Last week, I wrote about controversial research linking fallout from Japan’s earthquake-damaged Fukushima nuclear plant to infant deaths in the United States.
The research, which was harshly criticized by Scientific American’s Michael Moyer and others, was published in the peer-reviewed Journal of International Health Services, and I had asked the journal’s editor-in-chief Vicente Navarro for his response to the criticisms.
Navarro, professor of health policy at Johns Hopkins University’s Bloomberg School of Public Health, emailed me this comment today: Read more »
*This blog post was originally published at Reporting on Health - Barbara Feder Ostrov's Health Journalism Blog*
Many doctors roll their eyes whenever patients bring in a stack of research they printed out, stemming from a Google search of their symptoms. A piece by Dr. Zachary Meisel on TIME.com describes a familiar scenario:
The medical intern started her presentation with an eye roll. “The patient in Room 3 had some blood in the toilet bowl this morning and is here with a pile of Internet printouts listing all the crazy things she thinks she might have.”
The intern continued, “I think she has a hemorrhoid.”
“Another case of cyberchondria,” added the nurse behind me.
It’s time to stop debating whether patients should research their own symptoms. It’s happening already, and the medical profession would be better served to handle this new reality.
According to the Pew Internet and American Life Project, 61 percent of patients turn to the web to research health information. That number is from 2009, so presumably it’s higher today. Health information online is akin to the Wild, Wild West. Stories from questionable sites come up on Google as high — or higher — than information from reputable institutions. Read more »
*This blog post was originally published at KevinMD.com*