
The Pew Internet/Health FAQ |
Original post on e-Patients.net
The lessons learnt from Pew internet research report on e-patients.Susannah Fox is an Associate Director of the Pew Internet & American Life Project and principal author of the Project’s survey reports on e-patients and online health. Here, Susannah displays an almost naive view of a health consumer"s requirements and sounds arrogant at places, especially while talking of Privacy rights.
Read her <edited> views on Use of internet by e-patients.
Yes. Thanks to the internet, people increasingly expect to have access to information. They increasingly expect to be able to comment on and easily share information. And it turns out that participation matters as much as access.
- Is a cultural shift affecting health care?
The best they can, but probably not the way you think they should. Most people’s first stop for health information is a general search site. Google dominates the search market. A British Medical Journal article found that Google is a pretty good diagnostician. Very few people report bad outcomes from their online health research.
- How do people judge the quality of health information online?
Nobody’s “in charge” and to some degree, yes. The base of the internet population is broadening to include people with less education and lower health literacy/numeracy. E-patients with a high school degree or less are more likely than better-educated e-patients to say they were confused by the health information they found online. But note that the two groups are equally likely (and more likely) to say they felt confident to raise new questions or concerns with their doctor, too. Also read-*Medical Library Association’s consumer guide AND*Alicia White’s “Keep Calm and Carry On” advice for reading health news (PDF).
- Who’s in charge of vetting health information online? Shouldn’t we be concerned about this?
I don’t know, but Manhattan Research and ThinkHealth do.
- What are doctor’s attitudes?
The Center for Studying Health System Change’s study measuring “patient activation” is one indicator. The central role of family caregivers is not addressed in the study, however. Another indicator is the relentless popularity of health information online. Lots and lots of people are looking up information on all kinds of health topics.
- Are patients ready for this?
Daniel Solove’s taxonomy of the word “privacy” has forever changed my thinking about the changing nature of personal information. In fact, I try to avoid using the word at all (instead: confidentiality, security, anonymity…)
- What about privacy?
Deven McGraw, Director of the Health Privacy Project at CDT, is a good source on health privacy regulations and enforcement. Jules Polonetsky, Director of the Future of Privacy Forum, is a more general source.
Caution: “cyberchondria” is a loaded term. E-patients.net has hosted discussions of how to describe people who use the internet to gather health information. For example: Googlers vs. e-patients vs. cyberchondriacs.
- Does the internet cause cyberchondria?
I am watching the spread of wireless internet use very closely. Wireless access has a significant, independent effect on how someone uses the internet and it’s the trend I am most excited about tracking over the next year or so.
- What business opportunities are there in this field? What does the future hold?
Related articles
- Web 2.0 in health (neeleshbhandari.blogspot.com)
- Twitter in Health care (medical-communication.blogspot.com)
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