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1.
Rev Neurol ; 70(9): 323-328, 2020 05 01.
Artículo en Español | MEDLINE | ID: mdl-32329045

RESUMEN

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-CoV-2. 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.


TITLE: Herramientas de salud digital para superar la brecha de atención en epilepsia antes, durante y después de la pandemia de COVID-19.Introducción. La epilepsia es un trastorno neurológico crónico común que afecta 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-CoV-2. 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, telelectroencefalografía 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.


Asunto(s)
Infecciones por Coronavirus/epidemiología , Epilepsia/terapia , Aplicaciones Móviles , Pandemias , Atención al Paciente/métodos , Neumonía Viral/epidemiología , Telemedicina , Betacoronavirus , COVID-19 , Infecciones por Coronavirus/complicaciones , Atención a la Salud/tendencias , Humanos , Atención al Paciente/tendencias , Neumonía Viral/complicaciones , Cuarentena , SARS-CoV-2
2.
Neurologia (Engl Ed) ; 35(1): 1-9, 2020.
Artículo en Inglés, Español | MEDLINE | ID: mdl-28863828

RESUMEN

INTRODUCTION: Patients with temporal lobe epilepsy (TLE) perform poorly on semantic verbal fluency (SVF) tasks. Completing these tasks successfully involves multiple cognitive processes simultaneously. Therefore, quantitative analysis of SVF (number of correct words in one minute), conducted in most studies, has been found to be insufficient to identify cognitive dysfunction underlying SVF difficulties in TLE. OBJECTIVES: To determine whether a sample of patients with TLE had SVF difficulties compared with a control group (CG), and to identify the cognitive components associated with SVF difficulties using quantitative and qualitative analysis. METHODS: SVF was evaluated in 25 patients with TLE and 24 healthy controls; the semantic verbal fluency test included 5 semantic categories: animals, fruits, occupations, countries, and verbs. All 5 categories were analysed quantitatively (number of correct words per minute and interval of execution: 0-15, 16-30, 31-45, and 46-60seconds); the categories animals and fruits were also analysed qualitatively (clusters, cluster size, switches, perseverations, and intrusions). RESULTS: Patients generated fewer words for all categories and intervals and fewer clusters and switches for animals and fruits than the CG (P<.01). Differences between groups were not significant in terms of cluster size and number of intrusions and perseverations (P>.05). CONCLUSIONS: Our results suggest an association between SVF difficulties in TLE and difficulty activating semantic networks, impaired strategic search, and poor cognitive flexibility. Attention, inhibition, and working memory are preserved in these patients.


Asunto(s)
Epilepsia del Lóbulo Temporal/fisiopatología , Semántica , Conducta Verbal/fisiología , Adulto , Femenino , Humanos , Masculino , México , Análisis y Desempeño de Tareas
3.
Rev Neurol ; 65(6): 268-279, 2017 Sep 16.
Artículo en Español | MEDLINE | ID: mdl-28896001

RESUMEN

Drug-resistant epilepsy, a chronic condition with long-term consequences can be treated with surgery. The efficacy and safety of surgery for temporal lobe epilepsy have been established through a large number of retrospective and prospective cohort studies and two randomized controlled clinical trials. Despite the excellent outcomes reported after surgery, the literature suggests that this procedure is an underutilized treatment. While evidence is lacking as to why epilepsy surgery is underused, cited reasons include: failure of primary care physicians and neurologists to provide information and identify patients who could be referred for surgery; different levels of technology at various centers, resulting in different candidate selection strategies; the belief that epilepsy surgery is a risky procedure and that it should be only viewed as the last option; patient preference to avoid surgery; parents wanting to wait until their child is old enough to participate in the decision-making process regarding surgery; unwillingness of insurers to cover the expenses associated with presurgical evaluations or lack of insurance; racial and social disparities, among others. In this paper we review the available epidemiological data about lack of utilization of epilepsy surgery.


TITLE: Barreras de acceso a la cirugia de la epilepsia: revision de la bibliografia.La epilepsia farmacorresistente es una condicion cronica con consecuencias a largo plazo que puede ser tratada quirurgicamente. La eficacia y la seguridad de la cirugia de la epilepsia del lobulo temporal se han establecido a traves de un gran numero de estudios de cohorte retrospectivos y prospectivos y dos ensayos clinicos controlados aleatorizados. A pesar de los excelentes resultados comunicados con la cirugia, la bibliografia sugiere que este procedimiento es un tratamiento subutilizado. Aunque no existe evidencia de esto, entre algunos de los motivos descritos se apuntan el fallo de los medicos de atencion primaria y los neurologos en proveer informacion, identificar y remitir a los pacientes a un centro de cirugia; los diferentes niveles de tecnologia en los centros, lo que provoca distintas estrategias de seleccion de los candidatos; la creencia de que la cirugia de la epilepsia es un procedimiento arriesgado que deberia contemplarse solo como ultima opcion; la preferencia del paciente por evitar la cirugia; el deseo de los padres de esperar hasta que sus hijos sean lo suficientemente mayores para participar en el proceso de toma de decisiones; el hecho de que las aseguradoras no cubran los gastos asociados con las evaluaciones prequirurgicas o la carencia de un seguro medico, y la desigualdad racial y social, entre otros. En este articulo se revisan los datos epidemiologicos disponibles en relacion con la falta de acceso a la cirugia de la epilepsia.


Asunto(s)
Lobectomía Temporal Anterior , Epilepsia Refractaria/cirugía , Epilepsia del Lóbulo Temporal/cirugía , Accesibilidad a los Servicios de Salud , Humanos , Resultado del Tratamiento
4.
Rev Neurol ; 63(4): 165-75, 2016 Aug 16.
Artículo en Español | MEDLINE | ID: mdl-27439486

RESUMEN

Epileptic seizures are one of the main reasons for neurological visits in an emergency department. Convulsions represent a traumatic event for the patient and the family, with significant medical and social consequences. Due to their prevalence and impact, the initial management is of vital importance. Although following the first epileptic seizure, early recurrence diminishes after establishing treatment with antiepileptic drugs, the forecast for developing epilepsy and long-term outcomes are not altered by any early intervention. Detailed questioning based on the symptoms of the convulsions, the patient's medical history and a full electroencephalogram and neuroimaging study make it possible to define the risk of recurrence of the seizure and the possible diagnosis of epilepsy. Epileptic abnormalities, the presence of old or new potentially epileptogenic brain lesions, as well as nocturnal seizures, increase the risk of recurrence. Physicians must assess each patient on an individual basis to determine the most suitable treatment, and explain the risk of not being treated versus the risk that exists if treatment with antiepileptic drugs is established.


TITLE: Diagnostico y tratamiento de la crisis epileptica unica no provocada.Las crisis epilepticas son una de las principales causas de consulta neurologica en el servicio de urgencias. Un episodio convulsivo representa un evento traumatico para el paciente y la familia, con consecuencias medicas y sociales significativas. Por su prevalencia e impacto, el abordaje inicial es de vital importancia. Si bien despues de una primera crisis epileptica la recurrencia temprana disminuye con el inicio de farmacos antiepilepticos, el pronostico para el desarrollo de epilepsia y los desenlaces a largo plazo no se alteran por ninguna intervencion temprana. El interrogatorio detallado basado en la semiologia del episodio, los antecedentes del paciente y un estudio completo con electroencefalograma y neuroimagen permiten definir el riesgo de recurrencia de la crisis y el posible diagnostico de epilepsia. Las anormalidades epilepticas, la presencia de lesiones cerebrales con potencial epileptogeno antiguas o nuevas, asi como las crisis nocturnas, incrementan el riesgo de recurrencia. Los medicos deben evaluar a cada paciente de manera individual para determinar un tratamiento idoneo, explicando el riesgo de no tratar frente al riesgo existente con el inicio de farmacos antiepilepticos.


Asunto(s)
Epilepsia/diagnóstico , Epilepsia/terapia , Convulsiones/diagnóstico , Convulsiones/terapia , Anticonvulsivantes/uso terapéutico , Electroencefalografía , Humanos , Recurrencia
5.
Pharmacogenomics J ; 16(3): 286-92, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-26122019

RESUMEN

We aimed to explore the possible influence of CYP2C9 (*2, *3 and IVS8-109 A>T), CYP2C19 (*2, *3 and *17) and ABCB1 (1236C>T, 2677G>A/T and 3435C>T) on phenytoin (PHT) plasma concentrations in 64 Mexican Mestizo (MM) patients with epilepsy currently treated with PHT in mono- (n=25) and polytherapy (n=39). Genotype and allele frequencies of these variants were also estimated in 300 MM healthy volunteers. Linear regression models were used to assess associations between the dependent variables (PHT plasma concentration and dose-corrected PHT concentration) with independent variables (CYP2C9, CYP2C19 and ABCB1 genotypes, ABCB1 haplotypes, age, sex, weight, and polytherapy). In multivariate models, CYP2C9 IVS8-109 T was significantly associated with higher PHT plasma concentrations (t(64)=2.27; P=0.03). Moreover, this allele was more frequent in the supratherapeutic group as compared with the subtherapeutic group (0.13 versus 0.03, respectively; P=0.05, Fisher's exact test). Results suggest that CYP2C9 IVS8-109 T allele may decrease CYP2C9 enzymatic activity on PHT. More research is needed to confirm findings.


Asunto(s)
Anticonvulsivantes/sangre , Citocromo P-450 CYP2C19/genética , Citocromo P-450 CYP2C9/genética , Epilepsia/tratamiento farmacológico , Epilepsia/genética , Variantes Farmacogenómicas/genética , Fenitoína/sangre , Subfamilia B de Transportador de Casetes de Unión a ATP/genética , Subfamilia B de Transportador de Casetes de Unión a ATP/metabolismo , Adolescente , Adulto , Anciano , Anticonvulsivantes/administración & dosificación , Estudios de Casos y Controles , Distribución de Chi-Cuadrado , Citocromo P-450 CYP2C19/metabolismo , Citocromo P-450 CYP2C9/metabolismo , Monitoreo de Drogas , Epilepsia/sangre , Epilepsia/etnología , Femenino , Frecuencia de los Genes , Estudios de Asociación Genética , Genotipo , Humanos , Modelos Lineales , Masculino , México/epidemiología , Persona de Mediana Edad , Análisis Multivariante , Fenotipo , Fenitoína/administración & dosificación , Factores de Riesgo , Resultado del Tratamiento , Adulto Joven
6.
Epilepsy Behav ; 23(1): 52-6, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22154515

RESUMEN

Depression has a high prevalence among patients with temporal lobe epilepsy (TLE). A pilot study was carried out to evaluate group cognitive-behavioral therapy (CBT) as a treatment for depression in patients with TLE. Twenty-three outpatients with TLE and major depressive disorder, according to DSM-IV criteria, were enrolled and divided into two groups to receive 16 weekly sessions of CBT. The primary outcome measures were depression severity (assessed with the Beck Depression Inventory) and quality of life (measured with the Quality of Life in Epilepsy-31). Sixteen patients (70%) completed at least 80% of the sessions. From week 8, CBT had a significant positive effect on severity of depression that lasted until the end of treatment. A significant improvement in quality of life was also observed. CBT seems to be a useful intervention for treating depression and improving quality of life in patients with TLE.


Asunto(s)
Terapia Cognitivo-Conductual/métodos , Depresión/etiología , Depresión/rehabilitación , Epilepsia del Lóbulo Temporal/complicaciones , Adolescente , Adulto , Electroencefalografía , Epilepsia del Lóbulo Temporal/psicología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pruebas Neuropsicológicas , Proyectos Piloto , Escalas de Valoración Psiquiátrica , Calidad de Vida , Estadísticas no Paramétricas , Resultado del Tratamiento , Grabación de Cinta de Video , Adulto Joven
7.
Neurology ; 70(22 Pt 2): 2137-44, 2008 May 27.
Artículo en Inglés | MEDLINE | ID: mdl-18505993

RESUMEN

BACKGROUND: Juvenile myoclonic epilepsy (JME) accounts for 3 to 12% of all epilepsies. In 2004, the GENESS Consortium demonstrated four missense mutations in Myoclonin1/EFHC1 of chromosome 6p12.1 segregating in 20% of Hispanic families with JME. OBJECTIVE: To examine what percentage of consecutive JME clinic cases have mutations in Myoclonin1/EFHC1. METHODS: We screened 44 consecutive patients from Mexico and Honduras and 67 patients from Japan using heteroduplex analysis and direct sequencing. RESULTS: We found five novel mutations in transcripts A and B of Myoclonin1/EFHC1. Two novel heterozygous missense mutations (c.755C>A and c.1523C>G) in transcript A occurred in both a singleton from Mexico and another singleton from Japan. A deletion/frameshift (C.789del.AV264fsx280) in transcript B was present in a mother and daughter from Mexico. A nonsense mutation (c.829C>T) in transcript B segregated in four clinically and seven epileptiform-EEG affected members of a large Honduran family. The same nonsense mutation (c.829C>T) occurred as a de novo mutation in a sporadic case. Finally, we found a three-base deletion (-364--362del.GAT) in the promoter region in a family from Japan. CONCLUSION: Nine percent of consecutive juvenile myoclonic epilepsy cases from Mexico and Honduras clinics and 3% of clinic patients from Japan carry mutations in Myoclonin1/EFCH1. These results represent the highest number and percentage of mutations found for a juvenile myoclonic epilepsy causing gene of any population group.


Asunto(s)
Proteínas de Unión al Calcio/genética , Salud de la Familia , Mutación , Epilepsia Mioclónica Juvenil/genética , Canales de Cloruro CLC-2 , Canales de Cloruro/genética , Análisis Mutacional de ADN/métodos , Femenino , Genotipo , Honduras/epidemiología , Humanos , Japón , Masculino , México/epidemiología , Epilepsia Mioclónica Juvenil/epidemiología , Fenotipo , Regiones Promotoras Genéticas , Receptores de GABA-A/genética
8.
Neuropsychiatr Dis Treat ; 4(6): 1235-9, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19337463

RESUMEN

Different factors have been related with interictal anxiety, reported in 10%-25% of patients with epilepsy. We determined the frequency of interictal anxiety in 196 patients with active epilepsy in a cross-sectional survey to know which symptoms of anxiety were most frequently reported in patients with epilepsy and to analyze the factors associated with their presence. Patients were assessed with the Beck Depression Inventory (BDI), Montgomery-Asberg Depression Rating Scale (MADRS), and the Hamilton Anxiety Scale (HAMA). Data were analyzed with a logistic regression model. The HAMA ratings revealed that 38.8% experienced significant anxiety symptoms, as defined by a rating above 18 points. Use of primidone, depression, cryptogenic, and posttraumatic etiologies significantly predicted anxiety after logistic regression. Symptoms related to higher scores on HAMA were anxious mood, tension, insomnia, intellectual function, depressed mood, cardiovascular and genitourinary symptoms. Further studies should be performed to define the role of psychosocial factors in the development and evolution of anxiety among these patients.

9.
Childs Nerv Syst ; 23(8): 917-20, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17450365

RESUMEN

OBJECTS: To show the clinical results of a corpus callosotomy (CC) treatment using conformal stereotactic radiosurgery (SRS) on a patient with medically intractable multifocal epilepsy. MATERIALS AND METHODS: A 17-year-old male patient underwent corpus callosotomy conformal SRS using a dedicated linear accelerator (linac) with dynamic arcs technique. The prescribed dose was 36.0 Gy at the periphery of the rostrum, genu, and a half of the body of the corpus callosum (CCA). At 8 months after conformal SRS, the patient developed a significant brain edema and moderate transitory motor deficit, which were controlled with steroids. After 32 months follow-up, there is an improvement of 84% on drop attacks and generalized tonic-clonic seizures. CONCLUSIONS: Conformal SRS for corpus callosotomy with a single isocenter reproduce the results reported on literature using Gamma Knife-based SRS. The results show that this technique is safe and demonstrate its efficacy to control seizures.


Asunto(s)
Cuerpo Calloso/cirugía , Radiocirugia , Radioterapia Conformacional , Adolescente , Anticonvulsivantes/uso terapéutico , Edema Encefálico/etiología , Edema Encefálico/patología , Edema Encefálico/terapia , Cuerpo Calloso/patología , Resistencia a Medicamentos , Electroencefalografía , Epilepsia/cirugía , Humanos , Imagen por Resonancia Magnética , Masculino , Paresia/etiología , Aceleradores de Partículas , Complicaciones Posoperatorias/patología , Complicaciones Posoperatorias/terapia , Tomografía Computarizada por Rayos X
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