RESUMO
OBJECTIVES: To identify factors associated with poor prognoses in newborns with a prenatal diagnosis of gastroschisis in eight hospitals in Bogota, Colombia, from 2011 to 2022. METHODS: A multi-center retrospective case-control study was conducted on newborns with gastroschisis in eight hospitals in Bogota, Colombia. Poor prognosis was defined as the presence of sepsis, intestinal complications, or death. RESULTS: The study included 101 patients. Preterm newborns under 32 weeks had a poor neonatal prognosis (OR 6.78 95â¯% CI 0.75-319). Oligohydramnios (OR 4.95 95â¯% CI 1.15-21.32) and staged closure with silo (OR 3.48; 95â¯% CI 1.10-10.96) were risk factors for neonatal death, and intra-abdominal bowel dilation of 20-25â¯mm was a factor for the development of intestinal complications (OR 3.22 95â¯% CI 1.26-8.23). CONCLUSIONS: Intra-abdominal bowel dilation between 20 and 25â¯mm was associated with intestinal complications, while oligohydramnios was associated with the risk of perinatal death, requiring increased antenatal surveillance of fetal wellbeing. Management with primary reduction when technically feasible is recommended in these infants, considering that the use of silos was associated with higher mortality.
Assuntos
Gastrosquise , Humanos , Recém-Nascido , Colômbia/epidemiologia , Gastrosquise/diagnóstico , Gastrosquise/diagnóstico por imagem , Gastrosquise/epidemiologia , Gastrosquise/mortalidade , Feminino , Estudos Retrospectivos , Gravidez , Estudos de Casos e Controles , Prognóstico , Masculino , Fatores de Risco , Oligo-Hidrâmnio/epidemiologia , Oligo-Hidrâmnio/diagnóstico , Ultrassonografia Pré-Natal , Adulto , Recém-Nascido PrematuroRESUMO
Prenatal and perinatal risk factors for perinatal brain damage frequently produce brain injuries in preterm and term infants. The early diagnosis and treatment of these infants, in the period of higher brain plasticity, may prevent the neurological and cognitive sequels that accompany these lesions. The Neurodevelopmental Research Unit at the Institute of Neurobiology of the National Autonomous University of Mexico has taken this endeavor. A multidisciplinary approach is followed. Pediatric, neurologic and rehabilitation clinical studies, MRI, EEG, visual and auditory evoked responses, and Bayley II evaluations are carried out initially. Infants are followed up to 8 years, with periodic appointments for evaluation and treatment. Katona's neurohabilitation method is used for initial diagnosis and treatment. Selective visual and auditory attention are explored from 3 months of age. This method was created in the Unit and, if deficiencies are observed, the method also describes the treatment to avoid subsequent alterations of these processes. Deficiencies in the acquisition of language are evaluated from 4 months of age, implementing treatment through instructions to parents on how they should teach their children to speak. This method has also been developed in the Unit and is in its validation process. In the MRI, we pay special attention to subtle and diffuse patterns, due to the high frequency with which they appear in contemporary cohorts at a national and international level. More than 80% of these infants showed abnormal MRI findings that should be taken into consideration. The outcome of children at 8 years old showed that 78%, 76% and 78% of extremely preterm, very preterm and late preterm, respectively, had a normal neurodevelopment. In term infants, only 69% had a normal neurodevelopment; in this group, the majority of infants had very severe brain lesions. Conclusions: It is necessary to evaluate, at an early age, all newborns with prenatal and perinatal risk factors for brain damage. Special attention should be payed to all premature newborns and those newborns who have been discharged from the intensive care unit.
Assuntos
Lesões Encefálicas/diagnóstico , Lesões Encefálicas/reabilitação , Desenvolvimento Infantil/fisiologia , Diagnóstico Precoce , Intervenção Médica Precoce , Reabilitação Neurológica , Avaliação de Processos e Resultados em Cuidados de Saúde , Criança , Pré-Escolar , Feminino , Seguimentos , Humanos , Lactente , Recém-Nascido , Doenças do Recém-Nascido , Recém-Nascido Prematuro , Doenças do Prematuro , Unidades de Terapia Intensiva Neonatal , Imageamento por Ressonância Magnética , Masculino , México , Fatores de RiscoRESUMO
Environmental factors are at least as important as genetic factors for the development of obsessive-compulsive symptoms (OCS), but the identification of such factors remain a research priority. Our study aimed to investigate the association between a broad scope of potential risk factors and OCS in a large community cohort of children and adolescents. We evaluated 1877 participants and their caregivers at baseline and after 3 years to assess various demographic, prenatal, perinatal, childhood adversity, and psychopathological factors. Mean age at baseline was 10.2 years (SD 1.9) and mean age at follow-up was 13.4 years (SD 1.9). Reports of OCS at baseline and follow-up were analyzed using latent variable models. At preliminary regression analysis, 15 parameters were significantly associated with higher OCS scores at follow-up. At subsequent regression analysis, we found that eight of these parameters remained significantly associated with higher follow-up OCS scores while being controlled by each other and by baseline OCS scores. The significant predictors of follow-up OCS were: lower socioeconomic status (p = 0.033); lower intelligence quotient (p = 0.013); lower age (p < 0.001); higher maternal stress level during pregnancy (p = 0.028); absence of breastfeeding (p = 0.017); parental baseline OCS (p = 0.038); youth baseline anxiety disorder (p = 0.023); and youth baseline OCS scores (p < 0.001). These findings may better inform clinicians and policymakers engaged in the mental health assessment and prevention in children and adolescents.
Assuntos
Redes Comunitárias/normas , Transtorno Obsessivo-Compulsivo/psicologia , Psicopatologia/métodos , Criança , Estudos de Coortes , Comorbidade , Feminino , Seguimentos , Humanos , Masculino , Fatores de RiscoRESUMO
The cause of PHACE syndrome is unknown. In a study of 218 patients, we examined potential prenatal risk factors for PHACE syndrome. Rates of pre-eclampsia and placenta previa in affected individuals were significantly greater than in the general population. No significant risk factor differences were detected between male and female subjects.