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1.
Neurol Sci ; 2023 Oct 25.
Artigo em Inglês | MEDLINE | ID: mdl-37875597

RESUMO

Juvenile myoclonic epilepsy (JME) is the most common of the generalized genetic epilepsies, with multiple causal and susceptibility genes; however, its etiopathogenesis is mainly unknown. The toxic effects caused by xenobiotics in cells occur during their metabolic transformation, mainly by enzymes belonging to cytochrome P450. The elimination of these compounds by transporters of the ABC type protects the central nervous system, but their accumulation causes neuronal damage, resulting in neurological diseases. The present study has sought the association between single nucleotide genetic variants of the CYP2C9, CYP2C19, and ABCB1 genes and the development of JME in patients compared to healthy controls. The CC1236 and GG2677 genotypes of ABCB1 in women; allele G 2677, genotypes GG 2677 and CC 3435 in men; the CYP2C19*2A allele, and the CYP2C19*3G/A genotype in both sexes were found to be risk factors for JME. Furthermore, carriers of the TTGGCC genotype combination of the ABCB1 gene (1236/2677/3435) have a 10.5 times higher risk of developing JME than non-carriers. Using the STRING database, we found an interaction between the proteins encoded by these genes and other possible proteins. These findings indicate that the CYP450 system and ABC transporters could interact with other genes in the JME.

3.
Clin Epidemiol Glob Health ; 15: 101059, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35574431

RESUMO

Background: Inflammatory markers are pivotal for the diagnosis of coronavirus disease 2019 (COVID-19) and sepsis. This study compared markers between hospitalised patients with COVID-19 and those with bacterial sepsis. Methods: This retrospective single-centre cohort study included 50 patients with COVID-19 clinical stages II and III and 24 patients with bacterial sepsis. Both groups were treated according to the country's official standards. Leukocytes, C-reactive protein (CRP), ferritin, and D-dimer were registered at the time of patient's admission and 24, 48, and 72 h after initiating intrahospital treatment. Results: Upon admission, marker levels were high, with a significant decrease at 72 h after antibiotic therapy in the sepsis group. The leukocyte count was higher in deceased patients with sepsis. The mean ferritin levels were 1105 mcg/dl for COVID-19 and 525 mcg/dL for sepsis. Higher ferritin levels in COVID-19 (P = 0.001) seemed to be a predictor of higher mortality. Upon admission, the median D-dimer level was 0.68 mg/L for COVID-19 and 3 mg/L for patients with sepsis, whether recovered or deceased. As D-dimer, procalcitonin levels were higher in patients with sepsis (P = 0.001). CRP levels were equally elevated in both entities but higher in deceased patients with COVID-19. Conclusion: Ferritin was the main inflammatory marker for COVID-19, and leukocytes, procalcitonin, and D-dimer were the main markers of sepsis. Markers that were most affected in deceased patients were CRP for COVID-19 and leukocyte for sepsis. The therapeutic implications of these differences require further study.

5.
Rev. cienc. forenses Honduras (En línea) ; 8(1): 17-25, 2022. ilus., tab., map., graf.
Artigo em Espanhol | LILACS, BIMENA | ID: biblio-1399994

RESUMO

Introducción: El rol de la mujer en el área científica ha crecido con el paso de los años, pero aún persiste una gran brecha de género en ciencia. Para conocer y manejar esa brecha, es necesario hacer un mapeo de la situación de las mujeres investigadoras en Honduras. Objetivo: Describir la participación y contribuciones de las investigadoras hondureñas en la producción científica nacional según su perfil en Google Académico. Metodología: Se usó Power BI para analizar las variables sexo, institución, índice H, número de citaciones, número de publicaciones, año de la primera publicación, y áreas de investigación registradas en su perfil, utilizando la versión 2 del Ranking de Investigadores Hondureños según su Perfil de Google Académico disponible en https://bit.ly/38s6YuT, el cual es un registro depurado. Resultados: El 35% de todos los perfiles eran de mujeres, 41% vinculadas a las ciencias médicas y de la salud y en su mayoría (92%), afiliadas a universidades. Pese al creciente número de mujeres investigadoras registradas en Google Académico, el crecimiento no es simétrico respecto a los hombres. Solamente el 3.1% de las investigadoras tenía un índice H que supera los dos dígitos. Conclusión: A pesar de los avances, se mantiene la inequidad de género entre investigadores hondureños según la data de Google Académico. Se requiere de políticas públicas e institucionales, para corregir esa brecha...(AU)


Assuntos
Humanos , Feminino , Armazenamento e Recuperação da Informação , Ferramenta de Busca/métodos , Ferramenta de Busca , Papel de Gênero
9.
Artigo em Inglês | PAHO-IRIS | ID: phr-54462

RESUMO

To the Editor:To date, there have been around 178 million confirmed SARS CoV-2 infections, and more than 3 million deaths worldwide. The global war against COVID-19 has been fought mainly in three battlegrounds: the hospitals, the communities, and in the minds of people. As populations around the globe still struggle to establish or keep the public health strategies needed, they also face an infodemic, especially regarding vaccines.All vaccines can have rare adverse events, but during the pandemic, the report of isolated cases of blood clots associated to two of the anti-COVID vaccines that use adenovirus as a viral vector (AZD1222 and Johnson & Johnson) have raised concerns in the population, as well as emergency reviews, safety signals, and vaccination pauses. [...]


Assuntos
Trombose , COVID-19 , Vacinas contra COVID-19 , Coronavirus , Infecções por Coronavirus , Betacoronavirus , Vacinas , Vacinação
11.
J Public Health (Oxf) ; 43(2): e297-e298, 2021 06 07.
Artigo em Inglês | MEDLINE | ID: mdl-33512491

RESUMO

A recently published article of this journal stated that informatics solutions can guide better public health decision-making during the COVID 19 (Coronavirus Disease 2019) pandemic. Honduras is a country facing the COVID-19 pandemic with a weak health surveillance system while also fighting a dengue epidemic and the aftermath of two hurricanes that struck its territory in November 2020. In response, we as academics started a COVID-19 and Dengue Observatory combining several technological platforms and developing multidisciplinary research to help the country navigate the crisis. Mapping the pandemic and the natural disasters showed us that technology can be applied toward epidemiology to benefit communities in a time of need by quickly building a basic digital health surveillance system for Honduras.


Assuntos
COVID-19 , Tempestades Ciclônicas , Dengue , Dengue/epidemiologia , Honduras/epidemiologia , Humanos , Pandemias , SARS-CoV-2
13.
Rev. cienc. forenses Honduras (En línea) ; 7(1): 40-49, 2021. graf., tab
Artigo em Espanhol | LILACS, BIMENA | ID: biblio-1284617

RESUMO

Justificación: la webometría se ha usado para medir la actividad y visibilidad científica en los países. Objetivo: construir un ranking de investigadores hondureños según las citaciones en sus perfiles de Google Académico y su afiliación institucional. Metodología: se realizó una búsqueda sobre publicaciones científicas de investigadores e instituciones académicas e independientes de Honduras registradas en Google Académico. La información se organizó en Microsoft Excel y se analizó con la herramienta Tableau, con la cual también se creó un tablero interactivo para acceso público, mostrando frecuencias, porcentajes y promedios de las citaciones de los investigadores y otros criterios. Resultados: el 72% (110/151) de los investigadores con perfiles disponibles eran hombres; la Universidad Nacional Autónoma de Honduras lideró el porcentaje de investigadores con el 55.6% (84/151), seguida por la Universidad Tecnológica Centroamericana con el 13.9% (21/151) y la Escuela Agrícola Panamericana con el 12.6% (19/151). Los investigadores de la Escuela Agrícola Panamericana mostraron el mayor promedio de citaciones por investigador (390), seguida por los investigadores de la Universidad Nacional Autónoma de Honduras (179) y los de la Universidad Tecnológica Centroamericana (177). Los investigadores en los primeros 20 lugares, clasificados con el índice H, también pertenecían a estas universidades. Las disciplinas más frecuentemente reportadas por los investigadores fueron las ciencias sociales (27.2%), de la salud (22.53%), agrícolas (9.32%) y las naturales (8.6%). Conclusiones: el mayor número de investigadores con perfiles en Google Académico pertenecían a la Universidad Nacional Autónoma de Honduras, pero los investigadores de dos universidades privadas tuvieron un promedio de citación por autor casi igual o mayor a los de dicha institución. El tablero público de ranking de investigadores hondureños https://tabsoft.co/3wK3vym, puede orientar estrategias de visibilidad de los científicos del país...(AU)


Assuntos
Bibliometria , Indicadores de Produção Científica , Publicação Periódica , Bases de Dados de Citações
14.
Rev. neurol. (Ed. impr.) ; 70(9): 323-328, 1 mayo, 2020. graf, ilus, tab
Artigo em Espanhol | IBECS | ID: ibc-188036

RESUMO

INTRODUCCIÓN: La epilepsia es un trastorno neurológico crónico común que afecta a alrededor de 50 millones de personas en el mundo y abunda la bibliografía sobre la brecha de atención en salud a este sector de la población. Dicha brecha aumentará con la pandemia actual de COVID-19. OBJETIVO: Evaluar la disponibilidad actual de herramientas de salud digital para la atención a personas con epilepsia según la literatura médica mundial y su uso durante dicha pandemia. Desarrollo. Se hizo una revisión de las publicaciones en revistas científicas en la última década que tuvieran como tema principal el uso de herramientas de salud digital o telemedicina enfocada a la atención de los pacientes con epilepsia, incluyendo cuatro meses después de las cuarentenas nacionales por la aparición del virus SARS-CoV2. Se encontraron 17 publicaciones sobre el uso de telemedicina enfocada a la epilepsia. Las herramientas más utilizadas internacionalmente son las plataformas en línea, seguidas de las aplicaciones móviles, videoconferencias, sistemas de captación de crisis epilépticas, listas de verificación, algoritmos de comprensión de datos médicos, llamadas telefónicas, teleelectroencefalografía y mensajes de texto. Ninguna se publicó durante la presente pandemia. CONCLUSIONES: Hay poca bibliografía sobre herramientas de salud digital enfocadas a epilepsia, pero existen varias que pueden emplearse para luchar contra la brecha de atención, especialmente en esta pandemia mundial de COVID-19 que obliga a las personas y comunidades a mantenerse en cuarentena por la emergencia sanitaria. Es necesario eliminar barreras y facilitar el pronto acceso de los pacientes a estas nuevas tecnologías de información


INTRODUCTION: Epilepsy is a common chronic neurological disorder that affects around 50 million worldwide and there is an abundance of literature on the health care gap for this sector of the population. This gap will increase with the current pandemic due to COVID-19. AIM: To evaluate the current availability of digital health tools for the care of people with epilepsy according to the world medical literature and their use during said pandemic. Development. We reviewed the publications in scientific journals in the last decade that had as their main topic the use of digital health tools or telemedicine focused on the care of patients with epilepsy, including 4 months after the national quarantines due to the appearance of the virus SARS-CoV2. Seventeen publications were found on the use of telemedicine focused on epilepsy. The most widely used tools internationally are online platforms, followed by mobile applications, videoconferences, epileptic seizure capture systems, checklists, algorithms for understanding medical data, phone calls, tele-encephalography and text messages. None was published during the COVID-19 current pandemic. CONCLUSIONS: Although there is little literature on the use of digital health tools focused on epilepsy, there are several that can be used to fight the attention gap, especially in this global pandemic by COVID-19 that forces quarantines of people and communities for long periods. It is necessary to remove barriers and facilitate patient access to these new information technologies


Assuntos
Humanos , Infecções por Coronavirus/epidemiologia , Pneumonia Viral/epidemiologia , Betacoronavirus , Pandemias , Necessidades e Demandas de Serviços de Saúde , Acesso aos Serviços de Saúde/tendências , Epilepsia/terapia , Telemedicina/métodos , Telemedicina/tendências
15.
Rev. ecuat. neurol ; 28(1): 47-55, ene.-abr. 2019. tab, graf
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1013990

RESUMO

Resumen La circunferencia cefálica (CC) es una medición que detecta alteraciones del crecimiento adecuado del cerebro. Las curvas de CC más utilizadas mundialmente son las propuestas por los CDC, NCHS y OMS. A pesar de las críticas sobre la metodología para crearlas, se han hecho actualizaciones para corregir inconsistencias. Esto ha servido para detectar y tratar oportunamente problemas de tamaño craneal tanto en los extremos pequeños (microcefalia) o grandes (macrocefalia). Algunos autores opinan que existe la necesidad de contar con curvas regionales para mejorar el valor diagnóstico de éstas en cada población. Otros, como Kenton Holden y colaboradores, han propuesto nuevas curvas que consolidan diferentes bases de datos con el objetivo de reducir el riesgo de errores en el diagnóstico de microcefalia o macrocefalia leve. Es necesario estudiar cuál es el patrón de crecimiento craneal normal de niños/as latinoamericanos por cada región o país, así como conocer las diferencias interétnicas.


Abstract The cephalic circumference (CC) is a measurement that detects alterations in the proper growth of the brain. CC curves most used worldwide are those proposed by the CDC, NCHS and WHO. Despite criticism of the methodology used to create them, updates have been made to correct inconsistencies, and that has helped to detect and treat on time problems of cranial size at both the small (microcephaly) and large (macrocephaly) ends. Several authors have suggested that regional reference curves should be made, and others, like Kenton Holden and colleagues, have proposed new curves that consolidate different databases, aiming to reduce the risk of errors in the diagnosis of microcephaly or mild macrocephaly. It is necessary to study what the normal cranial growth pattern of Latin American children is for each region or country, as well as to determine the interethnic differences.

16.
Rev. ecuat. neurol ; 27(3): 63-68, sep.-dic. 2018. tab, graf
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1004047

RESUMO

RESUMEN El complejo esclerosis tuberosa (CET) es una enfermedad neurocutánea infrecuente y subdiagnosticada en zonas remotas donde usualmente no hay neurólogos disponibles. Una niña de 22 meses fue llevada a una clínica en una comunidad rural por un cuadro de epilepsia refractaria de causa no determinada, de inicio a los 18 meses de edad con episodios de oculogiros y espasmos epilépticos en extensión. Además presentaba angiofibromas perinasales y lesiones hipomelanóticas en tronco. El encefalograma interictal hecho en la comunidad mostraba actividad epiléptica multifocal y generalizada. La niña había sido llevada a la ciudad para una resonancia cerebral, la cual reveló hiperintensidades subcorticales multifocales y nódulos subependimarios. Por teleconsulta entre médicos de la comunidad y especialistas nacionales e internacionales se diagnosticó CET atípico con espasmos epilépticos de inicio tardío. Se sugirió tratamiento que logró control de las crisis y se estableció un plan de seguimiento. El caso muestra que las unidades de telemedicina en zonas rurales son una opción tecnológica para brindar acceso a atención especializada de las epilepsias.


ABSTRACT Tuberous sclerosis complex (TSC) is an uncommon neurocutaneous disease often underdiagnosed in remote areas where specialists in neurology are usually not available. A 22 month-old girl was taken to a clinic in a rural village presenting refractory epilepsy of undetermined cause that started at 18 months of age with upward eye deviation episodes and epileptic extensor spasms. She also presented perinasal angiofibromas and hypomelanotic skin lesions in trunk. The interictal encephalogram done in the community showed multifocal and generalized epileptic activity. The girl had been taken to the city for a brain magnetic resonance, which revealed multifocal subcortical hyperintensities and subependymal nodules. By teleconsult between community doctors and national and international specialists, atypical TSC with late onset epileptic spasms was diagnosed. The recommended treatment resulted in controlled seizures, and a follow-up plan was established. This case illustrates that telemedicine units in rural areas are a technological option to provide access to specialized epilepsy care.

17.
N Engl J Med ; 378(11): 1018-1028, 2018 03 15.
Artigo em Inglês | MEDLINE | ID: mdl-29539279

RESUMO

BACKGROUND: In juvenile myoclonic epilepsy, data are limited on the genetic basis of networks promoting convulsions with diffuse polyspikes on electroencephalography (EEG) and the subtle microscopic brain dysplasia called microdysgenesis. METHODS: Using Sanger sequencing, we sequenced the exomes of six members of a large family affected with juvenile myoclonic epilepsy and confirmed cosegregation in all 37 family members. We screened an additional 310 patients with this disorder for variants on DNA melting-curve analysis and targeted real-time DNA sequencing of the gene encoding intestinal-cell kinase ( ICK). We calculated Bayesian logarithm of the odds (LOD) scores for cosegregating variants, odds ratios in case-control associations, and allele frequencies in the Genome Aggregation Database. We performed functional tests of the effects of variants on mitosis, apoptosis, and radial neuroblast migration in vitro and conducted video-EEG studies in mice lacking a copy of Ick. RESULTS: A variant, K305T (c.914A→C), cosegregated with epilepsy or polyspikes on EEG in 12 members of the family affected with juvenile myoclonic epilepsy. We identified 21 pathogenic ICK variants in 22 of 310 additional patients (7%). Four strongly linked variants (K220E, K305T, A615T, and R632X) impaired mitosis, cell-cycle exit, and radial neuroblast migration while promoting apoptosis. Tonic-clonic convulsions and polyspikes on EEG resembling seizures in human juvenile myoclonic epilepsy occurred more often in knockout heterozygous mice than in wild-type mice (P=0.02) during light sleep with isoflurane anesthesia. CONCLUSIONS: Our data provide evidence that heterozygous variants in ICK caused juvenile myoclonic epilepsy in 7% of the patients included in our analysis. Variant ICK affects cell processes that help explain microdysgenesis and polyspike networks observed on EEG in juvenile myoclonic epilepsy. (Funded by the National Institutes of Health and others.).


Assuntos
Mutação , Epilepsia Mioclônica Juvenil/genética , Proteínas Serina-Treonina Quinases/genética , Adolescente , Animais , Teorema de Bayes , Estudos de Casos e Controles , Criança , Pré-Escolar , Cromossomos Humanos Par 6 , Modelos Animais de Doenças , Eletroencefalografia , Feminino , Heterozigoto , Humanos , Lactente , Recém-Nascido , Masculino , Malformações do Desenvolvimento Cortical/genética , Camundongos , Camundongos Knockout , Epilepsia Mioclônica Juvenil/fisiopatologia , Análise de Sequência de DNA , Adulto Jovem
18.
Rev. méd. hondur ; 85(3/4): 81-86, jul.-dic. 2017. tab, graf
Artigo em Espanhol | LILACS | ID: biblio-970037

RESUMO

Antecedentes: El cáncer de mama (CM) es causa frecuente de morbimortalidad en todo el mundo y Honduras no es excepción. Se ha hecho muchos esfuerzos por promover la detección y tratamiento temprano. Objetivo: Determinar los conocimien-tos, actitudes y prácticas en mujeres sobre el CM y su detección y tratamiento oportuno. Pacientes y métodos: Se realizó un estudio transversal descriptivo durante el primer trimestre del 2017. Se entrevistó a 100 pacientes consecutivas en las consultas externas de medicina general y ginecología en el Centro de Salud San Miguel, Hospital San Felipe de Tegucigalpa, Hospital General Santa Teresa de Comayagua. Las variables evaluadas fueron sociodemográicas, conceptos sobre cáncer de mama, práctica y método del autoexamen de mama y actitudes respecto a la importancia y la promoción del autoexamen. RESULTADOS: Todas las personas encuestadas han escuchado de cáncer de mama, su diagnóstico y tratamiento, pero cerca de un cuarto de ellas tenían conceptos incompletos sobre la importancia y método del autoexamen, sobredimensionando la importancia de los métodos de imagen. El 91% de entrevistadas tenia entre 21 y 50 años de edad y 92% airmó que se practica el eautoexamen al menos una vez al año. El método de tratamiento más conocido fue la cirugía (78%). Las entrevistadas opinaron que los médicos promocionan poco el autoexamen. Conclusión: La educación sobre CM y autoexamen de mama debería actualizarse en Honduras en base a los conocimientos, acti-tudes y prácticas entre nuestras mujeres, según la medicina basada en evidencia. Se propone un estudio línea base multicéntrico.


Assuntos
Humanos , Feminino , Neoplasias da Mama/prevenção & controle , Conhecimentos, Atitudes e Prática em Saúde , Saúde Pública , Autoexame de Mama/métodos
19.
Rural Remote Health ; 17(2): 3965, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28564548

RESUMO

INTRODUCTION: Honduras is the second poorest country in Central America, and roughly 50% of the population lives in rural areas. A telehealth network linking these areas to larger health centers may improve patient access to care, and physician access to educational opportunities. This pilot study assessed the feasibility of establishing a pediatric telehealth network between underserved clinics in Honduras and the Medical University of South Carolina (MUSC). METHODS: Two underserved Honduran clinics were identified and invited to participate in the telehealth network. Providers from these clinics connected remotely to educational conferences at MUSC, and received teleconsults from MUSC physicians and physicians from the other Honduran site. Honduran providers completed five-point Likert scale satisfaction surveys following participation in the conferences and teleconsults. RESULTS: Survey feedback was positive, with 100% of respondents stating they would utilize telemedicine in the future. Dissatisfaction was expressed subjectively in the survey comments with regards to poor Internet connectivity and unreliable electrical power. CONCLUSIONS: The establishment of a telehealth network between Honduras and MUSC is feasible, and rural providers were receptive to the clinical and educational opportunities this network provides. Future projects will expand telehealth capabilities to other Honduran sites and focus on intra-country collaboration to ensure sustainability.


Assuntos
Serviços de Saúde Rural/organização & administração , Telemedicina/organização & administração , Atitude do Pessoal de Saúde , Educação Médica Continuada/organização & administração , Honduras , Humanos , Internet , Avaliação de Programas e Projetos de Saúde , South Carolina , Telemedicina/instrumentação
20.
Genet Med ; 19(2): 144-156, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-27467453

RESUMO

PURPOSE: EFHC1 variants are the most common mutations in inherited myoclonic and grand mal clonic-tonic-clonic (CTC) convulsions of juvenile myoclonic epilepsy (JME). We reanalyzed 54 EFHC1 variants associated with epilepsy from 17 cohorts based on National Human Genome Research Institute (NHGRI) and American College of Medical Genetics and Genomics (ACMG) guidelines for interpretation of sequence variants. METHODS: We calculated Bayesian LOD scores for variants in coinheritance, unconditional exact tests and odds ratios (OR) in case-control associations, allele frequencies in genome databases, and predictions for conservation/pathogenicity. We reviewed whether variants damage EFHC1 functions, whether efhc1-/- KO mice recapitulate CTC convulsions and "microdysgenesis" neuropathology, and whether supernumerary synaptic and dendritic phenotypes can be rescued in the fly model when EFHC1 is overexpressed. We rated strengths of evidence and applied ACMG combinatorial criteria for classifying variants. RESULTS: Nine variants were classified as "pathogenic," 14 as "likely pathogenic," 9 as "benign," and 2 as "likely benign." Twenty variants of unknown significance had an insufficient number of ancestry-matched controls, but ORs exceeded 5 when compared with racial/ethnic-matched Exome Aggregation Consortium (ExAC) controls. CONCLUSIONS: NHGRI gene-level evidence and variant-level evidence establish EFHC1 as the first non-ion channel microtubule-associated protein whose mutations disturb R-type VDCC and TRPM2 calcium currents in overgrown synapses and dendrites within abnormally migrated dislocated neurons, thus explaining CTC convulsions and "microdysgenesis" neuropathology of JME.Genet Med 19 2, 144-156.


Assuntos
Proteínas de Ligação ao Cálcio/genética , Epilepsia Mioclônica Juvenil/genética , Convulsões/genética , Animais , Dendritos/patologia , Exoma , Frequência do Gene , Humanos , Camundongos , Camundongos Knockout , Mutação , Epilepsia Mioclônica Juvenil/fisiopatologia , National Human Genome Research Institute (U.S.) , Neurônios/patologia , Linhagem , Polimorfismo de Nucleotídeo Único , Convulsões/fisiopatologia , Sinapses/patologia , Estados Unidos
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