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1.
Glob Public Health ; 17(6): 1041-1054, 2022 06.
Artigo em Inglês | MEDLINE | ID: mdl-33736572

RESUMO

Since the end of the Cold War, health has gone from a peripheral concern in foreign policy negotiations to a prominent place on the global political agenda. While the rise of health onto the foreign policy agenda is by now old news, the driving forces behind its expansion into new political spheres remain understudied and undertheorized. This article builds on empirical findings from a four-country study of the integration of health into foreign policy, and proposes a conceptual approach to GHD to improve understanding of the conditions under which health is successfully positioned on the foreign policy agenda. Our approach consists of three dimensions: features of institutions and the interest various actors represent in GHD; the ideational environment in which GHD operates; and issue characteristics of the specific health concern entering foreign policy. Within each dimension, we identify specific variables that, in combination, make up the explanatory power of the proposed approach. The proposed approach does not relate to, or build upon, a single social sciences, public health, or international relations (IR) theory, but can be seen as a heuristic device to identify dimensions and variables that may shape why certain health issues rise onto the foreign policy agenda.


Assuntos
Diplomacia , Saúde Global , Política de Saúde , Humanos , Internacionalidade , Negociação , Política Pública
2.
Rheumatology (Oxford) ; 60(10): 4671-4680, 2021 10 02.
Artigo em Inglês | MEDLINE | ID: mdl-33528002

RESUMO

OBJECTIVES: GCA is a large vessel vasculitis (LVV) presenting with headache, jaw claudication, musculoskeletal and visual involvement. Current treatment is glucocorticoids and anti-IL-6 tocilizumab in refractory disease. The objective of this study was to explore the impact of GCA and its treatment on people's health-related quality of life (HRQoL), to inform the development of a disease-specific patient-reported outcome measure (PROM) for use in clinical trials and practice. METHODS: Participants from the UK and Australia, with biopsy- or imaging-confirmed GCA, were interviewed to identify salient aspects of HRQoL in relation to GCA and its treatment. Purposive sampling included a range of demographic and disease features (cranial, LVV-GCA and visual involvement). Inductive analysis identified individual themes of importance, then domains. Candidate questionnaire items were developed from the individual themes, refined by piloting, cognitive interviews and a linguistic translatability assessment. RESULTS: Thirty-six interviews were conducted to saturation with participants with GCA from the UK (25) and Australia (11). Mean age was 74 years, 23 (63.9%) were female, 13 (36.1%) had visual loss and 5 (13.9%) had LVV-GCA. Thirty-nine individual themes within five domains were identified: physical symptoms; activity of daily living and function; participation; psychological impact; and impact on sense of self and perception of health. Sixty-nine candidate items were developed from individual themes; piloting and refinement resulted in a 40-item draft questionnaire. CONCLUSION: This international qualitative study underpins the development of candidate items for a disease-specific PROM for GCA. The draft questionnaire is now ready for psychometric testing.


Assuntos
Arterite de Células Gigantes/psicologia , Medidas de Resultados Relatados pelo Paciente , Qualidade de Vida/psicologia , Idoso , Anticorpos Monoclonais Humanizados/uso terapêutico , Austrália , Efeitos Psicossociais da Doença , Autoavaliação Diagnóstica , Feminino , Estado Funcional , Arterite de Células Gigantes/tratamento farmacológico , Glucocorticoides/uso terapêutico , Humanos , Masculino , Pesquisa Qualitativa , Autoimagem , Participação Social/psicologia , Reino Unido
3.
Health Technol Assess ; 23(57): 1-130, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31601357

RESUMO

BACKGROUND: Fatigue is a major problem in rheumatoid arthritis (RA). There is evidence for the clinical effectiveness of cognitive-behavioural therapy (CBT) delivered by clinical psychologists, but few rheumatology units have psychologists. OBJECTIVES: To compare the clinical effectiveness and cost-effectiveness of a group CBT programme for RA fatigue [named RAFT, i.e. Reducing Arthritis Fatigue by clinical Teams using cognitive-behavioural (CB) approaches], delivered by the rheumatology team in addition to usual care (intervention), with usual care alone (control); and to evaluate tutors' experiences of the RAFT programme. DESIGN: A randomised controlled trial. Central trials unit computerised randomisation in four consecutive cohorts within each of the seven centres. A nested qualitative evaluation was undertaken. SETTING: Seven hospital rheumatology units in England and Wales. PARTICIPANTS: Adults with RA and fatigue severity of ≥ 6 [out of 10, as measured by the Bristol Rheumatoid Arthritis Fatigue Numerical Rating Scale (BRAF-NRS)] who had no recent changes in major RA medication/glucocorticoids. INTERVENTIONS: RAFT - group CBT programme delivered by rheumatology tutor pairs (nurses/occupational therapists). Usual care - brief discussion of a RA fatigue self-management booklet with the research nurse. MAIN OUTCOME MEASURES: Primary - fatigue impact (as measured by the BRAF-NRS) at 26 weeks. Secondary - fatigue severity/coping (as measured by the BRAF-NRS); broader fatigue impact [as measured by the Bristol Rheumatoid Arthritis Fatigue Multidimensional Questionnaire (BRAF-MDQ)]; self-reported clinical status; quality of life; mood; self-efficacy; and satisfaction. All data were collected at weeks 0, 6, 26, 52, 78 and 104. In addition, fatigue data were collected at weeks 10 and 18. The intention-to-treat analysis conducted was blind to treatment allocation, and adjusted for baseline scores and centre. Cost-effectiveness was explored through the intervention and RA-related health and social care costs, allowing the calculation of quality-adjusted life-years (QALYs) with the EuroQol-5 Dimensions, five-level version (EQ-5D-5L). Tutor and focus group interviews were analysed using inductive thematic analysis. RESULTS: A total of 308 out of 333 patients completed 26 weeks (RAFT, n/N = 156/175; control, n/N = 152/158). At 26 weeks, the mean BRAF-NRS impact was reduced for the RAFT programme (-1.36 units; p < 0.001) and the control interventions (-0.88 units; p < 0.004). Regression analysis showed a difference between treatment arms in favour of the RAFT programme [adjusted mean difference -0.59 units, 95% confidence interval (CI) -1.11 to -0.06 units; p = 0.03, effect size 0.36], and this was sustained over 2 years (-0.49 units, 95% CI -0.83 to -0.14 units; p = 0.01). At 26 weeks, further fatigue differences favoured the RAFT programme (BRAF-MDQ fatigue impact: adjusted mean difference -3.42 units, 95% CI -6.44 to - 0.39 units, p = 0.03; living with fatigue: adjusted mean difference -1.19 units, 95% CI -2.17 to -0.21 units, p = 0.02; and emotional fatigue: adjusted mean difference -0.91 units, 95% CI -1.58 to -0.23 units, p = 0.01), and these fatigue differences were sustained over 2 years. Self-efficacy favoured the RAFT programme at 26 weeks (Rheumatoid Arthritis Self-Efficacy Scale: adjusted mean difference 3.05 units, 95% CI 0.43 to 5.6 units; p = 0.02), as did BRAF-NRS coping over 2 years (adjusted mean difference 0.42 units, 95% CI 0.08 to 0.77 units; p = 0.02). Fatigue severity and other clinical outcomes were not different between trial arms and no harms were reported. Satisfaction with the RAFT programme was high, with 89% of patients scoring ≥ 8 out of 10, compared with 54% of patients in the control arm rating the booklet (p < 0.0001); and 96% of patients and 68% of patients recommending the RAFT programme and the booklet, respectively, to others (p < 0.001). There was no significant difference between arms for total societal costs including the RAFT programme training and delivery (mean difference £434, 95% CI -£389 to £1258), nor QALYs gained (mean difference 0.008, 95% CI -0.008 to 0.023). The probability of the RAFT programme being cost-effective was 28-35% at the National Institute for Health and Care Excellence's thresholds of £20,000-30,000 per QALY. Tutors felt that the RAFT programme's CB approaches challenged their usual problem-solving style, helped patients make life changes and improved tutors' wider clinical practice. LIMITATIONS: Primary outcome data were missing for 25 patients; the EQ-5D-5L might not capture fatigue change; and 30% of the 2-year economic data were missing. CONCLUSIONS: The RAFT programme improves RA fatigue impact beyond usual care alone; this was sustained for 2 years with high patient satisfaction, enhanced team skills and no harms. The RAFT programme is < 50% likely to be cost-effective; however, NHS costs were similar between treatment arms. FUTURE WORK: Given the paucity of RA fatigue interventions, rheumatology teams might investigate the pragmatic implementation of the RAFT programme, which is low cost. TRIAL REGISTRATION: Current Controlled Trials ISRCTN52709998. FUNDING: This project was funded by the NIHR Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 23, No. 57. See the NIHR Journals Library website for further project information.


Rheumatoid arthritis (RA) is a lifelong inflammatory condition affecting multiple joints, with fatigue as a major consequence. Cognitive­behavioural therapy (CBT) helps patients work out links between symptoms, behaviours and thoughts driving those behaviours (e.g. why someone pushes on when exhausted), and understanding these links helps patients make changes. A CBT programme for groups of RA patients, facilitated by a psychologist, reduces fatigue impact. However, few rheumatology teams have psychologists. The study tested whether or not rheumatology nurses and occupational therapists (OTs) could facilitate the programme [named RAFT, i.e. Reducing Arthritis Fatigue by clinical Teams using cognitive­behavioural (CB) approaches] after brief training. The study compared the RAFT programme with usual care for RA fatigue (i.e. a short discussion of an arthritis fatigue booklet). All 333 patients received usual care, and then half of the patients were allocated (by chance) to also attend the seven-session RAFT programme. The study compared the RAFT programme with usual care for effects on fatigue, quality of life, cost and value for money. In addition, the rheumatology nurse and OT RAFT tutors were interviewed for their views on the RAFT programme. The study found that patients' fatigue impact was reduced by both the RAFT programme and usual care at 6 months and 2 years, but patients undertaking the RAFT programme improved significantly more than those receiving usual care alone. Differences were seen for improvements in fatigue impact, fatigue coping, emotional fatigue and living with fatigue. Patients were very satisfied with the RAFT programme and attended most of the sessions. The study found no significant difference between the NHS costs of the RAFT programme and usual care. Neither the RAFT programme nor usual care changed quality of life; therefore, standard value-for-money tests showed no difference between them. Tutors found that the CB questioning approach of the RAFT programme was different from their usual problem-solving style, but helped patients make life changes, and the new CB skills improved tutors' wider clinical practice. In conclusion, the trial has shown that the RAFT programme has a small to medium effect on reducing fatigue impact in patients with RA and is a potentially low-cost intervention that can be delivered by rheumatology nurses and OTs rather than a psychologist.


Assuntos
Artrite Reumatoide/psicologia , Terapia Cognitivo-Comportamental/economia , Fadiga/prevenção & controle , Equipe de Assistência ao Paciente , Idoso , Artrite Reumatoide/enfermagem , Análise Custo-Benefício , Inglaterra , Feminino , Grupos Focais , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Terapia Ocupacional , Pesquisa Qualitativa , Autorrelato , País de Gales
4.
Cien Saude Colet ; 23(7): 2277-2290, 2018 Jul.
Artigo em Português, Inglês | MEDLINE | ID: mdl-30020381

RESUMO

This article examines the activities of national and international actors in Pharmaceutical Services (PS) in Mozambique from 2007 to 2012, focusing on the public provision of HIV/Aids, malaria and tuberculosis medicines. It describes how PS functions in the country, what actors are involved in this area and the relations among them, pursuing salient issues in the modus operandi of partners in cooperation. The methodology combines literature review, document survey and analysis and interviews. The theoretical and analytical framework was given by the policy analysis approach, focusing on the role of the State and its interrelations with other actors in foreign aid in PS, and also by the networks approach. It was concluded that the interactions among the actors involved is complex and characterised by operational fragmentation and overlapping of activities between entities, centralised medicine procurement in the hands of few agents, bypassing of national structures and disregard for the strengthening needed to bolster national health system autonomy. Despite some advances in the provision and availability of medicines for these diseases, external dependence is strong, which undermines the sustainability of PS in Mozambique.


Este artigo analisa a ação de atores nacionais e internacionais na Assistência Farmacêutica (AF) em Moçambique, no período de 2007 a 2012, com foco na provisão pública de medicamentos para HIV/Aids, malária e tuberculose. Descreve-se o funcionamento da AF no país; os atores que atuam nesse âmbito e as relações entre eles; discutem-se questões relevantes sobre o modus operandi dos parceiros de cooperação. A metodologia combinou: revisão bibliográfica, levantamento e análise documental e entrevistas. O marco teórico e analítico utilizou a análise de políticas públicas com foco no papel do Estado e suas inter-relações como os demais atores na ajuda externa na área farmacêutica e a abordagem de redes. Conclui-se que a interação entre os atores envolvidos é complexa, caraterizada pela fragmentação operacional e sobreposição de atividades entre diversos entes; centralização da aquisição de medicamentos na mão de poucos agentes; by pass das estruturas nacionais e desconsideração do necessário fortalecimento do sistema nacional de saúde para a construção de sua autonomia. A despeito de alguns avanços na provisão e disponibilidade de medicamentos para essas doenças, existe forte dependência externa nesse âmbito, o que obstaculiza a sustentabilidade da AF em Moçambique.


Assuntos
Cooperação Internacional , Assistência Farmacêutica/organização & administração , Fármacos Anti-HIV/administração & dosagem , Fármacos Anti-HIV/provisão & distribuição , Antimaláricos/administração & dosagem , Antimaláricos/provisão & distribuição , Antituberculosos/administração & dosagem , Antituberculosos/provisão & distribuição , Infecções por HIV/tratamento farmacológico , Política de Saúde , Humanos , Malária/tratamento farmacológico , Moçambique , Tuberculose/tratamento farmacológico
5.
Ciênc. Saúde Colet. (Impr.) ; 23(7): 2277-2290, jul. 2018. tab, graf
Artigo em Português | LILACS | ID: biblio-952693

RESUMO

Resumo Este artigo analisa a ação de atores nacionais e internacionais na Assistência Farmacêutica (AF) em Moçambique, no período de 2007 a 2012, com foco na provisão pública de medicamentos para HIV/Aids, malária e tuberculose. Descreve-se o funcionamento da AF no país; os atores que atuam nesse âmbito e as relações entre eles; discutem-se questões relevantes sobre o modus operandi dos parceiros de cooperação. A metodologia combinou: revisão bibliográfica, levantamento e análise documental e entrevistas. O marco teórico e analítico utilizou a análise de políticas públicas com foco no papel do Estado e suas inter-relações como os demais atores na ajuda externa na área farmacêutica e a abordagem de redes. Conclui-se que a interação entre os atores envolvidos é complexa, caraterizada pela fragmentação operacional e sobreposição de atividades entre diversos entes; centralização da aquisição de medicamentos na mão de poucos agentes; by pass das estruturas nacionais e desconsideração do necessário fortalecimento do sistema nacional de saúde para a construção de sua autonomia. A despeito de alguns avanços na provisão e disponibilidade de medicamentos para essas doenças, existe forte dependência externa nesse âmbito, o que obstaculiza a sustentabilidade da AF em Moçambique.


Abstract This article examines the activities of national and international actors in Pharmaceutical Services (PS) in Mozambique from 2007 to 2012, focusing on the public provision of HIV/Aids, malaria and tuberculosis medicines. It describes how PS functions in the country, what actors are involved in this area and the relations among them, pursuing salient issues in the modus operandi of partners in cooperation. The methodology combines literature review, document survey and analysis and interviews. The theoretical and analytical framework was given by the policy analysis approach, focusing on the role of the State and its interrelations with other actors in foreign aid in PS, and also by the networks approach. It was concluded that the interactions among the actors involved is complex and characterised by operational fragmentation and overlapping of activities between entities, centralised medicine procurement in the hands of few agents, bypassing of national structures and disregard for the strengthening needed to bolster national health system autonomy. Despite some advances in the provision and availability of medicines for these diseases, external dependence is strong, which undermines the sustainability of PS in Mozambique.


Assuntos
Humanos , Assistência Farmacêutica/organização & administração , Cooperação Internacional , Tuberculose/tratamento farmacológico , Infecções por HIV/tratamento farmacológico , Fármacos Anti-HIV/administração & dosagem , Fármacos Anti-HIV/provisão & distribuição , Política de Saúde , Malária/tratamento farmacológico , Moçambique , Antimaláricos/administração & dosagem , Antimaláricos/provisão & distribuição , Antituberculosos/administração & dosagem , Antituberculosos/provisão & distribuição
6.
Ann Rheum Dis ; 75(1): 142-7, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25261572

RESUMO

OBJECTIVES: Inflammatory arthritis (IA) can lead to anxiety, depression, pain and fatigue. Psychological support can improve quality of life and self-management; and European and American guidelines recommend support be offered. This study examined patient views on psychological support for their IA. METHODS: A questionnaire designed by researchers, patient partners and clinicians was administered to 2280 patients with IA. RESULTS: 1210 patients responded (53%): 74% women; mean age 59 years (SD 12.7); patient global 5 (2.3); disease duration <5 years (41%), 5-10 (20%), >10 (39%). Only 23% reported routinely being asked about social and emotional issues by a rheumatology professional, but 46% would like the opportunity to discuss psychological impact. If offered, 66% of patients reported they would use a self-management/coping clinic (63% pain management, 60% occupational therapy, 48% peer support groups, 46% patient education, 46% psychology/counselling). Patients want support with managing the impact of pain and fatigue (82%), managing emotions (57%), work and leisure (52%), relationships (37%) and depression (34%). Preferences are for support to be delivered by the rheumatology team (nurse 74%, doctor 55%) and general practitioners (GPs) (51%). Only 6% of patients stated that social and emotional issues were not relevant. CONCLUSIONS: Demand for psychological support is high; however, less than a quarter of patients reported being asked about social and emotional issues, suggesting a gap between needs and provision. The preference is for delivery from rheumatology clinicians and GPs, and research should establish whether they have the skills and resources to meet patients' needs.


Assuntos
Artrite Reumatoide/reabilitação , Preferência do Paciente , Qualidade de Vida , Apoio Social , Adaptação Psicológica , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Artrite Reumatoide/psicologia , Atenção à Saúde/organização & administração , Inglaterra , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Educação de Pacientes como Assunto/organização & administração , Autocuidado , Inquéritos e Questionários , Adulto Jovem
7.
Hist Cienc Saude Manguinhos ; 22(1): 115-41, 2015.
Artigo em Inglês, Português | MEDLINE | ID: mdl-25742102

RESUMO

This study centers on relationships among national and international actors in preparation of the first health policy document for East Timor, under the United Nations transitional administration, between 1999 and 2002. International cooperation support for the health system rehabilitation process during the post-conflict period is analyzed as part of reconstruction of the State in parallel with construction of the country's political and institutional framework. Knowledge, ideas, "ways of doing," and induced and accepted practices permeate an interplay of power relationships that condition both national political alliance-building and the architecture of international aid, pointing to input to a discussion of how these mechanisms interact at different conjunctures and times in different negotiating frameworks.


Assuntos
Política de Saúde , Cooperação Internacional , Política de Saúde/história , História do Século XX , Humanos , Cooperação Internacional/história , Timor-Leste , Nações Unidas , Guerra
8.
In. Giovanella, Lígia; Escorel, Sarah; Lobato, Lenaura de Vasconcelos Costa; Noronha, José Carvalho de; Carvalho, Antonio Ivo de. Políticas e sistema de saúde no Brasil. Rio de Janeiro, Editora Fiocruz, 2 ed., rev., amp; 2014. p.759-801.
Monografia em Português | LILACS, Sec. Est. Saúde SP | ID: lil-745047
9.
In. Pereira, João Márcio Mendes; Pronko, Marcela. A demolição de direitos: um exame das políticas do Banco Mundial para a educação e a saúde (1980-2013). Rio de Janeiro, Escola Politécnica de Saúde Joaquim Venâncio, 2014. p.183-232.
Monografia em Português | LILACS, BDS | ID: biblio-980619
13.
In. Giovanella, Lígia; Escorel, Sarah; Lobato, Lenaura de Vasconcelos Costa; Noronha, José Carvalho de; Carvalho, Antonio Ivo de. Políticas e sistema de saúde no Brasil. Rio de Janeiro, Fiocruz, 2 ed., rev., amp; 2012. p.759-801.
Monografia em Português | LILACS | ID: lil-670030
14.
Lancet ; 377(9779): 1778-97, 2011 May 21.
Artigo em Inglês | MEDLINE | ID: mdl-21561655

RESUMO

Brazil is a country of continental dimensions with widespread regional and social inequalities. In this report, we examine the historical development and components of the Brazilian health system, focusing on the reform process during the past 40 years, including the creation of the Unified Health System. A defining characteristic of the contemporary health sector reform in Brazil is that it was driven by civil society rather than by governments, political parties, or international organisations. The advent of the Unified Health System increased access to health care for a substantial proportion of the Brazilian population, at a time when the system was becoming increasingly privatised. Much is still to be done if universal health care is to be achieved. Over the past 20 years, there have been other advances, including investments in human resources, science and technology, and primary care, and a substantial decentralisation process, widespread social participation, and growing public awareness of a right to health care. If the Brazilian health system is to overcome the challenges with which it is presently faced, strengthened political support is needed so that financing can be restructured and the roles of both the public and private sector can be redefined.


Assuntos
Atenção à Saúde/história , Atenção à Saúde/organização & administração , Países em Desenvolvimento/história , Política , Cobertura Universal do Seguro de Saúde/história , Cobertura Universal do Seguro de Saúde/organização & administração , Adolescente , Adulto , Idoso , Brasil , Criança , Pré-Escolar , Atenção à Saúde/economia , Feminino , Financiamento Governamental/economia , Financiamento Governamental/organização & administração , Gastos em Saúde , Acessibilidade aos Serviços de Saúde/economia , Acessibilidade aos Serviços de Saúde/organização & administração , Necessidades e Demandas de Serviços de Saúde/economia , Necessidades e Demandas de Serviços de Saúde/organização & administração , História do Século XX , História do Século XXI , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Crescimento Demográfico , Fatores Socioeconômicos , Cobertura Universal do Seguro de Saúde/economia , Adulto Jovem
15.
Lancet ; 377(9782): 2042-53, 2011 Jun 11.
Artigo em Inglês | MEDLINE | ID: mdl-21561659

RESUMO

Brazil is a large complex country that is undergoing rapid economic, social, and environmental change. In this Series of six articles, we have reported important improvements in health status and life expectancy, which can be ascribed largely to progress in social determinants of health and to implementation of a comprehensive national health system with strong social participation. Many challenges remain, however. Socioeconomic and regional disparities are still unacceptably large, reflecting the fact that much progress is still needed to improve basic living conditions for a large proportion of the population. New health problems arise as a result of urbanisation and social and environmental change, and some old health issues remain unabated. Administration of a complex, decentralised public-health system, in which a large share of services is contracted out to the private sector, together with many private insurance providers, inevitably causes conflict and contradiction. The challenge is ultimately political, and we conclude with a call for action that requires continuous engagement by Brazilian society as a whole in securing the right to health for all Brazilian people.


Assuntos
Reforma dos Serviços de Saúde , Política de Saúde , Indicadores Básicos de Saúde , Pesquisa Biomédica , Brasil/epidemiologia , Seguro Saúde , Morbidade , Qualidade da Assistência à Saúde , Problemas Sociais , Fatores Socioeconômicos
18.
Comun. ciênc. saúde ; 20(2): 101-114, abr.-jun. 2009. graf, tab
Artigo em Português | MS | ID: mis-24483

RESUMO

A Assistência Oficial para o Desenvolvimento (AOD), estabelecida na década de 1960, representa recursos financeiros de governos de países industrializados destinados a governos dos chamados países em desenvolvimento com o propósito da promoção do desenvolvimento em vários setores. Apesar de o Brasil tradicionalmente receber AOD para a saúde, pouco se sabe sobre os países ou organismos multilaterais de onde se originam esses recursos, a sua dimensão em relação ao orçamento nacional de saúde, e os programas ou projetos beneficiados no Brasil. Levantar e analisar as tendências da AOD para a saúde do Brasil no período de 1997 a 2007, destacando os principais atores, a dimensão desses recursos em relação ao orçamento do Ministério da Saúde, e os programas e projetos apoiados no país. Os dados da AOD foram levantados a partir da base estatística Creditor Reporting System (CRS) da Organização para a Cooperação e Desenvolvimento Econômico (OECD). Os dados do orçamento do Ministério da Saúde foram levantados a partir dos relatórios de execução orçamentária providos pelo Conselho Nacional de Saúde (CNS). Os principais atores da AOD bilateral destinada à saúde do Brasil no período foram França, Estados Unidos, ReinoUnido, Japão e Alemanha. Em relação à AOD multilateral destacaram seo Fundo Global para o Combate à Aids, Tuberculose e Malária e o Fundo das Nações Unidas para a Infância. A grande parte dos recursos de AOD – mais da metade – foi destinada a inúmeros programas e projetos em atenção básica e em políticas e gestão administrativa. Apesar de ínfimos quando comparados ao orçamento executado do Ministérioda Saúde no mesmo período, tais recursos representam potencial deimpacto positivo. (AU)


Established in the 1960s, the Official Development Assistance (ODA) constitutes of financial resources flowing from governments of industrialized countries to governments of developing countries, aiming to promote the development of various sectors. Although Brazil has traditionally benefited from ODA little is known about the countries or multilateral organisms from which this resources are originated,its dimension in relation to the national health budget, and the projects and programs benefiting from it in Brazil. To identify and analyze ODA´s tendencies to the health sector in Brazil from 1997 to 2007, pointing out the main actors, the dimension of such resources in relation to the Ministry of Health budget,and the supported programs and projects in the country. ODA data were collected through the Creditor ReportingSystem (CRS) statistical database of the Organization for Economic Cooperation and Development (OECD). Data on the Minitry of Health budget were obtained through budget execution reports provided by the National Health Council (CNS). The main actors of the bilateral ODA to Brazil´s health sector in this period were France, United States of America,United Kingdom, Japan and Germany. Regarding the multilateralODA, stand out the Global Fund to Fight Aids, Tuberculosis and Malaria, and the UN Children’s Fund. Most of ODA resources – more than half – go to a number of programs and projects on primary health care and on policies and administrative management. Although close to insignificant, when compared to the Ministry of Health budget executionin the same period, these resources represent a potential of positive impact. (AU)


Assuntos
Cooperação Internacional , Financiamento Governamental , Gastos em Saúde
19.
Comun. ciênc. saúde ; 20(2): 101-114, abr.-jun. 2009. graf, tab
Artigo em Português | LILACS | ID: lil-552059

RESUMO

A Assistência Oficial para o Desenvolvimento (AOD), estabelecida na década de 1960, representa recursos financeiros de governos de países industrializados destinados a governos dos chamados países em desenvolvimento com o propósito da promoção do desenvolvimento em vários setores. Apesar de o Brasil tradicionalmente receber AOD para a saúde, pouco se sabe sobre os países ou organismos multilaterais de onde se originam esses recursos, a sua dimensão em relação ao orçamento nacional de saúde, e os programas ou projetos beneficiados no Brasil. Levantar e analisar as tendências da AOD para a saúde do Brasil no período de 1997 a 2007, destacando os principais atores, a dimensão desses recursos em relação ao orçamento do Ministério da Saúde, e os programas e projetos apoiados no país. Os dados da AOD foram levantados a partir da base estatística Creditor Reporting System (CRS) da Organização para a Cooperação e Desenvolvimento Econômico (OECD). Os dados do orçamento do Ministério da Saúde foram levantados a partir dos relatórios de execução orçamentária providos pelo Conselho Nacional de Saúde (CNS). Os principais atores da AOD bilateral destinada à saúde do Brasil no período foram França, Estados Unidos, ReinoUnido, Japão e Alemanha. Em relação à AOD multilateral destacaram seo Fundo Global para o Combate à Aids, Tuberculose e Malária e o Fundo das Nações Unidas para a Infância. A grande parte dos recursos de AOD – mais da metade – foi destinada a inúmeros programas e projetos em atenção básica e em políticas e gestão administrativa. Apesar de ínfimos quando comparados ao orçamento executado do Ministérioda Saúde no mesmo período, tais recursos representam potencial deimpacto positivo.


Established in the 1960s, the Official Development Assistance (ODA) constitutes of financial resources flowing from governments of industrialized countries to governments of developing countries, aiming to promote the development of various sectors. Although Brazil has traditionally benefited from ODA little is known about the countries or multilateral organisms from which this resources are originated,its dimension in relation to the national health budget, and the projects and programs benefiting from it in Brazil. To identify and analyze ODA´s tendencies to the health sector in Brazil from 1997 to 2007, pointing out the main actors, the dimension of such resources in relation to the Ministry of Health budget,and the supported programs and projects in the country. ODA data were collected through the Creditor ReportingSystem (CRS) statistical database of the Organization for Economic Cooperation and Development (OECD). Data on the Minitry of Health budget were obtained through budget execution reports provided by the National Health Council (CNS). The main actors of the bilateral ODA to Brazil´s health sector in this period were France, United States of America,United Kingdom, Japan and Germany. Regarding the multilateralODA, stand out the Global Fund to Fight Aids, Tuberculosis and Malaria, and the UN Children’s Fund. Most of ODA resources – more than half – go to a number of programs and projects on primary health care and on policies and administrative management. Although close to insignificant, when compared to the Ministry of Health budget executionin the same period, these resources represent a potential of positive impact.


Assuntos
Financiamento da Assistência à Saúde , Cooperação Internacional , Financiamento Governamental , Gastos em Saúde
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