RESUMO
Contemporary healthcare at all levels increasingly uses Artificial Intelligence (AI). However, since the various levels involve different tasks, have different data needs, and different ethical obligations, the AIs that are used have to be differently structured. Also, since healthcare construed as a commodity involves different ethical parameters from healthcare construed as a right, and different ethical systems entail logically distinct considerations, this also necessitates the need for differently structured AIs. What follows sketches how and why this is the case. It concludes with a brief look at why AIs programmed into quantum computers would not change this.
RESUMO
It is generally accepted that the global evolution of health information technology, both in design and usage, raises ethical issues that should be addressed. However, the terms in which this concern is expressed are shrouded in ambiguity. Even what constitutes an ethical issue itself is never clearly defined. The present discussion attempts to clarify the landscape and suggests how the concern should be addressed.
Assuntos
Tecnologia da Informação , Informática Médica , Big Data , HumanosRESUMO
The paper examines the issues of security and safety in Health Information Systems and focuses the need for the development of appropriate Guidelines for the effective use of IEC 61508 standard.
Assuntos
Segurança Computacional/normas , Sistemas de Informação/normas , Confidencialidade , Ética Profissional , União Europeia , Guias como Assunto , Humanos , Informática Médica , Sistemas Computadorizados de Registros MédicosRESUMO
The concept of data-space is fruitful in trying to understand the ethical rights and duties that surround the treatment of patient records. However, it also provides a solution to three apparently unconnected problems: the construction of expert diagnostic systems, the development of an internal security element within the sphere of permitted data-access for health care professionals, and the development of a professional quality assurance mechanism. This paper presents a model of how these diverse aims may be achieved. It does so by developing the notion of the logical form of data within a data-space and by showing how the path taken by a health care professional through a profession-relative data-space can provide checks for the security, quality and appropriateness of the path itself. The result is important in that it provides an integrated method for information specialists to meet their fiduciary obligations towards the patients whose records are in their care, and towards the institutions that employ them.
Assuntos
Sistemas Inteligentes , Garantia da Qualidade dos Cuidados de Saúde , Segurança Computacional , Ética , Humanos , Sistemas Computadorizados de Registros MédicosAssuntos
Atitude Frente a Saúde/etnologia , Tomada de Decisões , Ética Clínica , Terapia Intensiva Neonatal/normas , Programas Nacionais de Saúde/normas , Neonatologia/normas , Canadá , Efeitos Psicossociais da Doença , Comparação Transcultural , Alocação de Recursos para a Atenção à Saúde , Acessibilidade aos Serviços de Saúde , Humanos , Recém-Nascido , Consentimento Livre e Esclarecido , Terapia Intensiva Neonatal/economia , Terapia Intensiva Neonatal/legislação & jurisprudência , Internacionalidade , Programas Nacionais de Saúde/economia , Consentimento dos Pais , Seleção de Pacientes , Guias de Prática Clínica como Assunto , Qualidade de Vida , Valores Sociais , Estados UnidosRESUMO
Recent legislation has made physician practice profiles publicly available in many states of the United States. This paper examines the ethical reasoning underlying such a move. It concludes that, on balance, such an initiative is ethically appropriate and should be followed by other jurisdictions.
Assuntos
Ética Institucional , Serviços de Informação/normas , Defesa do Paciente , Padrões de Prática Médica/classificação , Serviços de Informação/legislação & jurisprudência , Licenciamento em Medicina , Relações Médico-Paciente , Estados UnidosAssuntos
Atitude Frente a Saúde , Ética Médica , Alocação de Recursos para a Atenção à Saúde/organização & administração , Modelos Econométricos , Valores Sociais , Análise Custo-Benefício , Direitos Humanos , Humanos , Programas Nacionais de Saúde , Avaliação das Necessidades , Avaliação de Resultados em Cuidados de Saúde/organização & administração , Defesa do Paciente , Filosofia Médica , Fatores SocioeconômicosRESUMO
Guidelines for the protection of electronic health care data frequently stipulate that national laws should be followed. This stipulation is subjected to analysis and critique. It is argued that it commits the fallacy of nationality, and suggests that appropriately constructed ethical guidelines for the protection of electronic health care data must focus solely on fundamental ethical principles as these are applied to the types of situations in which such electronic data are generated, used and ultimately disposed of. The relevance of economic considerations is also be addressed. An attempt is made to sketch a general ethical framework within which data protection guidelines could be situated.
Assuntos
Segurança Computacional , Ética Profissional , Sistemas Computadorizados de Registros Médicos/legislação & jurisprudência , Atenção à Saúde/economia , Atenção à Saúde/estatística & dados numéricos , Economia Médica , Guias como Assunto , Humanos , Sistemas Computadorizados de Registros Médicos/economiaRESUMO
The current global shortage of organs has prompted a series of proposals for improving organ retrieval rates. They include preferred recipient status for registered organ donors, payment for organs, presumed consent and required response. This paper examines the tenability of these proposals and points out their shortcomings. Taking the Canadian situation as an example, it argues further that the shortage is exacerbated by unethical and essentially illegal retrieval protocols that flout the law of informed consent. It is suggested that before any redrafting of laws and regulations is undertaken, these protocols should be revised.
Assuntos
Ética Médica , Obtenção de Tecidos e Órgãos/normas , Altruísmo , Canadá , Protocolos Clínicos , Comércio , Acessibilidade aos Serviços de Saúde , Humanos , Consentimento Presumido , Reembolso de Incentivo , Doadores de Tecidos/psicologia , Obtenção de Tecidos e Órgãos/economia , Obtenção de Tecidos e Órgãos/legislação & jurisprudência , Transplantes/provisão & distribuiçãoRESUMO
An electronic patient record consists of electronically stored data about a specific patient. It therefore constitutes a data-space. The data may be combined into a patient profile which is relative to a particular specialty as well as phenomenologically unique to the specific professional who constructs the profile. Further, a diagnosis may be interpreted as a path taken by a health care professional with a certain specialty through the data-space relative to the patient profile constructed by that professional. This way of looking at electronic patient records entails certain ethical implications about privacy and accessibility. However, it also permits the construction of artificial intelligence and competence algorithms for health care professionals relative to their specialties.
Assuntos
Confidencialidade , Ética , Sistemas Computadorizados de Registros Médicos , Humanos , Controle de QualidadeRESUMO
The Canadian health care system is a publicly funded system based on the philosophy that health is a right, not a commodity. The implementation of this perspective is hampered by the fact that the Canadian Constitution makes health care a matter of provincial jurisdiction, while most taxing powers lie in the hands of the federal government. Further problems arise because of Canada's geographic nature and a move to regionalization of provincial health care administration. The issue is compounded by recent developments in reproductive technologies, aboriginal health, changes in consent law, etc.
Assuntos
Programas Nacionais de Saúde/organização & administração , Canadá , Ética , Financiamento Governamental , Alocação de Recursos para a Atenção à Saúde , Política de Saúde , Acessibilidade aos Serviços de Saúde , Humanos , Indígenas Norte-Americanos , Programas Nacionais de Saúde/economia , Programas Nacionais de Saúde/legislação & jurisprudência , Opinião Pública , Justiça Social , Cobertura Universal do Seguro de Saúde , Listas de EsperaRESUMO
We propose an approach to macro allocation of health care resources that is compatible with the principles of the Canada Health Act. The approach is equitable and just and takes public support into account. It hinges on the provision of data on disease prevalence and incidence, on data on the effectiveness of intervention measures and of their cost. It is therefore a proposal that may be important as a direction for ongoing research even if it is not immediately feasible. The approach is analyzed with respect to selected related approaches.
Assuntos
Ética Médica , Alocação de Recursos para a Atenção à Saúde , Alocação de Recursos , Algoritmos , Canadá , Consenso , Humanos , Autonomia Pessoal , Valores SociaisAssuntos
Ética Médica , Programas Nacionais de Saúde/legislação & jurisprudência , Aborto Legal , Orçamentos/legislação & jurisprudência , Canadá , Eutanásia/legislação & jurisprudência , Alocação de Recursos para a Atenção à Saúde/economia , Alocação de Recursos para a Atenção à Saúde/legislação & jurisprudência , Humanos , Consentimento Livre e Esclarecido/legislação & jurisprudência , Prontuários Médicos/legislação & jurisprudência , Programas Nacionais de Saúde/economiaRESUMO
The development of uniform, ethical and internationally enforceable standards for handling computerised electronic patient records is a major requirement for the implementation of the next generation of health information systems. This paper develops a model code of ethics to address this issue.
Assuntos
Segurança Computacional/legislação & jurisprudência , Ética Profissional , Sistemas Computadorizados de Registros Médicos/legislação & jurisprudência , Canadá , Segurança Computacional/normas , Cooperação Internacional , Informática Médica , Sistemas Computadorizados de Registros Médicos/normas , Responsabilidade Social , Sociedades CientíficasRESUMO
With physicians in Canada under increasing threat of malpractice litigation, it has been suggested that adopting clinical practice guidelines (CPGs) as standards of care would free doctors from the fear of litigation initiated by dissatisfied patients. However, ethicist Eike-Henner Kluge argues that CPGs can only be considered general indicators of standards of care.