{"id":2661,"date":"2009-06-19T06:51:14","date_gmt":"2009-06-19T11:51:14","guid":{"rendered":"http:\/\/pmedicine.org\/epatients\/?p=2661"},"modified":"2017-05-17T08:59:59","modified_gmt":"2017-05-17T12:59:59","slug":"imagine-someone-had-been-managing-your-data-next-anecdote","status":"publish","type":"post","link":"https:\/\/participatorymedicine.org\/epatients\/2009\/06\/imagine-someone-had-been-managing-your-data-next-anecdote.html","title":{"rendered":"Imagine someone had been managing your data: next anecdote"},"content":{"rendered":"

Next anecdote about poorly managed medical data:<\/p>\n

Amen!<\/p>\n

Just had an incident where my SS# was attached to a different patient\u2019s name in the electronic med record. And the health facility will not tell me where the error occured, or how long someone else\u2019s name was linked to my ss# and my medical record. Discovered accidentally when the lead attendant called me by the wrong name\u2026. The hospital ethics person states only that they have taken care of it and counseled the individual involved!<\/p>\n

Then try reviewing your own EMR. They act like you are neurotic even though the reason is that your record had been mixed up with another person\u2026duh!<\/p>\n

Lots of errors\/lots of privacy issues.<\/p><\/blockquote>\n


\nThis is a new comment<\/a> that appeared Wednesday night on my April 1 post<\/a> about moving my data from my hospital’s system to Google Health. It’s from Kate Bosch, a Pacific Northwest resident who knew nothing about my story; she ran into her own mess and decided to see what she could learn. Good ol’ Google Blog Search brought her here.<\/p>\n

The front page Boston Globe article about my adventure focused on the newly emerging doubts about our data. (Aptly, it was titled Electronic Health Records Raise Doubts<\/a>.) There are at least two aspects to that doubt.<\/p>\n

The article talked about billing data, and how it’s a poor “proxy” (in engineering terms) for clinical reality. (When you can’t find real data for something, it’s sometimes valid to use an available substitute, which is referred to as a proxy.)<\/p>\n

But a deeper issue in my original post, much harder to change, is that no system will produce good results by itself: tools must be used properly.<\/strong> Buying a new hedge trimmer won’t guarantee gorgeous hedges, and among all the people you know who own a computer, I bet some get better results than others.<\/p>\n

More importantly, when it comes to putting data into a multi-user system, you will not get reliable data unless there are well controlled processes for how data gets into the system.<\/strong> That means teaching people to do things in a particular way. And in an established profession, that usually means changing people’s work habits. And that takes time.<\/p>\n

This is not rocket science, and it’s not unique to medicine. When I worked in the newspaper systems business, as that industry computerized, I saw at close range that changing an industry’s work habits can take a full generation.<\/em> (And I mean a generation of people, not generation of systems.)<\/p>\n

Think about that. Because we’re talking about how well others have been managing your medical data<\/em>. Are you ready to take responsibility?<\/p>\n

(Mind you, this doesn’t mean they’re “bad people.” It’s not trivial to design and stick to a good clean process. I know; I do that stuff in my day job. My point isn’t that the people are evil or anything, it’s that we are misguided if we assume<\/em> our data is probably correct; we should check it out. Another set of eyes never hurts, eh?)<\/p>\n

In my original post I wrote “I suspect processes for data integrity in healthcare are largely absent, by ordinary business standards.”<\/strong> This suspicion was validated by the Information Quality Trainwrecks blog<\/a>, a blog where data professionals talk about how to avoid such things. Reviewing the story, they said “problems that have been documented in the information quality literature for over a decade are at the root of an embarassing information quality trainwreck.”<\/p>\n

What to do? You and I must take control of our own data, because the industry may take twenty years to get there.<\/strong> Kate nailed it in a subsequent email:<\/p>\n

the deeper I question, the more of a mess it seems…In my estimation the EMR will only work if patients have full access to ALL their EMR<\/strong> and can catch mistakes as they happen. Also security and access should ideally rest with the patients wishes not the medical or\u00a0 insurance facility<\/strong>…<\/p>\n

A complete turnaround in medical staff thinking\u00a0 will be necessary though & I don’t think this will come easily\u00a0 judging on my own experience & how I was treated when I requested to review the EMR’s (something they claimed no-one had ever asked to do before).<\/p><\/blockquote>\n

Welcome, Kate. Have a seat – we got work to do.<\/p>\n

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

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