1000 resultados para Serviços de Assistência Domiciliar


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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Pós-graduação em Ginecologia, Obstetrícia e Mastologia - FMB

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OBJECTIVE: This study aimed to analyze the correlation between the levels of functional dependence of elderly living in the community, the burden related to care and the perception of quality of life in familiar caregivers. METHODS: This is an observational, descriptive and analytical study, using non probabilistic sampling selected by convenience in the period from December 2008 to May 2009, in the urban area of Curitiba and Colombo, state of Paraná, Brazil. Interviews were applied to caregivers, using demographic inquiry, functional evaluation of the aged, burden interview (Zarit-Burden-Interview) and quality of life instrument (WHOQOL-Bref). Spearman, Mann-Whitney and Kruskal Wallis coefficients were used to analyze the correlations between instruments and socio-demographic variables. Bivariate analyses identified which variables correlate with burden, and the most significant were included in a multiple linear regression. RESULTS: Forty-five caregivers were interviewed, mostly women (91.11%) with high educational level attending dependent elderly (66.77%). Moderate/severe burden was perceived in 75.55% of the sample. We found correlation between dependence, more severe burden in caregivers (r=-0.281, p=0.013) and worse perception of quality of life. The multiple linear regression identified strong association between burden related to care and psychological domain from WHOQOL-bref and time as caregiver (R²=0.58, p<0.001). CONCLUSION: In a sample of familiar caregivers, we identified correlations between lower burden related to care and better quality of life perceptions, as well as higher disability and less satisfactory quality of life perceptions.

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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Background: The possibility to acquire sexually transmitted diseases generates bio-psycho-social conflicts affecting daily life of women. Objective: To investigate the knowledge of women on the concept of being infected by the human papilloma virus (HPV) and to understand the significance they attributed to their condition as HPV carriers. Material and method: It is a qualitative study in which ten women were interviewed, after the result of a cytopathological exam suggesting HPV. Data were collected at the Center of Health School of the Universidade Estadual Paulista -UNESP-Brazil. Results: The significant items were: deception and preoccupation about the cure, since they indicate that it is very deceptive to be infected with an incurable disease by a person whom they trust; the method of having sexual relations and being infected again; the necessity of care and of being optimistic to face the disease and the threat of cervix cancer originating anxiety. Discussion: Orientations made by health professionals were efficacious to clarify the relationship with cancer development. It is possible to understand the necessity of assistance orientations and the opportunity to hear them, offering individualized quality care. This study also offers important elements to reinforce the educational role of health professionals, principally those referring to sexually transmitted infection and cancer, seeking prevention and early treatment with the offered information. However, there is no desire of finishing the subject regarding perception, thus there is much to discover about diseases related to human papilloma virus. Key words: women carriers of HPV, feelings attributed by women.

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The present study aims to identify families who have stock and are making use of medications, as well as assess the conditions of storage, security and use of these drugs. The study was conducted in a city of São Paulo, the interviews were conducted in households enrolled in one of ten units of the Estratégia de Saúde da Família (ESF) that the city provides and the sample was defined by means of stratified random sampling (134households, IC 95%). Data collection was conducted through interviews with a semistructured questionnaire during the first half of 2011. We interviewed 118 (88.0%) households, of which 112 (95.0%) had medications that were stored n insecure or inadequate places in 75.4% of households, non-prescription self-medication was a common practice in 46 (47 4%) households, and lack of identification and security of medications stored was observed in 60 (53.6%) households. Most households had stock of medicines, which were done improperly or unsecure, or have specialties with lack of identification and security, which can lead to poisoning or e ineffective therapy. The Pharmaceutical Assistance under SUS lacks social initiatives, with actions directed for medications users, which can be supplied by the presence of the pharmacist in the ESF, essential for the promotion of racional use of medicines, that, through the Pharmaceutical Care, can identify, correct and prevent possible problems related to drugs.

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OBJECTIVE: To understand the perception of nurses from the Family Health Strategy in relation to palliative care in the home. METHODS: A descriptive, exploratory study with a qualitative approach conducted with nine nurses from the Family Health Strategy of the municipality of Lavras - MG. Semi-structured interviews were conducted and data were subjected to content analysis. RESULTS: The various dimensions of care in the home context were identified, along with the performance and limitations of nurses in the care of the patient and his family at end of life. The capacity to establish a bond, by the proximity to people who receive their care, is a remarkable point of the action of these nurses with patients and families in end of life situations. CONCLUSION: The nurses consider the patient and his family as the unit of care, they have the opportunity to share solidarity, experiences and learning, not only from a professional standpoint, but above all, from a human one.

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Este trabalho investiga os limites à garantia constitucional do direito de defesa no Brasil, partindo de uma análise do uso do território paulista pela Defensoria Pública do Estado de São Paulo (DPESP), criada em 2006. Uma vez que as defensorias públicas oferecem assistência jurídica gratuita quase que exclusivamente aos pobres, o estudo de seus objetos e ações muito contribui para a compreensão destes limites. Assim, a pesquisa tem como objetivo testar a hipótese de que o uso do território paulista pela DPESP é expressão de como o sistema de justiça brasileiro não tem como prioridade a garantia constitucional do direito de defesa. Partindo de uma discussão teórica sobre a relação entre o território e o setor terciário, além da análise de uma série de mapas, o trabalho mostra como a localização das 41 unidades de atendimento da DPESP constitui um primeiro obstáculo ao acesso: na maior parte dos municípios atendidos, as unidades localizam-se nas áreas centrais enquanto os pobres habitam as periferias urbanas. Os deslocamentos representam um custo maior justamente para aqueles que mais necessitam dos serviços. A investigação em cada um dos municípios revela também a insuficiência no número de defensores. Ultrapassando a questão das localizações, a pesquisa analisa ainda os problemas estruturais, evidenciando que o sistema capitalista produz pobreza e concentração de renda, o Estado atende prioritariamente aos interesses empresariais e a justiça concentra seus esforços na garantia da ordem necessária aos negócios. Neste sentido, além de uma abordagem teórica a respeito do capitalismo, do Estado e da justiça, o trabalho recorre a dados empíricos do estado de São Paulo para evidenciar a produção estrutural de pobreza e a seletividade das ações estatais. Para teste da hipótese, são analisados igualmente os aspectos históricos da estruturação do direito na sociedade capitalista, destacando sua importância específica para a garantia dos interesses comerciais. Além disso, fundamentandose em pesquisa bibliográfica, a investigação sobre as origens dos serviços de assistência jurídica gratuita e da criação das defensorias públicas revela como estes são o resultado de difíceis embates políticos e que sua existência não é uma consequência natural do sistema legal pensado pelos ideólogos iluministas. A principal conclusão deste trabalho é que as dificuldades hoje enfrentadas pelas defensorias são, em grande medida, a expressão de uma estrutura social produtora de desigualdades e seletiva na aplicação da justiça. Neste sentido, a solução do problema do acesso à justiça aos mais pobres não se esgota na expansão dos serviços das defensorias. Este é apenas o começo, a partir do qual as desigualdades podem se tornar mais evidentes e as pessoas mais conscientes e exigentes de transformações sociais profundas.

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The present study aimed to understand the experience of being a family caregiver of a patient with Cerebrovascular Accident (CVA). The relevance of the study is to prove existence of a large number of caregivers of incapacitated patients, due to the CVA and it is not an academic research object, according to the literature. It is a qualitative research, which the guiding principle is the oral history of life, according to the theoretical foundation and operating of Meihy. Therefore, the following steps were highlighted: the target community, composed of all family caregivers of CVA patients; the colony, composed by family caregivers of CVA patients assisted by Home Care Service (HCS) of the Hospital José Pedro Bezerra (HJPB), in the city of Natal/RN; the network was composed of six caregivers who met the criteria for inclusion, and as zero point the first volunteer group. The population was composed of all family caregivers of patients attended by the HCS, of the HJPB having been addressed through interviews. For the empirical research there was the consent of that institution and approval by the Ethics Committee in Research of the Federal University of Rio Grande do Norte as CAAE 24569413.0.0000.5537 and, above all, with the acquiescence of employees in participating in the investigation, signing an informed consent. Of the empirical material, five categories of analysis were identified: the sense of being a caregiver; what has changed in the life of the caregiver; the feelings emerge in the relationship of care; the distance from family and friends; difficulties faced by the caregiver. The results show that the caregiver's life goes through profound transformations within the family as well as in all spheres of life. For the caregivers, assuming the care of a relative with CVA means renunciation and donation, compromising sometimes the individual projects and the family as a whole. In addition, they point out the confrontation of difficulties within the the assistance and humanization in healthcare, information, physical and emotional overload, as well as financial problems. Despite all the adversities that compromise the caregiver's life, it was possible to identify attitudes of resilience among caregivers, making them their daily life less strenuous and with more lightness. It is expected, therefore, that this research can contribute to a better orientation of professionals with the caregivers

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O presente trabalho teve como objectivo principal, analisar a agência do assistente social nos contextos da pobreza e exclusão social, tendo em conta que a mesma se desenvolve inserida numa estrutura social reguladora. Assim, pretendia-se compreender de que forma o assistente social, enquanto agente competente e capacitado de uma acção reflexiva, produz transformações e mudanças sociais nas relações que estabelece com outros agentes (utilizadores dos serviços de assistência social) considerando perspectivas de acção normalizante e/ou emancipatórias das situações de pobreza e exclusão social. Para isso, é feita uma exposição dos conceitos de cidadania e politica social uma vez que estas podem ser um meio para que os cidadãos possam ver reconhecidos os seus direitos de cidadania. Além disso, estabelece-se uma relação com estes conceitos e a pobreza e exclusão social, pois os indivíduos em situação de pobreza e exclusão social, estão desapossados de direitos, pelo que é urgente a criação de políticas e programas sociais eficazes para combater estes fenómenos sociais. O assistente social, enquanto técnico privilegiado na intervenção social, deve ser além de executor, participante na avaliação e elaboração dessas políticas. O trabalho apresenta ainda um estudo empírico utilizando como instrumento a medida do RSI, enquanto política actualmente definida pelo Estado como prioritária na intervenção realizada pelos assistentes sociais na pobreza e exclusão social.

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Mestrado em Marketing

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Tese (doutorado)—Universidade de Brasília, Centro de Desenvolvimento Sustentável, 2015.