e-Patient Dave

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March 10, 2013 By e-Patient Dave 3 Comments

Interesting new e-patient resource: Medivizor

Added 9/11/2013:  I do not endorse this product. I have no idea if the information it gathers is reliable. I add this because in a press release the company lists me in people who have “covered” their service; I want to be clear, as it says below, that although I wrote about it, I didn’t endorse it. Frankly it feels a bit dicey that a careful curator of information would be a little bit incautious about the meaning of words.

I get a lot of requests to look at new products, websites, services. If I were rich and retired (or tenured :-)) I’d spend my whole life exploring, but I’m not, so I can’t. This is one, though, that caught my eye, because it proposes to automate something that can normally only be done by peers: filter all the information out there and tell you what’s useful to you.

If this works out, it could become an essential resource for engaging patients and families.

Disclaimer: I haven’t been able to vet the site, testing it as someone with “skin in the game” because the company is currently only handling a few conditions. Also, I’m open to reports of similar products that claim to do what I describe here. This is a description of what interests me, not a final and absolute endorsement.

Okay, enough fine print:

Medivizor is a startup that culls literature and other resources, including the social web. They select portions relevant to you (based on a questionnaire and your feedback), rephrase it in ordinary language, and send it to you. As their site says:

[Read more…]

Filed Under: decision making, e-patient resources 3 Comments

March 4, 2013 By e-Patient Dave Leave a Comment

Biggest HIMSS news for families: CommonWell Health Alliance for getting our data to be where we need it

A quick note – mark my words, this is important –

At the big HIMSS health IT conference, six vendors of electronic health records have announced that they’ll be collaborating to share data as the Commonwell Health Alliance. That’s your data, our data, your family’s data.

Significantly missing from them is the Big Dog in the field, Epic, which is notoriously “all about us,” i.e. themselves.

Of course all the lesser dogs have a motivation in this – to band together and try to knock Big Dog off the top of the mountain.

Read about it here. Top EHR vendors join CommonWell Alliance to boost interoperability

My take: Market forces are starting to emerge. If underdog vendors can combine offer something the dominator doesn’t, that’s free enterprise working!
[Read more…]

Filed Under: Health data Leave a Comment

March 4, 2013 By e-Patient Dave 4 Comments

Let Patients Help, Cost-Cutting Edition: “Chaos behind a veil of secrecy”

One blog I read regularly is “Not Running A Hospital” by Paul Levy, formerly CEO of my hospital, Beth Israel Deaconess. Today’s post is A Tale of Two Blues, in which an MIT professor colleague recounts the insane, infuriating situation with his insurance company. His tale:

The last couple of months have been very heavy duty bad medical stuff for me.  Horrendous. So, I’ve been able to see the dysfunctional medical insurance system in action.   Do you understand how Blue Cross/Blue Shield actually works?  Out of, oh, maybe 80 transactions over 2 months — they managed to get one, as in the number 1, correct.  The rest are mistakes, mis-billings, computer errors, everything one can imagine.  And the only reason I can ever figure it out is because I am dogged and know something.  I can’t even begin to imagine the bone-head database that lurks behind all of it, along with inept programming, but whatever it is, the people running the place (sorry if I tread on toes) — up to and including all the executives, are simply, sorry to say, totally bonkers.  And they are just middlemen. They aren’t providing services, just managing to extract rents. Badly.

P.S. BTW, my running statistics on them, is that out of 540 transactions with them over the past 1.8 years, they have gotten two, as in the number 2, correct.   Not a good batting average. Why are they so inept?

As regular readers know, this general subject (not BC/BS of MA) has been one of my pet peeves lately, especially since I so often hear “Our costs are high because patients are irresponsible lazy slugs.” I summarized the past year’s posts in a comment there; I’m pasting it in here:

============

A quick preliminary response, Paul:

As I think you know, Paul, this is something I’ve been blogging about for the past year. [Read more…]

Filed Under: cost cutting edition 4 Comments

February 28, 2013 By e-Patient Dave Leave a Comment

Let My Data Go: the HIMSS Interop Showcase

Title slide: Let My Data Go

As regular readers know, I feel rather strongly about the power of information. As a data geek, a high tech innovation freak, and a fan of improving health and care, I want the power of data to be set free.

In health IT, that means exchanging data between systems – because if it’s locked up in one system, nobody else can add value to it. And at the point where it might save a life, it might not be there.

And when that’s you, or your daughter, or your mother, or even some male relative, that could make all the difference in the world.

You think video killed the radio star?  In my career in industry, I lived through disruptive innovation, when desktop publishing killed typesetting. I know what power there is when data gets lose and innovators can add value to it. We need that in medicine. And that’s interoperability.

That’s what I’ll be talking about at 4:00 pm Monday in the Interoperability Showcase Theater, at the big HIMSS (health IT) conference in New Orleans next week. If you’re a data geek, or if anyone you know consumes medical services, this issue is important to you. Come give it up for interop – to let my data go!

Filed Under: Events, Health data, public speaking Leave a Comment

February 27, 2013 By e-Patient Dave 6 Comments

Now online: full program “My Health Counts: e-Patients” and more

Last fall I wrote about a new program I’m in, on WNED-TV, the Buffalo PBS affiliate: “My Health Counts: e–Patients”. It also includes the e-patient stories of Lygeia Ricciardi (official consumer e-health guru at HHS) and Buffalo resident Tom Dixon, and is hosted by Susan Hunt.

The program aired Wednesday night for the first time, and is now available online. I’m thrilled with how it came out – the team at WNED, led by producer Christie May, did a phenomenal job. Here’s the video. (Email subscribers, click the headline to come online and view it.)

http://video.wned.org/videoPlayerInfo/2305112748

Watch e-Patients on PBS. See more from My Health Counts!.

Even better, the WNED team developed a terrific web page of related resources, including:

  • [Read more…]

Filed Under: Uncategorized 6 Comments

February 22, 2013 By e-Patient Dave 17 Comments

I’ve hung out my shingle – at last!

Photo of my first office signI’ve reached a milestone: after three years, my startup has reached breakeven. For the first time, I’m not living hand-to-mouth.

So I’m now able to have my first little office outside the home. I can go to work, and I can come home from work. See sign at right: my name, and my motto, “Let Patients Help.” I’ve hung out my shingle.

Thank you, clients and sponsors.

Words can barely express my gratitude to the people who helped me get started, through their early support when nobody had ever heard of me, and as far as I know nobody ever paid to hear a patient speak at a conference.

Who was first to offer me pay for a speech? Kent Bottles MD (@KentBottles), who at the time [Read more…]

Filed Under: Business of Patient Engagement 17 Comments

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