638 resultados para Ethical guidelines
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El presente trabajo abarca el desarrollo del sector salud en los últimos años enfocado hacia las Instituciones Prestadoras de Servicios en Colombia, así como la problemática actual de la empresa Médicos Asociados, a partir de la implementación del nuevo diseño organizacional basado en la administración sistémica, el desarrollo del Código de Buen gobierno y el Código de ética o comportamiento que se vienen trabajando desde el 2.007.
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With increasing calls for global health research there is growing concern regarding the ethical challenges encountered by researchers from high-income countries (HICs) working in low or middle-income countries (LMICs). There is a dearth of literature on how to address these challenges in practice. In this article, we conduct a critical analysis of three case studies of research conducted in LMICs.We apply emerging ethical guidelines and principles specific to global health research and offer practical strategies that researchers ought to consider. We present case studies in which Canadian health professional students conducted a health promotion project in a community in Honduras; a research capacity-building program in South Africa, in which Canadian students also worked alongside LMIC partners; and a community-university partnered research capacity-building program in which Ecuadorean graduate students, some working alongside Canadian students, conducted community-based health research projects in Ecuadorean communities.We examine each case, identifying ethical issues that emerged and how new ethical paradigms being promoted could be concretely applied.We conclude that research ethics boards should focus not only on protecting individual integrity and human dignity in health studies but also on beneficence and non-maleficence at the community level, explicitly considering social justice issues and local capacity-building imperatives.We conclude that researchers from HICs interested in global health research must work with LMIC partners to implement collaborative processes for assuring ethical research that respects local knowledge, cultural factors, the social determination of health, community participation and partnership, and making social accountability a paramount concern.
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With increasing calls for global health research there is growing concern regarding the ethical challenges encountered by researchers from high-income countries (HICs) working in low or middle-income countries (LMICs). There is a dearth of literature on how to address these challenges in practice. In this article, we conduct a critical analysis of three case studies of research conducted in LMICs.We apply emerging ethical guidelines and principles specific to global health research and offer practical strategies that researchers ought to consider. We present case studies in which Canadian health professional students conducted a health promotion project in a community in Honduras; a research capacity-building program in South Africa, in which Canadian students also worked alongside LMIC partners; and a community-university partnered research capacity-building program in which Ecuadorean graduate students, some working alongside Canadian students, conducted community-based health research projects in Ecuadorean communities.We examine each case, identifying ethical issues that emerged and how new ethical paradigms being promoted could be concretely applied.We conclude that research ethics boards should focus not only on protecting individual integrity and human dignity in health studies but also on beneficence and non-maleficence at the community level, explicitly considering social justice issues and local capacity-building imperatives.We conclude that researchers from HICs interested in global health research must work with LMIC partners to implement collaborative processes for assuring ethical research that respects local knowledge, cultural factors, the social determination of health, community participation and partnership, and making social accountability a paramount concern.
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Após considerações gerais sobre a ética na pesquisa envolvendo seres humanos, focaliza-se a possibilidade de ocorrências de injustiças, sob a égide de diversas formas de poder. Exemplificam-se situações concretas. Enfatiza-se a análise das possíveis injustiças à luz da Bioética, com destaque para multi e transdisciplinaridade. O autor se posiciona quanto às características atuais da Bioética, cuja ótica levou à elaboração das Diretrizes éticas para a pesquisa envolvendo seres humanos, no Brasil (Resolução 196/96 e complementares do Conselho Nacional de Saúde). Descreve-se a sistemática das atividades do Grupo Executivo de Trabalho - GET, designado pelo Conselho Nacional de Saúde (órgão de controle social na área da saúde), para elaborar as Diretrizes. É dado destaque à participação dos diversos segmentos da sociedade, evidenciando multi e transdiciplinaridade, sob a coordenação do GET, do qual o autor foi Presidente. Comentam-se os principais tópicos das Diretrizes brasileiras, enfocando-se a sua relação com o tema de poder e injustiça. Salienta-se o papel dos Comitês de Ética em Pesquisa - CEP e da Comissão Nacional de Ética em Pesquisa - CONEP.
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A infecção pelo vírus da imunodeficiência humana (HIV) atinge cada vez mais mulheres em idade reprodutiva, o que conseqüentemente favorece o crescimento da transmissão vertical. Com a proposta de se obter informações da situação epidemiológica das grávidas infectadas pelo HIV na maior maternidade pública do norte do Brasil, foi realizado um estudo descritivo, retrospectivo, envolvendo 770 grávidas atendidas na triagem obstétrica da Fundação Santa Casa de Misericórdia do Pará, no período entre 2004 a 2010. Após análise dos dados obtidos a partir de prontuários, sob os preceitos éticos recomendados, obteve-se os seguintes resultados: a prevalência e a incidência no período foram de 1,87% e 0,40%, respectivamente; a faixa etária predominante estava entre 18 e 23 anos (42,1%), sendo que 50,4% tinham ensino fundamental incompleto, 68,2% exerciam atividades do lar, 89% eram solteiras e a maioria procedia de municípios com mais de 50 mil habitantes (Belém, 53,9%; Ananindeua, 13,0%; Castanhal 4,8%; Paragominas, 3,6%; Tailândia, 3,5%; Barcarena 3,1%; Marituba, 2,9%; Abaetetuba, 1,8% e São Miguel do Guamá, 0,6%). O pré-natal foi realizado por 91,9% destas grávidas, com 4 a 6 consultas (61,0%), 85,2% procuraram as Unidades Básica de Saúde e 12,8% as Unidades de Referência Especializada ao atendimento e acompanhamento de mulher HIV positiva; 75,1% já sabiam antes da gravidez atual que estavam infectadas pelo HIV, 3,6%, tomaram conhecimento durante o pré-natal e 21,3% no momento do parto através do teste rápido, totalizando em 78,7% a cobertura do diagnóstico da infecção pelo HIV antes da chegada a maternidade, e destas 75,1% fezeram tratamento especifico durante o pré-natal. O parto cirúrgico foi o de maior ocorrência (85,1%); 89,7% das grávidas receberam Zidovudina profilática no parto, destas 85,1% fizeram parto cirúrgico e 14,9% parto normal. O conhecimento das variáveis epidemiológicas da maior casuística de grávidas infectadas pelo HIV da Amazônia brasileira, que chegaram a maternidade, permitiu concluir que o perfil de faixa etária, escolaridade, adesão ao pré-natal e número de consultas está compatível com os dados nacionais, entretanto, a maior procedência de grávidas de municípios de médio e grande porte opõem-se ao fenômeno da interiorização da epidemia à municípios menores como está sendo observado no país. Uma taxa de 21,3% de falta de cobertura diagnóstica de infecção pelo HIV no momento do parto, uma rotina em muitos serviços brasileiros, depõem contra a qualidade da execução dos programas de saúde e, sobretudo mostra que a equipe de assistência precisa melhorar o acolhimento às grávidas durante o pré-natal, independente do número de consultas, visto que o teste do HIV deve ser solicitado ainda na primeira consulta. Estas medidas devem ser reforçadas no Estado do Pará, que mostrou alta taxa de prevalência da infecção pelo HIV na gravidez, contrapondo-se as demais regiões do país onde há um decréscimo, o que tem favorecido a elevação do número de crianças infectadas pelo vírus HIV no Brasil.
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Pós-graduação em Serviço Social - FCHS
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Entire issue (large pdf file) Articles include: Improving Family Functioning through Family Preservation Services: Results of the Los Angeles Experiment. Family Preservation Journal. William Meezan and Jacquelyn McCroskey Idiographic Self-Monitoring Instruments to Empower Client Participation and Evaluate Outcome in Intensive Family Preservation Services. Barbara Peo Early Evaluating Family Preservation in Nevada: A University-State Agency Collaboration. Christine Bitoni and Joy Salmon The Family Partners Credit Card: A Token Economy System Adapted for Intensive Family Preservation Services to Enable Families to Manage Difficult Behavior of Adolescents. Jude Nichols and Barbara Peo Early Toward the Development of Ethical Guidelines for Family Preservation. David A Dosser Jr., Richard J. Shaffer, Michaux M. Shaffer, DeVault Clevenger, and Dustin K. Jefferies
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Objective: To summarize current knowledge about genetic susceptibility to mood disorders and examine ethical and policy issues that will need to be addressed if robustly replicated susceptibility alleles lead to proposals to screen and intervene with persons at increased genetic risk of developing mood disorders. Method: Empirical studies and reviews of the genetics of unipolar and bipolar depression were collected via MEDLINE and psycINFO database searches. Results: A number of candidate genes for depression have been identified, each of which increases the risk of mood disorders two- or threefold. None of the associations between these alleles and mood disorders have been consistently reported to date. Conclusions: Screening the population for genetic susceptibility to mood disorders is unlikely to be a practically useful policy (given plausible assumptions). Until there are effective treatments for persons at increased risk, screening is arguably unethical. Screening within affected families to advise on risks of developing depression would entail screening children and adolescents, raising potentially serious ethical issues of consent and stigmatization. Genetic research on depression should continue under appropriate ethical guidelines that protect the interests of research participants.
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The concepts of childhood are part of a cultural construction and vary throughout history politically, economically and socially. Nouns such as "childhood" and "child" did not exist as sense of unity in periods prior to modernity, reinforcing their historical character as concepts that have been socially constructed as profess the Historical Social Psychology, theoretical perspective which will support this research. The sociology of childhood distinguishes the terms and changes the approach toward the adult researcher approach with respect to children, aiming to give voice to the child. When it comes to defining the role of children in research, the researcher must take into consideration several relevant criteria such as age, gender, time, listening to the adults close to the children, the level of language and education and which children that will be heard in a group. It is from this discussion, considering the importance of children's participation in the research that are established the purpose of this work, namely, to analyze the theoretical and methodological aspects and ethical guidelines considered in the research process with children, by researchers at the UFRN, presenting as specific objectives: analyze and discuss, from research reports, the adopted ethical procedures and methods used in research with children. Set the goal, it was made a search of the UFRN Research Groups in SIGAA in order to select those which investigate children for participating in our survey. Among the centers of UFRN, we selected the Health Sciences Centre - CCSA, the Humanities Center, Letters and Arts - CCHLA, the Biosciences Center - CB and the Health Sciences Center - CCS, a total of 64 finalized reports to be analyzed. And here it is the observation that the foolish reports were not analyzed for ethical reasons as the guiding of this dissertation is the coordinator of the research group mentioned. In this study, we chose the documentary analysis of the finalized reports from UFRN research projects teachers / researchers as procedure to set up the corpus of the research. Data analysis was performed from the qualitative analysis in the following categories were established: the concept of childhood, concept of child, age of the subjects, the research context, theoretical and methodological care adopted and ethical care. It is hoped that this study will contribute with reflections on the ethical and theoretical and methodological care on research with children. The research showed how some of the results: significant number of reports excluded by repetition, most reports did not bring any closing remarks, no different procedures for children, with rare exceptions, the ethical issue was not mentioned in 50% of reports.
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Aim: To investigate the construction of cobalt-chromium removable partial dentures by commercial private dental laboratories. Methods: Ninety master casts for fabrication of cobalt-chromium removable partial dentures were obtained from three commercial laboratories randomly selected. Casts were assessed for dental arch treated, Kennedy classification, cast surveying, denture design information provided by the dentist, and mouth preparation (rest seat, guiding plane and retentive area). Dental technicians answered a questionnaire regarding qualification of assisted dentists, monthly number of framework castings, and use of dental surveyor. Mouth preparation was compared among laboratories using Kruskal-Wallis test (α=0.05). Results: The percentage of Kennedy class I was 16%, class II 19%, class III 56%, and class IV 9%. The majority of master cats (51%) examined was sent to dental laboratories without any design information and did not comply with ethical guidelines in the provision of RPD. Approximately half of the casts were considered “inappropriate” for guiding planes and retentive areas. One of the laboratories presented all casts “inappropriate” for rest seat distribution (p<0.001). Conclusions: Mouth preparation frequently failed for guiding planes, retentive areas and distribution of rest seats. It is necessary to provide students with adequate clinical experience at the dental school environment, which will actually be carried into the practice of dentistry.
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Aim: To investigate the construction of cobalt-chromium removable partial dentures by commercial private dental laboratories. Methods: Ninety master casts for fabrication of cobalt-chromium removable partial dentures were obtained from three commercial laboratories randomly selected. Casts were assessed for dental arch treated, Kennedy classification, cast surveying, denture design information provided by the dentist, and mouth preparation (rest seat, guiding plane and retentive area). Dental technicians answered a questionnaire regarding qualification of assisted dentists, monthly number of framework castings, and use of dental surveyor. Mouth preparation was compared among laboratories using Kruskal-Wallis test (α=0.05). Results: The percentage of Kennedy class I was 16%, class II 19%, class III 56%, and class IV 9%. The majority of master cats (51%) examined was sent to dental laboratories without any design information and did not comply with ethical guidelines in the provision of RPD. Approximately half of the casts were considered “inappropriate” for guiding planes and retentive areas. One of the laboratories presented all casts “inappropriate” for rest seat distribution (p<0.001). Conclusions: Mouth preparation frequently failed for guiding planes, retentive areas and distribution of rest seats. It is necessary to provide students with adequate clinical experience at the dental school environment, which will actually be carried into the practice of dentistry.
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From an ethical perspective, clinical research involving humans is only acceptable if it involves the potential for benefit. Various characteristics can be applied to differentiate research benefit. Often benefit is categorized in direct or indirect benefit, whereby indirect benefit might be further differentiated in collective or benefit for the society, excluding or including the trial patient in the long term. Ethical guidelines, such as the Declaration of Helsinki in its latest version, do not precisely favor a particular type of benefit.
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This document is designed to provide guidelines to professionals working with people who are HIV positive where the person living with HIV is placing other people at risk of infection through unprotected sexual intercourse or needle sharing, without informing his/her partner of the risk Download the Report here