The other day I went to an urgent care clinic, suffering from a problem which needed attention promptly. This clinic is part of the local integrated health system’s network, where I’ve been seen for nearly 20 years. This system uses Epic everywhere in its network to coordinate care.
I admittedly arrived rather late and close to when the clinic was going to close. But I truly didn’t want to make a wasteful visit to the ED, so I pressed on and presented myself to the receptionist. And sadly, that’s where things got a bit hairy.
The receptionist said: “We’ve already got five patients to see so we can’t see anyone else.” Uncomfortable as I was, I fought back with what seemed like logic to me: “I need help and a hospital would be a waste. Could someone please check my medical records? The doctors will understand what I need and why it’s urgent.”
The receptionist got the nurse, who said “I’m sorry, but we aren’t seeing any more patients today.” I asked, “But what about the acuity of a given case, such as mine for example? Can’t you prioritize me? It’s all in my medical records and I know you’re online with Epic!” She shook her head at me and walked away.
I sat in reception for a while, too irritated to walk out and too uncomfortable to let go of the issue. Man, it was no fun, and I called those folks some not-nice things in my mind – but more than anything else, wondered why they wouldn’t look at data on a well-documented patient like me for even a moment.
About 20 minutes before the place officially closed for the night, a nurse practitioner I know (let’s call him Ed) walked out into the waiting room and asked me what I needed. I explained in just a few words what I was after. Ed, who had reviewed my record, knew what I needed, knew why it was important and made it happen within five minutes. Officially, he wasn’t supposed to do that, but he felt comfortable helping because he was well-informed.
Truthfully, I realize this story is relatively trivial, but as I see it, it brings an important issue to the fore. And the issue is that even when seeing chronically-ill patients such as myself, whose comings and goings are well documented, providers can’t or won’t do much to exploit that data.
You hear a lot of talk about big data and analytics, and how they’ll change healthcare or even the world as we know it. But what about finding ways to better use “small data” produced by a single patient? It seems to me that clinicians don’t have the right tools to take advantage of a single patient’s history, or find it too difficult to do so. Either way, though, something must be done.
I know from personal experience that if clinicians don’t know my history, they can’t treat me efficiently and may drive up costs by letting me get sicker. And we need more Eds out there making the save. So let’s make the chart do a better job of mining patient’s data. Otherwise, having an EMR hardly matters.