{"id":3206,"date":"2009-09-21T21:03:05","date_gmt":"2009-09-22T02:03:05","guid":{"rendered":"http:\/\/pmedicine.org\/epatients\/?p=3206"},"modified":"2010-01-02T22:00:32","modified_gmt":"2010-01-03T03:00:32","slug":"gimme-my-damn-data","status":"publish","type":"post","link":"https:\/\/participatorymedicine.org\/epatients\/2009\/09\/gimme-my-damn-data.html","title":{"rendered":"Give patients (that’s you) access to all their (your) data – so they can help"},"content":{"rendered":"

Cross-posted from my website, ePatientDave.com<\/a> – the happy home for my new business!<\/em><\/p>\n

I’ve just returned from Toronto, where I gave the opening keynote at the Medicine 2.0 Congress<\/strong><\/a>. It was titled “Gimme My Damn Data,” which is an unconventional title for an opening address, but I meant it. Here’s why.<\/p>\n

\"Thanking<\/a>A new world of participatory medicine<\/a><\/strong> has been growing for years, largely unnoticed. In this new world, healthcare is not a one-way street: empowered patients are engaged in their care,<\/strong> actively collaborating with their physicians, sharing responsibility for their care.<\/p>\n

The healthcare providers (doctors, nurses, etc) are still the providers, but the patients share in both the knowledge and the responsibility for how it all turns out.<\/p>\n

And, certainly, the decision making.<\/p>\n

This requires that patients have access to their medical data.<\/strong> (Whose data is it, anyway?)
\n
\nAs my primary physician Danny Sands, MD MPH, says, “How can patients participate if they can’t see the data?” But in today’s world (America and, I’m told, many other countries), access to our health data is anything but easy.<\/p>\n

In the USA the HIPAA act guarantees that we can get it – but it can take months<\/em>, which is absurd in a crisis. And, law or no law, Deven McGraw of the Center for Democracy and Technology<\/a> reports that problems with data access are the #5 complaint <\/strong>in the entire Department of Health and Human Services.<\/span> #3\u00a0HIPAA complaint<\/strong>* reported to the Department of Health and Human Services.
\n* Deven updated this in an email, saying \u201cit\u2019s consistently the third based on this HHS source<\/a>.\u201d<\/em><\/p>\n

Clearly, what patients want and are asking for <\/em>is not an accomplished reality<\/strong> throughout the world today. This is unacceptable. Lives are at stake. <\/strong>I think people – especially sick people – have a right to take their records and seek care elsewhere. (And that’s beyond the basic issue of a person having access to their data on general principle. Imagine if you couldn’t see your banking information!)<\/p>\n

Some providers are great about this. My own medical records, which I can read anytime,<\/strong> are on PatientSite<\/a> at Beth Israel Deaconess. But there’s still no way for me to get all the data out: I can export some information, but not all. And my hospital’s much better than most: most have no way at all to give you your data – except by fax machine.<\/p>\n

There are many technical issues to be ironed out, not the least of which is what format the data should be in. I want to participate in projects<\/strong> to make something happen in this area, something all citizens can get their hands on. If you’d like to partner with me on such a project, contact me<\/a>.<\/p>\n

My slides from the talk should be online within a few days. I’m glad to say that my talk was well received, but to a certain extent I was preaching to the choir. We have much work to do.<\/p>\n

So yeah, I meant it: give us our data<\/em>, and I meant it strongly. No kidding: unleash our data!<\/strong><\/p>\n

It’ll take time. Let’s get to work.<\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

Cross-posted from my website, ePatientDave.com – the happy home for my new business! I’ve just returned from Toronto, where I gave the opening keynote at the Medicine 2.0 Congress. 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