Management of UWB picocell clusters : UCELLS project approach

International audienc

Gender, Age And Socio-Occupational Inequalities. Activa-Murcia Physical Activity Program

Este estudio ha recibido una ayuda en 2017 para la realización de Proyectos de Investigación Cuidados de Enfermería de la Fundación para la Formación e Investigación Sanitaria (FFIS) de la Región de Murcia. Número de Proyecto FFIS17/CE/01/02.[ES] El objetivo de este estudio fue describir las características diferenciales por sexo y edad en un Programa de actividad física (ACTIVA-Murcia) desde una perspectiva de género. Se realizó un estudio descriptivo mediante análisis secundario en 411 participantes de dos centros de salud de Murcia. El 62,3% fueron mujeres y el 71,8% tenían entre 45 y 64 años. Entre los hombres, el 57,8% estaban laboralmente activos y tenían una actividad física cuya mediana fue de 1.939,5 METs/semanales. Entre las mujeres, el 37,4% estaban activas laboralmente y realizaban una mediana de 1.386,0 METs/semanales. El motivo de ausencia a alguna sesión por enfermedad fue del 53,4% para las mujeres y el 30,4% para los hombres. Los profesionales deben considerar estas diferencias en la promoción de actividad física. [EN] The objective of this study was to describe the differential characteristics by sex and age in a physical activity Program (ACTIVA-Murcia) from a gender perspective. A descriptive study by secondary analysis was conducted on 411 participants from two municipality health centers in Murcia. 62.3% were women and 71.8% were between 45 and 64 years of age. Among men, 57.8% were working and they had a median physical activity of 1,939.5 METs/week. Among women, 37.4% were active in work, performing a median of 1,386.0 METs/week. The most declared reason of absence from any session was illness, as stated by 53.4% of women and 30.4% of men. Professionals should consider these differences in the promotion of physical activity.S

Macular dystrophies mimicking age-related macular degeneration

Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in the elderly population in the Western world. AMD is a clinically heterogeneous disease presenting with drusen, pigmentary changes, geographic atrophy and/or choroidal neovascularization. Due to its heterogeneous presentation, it can be challenging to distinguish AMD from several macular diseases that can mimic the features of AMD. This clinical overlap may potentially lead to misdiagnosis. In this review, we discuss the characteristics of AMD and the macular dystrophies that can mimic AMD. The appropriate use of clinical and genetic analysis can aid the clinician to establish the correct diagnosis, and to provide the patient with the appropriate prognostic information. An overview is presented of overlapping and distinguishing clinical features