912 resultados para Health public policies. Home care services. Hospital and home care


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Background: Globally there are few reports of the impairments, disabilities and medications used in people living with idiopathic Parkinson’s disease. Caregiver characteristics and caregiver burden have seldom been reported. We examined the health status in a large cohort of people living with Parkinson’s disease and their caregivers managed in a comprehensive health care setting.

Methods/Design: A prospective, cross sectional analysis of impairments, disabilities and Parkinson’s disease medication use was conducted in a sample of 100 people with Parkinson’s disease rated I-IV on the modified Hoehn & Yahr scale. Participants were recruited from the Victorian Comprehensive Parkinson Program in Melbourne, Australia. Their caregivers were invited to provide their views on the burden of care, services provided and support received.

Results: The severity of impairments and disabilities was strongly associated with disease duration (mean of 5.5 years). Those with long standing disease or more severe disease also used more Parkinson’s disease medications and participated in fewer social roles than people who were newly diagnosed or mildly affected. The severity of impairments was strongly correlated with limitations in performing activities of daily living. Limitations in performing daily activities were also found to be a significant contributing factor for health-related quality of life (PDQ-39 SI β=0.55, p=0.000; EQ-5D SI β=0.43, p=0.001). People with Parkinson’s disease lived at home with relatives. The average caregiver was a spouse or child providing approximately 3.5 hours of care per day, with the capacity to provide 9.4 hours per day and had provided care for four years. Additional support was high (63%) for 2.5 hours per day.

Conclusion: The comprehensive care setting of this cohort describes a relatively benign condition despite a wide range of disease duration and severity. This report provides a baseline with which to compare other delivery models.

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OBJECTIVES: Report the use of an objective tool, UK Gold Standards Framework (GSF) criteria, to describe the prevalence, recognition and outcomes of patients with palliative care needs in an Australian acute health setting. The rationale for this is to enable hospital doctors to identify patients who should have a patient-centred discussion about goals of care in hospital.

DESIGN: Prospective, observational, cohort study.

PARTICIPANTS: Adult in-patients during two separate 24 h periods.

MAIN OUTCOME MEASURES: Prevalence of in-patients with GSF criteria, documentation of treatment limitations, hospital and 1 year survival, admission and discharge destination and multivariate regression analysis of factors associated with the presence of hospital treatment limitations and 1 year survival.

RESULTS: Of 626 in-patients reviewed, 171 (27.3%) had at least one GSF criterion, with documentation of a treatment limitation discussion in 60 (30.5%) of those patients who had GSF criteria. Hospital mortality was 9.9%, 1 year mortality 50.3% and 3-year mortality 70.2% in patients with GSF criteria. One-year mortality was highest in patients with GSF cancer (73%), renal failure (67%) and heart failure (60%) criteria. Multivariate analysis revealed age, hospital length of stay and presence of the GSF chronic obstructive pulmonary disease criteria were independently associated with the likelihood of an in-hospital treatment limitation. Non-survivors at 3 years were more likely to have a GSF cancer (25% vs 6%, p=0.004), neurological (10% vs 3%, p=0.04), or frailty (45% vs 3%, p=0.04) criteria. After multivariate logistic regression GSF cancer criteria, renal failure criteria and the presence of two or more GSF clinical criteria were independently associated with increased risk of death at 3 years. Patients returning home to live reduced from 69% (preadmission) to 27% after discharge.

CONCLUSIONS: The use of an objective clinical tool identifies a high prevalence of patients with palliative care needs in the acute tertiary Australian hospital setting, with a high 1 year mortality and poor return to independence in this population. The low rate of documentation of discussions about treatment limitations in this population suggests palliative care needs are not recognised and discussed in the majority of patients.

TRIAL REGISTRATION NUMBER: 11/121.

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A crise por que passam os Hospitais Universitários – HU’s, incluindo o Hospital Universitário Gaffrée e Guinle, atualmente, deve ser analisada e entendida como decorrente da crise institucional por que passa o aparelho formador na área de saúde, da crise de financiamento e da estrutura de gastos do sistema de saúde e de condução das políticas públicas. No entanto, é possível estabelecer novas bases de parceria dos HU’s com os gestores do Sistema Único de Saúde - SUS, para construção dos instrumentos necessários tanto para a efetivação da hierarquização e regionalização dos serviços, como para novas diretrizes curriculares, contribuindo, assim, na superação de alguns fatores determinantes da crise. A lógica organizacional da inserção no Sistema Único de Saúde, força os HU’s a adaptarem-se ao atendimento da demanda espontânea e à necessidade de faturamento na tabela do SUS, com conseqüentes distorções no atendimento, desperdícios e pouca resolutividade do sistema, levando a um descompasso entre demanda, oferta, modelo assistencial, currículo e pesquisa.

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This paper discusses the process of training social workers in the environment of University Hospitals- UH s. These hospitals provide space for professional education aiming to achieve a critical and purposeful professional performance. As environments for training, producing knowledge and providing essential services to the public, these hospitals require all members of the healthcare team to have a continued education. Understanding that training has to be a priority and conceived as constant pursuit for update through the interaction of Teaching, Researching and EPO ( Education and Public Outreach). These dimensions provide approximations and domain of theoretical and methodological, giving special importance to understanding the social reality, a sine qua non condition to the work of the Social Service professional. The main goal of the research was to comprehend how the continuous professional education of the social worker occurs and it s relation with the articulations involving Teaching, Researching and EPO, as significant elements for the job of the social workers in the Hospital Universitário Ana Bezerra and Hospital Universitário Onofre Lopes/UFRN. The research was conducted through a literature review, documentary and field inquiries with semistructured interviews including the group of 09 (nine) social workers from the aforementioned hospitals, taking as a reference the quantitative and qualitative approach to analyze mediations that stand between the subject and the social context. The results indicate that social workers in these university hospitals have their insertion beyond the care provided to patients in performance in the areas of education through preceptorship to undergraduate students and social work residents in and extension projects with low insertion in area of research. We note that there is a recognition of the importance of a continuous education, indicating that the qualification of social worker is essential in transforming their daily professional practice to better monitor, critically explain the peculiarities of public health in its everyday showing of how unequally access is provided to the users of the public health system

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Com a finalidade de subsidiar gestores da área de saúde da mulher, na formulação de políticas públicas, voltadas ao desenvolvimento humano, realizou-se esta investigação, cujo objetivo foi avaliar a estrutura e o processo da atenção ao parto e ao neonato desenvolvido em região do interior paulista. Estudo epidemiológico, voltado para avaliação dos serviços de saúde, baseou-se na observação da assistência prestada pelo Sistema Único de Saúde em 12 maternidades e 134 partos, adotando-se padrões estabelecidos pelo Ministério da Saúde ou Organização Mundial de Saúde para comparação. Os resultados apontam problemas relacionados à estrutura em algumas maternidades, mostrando que práticas úteis ao parto normal ainda são pouco utilizadas, enquanto que outras prejudiciais ou ineficazes ainda são utilizadas rotineiramente. Reverter esse quadro será essencial para oferecer atendimento de qualidade às mulheres, com conseqüente redução nas taxas de mortalidade materna e neonatal, para que a região atinja as metas estabelecidas para ampliação do desenvolvimento humano no milênio.

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Includes bibliography

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There is a clear reported association between social disparity and oral health, for example, between dental caries and malnutrition in children. This fact is detected in several studies, and also found amongst the Brazilian population. However, several efforts have been made to improve the quality of life of the population and to achieve the 2015 Millennium Development Goals. Oral health is a branch to be improved among these goals. The Brazilian experience has been drawing the attention of authorities, insofar as there have been direct improvements in oral health through state oral health programs, and also indirect results by improving the quality of life of the population. Included within the Brazilian oral health programs are the Family Health Program and Smiling Brazil Program. The former is a global healthcare program which involves primary oral healthcare, while the latter is a specialized oral care program. Among the social programs that would indirectly improve oral health are Family Stipend and the Edmond and Lily Safra International Institute of Neuroscience of Natal (ELS-IINN). In conclusion, although oral health problems are related to socioeconomic factors, the implementation of primary oral health programs and programs to improve the population's quality of life may directly or indirectly improve the oral health scenario. This fact is being observed in Brazil, where the oral health policies have changed, and social programs have been implemented.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Prefacio de Alicia Bárcena y Luciano Sáez

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O presente trabalho teve como objetivo investigar as práticas pedagógicas docentes com crianças em tratamento oncológico no Hospital Ophir Loyola (HOL) em Belém, Pará. Optouse como estratégia de pesquisa pelo estudo de caso descritivo tendo como sujeitos seis professores que trabalham com crianças que fazem tratamento de saúde no referido hospital, os quais foram ouvidos por meio de entrevistas estruturadas. O estudo, em seu referencial teórico, buscou analisar a criança em tratamento oncológico e a educação escolar hospitalar em seus aspectos históricos, legais, didáticos e curriculares. Os dados coletados foram analisados pela técnica de análise de conteúdo, chegando-se às seguintes categorias temáticas: dinâmica de trabalho dos professores do HOL; práticas docentes com crianças em tratamento oncológico no HOL; dificuldades e facilidades nas práticas docentes no HOL e formação inicial e continuada dos professores do HOL. Após análise dessas categorias concluiu-se que a educação escolar do HOL desenvolve um saber sistematizado, devidamente planejado e adaptado às necessidades das crianças em tratamento oncológico. Os atendimentos pedagógicos são realizados em vários espaços, de acordo com as possibilidades e necessidades dos alunos. Quanto às dificuldades dos professores na execução de suas atividades, os docentes apontaram: o tempo de permanência da criança no hospital, a situação física e emocional do aluno, a falta de materiais didáticos, as dificuldades de memorização e atenção das crianças decorrentes das medicações, as interrupções das aulas para procedimentos clínicos diversos e a falta de tempo para planejamento das atividades, que interferem no processo ensino aprendizagem. Comprovou-se também a necessidade de maiores estudos sobre o cuidado da saúde emocional dos professores. No que diz respeito à formação inicial verificou-se que estes não tiveram nenhuma formação específica para trabalhar em ambiente não convencional de educação, mas que buscam formação contínua para dar conta das demandas que se apresentam nesse espaço. Os resultados da pesquisa poderão servir de referencial para a formação de professores e em estudos na área de educação e saúde, assim como concorrer para a ampliação de políticas públicas que beneficiem a educação escolar em ambiente hospitalar.

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Ao longo das últimas décadas diversos países, inclusive o Brasil têm implementado políticas de atenção em saúde mental, baseadas no elemento central comum de alteração do eixo da atenção do hospital para a comunidade, objetivando a continuidade do cuidado e a atenção integral, um processo de se costuma denominar de Reforma Psiquiátrica. Buscando compreender qual o modelo de assistência aplicado no Pará entre 2007 e 2010, o tradicional, manicomial ou o da reforma psiquiátrica e quais os resultados da política em termos de impacto?” esta pesquisa foi realizada, a partir de uma revisão bibliográfica sobre os processos de reforma psiquiátrica em vários países da Europa, da América Latina sem perder de vista as especificidades do Brasil e do Pará e uma análise sobre o papel do Estado, das políticas públicas sociais, dentre elas a política pública de Saúde e o Sistema Único de Saúde, além de análise de documentos e entrevistas com os executores das políticas. Como resultados foram observados avanços na política de saúde mental entre 2007 e 2010, tais como aumento (96%) no número de serviços, ainda que com a efetividade questionada tanto pela gestão quanto pelo movimento social, além de um estabelecimento de canal de diálogo entre gestão e movimento social através de conselhos gestores, ouvidorias internas e eventos de capacitação diversos. Por outro lado, os problemas estruturais persistem e de acordo com a análise efetuada têm relação com o contexto político-econômico vivenciado pelo Brasil de aprofundamento das desigualdades sociais e da negação dos direitos sociais, econômicos, culturais e ambientais instituídos na Constituição de 1988. Fica evidenciada, assim, a consolidação do processo de globalização neoliberal, com ações voltadas para a estabilidade econômica e focalização de políticas públicas sociais. Como alternativa a essa situação a autora apresenta o ponto de vista de que o SUS é um sistema em construção e que o desafio posto na atual conjuntura que tenha por objetivo superar as profundas desigualdades sociais através de um movimento de massas que retome as propostas de superação da crise e avance em propostas concretas.

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Pós-graduação em Serviço Social - FCHS

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This work analyses the mental health policy-making activity of the Brazilian National Health Agency (ANS), responsible for controlling health insurance companies. Three points are discussed: a) the framework of an economic and private health assistance regulatory activity, b) the ANS and its regulation activity and c) the rules produced by ANS in the mental health care field. It was concluded that, despite advances like the legal obligation to ensure medical treatment to all the diseases listed in ICD-10, the inclusion of suicidal patient damage and self-inflicted damage care, care provided by a multiprofessional team, the increase in the number of sessions with a psychologist, with an occupational therapist and of psychotherapy sessions, and mental health day hospitals included as part of the services offered, the authors identified specific regulatory gaps in this area. Some issues that ANS has to solve so that it can really play its institutional role of defending the public interest in the private health system are: the regulation of co-participation and franchise mechanisms, the increasing co-participation as a limitation of psychiatric hospitalization, and the limited number of crisis intervention psychotherapy sessions.

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Objectives: The Brazilian public health system does not provide electroconvulsive therapy (ECT), which is limited to a few academic services. National mental health policies are against ECT. Our objectives were to analyze critically the public policies toward ECT and present the current situation using statistics from the Institute of Psychiatry of the University of Sao Paulo (IPq-HCFMUSP) and summary data from the other 13 ECT services identified in the country. Methods: Data regarding ECT treatment at the IPq-HCFMUSP were collected from January 2009 to June 2010 (demographical, number of sessions, and diagnoses). All the data were analyzed using SPSS 19, Epic Info 2000, and Excel. Results: During this period, 331 patients were treated at IPq-HCFMUSP: 221 (67%) were from Sao Paulo city, 50 (15.2%) from Sao Paulo's metropolitan area, 39 (11.8%) from Sao Paulo's countryside, and 20 (6.1%) from other states; 7352 ECT treatments were delivered-63.0% (4629) devoted entirely via the public health system (although not funded by the federal government); the main diagnoses were a mood disorder in 86.4% and schizophrenia in 7.3% of the cases. Conclusions: There is an important lack of public assistance for ECT, affecting mainly the poor and severely ill patients. The university services are overcrowded and cannot handle all the referrals. The authors press for changes in the mental health policies.