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1.
Tidsskr Nor Laegeforen ; 138(17)2018 10 30.
Article in English, Norwegian | MEDLINE | ID: mdl-30378403

ABSTRACT

BACKGROUND: The interwar period was a time of comprehensive preventive health programmes in Norway. Physical exercise, nutritious diets, strict sleep regimens and better hygiene were at the centre of these efforts. A massive mobilisation of volunteers and professionals took place. The publication of House Maxims for Mothers and Children was part of this large-scale mobilisation, and consisted of ten posters with pithy health advice for hanging on the wall. Mothers were an important target group for health promotion. MATERIAL AND METHOD: The posters have previously received little attention in medical literature, but they can elucidate some features of life and the health propaganda of their time. We have used databases that provide access to newspapers, books and medical literature: Retriever, bokhylla.no, Oria, PubMed and Web of Science. RESULTS: It is hard to quantify the effect of this popular movement when compared to political measures to improve living conditions. In any case, mortality rates fell, life expectancy increased and the dreaded communicable diseases were largely defeated. Special efforts were targeted at children, also with good results. Infant mortality fell and schoolchildren became healthier, stronger, taller and cleaner. INTERPRETATION: The line between social hygiene and general disciplining is blurred, for example the boundary between a healthy diet and bourgeois norms. The education of mothers and children also included a normative aspect that concerned good manners and control.


Subject(s)
Consumer Health Information/history , Health Education/history , Health Promotion/history , Posters as Topic , Child , Child Health/history , History, 20th Century , Humans , Hygiene/history , Mothers/education , Mothers/history , Norway , Preventive Health Services/history , Public Health/history
2.
Yearb Med Inform ; Suppl 1: S42-7, 2016 May 20.
Article in English | MEDLINE | ID: mdl-27199196

ABSTRACT

OBJECTIVES: Consumer Health Informatics (CHI) is a rapidly growing domain within the field of biomedical and health informatics. The objective of this paper is to reflect on the past twenty five years and showcase informatics concepts and applications that led to new models of care and patient empowerment, and to predict future trends and challenges for the next 25 years. METHODS: We discuss concepts and systems based on a review and analysis of published literature in the consumer health informatics domain in the last 25 years. RESULTS: The field was introduced with the vision that one day patients will be in charge of their own health care using informatics tools and systems. Scientific literature in the field originally focused on ways to assess the quality and validity of available printed health information, only to grow significantly to cover diverse areas such as online communities, social media, and shared decision-making. Concepts such as home telehealth, mHealth, and the quantified-self movement, tools to address transparency of health care organizations, and personal health records and portals provided significant milestones in the field. CONCLUSION: Consumers are able to actively participate in the decision-making process and to engage in health care processes and decisions. However, challenges such as health literacy and the digital divide have hindered us from maximizing the potential of CHI tools with a significant portion of underserved populations unable to access and utilize them. At the same time, at a global scale consumer tools can increase access to care for underserved populations in developing countries. The field continues to grow and emerging movements such as precision medicine and the sharing economy will introduce new opportunities and challenges.


Subject(s)
Consumer Health Information/trends , Medical Informatics/trends , Telemedicine/trends , Consumer Health Information/history , Forecasting , Genomics , History, 20th Century , History, 21st Century , Medical Informatics/history , Precision Medicine/trends , Telemedicine/history
3.
J Paediatr Child Health ; 51(1): 16-20, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25586840

ABSTRACT

Medicine has seen dramatic changes in the last 50 years, and vaccinology is no different. Australia has made a significant contribution to world knowledge on vaccine-preventable diseases. Certain deadly diseases have disappeared or become rare in Australia following successful introduction of vaccines. As diseases become rarer, public knowledge about the diseases and their serious consequences has decreased, and concerns about potential vaccine side effects have increased. To maintain confidence in immunisations, sharing of detailed information about the vaccines and the diseases we are trying to prevent is integral to the continued success of our public health programme. Modern quality immunisation programmes need to communicate complex information to immunisation providers and also to the general community. Improving immunisation coverage rates and eliminating the gap in coverage and timeliness between Aboriginal and Torres Strait Islander peoples and non-Indigenous people has become a high priority.


Subject(s)
Bacterial Infections/history , Immunization Programs/history , Vaccination/history , Vaccines/history , Virus Diseases/history , Australia/epidemiology , Bacterial Infections/ethnology , Bacterial Infections/prevention & control , Consumer Health Information/history , Healthcare Disparities/ethnology , Healthcare Disparities/history , History, 20th Century , History, 21st Century , Humans , Native Hawaiian or Other Pacific Islander , Vaccination/adverse effects , Vaccines/adverse effects , Virus Diseases/ethnology , Virus Diseases/prevention & control
4.
J Med Libr Assoc ; 102(4): 271-80, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25349545

ABSTRACT

OBJECTIVES: Recently, government agencies in several countries have promoted information prescription programs to increase patients' understanding of their conditions. The practice has a long history and many publications, but no comprehensive literature reviews such as this. METHODS: Using a variety of high-precision and high-recall strategies, the researcher searched two dozen online bibliographic databases, citation databases, and repositories, as well as many print sources, to identify and retrieve documents for review. Of these documents, ninety relevant English-language case reports, research reports, and reviews published from 1930-2013 met the study criteria. RESULTS: Early to mid-twentieth century reports covered long-standing practices and used no rigorous research methods. The literature since the mid-1990s reports on short-term trial projects, especially of government-sponsored programs in the United States and United Kingdom. Although the concept of information prescription has been in the literature and practiced for decades, no long-term research studies were found. CONCLUSIONS: Most of the literature is anecdotal concerning small pilot projects. The reports investigate physician, patient, and librarian satisfaction but not changes in patient knowledge or behavior. Many twenty-first century projects emphasize materials and projects from specific government agencies and commercial enterprises. IMPLICATIONS: While the practice is commonly believed to be a good idea and there are many publications on the subject, few studies provide any evidence of the efficacy of information prescriptions for increased patient knowledge. Well-designed and executed large or long-term studies might produce needed evidence for professional practice.


Subject(s)
Consumer Health Information/statistics & numerical data , Information Dissemination , Information Storage and Retrieval , Libraries, Medical/organization & administration , Library Services/statistics & numerical data , Consumer Health Information/history , History, 20th Century , History, 21st Century , Humans , Information Dissemination/history , Information Storage and Retrieval/history , Libraries, Medical/history , Library Science/history , Library Services/history , Patient Education as Topic/history , Patient Education as Topic/statistics & numerical data
6.
Dynamis (Granada) ; 33(1): 43-67, 2013. ilus
Article in Spanish | IBECS | ID: ibc-120155

ABSTRACT

Las secciones periodísticas de preguntas y respuestas reflejan y contribuyen a las sociedades en que se publican, y pueden desempeñar roles tan diferentes como constituirse en una herramienta para mantener la normatividad social o, por el contrario, en un instrumento para el cambio de las normas sociales. En un contexto de complejas relaciones entre expertos y no-expertos dentro del movimiento libertario en la España del primer tercio del siglo XX, la sección «Preguntas y respuestas» (1930-1937) de la revista anarquista Estudios (1928-1937) se revela como un ejemplo particularmente ilustrativo de gestión multidimensional de conocimiento a través de la redefinición efectiva de la participación de muy diferentes colectivos. En este trabajo, analizamos el intercambio entre el médico Roberto Remartínez (1895-1977), coordinador de la sección, y los lectores, e identificamos las características de la puesta en práctica del ideario libertario de autogestión a través de prácticas comunicativas en las que intervienen conjuntamente expertos y no-expertos (AU)


Newspaper Q&A sections reflect and contribute to the social historical context in which they are published, and they may play roles as distinct as becoming a tool to sustain social arrangements or, conversely, being an instrument for social change. In a context of complex relations between experts and non-experts within the libertarian movement in Spain in the first third of the 20th century, the Q&A section («Preguntas y respuestas», 1930-1937) of the anarchist magazine Estudios (1928-1937) constitutes a particularly illustrative example of the multidimensional management of knowledge through the effective redefinition of the participation of quite different groups. In this paper, we analyze the exchange between physician Roberto Remartínez (1895-1977), the section coordinator, and its readers, and identify features of the implementation of the libertarian principles of self-management throughcommunication practices in which experts and non-experts jointly take part (AU)


Subject(s)
Humans , 50135 , Information Management/history , Knowledge Management , Spain , Information Services/history , Consumer Health Information/history , Information Dissemination/history
7.
Rev Soc Econ ; 69(2): 143-62, 2011.
Article in English | MEDLINE | ID: mdl-21941693

ABSTRACT

Through analysis of the French experience, this article explores the way economic policy has sought to encourage active, well-informed patients by giving them market power. The new status of the patient as consumer is based on two foundations: the endeavour to build a healthcare market and the activation of demand-based policies. The keystone of this new system is a conception of the market as a process constructed by economic policy. Recent measures such as the standardization of care and the introduction of incentives to respect a treatment pathway then constitute effective levers to establish a free-market rationale.


Subject(s)
Consumer Health Information , Economics , Patients , Power, Psychological , Standard of Care , Consumer Health Information/economics , Consumer Health Information/history , Consumer Health Information/legislation & jurisprudence , Economics/history , Economics/legislation & jurisprudence , France/ethnology , Health Care Sector/economics , Health Care Sector/history , Health Care Sector/legislation & jurisprudence , History, 20th Century , History, 21st Century , Patient Rights/history , Patient Rights/legislation & jurisprudence , Patients/history , Patients/legislation & jurisprudence , Patients/psychology , Standard of Care/economics , Standard of Care/history , Standard of Care/legislation & jurisprudence
8.
Fitoterapia ; 82(1): 5-10, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20837113

ABSTRACT

The Dietary Supplement Health and Education Act (DSHEA), enacted in 1994, had two primary goals: to ensure continued consumer access to a wide variety of dietary supplements, and to provide consumers with more information about the intended use of dietary supplements. It accomplished these goals, and more, without changing the fundamental regulatory status of dietary supplements as a category of foods. This article explores the history and reasoning behind the major provisions of the Act and reflects on the impact of each during 15 years of experience under DSHEA.


Subject(s)
Consumer Health Information/legislation & jurisprudence , Dietary Supplements , Legislation, Food , United States Food and Drug Administration , Consumer Health Information/history , Dietary Supplements/history , History, 20th Century , History, 21st Century , Humans , Legislation, Food/history , United States , United States Food and Drug Administration/history , United States Food and Drug Administration/legislation & jurisprudence , United States Food and Drug Administration/organization & administration
9.
J Asian Afr Stud ; 45(4): 387-405, 2010.
Article in English | MEDLINE | ID: mdl-20715334

ABSTRACT

This article investigates the extent of Human Immunodeficiency Virus/Acquired Immune Deficiency Syndrome Disclosures (HIV/AIDSD) in online annual reports by 200 listed companies from 10 African countries for the year ending 2006. Descriptive statistics reveal a very low level of overall HIV/AIDSD practices with a mean of 6 per cent disclosure, with half (100 out of 200) of the African companies making no disclosures at all. Logistic regression analysis reveals that company size and country are highly significant predictors of any disclosure of HIV/AIDS in annual reports. Profitability is also statistically significantly associated with the extent of disclosure.


Subject(s)
Acquired Immunodeficiency Syndrome , Annual Reports as Topic , Commerce , Disclosure , HIV , Public Health , Acquired Immunodeficiency Syndrome/ethnology , Acquired Immunodeficiency Syndrome/history , Africa/ethnology , Commerce/economics , Commerce/education , Commerce/history , Commerce/legislation & jurisprudence , Consumer Health Information/economics , Consumer Health Information/history , Consumer Health Information/legislation & jurisprudence , Delivery of Health Care/economics , Delivery of Health Care/history , Delivery of Health Care/legislation & jurisprudence , Disclosure/history , Disclosure/legislation & jurisprudence , History, 20th Century , History, 21st Century , Public Health/economics , Public Health/education , Public Health/history , Public Health/legislation & jurisprudence , Public Health Practice/economics , Public Health Practice/history , Public Health Practice/legislation & jurisprudence , Statistics as Topic/education , Statistics as Topic/history
10.
Can Public Policy ; 36(4): 521-34, 2010.
Article in English, French | MEDLINE | ID: mdl-21542210

ABSTRACT

As part of a larger e-health strategy, Canadian governments have invested millions in online health information services for the lay public. These services are intended to reduce demands on the primary health care system by encouraging greater individual responsibility for health and are often promoted using the language of personal empowerment. In this paper, we describe how lay searchers generally look for online health information and discuss the disempowering challenges they are likely to face in (a) locating Canadian government-sponsored health information sites and (b) finding useful information on these sites to address everyday health concerns. We conclude with several recommendations for policy changes.


Subject(s)
Consumer Health Information , Online Systems , Primary Health Care , Public Health Informatics , Public Policy , Canada/ethnology , Consumer Health Information/economics , Consumer Health Information/history , Consumer Health Information/legislation & jurisprudence , Government/history , History, 20th Century , History, 21st Century , Online Systems/economics , Online Systems/history , Online Systems/legislation & jurisprudence , Patients/history , Patients/legislation & jurisprudence , Patients/psychology , Power, Psychological , Primary Health Care/economics , Primary Health Care/history , Primary Health Care/legislation & jurisprudence , Public Health Informatics/economics , Public Health Informatics/education , Public Health Informatics/history , Public Health Informatics/legislation & jurisprudence , Public Policy/economics , Public Policy/history , Public Policy/legislation & jurisprudence
12.
Public Underst Sci ; 17(4): 461-72, 2008 Oct.
Article in English | MEDLINE | ID: mdl-19244867

ABSTRACT

Health issues and medical science receive a lot of attention on television. Of all the sciences, the European public is most interested in medicine, and the public uses television as their main source of information on science. There has been hardly any empirical research, however, into the historical development of the representation of medical science on television. The development of medical television was explored by carrying out a content analysis of Dutch non-fiction medical television programs spanning a period of 40 years. The speaking time allotted to experts has decreased over the years, while that allotted to laypeople has increased. We are seeing fewer references to sources and science and more expression of emotion and tension. The results suggest three periods of medical television: a scientific, a journalistic and a lay period. Medical television in 2000 shows a personified picture of patients against an instrumentalized and symbolized medical backdrop.


Subject(s)
Consumer Health Information/history , Journalism, Medical/history , Television/history , Consumer Health Information/trends , History, 20th Century , History, 21st Century , Netherlands , Television/trends
13.
Yearb Med Inform ; : 88-90, 2006.
Article in English | MEDLINE | ID: mdl-17051301

ABSTRACT

OBJECTIVES: To summarize current excellent research in the field of education and consumer informatics. METHOD: Synopsis of the articles selected for the IMIA Yearbook 2006. RESULTS: In the consumer informatics field current research focuses on meeting the informational needs of laypersons as well as health professionals with their specific demands and abilities. The selected papers' topics are genetic diseases and conditions, decision support for women considering genetic testing for the risk of breast cancer, history taking and advice for parents with children suffering from asthma, timed messages to motivate and support quit smoking efforts and the integration of health economics in medical education. CONCLUSIONS: The selected articles demonstrate examples of excellent research in consumer health informatics and medical education. The methods presented can contribute to the development of systems for the education of both laypersons and health professionals.


Subject(s)
Awards and Prizes , Consumer Health Information , Medical Informatics , Consumer Health Information/history , History, 21st Century , Medical Informatics/history , Societies, Medical
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