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1.
Ultrasound Obstet Gynecol ; 61(6): 728-733, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-36807360

RESUMO

OBJECTIVES: First, to investigate the correlation between prenatal presurgery anatomical and motor levels of the lesion with motor level at birth in cases undergoing prenatal repair of open spina bifida and, second, to identify factors leading to a loss of two or more motor levels between the presurgery and postnatal assessments. METHODS: This was an observational study of singleton pregnancies undergoing prenatal repair of open spina bifida, conducted between March 2011 and May 2022. All fetuses underwent an ultrasound assessment at 20-24 weeks of gestation to determine the motor and anatomical levels of the lesion before surgery. The anatomical level of the lesion was defined as the highest open posterior vertebral arch. The motor level was determined by systematic observation of the lower limb movements and was defined as the most distal active muscle present. Prenatal repair was performed at 23-26 weeks. At birth, motor level was assessed by a rehabilitation specialist by physical examination. Cases of intrauterine death or termination of pregnancy and those delivered at other sites were excluded from the neonatal assessment. The agreement between presurgery motor level and motor level at birth, and between presurgery anatomical level and motor level at birth, was assessed using the weighted kappa index (wκ). Logistic regression analysis was used to assess factors leading to a loss of two or more motor levels between the presurgery and postnatal assessments. RESULTS: Presurgery motor and anatomical levels were assessed in 61 fetuses at a median gestational age of 22.7 (interquartile range (IQR), 21.6-24.4) weeks. Prenatal repair was performed at a median gestational age of 24.6 (IQR, 23.7-25.7) weeks. Motor level at birth was assessed in 52 neonates after exclusion of nine fetuses due to loss to follow-up or fetal loss. There was moderate agreement between presurgery motor level and motor level at birth (wκ = 0.42; 95% CI, 0.21-0.63), with a median difference of 0 (IQR, -2 to 9) levels. Factors leading to a loss of two or more motor levels between the presurgery ultrasound assessment and postnatal examination were higher presurgery anatomical level (odds ratio (OR), 0.59 (95% CI, 0.35-0.98); P = 0.04) and larger difference between the anatomical and motor levels before surgery (OR, 1.85 (95% CI, 1.12-3.06); P = 0.017). None of the other ultrasound, surgery-related or neonatal variables assessed was associated significantly with a loss of two or more motor levels. There was slight agreement between the presurgery anatomical level of the lesion and motor level at birth (wκ = 0.07; 95% CI, -0.02 to 0.15). CONCLUSIONS: There is moderate agreement between fetal motor level of the lesion before prenatal repair of open spina bifida and motor level at birth, as opposed to only slight agreement between presurgery anatomical level and motor level at birth. A loss of two or more motor levels between the presurgery and postnatal assessments is associated with a higher presurgery anatomical level and with a larger difference between the presurgery anatomical and motor levels. Consequently, motor level, rather than the anatomical level, should be used for prenatal counseling. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.


Assuntos
Espinha Bífida Cística , Disrafismo Espinal , Gravidez , Recém-Nascido , Feminino , Humanos , Lactente , Espinha Bífida Cística/diagnóstico por imagem , Espinha Bífida Cística/cirurgia , Disrafismo Espinal/cirurgia , Feto , Parto , Idade Gestacional , Aconselhamento , Ultrassonografia Pré-Natal , Estudos Retrospectivos
2.
Enferm Infecc Microbiol Clin (Engl Ed) ; 40(10): 546-549, 2022 12.
Artigo em Inglês | MEDLINE | ID: mdl-36464472

RESUMO

INTRODUCTION: A newly identified SARS-CoV-2 variant, VOC202012/01 originating lineage B.1.1.7, recently emerged in the United Kingdom. The rapid spread in the UK of this new variant has caused other countries to be vigilant. MATERIAL AND METHODS: We based our initial screening of B.1.1.7 on the dropout of the S gene signal in the TaqPath assay, caused by the 69/70 deletion. Subsequently, we confirmed the B.1.1.7 candidates by whole genome sequencing. RESULTS: We describe the first three imported cases of this variant from London to Madrid, subsequent post-arrival household transmission to three relatives, and the two first cases without epidemiological links to UK. One case required hospitalization. In all cases, drop-out of gene S was correctly associated to the B.1.1.7 variant, as all the corresponding sequences carried the 17 lineage-marker mutations. CONCLUSION: The first identifications of the SARS-CoV-2 B.1.1.7 variant in Spain indicate the role of independent introductions from the UK coexisting with post-arrival transmission in the community, since the early steps of this new variant in our country.


Assuntos
COVID-19 , SARS-CoV-2 , Humanos , SARS-CoV-2/genética , Espanha/epidemiologia , COVID-19/diagnóstico , COVID-19/epidemiologia , Hospitalização
3.
Enferm. infecc. microbiol. clín. (Ed. impr.) ; 40(10): 546-549, dic. 2022. graf
Artigo em Inglês | IBECS | ID: ibc-212838

RESUMO

Introduction: A newly identified SARS-CoV-2 variant, VOC202012/01 originating lineage B.1.1.7, recently emerged in the United Kingdom. The rapid spread in the UK of this new variant has caused other countries to be vigilant. Material and methods: We based our initial screening of B.1.1.7 on the dropout of the S gene signal in the TaqPath assay, caused by the 69/70 deletion. Subsequently, we confirmed the B.1.1.7 candidates by whole genome sequencing. Results: We describe the first three imported cases of this variant from London to Madrid, subsequent post-arrival household transmission to three relatives, and the two first cases without epidemiological links to UK. One case required hospitalization. In all cases, drop-out of gene S was correctly associated to the B.1.1.7 variant, as all the corresponding sequences carried the 17 lineage-marker mutations. Conclusion: The first identifications of the SARS-CoV-2 B.1.1.7 variant in Spain indicate the role of independent introductions from the UK coexisting with post-arrival transmission in the community, since the early steps of this new variant in our country.(AU)


Introducción: Recientemente, ha surgido en Reino Unido una nueva variante de SARS-CoV-2, VOC202012/01, que origina el linaje B.1.1.7. Su rápida distribución en Reino Unido ha alertado a otros países a vigilar su presencia. Material y métodos: El rastreo inicial de la variante B.1.1.7 se basó en la ausencia de amplificación del gen S en el ensayo TaqPath, causado por la deleción 69/70. Todos los casos candidatos de corresponder a la variante B.1.1.7 con este criterio fueron posteriormente confirmados por secuenciación de genoma completo. Resultados: Describimos los primeros 3 casos importados de esta variante, desde Londres hasta Madrid, con la posterior transmisión domiciliaria de uno de estos casos a 3 familiares y, adicionalmente, los 2 primeros casos con la variante sin vínculo epidemiológico con Reino Unido. Uno de los casos requirió hospitalización. En todos los casos el criterio de no amplificación del gen S identificó con precisión la variante B.1.1.7, como demostró posteriormente la presencia de las 17 mutaciones marcadoras de este linaje. Conclusión: Las primeras identificaciones de la variante B.1.1.7 de SARS-CoV-2 indican un papel solapante de las introducciones independientes desde Reino Unido, con eventos de transmisión comunitaria, incluso desde los primeros momentos de la presencia de esta variante en nuestro país.(AU)


Assuntos
Humanos , Coronavírus Relacionado à Síndrome Respiratória Aguda Grave , Infecções por Coronavirus , Pandemias , Transmissão de Doença Infecciosa , Espanha , Doenças Transmissíveis , Microbiologia
4.
Sci Rep ; 12(1): 5986, 2022 04 08.
Artigo em Inglês | MEDLINE | ID: mdl-35396521

RESUMO

Rhythmic flickering visual stimulation produces steady-state visually evoked potentials (SSVEPs) in electroencephalogram (EEG) recordings. Based on electrode-level analyses, two dichotomous models of the underpinning mechanisms leading to SSVEP generation have been proposed: entrainment or superposition, i.e., phase-alignment or independence of endogenous brain oscillations from flicker-induced oscillations, respectively. Electrode-level analyses, however, represent an averaged view of underlying 'source-level' activity, at which variability in SSVEPs may lie, possibly suggesting the co-existence of multiple mechanisms. To probe this idea, we investigated the variability of SSVEPs derived from the sources underpinning scalp EEG responses during presentation of a flickering radial checkerboard. Flicker was presented between 6 and 12 Hz in 1 Hz steps, and at individual alpha frequency (IAF i.e., the dominant frequency of endogenous alpha oscillatory activity). We tested whether sources of endogenous alpha activity could be dissociated according to evoked responses to different flicker frequencies relative to IAF. Occipitoparietal sources were identified by temporal independent component analysis, maximal resting-state alpha power at IAF and source localisation. The pattern of SSVEPs to rhythmic flicker relative to IAF was estimated by correlation coefficients, describing the correlation between the peak-to-peak amplitude of the SSVEP and the absolute distance of the flicker frequency from IAF across flicker conditions. We observed extreme variability in correlation coefficients across sources, ranging from -0.84 to 0.93, with sources showing largely different coefficients co-existing within subjects. This result demonstrates variation in evoked responses to flicker across sources of endogenous alpha oscillatory activity. Data support the idea of multiple SSVEP mechanisms.


Assuntos
Eletroencefalografia , Potenciais Evocados Visuais , Encéfalo , Eletrodos , Humanos , Estimulação Luminosa
5.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33685741

RESUMO

INTRODUCTION: A newly identified SARS-CoV-2 variant, VOC202012/01 originating lineage B.1.1.7, recently emerged in the United Kingdom. The rapid spread in the UK of this new variant has caused other countries to be vigilant. MATERIAL AND METHODS: We based our initial screening of B.1.1.7 on the dropout of the S gene signal in the TaqPath assay, caused by the 69/70 deletion. Subsequently, we confirmed the B.1.1.7 candidates by whole genome sequencing. RESULTS: We describe the first three imported cases of this variant from London to Madrid, subsequent post-arrival household transmission to three relatives, and the two first cases without epidemiological links to UK. One case required hospitalization. In all cases, drop-out of gene S was correctly associated to the B.1.1.7 variant, as all the corresponding sequences carried the 17 lineage-marker mutations. CONCLUSION: The first identifications of the SARS-CoV-2 B.1.1.7 variant in Spain indicate the role of independent introductions from the UK coexisting with post-arrival transmission in the community, since the early steps of this new variant in our country.

6.
Opt Express ; 27(11): 16384-16394, 2019 May 27.
Artigo em Inglês | MEDLINE | ID: mdl-31163816

RESUMO

We discuss the properties of pure multipole beams with well-defined handedness or helicity, with the beam field a simultaneous eigenvector of the squared total angular momentum and its projection along the propagation axis. Under the condition of hemispherical illumination, we show that the only possible propagating multipole beams are "sectoral" multipoles. The sectoral dipole beam is shown to be equivalent to the non-singular time-reversed field of an electric and a magnetic point dipole Huygens' source located at the beam focus. Higher order multipolar beams are vortex beams vanishing on the propagation axis. The simple analytical expressions of the electric field of sectoral multipole beams, exact solutions of Maxwell's equations, and the peculiar behaviour of the Poynting vector and spin and orbital angular momenta in the focal volume could help to understand and model light-matter interactions under strongly focused beams.

7.
Phys Rev E ; 99(2-1): 022603, 2019 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-30934217

RESUMO

Previous research has shown that gold nanoparticles immersed in water in an optical vortex lattice formed by the perpendicular intersection of two standing light waves with a π/2rad phase difference will experience enhanced dispersion that scales with the intensity of the incident laser. We show that flexible nanoscale dumbbells (created by attaching two such gold particles by means of a polymer chain) in the same field display different types of motion depending on the chain length and field intensity. We have not disregarded the secondary optical forces due to light scattering. The dumbbells may disperse, rotate, or remain trapped. For some values of the parameters, the (enhanced) dispersion possesses a displacement distribution with exponential tails, making the motion anomalous, though Brownian.

8.
Prev Med ; 114: 149-155, 2018 09.
Artigo em Inglês | MEDLINE | ID: mdl-29958860

RESUMO

In a cross-sectional study carried out in El Salvador between February 2016 and July 2017, self-sampling and human papillomavirus (HPV) testing was found to be highly acceptable among 2019 women who had not attended a cervical cancer screening in at least 3 years. Within this population, HPV positivity rates differed according to age, marital status, number of children, and lifetime sexual partners. The proportion of women who tested HPV positive or who were diagnosed with cervical intraepithelial neoplasia grade 2 (CIN2) or more severe diagnoses (CIN2+) was similar to the general population of the area. Among the reasons for failing to participate in previous screening programs, non-attending women described logistic concerns, but also erroneous beliefs regarding HPV and cervical cancer, misconceptions regarding the screening procedure, discomfort with male providers, and confidentiality fears. The aim of this study was to identify opportunities and challenges that emerged from the use of self-sampling and HPV testing as part of a public cervical cancer control effort in a low-resource setting.


Assuntos
Detecção Precoce de Câncer , Infecções por Papillomavirus/diagnóstico , Manejo de Espécimes/métodos , Displasia do Colo do Útero/diagnóstico , Neoplasias do Colo do Útero/prevenção & controle , Adulto , Estudos Transversais , Detecção Precoce de Câncer/métodos , El Salvador , Feminino , Humanos , Programas de Rastreamento/métodos , Pessoa de Meia-Idade , Papillomaviridae/isolamento & purificação , População Rural , Esfregaço Vaginal/métodos
9.
J Dev Orig Health Dis ; 8(5): 556-565, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28789711

RESUMO

Fetal growth restriction (FGR) and preterm birth are frequent co-morbidities, both are independent risks for brain injury. However, few studies have examined the mechanisms by which preterm FGR increases the risk of adverse neurological outcomes. We aimed to determine the effects of prematurity and mechanical ventilation (VENT) on the brain of FGR and appropriately grown (AG, control) lambs. We hypothesized that FGR preterm lambs are more vulnerable to ventilation-induced acute brain injury. FGR was surgically induced in fetal sheep (0.7 gestation) by ligation of a single umbilical artery. After 4 weeks, preterm lambs were euthanized at delivery or delivered and ventilated for 2 h before euthanasia. Brains and cerebrospinal fluid (CSF) were collected for analysis of molecular and structural indices of early brain injury. FGRVENT lambs had increased oxidative cell damage and brain injury marker S100B levels compared with all other groups. Mechanical ventilation increased inflammatory marker IL-8 within the brain of FGRVENT and AGVENT lambs. Abnormalities in the neurovascular unit and increased blood-brain barrier permeability were observed in FGRVENT lambs, as well as an altered density of vascular tight junctions markers. FGR and AG preterm lambs have different responses to acute injurious mechanical ventilation, changes which appear to have been developmentally programmed in utero.


Assuntos
Lesões Encefálicas/patologia , Lesões Encefálicas/fisiopatologia , Retardo do Crescimento Fetal/patologia , Retardo do Crescimento Fetal/fisiopatologia , Nível de Saúde , Respiração Artificial/efeitos adversos , Animais , Animais Recém-Nascidos , Lesões Encefálicas/etiologia , Feminino , Previsões , Ovinos
10.
J Matern Fetal Neonatal Med ; 30(19): 2301-2305, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27997256

RESUMO

OBJECTIVE: To assess the reliability of the interpretation of a new technique for the ultrasound evaluation of the level of neurological lesion in fetuses with myelomeningocele. METHODS: Observational study including myelomeningocele fetuses, referred to our center for the sonographic assessment of the fetal lower-limb movements, made and recorded by an expert in Maternal-fetal medicine and a specialist in Rehabilitation. Two observers, with different levels of expertise and blinded to each other's results, interpreted each recorded scan two different times. The agreement for the segmental levels assigned between the observers and the gold standard, the inter-observer and intra-observer reproducibility were tested using the weighed Kappa (wκ) index. RESULTS: Twenty-eight scans were recorded and evaluated. The agreement between the observers and the gold standard remained constant for the expert observer (wκ = 0.82) and increased (wκ = 0.66-wκ = 0.72) for the other one. The inter-observer and the intra-observer variability for the expert observer were wκ = 0.72 and wκ = 0.94, respectively. DISCUSSION: The agreement for the prenatal evaluation of the segmental neurological level was excellent, after a short training period, for observers with different degrees of expertise. The interpretation of this technique is reproducible enough and this supports its value for the prediction of postnatal motor function in myelomeningocele fetuses.


Assuntos
Meningomielocele/diagnóstico por imagem , Ultrassonografia Pré-Natal , Feminino , Humanos , Variações Dependentes do Observador , Gravidez
11.
Ultrasound Obstet Gynecol ; 47(2): 162-7, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26306897

RESUMO

OBJECTIVES: To report our preliminary experience in the use of prenatal ultrasound examination to assess lower-limb movements in fetuses with myelomeningocele. We aimed to determine the accuracy of this method to establish the segmental level of neurological lesion, as this is the best known predictor of the future ability to walk. METHODS: This was a preliminary, observational study including fetuses with myelomeningocele operated on prenatally. The patterns of movements present and absent in the affected fetuses' lower limbs were evaluated systematically by ultrasound examination. According to the known nerve function associated with each muscle group, the segmental level of neurological lesion was established before birth. The agreement for the segmental levels assigned, between the prenatal ultrasound technique and the classical neurological clinical examination after birth (gold standard), was tested using the weighed kappa (wκ) index. RESULTS: Seventy-one fetuses with myelomeningocele were evaluated at the Hospital Universitari Vall d'Hebron. After counseling, the parents opted for prenatal surgery (26 cases), termination of pregnancy (43 cases) or postnatal repair (two cases). Five patients did not fulfil the inclusion criteria for prenatal surgery and three were excluded after birth. In the 18 fetuses that underwent surgery and were analyzed, the agreement between prenatal and postnatal segmental levels assigned was 91.7% for the right limb (wκ = 0.80) and 88.9% for the left limb (wκ = 0.73). CONCLUSIONS: The agreement found between prenatal and postnatal assignment of level of lesion in this preliminary study suggests that neurological sonographic evaluation is feasible before birth. This may provide accurate individualized information about the motor function and future ambulation prognosis of fetuses with myelomeningocele.


Assuntos
Movimento Fetal , Feto/fisiopatologia , Transtornos Neurológicos da Marcha/diagnóstico por imagem , Meningomielocele/diagnóstico por imagem , Ultrassonografia Pré-Natal/métodos , Adulto , Feminino , Transtornos Neurológicos da Marcha/embriologia , Transtornos Neurológicos da Marcha/etiologia , Idade Gestacional , Humanos , Extremidade Inferior/diagnóstico por imagem , Extremidade Inferior/embriologia , Meningomielocele/complicações , Meningomielocele/embriologia , Valor Preditivo dos Testes , Gravidez , Prognóstico , Reprodutibilidade dos Testes
13.
Nature ; 519(7544): 436-8, 2015 Mar 26.
Artigo em Inglês | MEDLINE | ID: mdl-25810204

RESUMO

Powerful winds driven by active galactic nuclei are often thought to affect the evolution of both supermassive black holes and their host galaxies, quenching star formation and explaining the close relationship between black holes and galaxies. Recent observations of large-scale molecular outflows in ultraluminous infrared galaxies support this quasar-feedback idea, because they directly trace the gas from which stars form. Theoretical models suggest that these outflows originate as energy-conserving flows driven by fast accretion-disk winds. Proposed connections between large-scale molecular outflows and accretion-disk activity in ultraluminous galaxies were incomplete because no accretion-disk wind had been detected. Conversely, studies of powerful accretion-disk winds have until now focused only on X-ray observations of local Seyfert galaxies and a few higher-redshift quasars. Here we report observations of a powerful accretion-disk wind with a mildly relativistic velocity (a quarter that of light) in the X-ray spectrum of IRAS F11119+3257, a nearby (redshift 0.189) optically classified type 1 ultraluminous infrared galaxy hosting a powerful molecular outflow. The active galactic nucleus is responsible for about 80 per cent of the emission, with a quasar-like luminosity of 1.5 × 10(46) ergs per second. The energetics of these two types of wide-angle outflows is consistent with the energy-conserving mechanism that is the basis of the quasar feedback in active galactic nuclei that lack powerful radio jets (such jets are an alternative way to drive molecular outflows).

14.
Eur J Cancer ; 51(5): 632-41, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25686481

RESUMO

PURPOSE: Activation of proto-oncogenes and inactivation of tumour suppressor genes are the major genetic alterations involved in carcinogenesis. The increase in methylation at the promoter region of a tumour suppressor gene can lead to gene inactivation, selecting cells with proliferative advantage. Thus, promoter hypermethylation is considered a marker in a variety of malignant tumours, including oral cavity. EXPERIMENTAL DESIGN: The methylation pattern of eight genes was evaluated in 40 oral cavity squamous cell carcinomas (OSCCs) and 40 saliva samples from healthy individuals by Q-MSP. Different combinations of genes were also assessed in order to identify gene panels that could better distinguish between OSCC and saliva samples. RESULTS: CCNA1, DAPK, DCC and TIMP3 methylation were highly specific for being found in the OSCC samples. Moreover, the combination of these genes improved detection when compared with single markers, reaching values of 92.5% for sensitivity and specificity (when using the panel CCNA1, DCC, TIMP3). Moreover, DAPK, DCC and TIMP3 were hypermethylated in nearly 90% of clinically T1 and T2 cases. CONCLUSION: The pursuing of this panel of hypermethylated genes is an important tool for the detection of individuals with OSCC. Moreover, the identification of these markers in early stages of OSCC shows the feasibility of using the panel on saliva as possible biomarkers for early diagnosis. The lack of association between the methylation status of these genes and clinical characteristics shows that they are able to distinguish OSCC cases irrespective of social and clinical factors (gender, age, human papillomavirus (HPV) status, clinical stage, vascular embolisation and perineural invasion).


Assuntos
Biomarcadores Tumorais/genética , Carcinoma de Células Escamosas/genética , Metilação de DNA , Epigênese Genética , Testes Genéticos/métodos , Neoplasias de Cabeça e Pescoço/genética , Neoplasias Bucais/genética , Adulto , Idoso , Brasil , Estudos de Casos e Controles , Ciclina A1/genética , Receptor DCC , Proteínas Quinases Associadas com Morte Celular/genética , Estudos de Viabilidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Regiões Promotoras Genéticas , Receptores de Superfície Celular/genética , Reprodutibilidade dos Testes , Carcinoma de Células Escamosas de Cabeça e Pescoço , Inibidor Tecidual de Metaloproteinase-3/genética , Proteínas Supressoras de Tumor/genética
15.
Oral Oncol ; 50(6): 587-92, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24656975

RESUMO

Head and neck cancer is a collective term that describes malignant tumors of the oral cavity, pharynx, and larynx characterized by high incidence and mortality rates. Although most HNSCC originate from the mucosal surface of the upper aerodigestive tract, where they can be easily detected during a routine clinical examination. Often the definitive diagnosis is delayed because of the difficulty in differentiating from other similar lesions. Activation of proto-oncogenes and inactivation of tumor suppressor genes are the major molecular alterations involved in carcinogenesis. In addition, epigenetic changes can alter the expression of critical genes important in the development of a variety of cancers. The detection of aberrant gene promoter methylation as a tool for the detection of tumors or its use as prognostic marker have been described for many different cancers including HNSCC. The search for biomarkers has as its main aim the evaluation and measurement of the status of normal and pathological biological processes as well as pharmacological responses to certain treatments. The tracking of these biomarkers is an important part for the identification of individuals in the early stages of head and neck cancer for its diagnostic and prognostic relevance reflecting in high survival rates, better quality of life and less cost to the healthcare system. Therefore, assuming that cancer results from genetic and epigenetic changes, analyzes based on gene methylation profile in combination with the pathological diagnosis would be useful in predicting the behavior of these head and neck tumors.


Assuntos
Biomarcadores Tumorais/metabolismo , Carcinoma de Células Escamosas/metabolismo , Metilação de DNA , Neoplasias de Cabeça e Pescoço/metabolismo , Carcinoma de Células Escamosas/genética , Carcinoma de Células Escamosas/patologia , Epigênese Genética , Neoplasias de Cabeça e Pescoço/genética , Neoplasias de Cabeça e Pescoço/patologia , Humanos
16.
Phys Rev Lett ; 110(2): 028901, 2013 Jan 11.
Artigo em Inglês | MEDLINE | ID: mdl-23383948
17.
Child Abuse Negl ; 37(1): 77-85, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23306145

RESUMO

OBJECTIVES: Research from developed countries shows that child maltreatment increases the risk for substance use and problems. However, little evidence on this relationship is available from developing countries, and recognition of this relationship may have important implications for substance demand reduction strategies, including efforts to prevent and treat substance use and related problems. Latin America and the Caribbean is a rich and diverse region of the world with a large range of social and cultural influences. A working group constituted by the Inter-American Drug Abuse Control Commission and the Center for Addiction and Mental Health in June, 2010 identified research on this relationship as a priority area for a multinational research partnership. METHODS: This paper examines the association between self-reported child maltreatment and use in the past 12 months of alcohol and cannabis in 2294 university students in seven participating universities in six participating countries: Colombia, El Salvador, Jamaica, Nicaragua, Panama and Uruguay. The research also considers the possible impact of religiosity and minimal psychological distress as factors contributing to resiliency in these samples. RESULTS: The results showed that experience of maltreatment was associated with increased use of alcohol and cannabis. However, the effects differed depending on the type of maltreatment experienced. Higher levels of religiosity were consistently associated with lower levels of alcohol and cannabis use, but we found no evidence of an impact of minimal psychological distress on these measures. CONCLUSIONS: This preliminary study shows that the experience of maltreatment may increase the risk of alcohol and cannabis use among university students in Latin American and Caribbean countries, but that higher levels of religiosity may reduce that risk. More work to determine the nature and significance of these relationships is needed.


Assuntos
Consumo de Bebidas Alcoólicas/epidemiologia , Maus-Tratos Infantis/estatística & dados numéricos , Abuso de Maconha/epidemiologia , Adaptação Psicológica , Adulto , Consumo de Bebidas Alcoólicas/psicologia , Criança , Maus-Tratos Infantis/psicologia , Colômbia/epidemiologia , El Salvador/epidemiologia , Feminino , Humanos , Jamaica/epidemiologia , Masculino , Abuso de Maconha/psicologia , Nicarágua/epidemiologia , Panamá/epidemiologia , Religião , Fatores de Risco , Autorrelato , Estudantes/estatística & dados numéricos , Universidades , Uruguai/epidemiologia , Adulto Jovem
18.
Rev. neurol. (Ed. impr.) ; 53(10): 607-618, 16 nov., 2011. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-92042

RESUMO

Un aspecto crítico en todos los modelos experimentales de patologías del sistema nervioso es la evaluación del pronóstico neurológico final. En el caso de una lesión cerebral isquémica focal, además de la determinación del tamaño de la lesión, una valiosa herramienta es la evaluación del déficit funcional final. Ello se debe al hecho de que el daño isquémico produce diferentes grados de deterioro sensoriomotor y cognitivo, que pueden proporcionar información sobre la ubicación y el tamaño de la lesión y sobre la eficacia de los tratamientos neuroprotectores después del daño agudo. Además, la magnitud de estas alteraciones también puede ser útil para predecir el resultado final y para evaluar terapias reparadoras a largo plazo. Con este fin se ha desarrollado una amplia gama de tests que permite la cuantificación de todos estos síntomas neurológicos. Esta revisión tiene como intención recopilar los tests de comportamiento más útiles diseñados para evaluar los síntomas neurológicos en los estudios de isquemia cerebral focal experimental en roedores inducida por oclusión de la arteria cerebral media, el modelo más utilizado para el estudio del ictus isquémico (AU)


A critical aspect in all models is the assessment of the final outcome of the modelling procedure. In the case of a focal ischaemic brain injury, apart from the determination of the size of the lesion, another valuable tool is the evaluation of the final functional deficit. Indeed, ischaemic damage leads to the appearance of different degrees of sensoriomotor and cognitive impairments, which may yield useful information on location and size of the lesion and on the efficacy of neuroprotective treatments after the acute injury. In addition, the magnitude of these impairments may also be useful to predict final outcome and to evaluate neuro-restorative therapies in a long-term scenario. To this aim, a wide range of tests has been developed which allow the quantification of all these neurological symptoms. This review intends to compile the most useful behavioural tests designed to assess neurological symptoms in studies of focal experimental cerebral ischemia in rodents induced by middle cerebral artery occlusion, the most commonly used model of ischaemic stroke (AU)


Assuntos
Animais , Exame Neurológico/métodos , Isquemia Encefálica/fisiopatologia , Transtornos das Habilidades Motoras/diagnóstico , Modelos Animais de Doenças , Fármacos Neuroprotetores/uso terapêutico , Transtornos Mentais/diagnóstico , Transtornos da Memória/diagnóstico
19.
Trauma (Majadahonda) ; 22(3): 148-154, jul.-sept. 2011. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-91015

RESUMO

Objetivo: Valorar la evolución a largo plazo de las fracturas tóraco-lumbares tratadas exclusivamente por vía posterior y comprobar la pérdida de corrección. Material y métodos: Basamos el estudio sobre 91 pacientes, operados mediante instrumentación posterior y artrodesis póstero-lateral, durante un periodo de tiempo de 15 años, que presentaban fracturas tóraco-lumbares sin lesión neurológica. Se analizaron estadísticamente la evolución de la cifosis y del aplastamiento vertebral en la radiografía lateral, con un periodo mínimo de 6 años. Resultados: No encontramos diferencias en la evolución clínica, estancia hospitalaria en relación con la edad o el sexo. Sin embargo, hallamos diferencias de las complicaciones con el uso de instrumentaciones largas y tanto en las instrumentaciones cortas como largas hubo perdida de corrección a lo largo del tiempo que fue mayor en las cortas. Conclusión: La radiografía simple lateral de columna es útil en el seguimiento y control de la evolución en el plano sagital de las fractura tóraco-lumbares, siendo el parámetro más sensible el ángulo de la fractura (AU)


Objective: To assess long term outcome of thoracic and lumber fractures treated only by the posterior approach and verify loss of correction. Material and Methods: The study was based on 91 patients with thoracic and lumbar fractures with no neurological damage operated on with posterior instrumentation and posterolateral arthrodesis over a period of 15 years. The clinical course of kyphosis and vertebral crushing on the lateral X-ray was statistically analyzed over a period of at least 6 years. Results: We did not find any differences in clinical course or hospital stay with regard to age or sex. However, we did find differences in complications with the use of long instrumentation and both in the long and short instrumentation there was a loss of correction over time that was greater with the short instrumentation. Conclusion: Plain X-ray of spine is useful for the follow up and control of the course in the sagittal plane of thoracic and lumbar fractures, the most sensitive parameter being fracture angle (AU)


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Adulto Jovem , Adulto , Pessoa de Meia-Idade , Traumatismos Torácicos/epidemiologia , Vértebras Lombares/lesões , Artrodese/métodos , Artrodese/tendências , Radiografia Torácica/métodos , Radiografia Torácica , Antibioticoprofilaxia/métodos , Traumatismos Torácicos/complicações , Antibioticoprofilaxia/tendências , Antibioticoprofilaxia , /estatística & dados numéricos , /tendências , /métodos
20.
J Med Microbiol ; 60(Pt 11): 1685-1688, 2011 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21680765

RESUMO

We report a case of concurrent diphtheria and infectious mononucleosis in an 11-year-old Brazilian child. Two days after specific treatment for diphtheria was started the patient was discharged following clinical recovery. This case highlights the difficulties in the clinical diagnosis of diphtheria in partially immunized individuals, and for the management and control of diphtheria in developing countries.


Assuntos
Antibacterianos/uso terapêutico , Corynebacterium diphtheriae/imunologia , Antitoxina Diftérica/uso terapêutico , Difteria/complicações , Mononucleose Infecciosa/complicações , Criança , Difteria/tratamento farmacológico , Difteria/imunologia , Humanos , Mononucleose Infecciosa/imunologia , Masculino
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