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2.
Medicine (Baltimore) ; 100(7): e24871, 2021 Feb 19.
Artigo em Inglês | MEDLINE | ID: mdl-33607861

RESUMO

BACKGROUND: Idiopathic short stature (ISS) causes a high economic burden worldwide. As part of a research project that synthesizes economic evidence for Korean medicine treatment of ISS, we describe the methods that will be used for the comprehensive review of articles that analyze health-related economic evaluation for available interventions for ISS using a systematic review methodology. METHODS: Eight electronic English, Korean, and Chinese databases will be searched from their inception until December 2020 to identify studies on the economic evaluation of available interventions on ISS, without language, study design, or publication status restrictions. From the included studies, the effectiveness, utility, and cost data will be collected as the outcome measures by two researchers independently. Descriptive analysis of individual studies will be conducted. If it is judged that the interventions and outcomes of the included studies are sufficiently homogeneous, we will attempt a quantitative synthesis through meta-analysis using Review Manager version 5.4 software (Cochrane, London, UK). RESULTS: This study will summarize the evidence regarding the economic evaluation of available interventions for ISS. CONCLUSIONS: The findings of this review will help clinicians and patients in evidence-based decision-making in clinical settings and help policy makers develop effective policies and distribute resources based on the available evidence.


Assuntos
Análise Custo-Benefício , Nanismo , Feminino , Humanos , Masculino , Acupuntura/métodos , Pessoal Administrativo/legislação & jurisprudência , Tomada de Decisão Clínica/ética , Efeitos Psicossociais da Doença , Análise Custo-Benefício/métodos , Gerenciamento de Dados , Nanismo/economia , Nanismo/epidemiologia , Nanismo/terapia , Recursos em Saúde/provisão & distribuição , Medicina Herbária/métodos , Hormônio do Crescimento Humano/uso terapêutico , Ensaios Clínicos Controlados não Aleatórios como Assunto , Ensaios Clínicos Controlados Aleatórios como Assunto , República da Coreia/epidemiologia , Metanálise como Assunto , Revisões Sistemáticas como Assunto
3.
Acad Med ; 95(1): 13-15, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31599757

RESUMO

Government funding and policies are critical to academic medicine. Publicfunds sustain the education, research, and patient care missions of medical schools and teaching hospitals, and regulations govern the fulfillment of those missions. Consequently, both individuals and institutions often need to engage with those who develop these policies, including through lobbying. Lobbying fulfills a constitutionally protected right to petition the government for a redress of grievances, despite perceptions that it is instead only back-room dealing and insider influence. As an important part of the system of government in the United States, lobbying is subject to complex regulations, and failure to comply can result in substantial penalties, particularly for tax-exempt entities, of which almost all medical schools and the large majority of teaching hospitals are. In this Invited Commentary, the author briefly summarizes these regulations to complement the article in this issue by Lynch and colleagues. He then argues that while regulatory compliance is essential, it is not the same as lobbying effectively. For individual academic researchers to do that involves a number of considerations, including whether to coordinate their efforts with those of their institution to leverage the expertise and resources of the institution, to maximize their chances for success with policymakers.


Assuntos
Pessoal Administrativo/legislação & jurisprudência , Financiamento Governamental/legislação & jurisprudência , Faculdades de Medicina/economia , Política de Saúde/legislação & jurisprudência , Hospitais de Ensino , Humanos , Manobras Políticas , Estados Unidos/epidemiologia
4.
Acad Med ; 95(1): 44-51, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31599758

RESUMO

Medical school faculty and their colleagues in schools of nursing, public health, social work, and elsewhere often research issues of critical importance to health and science policy. When academics engage with government policymakers to advocate for change based on their research, however, they may find themselves engaged in "lobbying," thereby entering a complex environment of legal requirements and institutional policies that they may not fully understand. To promote academic advocacy, this article explains what is and is not legally permitted when it comes to engaging with policymakers and encourages academic institutions to facilitate permissible advocacy activities.U.S. law permits academic researchers to conduct certain types of policy-focused advocacy without running afoul of legal restrictions on lobbying. Academics acting in their personal capacities and with their own resources may freely engage with policymakers in any branch of government to provide their expertise and advocate for desired outcomes. When acting in their professional capacities, academics are free to engage in most advocacy activities directed to the executive and judicial branches, and they also may advocate to influence legislation and legislators within certain limits that are particularly relevant to academic work. In all cases, academics must take care to not use restricted funds for lobbying.Academic researchers have an important role to play in advancing evidence-based health and science policy. They should familiarize themselves with legal restrictions and opportunities to influence policy based on their research, and their institutions should actively support them in doing so.


Assuntos
Política de Saúde/legislação & jurisprudência , Manobras Políticas , Ciência/legislação & jurisprudência , Academias e Institutos/organização & administração , Pessoal Administrativo/legislação & jurisprudência , Pessoal Administrativo/normas , Defesa do Consumidor/legislação & jurisprudência , Prática Clínica Baseada em Evidências/legislação & jurisprudência , Docentes de Medicina/normas , Apoio Financeiro , Programas Governamentais , Humanos , Saúde Pública/legislação & jurisprudência , Pesquisadores/legislação & jurisprudência , Faculdades de Medicina/normas , Escolas de Enfermagem/normas , Serviço Social , Estados Unidos/epidemiologia
6.
Australas J Ageing ; 38 Suppl 2: 83-89, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31496058

RESUMO

OBJECTIVE: To explore how Australian residential dementia aged care providers respond to regulation via organisational culture, level, processes and interpretation. METHODS: Observation took place in three provider organisations. Qualitative, semi-structured in-depth interviews were conducted with aged care staff (n = 60) at three different levels of each organisation: senior management from three head offices (n = 17), facility management (n = 13) and personal care workers (n = 30) from eight residential care facilities. RESULTS: Orientations towards regulation included the following: "above and beyond;" "pushing back;" and "engineering out." Regulation was interpreted differently depending on the level of authority within an organisation where boundaries were managed according to strategic, operational and interactional priorities. DISCUSSION: Examining regulation within an organisational context and at different staff levels suggests ways to balance dementia care with regulatory control. Both generate stress, mitigated by culture and interdependent role differentiation.


Assuntos
Acreditação/legislação & jurisprudência , Pessoal Administrativo/legislação & jurisprudência , Demência/terapia , Pessoal de Saúde/legislação & jurisprudência , Serviços de Saúde para Idosos/legislação & jurisprudência , Instituição de Longa Permanência para Idosos/legislação & jurisprudência , Casas de Saúde/legislação & jurisprudência , Formulação de Políticas , Acreditação/organização & administração , Pessoal Administrativo/organização & administração , Pessoal Administrativo/psicologia , Atitude do Pessoal de Saúde , Austrália , Demência/diagnóstico , Demência/psicologia , Fidelidade a Diretrizes , Pessoal de Saúde/organização & administração , Pessoal de Saúde/psicologia , Serviços de Saúde para Idosos/organização & administração , Instituição de Longa Permanência para Idosos/organização & administração , Humanos , Entrevistas como Assunto , Descrição de Cargo , Casas de Saúde/organização & administração , Estresse Ocupacional/etiologia , Cultura Organizacional , Papel Profissional , Pesquisa Qualitativa , Local de Trabalho/legislação & jurisprudência
10.
Issue Brief (Commonw Fund) ; 2019: 1-11, 2019 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-30990594

RESUMO

Issue: Pharmacy benefit managers (PBMs) are responsible for negotiating payment rates for a large share of prescription drugs distributed in the U.S. Recently, policymakers have expressed concern that certain PBMs' business practices may not be consistent with public policy goals to improve the value of pharmaceutical spending. Goal: We sought to explain key controversies related to PBM practices and their roles in driving value in the pharmaceutical market. Methods: Literature review and feedback from top experts on PBM business practices and potential policy solutions. Key Findings and Conclusion: In some cases, PBMs' use of rebates has contributed to high pharmaceutical costs, yet proposed solutions to the rebate controversy--including passing the rebate through to payers or patients--will not on their own reduce overall pharmaceutical spending without other policies that drive toward value. Policymakers seeking to reform pharmaceutical reimbursement beyond the practice of rebates will need to consider these changes in light of the recent mergers between PBMs and insurers and the entry of new market competitors.


Assuntos
Pessoal Administrativo/economia , Pessoal Administrativo/legislação & jurisprudência , Benefícios do Seguro/economia , Benefícios do Seguro/legislação & jurisprudência , Seguro de Serviços Farmacêuticos/economia , Seguro de Serviços Farmacêuticos/legislação & jurisprudência , Previsões , Formulários Farmacêuticos como Assunto , Setor de Assistência à Saúde/tendências , Humanos , Reembolso de Seguro de Saúde/economia , Reembolso de Seguro de Saúde/legislação & jurisprudência , Medicare Part D/economia , Medicare Part D/legislação & jurisprudência , Estados Unidos
11.
Sci Eng Ethics ; 25(4): 1147-1165, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-29721846

RESUMO

Corruption in the construction industry is a serious problem in China. As such, fighting this corruption has become a priority target of the Chinese government, with the main effort being to discover and prosecute its perpetrators. This study profiles the demographic characteristics of major incidences of corruption in construction. It draws on the database of the 83 complete recorded cases of construction related corruption held by the Chinese National Bureau of Corruption Prevention. Categorical variables were drawn from the database, and 'association rule mining analysis' was used to identify associations between variables as a means of profiling perpetrators. Such profiling may be used as predictors of future incidences of corruption, and consequently to inform policy makers in their fight against corruption. The results signal corruption within the Chinese construction industry to be correlated with age, with incidences rising as managers' approach retirement age. Moreover, a majority of perpetrators operate within government agencies, are department deputies in direct contact with projects, and extort the greatest amounts per case from second tier cities. The relatively lengthy average 6.4-year period before cases come to public attention corroborates the view that current efforts at fighting corruption remain inadequate.


Assuntos
Indústria da Construção/economia , Indústria da Construção/ética , Indústria da Construção/legislação & jurisprudência , Comportamento Criminoso , Demografia , Pessoal Administrativo/economia , Pessoal Administrativo/ética , Pessoal Administrativo/legislação & jurisprudência , Adulto , Fatores Etários , Idoso , China , Cidades , Mineração de Dados , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estatísticas não Paramétricas
14.
Lancet Psychiatry ; 4(6): 501-506, 2017 06.
Artigo em Inglês | MEDLINE | ID: mdl-28219609

RESUMO

Neuroscientific explanations of gambling disorder can help people make sense of their experiences and guide the development of psychosocial interventions. However, the societal perceptions and implications of these explanations are not always clear or helpful. Two workshops in 2013 and 2014 brought together multidisciplinary researchers aiming to improve the clinical and policy-related effects of neuroscience research on gambling. The workshops revealed that neuroscience can be used to improve identification of the dangers of products used in gambling. Additionally, there was optimism associated with the diagnostic and prognostic uses of neuroscience in problem gambling and the provision of novel tools (eg, virtual reality) to assess the effectiveness of new policy interventions before their implementation. Other messages from these workshops were that neuroscientific models of decision making could provide a strong rationale for precommitment strategies and that interdisciplinary collaborations are needed to reduce the harms of gambling.


Assuntos
Pessoal Administrativo/legislação & jurisprudência , Transtornos Disruptivos, de Controle do Impulso e da Conduta/psicologia , Jogo de Azar/psicologia , Neurociências/métodos , Depressores do Apetite/uso terapêutico , Tomada de Decisões , Manual Diagnóstico e Estatístico de Transtornos Mentais , Transtornos Disruptivos, de Controle do Impulso e da Conduta/tratamento farmacológico , Jogo de Azar/tratamento farmacológico , Jogo de Azar/economia , Jogo de Azar/epidemiologia , Redução do Dano , Humanos , Naloxona/uso terapêutico , Naltrexona/análogos & derivados , Naltrexona/uso terapêutico , Antagonistas de Entorpecentes/uso terapêutico , Neurociências/economia , Saúde Pública/legislação & jurisprudência
16.
Int J Health Policy Manag ; 5(6): 355-63, 2016 Feb 09.
Artigo em Inglês | MEDLINE | ID: mdl-27285513

RESUMO

BACKGROUND: Global health policy is created largely through a collaborative process between development agencies and aid-recipient governments, yet it remains unclear whether governments retain ownership over the creation of policy in their own countries. An assessment of the power structure in this relationship and its influence over agenda-setting is thus the first step towards understanding where progress is still needed in policy-making for development. METHODS: This study employed qualitative policy analysis methodology to examine how health-related policy agendas are adopted in low-income countries, using Tanzania as a case study. Semi-structured, in-depth, key informant interviews with 11 policy-makers were conducted on perspectives of the agenda-setting process and its actors. Kingdon's stream theory was chosen as the lens through which to interpret the data analysis. RESULTS: This study demonstrates that while stakeholders each have ways of influencing the process, the power to do so can be assessed based on three major factors: financial incentives, technical expertise, and influential position. Since donors often have two or all of these elements simultaneously a natural power imbalance ensues, whereby donor interests tend to prevail over recipient government limitations in prioritization of agendas. One way to mediate these imbalances seems to be the initiation of meaningful policy dialogue. CONCLUSION: In Tanzania, the agenda-setting process operates within a complex network of factors that interact until a "policy window" opens and a decision is made. Power in this process often lies not with the Tanzanian government but with the donors, and the contrast between latent presence and deliberate use of this power seems to be based on the donor ideology behind giving aid (defined here by funding modality). Donors who used pooled funding (PF) modalities were less likely to exploit their inherent power, whereas those who preferred to maintain maximum control over the aid they provided (ie, non-pooled funders) more readily wielded their intrinsic power to push their own priorities.


Assuntos
Pessoal Administrativo/legislação & jurisprudência , Política de Saúde/legislação & jurisprudência , Formulação de Políticas , Poder Psicológico , Países em Desenvolvimento , Humanos , Entrevistas como Assunto , Pobreza , Tanzânia
19.
Health Aff (Millwood) ; 33(1): 11-9, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24395930

RESUMO

Communication-and-resolution programs (CRPs) in health care organizations seek to identify medical injuries promptly; ensure that they are disclosed to patients compassionately; pursue timely resolution through patient engagement, explanation, and, where appropriate, apology and compensation; and use lessons learned to improve patient safety. CRPs have existed for years, but they are being tested in new settings and primed for broad implementation through grants from the Agency for Healthcare Research and Quality. These projects do not require changing laws. However, grantees' experiences suggest that the path to successful dissemination of CRPs would be smoother if the legal environment supported them. State and federal policy makers should try to allay potential defendants' fears of litigation (for example, by protecting apologies from use in court), facilitate patient participation (for example, by ensuring access to legal representation), and address the reputational and economic concerns of health care providers (for example, by clarifying practices governing National Practitioner Data Bank reporting and payers' financial recourse following medical error).


Assuntos
Pessoal Administrativo/legislação & jurisprudência , Comunicação , Setor de Assistência à Saúde/legislação & jurisprudência , Política de Saúde/legislação & jurisprudência , Imperícia/legislação & jurisprudência , Negociação , Compensação e Reparação/legislação & jurisprudência , Órgãos Governamentais/legislação & jurisprudência , Pesquisa sobre Serviços de Saúde/legislação & jurisprudência , Humanos , Responsabilidade Legal , National Practitioner Data Bank , Defesa do Paciente/legislação & jurisprudência , Formulação de Políticas , Qualidade da Assistência à Saúde/legislação & jurisprudência , Estados Unidos
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