 11,1-30,2%). A MH estava presente em 54% dos fetos (IC95%: 41,3-65,1%). A circunferência abdominal fetal estava normal em 46 (73%) fetos, e destes, 50% apresentavam MH. Conclusão: A prevalência de MH em fetos de gestantes portadoras de DMG antes do tratamento foi de 54% (IC95% 41,3-65,1%).

Preeclampsia y defecto cardiaco fetal: ¿existe una asociación? revisión de la evidencia / Preeclampsia and fetal heart defect: is there an association? evidence review

Introducción: La preeclampsia (PE) es un desorden multisistémico complejo causado por una angiogénesis anormal placentaria. La cardiopatía congénita (CC) es uno de los defectos estructurales más comunes en neonatos. Recientemente, diversos estudios han identificado un desequilibrio en los niveles de factores proangiogénicos y antiangiogénicos en sangre umbilical de neonatos con CC similares a los hallados en sangre de mujeres con PE, lo que sugiere una posible asociación. Objetivo: Revisar la evidencia científica disponible sobre la relación entre la PE y el desarrollo de CC en neonatos. Métodos: Se realizó una búsqueda en las bases de datos Scopus y Medline/Pubmed utilizando los términos "pre-eclampsia" y "congenital heart defects", se seleccionaron 4 artículos que relacionaban las variables PE y CC, los cuales fueron revisados a texto completo. Únicamente se encontraron trabajos de tipo observacional analítico (1 estudio de prevalencia, 1 estudio de casos y controles y 2 estudios de cohortes), publicados entre el 2014 y 2016. Resultados: La PE de inicio temprano (<34 semanas) fue el factor de riesgo más importante asociado al desarrollo de CC en neonatos. La severidad de un defecto cardiaco se asocia con la intensidad y el momento de inicio de los desequilibrios en los factores angiogénicos. Conclusión: Encontramos evidencia relevante de la asociación entre PE y CC. La condición hipertensiva y los cambios endoteliales condicionados por ésta, estarían relacionados con el aumento de riesgo para el desarrollo de la CC antes que la exposición a medicamentos antihipertensivos.

Introduction: Preeclampsia (PE) is a complex multisystem disorder caused by an abnormal placental angiogenesis. Congenital heart disease (CHD) is one of the most common structural defects in newborn infants. Recently, several studies have identified an imbalance in the levels of proangiogenic and antiangiogenic factors in umbilical blood of newborn infants with CHD similar to those found in the blood of women with PE, suggesting a possible association. Objective: To review the available scientific evidence about the relationship between the PE and the development of CHD in newborn infants. Method: A search was conducted in Scopus and Medline/PubMed databases using the terms "pre-eclampsia" and "congenital heart defects". Four articles that linked PE and CHD were selected and reviewed in full text. Only analytical observational studies were found (1 prevalence study, 1 case-control study and 2 cohort studies), published between 2014 and 2016. Results: Early onset PE (<34 weeks) was the most important risk factor for the development of CHD in newborn infants. The severity of a heart defect is associated with the intensity and the onset time of imbalances in the angiogenic factors. Conclusion: We found relevant evidence on the possible association between PE and CHD. Hypertensive condition and endothelial changes conditioned by this seem to be linked to increased risk for the development of CHD instead of exposure to antihypertensive drugs.

DENGUE DURING PREGNANCY: ASSOCIATION WITH LOW BIRTH WEIGHT AND PREMATURITY

The aim of this study was to evaluate the effects of dengue virus infection during pregnancy and its correlation with low birth weight, prematurity, and asphyxia. A non-concurrent cohort study reveals the association of dengue during pregnancy with prematurity and low birth weight, when birth occurred during the maternal-fetal viremia period (p = 0.016 and p < 0.0001, respectively).

Prevalência de infecções congênitas e perinatais em gestantes HIV positivas da região metropolitana de Belo Horizonte / Prevalence of congenital and perinatal infection in HIV positive pregnant in Belo Horizonte metropolitan region

OBJETIVOS: Avaliar a prevalência de toxoplasmose, rubéola, citomegalovirose, hepatites B e C e sífilis (Torchs) em uma coorte de gestantes, bem como identificar os fatores sociodemográficos, clínicos e laboratoriais.MÉTODOS: Entre 1998 e 2013, foram atendidas 1.573 gestantes com sorologia positiva para o HIV em área metropolitana do Brasil, das quais 704 (44,8%) foram submetidas a algum dos testes sorológicos. Gestantes Torchs positivas (Gtp) foram consideradas aquelas com resultado positivo para uma dessas infecções, e gestantes Torchs negativas (Gtn) aquelas com resultados negativos para todas elas. As variáveis maternas investigadas foram: idade, estado civil, escolaridade, momento e forma de contágio da infeccção pelo HIV, contagem de linfócitos TCD4+, carga viral plasmática do HIV próxima ao parto e uso de terapia antirretroviral durante a gestação. As variáveis neonatais investigadas foram ocorrência de: transmissão vertical, prematuridade, baixo peso ao nascimento, complicações fetais, aborto e óbito fetal. Foram utilizadas razões de chance com intervalo de confiança de 95% para quantificar a associação entre as variáveis maternas e neonatais e a presença de Torchs.RESULTADOS: Entre as 704 gestantes, 70 (9,9%; IC95% 7,8-12,4) tinham alguma sorologia positiva para Torchs. Foram encontradas taxas: 1,5% (10/685) para a toxoplasmose; 1,3% (8/618) para rubéola; 1,3% (8/597) para citomegalovirose; 0,9% (6/653) para hepatite B e 3,7% (20/545) para hepatite C; e 3,8% (25/664) para sífilis. A transmissão vertical do HIV entre as gestantes Gtp foi 4,6% e de 1,2% entre as Gtn. As variáveis associadas à presença de Torchs na análise univariada foram: uso de terapia antirretroviral, transmissão vertical do HIV, baixo peso ao nascimento e complicações fetais.CONCLUSÃO: A prevalência das Torchs mostrou-se elevada para algumas infecções. Conclui-se que é importante manter o rastreamento de Torchs na gravidez, especialmente nas gestantes HIV positivas, para que se possa estabelecer diagnóstico e tratamento, e/ou medidas preventivas para evitar a transmissão materno-fetal.

PURPOSE: To evaluate the prevalence of toxoplasmosis, rubella, cytomegalovirus, hepatitis B&C and syphilis (Torchs) in a cohort pregnant women and to identify the sociodemographic, clinical and laboratory factors.METHODS: A total of 1,573 HIV-infected pregnant women from a Brazilian metropolitan region were studied between 1998 and 2013. The results of serological tests were available for 704 (44.8%) pregnant women. Pregnant women were considered to be Torchs positive (Gtp) when they had positive results for at least one of these infections, and to be Torchs negative (Gtn) when they had negative results for all of them. Maternal covariables were: age, marital status, educational level, time and mode of infection, CD4 lymphocyte count, viral load at delivery, and use of antiretroviral therapy (ARV). Neonatal covariables were: HIV infection, prematurity, low birth weight, neonatal complications, abortion and neonatal death. Odds ratios with 95% confidence interval were used to quantify the association between maternal and neonatal variables and the presence of Torchs.RESULTS: Among 704 pregnant women, 70 (9.9%; 95%CI 7.8-12.4) had positive serological tests for any Torchs factor. The individual prevalence rates were: 1.5% (10/685) for toxoplasmosis; 1.3% (8/618) for rubella; 1.3% (8/597) for cytomegalovirus; 0.9% (6/653) for hepatitis B and 3.7% (20/545) for hepatitis C; and 3.8% (25/664) for syphilis. The HIV Vertical HIV transmission was 4.6% among Gtp pregnant women and 1.2% among Gtn women. Antiretroviral therapy (ARV), vertical transmission, low birth weight and neonatal complications were significantly associated with Torchs positivity in univariate analysis.CONCLUSIONS: The Torchs prevalence found in the study was high for some infections. These findings emphasize the need to promote serological Torchs screening for all pregnant women, especially HIV-infected women, so that an early diagnosis can be made and treatment interventions can be implemented to prevent vertical HIV transmission.

Detección ecográfica de anomalías congénitas en 76.155 nacimientos en Bogotá y Cali, 2011-2012 / Ultrasound detection of congenital anomalies in 76,155 births in the cities of Bogotá and Cali, 2011-2012

Introducción. Las anomalías congénitas afectan de 2 a 3 % de los nacidos vivos en Colombia y, actualmente, son la principal causa de mortalidad en menores de un año en Bogotá y la tercera causa de mortalidad en menores de un año en Cali; en el mundo son causa importante de mortalidad y morbilidad fetal e infantil. Algunas anomalías congénitas pueden detectarse por la ecografía obstétrica, lo que permite establecer su manejo. Objetivo. Determinar la tasa de detección de anomalías congénitas mediante ecografía obstétrica y la tasa de falsos positivos, comparando poblaciones de Bogotá y Cali atendidas en servicios de salud de diferentes niveles de complejidad. Materiales y métodos. Se vigilaron 76.155 nacimientos en las ciudades de Cali y Bogotá en la modalidad de caso control basada en la metodología del Estudio Colaborativo Latinoamericano de Malformaciones Congénitas (ECLAMC), durante el periodo de enero de 2011 a diciembre de 2012. Resultados. Se encontró una tasa de infantes malformados de 2,08 %. La tasa de detección de anomalías congénitas diagnosticables fue de 31,45 % en los casos sobre los que se tenía información de control prenatal. La tasa encontrada fue menor a las reportadas en la literatura científica. Las anomalías congénitas más detectadas fueron las del sistema nervioso central y las urogenitales. Conclusiones. La baja tasa de detección evidencia la necesidad de mejorar la calidad de la ecografía para tener mayor sensibilidad y un diagnóstico prenatal adecuado que contribuya a la disminución de la morbilidad y la mortalidad, y a brindar una mejor atención al recién nacido con malformaciones.

Introduction: Congenital anomalies affect 2 to 3% of live births in Colombia and they are currently the leading cause of death in children under 1 year of age in Bogotá, and the third cause of death in children under 1 year of age in Cali. Congenital anomalies are a major factor contributing to fetal and infant mortality and morbidity in the world. Some congenital anomalies can be detected by obstetric ultrasonography, thus helping to decide on the best way to manage them. Objective: To determine the rate of detection of congenital anomalies by obstetric ultrasound and the false positive rate comparing infants born with birth defects in Bogota and Cali treated at health care facilities of different levels of complexity. Materials and methods: We monitored 76,155 births in the cities of Cali and Bogotá based on a case-control model following the methodology of the Latin American Collaborative Study of Congenital Malformations (ECLAMC) from January 2011 to December 2012. Results: The rate of malformed infants was 2.08%. The detection rate of diagnosable congenital anomalies was 31.45% among cases that had information about prenatal care. This rate is lower than that reported in the literature. Most of the congenital anomalies detected were of the central nervous system and of the genitourinary system. Conclusions: The low detection rate highlights the need to improve the quality of ultrasound to have greater sensitivity for adequate prenatal diagnosis that will contribute to the reduction of morbidity and mortality and allow for better care of newborns with malformations.

Variaveis perinatais e associacao de recem-nascidos de muito baixo peso ao nascer em hospital publico universitario do Brasil / Perinatal variables and association with very low birthweight newborns in a Brazilian public university hospital

OBJETIVO: Verificar a associação de variáveis perinatais com o nascimento de recém-nascidos pré-termo de muito baixo peso ao nascer (MBPN). MÉTODOS: Foi um estudo retrospectivo com análise de prontuários de recém-nascidos (RN) de parto pré-termo espontâneo com admissão em unidade de terapia intensiva neonatal. Os RN pré-termo foram distribuídos em dois grupos: grupo muito baixo peso ao nascer (MBPN; peso <1.500g) e grupo baixo peso ao nascer (BPN; peso ≥1.500g e <2.500g). Foram pesquisadas variáveis de pré-natal maternas de intercorrências durante a gestação e parto/periparto e intercorrências fetal/neonatal. Foi realizada análise estatística por meio do teste exato de Fisher ou χ2, com cálculo do risco relativo (RR), considerando valor p≤0,05 e teste t de Student para comparação das médias dos grupos. RESULTADOS: As comorbidades hemorrágicas (p=0,006; RR=1,2) e hipertensivas (p=0,04; RR=1,5), parto operatório (p=0,001; RR=0,5), idade gestacional <33 semanas (p<0,001; RR=16,7) e Apgar de 1° e 5° minuto (p=0,006; RR=1,6; p=0,01; RR=1,9) estiveram associadas à ocorrência de MBPN. Os RN com MBPN apresentaram associação significativa para ocorrência de comorbidades metabólicas (p=0,01; RR=1,8), neurológicas (p=0,01; RR=1,7) e infecciosas (p=0,001; RR=1,9), período de internação >4 semanas (p=0,02; RR=1,8) e óbito neonatal precoce (p=0,001; RR=2,9). CONCLUSÕES: Fatores como comorbidades hipertensivas e hemorrágicas durante a gestação e parto com idade gestacional inferior a 33 semanas foram associadas ao nascimento de recém-nascidos de MBPN. Esse grupo de recém-natos também apresentou RR elevado para a ocorrência de óbito neonatal precoce. .

PURPOSE: To investigate the association of perinatal variables with the birth of very low birth weight (VLBW) preterm newborns. METHODS: It was a retrospective study of the medical records of infants born after spontaneous preterm labor with admission to a neonatal intensive care unit. Preterm infants were divided into two groups: very low birth weight (VLBW) group (weight <1,500 g) and low birth weight (LBW) group (weight ≥1,500 g and <2,500 g). Prenatal variables such as maternal complications during pregnancy and childbirth/postpartum, and fetal/neonatal complications were investigated. Statistical analysis was performed using the Fisher exact test or χ2 test, with calculation of relative risk (RR), and the Student t test for comparison of group means, with the level of significance set at p≤0.05. RESULTS: Hemorrhagic comorbidities (p=0.006; RR=1.2) and hypertension (p=0.04; RR=1.5), surgical delivery (p=0.001; RR=0.5), gestational age <33 weeks (p< 0.001; RR=16.7) and Apgar score at 1st and 5th minute (p=0.006; RR=1.6; p=0.01; RR=1.9) were associated with the occurrence of VLBW. Infants with VLBW had a significant association with the occurrence of metabolic comorbidities (p=0.01; RR=1.8), neurological (p=0.01; RR=1.7) and infectious diseases (p=0.001; RR=1.9), hospitalization >4 weeks (p=0.02; RR=1.8) and early neonatal death (p=0.0001; RR=2.9). CONCLUSIONS: Factors such as hypertension and bleeding comorbidities during delivery and management of gestational age of less than 33 weeks were associated with the birth of VLBW newborns. This group of infants also showed higher RR for the occurrence of early neonatal death. .

Glicemia de jejum do primeiro trimestre e fatores de risco de gestantes com diagnóstico de diabetes melito gestacional / First trimester fasting glycemia and risk factors of pregnant women diagnosed with gestational diabetes mellitus

OBJETIVO: Avaliar a incidência de repercussões materno-fetais e controle glicêmico em gestantes com diagnóstico de Diabetes Melito Gestacional (DMG) tendo como corte a glicemia de jejum de 85 mg/dL no primeiro trimestre e correlacionar com fatores de risco. MÉTODOS: Foram revisados os prontuários das gestantes acompanhadas no ambulatório de Pré-Natal de Alto Risco (PNAR) no período de janeiro de 2011 a março de 2012 e selecionadas aquelas com diagnóstico de DMG para contato e verificação do cartão de pré-natal. Foram colhidos dados de idade, paridade, glicemia de jejum do primeiro trimestre, valor do Teste Oral de Tolerância à Glicose (TOTG), Índice de Massa Corpórea (IMC), via de parto, forma de controle, repercussões fetais e fatores de risco para DMG. A análise estatística foi realizada no software PSPP 0.6.2 e consistiu de análise descritiva de frequências, teste do χ2 para variáveis categóricas, teste t de Student para amostras independentes e teste de Pearson para as correlações com nível de significância de 5%. RESULTADOS: Das 408 gestantes atendidas, 105 tinham diagnóstico de Diabetes Melito Gestacional (DMG) e 71 tinham prontuários completos ou responderam ao contato para fornecer as informações faltantes. No grupo DMG-jejum <85, (com glicemia de jejum <85 mg/dL na primeira consulta no primeiro trimestre) foram incluídas 29 gestantes (40,8%) e no grupo DMG-jejum>85 (glicemia de jejum >85 mg/dL na primeira consulta, no primeiro trimestre) 42 gestantes (59,1%). Observou-se que poucas pacientes (5 no grupo DMG-jejum <85 e 3 no grupo DMG-jejum>85) não apresentavam fatores de risco para DMG. Houve maior frequência da necessidade de controle com insulina nas pacientes do grupo DMG-jejum >85. Não houve diferença significativa quanto às repercussões fetais e via de parto entre os grupos. CONCLUSÃO: A glicemia de jejum do primeiro trimestre, tendo como ponto de corte o valor 85 mg/dL, isoladamente, ou associado a fatores de risco, não seria bom preditor isolado de repercussões materno-fetais do DMG.

PURPOSE: To evaluate the incidence of maternal and fetal repercussions and glycemic control in women with Gestational Diabetes Mellitus (GDM) using a fasting glucose of 85 mg/dL in the first trimester as a cut-off point and to correlate it with risk factors. METHODS: The medical records of pregnant women followed in the outpatient antenatal high-risk service (PNAR) of HRAN from January 2011 to March 2012 were reviewed and those women diagnosed with GDM were selected for contact and for prenatal card verification. We collected data of age, parity, fasting glucose during the first quarter, the value of the Oral Glucose Tolerance Test (OGTT), Body Mass Index (BMI), mode of delivery, form of control, effects and fetal risk factors for GDM. Statistical analysis was performed using the PSPP 0.6.2 software and consisted of descriptive analysis of frequencies, χ2 test for categorical variables, Student's t-test for independent samples, and Pearson test for correlations, with the level of significance set at 5%. RESULTS: From 408 pregnant women enrolled, 105 were diagnosed with GDM and 71 had complete records or answered to the contact in order to provide the missing information. The GDM-fasting <85 (fasting glucose <85 mg/dL at the first prenatal visit, in the first trimester) group consisted of 29 (40.8%) women and the GDM-fasting >85 (fasting glucose >85 mg/dL at the first prenatal visit, in the first trimester) consisted of 42 (59.1%) women. It was observed that few patients (five in the GDM-fasting <85 group and three in the GDM-fasting >85 group) had no risk factors for GDM. There was a major need for control with insulin in patients of the GDM-fasting >85 group. There was no significant difference related to fetal impact or mode of delivery between the groups. CONCLUSIONS: The first trimester fasting glycemia, with a cut-off value of 85 mg/dL alone or associated with risk factors, does not seem to be a good single predictor of the maternal-fetal effects of GDM.

Impacto de la altura en el embarazo y en el producto de la gestación / Impact of high altitude on pregnancy and newborn parameters

Esta revisión describe los procesos asociados con mantener un embarazo en mujeres nacidas al nivel del mar que cursan su embarazo en la altura; en aquellas que viajan intermitentemente, o las que nacen y residen en la altura. La literatura examinada demuestra que la frecuencia de malformaciones congénitas es elevada en la altura; que las tasas de mortalidad fetal tardía, nacidos pequeños para su edad gestacional, y preeclampsia se encuentran incrementadas en la altura, asociadas a valores altos de hemoglobina materna (>14,5 g/dL). En conclusión, el embarazo en una mujer expuesta de forma aguda, intermitente o permanente a las grandes alturas, genera mayores riesgos en comparación con un embarazo desarrollado a nivel del mar.

This review describes adverse outcomes in pregnancy after brief, intermittent, or permanent residence at high altitudes. Review of literature shows that congenital malformations rates are higher at high altitudes. Additionally, rates of stillbirths, small size for gestational age, and preeclampsia are increased in populations living at high altitudes and are associated with high maternal hemoglobin levels (>14.5 g/dl). In conclusion, a pregnant woman exposed briefly, intermittently, or permanently to high altitudes results in increased risk of adverse outcomes when compared to pregnancies observed at sea level.

Resultados perinatales relacionados con trastornos hipertensivos del embarazo / Perinatal results related to pregnancy hypertensive disorders

Introducción: los trastornos hipertensivos del embarazo se relacionan con una elevada morbilidad y mortalidad perinatal. Objetivo: determinar la incidencia de resultados perinatales desfavorables asociada con los distintos trastornos hipertensivos del embarazo. Métodos: estudio observacional descriptivo prospectivo, realizado en el Hospital General Docente Enrique Cabrera, del 1ro. de enero al 31 de diciembre de 2010. La muestra fue de 108 pacientes con diagnóstico de hipertensión y en ellas se determinó, edad gestacional al parto, peso y apgar del neonato, diagnóstico de sufrimiento fetal y necesidad de cuidados intensivos neonatales. Se usaron porcentajes y test de Chi-cuadrado para variables cualitativas, utilizando el sistema estadístico para Windows SPSS-11.5. Resultados: la prematuridad fue más frecuente en las pacientes con eclampsia (4/100 por ciento) y preeclampsia (16/66,7 por ciento), el peso medio de los neonatos fue inferior en las pacientes con eclampsia (1540 ± 1160), hipertensión crónica con preeclampsia sobreañadida (2226,2 ± 1236,2) y preeclampsia (2442 ± 917), la mayor frecuencia de mortinatos, ocurrió en las pacientes con eclampsia y en aquellas con preeclampsia sobreañadida (25 por ciento cada una). Conclusiones: la preeclampsia-eclampsia se asoció con elevada morbilidad y mortalidad perinatal, durante el periodo estudiado

Introduction: The pregnancy hypertensive disorders are related to a high perinatal morbidity and mortality. Objective: To determine the incidence of the unfavourable perinatal results associated with different pregnancy hypertensive disorders. Methods: A prospective, descriptive and observational study was conducted in the Enrique Cabrera Teaching and General Hospital from January 1 to December 31, 2020. Sample included 108 patients diagnosed with hypertension and in them it was possible to determine the gestational age at delivery, weight and Apgar score of the neonate, diagnosis of fetal suffering and the need of neonatal intensive cares. Percentages and Chi² test were used for qualitative variables, using the statistical system for Window SPSS-11.5. Results: Prematurity was more frequent in patients presenting with eclampsia (4/100 percent) and pre-eclampsia (16/66,7 percent), the mean weight of neonates was lower in patients with eclampsia (1540 ± 1160), chronic hypertension with addition of pre-eclampsia (2226 ± 1236,2) and pre-eclampsia (2442 ± 917, the great frequency of stillbirths occurred in patients presenting with eclampsia and in those with addition of pre-eclampsia (25 percent each). Conclusions: The pre-eclampsia-eclampsia is associated with a high perinatal morbidity and mortality over the study period

Detección ecográfica y pronóstico de la ventriculomegalia fetal / Ultrasound detection and prognosis of fetal ventriculomegaly

Antecedentes: La ventriculomegalia fetal es un signo ecográfico muy sensible para las alteraciones del sistema nervioso central fetal. La morbilidad asociada a la misma depende principalmente de la etiología y de la presencia de otras malformaciones asociadas. Si es aislada y no progresiva se puede preveer un resultado posnatal favorable hasta en el 70 por ciento de los casos aunque hay una gran disparidad de cifras entre distintos centros y autores. Objetivo: Establecer la relación entre ventriculomegalia y pronóstico perinatal. Método: Se han revisado 60 casos diagnosticados mediante ecografía prenatal en el Hospital Universitario de Canarias siguiendo los criterios ecográficos de ventriculomegalia (astas posteriores mayores de 10 mm). Se realizaron cariotipos y serología materna y en líquido amniótico para completar el estudio. Resultados: Hubo un total de 23 interrupciones voluntarias de la gestación y 28 recién nacidos sin secuelas (47 por ciento). Un 70 por ciento de las ventriculomegalias aisladas correspondieron a recién nacidos sin secuelas. El 10 por ciento de las ventriculomegalias aparecieron en fetos con aneuploidías. Conclusión: El pronóstico fue favorable en los casos de ventriculomegalia no progresiva y aislada. La medida de la ventriculomegalia no predice el resultado. La variabilidad de resultados en la literatura obliga a cada centro a disponer de sus protocolos y datos para aconsejar a la pareja que ha de tomar una decisión sobre el futuro de su embarazo.

Background: Fetal ventriculomegaly is the most sensitive sonographic sign for central nervous system anomalies. Neonatal morbidity and mortality depends on the etiology of the ventriculomegaly and the presence of other malformations. Isolated non-progressive ventriculomegaly is associated with 70 percent favorable results, with a great disparity among studies. Aims: To establish the relationships between ventriculomegaly and perinatal outcome. Methods: The authors reviewed 60 cases of prenatally diagnosed fetal ventriculomegaly in the Canary Islands University Hospital. An ultrasonographic measurement of the lateral ventricles of 10 mm or more was considered as ventriculomegaly. Fetal and maternal serology was performed as well as fetal karyotyping. Results: 23 patients decided to terminate the pregnancy due to unfavorable prognosis. In 28 cases outcome was favorable. 70 percent of isolated ventriculomegaly corresponded to healthy newborns. 10 percent of the fetuses had aneuploidies. Conclusion: Prognosis is favorable if ventriculomegaly is isolated and non-progressive. Measurement of the lateral ventricle does not predict outcome. Disparity of results in literature makes it necessary for each Hospital to rely on their own data and guidelines to assess parents on the fate of the pregnancy.

Fetomaternal and neonatal outcome of triplet pregnancy. promising results

To determine the fetomaternal and neonatal outcomes in triplet pregnancy. A retrospective review of 32 triplet pregnancies between January 2007 to December 2009 was carried out. This study was conducted at the Department of Obstetrics and Gynecology, Abha Maternity Hospital, Abha, Kingdom of Saudi Arabia. In this study, the most common complication was preterm labor, while other complications examined were not dramatically increased. The most common complication observed in neonates were respiratory distress syndrome with good neonatal outcome. The study demonstrated high perinatal mortality, mostly due to extreme low gestational age at delivery. We found a good maternal and neonatal outcome in patients who conceived with triplet, although the sample size is small due to a rare incidence of triplet gestation. This finding is helpful in counseling patients who had conceived triplets in terms of preterm delivery, mode of delivery, and the need for embryo reduction at earlier stages of pregnancy, as well as performing a prophylactic cervical cerclage

Factores antenatales de riesgo de parálisis cerebral / Prenatal risk factors of cerebral palsy

Se ha considerado que las causas antenatales constituyen la gran mayoría de las causas de parálisis cerebral (PC) en países industrializados. Realizar una actualización sobre los factores antenatales de riesgo de PC fue el objetivo de este trabajo. En la etiología de la PC se debe partir de la diferenciación entre factores de riesgo causales e indicadores tempranos de enfermedad. A su vez, existen causas conocidas, factores de riesgo y patrones causales de PC, estos últimos no bien conocidos aún. Dentro de las causas antenatales de PC se encuentran las infecciones, malformaciones, accidentes cerebro vasculares isquémicos, enfermedades genéticas y trastornos metabólicos. Muchos patrones causales de PC tienen un origen prenatal, sin embargo, no se debe sobrevalorar el papel de las causas antenatales, puesto que análisis actuales a partir de estudios neuroimaginológicos y epidemiológicos muestran que el momento causal antenatal está presente solo en aproximadamente un tercio de los casos con PC congénita. La determinación de factores de riesgo de PC constituye únicamente un acercamiento inicial en la creación y/o confirmación de hipótesis causales, y su utilidad es limitada cuando lo que se persigue es la prevención a nivel poblacional. Si bien han sido determinados múltiples factores de riesgo causales de PC, todavía queda un gran camino por recorrer en el estudio de su etiopatogenia

It has been considered that the prenatal causes are the main provoking cerebral palsy (CP) in industrial countries. The aim of present paper was to update the prenatal risk factors of CP. The etiology of this entity came from the differentiation among the causal and early indicators risk factors of disease. At the same time, there are known causes, risk factors and causal patterns of CP, these latter are even so not known. Included in prenatal causes of CP are the infections, malformations, ischemic strokes, genetic diseases and metabolic disorders. Many causal patterns of CP have as prenatal origin; however, we must not to overestimate the role of prenatal causes since the current analyses from neuro-imaging and epidemiological studies show that the prenatal causal moment is present in only a third of cases presenting with congenital CP. The determination of CP risk factors is solely a initial approach in creation and/or confirmation of causal hypotheses and its usefulness is limited when the aim is the prevention at population scale. Although many causal risk factors of CP have been determined, still there is a long way for covering in study of its pathogeny

Translucencia nucal aumentada y cariotipo normal / Increased nuchal translucency and normal kariotype

Antecedentes: La exploración ecográfica entre las semanas 11 y 14 tiene un papel fundamental en el cribado de anomalías cromosómicas, siendo la medida de la translucencia nucal un método bien establecido y ampliamente aceptado para este fin. Objetivo: Evaluar retrospectivamente la evolución de los fetos con translucencia nucal aumentada y cariotipo normal. Método: Se recogieron los datos de 104 fetos con TN >percentil 95 (p95) entre las semanas 11 y 14, evaluados en nuestro centro. En los 61 que resultaron eu-ploides, se estudió la incidencia de anomalías estructurales diagnosticadas tanto prenatalmente como tras el nacimiento, así como las pérdidas fetales anteparto. De estos fetos, nacieron sanos el 80 por ciento cuando la TN estaba entre p95 y 3,4 mm, el 50 por ciento con TN entre 3,5 y 4,4 mm, el 30 por ciento con TN entre 4,5 y 5,4 mm, y el 18 por ciento con TN > 5,5 mm. Entre los 4 recién nacidos euploides con patología, hubo 3 con cardiopatía. Conclusión: La presencia de TN aumentada entre las 11 -14 semanas en fetos euploides se asocia a un incremento del riesgo de anomalías estructurales mayores, principalmente cardiacas. La prevalencia de malformaciones aumenta significativamente con TN >3,5 mm, y el pronóstico gestacional adverso empeora conforme aumenta la medida de la TN.

Background: Ultrasound scan has a main role at the 11-14 weeks screening for chromosomal abnormalities. The measurement of nuchal translucency (NT) thickness is a widespread stablished method to achieve this target. Objective: To assess retrospectively the outcome of fetuses with increased nuchal translucency and normal karyotype. Method: Data were collected from 104 fetuses with NT > 95th percentile at 11 to 14 weeks of gestation, followed in our institution. The sixty one euploid fetuses were studied in order to determine the incidence of structural abnormalities, diagnosed either before or after delivery, as well as antenatal fetal loss. Among these fetuses, there were no malformations at birth in 80 percent for NT between the 95th percentile and 3.4 mm; 50 percent for NT between 3.5 and 4.4 mm; 30 percent for NT of 4.5-5.4 mm; and 18 percent for NT > 5.5 mm. There were 4 euploid newborns with some kind of structural defect at birth, 3 of them presented a cardiac malformation. Conclusion: The presence of increased NT at 11-14 weeks scan in euploid fetuses it's associated with a higher risk of major structural abnormalities, mainly cardiac ones. The prevalence of malformations is significantly increased for NT > 3.5 mm, and the adverse perinatal outcome is directly associated with the thickness of NT.

Hipertireoidismo na gravidez: repercussões materno-fetais / Hyperthyroidism during pregnancy: maternal-fetal outcomes

OBJETIVO: avaliar a experiência do Hospital das Clínicas da Faculdade de Medicina de Botucatu da Universidade Estadual Paulista "Júlio de Mesquita Filho", no acompanhamento de gestantes com hipertireoidismo. MÉTODOS: foram estudadas, retrospectivamente, 60 pacientes, divididas em grupos com hipertireoidismo compensado (GHC=24) e com hipertireoidismo descompensado (GHD=36) e comparadas quanto a características clínico-laboratoriais e intercorrências. Para análise dos resultados, foram utilizados o teste t de Student, as tabelas de contingência, regressão linear múltipla e regressão logística múltipla, com nível de significância de 5,0 por cento. RESULTADOS: propiltiouracil (PTU) foi usado por 94,0 por cento do GHD e 42,0 por cento do GHC (p<0,0001); complicações maternas próximas ao parto ocorreram em 20,6 por cento do GHD e 11,8 por cento do GHC, sendo que o GHD apresentou três óbitos fetais. Influenciaram nestes: idade materna, nível de T4L (nT4L) e dose de PTU (dPTU) mais elevados, no terceiro trimestre (p=0,007); restrição de crescimento intra-uterino, influenciada por nT4L e dPTU do terceiro trimestre, ocorreu em nove casos do GHD e três do GHC, e oligoâmnio ocorreu em 12 pacientes (83,3 por cento do GHD, 16,7 por cento do GHC), influenciado por idade e nT4L do terceiro trimestre (p=0,04); a idade gestacional no parto foi de 34,4±4,6 semanas no GHD e 37,0±2,5 no GHC, influenciada pelo nT4L do terceiro trimestre (p<0,05). CONCLUSÕES: o GHD apresentou resultados menos satisfatórios que o GHC, influenciados por nT4L e dPTU elevados no terceiro trimestre e por idade mais avançada de algumas gestantes.

PURPOSE: to evaluate the experience of Hospital das Clínicas da Faculdade de Medicina de Botucatu da Universidade Estadual Paulista "Júlio de Mesquita Filho", in the follow-up of pregnant women with hyperthyroidism. METHODS: Sixty patients, divided in groups with compensated hyperthyroidism (CHG=24) and with uncompensated hyperthyroidism (UHG=36) were retrospectively studied and compared concerning clinical-laboratorial characteristics and intercurrences. The t-Student test, contingency tables, multiple linear regression and multiple logistic regression with significance level at 5.0 percent were used. RESULTS: propylthiouracil (PTU) was used by 94.0 percent of UHG and by 42.0 percent of CHG (p<0.0001); maternal complications close to delivery have occurred in 20.6 percent of UHG and in 11.8 percent of CHG, and UHG presented three fetal deaths, influenced by the mother age, higher level of T4L (lT4L) and of PTU dose (PTUd) in the third trimester (p=0.007); restriction of intra-uterine growth, influenced by lT4L and PTUd in the third trimester has occurred in nine UHG and in three CHG cases, and oligoamnios has occurred in 12 patients (83.3 percent of UGH and 16.7 percent of CGH), influenced by age and lT4L in the third trimester (p=0.04); the gestational age at delivery was 34.4±4.6 weeks in UHG and 37.0±2.5 in CHG, influenced by the T4Ll in the third trimester (p<0.05). CONCLUSIONS: the UHG has presented less satisfactory results than CHG, influenced by high lT4L and PTUd in the third trimester, and by more advanced age of some pregnant women.

Diagnóstico citogenético prenatal: experiencia de 10 años en el Hospital Regional Rancagua / Prenatal diagnosis and cytogenetics: 10 year experience in a regional hospital

Objective: To present a 10-year experience with prenatal karyiotyping in cases of fetal malformations in a Regional NHS hospital. Methods: Pregnancies complicated with congenital abnormalities detected prenatally by ultrasonography and undergoing an invasive procedure for fetal Karyotyping were reviewed. Information on maternal demographics, number and type of procedure, indications, complications, and cytogenetic results was obtained by reviewing the ultrasound reports and medical records. Results: In the 10- year period from January 1997 to December 2006, 1.139 pregnancies complicated by a fetal structural anomaly were evaluated in our unit. In 270 cases, an invasive procedure for fetal karyotyping was carried out, including 212 (78 percent) fetal blood sampling procedures, 43 (16 percent) amniocenteses, 8 ( 3 percent) chronic villus sampling procedures. In 178 (66 percent) the karyotype result was reported as normal, in 68 (25 percent) as abnormal, in 22 (8 percent) there was a culture failure, and in 2 (1 percent) a failed procedure. Among the 68 chromosomal abnormalities, 32 percent were trisomy 21 (n=22), 32 percent trisomy 18 (n=22), and 25 percent a monosomy X(n=17). In the remaining cases there was a trisomy 13, trisomy 14, triploidy, or a chromosomal structural defect. In the first 4 years, the detection rate of a chromosomal defect was approximately 15 percent, which increased to 35 percent in the last 6 years, without a significant increase in the number of procedures. Conclusions: Our unit deals with more than 100 cases of fetal malformations per year. The implementation of a cytogenetic laboratory allows the provision of critical information for the subsequent management of the pregnancy and future genetic counseling. Overall, 25 percent of the procedures yielded an abnormal result. With increasing experience, the efficiency is improving considerable without a concomitant increase in the number of procedures.

Objetivo: Presentar la experiencia acumulada de 10 años con el diagnóstico citogenético prenatal en fetos con malformaciones congénitas detectados por ultrasonografía en un hospital base del sector público. Métodos : Se revisó nuestra base de datos seleccionando aquellas pacientes evaluadas exclusivamente por malformaciones fetales únicas o múltiples que fueron sometidas a estudio citogenético prenatal. Se recolectó la información demográfica y clínica, evaluando el número total de procedimientos por año, la relación normales/anormales, el rendimiento por tipo de muestra, el porcentaje de procedimientos frustros en la toma de muestra y la fallas del cultivo. Resultados: En el período entre enero de 1997 y diciembre del 2006, se evaluaron 1.139 embarazos complicados con malformaciones congénitas, en los cuales se realizaron 270 procedimientos invasivos prenatales. De ellos 212 (78 por ciento) fueron cordocentesis, 43 (16 por ciento) amniocentesis, 8 (3 por ciento) biopsias placentarias y 7 (3 por ciento) biopsia de vellosidades coriales. En 178 (66 por ciento) casos el cariograma fue informado como normal en 68 (25 por ciento) como anormal, en 22 (8 por ciento) no hubo crecimiento de cultivo celular y en 2 (1 por ciento) hubo una punción frustra. De los 68 resultados anormales, un 32 por ciento corresponden a trisomías 21 (n=22), un 32 por ciento a trisomías 18 (n= 22) y un 25 por ciento a monosomía del cromosoma X (n=17). El 10 por ciento restante corresponde a anomalías del cromosoma 13 ó 14, triploidías o defectos estructurales rearreglos cromosómicos. De un promedio de resultados anormales de un 15 por ciento en los primeros 4 años del estudio, se mejoró la detección a un 35 por ciento en los últimos 6 años, sin un aumento significativo en el número de procedimientos. Conclusiones: Nuestra Unidad de Ultrasonografía maneja un volumen superior a los 100 casos de anomalías fetales anuales...

Prenatal diagnosis of renal disease

INTRODUCTION: The purpose of this study is to report the range of renal congenital anomalies identified by ultrasonography and to analyze the indications for the ultrasound study that lead to their diagnosis. MATERIALS AND METHODS: All cases of renal malformations diagnosed at our institution from June 2001 through May 2004 were evaluated retrospectively. The indications for sonographic evaluation were reviewed. Cases were divided into those referred for routine ultrasound screening and those referred with other indications. Results were expressed as percents of total. RESULTS: A total of 117 cases of renal congenital anomalies were identified, in 14 cases (11.9), other congenital anomalies were also present. Hydronephrosis was the most common diagnosis detected in 64 cases (54.7). There were 21 lethal renal anomalies identified (17.9). Multicystic dysplastic kidneys were present in 21 cases (17.9). Renal agenesis was identified in 15 cases (12.8). Other detected anomalies were: bladder outlet obstruction 15 (12.8), echogenic kidneys 13 (11.1), ectopic ureteral implantation 2 (1.7), renal cysts 1 (0.8), pelvic kidney 3 (2.6), double collecting system 1 (0.8), and unilateral atrophic kidney 1 (0.8). A total of 94 cases (80.3) had no indications for sonographic evaluation other than routine screening. CONCLUSIONS: Relying on risk factors as indications for ultrasound studies will not detect the majority of congenital anomalies, especially those associated to the urogenital system, a group of conditions that may particularly benefit form prenatal detection.