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Healthcare Groups Want Meaningful Use Evaluated Before Stage 3

Posted on January 16, 2013 I Written By

Anne Zieger is a healthcare journalist who has written about the industry for 30 years. Her work has appeared in all of the leading healthcare industry publications, and she's served as editor in chief of several healthcare B2B sites.

Though the final rules for Meaningful Use Stage 3 aren’t due to take effect until 2016, ONC has already made the draft rules available for public comment.  And comments, to be sure, the agency is getting.

While various groups have chosen their own details to critique, the general consensus seems to be that ONC is getting ahead of itself and ought to give Meaningful Use Stage 1 and 2 a good hard look first.

Accordng to a nice summary from iHealthBeat, here’s where some of the major healthcare groups stand:

* The American Hospital Association is recommending that ONC fund a comprehensive evaluation of MU generally, and while it does, hold off on finalizing Stage 3 recommendations.

*  CHIME, too, is asking ONC to evaluate the existing Meaningful Use program to decide whether achieving stage 3 is realistically possible by 2016.

* The Federation of American Hospitals is also arguing that ONC needs to evaluate current Meaningful Use requirements.  Also, in its letter to ONC, the group argues that the existing structure of two years per stage doesn’t cut it.

* The AMA weighed in with its own recommendation that ONC evaluate Meaningful Use as is before moving ahead. It also suggested changing some thresholds to  make them more reachable; greater flexibility in program requirements; change the certification process to address usability; and improve HIT’s capability to share patient data.

Personally, I think the idea of doing an extensive Meaningful Use evalulation sounds like a good one, and I hope ONC actually does so.  When you’re setting new standards that affect so many providers, why not gather some data on how existing standards work?

Thirty-Five Percent of Americans Consult Internet For Health Information

Posted on I Written By

Katie Clark is originally from Colorado and currently lives in Utah with her husband and son. She writes primarily for Smart Phone Health Care, but contributes to several Health Care Scene blogs, including EMR Thoughts, EMR and EHR, and EMR and HIPAA. She enjoys learning about Health IT and mHealth, and finding ways to improve her own health along the way.

Every  morning before I get out of bed, I look at all the headlines on my news widget. The last section I usually look at is the health news. Today, a headline caught my attention — it said something about thirty-five percent of American adults consult “Dr. Google” to diagnose illness. This definitely sounded like something up my alley, so I read it, and wanted to share the information here.

I couldn’t find the article that I originally read, but this one from provided the same information. Just today, findings from The Pew Research Center’s Internet and American Life Project were published. Here are some of the most interesting findings:

  • 59 percent of adults using the Internet have looked online for health info in the past year
  • 35 percent have sought out information online, specifically trying to diagnose theirs, or someone elses’, medical condition
  • After apparently finding out what their condition was online, 46 percent felt they should seek help from a health provider, 38 percent felt they could treat it at home, and 11 percent said it was in between.
  • 41 percent had a doctor confirm the condition, thirty five percent didn’t consult a physician, and 18 percent were corrected by their physician on what the condition was.

I thought this was all pretty interesting. The study also found that women are more likely to look information up online about health. That sounds about right to me — I don’t think my husband has EVER looked up something about a medical condition online, while I probably do every other day.

I think the fact that almost half of those that looked up information were able to have the condition they “diagnosed” themselves with confirmed with a physician shows how information found online is getting better. The authors did say this though, about these findings:

It is important to note what these findings mean — and what they don’t mean. Historically, people have always tried to answer their health questions at home and made personal choices about whether and when to consult a clinician. Many have now added the internet to their personal health toolbox, helping themselves and their loved ones better understand what might be ailing them. This study was not designed to determine whether the internet has had a good or bad influence on health care. It measures the scope, but not the outcome, of this activity.

What I think this study does show, however, is that it’s now more important than ever to make sure there’s good, reliable information out there for people to consult. A decent percentage of the people surveyed didn’t seek medical attention after their self-diagnosis, and it would be unfortunate if someone got incorrect information and really did need to see a doctor.

If anything, I’m just happy to see that there are others who consult Dr. Google as much as I do!