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4.
Hist. ciênc. saúde-Manguinhos ; 26(1): 71-84, Jan.-Mar. 2019.
Article in Portuguese | LILACS | ID: biblio-989865

ABSTRACT

Resumo Não há uma visão clara na historiografia internacional sobre a participação do Brasil na Conferência de Washington de 1884. No Brasil há uma interpretação de que o voto brasileiro acompanhou a França, por razões de subordinação. Este texto pretende estabelecer um diálogo com essas produções, ao trazer fontes inéditas sobre o tema, como as cartas trocadas por Luiz Cruls, tanto com o imperador como com sua esposa, bem como notícias de periódicos, anais e relatórios. Neste artigo foi utilizada uma abordagem da história da ciência, preocupada com os processos de institucionalização da astronomia no Brasil em meio a um debate mundial sobre padronização e universalização da ciência.


Abstract There is no clear picture in the international historiography of Brazil's participation at the International Prime Meridian Conference in Washington of 1884. In Brazil there exists the prevailing interpretation that the Brazilian vote accompanied France for reasons of subordination. This work seeks to analyze this interpretation, by scrutinizing unpublished sources on the subject, such as the letters exchanged by Luiz Cruls both with the emperor and with his wife, as well as news articles in journals, annals and reports. In this article, an approach to the history of science was adopted that was concerned with the processes of institutionalization of astronomy in Brazil in the midst of a worldwide debate on the standardization and universalization of science.


Subject(s)
Humans , Telemedicine/legislation & jurisprudence , Telemedicine/trends , Guidelines as Topic , Brazil , Telemedicine/standards , Codes of Ethics , Ethics, Medical , Health Planning Councils/legislation & jurisprudence
8.
Pharm. pract. (Granada, Internet) ; 12(3): 0-0, jul.-sept. 2014. tab
Article in English | IBECS | ID: ibc-126742

ABSTRACT

Background: Counter counseling is an important part of community pharmacies service delivery. Difficulties arise because customers appear less interested than the staff in discussing their medicine. It is unclear how individual pharmacies differ with regard to overcoming these obstacles. Objective: This study explores differences in the communication practices of pharmacies with regard to engaging customers in medicine dialogues. Methods: The work of Stevenson et al. describing five types of interaction scenarios at the counter was used for structured overt non-participant observations of 100 encounters in each of five Danish pharmacies. Variation in pharmacies success in engaging customers in medicine dialogues were calculated using descriptive statistics, and the statistical significance of observed differences across pharmacies was analyzed using odds ratios (OR). Results: Considerable differences between the pharmacies were identified. Differences exist in how often pharmacy staff attempts to encourage customers to participate in medication dialogues and how often they succeed. The pharmacies serving the most customers per day were the most successful. A possible link between a low number of refill customers offered counseling and ‘success rate’ was identified. Conclusions: The pharmacies showed considerable variation in attempts to engage customers in medication dialogues at the counter and success in doing so. The reasons for the identified patterns are unclear (AU)


Antecedentes: El consejo de mostrador es una parte importante de la provisión de servicios en farmacias comunitarias. Las dificultades aparecen porque los clientes parecen estar menos interesados que el personal en discutir sobre sus medicamentos. No está claro cómo se diferencian las farmacias para superar estos obstáculos. Objetivo: Este estudio explora las diferencias en las prácticas de comunicación de farmacias en relación a atraer clientes a diálogos sobre medicamentos. Métodos: Se usó el trabajo de Stevenson et al. que describe cinco tipos de escenarios de interacción en el mostrador para 100 observaciones estructuradas, abiertas y sin participación de encuentros en cinco farmacias danesas. Se calculó mediante estadística descriptiva la variación en el éxito en atraer clientes a diálogos sobre medicamentos, y la significación estadística de las diferencias encontradas se analizó usando odds ratios (OR). Resultados: Se identificaron diferencias considerables entre las farmacias. Existían diferencias en la frecuencia en que el personal de la farmacia intenta animar a los clientes a participar en diálogos sobre la medicación y en la frecuencia en que tenían éxito. Las farmacias que atendían más clientes por día tenían más éxito. Se identificó un posible nexo entre un bajo número de clientes a los que se les ofrece consejo y la ‘tasa de éxito’. Conclusión: Las farmacias mostraron variaciones considerables en los intentos de atraer clientes a diálogos sobre medicación en el mostrador y en el éxito en hacerlo. Las causas de los patrones identificados son inciertas (AU)


Subject(s)
Humans , Male , Female , Middle Aged , Pharmacies/organization & administration , Pharmaceutical Services/organization & administration , Health Planning Councils/legislation & jurisprudence , Health Planning Councils/organization & administration , Professional Practice/organization & administration , Pharmaceutical Services/trends , Pharmaceutical Services , Odds Ratio , Denmark/epidemiology
13.
S Afr Med J ; 102(3 Pt 1): 115-7, 2012 Feb 23.
Article in English | MEDLINE | ID: mdl-22380892

ABSTRACT

The Health Professions Council of South Africa (HPCSA)'s top management has ordered a probe of all foreign-qualified specialist registrations going back at least a decade, and instituted a 'double verification' mechanism for all future such applications following a dramatic system failure.


Subject(s)
Foreign Medical Graduates , Neurosurgery , Specialty Boards/standards , Foreign Medical Graduates/legislation & jurisprudence , Foreign Medical Graduates/standards , Health Personnel/legislation & jurisprudence , Health Personnel/standards , Health Planning Councils/legislation & jurisprudence , Health Planning Councils/standards , Humans , Neurosurgery/education , Public Health/legislation & jurisprudence , Public Health/standards , Quality of Health Care/standards , South Africa , Workforce
15.
Cad. saúde pública ; 27(12): 2315-2326, dez. 2011.
Article in Portuguese | LILACS | ID: lil-610713

ABSTRACT

Este artigo apresenta um modelo de avaliação da participação popular em sistemas municipais de saúde. Trata-se de pesquisa avaliativa cuja construção da matriz utilizou o referencial teórico da legislação existente que orienta a participação popular na formulação de estratégias e no controle da execução das políticas de saúde. Os indicadores e medidas foram validados por técnica de consenso com especialistas. O modelo proposto tem 26 indicadores divididos em cinco dimensões avaliativas, que refletem a adequação à legislação da estrutura, organização, representatividade, participação no planejamento em saúde e autonomia dos Conselhos Municipais de Saúde. Sua aplicabilidade foi testada em 24 municípios de Santa Catarina, Brasil. Os dados analisados indicaram os melhores resultados para a dimensão "sistema de planejamento do SUS", e os piores para as dimensões "estrutura e autonomia". Apenas dois municípios apresentaram bom resultado para o indicador sintético final. Foi demonstrada a viabilidade e adequação do modelo de avaliação proposto.


This article presents a model for the evaluation of community participation in municipal (county) health systems. The theoretical basis for this evaluative study was the existing Brazilian legislation on community participation in drafting health strategies and overseeing health policy implementation. The indicators and measures were validated using the expert consensus technique. The proposed model has 26 indicators divided into five evaluative dimensions that reflect the legislation's adequacy for the structure, organization, representativeness, health planning participation, and autonomy of the Municipal Health Councils. Its applicability was tested in 24 municipalities in Santa Catarina State, Brazil. The data analysis indicated the best results for the dimension "planning system in the Unified National Health System" and the worst for "structure" and "autonomy". Only two municipalities showed good results for the final summary indicator. The study demonstrated the feasibility and adequacy of the proposed evaluation model.


Subject(s)
Humans , Community Participation , Health Planning Councils/organization & administration , National Health Programs/organization & administration , National Health Systems , Brazil , Health Policy , Health Planning Councils/legislation & jurisprudence , Local Government , National Health Programs/legislation & jurisprudence
16.
J Palliat Med ; 14(11): 1240-5, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21988487

ABSTRACT

Mechanisms are needed to foster discussion of policy choices about end-of-life care, identify areas of general agreement, and clarify possible areas of disagreement. The Maryland State Advisory Council on Quality Care at the End of Life (MSAC), created by legislation as a permanent part of Maryland government, is one such mechanism. We describe the rationale for creating the MSAC, its operational features, and some of its successes and challenges. Given state-to-state variation in many aspects of health care organization and financing, we do not present the MSAC as a model to be adopted in every state. The MSAC's body of work over 8 years indicates that the model can be an effective catalyst for positive change in end-of-life policy making. Reformers elsewhere should consider this model, with an eye to both the MSAC's accomplishments and areas in which a different approach might be more fruitful.


Subject(s)
Health Planning Councils/organization & administration , Health Policy/legislation & jurisprudence , Palliative Care/standards , Quality Assurance, Health Care/standards , Terminal Care/standards , Health Planning Councils/legislation & jurisprudence , Humans , Maryland , Palliative Care/legislation & jurisprudence , Policy Making , Quality Assurance, Health Care/legislation & jurisprudence , Terminal Care/legislation & jurisprudence
17.
BMC Health Serv Res ; 11: 215, 2011 Sep 12.
Article in English | MEDLINE | ID: mdl-21910899

ABSTRACT

BACKGROUND: Legislation demands the establishment of client councils in Dutch nursing homes and residential care facilities. The members of those councils are residents or their representatives. Client councils have the right to participate in the strategic management of long-term care facilities. More specifically, they need to be consulted regarding organisational issues and a right to consent on issues regarding daily living of residents, including CQ-index research. CQ-index research concerns a method that measures, analyses and report clients' experiences about the quality of care. Research questions were: 'Do client councils exercise their rights to be consulted and to give their consent?' and 'What is the role of client councils in the process of measuring clients' experiences with the CQ-index and what is their opinion about the CQ-index?' METHODS: Postal questionnaires were sent to members of 1,540 client councils of Dutch nursing homes and residential care facilities. The questionnaire focussed on background information and client councils' involvement in decision-making and strategic management. RESULTS: The response rate was 34% (n = 524). Most councils consisted of seven members (range: 5 to 12 members). One out of four members participating in the client councils were clients themselves. Although councils have a legal right to be consulted for organisational issues like finance, vision, annual report, and accommodation, less than half the councils (31-46%) reported that they exercised this right. The legal right to consent was perceived by 18 to 36% of the councils regarding client care issues like food and drink, complaints registration, respectful treatment, and activities. For CQ-index research, only 18% of the client councils perceived a right to consent. Their rights to choose an approved contractor -who performs CQ-index research- and indicating improvement priorities, were hardly used. CONCLUSIONS: Client councils play a rather passive role in determining the policy on quality of long-term care. Therefore, specific attention and actions are needed to create a more proactive attitude in councils towards exercising their rights, which are already supported by legislation.


Subject(s)
Nursing Homes/organization & administration , Patient Participation/legislation & jurisprudence , Patient Rights , Total Quality Management , Cross-Sectional Studies , Female , Health Planning Councils/legislation & jurisprudence , Humans , Long-Term Care/legislation & jurisprudence , Male , Netherlands , Patient Satisfaction , Public Relations , Residential Facilities/organization & administration , Surveys and Questionnaires
19.
Cad Saude Publica ; 27(12): 2315-26, 2011 Dec.
Article in Portuguese | MEDLINE | ID: mdl-22218575

ABSTRACT

This article presents a model for the evaluation of community participation in municipal (county) health systems. The theoretical basis for this evaluative study was the existing Brazilian legislation on community participation in drafting health strategies and overseeing health policy implementation. The indicators and measures were validated using the expert consensus technique. The proposed model has 26 indicators divided into five evaluative dimensions that reflect the legislation's adequacy for the structure, organization, representativeness, health planning participation, and autonomy of the Municipal Health Councils. Its applicability was tested in 24 municipalities in Santa Catarina State, Brazil. The data analysis indicated the best results for the dimension "planning system in the Unified National Health System" and the worst for "structure" and "autonomy". Only two municipalities showed good results for the final summary indicator. The study demonstrated the feasibility and adequacy of the proposed evaluation model.


Subject(s)
Community Participation , Health Planning Councils/organization & administration , National Health Programs/organization & administration , Brazil , Health Planning Councils/legislation & jurisprudence , Health Policy , Humans , Local Government , National Health Programs/legislation & jurisprudence
20.
Cien Saude Colet ; 15(5): 2431-6, 2010 Aug.
Article in Portuguese | MEDLINE | ID: mdl-20802875

ABSTRACT

The present study has a documentary character and analyzes the resolutions registered in minutes of meetings of a Health Council, as a form to characterize the social control in health carried through for this instance. The majority of the resolutions were referred to the approval of Programs and Projects, arising from the Secretariat of Health, regarding the reform, material and equipment acquisition for units of health, the qualification of existing services or the creation of new services. The study suggests that the practical one of this council seems to be bureaucratic, without any proposal of politics of health for the council is visualized. The way the resolutions have being legalized does not characterize its guiding not even the visibility of the actions for the population in general. In the studied case, it is signaled that the mere regular functioning of this council does not guarantee that exist effective social control.


Subject(s)
Health Planning Councils/legislation & jurisprudence , Social Control, Formal , Brazil
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