RESUMEN
BACKGROUND: Associations between maternal periconceptional exposure to disinfection by-products (DBPs) in drinking water and neural tube defects (NTDs) in offspring are inconclusive, limited in part by exposure misclassification. METHODS: Maternal interview reports of drinking water sources and consumption from the National Birth Defects Prevention Study were linked with DBP concentrations in public water system monitoring data for case children with an NTD and control children delivered during 2000-2005. DBPs analyzed were total trihalomethanes, the five most common haloacetic acids combined, and individual species. Associations were estimated for all NTDs combined and selected subtypes (spina bifida, anencephaly) with maternal periconceptional exposure to DBPs in public water systems and with average daily periconceptional ingestion of DBPs accounting for individual-level consumption and filtration information. Mixed effects logistic regression models with maternal race/ethnicity and educational attainment at delivery as fixed effects and study site as a random intercept were applied. RESULTS: Overall, 111 case and 649 control children were eligible for analyses. Adjusted odds ratios for maternal exposure to DBPs in public water systems ranged from 0.8-1.5 for all NTDs combined, 0.6-2.0 for spina bifida, and 0.7-1.9 for anencephaly; respective ranges for average daily maternal ingestion of DBPs were 0.7-1.1, 0.5-1.5, and 0.6-1.8. Several positive estimates (≥1.2) were observed, but all confidence intervals included the null. CONCLUSIONS: Using community- and individual-level data from a large, US, population-based, case-control study, we observed statistically nonsignificant associations between maternal periconceptional exposure to total and individual DBP species in drinking water and NTDs and subtypes.
Asunto(s)
Desinfección , Agua Potable , Exposición Materna , Defectos del Tubo Neural , Humanos , Femenino , Agua Potable/efectos adversos , Defectos del Tubo Neural/etiología , Defectos del Tubo Neural/epidemiología , Embarazo , Exposición Materna/efectos adversos , Exposición Materna/estadística & datos numéricos , Desinfección/métodos , Adulto , Estudios de Casos y Controles , Desinfectantes/efectos adversos , Desinfectantes/análisis , Purificación del Agua/métodos , Trihalometanos/análisis , Trihalometanos/efectos adversos , Masculino , Contaminantes Químicos del Agua/análisis , Contaminantes Químicos del Agua/efectos adversos , Efectos Tardíos de la Exposición Prenatal , Disrafia Espinal/etiología , Disrafia Espinal/epidemiologíaRESUMEN
OBJECTIVE: To investigate the association between Chlamydia trachomatis (CT) infection seropositivity and gastroschisis. STUDY DESIGN: In this case-control study we enrolled pregnant women either prenatally diagnosed with gastroschisis (cases, n=33) or with a normal ultrasound (controls, n=66). Both groups attended the University of Utah's Maternal Fetal Medicine Diagnostic Center for their diagnostic ultrasound or because of a community obstetrician referral. Participants completed a structured interview on potential risk factors. Anti-CT immunoglobulin (IgG)1 and IgG3 were measured by a CT elementary body enzyme-linked immunosorbent assay. RESULT: Median age at sexual debut was lower and reported sexual partner number higher in cases compared with controls. Risk factors for gastroschisis included having ⩾ 3 sexual partners (odds ratio (OR)=3.3, 95% CI 1.2, 9.4), change in partner from the previous pregnancy (OR=3.6, 95% CI 0.9, 13.9) and anti-CT IgG3 seropositivity (age-adjusted OR=3.9, 95% CI: 1.1, 13.2). CONCLUSION: Anti-CT IgG3 seropositivity was associated with greater than a threefold risk for gastroschisis.
Asunto(s)
Infecciones por Chlamydia/complicaciones , Chlamydia trachomatis/inmunología , Gastrosquisis/etiología , Inmunoglobulina G/inmunología , Complicaciones Infecciosas del Embarazo/diagnóstico , Ultrasonografía Prenatal , Adulto , Estudios de Casos y Controles , Infecciones por Chlamydia/diagnóstico , Intervalos de Confianza , Ensayo de Inmunoadsorción Enzimática , Femenino , Gastrosquisis/diagnóstico por imagen , Gastrosquisis/epidemiología , Edad Gestacional , Humanos , Incidencia , Recién Nacido , Masculino , Oportunidad Relativa , Embarazo , Complicaciones Infecciosas del Embarazo/inmunología , Medición de Riesgo , Pruebas Serológicas , Estadísticas no Paramétricas , Estados Unidos/epidemiologíaRESUMEN
The objective of this study was to explore how a parent-to-parent support network could impact parents of a child with a structural birth defect by specifically looking at parents' continued needs, aspects influencing their participation in support networks, and their recommendations. Structural birth defects occur in approximately 3 % of all infants, representing a significant public health issue. For many reasons, parents are uniquely qualified to provide support to each other. Data were collected retrospectively through a qualitative approach of focus groups or one-on-one interviews. Thirty one parents of infants registered in the Utah Birth Defect Network participated in the study. Three themes emerged, "current sources and inconsistencies in parent-to-parent-support," "aspects that influence participation in parent-to-parent network," and "recommendations for a parent-to-parent program." Health care providers need to be aware of the services and inform parents about these options. A statewide parent-to-parent network integrated into all hospitals would be a valuable resource to facilitate sharing of issues related to caring for an infant or child with a birth defect.
Asunto(s)
Anomalías Congénitas/psicología , Necesidades y Demandas de Servicios de Salud , Padres/psicología , Apoyo Social , Preescolar , Anomalías Congénitas/fisiopatología , Femenino , Humanos , Lactante , MasculinoRESUMEN
Data were used to determine the population prevalence of aneuploidy and additional anatomic abnormalities in fetuses with open spina bifida. The ability of sonography to predict aneuploidy and identify additional anatomic abnormalities in euploid fetuses was assessed. All cases of spina bifida occurring in the state of Utah from 1995 through 1997 were reviewed using Utah Birth Defect Network data, including stillborn, liveborn, and terminated cases. Chromosomes were known in 45 of 51 cases of open spina bifida. Of the 45 fetuses, 6 (13%) were aneuploid. Major anatomic abnormalities were present in four of six (67%) cases, and two of six (33%) cases had additional anomalies that could be missed sonographically. Of 39 euploid fetuses, 12 (31%) had additional abnormalities, but only half likely would be detected sonographically. Our 4% risk of aneuploidy in sonographically isolated spina bifida is substantially higher than the risk associated with advanced maternal age (0.37%).