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1.
Yakugaku Zasshi ; 141(3): 377-380, 2021.
Article in Japanese | MEDLINE | ID: mdl-33642507

ABSTRACT

Nowadays, approximately 90 percent of the general population in Japan uses the internet and many of them look for health-related information. However, there have been serious concerns about the contents and credibility of these information. Among "mixture of wheat and chaff", information provided by the public domains are expected as accurate and reliable ones. This article reviews five public websites that provide health or health care information for users including the general population: Minds by the Japan Council for Quality Health Care, e-health net, evidence-based Japanese Integrative Medicine (eJIM), Cancer Information Service by the National Cancer Center, Center for Cancer Control and Information Services, Information system on safety and effectiveness for health foods (HF net) by National Institute of Health and Nutrition. These websites show their running policy transparently and have constructed collaborative relationships with each domain experts, and from the people who are not related with the healthcare field including patients in some cases. Each of them is content-rich and well-organized as an individual unit. The organizations that run these websites share the common goal that provides the general population with quality health-related information, however, cooperation have been limited. To increase awareness among the public, it is worthy considering joint efforts of these organizations in future.


Subject(s)
Consumer Health Informatics , Consumer Health Information , Delivery of Health Care , Internet , Community Networks , Consumer Health Informatics/organization & administration , Consumer Health Informatics/trends , Consumer Health Information/organization & administration , Consumer Health Information/trends , Food Safety , Functional Food , Humans , Japan , Risk Reduction Behavior
2.
Yearb Med Inform ; 28(1): 158-164, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31419828

ABSTRACT

OBJECTIVES: To present the breadth and depth of Consumer Health Informatics (CHI) initiatives and in particular, identify areas to further enhance such solutions with the incorporation of advances in artificial intelligence (AI). METHODS: A literature review was conducted. Inclusion criteria focused on barriers and facilitators as well as key milestones for CHI over the last 10 years. In addition, significant international initiatives in regions and /or countries and opportunities to incorporate the advances of AI also made up the inclusion criteria. Exclusion criteria included factors that made reach/range of solutions to individuals or groups of individuals less than 50 people. Journals in Medline were accessed as well as the grey literature. RESULTS: 200 papers were identified but this was narrowed to 25 due to repetitions and similarities of the types of solutions presented. From this, it was possible to identify key barriers and facilitators including: socio-political factors, financial factors, infrastructure, as well as levels of health literacy. CONCLUSIONS: The relatively nascent domain of CHI has developed and is growing. Full benefits will only be realized when more precision solutions that incorporate AI advances will be designed. The example of RxPredict is provided as a case vignette to illustrate.


Subject(s)
Consumer Health Informatics , Telemedicine , Artificial Intelligence , Consumer Health Informatics/economics , Consumer Health Informatics/trends , Electronic Health Records , Patient Portals
4.
Annu Int Conf IEEE Eng Med Biol Soc ; 2019: 4283-4288, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31946815

ABSTRACT

Diabetes-related consumer health information technology (CHIT) has been designed to facilitate self-management practices, and its use has improved health outcomes for many consumers. This analysis sought to identify tendencies in diabetes-related CHIT research from 2010-2015 to help researchers find novel research topics, periodicals, collaborators, and funding agencies and experts and lay consumers to find scholarly information. Six search engines encompassing computer science, engineering, and medicine yielded potential diabetes-related CHIT publications. Abstracts and full texts were screened based on inclusion and exclusion criteria. Information on year, periodical, periodical domain, keywords, author location, author institutions, authors, and funding agencies were collected from included publications. The screening process yielded 1551 publications. Studies were published in a core of twenty periodicals, commonly comprising medicine or technology domains. "Telemedicine" was the most frequently used keyword. Harvard University, Dr. Eirik Årsand, and the National Institute of Diabetes and Digestive Kidney Diseases were the most frequent author institution, author, and funding agency, respectively, associated with publications. This analysis revealed potential for novel research on the sociology and economics of diabetes-related CHIT, among other topics. A lack of collaboration between top authors in the field indicates potential for new, impactful collaborations. Ongoing bibliometric research will be necessary to assess changes in this field. The opportunity exists to inform lay consumers and researchers through bibliometric analyses of other consumer health informatics topics.


Subject(s)
Consumer Health Informatics/trends , Diabetes Mellitus , Publications , Bibliometrics , Humans , Search Engine
5.
J Drugs Dermatol ; 17(4): 482-484, 2018 04 01.
Article in English | MEDLINE | ID: mdl-29601627

ABSTRACT

Forty-two percent of Americans search for health-related information on social media platforms, and forty-five percent of consumers report that social media health information influences their decision to seek care.


Subject(s)
Consumer Health Informatics/trends , Dermatology/trends , Social Media/trends , Consumer Health Informatics/methods , Dermatology/education , Dermatology/methods , Humans
6.
Yearb Med Inform ; 26(1): 152-159, 2017 Aug.
Article in English | MEDLINE | ID: mdl-29063559

ABSTRACT

Objectives: Consumer Health Informatics (CHI) and the use of Patient-Generated Health Data (PGHD) are rapidly growing focus areas in healthcare. The objective of this paper is to briefly review the literature that has been published over the past few years and to provide a sense of where the field is going. Methods: We searched PubMed and the ACM Digital Library for articles published between 2014 and 2016 on the topics of CHI and PGHD. The results of the search were screened for relevance and categorized into a set of common themes. We discuss the major topics covered in these articles. Results: We retrieved 65 articles from our PubMed query and 32 articles from our ACM Digital Library query. After a review of titles, we were left with 47 articles to conduct our full article survey of the activities in CHI and PGHD. We have summarized these articles and placed them into major categories of activity. Within the domain of consumer health informatics, articles focused on mobile health and patient-generated health data comprise the majority of the articles published in recent years. Conclusions: Current evidence indicates that technological advancements and the widespread availability of affordable consumer-grade devices are fueling research into using PGHD for better care. As we observe a growing number of (pilot) developments using various mobile health technologies to collect PGHD, major gaps still exist in how to use the data by both patients and providers. Further research is needed to understand the impact of PGHD on clinical outcomes.


Subject(s)
Consumer Health Informatics , Health Records, Personal , Telemedicine , Consumer Health Informatics/trends , Humans , Information Seeking Behavior , Professional-Patient Relations
7.
J Am Board Fam Med ; 29 Suppl 1: S69-71, 2016.
Article in English | MEDLINE | ID: mdl-27387169

ABSTRACT

A recurring conference theme was the essential place of social justice within family medicine, especially the need to focus on denominator populations, exalt the personal and caring qualities of doctoring, and address social determinants of health. Many expressed solidarity with "community," but it is not always easy to define community in our large and diverse nation. Exhortations for health advocacy were frequently voiced, but putting these into meaningful action agendas is a challenge. There was general agreement that medicine is in flux and that the many expressions of "commodity-centered consumerism" have altered organization and financing. The increasing demands by "consumers", who want low cost, instant availability, and shared decision-making, and yet change doctors when health plans alter coverage also differentially impact high-volume, low-margin specialties such as family medicine. Additional challenges were the electronic health record and calibrating an appropriate work/life balance. Five action steps are recommended: 1) speak out on the important social and moral issues; 2) be the experts on personal care; 3) make common cause with potential allies; 4) help institutions perceive the value of generalism; and 5) help find ways to enrich generalist disciplines to increase the joy of medicine and decrease the threat of burn out.


Subject(s)
Family Practice/ethics , Physicians, Family/ethics , Primary Health Care/ethics , Social Justice , Academic Medical Centers , Consumer Advocacy/trends , Consumer Health Informatics/trends , Electronic Health Records , Family Practice/trends , Humans , Physicians, Family/trends , Primary Health Care/trends , Social Determinants of Health , Social Media , United States
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