RESUMO
BI-RADS is a communication and data tracking system that has evolved since its inception as a brief mammography lexicon and reporting guide into a robust structured reporting platform and comprehensive quality assurance tool for mammography, ultrasound, and MRI. Consistent and appropriate use of the BI-RADS lexicon terminology and assessment categories effectively communicates findings, estimates the risk of malignancy, and provides management recommendations to patients and referring clinicians. The impact of BI-RADS currently extends internationally through six language translations. A condensed version has been proposed to facilitate a phased implementation of BI-RADS in resource-constrained regions. The primary advance of the 5th edition of BI-RADS is harmonization of the lexicon terms across mammography, ultrasound, and MRI. Harmonization has also been achieved across these modalities for the reporting structure, assessment categories, management recommendations, and data tracking system. Areas for improvement relate to certain common findings that lack lexicon descriptors and a need for further clarification of proper use of category 3. BI-RADS is anticipated to continue to evolve for application to a range of emerging breast imaging modalities.
Assuntos
Mama/diagnóstico por imagem , Mamografia , Imagem Multimodal , Neoplasias da Mama/diagnóstico por imagem , Feminino , Previsões , Gestão da Informação em Saúde/métodos , Gestão da Informação em Saúde/tendências , Humanos , Imageamento por Ressonância Magnética/métodos , Imageamento por Ressonância Magnética/tendências , Mamografia/métodos , Mamografia/normas , Mamografia/tendências , Imagem Multimodal/métodos , Imagem Multimodal/tendências , Ultrassonografia Mamária/métodos , Ultrassonografia Mamária/tendênciasRESUMO
The recent opening of massive health databases, as well as the development of methods and tools adapted to their data processing, questions the French model of "morbidity registry". In France in 2019, nearly 61 health registries were operating. As defined by law, these registries identify exhaustively all patients with a given disease in a given territory. Established several decades ago, these registries are part of the French surveillance system that is used for research and evaluation purposes. Since the advent of recent technological progress, large-scale databases are made available to researchers and it is possible with these databases to answer questions initially assigned to the registries. What is the place of such registries in this new context: are they obsolete or still useful? Should they be opposed to the new tools or are they complementary to them, and if so, what is their place in the new French public health ecosystem? The objective of this work was to assess the roles and missions of existing registries and to reflect on their positioning in this new environment. The French model of registry is sometimes questioned because of the complexity of its circuits, requiring a significant amount of human resources. However, the data that constitute them, validated by cross-checking information from several sources, are of very high quality, and make it possible to validate the data in the new databases (National Health Data System (NSDS) or Hospital Data Warehouses). Registries and new databases are in fact complementary, and far from jeopardizing this model, the recent opening of these databases represents an opportunity for registries to modernize their operations and respond to new missions.
Assuntos
Big Data , Bases de Dados Factuais/tendências , Morbidade , Saúde Pública/tendências , Sistema de Registros , Big Data/provisão & distribuição , Bases de Dados Factuais/normas , Bases de Dados Factuais/provisão & distribuição , Registros Eletrônicos de Saúde/organização & administração , Registros Eletrônicos de Saúde/normas , Registros Eletrônicos de Saúde/tendências , França/epidemiologia , Gestão da Informação em Saúde/organização & administração , Gestão da Informação em Saúde/normas , Gestão da Informação em Saúde/tendências , Humanos , Disseminação de Informação/métodos , Modelos Organizacionais , Prática Profissional/organização & administração , Prática Profissional/normas , Prática Profissional/tendências , Papel Profissional , Saúde Pública/estatística & dados numéricos , Sistema de Registros/normas , Sistema de Registros/estatística & dados numéricosRESUMO
As a prelude to his keynote speech at the forthcoming Health Libraries Group conference, Sean McNamara, Head of CILIP Scotland, provides an insight into the work being undertaken with health librarians in Scotland and considers how CILIP Scotland might support the health information sector in the coming years.
Assuntos
Gestão da Informação em Saúde/métodos , Bibliotecas Médicas/tendências , Biblioteconomia/métodos , Gestão da Informação em Saúde/tendências , HumanosRESUMO
The 2020 virtual issue of the Health Information and Libraries Journal (HILJ) is published to link to the CILIP Health Libraries Group Conference which was to take place in Scotland 22-25th July. Whilst the conference was postponed in light of the coronavirus (COVID-19) pandemic, its themes of (i) Working in Partnership; (ii) Resilience and Well-being; (iii) Public and Patient involvement; (iv) Quality Impact and Metrics; and (v) Improvement and Innovation have nevertheless provided the basis on which to compile this virtual issue. Overarching these themes is a core value of the HIL profession, to provide relevant, timely and sustainable information services, and the articles selected from HILJ (2018 through to March 2020) contribute to the aim of meeting and going beyond these goals under the conference banner of 'not your average day in the office'. The virtual issue mirrors the format of a regular issue of HILJ, a review article, four original articles and three from our regular features: 'Dissertations into Practice', 'International Perspectives and Initiatives' and 'Teaching and Learning in Action'. The authors come from Canada, China, Croatia, Sweden and the UK. All articles included in this issue are available online.
Assuntos
Infecções por Coronavirus/epidemiologia , Gestão da Informação em Saúde/tendências , Serviços de Biblioteca/tendências , Pneumonia Viral/epidemiologia , Papel Profissional , Betacoronavirus , COVID-19 , Congressos como Assunto , Humanos , Internacionalidade , Pandemias , SARS-CoV-2 , EscóciaRESUMO
The 2019 virtual issue of the Health Information and Libraries Journal (HILJ) is published to link to the 2019 EAHIL Workshop taking place in Basel, Switzerland on 17-20 June 2019. The workshop is structured around six topics: (i) Roadmap of our Profession; (ii) Technology Uptake; (iii) Ecology of Scholarly Communications; (iv) Impact + Assessment; (v) Benchmarking + Advocacy; (vi) Evidence-Based Practice. These themes have been used to compile this virtual issue, which contains published articles selected from HILJ from the March 2019 issue through to June 2017. The virtual issue mirrors the format of a regular issue of HILJ, namely a review article, five original articles and articles from our three regular features: 'Dissertations into Practice', 'International Perspectives and Initiatives' and 'Teaching and Learning in Action'. The authors come from the UK, Canada, Australia, Italy, Iran and Belgium. All articles included in this virtual issue are available free online.
Assuntos
Gestão da Informação em Saúde/educação , Biblioteconomia/tendências , Educação/métodos , Prática Clínica Baseada em Evidências/métodos , Prática Clínica Baseada em Evidências/tendências , Gestão da Informação em Saúde/tendências , Humanos , Papel Profissional , SuíçaRESUMO
Steady changes in society present challenges to constructive cooperation between stakeholders in the diverse PH landscape of Germany through individualism, globalisation, medical progress, digitalisation, etc. Working group 8 therefore suggests that the PH community should build new internal structures, in order to be able to respond jointly to external challenges, facilitate networking amongst the actors and speak with one voice, when needed. The suggestion is to establish an office that has the task to organise further meetings, harmonize written joint statements and moderate the dialogue amongst peers.
Assuntos
Redes de Comunicação de Computadores/tendências , Gestão da Informação em Saúde/tendências , Programas Nacionais de Saúde/tendências , Saúde Pública/tendências , Mídias Sociais/tendências , Berlim , Big Data , Diversidade Cultural , Previsões , Alemanha , Política de Saúde/tendências , HumanosRESUMO
The 2017 virtual issue of the Health Information and Libraries Journal (HILJ) is published to link to the 12th International Congress on Medical Librarianship and the 2017 EAHIL Workshop taking place in Dublin, Ireland on 12-16 June 2017. The conference title is Diversity in Practice: integrating, inspiring and innovative and it is exploring how health science librarianship, in all its diversity, is integrating, inspiring and innovating practice. These themes have been used to compile this virtual issue, which contains published articles selected from HILJ from the June 2014 issue through to September 2016. The virtual issue mirrors the format of a regular issue of HILJ, namely a review article, six original articles and our three regular features: 'Dissertations into Practice', 'International Perspectives and Initiatives' and 'Teaching and Learning in Action'. All articles included in this virtual issue are available free online.
Assuntos
Gestão da Informação em Saúde/métodos , Biblioteconomia/educação , Gestão da Informação em Saúde/normas , Gestão da Informação em Saúde/tendências , Humanos , Biblioteconomia/tendências , RedaçãoRESUMO
The ethical landscape in the field of genomics is rapidly shifting. Plummeting sequencing costs, along with ongoing advances in bioinformatics, now make it possible to generate an enormous volume of genomic data about vast numbers of people. The informational richness, complexity, and frequently uncertain meaning of these data, coupled with evolving norms surrounding the sharing of data and samples and persistent privacy concerns, have generated a range of approaches to the ethical management of genomic information. As calls increase for the expanded use of broad or even open consent, and as controversy grows about how best to handle incidental genomic findings, these approaches, informed by normative analysis and empirical data, will continue to evolve alongside the science.
Assuntos
Genômica/ética , Gestão da Informação em Saúde/ética , Gestão da Informação em Saúde/tendências , Humanos , Consentimento Livre e Esclarecido/ética , PrivacidadeRESUMO
In today's era of aging society, people want to handle personal health care by themselves in everyday life. In particular, the evolution of medical and IT convergence technology and mobile smart devices has made it possible for people to gather information on their health status anytime and anywhere easily using biometric information acquisition devices. Healthcare information systems can contribute to the improvement of the nation's healthcare quality and the reduction of related cost. However, there are no perfect security models or mechanisms for healthcare service applications, and privacy information can therefore be leaked. In this paper, we examine security requirements related to privacy protection in u-healthcare service and propose an extended RBAC based security model. We propose and design u-healthcare service integration platform (u-HCSIP) applying RBAC security model. The proposed u-HCSIP performs four main functions: storing and exchanging personal health records (PHR), recommending meals and exercise, buying/selling private health information or experience, and managing personal health data using smart devices.
Assuntos
Segurança Computacional/tendências , Confidencialidade/normas , Gestão da Informação em Saúde/métodos , Sistemas de Informação em Saúde/tendências , Informática Médica/métodos , Acesso à Informação , Segurança Computacional/normas , Gestão da Informação em Saúde/tendências , Informática Médica/tendênciasRESUMO
BACKGROUND: Anesthesia information management systems (AIMS) are electronic health records that automatically import vital signs from patient monitors and allow for computer-assisted creation of the anesthesia record. When most recently surveyed in 2007, it was estimated that at least 16% of U.S. academic hospitals (i.e., with an anesthesia residency program) had installed an AIMS. At least an additional 28% reported that they were in the process of implementing, or searching for an AIMS. In this study, we updated the adoption figures as of May 2013 and examined the historical trend of AIMS deployment in U.S. anesthesia residency programs from the perspective of the theory of diffusion of technologic innovations. METHODS: Questionnaires were sent by e-mail to program directors or their identified contact individuals at the 130 U.S. anesthesiology residency programs accredited as of June 30, 2012 by the Accreditation Council for Graduate Medical Education. The questionnaires asked whether the department had an AIMS, the year of installation, and, if not present, whether there were plans to install an AIMS within the next 12 months. Follow-up e-mails and phone calls were made until responses were obtained from all programs. Results were collected between February and May 2013. Implementation percentages were determined using the number of accredited anesthesia residency programs at the start of each academic year between 1987 and 2013 and were fit to a logistic regression curve using data through 2012. RESULTS: Responses were received from all 130 programs. Eighty-seven (67%) reported that they currently are using an AIMS. Ten programs without a current AIMS responded that they would be installing an AIMS within 12 months of the survey. The rate of AIMS adoption by year was well fit by a logistic regression curve (P = 0.90). CONCLUSIONS: By the end of 2014, approximately 75% of U.S. academic anesthesiology departments will be using an AIMS, with 84% adoption expected between 2018 and 2020. Historical adoption of AIMS has followed Roger's 1962 formulation of the theory of diffusion of innovation.
Assuntos
Centros Médicos Acadêmicos/métodos , Serviço Hospitalar de Anestesia/métodos , Gestão da Informação em Saúde/métodos , Internato e Residência/métodos , Diretores Médicos , Inquéritos e Questionários , Centros Médicos Acadêmicos/tendências , Serviço Hospitalar de Anestesia/tendências , Gestão da Informação em Saúde/tendências , Humanos , Internato e Residência/tendências , Diretores Médicos/tendências , Estados UnidosAssuntos
Congressos como Assunto , Gestão da Informação em Saúde , Congressos como Assunto/normas , França , Reforma dos Serviços de Saúde/tendências , Gestão da Informação em Saúde/legislação & jurisprudência , Gestão da Informação em Saúde/métodos , Gestão da Informação em Saúde/organização & administração , Gestão da Informação em Saúde/tendências , História do Século XXI , Humanos , Corpo Clínico/educação , Corpo Clínico/organização & administração , Corpo Clínico/normas , Corpo Clínico/tendências , Avaliação de Programas e Projetos de Saúde/métodos , Avaliação de Programas e Projetos de Saúde/normas , Parcerias Público-Privadas/organização & administração , Parcerias Público-Privadas/tendências , Sociedades Médicas/organização & administração , Sociedades Médicas/normasRESUMO
BACKGROUND: The provision of residential aged care is underpinned by information, and is reliant upon systems that adequately capture and effectively utilise and communicate this information. The aim of this study was to explicate and quantify the volume and method by which information is collected, exchanged within facilities and with external providers, and retrieved from facility information systems and hospitals. METHODS: A survey of staff (n = 119), including managers, health informatics officers (HIOs), quality improvement staff, registered nurses (RNs), enrolled nurses (ENs)/endorsed enrolled nurses (EENs) and assistants in nursing (AINs) was carried out in four residential aged care facilities in New South Wales and Victoria, Australia. Sites varied in size and displayed a range of information technology (IT) capabilities. The survey investigated how and by whom information is collected, retrieved and exchanged, and the frequency and amount of time devoted to these tasks. Descriptive analysis was performed using SPSS, and open responses to questions were coded into key themes. RESULTS: Staff completed a median of six forms each, taking a median of 30 min per shift. 68.8% of staff reported transferring information from paper to a computer system, which took a median of 30 min per shift. Handover and face-to-face communication was the most frequently used form of information exchange within facilities. There was a large amount of faxing and telephone communication between facility staff and General Practitioners and community pharmacists, with staff reporting sending a median of 2 faxes to pharmacy and 1.5 faxes to General Practitioners, and initiating 2 telephone calls to pharmacies and 1.5 calls to General Practitioners per shift. Only 38.5% of respondents reported that they always had information available at the point-of-care and only 35.4% of respondents reported that they always had access to hospital stay information of residents after hospital discharge. CONCLUSIONS: This survey identified a high volume of information exchange activities, as well as inefficient procedures, such as the transfer of information from paper to computer systems and the reliance upon faxes for communication with external providers. These findings contribute to evidence for the need for interoperable IT systems to allow more efficient and reliable information exchange between facilities and external providers.