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1.
Neumol. pediátr. (En línea) ; 18(2): 37-39, 2023. ilus, tab
Article in Spanish | LILACS | ID: biblio-1444103

ABSTRACT

En las alturas, sobre todo a 2500 metros sobre el nivel del mar, la cantidad absoluta de oxígeno va decreciendo y por lo tanto la cantidad disponible para el intercambio gaseoso disminuye, produciéndose una vasoconstricción hipóxica pulmonar (VHP). La VHP asociada a la hipoxia hipobárica de la altura produce un aumento de la presión pulmonar que es mayor en los lactantes y a mayores alturas. No hay valores únicos de saturación de oxígeno (SatO2) en la altura, porque ésta va disminuyendo según el mayor nivel de altura, aumenta con la edad, y la brecha entre la vigilia y sueño es grande (sobre todo en los primeros meses de vida). El 25% de los niños sanos que viven en altura tienen valores de SatO2 significativamente menores que el 75% restante. Los valores normales de los índices de apnea/hipopnea son distintos a los de nivel del mar. El edema pulmonar de las alturas es una patología frecuente, que se produce por un incremento desproporcionado en la VHP reflejando una hiperactividad del lecho vascular pulmonar ante la exposición aguda a la hipoxia hipobárica. Tiene cuatro fenotipos, es infrecuente en menores de 5 años y rara vez es mortal, la sospecha clínica y el manejo oportuno con oxigeno es la clave. Finalmente, en la altura los valores normales de la función pulmonar de la espirometría, oscilometría de impulso y capacidad de difusión son distintos que a nivel del mar.


At high altitude, especially > 2,500 meters above sea level, the absolute amount of oxygen decreases and therefore the amount available for gas exchange decreases, producing hypoxic pulmonary vasoconstriction (VHP). VHP associated with high-altitude hypobaric hypoxia produces an increase in pulmonary pressure that is greater in infants and at higher altitudes. There are no single values of oxygen saturation (SatO2) at altitude, because it decreases with the highest level of altitude, increases with age, and the gap between wakefulness and sleep is large (especially in the first months of life). Around 25% of healthy children living at altitude have SatO2 values significantly lower than the remaining 75%. The normal values of the apnea/hypopnea indices are different from those at sea level. High altitude pulmonary edema is a frequent pathology that is produced by a disproportionate increase in VHP reflecting hyperactivity of the pulmonary vascular bed in the face of acute exposure to hypobaric hypoxia, it has four phenotypes, it is uncommon in children under 5 years of age, and it is rarely fatal, the clinical suspicion and timely management with oxygen is the key. Finally, at high altitude, the normal values of lung function from spirometry, impulse oscillometry, and diffusing capacity are different from those at sea level.


Subject(s)
Humans , Child , Adolescent , Pulmonary Edema/physiopathology , Altitude , Altitude Sickness/physiopathology , Respiratory Function Tests , Oxygen Saturation , Hypoxia/physiopathology
2.
Medicentro (Villa Clara) ; 26(3): 583-597, jul.-set. 2022. graf
Article in Spanish | LILACS | ID: biblio-1405658

ABSTRACT

RESUMEN Introducción: Las infecciones cutáneas por Staphylococcus aureus, se presentan con alta frecuencia en la comunidad. La forma superficial de esta es la foliculitis. Una extensión hacia el tejido subcutáneo da como resultado la formación de una lesión supurativa local llamada forúnculo. Aproximadamente el 20 % de los pacientes con forúnculo presentan una o más recidivas durante el año siguiente, y cierto número presenta forunculosis recidivante crónica durante meses o años. Objetivo: Conocer el comportamiento de los niveles de IgE y las subclases de IgG expresadas en pacientes y controles, para inferir el patrón de la respuesta inmune a la infección. Métodos: Se realizó un estudio prospectivo donde se determinaron las subclases de inmunoglobulina G (IgG) y los niveles de inmunoglobulina E (IgE) en suero de 25 enfermos con lesiones cutáneas por Staphylococcus aureus, y 25 controles sanos, provenientes del banco de sangre. Se elaboró un antígeno (Bacterina de Staphylococcus aureus) y en su enfrentamiento se procedió con la metodología de normalización y validación de ensayos inmunoenzimáticos para cuantificar IgG humana. Los resultados se expresaron en densidades ópticas y gráficamente como la relación matemática (IgG1/3) para Th1 e (IgE/IgG4) para Th2, en el suero de los pacientes. Resultados: Se obtuvo respuesta IgG1 e IgG4 en pacientes y controles y respuesta IgE anti Staphylococcus aureus en pacientes. Conclusiones: Como Staphylococcus aureus es flora normal de la piel, los controles ya han tenido contacto con él, lo que provoca el desarrollo de respuesta Th1 (IgG1) y anticuerpos bloqueadores (IgG4). Contrariamente, los enfermos desarrollan respuesta Th2 (IgE) y la infección.


ABSTRACT Introduction: Staphylococcus aureus skin infections occur with high frequency in the community. Folliculitis is its superficial form. An extension into the subcutaneous tissue results in the formation of a local suppurative lesion known as a furunculosis. Approximately 20% of patients with a furuncle have one or more recurrences over the next year, and a certain number have chronic relapsing furunculosis for months or years. Objective: to know the manifestation of IgE levels and IgG subclasses expressed in patients and controls, to infer the pattern of the immune response to infection. Methods: we conducted a prospective study where immunoglobulin G (IgG) subclasses and immunoglobulin E (IgE) levels were determined in serum of 25 ill patients with Staphylococcus aureus skin lesions, and 25 healthy controls, from the blood bank. An antigen (Staphylococcus aureus bacterin) was elaborated and in its confrontation, the normalization and validation methodology of immunoenzymatic assays to quantify human IgG was carried out. The results were expressed in optical densities and graphically as the mathematical ratio (IgG1/3) for Th1 and (IgE/IgG4) for Th2, in the serum of the patients. Results: IgG1 and IgG4 responses were obtained in patients and controls, and anti-Staphylococcus aureus IgE responses in patients. Conclusions: the controls have already had contact with Staphylococcus aureus, as it is normal flora of the skin, which causes the development of Th1 response (IgG1) and antibodies blockers (IgG4). On the contrary, ill patients develop a Th2 response (IgE) and the infection.


Subject(s)
Furunculosis/immunology , Immunoglobulin G
3.
Adv Rheumatol ; 61: 2, 2021. tab, graf
Article in English | LILACS | ID: biblio-1152742

ABSTRACT

Abstract Large epidemiologic and clinical estimates of spondyloarthritis (SpA) in Latin America are not available. In this narrative review, our goal was to descriptively summarize the prevalence and features of SpA in Latin America, based on available small studies. A review of peer-reviewed literature identified 41 relevant publications. Of these, 11 (mostly based on Mexican data) estimated the prevalence of SpA and its subtypes, which varied from 0.28 to 0.9% (SpA), 0.02 to 0.8% (ankylosing spondylitis), 0.2 to 0.9% (axial SpA), and 0.004 to 0.08% (psoriatic arthritis). Demographic and/or clinical characteristics were reported in 31 of the 41 publications, deriving data from 3 multinational studies, as well as individual studies from Argentina, Brazil, Chile, Colombia, Costa Rica, Mexico, Peru, Uruguay, and Venezuela. Data relating to treatment, disease manifestations (articular and extra-articular), and comorbidities were summarized across the countries. Available data suggest that there is a variability in prevalence, manifestations, and comorbidities of SpA across Latin America. Basic epidemiologic and clinical data are required from several countries not currently represented. Data relating to current treatment approaches, patient outcomes, and socioeconomic impact within this large geographic region are also needed.(AU)


Subject(s)
Humans , Spondylarthritis/epidemiology , Prognosis , Spondylitis, Ankylosing/epidemiology , Arthritis, Psoriatic/epidemiology , Demography , Prevalence , Risk Factors , Latin America/epidemiology
4.
J. pediatr. (Rio J.) ; 95(supl.1): S10-S22, 2019. tab
Article in English | LILACS | ID: biblio-1002480

ABSTRACT

Abstract Objectives: To assess the impact of asthma and its treatment (inhaled corticosteroids and other control medications) on growth. Data sources: The authors searched PubMed (up to August 24, 2018) and screened the reference lists of retrieved articles. Systematic reviews and meta-analysis were selected. If there was no such article, the authors selected either randomized clinical trials or observational studies. Data synthesis: A total of 37 articles were included in this review. The findings from 21 studies suggest that asthma per se, especially more severe and/or uncontrolled cases, can transitorily impair child's growth. Two Cochrane reviews of randomized clinical trials showed a small mean reduction in linear growth (-0.91 cm/year for beclomethasone, -0.59 cm/year for budesonide, and -0.39 cm/year for fluticasone) in the first year of treatment with inhaled corticosteroids in prepubertal children with persistent asthma. The effects were likely to be molecule- and dose-dependent. A recent review showed that most of "real-life" observational studies had not found significant effects of inhaled corticosteroids on growth in asthmatic children. Fifteen studies showed that the maintenance systemic corticosteroids could cause a dose-dependent growth suppression in children with severe asthma, but other controllers (cromones, montelukast, salmeterol, and theophylline) had no significant adverse effects no growth. Conclusions: Severe and/or uncontrolled asthma can transitorily impair child's growth. Regular use of inhaled corticosteroids may cause a small reduction in linear growth in children with asthma, but the well-established benefits of inhaled corticosteroids in controlling asthma outweigh the potential adverse effects on growth. Use of the minimally effective dose of inhaled corticosteroids and regular monitoring of child's height during inhaled corticosteroids therapy are recommended.


Resumo Objetivos: Avaliar o impacto da asma e seu tratamento (corticosteroides inalados e outros medicamentos de controle) no crescimento. Fontes de dados: Uma busca foi feita no PubMed (até 24 de agosto de 2018) e foram triadas as listas de referência dos artigos recuperados. Revisões sistemáticas e metanálises foram selecionadas. Se não houvesse tal artigo, ensaios clínicos randomizados ou estudos observacionais eram selecionados. Síntese dos dados: Trinta e sete artigos foram incluídos nesta revisão. Os achados de 21 estudos sugerem que a asma por si só, especialmente os casos mais graves e/ou descontrolados, podem prejudicar o crescimento da criança. Duas revisões Cochrane de ensaios clínicos randomizados mostraram uma pequena redução média no crescimento linear (−0,91 cm/ano para beclometasona, −0,59 cm/ano para budesonida e −0,39 cm/ano para fluticasona) no primeiro ano de tratamento com corticosteroides inalados em crianças pré-púberes com asma persistente. Os efeitos pareciam ter efeito dose- e molécula-dependente. Uma revisão recente mostrou que a maioria dos estudos observacionais da "vida real" não encontrou efeitos significativos dos corticosteroides inalados no crescimento de crianças asmáticas. Quinze estudos mostraram que a manutenção de corticosteroides sistêmicos poderia causar uma supressão do crescimento dose-dependente em crianças com asma grave, mas outros controladores (cromonas, montelucaste, salmeterol e teofilina) não tiveram efeitos adversos significativos no crescimento. Conclusões: A asma grave e/ou descontrolada pode prejudicar o crescimento da criança. O uso regular de corticosteroides inalados pode causar uma pequena redução no crescimento linear em crianças com asma, mas os benefícios bem estabelecidos dos corticosteroides inalados no controle da asma superam os potenciais efeitos adversos no crescimento. Recomenda-se o uso de doses minimamente eficazes de corticosteroides inalados e o monitoramento regular da altura da criança durante a terapia com corticosteroides inalados.


Subject(s)
Humans , Child , Asthma/drug therapy , Adrenal Cortex Hormones/administration & dosage , Anti-Asthmatic Agents/adverse effects , Growth Disorders/chemically induced , Severity of Illness Index , Anti-Asthmatic Agents/administration & dosage , Evidence-Based Medicine
6.
Medisan ; 21(11)nov. 2017. tab
Article in Spanish | LILACS | ID: biblio-894574

ABSTRACT

Se realizó un estudio descriptivo y transversal de 30 pacientes con mediastinitis aguda por perforación esofágica, operados en el Hospital Provincial Docente Clinicoquirúrgico Saturnino Lora Torres de Santiago de Cuba, con vistas a caracterizarles desde los puntos de vista clínico, diagnóstico y quirúrgico, desde enero de 1990 hasta agosto de 2016. La incidencia de la enfermedad fue de 37,9 por cada 100 000 habitantes con predominio de los pacientes jóvenes, en los cuales la esofagoscopia terapéutica por cuerpo extraño de difícil extracción fue la causa más frecuente de la perforación torácica, acompañada de síntomas y signos de síndrome esofágico y de sepsis, asociada a la presencia de estafilococos y estreptococos. La tomografía computarizada constituyó el examen de mayor valor para el diagnóstico, en tanto, los diferentes hallazgos durante la intervención quirúrgica estuvieron en dependencia del grado de infección mediastinal. Se necesita un conocimiento exhaustivo de los antecedentes, la clínica y posibles resultados de los exámenes complementarios para asumir una conducta rápida y eficaz, a fin de lograr la disminución de la mortalidad por dicha afección


A descriptive and cross-sectional study of 30 patients with acute mediastinitis due to esophageal perforation, who were surgically intervened at Saturnino Lora Torres Teaching Clinical Surgical Provincial Hospital was carried out in Santiago de Cuba from January, 1990 to August, 2016, aimed at characterizing them from the clinical, diagnostic and surgical points of view. The incidence of the disease was 37.9 out of 100 000 inhabitants with the young patients prevalence, in which the therapeutic esophagoscopy due to strange body of difficult extraction was the most frequent cause in the thoracic perforation, accompanied by symptoms and signs of esophageal syndrome and sepsis, associated with the staphylococci and streptococci presence. The computerized axial tomography constituted the exam of more value for the diagnosis, as long as, the different findings during the surgical intervention were in dependence of the grade of mediastinal infection. An exhaustive knowledge of the history, clinic and possible results of the complementary exams is necessary to assume a quick and effective behaviour, in order to achieve the decrease of mortality due to this disorder


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Aged , Aged, 80 and over , Surgical Procedures, Operative , Morbidity , Esophageal Perforation/mortality , Mediastinitis/epidemiology , Secondary Care , Epidemiology, Descriptive , Cross-Sectional Studies , Foreign Bodies/complications , Mediastinitis
7.
Bol. méd. Hosp. Infant. Méx ; 73(6): 372-379, Nov.-Dec. 2016. tab, graf
Article in English | LILACS | ID: biblio-951255

ABSTRACT

Abstract: Iron is essential for cell growth and is imported into cells in part through the action of transferrin (Tf), a protein that binds its receptor (TfR1 or CD71) on the surface of a cell, and then releases iron into endosomes. TfR1 is a single pass type-II transmembrane protein expressed at basal levels in most tissues. High expression of TfR1 is typically associated with rapidly proliferating cells, including various types of cancer. TfR1 is targeted by experimental therapeutics for several reasons: its cell surface accessibility, constitutive endocytosis into cells, essential role in cell growth and proliferation, and its overexpression by cancer cells. Among the therapeutic agents used to target TfR1, antibodies stand out due to their remarkable specificity and affinity. Clinical trials are being conducted to evaluate the safety and efficacy of agents targeting TfR1 in cancer patients with promising results. These observations suggest that therapies targeting TfR1 as direct therapeutics or delivery conduits remain an attractive alternative for the treatment of cancers that overexpress the receptor.


Resumen: El hierro es esencial para el crecimiento celular. Es transportado dentro de las células con la ayuda de la transferrina (Tf), proteína que se une a su receptor (TfR1 o CD71) en la superficie celular y libera el hierro dentro de los endosomas. El TfR1 es una proteína de membrana tipo II que se sobreexpresa en muchos tejidos debido al requerimiento de las células para importar hierro unido a Tf. La sobreexpresión de TfR1 se ha asociado con células que proliferan rápidamente, incluyendo los diferentes tipos de cáncer. El TfR1 se ha empleado como blanco terapéutico por diversos motivos: su accesibilidad a la superficie celular, su capacidad de internalizarse constitutivamente en las células, su papel esencial en el crecimiento y la proliferación celular, así como por su sobreexpresión en las células tumorales proliferantes. Entre los agentes terapéuticos dirigidos contra el TfR1 destacan los anticuerpos, por su alta especificidad, estabilidad y propiedades estructurales. Se han realizado diversos ensayos clínicos para evaluar la seguridad y la eficacia de los anticuerpos que reconocen el TfR1 en pacientes con cáncer y se han obtenido resultados prometedores. Estas observaciones sugieren que las terapias con fundamento en el reconocimiento de TfR1, ya sea como terapia directa o empleados como acarreadores, representan una alternativa muy atractiva de tratamiento contra los diferentes tipos de cáncer que sobreexpresan este receptor.

8.
Rev. chil. pediatr ; 87(5): 335-342, oct. 2016. ilus, graf
Article in Spanish | LILACS | ID: biblio-830161

ABSTRACT

La evidencia indica que la exposición a diversas condiciones ambientales en etapas tempranas de la vida puede inducir alteraciones persistentes en el epigenoma. Los estudios epigenómicos en sujetos obesos han permitido evaluar el papel de los mecanismos epigenéticos en el origen y desarrollo de la obesidad. La presente revisión aborda estudios que dan cuenta de la asociación entre la obesidad y metilación global del genoma (ADN), analizando el potencial impacto de intervenciones previas y posteriores al nacimiento que afectan la metilación del ADN y la obesidad en etapas más avanzadas de la vida. Estudios realizados principalmente en leucocitos, han logrado identificar sitios del ADN diferencialmente metilados asociados con obesidad. Estudios hasta la fecha no han demostrado que dichos cambios en metilación sean revertidos luego de bajar de peso. Esto contrasta con resultados iniciales en este campo, que sugieren que existirían marcadores epigenéticos presentes desde el nacimiento que permitirían definir el riesgo de obesidad durante el curso de la vida. La evidencia actual sugiere que algunas marcas epigenéticas son modificables, basándonos en la exposición en la vida intrauterina y también por los hábitos dietarios y de actividad fisica durante las etapas del crecimiento y en la adultez. Esto sugiere que existe la oportunidad de intervenir durante la gestación o en la vida posnatal temprana, que modificaría los perfiles epigenéticos desfavorables e idealmente contribuiría a prevenir la obesidad en los sujetos o poblaciones susceptibles.


Current evidence supports the notion that exposure to various environmental conditions in early life may induce permanent changes in the epigenome that persist throughout the life-course. This article focuses on early changes associated with obesity in adult life. A review is presented on the factors that induce changes in whole genome (DNA) methylation in early life that are associated with adult onset obesity and related disorders. In contrast, reversal of epigenetic changes associated with weight loss in obese subjects has not been demonstrated. This contrasts with well-established associations found between obesity related DNA methylation patterns at birth and adult onset obesity and diabetes. Epigenetic markers may serve to screen indivuals at risk for obesity and assess the effects of interventions in early life that may delay or prevent obesity in early life. This might contribute to lower the obesity-related burden of death and disability at the population level. The available evidence indicates that epigenetic marks are in fact modifiable, based on modifications in the intrauterine environment and changes in food intake, physical activity and dietary patterns patterns during pregnancy and early years of adult life. This offers the opportunity to intervene before conception, during pregnancy, infancy, childhood, and also in later life. There must be documentation on the best preventive actions in terms of diet and physical activity that will modify or revert the adverse epigenetic markers, thus preventing obesity and diabetes in suceptible individuals and populations.


Subject(s)
Humans , Adult , Epigenesis, Genetic , Diabetes Mellitus, Type 2/epidemiology , Obesity/epidemiology , Exercise/physiology , Weight Loss/physiology , DNA Methylation , Diabetes Mellitus, Type 2/genetics , Diabetes Mellitus, Type 2/prevention & control , Diet , Eating/physiology , Obesity/genetics , Obesity/prevention & control
9.
Comunidad salud ; 14(1): 41-51, jun. 2016. ilus
Article in Spanish | LILACS | ID: biblio-828628

ABSTRACT

Chikungunya en la mujer embarazada constituye un estado nosológico que pone en peligro la vida materno-infantil durante el periodo perinatal. Con el objetivo de determinar el perfil clínico epidemiológico de embarazadas con Chikungunya bajo vigilancia epidemiológica, se realizo un estudio descriptivo y epidemiológico retrospectivo con una muestra de fichas epidemiológicas de 100 embarazadas con Chikungunya durante el segundo semestre del año 2014.Los datos obtenidos fueron procesados y analizados utilizando medidas de tendencia central, porcentajes e intervalos de confianza. Los resultados indican un promedio de 27 años de edad, siendo el eje Metropolitano de la ciudad de Maracay el de mayor incidencia con 86% de los casos de la entidad federal. El promedio del tiempo de embarazo fue entre las semanas 36 y 40 en 30% de ellas. La red pública representó 53% de las referencias. Las manifestaciones clínicas incluyen fiebre 94%, artralgias 84%, cefalea 75%, erupción cutánea 64%, náuseas y vómitos 45% y 43% respectivamente y disminución sustancial del hematocrito. En la evolución de las gestantes con Chikungunya no se encontró un comportamiento distinto al de la triada clínica de la enfermedad. Se evidenció un buen control prenatal con un estándar normal de 6 controles prenatales. Un bajo porcentaje de las embarazadas ingresó a la unidad de cuidados intensivos. Las complicaciones más frecuentes fueron la preeclamsia grave y la amenaza de parto pretérmino. El mal llenado de las fichas e historias clínicas impidió conocer con detalle los avances significativos en la toma de decisiones con respecto a la enfermedad.


Chikungunya in pregnant women is a nosological state that endangers life maternal and child during the perinatal period. In order to determine the clinical and epidemiological profile of pregnant women with Chikungunya under epidemiological surveillance, descriptive and retrospective epidemiological study with a sample of 100 pregnant epidemiological chips with Chikungunya was conducted during the second half of the year 2014.Los data were processed and analyzed using measures of central tendency, percentages and confidence intervals. The results indicate an average of 27 years of age, being the Metropolitan axis of the city of Maracay the highest incidence with 86% of cases the federal entity. The average length of pregnancy was between weeks 36 and 40 in 30% of them. The public network represented 53% of the references. Clinical manifestations include fever 94%, arthralgia 84%, headache 75%, 64% rash, nausea and vomiting 45% and 43% respectively and substantially decreased hematocrit. In the evolution of pregnant women with Chikungunya a different triad clinical behavior of the disease was found. good prenatal care with a normal standard 6 prenatal visits was evident. A low percentage of pregnant entered the intensive care unit. The most frequent complications were severe preeclampsia and preterm labor. The poor completion of clinical histories and files kept detailed knowledge significant advances in making decisions regarding the disease.

10.
Rev. chil. pediatr ; 87(2): 88-95, abr. 2016. ilus
Article in Spanish | LILACS | ID: lil-783489

ABSTRACT

Las enfermedades alérgicas y el asma son el resultado de complejas interacciones entre la predisposición genética y factores ambientales. El asma es una de las enfermedades crónicas más prevalentes en niños. En este artículo se revisan algunos factores ambientales como la exposición a alérgenos, tabaco, bacterias, componentes microbianos, dieta, obesidad y estrés, que intervienen durante la vida intrauterina y la infancia en la regulación epigenética de las enfermedades alérgicas y el asma. La revisión se realiza en tres tipos de modelos: in-vitro, animales y humanos.


Allergic diseases and asthma are the result of complex interactions between genetic predisposition and environmental factors. Asthma is one of the most prevalent chronic disease among children. In this article we review some environmental factors like: allergen exposition, tobacco, bacteria, microbial components, diet, obesity and stress, which influences during intrauterine and infancy life in the epigenetic regulation of asthma and allergic diseases. The review has been done in three models: in-vitro, animal and human.


Subject(s)
Humans , Animals , Child , Asthma/etiology , Epigenesis, Genetic , Hypersensitivity/etiology , Asthma/genetics , Risk Factors , Genetic Predisposition to Disease , Environment , Hypersensitivity/genetics
11.
Rev. chil. pediatr ; 87(1): 4-10, feb. 2016. ilus, tab
Article in Spanish | LILACS | ID: lil-779467

ABSTRACT

La asociación entre factores ambientales presentes durante el desarrollo embrionario/fetal y enfermedades que puedan presentarse durante la vida representa un campo de creciente interés. En este contexto la evidencia actual apoya fuertemente que alteraciones en el crecimiento intrauterino y durante los primeros años de vida presentan una fuerte influencia en el riesgo de padecer enfermedades crónicas que en muchos casos pudiera ser mayor que la carga genética del paciente. La persistencia y reproducibilidad de los fenotipos asociados a alteraciones en el desarrollo temprano sugieren la participación de mecanismos moleculares que registran dichas modificaciones (i.e. mecanismos epigenéticos) generando una «reprogramación¼ celular y fisiológica. Esta revisión es la introducción a una serie de 5 artículos en torno a la participación de los mecanismos epigenéticos en el desarrollo de enfermedades crónicas (i.e. cardiovasculares, metabólicas, asma/alergias y cáncer) y su relación con el origen de dichas enfermedades en etapas tempranas del desarrollo. El objetivo de esta serie es mostrar el estado actual de esta área de la investigación y presentar los desafíos e interrogantes futuros en los cuales la pediatría tiene un papel preponderante, desarrollando estrategias para la prevención, detección precoz y seguimiento.


Current evidence supports the notion that alterations in intrauterine growth and during the first years of life have a substantial effect on the risk for the development of chronic disease, which in some cases is even higher than those due to genetic factors. The persistence and reproducibility of the phenotypes associated with altered early development suggest the participation of mechanisms that would record environmental cues, generating a cellular reprogramming (i.e. epigenetic mechanisms). This review is an introduction to a series of five articles focused on the participation of epigenetic mechanisms in the development of highly prevalent chronic diseases (i.e. cardiovascular, metabolic, asthma/allergies and cancer) and their origins in the foetal and neonatal period. This series of articles aims to show the state of the art in this research area and present the upcoming clues and challenges, in which paediatricians have a prominent role, developing strategies for the prevention, early detection and follow-up.


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Infant , Epigenesis, Genetic/genetics , Fetal Development/genetics , Pediatricians/organization & administration , Physician's Role , Chronic Disease , Reproducibility of Results , Genetic Predisposition to Disease
12.
Estud. psicol. (Natal) ; 20(1): 12-21, jan.-mar. 2015. tab
Article in Portuguese | LILACS | ID: lil-755073

ABSTRACT

A adolescência é uma fase desenvolvimental marcada por desafios. No sentido de conhecer melhor as estratégias que os adolescentes utilizam para lidar com o stress, pretendeu-se com este estudo apresentar as propriedades psicométricas da Escala de Estratégias de Coping na Adolescência (Burnett & Fanshawe, 1997), testada junto de uma amostra de adolescentes portugueses, explorando diferenças em função do género e da idade. Os resultados permitiram encontrar uma estrutura factorial válida e com consistência interna genericamente adequada. Os dados permitem perceber diferenças nas estratégias de coping, com as moças a procurar mais apoio dos outros e melhoria pessoal, enquanto os rapazes utilizam mais frequentemente drogas ou o humor. Em função da idade verificouse uma relação positiva com o uso de substâncias e diminuição da procura de apoio da família e de profissionais. Os dados são discutidos à luz da literatura e implicações para a prática são apresentadas.


Adolescence is a developmental period marked by challenges. In order to better understand the strategies that adolescents use to cope with stress, it is intended with this study to present the psychometric properties of the Adolescent Coping Strategies Scale (Fanshawe & Burnett, 1997), tested with a sample of Portuguese adolescents, exploring differences by gender and age. The results allowed to find a valid and generally adequate internal consistency factor structure. The data allow to discern differences in coping strategies, with the girls to seek more support from others and personal improvement, while boys more often use of drugs or humor. We found a positive relationship between age and substance use and decreased demand for support from family and professionals. The data are discussed according to literature and implications for practice are presented.


La adolescencia es un periodo de desarrollo marcado por los desafíos. En el presente estudio se presentan las propiedades psicométricas de la Escala de Estrategias de Afrontamiento en la Adolescencia (Fanshawe y Burnett, 1997) con el fin de comprender mejor las estrategias que utilizan los adolescentes para hacer frente al estrés. El instrumento ha sido probado en una muestra de adolescentes portugueses, explorando las diferencias por sexo y edad. Los resultados permitieron encontrar una estructura factorial con una consistencia interna válida y adecuada. Los datos permiten discernir las diferencias en las estrategias de supervivencia, donde las chicas tienden a buscar más apoyo de los demás y la mejora personal, mientras que los chicos emplean más a menudo el consumo de drogas o el demanda del humor. Dependiendo de la edad se verifica una relación con el consumo de sustancias y la disminución de la demanda de apoyo familiar y profesional. Los datos se analizan en base a la literatura y se presentan las implicaciones para la práctica.


Subject(s)
Humans , Male , Female , Adolescent , Psychometrics , Stress, Physiological , Adolescent
13.
Arch. argent. pediatr ; 111(2): 0-0, Apr. 2013. ilus
Article in Spanish | LILACS | ID: lil-671997

ABSTRACT

La tos crónica es un síntoma de diversos procesos patológicos de origen respiratorio o extrarrespiratorio, con impacto negativo en la calidad de vida del niño y su familia. El pediatra debe guiar su acción en busca del diagnóstico etiológico. Una cuidadosa historia clínica es clave para el diagnóstico y una guía para solicitar los estudios complementarios necesarios para la detección de las causas definitivas. La exacta identificación etiológica de la tos crónica debe ser seguida de un tratamiento específico. El abordaje sintomático con antitusivos y mucolíticos es excepcionalmente necesario y debería reservarse para algunas situaciones de tos inespecífica sin causa aparente.


Chronic cough is a symptom of various respiratory and non-respiratory conditions with negative impact on quality of life of children and their families. The pediatricians should focus their efforts in search for etiological diagnosis. A careful medical history and physical examination are the mainstays of diagnosis and guidance to further studies that may contribute to detection of final causes. The etiological identification of chronic cough must be followed by specific treatment. The symptomatic approach with antitussives and mucolytic drugs is exceptionally necessary and should be considered for some situations of nonspecific cough without any specific disease association.


Subject(s)
Child , Humans , Cough/diagnosis , Cough/therapy , Algorithms , Chronic Disease , Cough/etiology
14.
MedUNAB ; 15(1): 63-67, 2012.
Article in Spanish | LILACS | ID: biblio-998565

ABSTRACT

La urticaria pigmentosa es una de las formas más comunes de las mastocitosis, las cuales corresponden a una serie de procesos caracterizados por un aumento anormal de los mastocitos en diversos órganos y tejidos corporales. En la urticaria pigmentosa la manifestación es exclusiva de la piel, caracterizada por la presencia de lesiones maculopapulares de 2.5 a 5 mm de diámetro, de un color que puede oscilar entre rojo y café, distribuyéndose generalmente en tronco y extremidades respetando palmas y plantas. Cerca de la mitad de los lesiones presenta rubor localizado, prurito y ampollas. Su incidencia y prevalencia son desconocidas; sin embargo, su aparición es más común en niños que en adultos. El diagnóstico depende en gran manera de un adecuado examen físico complementado con estudios de laboratorio e histopatología. El tratamiento de elección constituye la administración de antihistamínicos orales. [Ávila JA, Cala JC, Gelvis JA, Torres V, Mosquera H. Urticaria pigmentosa en el adulto. MedUNAB 2012; 15:63-67].


Urticaria pigmentosa is one of the most common forms of mastocytosis, which correspond to a series of processes characterized by an abnormal increase of mast cells in different organs and tissues. Urticaria pigmentosa has an unique manifestation in the skin, characterized by maculopapular lesions 2.5 to 5 mm in diameter, of a color that can range from red and brown, usually distributed on the trunk and limbs respecting the palms and soles. Half of the lesions presented blush on a specific site, pruritus and blisters. The incidence and prevalence are unknown but their appearance is more common in children than in adults. Diagnosis depends on an properly physical examination with laboratory test and histopathological analysis. The treatment of choice is the administration of oral antihistamines. [Ávila JA, Cala JC, Gelvis JA, Torres V, Mosquera H. Urticaria pigmentosa in adult. MedUNAB 2012; 15:63-67].


Subject(s)
Urticaria Pigmentosa , Mastocytosis , Adult , Mastocytosis, Cutaneous
17.
Rev. méd. Chile ; 137(11): 1457-1462, nov. 2009. tab, graf
Article in Spanish | LILACS | ID: lil-537008

ABSTRACT

Background: Cardiac dyssynchrony is common in advanced heart failure (HF), but the changes in cardiac synchrony after myocardial infarction (MI) have not been adequately descríbed. Aim: To study the relationship between cardiac synchrony and left ventricular remodeling after acute myocardial infarction. Material and methods: Forty nine patients aged 59±10 years (77 percent men) with a first episode of a ST segment elevation MI, were studied. Scintigraphic left ventricular function and synchrony analyses were performed at baseline and after a six months follow-up. Determinations were compared with 33 healthy subjects. Results: At baseline, patients with MIhad a decreased left ventricular ejection fraction (LVEF) and significant dyssynchrony, when compared with controls. LVEF was 36.4 percent±10 percent, left ventricular end-diastolic volume (LVEDV) 127±38 mL, interventricular delay (IEV) 29±35 miliseconds (ms), and intraventricular delay (IAV), 234±89 ms. After 6 months, LVEF significantly improved (38 percent±10 percent, p =0.042) without significant changes in LVEDV (129±32 mL, p =0.97), IEV (24±17, p =0.96) or IAV (231±97, p =0.34). At baseline there were significant correlations between IAV and LVEF, and between IAV and LVEDV (r =0.48, p =0.001 and r =0.41, p =0.004, respectively). These correlations remained significant after 6 months. There was a positive correlation between IAV and LVEDV changes at six months (r =0.403, p =0.04). Conclusions: The development of cardiac dyssynchrony correlates with adverse left ventricular remodeling after MI.


Subject(s)
Female , Humans , Male , Middle Aged , Myocardial Infarction/complications , Ventricular Dysfunction, Left/etiology , Ventricular Remodeling/physiology , Epidemiologic Methods , Myocardial Infarction/physiopathology , Stroke Volume/physiology , Ventricular Dysfunction, Left/pathology , Ventricular Dysfunction, Left/physiopathology , Ventricular Dysfunction, Left
18.
Neumol. pediátr ; 4(supl): 37-51, 2009. tab, graf
Article in Spanish | LILACS | ID: lil-640053

ABSTRACT

La bronquiolitis obliterante (BO) es un síndrome clínico poco frecuente en niños, caracterizado por la obstrucción crónica al flujo de aire asociado a cambios inflamatorios y distintos grados de fibrosis en la vía aérea pequeña. Si bien existen muchas etiologías, la causa mas frecuente se asocia a infeccionesrespiratorias virales, principalmente adenovirus. No existe un consenso para establecer su diagnóstico; sin embargo, se considera un espectro de síntomas persistentes asociados a un patrón en mosaico, bronquiectasias y atelectasias persistentes. El rol de la biopsia pulmonar ha sido cuestionado por subajo rendimiento, invasividad y complicaciones. No existe un tratamiento específico por lo que elmanejo es soporte. Probablemente la mejor estrategia constituya el empleo de antibióticos en forma agresiva, soporte kinésico y nutricional constante y una precoz rehabilitación pulmonar. Estas guías clínicas representan un esfuerzo multidisciplinario, basado en evidencias actuales para brindarherramientas prácticas para el diagnóstico y cuidado de niños y adolescentes con BO post infecciosa.


Subject(s)
Humans , Adolescent , Child , Bronchiolitis Obliterans/diagnosis , Bronchiolitis Obliterans/therapy , Pulmonary Medicine/standards , Bronchiolitis Obliterans/etiology , Bacterial Infections/complications , Virus Diseases/complications
19.
Rev. méd. Chile ; 135(11): 1456-1462, nov. 2007. graf, tab
Article in Spanish | LILACS | ID: lil-472846

ABSTRACT

Hypokalemia (serum K+ < 3.5 mEq/1) is a potentially serious adverse effect of diuretic ingestión. We report a 27 year-old woman admitted with muscle weakness, a serum potassium of 2.0 mEq/1, metabolic alkalosis and EKG abnormalities simulating cardiac ischemia, that reverted with potassium chloride administration. She admitted high dose furosemide self-medication for edema. Glomerular filtration rate, tubular sodium reabsortion, potassium secretion, the renin-aldosterone system, total body water distribution and capillary permeability, were studied sequentially until 90 days after her admission. There was hyperactivity of the renin-aldosterone axis, reduction in extracellular and intracellular volumes, normal capillary permeability and high sodium tubular reabsorption, probably explained by a "rebound" salt retention associated with her decreased extracellular volume.


Subject(s)
Adult , Female , Humans , Diuretics/adverse effects , Furosemide/adverse effects , Hypokalemia/chemically induced , Hypovolemia/chemically induced , Self Medication/adverse effects , Edema/drug therapy , Electrocardiography/drug effects , Potassium Chloride/therapeutic use
20.
Rev. venez. cir. ortop. traumatol ; 38(1): 13-17, jun. 2006. ilus, tab
Article in Spanish | LILACS | ID: lil-513410

ABSTRACT

El presente trabajo tiene como objetivo revisar las historias clínicas de todos los pacientes intervenidos quirúrgicamente de prótesis de cadera, en un período de 5 años para determinar que prótesis se complicaron con fracturas periprotésicas; obteniéndose un total de 190 pacientes; de las cuales 12 tuvieron fracturas alrededor de la prótesis, 03 casos intraoperatorios. 05 ocurrieron en prótesis total y 7 en prótesis parcial. Los 12 casos se presentaron en prótesis cementadas. Todas las fracturas ocurrieron alrededor del vástago femoral y fueron clasificadas según la región anatómica comprometida en: Tipo 1 Proximal: 03 casos, Tipo T1 Medio: 05 casos, Tipo III Distal: 04 casos, prótesis de tallo largo: 04 casos, cerclaje:03 casos, placa BMP: 1 caso.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged, 80 and over , Hip Fractures/surgery , Hip Fractures/pathology , Hip Prosthesis , Arthroplasty, Replacement, Hip/methods , Orthopedics , Traumatology
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