Jimison, H. (2005) Ethical Issues in Consumer Health Informatics, in Deborah Lewis, Gunther Eysenbach, Holly B. Jimison, Rita Kukafka and P. Zoie Stavri (Eds.) Consumer Health Informatics. Informing Consumers and Improving Health Care, Springer, New York, NY, 143-149....
“The issues related to MH due to the excessive use of DT and the internet became a significant challenge in the Metaverse.” Its emergence has raised concerns regarding the possible effects of immersive digital platforms on human MH (Usmani et al.2022). Although there is early optimism, it ...
The continued deployment of new and evermore powerful information technology (IT) and information systems (IS) presents an increasingly important ethical challenge within the healthcare field for IT, business, and healthcare professionals. The increased use of the Internet by those...
The continued deployment of new and evermore powerful information technology (IT) and information systems (IS) presents an increasingly important ethical challenge within the healthcare field for IT, business, and healthcare professionals. The increased use of the Internet by those...
This chapter will address ethical issues in consumer informatics and online content, including quality assurance, privacy and security concerns, consent and governance, and the important role consumer information plays in shared decision-making. If privacy concerns have slowed the progress of research, ...
This chapter explores a wide range of ethical, legal, and social issues in mental health informatics. The topics covered are broadly categorized into four groups: (1) ethical issues related to artificial intelligence in mental healthcare, (2) issues related to mobile health and eHealth ...
It also argues that a corresponding certification process for health care institutions and software developers should be initiated.Eike-Henner W. KlugeMEDINFOKluge EH. The need for global certification in the field of health informatics: some ethical issues. Medinfo 2007; 12:233-236....
Common issues raised by IRBs included: (a) attempting to strike a balance between the degree of detail and readability needed for informed consent, (b) the process for determining actionable genes in pediatric populations, (c) the specific language detailing the full range of potential risks, (...