Estrés laboral y estilos de afrontamiento en tiempos de pandemia en trabajadores de una empresa de telecomunicaciones de Lima, 2021

Diversos estudios han demostrado los efectos negativos del estrés laboral sobre la salud física y mental de la población económicamente activa, también se indica que si no es tratada a tiempo puede desencadenar en trastornos psicosomáticos graves y severos; por tal motivo, el objetivo del trabajo fue determinar la relación que existe entre el estrés laboral y los estilos de afrontamiento en tiempos de pandemia en un grupo de trabajadores de una empresa de telecomunicaciones de la ciudad de Lima, 2021. El trabajo se enmarcó dentro del enfoque cuantitativo, de tipo básico, nivel correlacional y diseño no experimental de corte transversal correlacional. Los instrumentos utilizados para la recolección de datos fueron: la Escala de Estrés Laboral OIT–OMS y el Cuestionario de Modos de Afrontamiento al Estrés COPE; se trabajó con una muestra de 80 personas adultas entre varones y mujeres, quienes fueron asignados mediante el tipo de muestreo censal. Los resultados indican una prevalencia del nivel bajo de estrés laboral, la estrategia de afrontamiento prevalente es la denominada Reinterpretación positiva y crecimiento, la estrategia menos utilizada es la postergación del afrontamiento. Como conclusión general se observa que no existe relación significativa entre las variables estrés laboral y los estilos de afrontamiento en un grupo de trabajadores de una empresa de telecomunicaciones de la ciudad de Lima, 2021. Por la relevancia de los resultados del presente estudio se sugiere que la universidad publique a través de los canales de comunicación pertinentes

Neuromyelitis optica: a challenging diagnosis at secondary hospital

Known since the 19th century, neuromyelitis optica (NMO), or Devic’s disease, is an idiopathic immune-mediated inflammatory demyelinating disease of the central nervous system selectively affecting the optic nerve and spinal cord. Commonly diagnosed in demyelinating diseases reference centers, we report an 18-year-old female patient who sought medical attention with a 3-month history of weight loss, headache, and vomiting, followed by diplopia, a burning sensation over the lower limbs, and difficulty walking. A few days prior to hospital admission, the muscle strength in her lower limbs became worse and ascended to the upper limbs associated with sensory changes in the trunk and voiding dysfunction. At admission, the neurological examination was consistent with a spinal cord syndrome. After few days of hospitalization, she was tetraplegic with severe signs of brainstem involvement requiring mechanical ventilatory support. Intravenous methylprednisolone and cyclophosphamide were promptly started after ruling out the diagnosis of infectious disease and cord compression. Due to no substantial early improvement, intravenous immunoglobulin was also used. From then on, the neurological status gradually improved. Magnetic resonance imaging showed extensive demyelinating features in the spinal cord, and the serum IgG autoantibody was negative. The patient was referred to a tertiary neurological reference center where she remains under treatment

Adult-onset opsoclonus-myoclonus-ataxia syndrome as a manifestation of brazilian lyme disease-like syndrome: a case report and review of literature

Described in 1962, the opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare, neurologically debilitating disorder with distinct characteristics that may begin in childhood or adult life. Although many cases remain without etiological diagnosis, others are related to neoplasms and infectious diseases. We report a 41-year-old previously healthy male with an 8-day history of headache, vertigo, nausea, vomiting, and nystagmus. After a normal brain computed tomography and lymphocytic pleocytosis in cerebral spinal fluid (CSF), intravenous acyclovir therapy was initiated in the emergency room. On the third day of hospitalization, the diagnosis of OMAS was made based on the presence of chaotic and irregular eye movements, dysarthric speech, gait instability, generalized tremor, and myoclonic jerks. In the face of his neurological worsening, ampicillin followed by nonspecific immunotherapy (methylprednisolone and intravenous immunoglobulin) was prescribed, with mild clinical improvement. After a thorough laboratory workup, the definite diagnosis of neuroborreliosis was established and ceftriaxone (4 g/daily/3wks) and doxycycline (200 mg/day/2 mo) was administered. Toward the end of the ceftriaxone regimen, the neurologic signs substantially improved. We believe this to be the first case description of OMAS as clinical presentation of Brazilian Lyme disease-like syndrome (Baggio-Yoshinari syndrome)

ANÁLISE DAS DISSERTAÇÕES DE MESTRADO EM SERVIÇO SOCIAL DA UNESP/FRANCA

Neste artigo temos por objetivo compreender como a temática família foi estudada nas dissertações de mestrado do programa de Pós Graduação em Serviço Social na UNESP Franca, entre os anos de 2004 a 2013. Buscamos analisar como  cada pesquisador dialogou com a temática, quais as principais contribuições da pesquisa para a sociedade e quais reflexões nos proporcionaram. Procuramos compreender como a família está caracterizada e como está configurada no século XXI a partir das leituras das dissertações defendidas nesse período

Do Saber ao Criar: experiências tecnoromanas na Villa de Milreu

O programa DiVaM pretende contribuir para destacar a importância das comunidades locais na valorização do património cultural, indo ao encontro dos princípios da “Convenção de Faro”, pois tenta promover o património cultural como factor de aproximação, de diálogo, de coesão social e de uma cidadania cada vez mais inclusiva. O Centro Ciência Viva do Algarve, no âmbito deste programa, levou “experiências” às ruínas de Milreu pelo quarto ano consecutivo, tendo-se considerado imperativo dedicar pela primeira vez um dia inteiro ao público escolar. A presente comunicação visa dar a conhecer as atividades desenvolvidas.info:eu-repo/semantics/publishedVersio

Comparison of seven prognostic tools to identify low-risk pulmonary embolism in patients aged <50 years

publishersversionPeer reviewe

Mucopolysaccharidosis I, II, and VI: Brief review and guidelines for treatment

Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosomal enzymes involved in the glycosaminoglycan (GAG) breakdown pathway. This metabolic block leads to the accumulation of GAG in various organs and tissues of the affected patients, resulting in a multisystemic clinical picture, sometimes including cognitive impairment. Until the beginning of the XXI century, treatment was mainly supportive. Bone marrow transplantation improved the natural course of the disease in some types of MPS, but the morbidity and mortality restricted its use to selected cases. The identification of the genes involved, the new molecular biology tools and the availability of animal models made it possible to develop specific enzyme replacement therapies (ERT) for these diseases. At present, a great number of Brazilian medical centers from all regions of the country have experience with ERT for MPS I, II, and VI, acquired not only through patient treatment but also in clinical trials. Taking the three types of MPS together, over 200 patients have been treated with ERT in our country. This document summarizes the experience of the professionals involved, along with the data available in the international literature, bringing together and harmonizing the information available on the management of these severe and progressive diseases, thus disclosing new prospects for Brazilian patients affected by these conditions

Nucleases as a barrier to gene silencing in the cotton boll weevil, Anthonomus grandis.

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Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

Background: Approximately 450 000 children are born with familial hypercholesterolaemia worldwide every year, yet only 2·1% of adults with familial hypercholesterolaemia were diagnosed before age 18 years via current diagnostic approaches, which are derived from observations in adults. We aimed to characterise children and adolescents with heterozygous familial hypercholesterolaemia (HeFH) and understand current approaches to the identification and management of familial hypercholesterolaemia to inform future public health strategies. Methods: For this cross-sectional study, we assessed children and adolescents younger than 18 years with a clinical or genetic diagnosis of HeFH at the time of entry into the Familial Hypercholesterolaemia Studies Collaboration (FHSC) registry between Oct 1, 2015, and Jan 31, 2021. Data in the registry were collected from 55 regional or national registries in 48 countries. Diagnoses relying on self-reported history of familial hypercholesterolaemia and suspected secondary hypercholesterolaemia were excluded from the registry; people with untreated LDL cholesterol (LDL-C) of at least 13·0 mmol/L were excluded from this study. Data were assessed overall and by WHO region, World Bank country income status, age, diagnostic criteria, and index-case status. The main outcome of this study was to assess current identification and management of children and adolescents with familial hypercholesterolaemia. Findings: Of 63 093 individuals in the FHSC registry, 11 848 (18·8%) were children or adolescents younger than 18 years with HeFH and were included in this study; 5756 (50·2%) of 11 476 included individuals were female and 5720 (49·8%) were male. Sex data were missing for 372 (3·1%) of 11 848 individuals. Median age at registry entry was 9·6 years (IQR 5·8-13·2). 10 099 (89·9%) of 11 235 included individuals had a final genetically confirmed diagnosis of familial hypercholesterolaemia and 1136 (10·1%) had a clinical diagnosis. Genetically confirmed diagnosis data or clinical diagnosis data were missing for 613 (5·2%) of 11 848 individuals. Genetic diagnosis was more common in children and adolescents from high-income countries (9427 [92·4%] of 10 202) than in children and adolescents from non-high-income countries (199 [48·0%] of 415). 3414 (31·6%) of 10 804 children or adolescents were index cases. Familial-hypercholesterolaemia-related physical signs, cardiovascular risk factors, and cardiovascular disease were uncommon, but were more common in non-high-income countries. 7557 (72·4%) of 10 428 included children or adolescents were not taking lipid-lowering medication (LLM) and had a median LDL-C of 5·00 mmol/L (IQR 4·05-6·08). Compared with genetic diagnosis, the use of unadapted clinical criteria intended for use in adults and reliant on more extreme phenotypes could result in 50-75% of children and adolescents with familial hypercholesterolaemia not being identified. Interpretation: Clinical characteristics observed in adults with familial hypercholesterolaemia are uncommon in children and adolescents with familial hypercholesterolaemia, hence detection in this age group relies on measurement of LDL-C and genetic confirmation. Where genetic testing is unavailable, increased availability and use of LDL-C measurements in the first few years of life could help reduce the current gap between prevalence and detection, enabling increased use of combination LLM to reach recommended LDL-C targets early in life