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Executive Interview: From Data Exchange to Data Utility with Dr. Steven Lane and Mike Cordeiro
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I'm Bill Russell, creator of this Week Health, where our mission is to transform healthcare, one connection at a time. This is an executive interview
quick powerful Conversations with Leaders Driving Change. So let's get started.
r Director, interoperability [:This has been a passion project for me since I got into healthcare back in 2011. I came in from outside the industry and it just felt to me like I worked in banking and everything else. It's like this interoperability thing should be pretty easy. And then when I got into healthcare, I realized this is not quite as simple as I.
Thought it was going to be, but interoperability efforts have really come a long way in just the last few years. Where are you seeing this impact healthcare the most at this point?
Steven: that's a great way, to start the conversation. I think, you know, as a practicing physician, I can tell you it absolutely impacts care at the bedside, you know, or in the doctor's office.
e that moving forward, we're [:People have really integrated this into their workflows. So when I see patients, routinely, I have access to data not only from my own institution, but from other institutions and facilities where the patients receive care. And this is important in so many settings. I mean, in primary care where I work, where patients move around and see multiple specialists.
In the acute care setting, whether you're talking about the emergency department, where people will drop in, and you really need rapid real-time access to data in order to provide safe and effective care. Maternity care is a great example where prenatal care. Delivery care, postnatal and pediatric care are often provided in different institutions, and we need to move that data around and make it available.
allenges of value-based care [:Seen historically that when you provide clinicians and institutions with more data, sometimes they don't know what to do with it. It's more data than they can manage cognitively. And with AI where you can actually review that data, come up with actionable insights and help to inform the care that it's proving to be tremendously important.
We're seeing today providers increasingly integrating AI tools into their decision making and their patient care processes. But oftentimes that involves. You know, hopping between applications or picking your favorite app. But what we need to see, what we wanna see is those tools integrated into the daily clinical workflow where the AI will be able to review all the data both locally.
Externally [:Mike: Yeah I couldn't agree more. It's definitely been a journey from the e HR perspective, you know, and kind of from my vantage point we've, you know, moved beyond, you know, static documents like the CCD and the expectation today and time from interoperability standpoint is real time data exchange.
It's structured and it's essentially meant to have utility around it. Like you said, Dr. Lane removing the cognitive load on clinicians and surfacing insights directly at that point of care. MEDITECH you know, we launched Traverse Exchange, our own data sharing network first in Canada now in the States.
ose insights directly within [:I think the other kind of key component here too is, and it's importantly is that government backed frameworks like tef are leveraged, are leveling, you know, the playing field. So they remove the historical barriers that force community health systems to consider mergers, to gain access to, to, to data.
And now will these national networks and frameworks in place organizations, whether they're independent or part of a larger system, can participate fully in, in in data sharing. So I think it's been a, a. A pretty big shift overall, you know, a shift towards scalability, sustainability and kind of equity as it relates to healthcare data.
ctured data, we now have us, [:You know, what are the barriers keeping the data from being actionable and what shifts are needed to move from data collection and data movement to really data utility, for the clinicians.
Steven: So a lot of work is being done on those very issues. Data usability is the word that has caught on.
And the idea is, yes, you can get your hands on huge volumes of data, but if it's not structured, if it's not normalized, if it's not de-duplicated it's very difficult to really see it. in A holistic way so that you can make decisions. I think you pointed out that the structure of the data is very important and we need to be able to normalize that if we're going to be able to integrate even data generated within a single provider or health system, but certainly when you're going across systems.
ge of integrating externally [:What are their medical problems? What are their allergies? Who's on their care team? All these things are incredibly important. The data exchange brings you that data, but if you're having to sift through it, as you said, PDFs, you know, or even CCDs, you know, it's very difficult. What you need is to be able to receive the data, either receive it discreetly or receive it in a document format, and then tear it apart into the individual elements.
You know, these days where using the FHIR the fast healthcare interoperability, resources, standards for that and then you can bring all of that data together at the point of care to inform what's going on.
Mike: Yeah, I definitely agree, and I think there's kind of been a shift, right? So interoperability, you know.
iving health it forward, you [:But once you have it, like you were saying, you need to have, understand the intent of that data, have structure, have codes behind it so you actually use it. And drive insights from it. So, so it's not just about, you know, putting the plumbing in place to exchange the data, but putting the utility a, around the data, either through AI or more advanced technologies around, you know, bringing surfacing insights and using the data to drive operations, right?
So, data needs to be part of an organization's in my opinion or overall strategy. It's not just about collecting it, but it's collecting it with intent, making sure that you have the tools behind it so you can codify it and then use it.
Bill Russell (2): Can we talk about one of the banes of my existence was we had partnerships with with payers and we had different programs and whatnot, and interoperability.
We had to figure out ways to [:We're getting closer to solving this, but it was a significant problem for me when we were setting this up back in the day.
Steven: I mean, the cost is huge. The. Investment that we all make in exchanging data between payers and providers is really unconscionable. You know, we came to this point very organically.
You know, we started sending documents, we data files, you know, we built pipes. Everyone was trying to develop ways to make, Billing and payments much more efficient. And they came up with all kinds of creative ways. There were some standards that HIPAA brought us at standardized transactions, but we still see a very bespoke landscape, where different payers have different solutions that they use, different vendors.
ent exchange purpose is real [:Can also benefit the payers. The Da Vinci Project. I'm sure you're aware Bill has done a lot of work on FIHR based exchange between payers and providers. I've helped to support that work. There are tremendous opportunities for cost savings and efficiencies in getting that exchange to be more standardized and more integrated.
And from a clinician's perspective, I wanna know what the payer knows about the patient. Oftentimes the payer knows that a care gap was closed. For example, the patient may receive a mammogram or a pap smear or colonoscopy somewhere, and it's not available to me, through the clinical data connections that I have, but they can tell me that they paid for it and then I know that it was taken care of.
So [:Mike: Yeah, I think that's a great example because that's something that some of our clients are asking us for today and time as well is, you know, at the point someone presents for a wellness visit, being able to query that payer.
Get that care gap information. So it can be closed, during the episode. But I think, like, to just double click on a few things that Dr. Lane talked about I definitely see an uptick in, you know, the curiosity around payer provider interoperability. And I think that shift from fee for service to value-based care is probably gonna kind of drive more of that curiosity as health plans become participatory in, in, in patient care.
But I think. In my opinion for this really to evolve I think there needs to be some trust and transparency around providers and payers, you know, relative to that data. I often hear the the fear that, you know, if I overshare my denials will go up, you know, so having that transparency around the data and how it's used and the impact it can have on the patient.
Care [:Steven: I think if I may, you know, the concern about denials is real. But I think on a broader level, providers have historically been reticent about sharing data with payers because they're worried about their contract rates, they're worried about their patients and how they're being underwritten.
And, you know, there's this thought that the. the provider is protecting the patient from the payer. You know, in an era of value-based care, those. Relationships change and we should be seeing more collaboration and cooperation. The other thing that comes up a lot is under hipaa, so long as you receive data for a permitted purpose, you can then repurpose that data and use it in any way you want.
et. So I think there's still [:And so I think providers are changing their feelings about this because they really can't move forward until these. Barriers are lowered and remove the burden from workflows like prior auth.
Mike: I a hundred percent agree with that and I think, you know, one of the things I didn't mention, and as I'm having conversations with provider organizations and payers and in.
Especially on the payer side when asked like, how do we continue to be able to automate some of these data sharing processes? You know, it, I think it's an education thing, right? So there's some responsibility on the side of the health plan to help educate relative to what the value adds are for automating this and putting transparency around how that data is being shared and used and ultimately keeping the patient and always in mind.
I learned recently is, some [:Bill Russell (2): it's one of those things of we didn't know what we didn't know. We used to have a, a a technology gap which kept us from doing interoperability well, technology and policies. And now that we're able to move the data as seamlessly as we are now, we're learning that there are there, there's other barriers to sharing that data and fears and concerns.
I, along those lines, I wanna talk about the patients. I interviewed a patient whose son had uh, cancer and it was interesting to talk to her about how she was using ai and she said every, every diagnosis, everything she gets from a physician now she's putting through ai. And I think that's becoming more and more the norm of saying, oh, I've been prescribed this medication.
What [:That was always the promise the that we were gonna empower the patients with data and they were going to start to participate in their health journey. So I'd love to hear from you guys. where are we at and what does this mean for the patient?
Mike: Yeah. I definitely think that patients are becoming kind of the central players in that, you know, I think frameworks like TEFCA have definitely been able to enable that because of doubling down on that trust element relative to that framework. And those use cases. So individual access services for instance, you know, patients have control over their data, right? They have the right to gain access to their records.
their progress or be able to [:So I think that it's not just about data access um, for the patients, but now that they have access is how they're using that data to help. Inform their care decisions and talk to their providers. But I think Dr. Lane definitely has some perspective here as well.
Steven: we implemented one of the very first patient portals 25 years ago.
We've been at this again for a long time. It's kind of similar timeframe to interoperability and patients getting access, you know, was a very new idea then. And then with the legislation that was passed by the government, you know, we opened up that access further. Really, you know, making the prohibitions on information blocking, making data available to patients in more real time.
of their data holders. Being [:Very different than portals. I mean, if you've seen a dozen different providers over the last 10 years, you know, you might have 10 different portals and you can't integrate that data. But with IAS, you can bring that data down discreetly in a fire format work with a vendor that will allow you to make full use of that.
As you mentioned, you came from financial services, it's like being able to connect all your bank accounts, you know, and see all of your data in one graph, in one timeline. What have you do? Planning. That's where we're heading with patient. Access to their own data.
ago, we're gonna be seeing a [:It's further changing the provider patient relationship. You know, where patients, some patients at least, are much more informed and come in, you know, and that can challenge providers. I mean, you have to, we all have to grow in our capabilities of how to leverage the data for good.
Bill Russell (2): You know, I've had an Anish Chopra on the show a couple times, and we talk a lot about the different stakeholders here and get gaining alignment of these stakeholders has been a challenge. And but it's not only that it's shared accountability across the entire ecosystem.
what mechanisms, models could actually drive shared ownership of. Of the data quality, utility and innovation across the payers, providers tech partners, I guess is the question?
Mike: Yeah. I mean, I think from my perspective, you know, the industry is the mechanism for moving this forward.
hallenge of, of data quality [:So I, I think it's. It's a coalition of many to kind of move this forward. I think, you know, CMS is kind of, looked at this and that's kind of part of their framework right now with the CMS aligned networks is bringing in a coalition of, you know, big tech EHRs payers.
So, anyone participating in the healthcare ecosystem to help drive this innovation forward and provide this governance and standardization around it.
Steven: So Bill you asked about, you know, how do we manage the governance of the data. We've talked a couple times about the Sequoia Project and their data usability initiative and two versions now of implementation guides that have been published.
And we're starting to see. [:Bright folks have come together and really started to say, how can we quantify data quality? And once we do, how do we measure it? How do we remediate it? How do we improve it as part of this framework based exchange. So I think we're gonna see real progress in data quality. And again, that makes a huge difference whether you're, you know, in the office at the bedside.
p us to be able to identify, [:Where is it bad? But it's really the patients that know what their health story is. I think we are increasingly, as you, we were discussing before, seeing patients accessing their data, but then saying, Hey, this isn't up to date, or this isn't accurate, or this isn't my data, it's somebody else, you know, who has this, maybe has the same name.
So I think patient access is going to drive data quality in the, you know, different way than AI is gonna drive it in a different way that PO than population health. But there are a lot of reasons for us to be focused on the quality of the data.
Bill Russell (2): looking forward for MEDITECH.
What's the vision for advancing healthcare delivery through data networks and interoperability?
Mike: Yeah. So I mean, one of our mission is just not to respond to change, but actually designing the next generation of data-driven care. So, interop really is just no longer about connecting hospitals.
nd all of these nuanced data [:You know, so our vision is about enabling timely, actionable insights, whether for a single patient or entire population. So the objective is to provide better care in a better patient experience.
Bill Russell (2): Fantastic, Dr. Lane. Mike, I really appreciate your time. Really appreciate you guys uh, sharing your experience and the progress that we're making.
This is an definitely an exciting time to, uh, to be in healthcare.
Mike: Awesome. Thanks for having me.
Steven: Thank you so much.
Together we're transforming [:Thanks for listening. That's all for now.