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INTRODUCTION: Physical trauma is one of the most common causes of death and disability in children's development and adolescents. By consequence, pediatric trauma is a topic that needs further studies. OBJECTIVE: The identification of factors associated with child and adolescent victims of trauma treated at a referral center in Southern Brazil relating to trauma in children and adolescents from birth to age 14 years treated in a hospital emergency room. METHODS: A retrospective study using secondary data from a hospital service, performed the analysis of associated factors among 375 children and adolescents (range 0-14 years) admitted to the emergency room for any kind of physical trauma and the variables described about the traumas. The period was June 14 to December 14, 2013. RESULTS: Most patients were male (65.1%), white (89.1%); they were attended nightly (45.9%) and belonging to the age group 10-14 years (40.3%), head and neck prevailed in number occurrences with 33.6% of cases, followed by the upper and lower limbs 27.7% and 26.9%, respectively. Falls represented 45.6% of cases, followed by exposure to inanimate mechanical forces (12%) and exposure to animated mechanical forces (5.9%). The neurosurgery service was the most referenced for younger age groups, while for the older groups were the maxillofacial services (p = 0.001). CONCLUSION: This study showed results that draw the community’s attention not only academic, but also to call the attention of caregivers to work with constant prevention alternatives to the monitoring of the course of children’s development.

BACKGROUND Nasoethmoidal meningocele is considered an uncommon type of cephalocele, and congenital cystic adenomatoid malformation (CCAM) is a rare lung disorder characterized by overgrowth of the terminal bronchioles. CASE We report the unusual association between a nasoethmoidal meningocele and CCAM type II in a fetus exposed to valproic acid and misoprostol. The mother was an 18-year-old woman on her first pregnancy. She had a history of absence seizures since she was 5 years old. She took valproic acid from the beginning of the gestation until the end of the third month. At the end of the third month, she attempted interruption of her pregnancy using misoprostol. The fetal nasoethmoidal meningocele and CCAM type II were identified through morphological ultrasound examination and magnetic resonance imaging. A genome-wide study detected one copy number variation classified as rare, entirely contained into the SPATA5 gene. However, it does not seem to be associated to the clinical findings of the patient. CONCLUSION To our knowledge, there is only one case reported in the literature showing the same association between a nasoethmoidal meningocele and CCAM. Thus, the malformations observed in our patient may be related to the gestational exposures. Also, we cannot rule out that the patient may present the same condition characterized by a cephalocele and CCAM described by some authors, or even an undescribed entity, because some hallmark features, such as laryngeal atresia and limb defects, were not observed in our case. Further reports will be very important to better understand the associations described in our study.

Several countries, as Brazil, have public policies for periconceptional folic acid supplementation (FAS) in order to prevent unfavorable outcomes. Our aim was to evaluate the FAS situation in a public reference hospital from Southern Brazil. This study included all mothers who had children born at the Hospital Materno Infantil Presidente Vargas, RS, Brazil, in a 1-year period. Data collection was conducted through interviews with application of a clinical protocol and analysis of the patients' records. FAS was defined as the use of folic acid in any period of the periconceptional period, irrespective of the duration and amount. We also classified those mothers who correctly followed the national recommendation proposed by the Health Ministry of Brazil. The sample consisted of 765 mothers evaluated soon after childbirth. Their ages ranged from 12 to 45 years (mean 25.2 years). The overall level of FAS was 51.5%, and the use according to the national recommendation occurred in only 1.6%. Factors associated with non-FAS consisted of lower maternal age (p = .009) and maternal schooling (p = .023), higher number of pregnancies (p = .003), fewer prenatal visits (p = .050) and later prenatal care onset (p = .037). Periconceptional FAS in our midst seems to be very far from the ideal goal. Susceptible groups appeared to be mothers who were younger, less educated, multiparous, and had inadequate prenatal care. We believe that efforts of education and awareness should be especially targeted for these groups. These recommendations should also be strengthened among those who prescribe the FAS.

Background There are few studies assessing the birth measures of patients with congenital heart disease (CHD). Our aim to evaluate their progression and impact over the outcome. Methods The cases consisted of patients with CHD during their first hospitalization in a reference cardiac and pediatric intensive care unit (ICU) from Southern Brazil. Controls were composed of patients with no clinical evidence of CHD hospitalized soon after cases. The cases underwent high-resolution karyotype and fluorescence in situ hybridization (FISH) for 22q11 microdeletion. We analyzed birth weight, length and head circumference of patients of both groups. For CHD patients, we evaluated their progression and impact until hospitalization at ICU. Results Our sample was composed of 198 cases and controls. We observe a difference in birth weight of CHD patients only in relation to general population. There was a significant increase in children with CHD and weight below the lower limit from birth until the hospitalization at ICU, and this occurred more in those without complex CHD. Syndromic patients and with an extracardiac malformation also presented a greater difficulty to maintain not only the weight but also the length/height until the hospitalization. Individuals with weight below the lower limit at hospitalization who died had a tendency to present longer stay at ICU. Conclusions Some CHD patients, especially without complex defects, and with syndromic aspect and a major extracardiac malformation, present a higher difficult to maintain their weight and growth, and, therefore, may be at risk and should be more closely monitored.

Warfarin is a synthetic oral anticoagulant that crosses the placenta and can lead to a number of congenital abnormalities known as fetal warfarin syndrome. Our aim is to report on the follow-up from birth to age 8 years of a patient with fetal warfarin syndrome. He presented significant respiratory dysfunction, as well as dental and speech and language complications. The patient was the second child of a mother who took warfarin during pregnancy due to a metallic heart valve. The patient had respiratory dysfunction at birth. On physical examination, he had a hypoplastic nose, pectus excavatum, and clubbing of the fingers. Nasal fibrobronchoscopy showed upper airway obstruction due to narrowing of the nasal cavities. He underwent surgical correction with Max Pereira graft, zetaplasty, and osteotomies for the piriform aperture. At dental evaluation, he had caries and delayed eruption of the upper incisors. Speech and language assessment revealed high palate, mouth breathing, little nasal patency, and shortened upper lip. Auditory long latency and cognitive-related potential to auditory stimuli demonstrated functional changes in the cortical auditory pathways. We believe that the frequency of certain findings observed in our patient may be higher in fetal warfarin syndrome than is appreciated, since a significant number result in abortions, stillbirths, or children evaluated in the first year of life without a follow-up. Thus, a multidisciplinary approach and long-term monitoring of these patients may be necessary. © 2015 Wiley Periodicals, Inc.

a Graduate Program in Pathology, Universidade Federal de Ciencias da Saude de Porto Alegre (UFCSPA), RS, Brazil b Graduation in Medicine, Universidade Federal de Ciencias da Saude de Porto Alegre (UFCSPA), RS, Brazil c Graduation in Nursing, Universidade Federal de Ciencias da Saude de Porto Alegre (UFCSPA), RS, Brazil d School of Medicine, Division of Medical Oncology, University of Colorado Denver, CO, USA e Clinical Genetics, Universidade Federal de Ciencias da Saude de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, Brazil f Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), RS, Brazil

La muerte por suicidio paso a ocupar la tercera posici—n entre las causas mas frecuentes en la poblaci—n de 15 a 44 a–os de edad. La muerte autoinflingida posee significados que requieren comprensi—n y atenci—n . El objetivo de este estudio fue conocer las vivencias y los sentimientos de los usuarios de coca’na dentro de la relaci—n de dependencia qu’mica y suicidio. Este es un estudio cualitativo, realizado entre agosto del 2012 y febrero del 2013. Los 18 individuos que cumplieron con los criterios para episodio depresivo respondieron a una entrevista semiestructurada para el riesgo de suicidio, por el Mini International Neuropsychiatric Interview. En el an‡lisis de los contenidos narrados, se establecieron tres categor’as: historia anterior, tentativas de suicidio y depresi—n. Los resultados fueron evaluados procurando reflexionar y comprender las vivencias expuestas por los usuarios. Este estudio apoya la comprensi—n de significados de las vivencias y sentimientos de los usuarios de coca’na/crack ante el riesgo de suicidio.