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1.
Interface (Botucatu, Online) ; 28: e230178, 2024. graf
Article in Portuguese | LILACS-Express | LILACS | ID: biblio-1534628

ABSTRACT

Avaliamos, em conjunto com profissionais dos serviços, os desafios à implementação do modelo biopsicossocial nos Centros Especializados em Reabilitação. Por meio da articulação da Avaliação de Quarta Geração e Roda de Conversa (Método Paideia), abordamos os modelos implementados de assistência à pessoa com deficiência, partindo das seguintes questões: trabalhar em reabilitação; prontuário e avaliação; atendimento compartilhado e qualificação da alta. Do conteúdo das rodas emergiram três categorias empíricas: o processo de trabalho em reabilitação; o trabalho em rede; o modelo de cuidado. A identificação de entraves e facilitadores poderá favorecer a plena implementação do modelo biopsicossocial na atenção às pessoas com deficiência, gerando subsídios para o avanço rumo à integralidade do cuidado às pessoas com deficiência representado neste modelo.


We assessed challenges in implementing the biopsychosocial model in specialized rehabilitation centers together with the professionals working in these services. Using fourth generation assessment and conversation circles (the Paideia method), we explored models of care for people with disabilities focusing on the following issues: working in rehabilitation; health records and evaluation; shared appointments; and improving discharge. Three empirical categories emerged from the conversation circles: rehabilitation work processes; the network-based approach; and the care model. The identification of constraints and enabling factors can help promote the effective implementation of the biopsychosocial model, generating important insights to help drive progress towards the delivery of comprehensive care to people with disabilities represented in this model.


Evaluamos en conjunto con profesionales de los servicios, los desafíos para la implementación del modelo biosicosocial en los centros especializados en rehabilitación. Por medio de la articulación de la Evaluación de Cuarta Generación y Rueda de Conversación (Método Paideia), abordamos los modelos implementados de asistencia a la persona con discapacidad, partiendo de las siguientes cuestiones: trabajar en rehabilitación; historial médico y evaluación; atención compartida y calificación del alta. Del contenido de las ruedas surgieron tres categorías empíricas: el proceso de trabajo en rehabilitación; el proceso en red; el modelo de cuidado. La identificación de obstáculos y facilitadores podrá favorecer la plena implementación del modelo biosicosocial en la atención a las personas con discapacidad, generando subsidios para el avance hacia la integralidad del cuidado a las personas con discapacidad representado en este modelo.

2.
Psicol. ciênc. prof ; 43: e250490, 2023.
Article in Portuguese | LILACS, INDEXPSI | ID: biblio-1448944

ABSTRACT

As dificuldades e barreiras enfrentadas no processo de inclusão de pessoas com deficiência (PcD) nas organizações incitam o desenvolvimento de pesquisas. Este estudo compreendeu a percepção de psicólogos organizacionais sobre a inclusão de PcD em empresas. Dezoito psicólogos atuantes na área de gestão de pessoas de empresas das sete regiões do estado do Rio Grande do Sul responderam a uma entrevista individual. A média de idade dos participantes foi de 33,17 anos, atuavam em empresas de diferentes segmentos, eram predominantemente do sexo feminino e possuíam pós-graduação em áreas relacionadas. Os relatos dos psicólogos alertaram para o fato de que, em suas graduações, o conteúdo sobre deficiência humana e, especificamente, inclusão no mercado de trabalho foi escasso ou inexistente. Essa lacuna na formação, de egressos de diferentes instituições de ensino superior, é relatada desde os anos de 1990. Para esses psicólogos, barreiras atitudinais e organizacionais são frequentemente enfrentadas no processo de inclusão, tais como o despreparo das empresas, gestores e colaboradores para receber as PcD, os poucos programas voltados a uma prática efetiva de inclusão e não somente ao cumprimento da legislação, além das dificuldades dos próprios profissionais em identificar os potenciais e as limitações que a PcD apresenta e de adaptá-la de maneira correta ao trabalho. O psicólogo organizacional pode contribuir para um processo adequado de inclusão por meio de práticas, tais como treinamentos e sensibilizações, que fomentem a informação e diminuam a discriminação e as dificuldades.(AU)


Difficulties and barriers to including people with disabilities (PwDs) in organizations drives research development. This study sought to understand how organizational psychologists perceived the inclusion of PwDs in organizations. Eighteen organizational psychologists who work in people management for companies in the seven regions of the state of Rio Grande do Sul participated in an individual interview. Most interviewees were female, with average age of 33.17 years, had a postgraduate degree in the field, and worked in companies from different segments. During the interviews, the psychologists called attention to the little or nonexistent content on human disability and, specifically, inclusion in the labor market covered in the graduate course. This gap has been reported by graduates from different higher education institutions since the 1990s. According to the respondents, attitudinal and organizational barriers are often faced in the inclusion process, such as the unpreparedness of companies, managers, and employees to welcome PwD, the few programs aimed at an effective inclusion and not only to comply with the law, as well as the difficulties of the professionals themselves to identify the potentials and limitations that PwD present and to adapt them correctly to the work. Organizational psychologists can contribute to an adequate inclusion process by developing training and sensibilization activities that foster information and reduce discrimination and difficulties.(AU)


Las dificultades y barreras enfrentadas en el proceso de inclusión de personas con discapacidad (PcD) en las organizaciones fortalecen el desarrollo de la investigación. Este estudio entendió la percepción de los psicólogos organizacionales acerca de la inclusión de las PcD en las empresas. Dieciocho psicólogos que trabajan en el área de gestión de personas en empresas de las siete regiones del estado de Rio Grande do Sul (Brasil) respondieron a una entrevista individual. Los participantes tenían una edad promedio de 33,17 años, trabajaban en empresas de diferentes segmentos, eran predominantemente mujeres y tenían un posgrado en el área. Los informes de los psicólogos alertaron sobre el hecho de que el contenido sobre discapacidad humana y, específicamente, su inclusión en el mercado laboral era escaso o inexistente durante su formación académica. Esta brecha en la formación de los egresados de diferentes instituciones de educación superior se reporta desde los 1990. Para estos psicólogos, a menudo ocurren barreras organizacionales y de actitud en el proceso de inclusión de las PcD, como la falta de preparación de las empresas, gerentes y empleados para recibirlas, pocos programas destinados a una práctica efectiva de la inclusión, no solo al cumplimiento de la ley, y las dificultades de los profesionales para identificar las potencialidades y limitaciones y adecuarlas correctamente al trabajo. El psicólogo organizacional puede contribuir a un proceso de inclusión adecuado, con prácticas de capacitación y sensibilización que brindan información y reducen la discriminación y dificultades.(AU)


Subject(s)
Humans , Male , Female , Personnel Management , Architectural Accessibility , Organizations , Disabled Persons , Social Inclusion , Organization and Administration , Organizational Innovation , Personnel Selection , Prejudice , Psychology , Psychology, Industrial , Public Policy , Quality of Life , Salaries and Fringe Benefits , Self Concept , Social Behavior , Social Environment , Social Justice , Social Responsibility , Social Security , Social Welfare , Socialization , Societies , Stereotyping , Awareness , Task Performance and Analysis , Unemployment , Vocational Guidance , Occupational Health Program , Decision Making, Organizational , Handicapped Advocacy , Adaptation, Psychological , Organizational Culture , Occupational Health , Staff Development , Civil Rights , Employment, Supported , Workplace , Efficiency, Organizational , Constitution and Bylaws , Cultural Diversity , Legislation , Personal Autonomy , Whistleblowing , Disability Evaluation , Absenteeism , Economics , Education , Ego , Employee Grievances , Employee Incentive Plans , Employment , Workforce , Health of Specific Groups , Health of the Disabled , Job Market , Occupational Health Policy , Social Stigma , Social Discrimination , Work Performance , Social Workers , Occupational Stress , Work Engagement , Respect , e-Accessibility , Public Nondiscrimination Policies , Social Integration , Right to Work , Empowerment , Teleworking , Disinformation , Sociodemographic Factors , Citizenship , Diversity, Equity, Inclusion , Working Conditions , Health Promotion , Ergonomics , Human Rights , Job Application , Job Satisfaction , Labor Unions , Leadership , Life Change Events
3.
Rev. chil. ter. ocup ; 23(1): 37-48, jun. 2022. tab
Article in Spanish | LILACS | ID: biblio-1398792

ABSTRACT

Introducción: La baja contratación de personas con discapacidad, falta de oportunidades y discriminación, en un país post inclusión, está condicionada por diversas barreras, factores o preocupaciones de las empresas y empleadores, las cuales dificultan la inclusión laboral debido a diferentes apreciaciones de índole personal y cultural. Objetivo: La presente investigación tiene por objetivo describir factores legales, de imagen, sociales y económicos que determinan la contratación de personas con discapacidad, según la percepción de los gerentes, administradores y jefes de recursos humanos de empresas de la ciudad de Chillán. Metodología: Para llevar a cabo dicho análisis, se consideró a 50 representantes de 50 empresas de la ciudad, pertenecientes a los rubros del comercio, servicios básicos y otros rubros, los cuales entregaron la percepción sobre los factores a través de una encuesta de auto aplicación. Resultados: Los análisis de los resultados demostraron una tendencia generalizada de la muestra sobre el factor social, identificándolo como un determinante sobre la contratación de personas con discapacidad. Discusión: Se concluyó que el factor social seguido del factor económico, mayormente determinan la contratación de personas con discapacidad, independiente del rubro empresarial, tamaño de las empresas y experiencias previas en la contratación de personas discapacitadas.


Introduction: The low hiring, lack of opportunities and discrimination of people with disabilities, in a post-inclusion country, is conditioned by various barriers, factors or concerns in companies and employers, which hinder labor inclusion, due to different views from a personal and cultural nature. Aim: To describe legal, image, social and economic factors that determine the hiring of people with disabilities, according to the perception of managers, chief of staff and human resources manager of companies in the city of Chillán. Methods: To carry out this analysis, 50 representatives of 50 companies in the city, belonging to the trade, basic services and other items were considered. Participants gave their perception of the factors, through a self-application survey. Results: The analysis of the results showed a general trend in the sample, regarding the social factor, identifying it as a determining factor in hiring people with disabilities. Discussion: It was concluded that the social factor followed by the economic factor, mainly determine the hiring of people with disabilities, regardless the business category, size of the companies and previous experiences in hiring people with disabilities.


Subject(s)
Humans , Male , Female , Adult , Personnel Selection , Disabled Persons , Socioeconomic Factors , Chile , Cross-Sectional Studies , Surveys and Questionnaires , Administrative Personnel , Workforce
4.
Cad. Saúde Pública (Online) ; 38(6): e00142021, 2022. tab, graf
Article in Portuguese | LILACS | ID: biblio-1384264

ABSTRACT

O objetivo do presente estudo foi investigar a associação entre capital social e a incapacidade funcional, numa perspectiva longitudinal, utilizando dados da coorte de idosos de Bambuí, Minas Gerais, Brasil. A linha de base do estudo foi composta por todos os idosos sobreviventes e livres de incapacidade no sétimo ano de seguimento (2004), acompanhados até 2011. A variável desfecho foi a incapacidade funcional para as ABVD (atividades básicas de vida diária) e AIVD (atividades instrumentais de vida diária), analisadas separadamente. A exposição de interesse foi o capital social, mensurado por meio de seus componentes cognitivo (coesão e suporte social) e estrutural (participação social e satisfação com a vizinhança). Variáveis sociodemográficas, de condições de saúde e de hábitos de vida foram utilizadas para efeitos de ajuste, e a ocorrência de óbito foi considerada evento competitivo. A hipótese de associação entre capital social e incapacidade funcional foi testada por meio do modelo de riscos competitivos, que fornece hazard ratios (HR) e intervalos de 95% de confiança (IC95%). Após a análise multivariada, o capital social, em seu componente estrutural, esteve associado à incapacidade funcional. Idosos insatisfeitos com a vizinhança apresentaram risco maior de desenvolver incapacidade funcional para AIVD (HR = 2,36; IC95%: 1,31-4,24), em relação às suas contrapartes. Os resultados desse estudo sugerem que a incapacidade funcional está associada a outros aspectos que não somente da saúde, evidenciando a necessidade de desenvolver políticas e intervenções que abarquem aspectos ligados ao ambiente físico e social em que o idoso está inserido.


This study aimed to investigate the association between social capital and functional disability, based on a longitudinal perspective, using data from the cohort of older adults from Bambuí, Minas Gerais State, Brazil. The baseline of this study was composed of all surviving and disability-free - up until the seventh year of follow-up (2004) - older adults who were followed up until 2011. The outcome variable was functional disability for basic activities of daily living (ADL) and instrumental activities of daily living (IADL), separately analyzed. Social capital was the exposure of interest, measured through its cognitive (cohesion and social support) and structural (social participation and satisfaction with the neighborhood) components. Sociodemographic variables, health conditions, and lifestyle habits were used for adjustment purposes, and the occurrence of death was considered a competitive event. The hypothesis of association between social capital and functional disability was tested using the competing risk model, which provides hazard ratios (HR) and a 95% confidence interval (95%CI). After multivariate analysis, social capital - in its structural component - was associated with functional disability. Older adults who were dissatisfied with the neighborhood had a higher risk of developing functional disability for IADL (HR = 2.36; 95%CI: 1.31-4.24), in relation to their counterparts. This study results suggest that functional disability is associated with aspects other than health, evidencing the need for the development of policies and interventions that support aspects related to the physical and social environment in which older adults live.


El objetivo de este estudio fue investigar la asociación entre el capital social y la discapacidad funcional desde una perspectiva longitudinal, utilizando datos de la cohorte de ancianos de Bambuí, Minas Gerais, Brasil. La línea de base de este estudio estaba compuesta por todos los supervivientes de edad avanzada y sin discapacidad en el séptimo año de seguimiento (2004), seguidos hasta 2011. La variable de resultado fue la discapacidad funcional para las ABVD (actividades básicas de la vida diaria) y las AIVD (actividades instrumentales de la vida diaria), analizadas por separado. La exposición de interés fue el capital social, medido a través de sus componentes cognitivo (cohesión y apoyo social) y estructural (participación social y satisfacción con el barrio). Se utilizaron variables sociodemográficas, de condiciones de salud y de estilo de vida para los efectos de ajuste, y la ocurrencia de la muerte se consideró un evento competitivo. La hipótesis de asociación entre el capital social y la discapacidad funcional se probó mediante el modelo de riesgos competitivos, que proporciona tasas de riesgo (hazard ratios, HR) e intervalos del 95% de confianza (IC95%). Tras el análisis multivariante, el capital social en su componente estructural se asoció con la discapacidad funcional. Los ancianos insatisfechos con su vecindario tenían un mayor riesgo de desarrollar una discapacidad funcional para las AIVD (HR = 2,36; IC95%: 1,31-4,24) en comparación con sus homólogos. Los resultados sugieren que la discapacidad funcional está asociada a otros aspectos además de la salud, lo que pone de manifiesto la necesidad de desarrollar políticas e intervenciones que abarquen aspectos relacionados con el entorno físico y social en el que se insertan las personas mayores.


Subject(s)
Humans , Aged , Disabled Persons/psychology , Social Capital , Brazil , Activities of Daily Living/psychology , Longitudinal Studies , Independent Living
5.
Rev. bras. educ. espec ; 28: e0074, 2022. tab, graf
Article in Portuguese | LILACS-Express | LILACS | ID: biblio-1351693

ABSTRACT

RESUMO: Estudos têm sido desenvolvidos em contextos de trabalho, os quais enfatizam a importância de privilegiar a diversidade e desenvolver práticas de inclusão, com vistas à igualdade de direitos e ao acolhimento de múltiplas etnias, gêneros e pessoas com deficiências. Nesse sentido, o presente estudo teve como objetivo analisar a produção científica brasileira acerca da diversidade e da inclusão de pessoas com deficiência visual em contextos de trabalho. Ele consiste em uma revisão sistemática de artigos científicos, publicados até o ano de 2020, em duas bases eletrônicas de dados. Após busca sistemática, três artigos foram identificados, descritos e analisados por meio das categorias "potencialidades" e "dificuldades do processo de inclusão". A produção científica identificada, talvez por estar em seu estágio inicial, reafirma a importância da educação, das políticas públicas, das legislações e da inserção ou reintegração em ambientes de trabalho, que podem ser consideradas etapas, ainda que fundamentais, anteriores ao processo de inclusão. Ademais, são enfatizadas as dificuldades enfrentadas pelas pessoas com deficiência visual no trabalho, não dedicando maior atenção às potencialidades desse processo de inserção para as pessoas, assim como para as organizações e a sociedade. Destaca-se a importância de propostas educacionais voltadas à promoção da inclusão, que envolvam, para além dos espaços formalmente reconhecidos como educacionais, os contextos de trabalho. Assim sendo, entende-se que estudos como este podem fomentar a ampliação da produção de conhecimento, bem como as discussões para a criação de políticas e de práticas de inclusão culturalmente sensíveis às pessoas com deficiência visual no mundo do trabalho.


ABSTRACT: Studies have been developed in work contexts, which emphasize the importance of privileging diversity and developing practices of inclusion, with a view to equal rights and the welcoming of multiple ethnicities, genders and people with disabilities. In this sense, this study aimed to analyze the Brazilian scientific production about diversity and inclusion of people with visual impairment in work contexts. It consists of a systematic review of scientific articles, published until 2020, in two electronic databases. After a systematic search, three articles were identified, described and analyzed using the categories "potentialities" and "difficulties of the inclusion process". Te identified scientific production, perhaps because it is in its initial stage, reaffirms the importance of education, public policies, legislation and insertion or reintegration into work environments, which can be considered stages, albeit fundamental, prior to the inclusion process. In addition, the difficulties faced by people with visual impairments at work are emphasized, not paying more attention to the potentialities of this insertion process for people, as well as for organizations and society. Te importance of educational proposals aimed at promoting inclusion is highlighted, which involve, in addition to spaces formally recognized as educational, the work contexts. Terefore, it is understood that studies as this one can foster the expansion of knowledge production, as well as discussions to create culturally sensitive inclusion policies and practices for people with visual impairments in the world of work.

6.
Medisan ; 25(6)2021. tab, ilus
Article in Spanish | CUMED, LILACS | ID: biblio-1356469

ABSTRACT

Introducción: La Organización Mundial de la Salud estima que, a escala mundial, 15 % de la población vive con alguna forma de discapacidad, pero se espera un aumento de su prevalencia. Objetivo: Determinar los niveles de agotamiento psicológico o síndrome de burnout en los cuidadores familiares de personas con discapacidad, vinculadas a un proyecto de atención comunitaria. Métodos: Se realizó un estudio descriptivo y transversal de 150 cuidadores familiares de personas con discapacidad, quienes contaban con el apoyo de la Fundación de Atención y Desarrollo Integral a la Niña, Niño, Adolescente y la Familia, radicada en la ciudad de Portoviejo, provincia de Manabí, Ecuador, desde enero hasta mayo del 2019. Para determinar el nivel de agotamiento psicológico se utilizó el cuestionario Maslach Burnout Inventory, que consta de 22 ítems divididos en 3 subescalas: agotamiento emocional, despersonalización y realización personal en el trabajo. También se registraron datos como sexo, procedencia y tipo de discapacidad. Resultados: Predominó el sexo femenino (121 para 80,6 %). El agotamiento psicológico resultó de medio a alto en más de 70,0 % de los cuidadores y el componente cansancio emocional alto fue el más frecuente, seguido de la despersonalización. La realización personal se consideró de baja a media en más de 85,0 % de los encuestados. Conclusiones: Se constató una tendencia al incremento del cansancio emocional en cuidadores de personas con discapacidad, lo cual pudo asociarse con el tipo de minusvalía presente.


Introduction: The Health World Organization estimates that, worldwide, the 15 % of the population lives with some form of disability, but an increase of its prevalence is expected. Objective: To determine the levels of psychological exhaustion or burnout syndrome in the family caregiver of disabled people, linked to a project of community care. Methods: A descriptive and cross-sectional study of 150 family caregiver of disabled people was carried out. They had the support of the Foundation of Integral Care and Development to the Girl, Boy, Adolescent and Family, settled in Portoviejo city, Manabí province, Ecuador, from January to May, 2019. To determine the level of psychological exhaustion the Maslach Burnout Inventory questionnaire was used that consists of 22 articles divided into 3 subscales: emotional exhaustion, depersonalization and personal realization at work. They also registered data as sex, origin and type of disability. Results: There was a prevalence of the female sex (121 for 80.6 %). The psychological exhaustion was from mean to high in more than 70.0 % of the caregiver and the high emotional fatigue component was the most frequent, followed by depersonalization. The personal realization was considered from low to mean in more than 85.0 % of those interviewed. Conclusions: A tendency to the increment of the emotional fatigue in caregiver of people with disability was verified, which could be associated with the type of disability.


Subject(s)
Caregivers , Disabled Persons , Burnout, Psychological
7.
Rev. cuba. invest. bioméd ; 40(3)sept. 2021. ilus, tab
Article in Spanish | LILACS, CUMED | ID: biblio-1408564

ABSTRACT

Introducción: Existe la tendencia mundial del aumento de población adulta mayor. Colombia no es un país ajeno a esta situación. Objetivo: Determinar las condiciones crónicas de salud asociadas al desarrollo de discapacidad en adultos mayores de la ciudad de Santiago de Cali, Colombia. Métodos: Estudio transversal en el que participaron 322 adultos mayores, seleccionados con muestreo aleatorio estratificado proporcional. Se aplicó la Encuesta de Salud, Bienestar y Envejecimiento Colombia, en su sección 8, y el WHODAS 2.0, versión de 36 preguntas. Resultados: El 90,4 por ciento de los participantes en el estudio eran mujeres, la mediana de edad fue de 70 años. La media de discapacidad global fue de 9,39 ± 10,2 puntos. La movilidad obtuvo la mayor puntuación 13,80 ± 17,79 (escala de 0-100 puntos) y las de menor puntuación fueron AVD-trabajo remunerado y participación (2,240 ± 11,15 puntos). La hipertensión arterial fue el padecimiento con mayor prevalencia. Los adultos que han sufrido embolias reportaron el mayor nivel de discapacidad (18,395), seguido de los que manifestaron haber tenido algún tipo de alteración mental (14,15 por ciento ). El dominio con mayor significancia estadística fue la participación, más afectada en los adultos con diabetes, ataques al corazón, embolia cerebral, artritis, osteoporosis y cataratas. Conclusiones: Hubo presencia de enfermedades crónicas en los sistemas cardiovascular, pulmonar y músculo-esquelético, aunque se reportaron niveles bajos discapacidad. Las actividades de la vida diaria más complejas son las que primero presentan dificultad; además, la movilidad es crucial para el funcionamiento de los adultos mayores(AU)


Introduction: Increase in the number of older adults is a current worldwide tendency. Colombia is not an exception. Objective: Determine the chronic health conditions associated to the development of disability in older adults from the city of Santiago de Cali, Colombia. Methods: A cross-sectional study was conducted of 322 older adults selected by proportional stratified random sampling. Data were obtained with the survey Health, Wellbeing and Aging Colombia, section 8, and the tool WHODAS 2.0, 36-item version. Results: Of the participants in the study, 90.4 percent were women; mean age was 70 years. Mean global disability was 9.39 ± 10.2 points. Mobility obtained the highest score (13.80 ± 17.79 on a 0-100 scale), whereas the lowest ranking variables were ADL - paid work and participation (2.240 ± 11.15 points). Arterial hypertension was the most common condition. Patients who had had embolisms reported the highest level of disability (18.395), followed by those reporting having had some sort of mental disorder (14.15 percent). The domain with the greatest statistical significance was participation, which was more affected in adults with diabetes, heart attacks, cerebral embolism, arthritis, osteoporosis and cataract. Conclusions: A presence was observed of chronic diseases of the cardiovascular, respiratory and musculoskeletal systems, though low disability levels were reported. The most complex activities of daily living are the first to present difficulty. On the other hand, mobility is crucial for the functioning of older adults(AU)


Subject(s)
Humans , Aged , Activities of Daily Living , Exercise , Health Status , Heart , Chronic Disease , Cross-Sectional Studies , Sports for Persons with Disabilities , Health Services for the Aged
8.
Rev. bras. ativ. fís. saúde ; 26: 1-11, mar. 2021. tab, fig, quad
Article in Portuguese | LILACS | ID: biblio-1282852

ABSTRACT

Visando orientar a população dos benefícios da prática de atividade física à saúde, pesquisadores nacionais, em parceria com o Ministério da Saúde, elaboraram o Guia de Atividade Física para a População Brasileira (Guia). O objetivo deste estudo foi apresentar o processo de elaboração das recomendações brasileiras de atividade física para pessoas com deficiência (PCD). O processo de elaboração das recomendações específicas para PCD foi liderado por um grupo de trabalho com nove pesquisadores/profissionais que realizaram reuniões semanais, e que conduziram revisões sistemáti-cas e escutas com PCD, familiares, gestores, profissionais da saúde, professores e pesquisadores. Na revisão sistemática, um total de 83 estudos foram revisados e incluídos. As escutas foram realizadas por meio de formulários eletrônicos enviados por e-mail para profissionais, gestores, professores e pesquisadores que trabalhavam com PCD e de escutas virtuais, as quais foram conduzidas em dois momentos: (a) com PCD, familiares e profissionais; (b) com professores, gestores; e pesquisadores da temática. Baseado nos resultados das revisões sistemáticas e das escutas, as recomendações de atividade física para PCD foram elaboradas considerando o tempo mínimo de atividade física de acordo com faixas etárias, domínios da atividade física e recomendações para redução do comporta-mento sedentário. Portanto, o presente trabalho apresentou as estratégias e as etapas utilizadas para a elaboração do Guia, com recomendações de atividade física para PCD, as quais podem ser aliadas a políticas públicas, ambientes e oportunidades de atividade física, tornando-se estratégia essencial para o engajamento de PCD em atividades físicas


Aiming to guide the population of the physical activity benefits to health, national researchers, in partnership with the Health Ministry, have elaborated the Physical Activity Guide for the Brazilian population. The aim of this study is to present the process of elaborating Brazilian physical activity recommendations for people with disabilities (PWD). The process of elaborating specific recommendations for PWD has included the participation of nine researchers/professionals who held weekly meetings, systematic reviews, and focus groups with PWD, caregivers, healthcare managers, professionals, and researchers. In the systematic review, a total of 83 studies were included and reviewed. The focus groups were performed using an electronic form sent by e-mail to health professionals, managers, and researchers who worked with PWD and virtual focus groups, which were conducted in two moments: (a) with PWD, caregivers, and professionals; (b) with pro-fessors and researchers on the theme. Based on the results of systematic reviews and focus groups, the physical activity recommendations for PWD were developed considering the minimum physical activity time accord-ing to age group, types of physical activity, and recommendations for reducing sedentary behavior. Therefore, the present work presented recommendations for physical activity for PWD, which can be combined with public policies, environments, and opportunities for physical activity, becoming an essential strategy for the engagement of PWD in physical activities


Subject(s)
Global Health Strategies , Exercise , Disabled Persons , Sedentary Behavior
9.
Ciênc. Saúde Colet. (Impr.) ; 25(7): 2859-2870, Jul. 2020. tab, graf
Article in English, Portuguese | LILACS, ColecionaSUS, SES-SP | ID: biblio-1133090

ABSTRACT

Resumo Este estudo objetiva identificar os fatores que dificultam o acesso de crianças e adolescentes com deficiência física ao tratamento fisioterapêutico, em estabelecimentos credenciados ao Sistema Único de Saúde em Curitiba, Paraná, Brasil. Trata-se de um estudo transversal que entrevistou gestores, fisioterapeutas, pais e/ou responsáveis por crianças com deficiência física. A percepção de dificuldades de cada um dos grupos de entrevistados foi comparada por meio de estatísticas descritivas, considerando as dimensões: disponibilidade, poder de pagamento, informação e aceitabilidade. Considerando a dimensão disponibilidade, identificaram-se como dificuldades: distância entre o estabelecimento e a residência dos usuários, pouca oferta de serviços e fila de espera. Em relação ao poder de pagamento, observou-se a falta de recursos financeiros entre os pais. Nas dimensões informação e aceitabilidade, a falta de informação acerca do diagnóstico e a negação foram referidas pelos participantes. Conclui-se que o serviço de fisioterapia não tem sido garantido em tempo favorável ao desenvolvimento motor das crianças, de modo que se faz necessário rever a organização e distribuição dos serviços, bem como são essenciais políticas efetivas que garantam a sua utilização.


Abstract This study aims to identify the factors that hinder physically disabled children and adolescent's access to physiotherapy in establishments accredited by the Unified Health System in Curitiba, Paraná, Brazil. This is a cross-sectional study that interviewed managers, physiotherapists, parents or guardians of children with physical disabilities. The perception of difficulties of each interviewed group was compared through descriptive statistics, considering the following realms: availability, purchasing power, information and acceptability. Considering the realm of availability, we identified the following hindrances: distance between the physiotherapy location and user's residence, inadequate supply of services and waiting list. Regarding the purchasing power, we observed the lack of financial resources among parents. Regarding information and acceptability, the lack of information about diagnosis and denial were reported by participants. We can conclude that the physiotherapy service has not been timely assured to children's motor development, so it is necessary to review the organization and distribution of services, and effective policies are required to ensure their use.


Subject(s)
Humans , Child , Adolescent , Disabled Persons , Physical Therapists , Brazil , Cross-Sectional Studies , Physical Therapy Modalities
10.
Ciênc. Saúde Colet. (Impr.) ; 25(3): 1083-1090, mar. 2020. tab
Article in Portuguese | LILACS | ID: biblio-1089473

ABSTRACT

Resumo O objetivo do estudo foi verificar a ocorrência de mudanças na capacidade funcional e no desempenho físico de idosos comunitários e seus fatores determinantes, em um período de dois anos. Foi realizado estudo quantitativo, do tipo inquérito domiciliar, observacional e longitudinal, em 2014 e 2016, com 380 idosos residentes em Uberaba, Minas Gerais. Foram utilizados os instrumentos: Mini Exame do Estado Mental e questionários com dados sociodemográficos/econômicos, clínicos e de hábito de vida. A capacidade funcional foi avaliada por meio do Índice de Katz e da escala de Lawton e Brody. O desempenho físico foi verificado através da Short Physical Performance Battery. Procedeu-se a análise descritiva, bivariada e de regressão linear múltipla, com nível de significância de α < 0,05. Os resultados mostraram que no período de dois anos ocorreu redução da capacidade funcional para as atividades instrumentais da vida diária e do desempenho físico. Os fatores determinantes comuns aos desfechos foram: faixa etária, atividade profissional e prática de atividade física. A escolaridade foi específica somente para as atividades instrumentais da vida diária, e o sexo e o número de medicamentos para o desempenho físico.


Abstract This study aimed to verify the occurrence of changes in the functional capacity and physical performance of community-dwelling elderly and its determining factors over a two-year period. This is a quantitative, observational and longitudinal household survey conducted in 2014 and 2016, with the participation of 380 elderly from Uberaba, Minas Gerais. The following instruments were used: The Mini-Mental State Examination and questionnaires with sociodemographic/economic, clinical and life habits data. The functional capacity was evaluated through the Katz Index and Lawton-Brody's scale. Physical performance was verified through the Short Physical Performance Battery. A descriptive, bivariate and linear multiple regression analysis was conducted, with a significance level of α < 0.05. The results showed reduced functional capacity for the instrumental activities of daily living and physical performance in a two-year period. The determining factors for both outcomes were age group, occupational activity, and physical activity. Schooling was a specific factor only for the instrumental activities of daily living, and gender and the number of medicines used, for physical performance.


Subject(s)
Humans , Male , Female , Aged , Aged, 80 and over , Activities of Daily Living , Independent Living , Physical Functional Performance , Geriatric Assessment/methods , Longitudinal Studies , Middle Aged
11.
Arch. argent. pediatr ; 117(3): 183-187, jun. 2019. graf, tab
Article in English, Spanish | LILACS, BINACIS | ID: biblio-1001194

ABSTRACT

La discapacidad es un problema de salud pública que afecta las oportunidades de desarrollo integral del individuo. El objetivo del trabajo fue estimar la prevalencia e incidencia anual y de las categorías diagnósticas asociadas a discapacidad total y por grupos etarios a partir de la tramitación del Certificado Único de Discapacidad. Estudio analítico de una cohorte de niños/as de 0 a 18 años perteneciente a un hospital universitario del Área Metropolitana de Buenos Aires, entre enero de 2010 y diciembre de 2017. Sobre un total de 22 750 afiliados activos, 726 pacientes tramitaron el Certificado Único de Discapacidad; la prevalencia fue del 3,2 % (IC 95 %: 2,9-3,4). La incidencia acumulada anual aumentó desde 2012 (0,22 %; IC 95 %: 0,1-0,19) hasta 2017 (0,59 %; IC 95 %: 0,5-0,7). Las discapacidades mentales constituyeron el 80 % (n = 576). En este estudio se observó un aumento de la incidencia de discapacidad y de la categoría de discapacidad mental.


Disability is a public health problem that affects an individual's comprehensive development opportunities. The objective of this study was to estimate the annual incidence and prevalence and the diagnostic categories associated with total disability and age groups based on the application for a Unique Certificate of Disability. This was an analytical cohort study in children aged 0-18 years conducted at a teaching hospital of the Metropolitan Area of Buenos Aires between January 2010 and December 2017. Among 22 750 active members, 726 patients applied for a Unique Certificate of Disability; the prevalence was 3.2 % (95 % confidence interval [CI]: 2.9-3.4). The annual cumulative incidence increased from 2012 (0.22 %, 95 % CI: 0.1-0.19) to 2017 (0.59 %, 95 % CI: 0.5-0.7). Mental disabilities accounted for 80 % (n = 576). This study showed an increase in the incidence of disability and also the mental disability category.


Subject(s)
Humans , Infant , Child, Preschool , Child , Adolescent , Pediatrics , Epidemiology , Disabled Persons , Autism Spectrum Disorder , Intellectual Disability
12.
Rev. bras. educ. espec ; 24(4): 517-534, out.-dez. 2018.
Article in Portuguese | LILACS | ID: biblio-977529

ABSTRACT

RESUMO: Este artigo trata de um estudo retrospectivo sobre estratégias comunitárias para inclusão de Pessoas com Deficiência (PcD) no trabalho, realizadas por projeto de extensão universitária em parceria com a Unidade Básica de Saúde, entre 2012 e 2016. A pesquisa documental identificou o perfil dos atendidos e as ações compreenderam o apoio em grupo (34 encontros) e individual/familiar (172 atendimentos/20 visitas ao local de trabalho). Houve investimento na constituição de rede comunitária de suporte com atores públicos e privados. Dentre os 22 participantes, 10 iniciaram atividade remunerada, 6 estavam desempregados e 6 não iniciaram atividade remunerada nem tinham experiência prévia; tinham em média 29 anos e, majoritariamente, apresentavam deficiência intelectual, pouca escolaridade ou experiência de trabalho. O grupo possibilitou conhecer as necessidades dos participantes, abordar questões coletivas sobre o tema e compartilhar informações. Os apoios individuais foram essenciais para tratar necessidades singulares, considerando a inexistência de política de apoio à permanência de PcD nas empresas. A criação de rede entre os envolvidos possibilitou interlocução entre serviços para enfrentamento das questões. Houve diálogo com a proposta do Emprego Apoiado e Reabilitação Baseada na Comunidade. Esses aspectos facilitaram processos personalizados, demonstrando a importância e a viabilidade de iniciativas comunitárias que poderiam indicar políticas públicas de acesso a direitos.


ABSTRACT: This paper is about a retrospective study on community strategies for inclusion of People with Disabilities (PwD) at work, carried out by a university extension project in partnership with the Basic Health Unit between 2012 and 2016. The documentary research identified the profile of those served and the actions included support in group (34 encounters) and individual/family (172 assistance meetings/20 visits to the workplace). There was investment in the constitution of a community support network with public and private actors. Among the 22 participants, 10 started paid work, 6 were unemployed and 6 did not start paid work or had previous experience; the average age was 29 years and, mostly, had intellectual disability, little schooling or work experience. The group made it possible to meet the needs of the participants, to address collective issues and share information. Individual support was essential to address unique needs, considering the lack of a policy to support the permanence of PwD in companies. The creation of a network among those involved allowed the interlocution between services to deal with the issues. There was dialogue with the proposal of Supported Employment and Community Based Rehabilitation. These aspects facilitated personalized processes, demonstrating the importance and feasibility of community initiatives that may indicate public policies of access to rights.

13.
Indian J Lepr ; 2018 Sep; 90(3): 177-188
Article | IMSEAR | ID: sea-195012

ABSTRACT

This study has been carried out to verify the association between physical disability, activity limitation and social participation of people who had leprosy. This is an ecological analytical study, carried out from 2003 to 2014 in eleven cities belonging to the Epidemiological Surveillance Group of Taubaté-SP, Brazil. Individuals who had leprosy and were discharged after cure were evaluated through simplified neurological assessment, disability grade, activity limitation and social participation. Two hundred and ten people were assessed, with average age of 55.62 years. Among them, 72.86% individuals reported some health problem and the majority complained of pain. The prevalent operational classification for leprosy was multibacillary (70.48%). 156 individuals (75.29%) presented with physical disability, either in moderate or severe grade, and 60.48% had some level of activity limitation. The most frequent degree of social restriction (19.52%) was mild. There was strong correlation between social participation and activity limitation (r=0.5798; p<0.0001). To conclude, both physical disabilities as well as activity limitations were frequent in these persons. Activity limitation was significantly associated with multibacillary forms, physical disabilities, low educational level and pain. As for decreased social participation, the association was more evident among people who had family income less than three minimum wages, with visible physical damages and presence of severe pain.

14.
Interface (Botucatu, Online) ; 22(64): 109-120, jan.-mar. 2018.
Article in Portuguese | LILACS | ID: biblio-893459

ABSTRACT

Este estudo objetivou analisar as percepções dos trabalhadores da Estratégia Saúde da Família sobre a saúde da pessoa com deficiência que vive no campo. Trata-se de uma pesquisa de abordagem qualitativa, com o desenho de cunho etnometodológico. Foi realizada observação participante e debates por meio da roda, com registro em diário de campo, e entrevistas semiestruturadas em uma Unidade Básica de Saúde de Grão Mogol, Minas Gerais. Na análise, combinaram-se os dados coletados para triangulação. Os resultados evidenciam que as políticas desenvolvimentistas e a inserção das políticas públicas estão incidindo sobre a saúde das populações do campo. A deficiência está ancorada no modelo biomédico e a dimensão da caridade se ressalta nas ações em saúde. O desenho da Rede de Cuidados à Pessoa com Deficiência deve ser repactuado a fim de enfrentar as barreiras de acesso à saúde.(AU)


This study aimed to analyze the perceptions of Family Health Strategy workers about people with disabilities living in rural areas. This was a qualitative research with an ethnomethodological design. Data was collected through participant observation, discussion roundtables, field notes and semi-structured interviews at the Primary Health Care Service in the city of Grão Mongol, state of Minas Gerais. The analysis was supported by triangulation methods. The results show that the developmental policies and implementation of public policies are impacting the health of populations in the rural areas. Disability is described based on biomedical model, and charity perspective is evident in health care activities. The Health Care Network for People with Disabilities should be subject of new agreements to lower health access barriers.(AU)


El objetivo de este estudio fue analizar las percepciones de los trabajadores de la Estrategia Salud de la Familia sobre la salud de la persona con deficiencia que vive en el campo. Se trata de una investigación de abordaje cualitativo con diseño de cuño etno-metodológico. Se realizó una observación participativa y círculo de debates, con registro en diario de campo y entrevistas semi-estructuradas en una Unidad Básica de Salud de Grão Mogol, Estado de Minas Gerais. En el análisis se combinaron los datos colectados para triangulación. Los resultados mostraron que las políticas desarrollistas y la inserción de las políticas públicas inciden sobre la salud de las poblaciones del campo. La discapacidad está anclada en el modelo biomédico y la dimensión de la caridad se subraya en las acciones de salud. El diseño de la Red de Cuidados a la Persona con Discapacidad debe ser objeto de un nuevo pacto con la finalidad de enfrentar las barreras de acceso a la salud.(AU)


Subject(s)
Humans , Male , Female , Disabled Persons , Health Workforce , Primary Health Care , Rural Health/legislation & jurisprudence , Family Health , Unified Health System
15.
Ciênc. Saúde Colet. (Impr.) ; 23(11): 3965-3978, Oct. 2018. tab
Article in Portuguese | LILACS | ID: biblio-974723

ABSTRACT

Resumo O artigo discute a questão da proteção social frente às demandas apresentadas no tratamento oncológico infanto/juvenil no Brasil. Tem como objetivo problematizar os avanços e os limites do sistema de proteção social brasileiro frente às demandas sociais decorrentes do tratamento oncológico infanto/juvenil que ultrapassam os limites específicos da atenção à saúde. Trata-se de estudo qualitativo que foi estruturado com base na análise de documentos oficiais, Leis, Decretos, Portarias e Políticas e da literatura destinados às crianças e adolescentes em tratamento de câncer cujas consequências incapacitantes produzem demandas sociais que impactam, sobretudo, a vida familiar. O trabalho apresenta as políticas sociais como um recurso fundamental ao tratamento, considerando a demanda por renda e deslocamento, de modo a possibilitar uma efetiva atenção à saúde. Entretanto, as reflexões apontam haver na atualidade uma retração das políticas sociais pelo Estado que se exprimi na focalização e no repasse de suas responsabilidades a outros setores da sociedade civil.


Abstract This article discusses the issue of social protection against the demands presented in the treatment of children and adolescents in Brazil. It aims to problematize the advances and limits of the Brazilian social protection system in face of the social demands arising from the treatment of children and adolescents that go beyond the specific limits of health care. It is a qualitative study that was structured based on the analysis of official documents, Laws, Decrees, Ordinances and Policies and the literature destined to children and adolescents in cancer treatment whose incapacitating consequences produce social demands that impact, above all, family life. The paper presents social policies as a fundamental resource for treatment, considering the demand for income and displacement, in order to enable an effective health care. However, the reflections indicate that there is now a retraction of social policies by the State that was expressed in the focus and transfer of responsibilities of the State to other sectors of civil society.


Subject(s)
Humans , Child , Adolescent , Public Policy , Delivery of Health Care/legislation & jurisprudence , Health Policy , Neoplasms/therapy , Brazil , Delivery of Health Care/organization & administration
16.
Psicol. ciênc. prof ; 37(3): 799-814, jun.- sept.2017.
Article in Spanish | LILACS, INDEXPSI | ID: biblio-883348

ABSTRACT

Mediante pesquisa bibliográfica realizada nas principais bases de dados disponíveis atualmente, este ensaio discute a situação atual da inclusão de pessoas com deficiência no mercado de trabalho, destacando os obstáculos e desafios presentes na realidade brasileira. Discute ainda a atuação do Psicólogo Organizacional e do Trabalho (POT) neste contexto, postulando sobre a importância de seu comprometimento com as transformações necessárias, tanto na sociedade quanto nas organizações de trabalho, para que tenhamos uma cultura verdadeiramente inclusiva. Embora essa temática venha sendo amplamente discutida, o presente estudo concluiu que ainda temos muito a avançar, considerando, sobretudo, as questões culturais que, somadas ao despreparo das organizações e dos gestores organizacionais para lidarem com os trabalhadores com deficiência, representam os maiores obstáculos à inclusão. Embora devamos reconhecer que no Brasil houve avanços, em especial após a promulgação, em 1991, da chamada Lei de Cotas, diversas pesquisas têm apontado para a dificuldade, por parte das organizações, em cumpri-la. Entendemos que o POT deva ser um profissional preparado técnica e eticamente para, juntamente com outros profissionais, promover ações na direção de um processo efetivo de inclusão dessa população nos contextos de trabalho, favorecendo não somente as pessoas envolvidas, como também, as próprias organizações....(AU)


Through bibliographical research carried out in the major databases available today, this paper discusses the current situation of inclusion of people with disabilities in the labor market, highlighting present obstacles and challenges in the Brazilian reality. It also discusses the role of the Work and Organizational Psychologists (WOP) in this context, suggesting the importance of their commitment to the necessary changes, both in society and work organizations, so that we have a truly inclusive culture. Although this theme has been widely discussed, the study found that we still have long way to go, considering all the cultural issues that, added to the unpreparedness of organizations and organizational managers to deal with employees with disabilities, represent major obstacles to inclusion. While we must recognize that there has been progress in Brazil, especially after the promulgation in 1991 of the so-called "Quota" Law, several studies have pointed to the difficulty of organizations in fulfilling it. We understand that the WOP should be a ethically and technically prepared professional for, along with other professionals, promoting actions towards an effective process of inclusion of this population in the contexts of work, not only favoring the people involved, but also the organizations....(AU)


Mediante investigación bibliográfica realizada en las principales bases de datos disponibles hoy, este trabajo analiza la situación actual de la inclusión de personas con discapacidad en el mercado laboral, poniendo de relieve los obstáculos y desafíos presentes en la realidad brasileña. También se discute el papel del Psicólogo Organizacional y del Trabajo (POT) en este contexto, resaltando la importancia de su compromiso con los cambios necesarios en la sociedad y en las organizaciones para que tengamos una cultura verdaderamente incluyente. Aunque este tema venga siendo ampliamente discutido, el estudio encontró que todavía nos queda mucho camino por recorrer, considerando especialmente las cuestiones culturales que, añadidas a la falta de preparación de las organizaciones y los gerentes de la organización para hacer frente a los empleados con discapacidad, representan los principales obstáculos a la inclusión. Si bien hay que reconocer que en Brasil se han registrado avances, especialmente después de la promulgación en 1991 de la llamada Ley de Cuotas, varios estudios han señalado la dificultad de las organizaciones en cumplirla. Entendemos que el POT debe ser un profesional técnica y éticamente preparado, junto con otros profesionales, para promover acciones hacia un proceso efectivo de inclusión de esta población en los contextos de trabajo, favoreciendo no solo a las personas involucradas, sino también a las organizaciones....(AU)


Subject(s)
Humans , Male , Female , Disabled Persons , Psychology , Work
17.
Motriz (Online) ; 23(2): e101703, 2017. tab
Article in English | LILACS | ID: biblio-841843

ABSTRACT

Abstract Aims This study aimed to identify Brazilian wheelchair tennis athletes' quality of life and to compare the perception scores between competitive and elite athletes. Methods Participants were wheelchair tennis athletes (N = 31) from Brazil (males = 25, females = 6) divided into two groups: competitive and elite. Data was collected using the Brazilian version of the WHOQOL-Bref. The WHOQOL-Bref asks two general questions, and is thereafter divided into four main domains: 1) physical, psychological, social, and environment, which give us an understanding of their overall quality of life perception. Results The results showed that overall, 29 out of the 31 athletes perceived their quality of life positively, regardless of the competitive level. However, statistically higher perceptions were found in the physical domain and the total score of quality of life of the elite group. Conclusion The findings of this study suggest that even though participation in high-performance adapted sports may offer a stressful and exhausting environment, elite wheelchair tennis athletes from Brazil perceive themselves as having a better QoL than competitive athletes.(AU)


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Athletic Performance/psychology , Disabled Persons/psychology , Quality of Life , Sports for Persons with Disabilities , Tennis , Brazil
18.
Chinese Mental Health Journal ; (12): 195-202, 2017.
Article in Chinese | WPRIM | ID: wpr-505871

ABSTRACT

Objective:To describe health service use and trend of treatment and rehabilitation rates among people with psychiatric disability from 2007 to 2013.Methods:Data collected by the 2006 Second China National Sample Survey and the 2007-2013 National Disability Monitoring Survey were utilized and analyzed.The 2006 National Sample Survey on Disabilities investigated 2 526 145 non-institutionalized representative civilians in 734 counties across mainland China.Psychiatric disability was diagnosed by clinical psychiatrists according to ICD-10 and WHO DAS Ⅱ criteria.The 2007 to 2013 National Disability Monitoring Survey selected 1 to 2 study sites among each of the 734 study counties that had been investigated by the Second China National Sample Survey.Information on living conditions,health service use,education and employment were recorded.Results:The data showed that treatment and rehabilitation rates for people with psychiatric disability had largely increased from 2007 to 2013 among adults aged 18 years or older,with the treatment and rehabilitation rates from 49.52% and 21.8% to 66.9% and 58.7% respectively,and the rates among those with 17 years or younger from 23.5% to 43.9%.However,with regard to the effect of the treatment and rehabilitation services,a much larger proportion of people with psychiatric disability reported that the effect was soso instead of good or very good.In addition,among those who received rehabilitation service,most received day care or psychotherapy service,only less than 8% participated work therapy,farming therapy or working skill trainings.Conclusion:The results suggest treatment and rehabilitation rates among people with psychiatric disability are largely increased from 2007 to 2013,while the quality of the service needs further attention.

19.
Chinese Journal of Rehabilitation Theory and Practice ; (12): 971-975, 2017.
Article in Chinese | WPRIM | ID: wpr-614237

ABSTRACT

According to the United Nations' definition of a three-stage aging society, China has entered into the aging society since 2000. As for the reason resulting in dysfunction of aged people, this paper points out that the majority is due to degenerative changes of the organs to cause the ability a gradual decline, besides the reason resulted from old-age disease. They are neither patients caused by diseases, nor people with disablities reaching the threshold on the continuum of disability;they might be called as aged people with disability. The re-habilitation of the aged people mainly relies on assistive technologies to improve the ability of activity and participation. The needs of assis-tive technology for old people as well as the role and selection principles of assistive technologies in rehabilitation of aged people are intro-duced in the paper. Finally, an overview of assistive technology for aged people is introduced in the paper.

20.
An. bras. dermatol ; 91(3): 311-317, tab, graf
Article in English | LILACS | ID: lil-787289

ABSTRACT

Abstract: Background: Leprosy is an infectious chronic condition associated with potentially serious physical, social and psychological impacts. Objectives: To characterize the clinical and epidemiological profile of leprosy patients treated from 2007 to 2011 in the University Hospital of Ceará, Northeastern Brazil. Methods: This is a retrospective and descriptive study. The study population consisted of residents in the state of Ceará treated in a dermatology clinic between 2007-2011. Clinical and epidemiological data analyzed were obtained from medical records and from the database of national Information System for Notifiable Diseases. Results: 475 cases were analyzed, mostly women (51.8%), aged 45-59 years (35.0%) - mean of 45.2 years at diagnosis - with 6.3% of children under 15 , with low education (73.7%), white color (68.8%), residency in the city of Fortaleza (82.3%), and no defined work occupation (59.6%). At diagnosis, most patients were multibacillary (MB) (65.5%), had borderline clinical form (48.0%), and 22.7% had physical disability (8.0% with grade 2), predominantly in MB cases (p <0.001). We observe worsening of disability in 5.1% of cases post-MDT. The proportion of cases with reactional episodes was 42.7%, mainly during MDT (51.2%). Conclusion: This is the first study conducted in this hospital context, revealing late diagnosis, high burden of disease, hidden endemicity, and high social vulnerability in the state of Ceará. This study reinforces the need to strengthen health care network for timely diagnosis and treatment, aiming at longitudinality of assistance.


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Aged , Aged, 80 and over , Young Adult , Leprosy/diagnosis , Leprosy/epidemiology , Brazil/epidemiology , Medical Records/statistics & numerical data , Retrospective Studies , Databases, Factual/statistics & numerical data , Disabled Persons/statistics & numerical data , Sex Distribution , Age Distribution , Delayed Diagnosis , Hospitals, University , Leprosy/physiopathology
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