Advances in natural language-processing and the ability to read large volumes of data are creating new insights for clinicians.
This article first appeared in the November 2015 issue of HealthLeaders magazine.
Steve Morgan, MD
Until now, the electronic health record has been largely about structuring data to drive initiatives such as value-based care and population health. But now technology is unlocking unstructured information from clinical narratives, making it useful and actionable.
"It's still a work in progress, but a necessary piece of technology that we need to learn to leverage to fully get information out of our EMRs," says Steve Morgan MD, senior vice president and chief medical information officer for Carilion Clinic, an integrated delivery network headquartered in Roanoke, Virginia.
Carilion's first effort to tap unstructured EHR information was to attempt predictive analytics on its congestive heart failure population, Morgan says. Using a previously developed algorithm, the clinic engaged with EHR vendor Epic and data analytics vendor IBM to perform regression analysis on patients with specific risk factors, to see if they later developed heart failure, and then applied these risk factors to the larger cohort patients who may not yet have symptoms, as a way to establish a larger at-risk cohort.
When the analysis confirmed that the patients treated had, indeed, developed heart failure based on the early indicators, Carilion and its vendors began to refine the model.
To increase the model's accuracy, Carilion, Epic, and IBM together developed a proof of concept using the natural language-processing capabilities of IBM's Watson technology, which is capable of quickly reading large volumes of unstructured documents and producing assessments.
By doing so, Carilion was able to add 3,000 more patients into its predictive model for a total of 8,000 patients, Morgan says.
"It was fairly significant," he says. "It was not unanticipated, because we knew, based on where we were at the time when we looked back over that data, that one of the key elements that we did not and now do capture discretely was a piece of data called ejection fraction, which really tells you about heart function. It did give us some guidance on where we might be able to change workflows to capture the data discretely going forward."
Parveen Chand, MHA
Carilion has ongoing research to determine better ways to approach patients in the larger at-risk cohort. "We would like to be able to release this list to our providers and say these are folks we have identified as being at risk," Morgan says. "Here are the areas that you need to focus on with these individuals. Could these patients have different medications that could be added? Could these patients be treated in a different way? We know that a lot of these folks, and no surprise, needed some behavior modification in their lifestyle such as smoking cessation and weight reduction."
The staffing investment on Carilion's part in the unstructured data initiative was minimal. "We had one analyst that worked directly with IBM," Morgan says. "There was also an analyst from Epic that was involved. We also had, just to be able to feed the information, some of our database administrators involved, and to be able to generate the reports, but it was a true collaborative between the three entities, trying to figure out how we can leverage this type of technology."
Carilion is preparing to have discussions with IBM about using this technology to find specific diagnoses in unstructured text in pathology reports, as a foundation for building decision-support systems to live inside the Epic EHR for providers, Morgan says.
Morgan notes that he often discusses the untapped potential of unstructured data with other CMIOs and CIOs. "We all struggle with the same problem with EMRs," he says. "Do you try to push physicians and providers and nurses into documenting into discrete data blocks, or do you give more leeway to be able to do transcription or voice recognition?"
Personal insights
Eskenazi Health, anchored by a 315-bed campus in Indianapolis, recently piloted an initiative using Watson to analyze the contents of call center conversations, not just for the words being said but also "the duration of the phone call, the sentence structure that's being used, the pitch and tone of the voice—to basically look at all that information against Watson analytics and what Watson has categorized as personal insights or persona insights," says Parveen Chand, MHA, FACHE, chief operating officer of Eskenazi Health.
Shannon Werb
"If we can potentially discern whether or not you are a patient that's at risk of leaving our system, and I know that because we've got a voice profile on you, I may want to tweak my conversation a little differently," Chand says.
Chand says that with a payer mix that is highly government- or self-pay-dependent, Eskenazi is looking for new ways to engage its community. "We see unstructured data as really a new pathway for us to mine and better refine our current relationships we actually have with our patients, as well as exploring new markets," Chand says.
With Patient Insights, an application by Indianapolis-based hc1.com that uses Watson's data, Eskenazi can also identify and address at-risk populations.
One sign of such populations turns out to be no-show rates for appointments. With such rates previously running as high as 40%, "you can already imagine what that means for staffing, what that means for physician resources and clinical resources overall," Chand says.
Using hc1 since February to analyze daily incoming admission, scheduling, discharge, and transfer feeds, Eskenazi identified such patients and ways to engage them via text blasts and reminder notifications. "We have seen at least a 10% to a 15% drop in our no-show rates," Chand says. "In some of our clinics we're down to 25% no-show rates now. And a few others, we're actually down to 8%." The urgent need to get this no-show rate under control was emphasized in January when Indiana passed Healthy Indiana Plan 2.0, the state's equivalent to Medicaid expansion, he adds.
Other potential data sources for Watson to feed hc1 include analysis from social media accounts that patients have chosen to make public on services such as Twitter, Tumblr, Pinterest, or Facebook, Chand says. Such analyses could trigger invitations from Eskenazi to patients for classes of special interest to them, he says.
Part of utilizing such assembled knowledge includes properly safeguarding aggregated patient data as part of HIPAA, Chand notes. "The pure number of lab results that are sitting out there in all these information exchanges across the country, that's an endless potential for things like fast-tracking drug delivery and moving clinical trials along faster," he says.
Imaging insights
Radiology reports represent a huge repository of unstructured data, and a national virtual radiology practice is using natural language processing from SyTrue to improve quality and identify unnecessary imaging orders.
Based in Eden Prairie, Minnesota, Virtual Radiologic supplies virtual radiology services to more than 2,000 healthcare facilities, mostly in the United States. With more than 350 radiologists working as independent contractors, vRad is able to provide specialized radiology services, says CIO Shannon Werb.
"Overutilization of radiation and overutilization of imaging in the ER is a common topic, especially with pediatric patients."
"We're estimating to complete close to 6 million examinations this year, so we ingest a significant amount of information—order information metadata, images, prior reports—and present that to the radiologist," he says. "Ultimately what they produce by work product is that report. Historically that report has been highly unstructured and it hasn't been able to be leveraged. That's what we're trying to do with natural language processing."
To produce meaningful reports for its clients, vRad needs to ensure all procedure data is consistent—for example, all of its client hospitals use the same name for an "x-ray of the foot"—which is not usually a common practice. One hospital's "x-ray of the foot" could be a "lower-extremity study" at the hospital across the street, Werb says. Normalized, standard data is the essence of producing meaningful reports, and vRad's internally developed data normalization tool called vCoder provides that consistency, he says.
The SyTrue technology and vCoder were able to create a determination if a particular imaging referral was warranted, Werb says.
"The radiology industry and hospitals are grappling with things like clinical decision support and training the ER physicians around appropriateness criteria," he says. "Overutilization of radiation and overutilization of imaging in the ER is a common topic, especially with pediatric patients."
One result: Healthcare organizations can increase their training of physicians in appropriateness criteria for referrals for advanced imaging.
Werb acknowledges that some vendors already utilize natural language processing purely around billing, but he asserts that the vRad practice is part of a new generation of virtual services that focus more on the clinical informatics side.
Analyzing the radiology report's unstructured text, vRad can distinguish between incidental findings such as a benign cyst in a patient's lung, and an acute critical finding such as an intracranial hemorrhage in the patient's brain, Werb says.
From its internal data warehouse, vRad can help its healthcare customers "tell stories about their internal performance, maybe our performance for the services we're offering them, or their performance for the services that they're offering their hospital customers."
The investment in natural language processing technology isn't cost-free, but Werb believes it pays for itself over time.
"Are we seeing a return on our investment I can measure in actual dollars? No. But are we seeing the results associated with the implementation, and how it's driving a better experience from our clients? Absolutely."
Perhaps another telling indication of vRad's success: In May, the 14-year-old company was acquired for $500 million by Mednax, Inc., a publicly traded company that provides maternal-fetal, newborn, pediatric subspecialty, and anesthesia physician services.
"We recognize that improving quality of radiology services could result in a downturn in volume," Werb says. "We make decisions in our business based upon providing the best possible patient care, so we believe solutions like this allow us to continue to drive toward that goal. Now, imaging volume and imaging procedure volume continue to be on the increase, but as we move to more of a fee-for-value-based model, I think solutions like NLP are going to help us significantly.
"They may have thousands of images hung on the screen—the current study," he says. "They may have literally tens of thousands of images of prior studies. They may have many or dozens of prior reports and clinical history in front of them. And they need to evaluate that in an emergent situation in a very rapid time and, of course, produce very high-quality, accurate diagnoses for patients. We think when you put NLP in the front, we could interpret that information for them and drive their eyes to the most relevant prior reports and the most relevant elements in the clinical history. We think that would allow our physicians to provide a better service with a more rapid turnaround time."
While it has been an elusive goal for years, the costs associated with not having standardization are mounting and "interoperability is becoming the main act" for healthcare leaders, says an HIT expert.
This article first appeared in the November 2015 issue of HealthLeaders magazine.
Interoperability of electronic health records and other healthcare IT systems remains elusive. Healthcare organizations clamor for it and the federal government voices support, but until very recently providers and vendors have lacked incentive to do more than create isolated networks. Yet many providers around the country are creating their own workarounds to achieve at least partial interoperability. These efforts take a lot of work, but technology leaders undertake them in pursuit of cost savings and patient safety.
The Institute for Electrical and Electronics Engineering defines interoperability as "the ability of two or more systems or components to exchange information and to use the information that has been exchanged," and that is the commonly agreed-on aspiration of all stakeholders in healthcare.
"There is a cost for the lack of standardization and the lack of interoperability," says Jonathan B. Perlin, MD, PhD, MSHA, FACP, FACMI, who is chief medical officer and president of clinical services for Nashville-based Hospital Corporation of America, which includes 168 hospitals and 113 freestanding surgery centers in 20 states and England, and reported revenues of about $37 billion in 2014. "Organizations, ours included, are compelled to create workarounds to make different devices or different information systems share the information. We need standards that get us to plug-and-play."
It's clear that there's no easy way to share patient health data, but to turn to the last resort of heavy government regulation seems an ill-considered remedy.
Even though there is ample evidence that hospital providers themselves are the biggest source of information blocking, the inability for patients' electronic health records to follow them wherever they receive care, allegation persists that EHR vendors, Epic in particular, are a major part of the problem.
The Office of the National Coordinator for Health Information Technology brought freshcredence to this allegation in its April 2015 report to Congress. "As more fully defined in this report, information blocking occurs when persons or entities knowingly and unreasonably interfere with the exchange or use of electronic health information," the report states.
"In 2014, ONC received approximately 60 unsolicited reports of potential information blocking. In addition, ONC staff reviewed many additional anecdotes and accounts of potential information blocking found in various public records and testimony, industry analyses, trade and public news media, and other sources," the report says.
Daniel Barchi
It found a wide variation in fees charged by a number of EHR software providers to permit information to flow to and from their EHR software. Perhaps it comes as no coincidence that the same month that ONC issued its report, Epic announced it would waive its transaction fees for information flow, and Cerner announced it would waive similar fees to exchange data through its connections to Commonwell Alliance through the end of 2017.
Recently, I became aware of a new freely available exchange between Epic and Yale-New Haven Hospital, about six months ago. The hospital, which runs Epic, now integrates the Athenanet network with Epic's CareEverywhere record-sharing network.
Implementation is 'Challenging Work' Today, Yale-New Haven Hospital physicians are able to see Athena-generated CCDs appear in CareEverywhere's list of organizations containing CCDs about the patient in question (albeit listed under "other organizations," rather than "Epic organizations").
"Implementing these large, integrated EMRs and making all the connections is challenging work," says Daniel Barchi, who until Monday was chief information officer at Yale-New Haven Hospital. (Today, Dec 1, is his first day as CIO of NewYork-Presbyterian Hospital, taking the place of retiring CIO, Aurelia Boyer.)
After Yale-New Haven started rolling out the Epic EHR in 2011, "and finally being up on all of our sites and physician practices in 2014, then we turned our attention to this type of interoperability, so it's not a conscious decision not to have done it before this," Barchi says.
He takes issue with a Politico story quoting him as saying that Epic is the de facto health information exchange for the state of Connecticut. In an email he sent me after our conversation, Barchi clarified:
"I said that HIEs have not lived up to their promise and that what we did at Yale New Haven Health was to leverage all of the tools we have available (HIEs, APIs, interfaces, shared access to the EMR, patient portals, and data sharing through the EMR) to share data."
"It's just now that we and other health systems around the nation are getting to this important work. It's because we really believe that the data is the patients', and we are merely stewards of that data, so if you believe that the data is the patient's data, and we're responsible for protecting it and then giving it to the people who need to use it to care for those patients."
Although Barchi does not yet have data on how many records have flowed specifically between Epic and Athena at Yale-New Haven Hospital so far, overall, the hospital has shared 131,000 patient records in the past 12 months, with more than 500 healthcare institutions across the U.S.
Patient Consent Required "It's also important to reinforce the point that you've made that there is no easy way to share data," Barchi says. "Everywhere that you share data takes work, and it's people who are building interfaces or making the API connections, and then maintaining those. So we all wish that it was easier and more secure. Because it's not, it's upon us to do the work by building these interfaces and making these API and FHIR connections, and then maintaining them and watching to make sure that they're safe and secure."
The patient experience of records which flow slowly (if at all) is also distorted by patients' own lack of understanding that data does not flow unless there is patient consent first. A friend of mine was perturbed recently to learn that in order to get his Epic-based medical records from the Cleveland Clinic to Kaiser Permanente, he had to go not to his doctor, but to Kaiser's medical records department, to sign some consent forms.
The good news is, that once patients sign the consents, and once initial connections are established, as in the case of Athena-Epic, data then continues to flow without further patient consents being required.
Also worth noting is the fact that Epic has already enabled similar sharing with rival EHR brands eClinicalWorks and Greenway Health. It's also interesting to note that Epic and Athenahealth (along with Cerner) garnered top ratings in KLAS' inaugural interoperability report released in October.
I wish I could believe that podium-pounding elected officials in Washington haven't sometimes reduced this issue to a political one, but stories like Yale-New Haven Hospital's, and my friend's, have me believing that this issue sometimes has been over-simplified for political gain.
The danger remains that Congress will insert some sort of blunt instrument into legislation such as the 21st Century Cures Act, putting regulations in place even as the need for such heavy-handed legislation appears to be in question.
I do believe that patients and all providers need to continue to push and challenge each other to understand the underlying issues that made 2015 the Year of Information Blocking and What To Do About It. As I've noted, someone has to pay for health information exchange. In addition, the final shape of the nation's EHR-sharing networks remains more of a rough outline than a clear roadmap.
One final point. Nothing I've said here means we don't have to watch the behavior of players who wield a lot of market making-or-breaking power. That applies to technology players as well as to healthcare players. I hope that the more freely information flows, the more educated patients and physicians alike can become, and the easier it will be to take their business where they wish without interoperability issues being an impediment.
To a certain extent, the standards set forth in meaningful use stage 2, notably the Continuity of Care Document and the Direct messaging protocol, appear to be proving increasingly useful to the soaring amount of sharing now occurring. More needs to be done, but to turn to the last resort of heavy government regulation seems an ill-considered remedy at this point.
The filmmaker's objective was not to start a patient-led movement for better health information exchanges. But the way audiences react when they learn their EHRs are largely unable to be shared may spur them into action.
One may pound podiums in Congress or write convincingly about the sorry state of interoperability among healthcare IT systems, but Kevin Johnson, MD, made a movie, and judging by audience reaction at early screenings, he may be awakening the public at large about this mess.
Patients who believe that their electronic health records can already follow them wherever they go in the U.S. have been leaving the screenings "shocked and angry," Johnson told a post-screening audience at last week's annual symposium of the American Medical Informatics Association in San Francisco.
In fact, Johnson says, 70% of U.S. patients believe medical records follow them, when in fact the sad truth today is that only 25% of the U.S. is covered by health information exchanges.
To change this, Johnson produced No Matter Where, a documentary supported by funding from the Office of the National Coordinator, from the state of Tennessee, and from other sources.
A centerpiece of the film is the contrast between two very different disasters—Hurricane Katrina in New Orleans in 2005, where paper records on 800,000 patients were destroyed by storm and flood—and the tornado that hit Moore Medical Center in Oklahoma in 2013, where the local HIE preserved medical records and followed Moore patients to surrounding area hospitals without skipping a beat.
A More Impactful Way to Communicate
So who is Kevin Johnson? "I'm a pediatrician," he says. "I've been doing clinical informatics research since basically 1989." After stints at Johns Hopkins and Stanford, he ended up at Vanderbilt, where he is currently assistant vice chancellor for health IT, Cornelius Vanderbilt professor and chair of biomedical informatics, and professor of pediatrics.
Eventually, he realized that research papers end up having too limited an impact. So, inspired by TED talks, he turned to the idea of "vision videos" to communicate new ideas. This led him to focus on the nation's effort to make healthcare data interoperable, or at least to have it follow patients—the very essence of health information exchanges.
Eventually, the film focuses on a woman who lost her husband too soon to cancer as a result of uncoordinated care between his primary care physician and his oncologist. Leigh Sterling then leveraged her executive experience outside of healthcare to become an HIE champion as executive director of the East Tennessee Health Information Network (etHIN) in Knoxville.
But Sterling's effort to sustain and grow etHIN exposed a major challenge made clear in the film. We watch HIEs struggle to be born and grow, only to succumb to the well-documented business and technical challenges of HIEs. Given Sterling's strong motivation for joining the cause, it's heart-wrenching.
Kevin Johnson, MD
Johnson's biggest challenge was conveying the information about HIEs "in a way that my mother actually understands the issues," he says. "That was the metric." A narrator helps, as do vivid animations, graphics, and humor, making what can be an impenetrable subject as accessible as possible on film.
The objective of making the film was not to start a national patient-led movement for HIEs, although Johnson hopes that this could be one outcome of the many screenings he is in the midst of holding around the country.
"It's almost like we don't expect the technology that's in all other aspects of our lives to be there," in healthcare, says Judy Murphy, who at the time of filming in 2014 was chief nursing officer at the ONC. (She has since moved on to become CNO of IBM Healthcare). "I think when you sit there and you do online banking, and you book your flights, and you check into your flights, and not only on the Internet, but on mobile devices now, people are starting to realize, because of what goes on in other aspects of their lives, that they could have this in healthcare."
"We realized, the places where we'll find HIE happening, it's kind of like the Sistine Chapel floor. You realize you're walking on it, but you pay no attention to it," Johnson says. Yet, the movie also points out HIE technology's limitations. In one segment, physicians in Montana struggle to learn how to use the nascent HIE alongside their electronic health records. Six months later, Montana's HIE was dead.
On the other hand, a line in the film prompted some immediate action at the highest levels of government. In revisiting New Orleans ten years after Katrina, the filmmakers discovered that two thirds of the state of Louisiana did not belong to the state's HIE.
"It's better now," Johnson says. ONC National Coordinator Karen DeSalvo, MD, former health commissioner of New Orleans, "was quick to clarify this point with me when we put that on film," he says. "It's better now. This is a film about an ongoing process."
At one point, the film touches on the pressure being put upon small practices not only to computerize, but to belong to HIEs even if they do not see the value if the HIE doesn't contain sufficient information on patients.
A Few Omissions
For that matter, there is no mention of the EHR vendor-driven Health Information Service Provider model which has really taken the wind out of HIE sails around the country. While the country now struggles to connect these HISPs to each other, it's clear that in the effort to simplify a complex story, Johnson has failed to account for a huge reason that HIEs are failing: EHR vendors continue to promise to take care of everything for physicians, even as those physicians are increasingly winding up being acquired by large healthcare systems.
The film also lacks many voices of hospital and healthcare system executives, some of whom I am guessing gave the kind of long-winded answers to questions which does not make good cinema. Johnson confirms that much of what they had to say wound up on the cutting room floor.
Still, it's riveting to see the stories of Sterling and others on the big screen, with an appropriate focus on what patients want and need, not just physicians. It remains to be seen if this grass-roots effort, abetted by ONC funding and a passionate filmmaker, can shock and outrage the public sufficiently to make a difference.
While it has been an elusive goal for years, the costs associated with not having standardization are mounting and "interoperability is becoming the main act" for healthcare leaders, says an HIT expert.
This article appears in the November 2015 issue of HealthLeaders magazine.
Interoperability of electronic health records and other healthcare IT systems remains elusive. Healthcare organizations clamor for it and the federal government voices support, but until very recently providers and vendors have lacked incentive to do more than create isolated networks. Yet many providers around the country are creating their own workarounds to achieve at least partial interoperability. These efforts take a lot of work, but technology leaders undertake them in pursuit of cost savings and patient safety.
Jonathan B. Perlin, MD, PhD, MSHA, FACP, FACMI
The Institute for Electrical and Electronics Engineering defines interoperability as "the ability of two or more systems or components to exchange information and to use the information that has been exchanged," and that is the commonly agreed-on aspiration of all stakeholders in healthcare.
"There is a cost for the lack of standardization and the lack of interoperability," says Jonathan B. Perlin, MD, PhD, MSHA, FACP, FACMI, who is chief medical officer and president of clinical services for Nashville-based Hospital Corporation of America, which includes 168 hospitals and 113 freestanding surgery centers in 20 states and England, and reported revenues of about $37 billion in 2014. "Organizations, ours included, are compelled to create workarounds to make different devices or different information systems share the information. We need standards that get us to plug-and-play."
In April, at the request of the U.S. Congress, the Office of the National Coordinator for Health Information Technology (ONC) issued its Report on Health Information Blocking, which concludes, "based on the evidence and knowledge available, it is apparent that some healthcare providers and health IT developers are knowingly interfering with the exchange or use of electronic health information in ways that limit its availability and use to improve health and health care."
The result of so-called information blocking, which has become a cause célèbre, is an additional layer of data charges.
"Clearly, the support that the government provided created extraordinary investment in health IT with the promise and the aspiration that information would flow along a superhighway to follow and inform patient care," Perlin says. "The promise was a superhighway, not a toll road."
Beyond the road map
The ONC is focused on this problem with its 10-year interoperability road map, initially released in January. But it is difficult to pinpoint just how much the lack of more seamless interoperability is costing U.S. healthcare. Health system executives are unable to produce a firm dollar figure, and various reports tend to lump interoperability costs in with the rest of the higher costs that uncoordinated, fee-for-service care imposes upon the industry.
A Robust Health Data Infrastructure, a 2014 report prepared for the Agency for Healthcare Research and Quality by JASON, an independent scientific advisory group, estimates that if data mining and predictive analytics could work on interoperable health information, it should be possible to reduce significantly the estimated $60 billion–$100 billion of annual healthcare fraud in the United States.
David Allard, MD
And perhaps more important, the report states that "the data also will contribute to improved understanding of the economics of healthcare delivery, both in the aggregate and for particular instantiations that either outperform or underperform the aggregate in achieving beneficial outcomes."
Choosing Wisely, an initiative of the American Board of Internal Medicine Foundation, aims to reduce the over-ordering of tests and procedures. "Think of interoperability as being a key way to reduce the extra ordering of tests," says David Allard, MD, chief medical information officer of Henry Ford Health System, a five-hospital system whose flagship Detroit hospital has 877 beds. Such reductions would save Henry Ford "probably tens of millions dollars" annually by following the recommendations of the initiative, he says.
Why interoperability is difficult
Studies published in 2010 and 2014 by the President's Council of Advisors on Science and Technology list numerous scenarios where enhanced health IT interoperability could benefit the United States. So why does the nation continue to come up short on interoperability?
The answer is complex, but part of it is that interoperability already exists in many forms—much as before the Internet coalesced it was a series of networks that eventually became joined together by common protocols. The good news: Healthcare already has a set of such common protocols that routinely pass information between information systems not well-known for exchanging and using each other's information. Some of these common protocols were set in place by the federal meaningful use incentive program. The bad news: The protocols are unevenly adopted, reciprocal use agreements to "share and share alike" patient information with consent still require too much negotiation, and shared use cases often emerge only when providers discover or develop common business incentives to share information with each other. Such use cases are still rare.
"Many of our healthcare organizations don't really want to share data because they'd be sharing it with a competitor, and that would cost them money," says Dean F. Sittig, PhD, a medical informatics professor at University of Texas Health Science Center and School of Biomedical Informatics and a member of the UT-Memorial Hermann Center for Healthcare Quality and Safety.
Marc Probst
"It's all too slow," says Marc Probst, chief information officer at Intermountain Healthcare, the 22-hospital system headquartered in Salt Lake City, which has been in the process of installing Cerner EHR software systemwide. "We're putting too much trust in the industry to pull it off on their own versus strong direction and mandates from the government. I am stating this as an über-conservative, but we are losing lives due to our inability to implement meaningful standards."
Others note that government intervention brings its own set of concerns to the interoperability debate. "More recently, we've had congressmen and senators talking about interoperability," Sittig says. "That's out of their league. A lot of our problems with interoperability surround [a] lack of agreed-upon uses. We have standards. We just don't agree to use the standards."
More than a technical challenge
"Technologically, we can share data," says Joel Vengco, vice president of information and technology and chief information officer of Baystate Health, a six-hospital system headquartered in Springfield, Massachusetts, in the state's Pioneer Valley region. "We can open up, create an API [application program interface]. The challenge is not technical, but rather about the vendor community working with its users to ensure cost-effective interoperability.
Joel Vengco
"We've got an Epic organization right now in our region," Vengco says. "They desperately want to connect to the Pioneer Valley Information Exchange, but the issue for them is that they are charged per transaction." The PVIX portal is an electronic way for member providers to access patient medical information.
A patchwork of networks—some private HIEs, some public HIEs, and some EHR vendor–operated HIEs—does allow relatively inexpensive and convenient record location services within each network. In Michigan, for instance, a high concentration of Epic EHR usage has allowed Epic's Care Everywhere platform to flow EHR data among 11 healthcare systems in the state, as well as other health
systems across the country running Epic.
"We were probably the earliest adopter in this market with Epic," says Subra Sripada, executive vice president, chief transformation officer, and system CIO of Beaumont Health, a three-hospital system in southeastern Michigan that reported total revenue of about $2.4 billion in 2013. "About three years ago, I reached out to my fellow CIOs to say, 'We are competitors in the market, but we shouldn't be competing on data.' "
Subra Sripada
Just on its own, in the first half of 2015, Beaumont shared 511,000 records with other healthcare systems in the United States via Care Everywhere, Sripada adds. "We can pull data from anybody that has Epic across the country, and they can pull data from us" due to Epic's reciprocal use agreements, which all Epic customers agree to when they activate Care Everywhere.
"We spend an awfully large amount of time trying to get records from other organizations, and we've found that we do notice a decrease in that since we've put in Epic," Henry Ford's Allard says. "We're now exchanging somewhere around 750,000 documents per quarter with other organizations [running Epic] for the purpose of getting health information on our patients that we're actively taking care of, and we're just not spending the amount of time at that [as we had to in the past]."
Common ground among competitors
When traditional competitors find common cause, technology barriers to interoperability can be overcome, even when no common EHR or HIE exists between the two. For instance, Detroit Medical Center—which includes eight hospitals, 140 clinics, more than 2,000 licensed beds, and 3,000 affiliated physicians—is in the process of negotiating a reciprocal use agreement with nearby Henry Ford that will allow each provider to exchange continuity-of-care documents, even though Detroit Medical Center runs Cerner EHR software, not Epic.
Henry Ford's pediatric practices are performed at Detroit Medical Center, says Mary Alice Annecharico, RN, Henry Ford's senior vice president and chief information officer. "We have an absolute need to be able to share clinical information with them on a regular and consistent basis," she says.
Once the reciprocal use agreement is finalized, electronic documents based on Health Level Seven International's Consolidated Clinical Document Architecture (CCDA) will begin flowing between Detroit Medical Center and Henry Ford, Allard says.
The technological foundation for such transfers was laid when both Cerner and Epic software were required to support CCDA as part of being certified in the meaningful use federal incentive program. Rather than requiring a third-party HIE, the communication will occur via existing support provided by Epic's Care Everywhere and Cerner's Resonance connectivity capabilities.
"Interoperability is becoming the main act," says Joe Francis, chief information officer of Detroit Medical Center. "We have a Pioneer accountable care organization here. I need to know everything that's going on with my patient, no matter which venue of care they're in, so interoperability becomes the underlying driver for being able to do that. We have 38 hospitals in southeast Michigan, as well as umpteen clinics. So a patient can go anywhere. Getting that information from those other organizations so you can build those missing pieces into your record of that patient—that's what I consider interoperability."
The need for a patient identifier
Dean F. Sittig, PhD
Lack of a nationwide patient identity standard is one area where Congress has made its own blocking law that continues to bedevil healthcare interoperability efforts. "We don't have a good way of identifying patients across systems," Sittig says. By federal law, the U.S. Department of Health and Human Services is prohibited from establishing a national patient identifier until legislation is enacted specifically approving the standard.
The blocking law was pushed by privacy advocates, but such concerns can be mitigated, Sittig says.
"We're not going to have true interoperability until we have a unique patient identifier, or at least a way for people who want to share their records to obtain a unique patient identifier," Sittig says. "The government wouldn't have to give this out. The government could just make a way for me to get one. I can get an employee identification number from my private business, so I don't have to use my Social Security number. There's lots of ways the government could give out a number, and then I could just give that number to every healthcare provider I went to, so they could share the data. It's a better solution than we've got now for sharing data."
Sittig also notes that many patients do not want their data shared. "I've always worked in hospitals or for healthcare, and I know there's a lot of employees that won't go to their own organization for healthcare because they don't want their employer to know what's wrong with them," he says.
Different routes to interoperability
Effective as a way to move beyond the privacy concerns and shortcomings of paper or faxed documents, CCDA represents one of meaningful use stage 2's major interoperability common denominators and also is in widespread use as a way to share EHR data via HIEs around the country.
Certain HIEs also offer record location services that, combined with methods of expressing patient consent to share information with other providers involved in their care, allow providers to query patient data that might reside at various hospitals or clinics. Such services are also core elements of Care Everywhere and another patient record information–sharing network, CommonWell Health Alliance, a set of services promoted initially by a group of EHR vendors, with the notable exception of Epic.
John Halamka, MD
State HIEs offer their own variants. The Massachusetts Health Information Highway, known as Mass HIway, launched in 2012, initially permitting the encrypted pushing of messages containing medical records. This pushing technology leveraged the Direct protocol, an EHR secure messaging standard required of all meaningful use stage 2–certified software, for use in many short-term interoperability initiatives. In 2014, the Mass HIway then added query-and-retrieve capability throughout the state.
More than 500 organizations in Massachusetts currently participate in Mass HIway. Physicians who belong to the Mass HIway can, with a click display, request records that may reside in an incompatible EHR, which may allow the treating physicians to avoid duplicative or expensive tests when making their diagnoses.
"We've really been on a tear," says John Halamka, MD, chief information officer of Beth Israel Deaconess Medical Center—a Boston-based 649-bed teaching hospital. He also is a member of the governing health information technology council of the Mass HIway. "In April, we did 2 million transactions and we are completely financially viable."
Low cost to providers has driven adoption of Mass HIway, Halamka says. "We went to Blue Cross Blue Shield of Massachusetts and Partners HealthCare and Beth Israel Deaconess and said, 'Would you be willing to pay 10 times the cost of the service so that we can charge two-doctor practices $5 a month?' That's what we did. I'm more than happy to pay $50,000 a year because, boy, the value I get from healthcare information exchange is enormous, and by doing that, the big guys subsidize the little guys. Even at that price point, once you get enough volume, the whole thing works and the HIE, the HIway, doesn't go broke."
Another aspect of Mass HIway that lowers its operating costs: Unlike many other HIEs, the HIway does not act as a central repository of health information, leaving that job to other service providers who charge separately for those services.
Interoperability can also follow a different path to drive a sufficient number of healthcare organizations to participate on a statewide level. In Michigan, a high priority was to alert care providers when their patients were going to the hospital or the emergency department.
The solution, coordinated at the state level, arose from state legislation mandating an exchange initiated by the sender (a push exchange) of an admission-discharge-transfer (ADT) message from hospitals and emergency rooms—and the nine regional HIEs in the state to which they belonged—to doctors, specialists, therapists, and other patient-authorized providers. While not as comprehensive as some of the data exchanged via CCDAs, ADT updates are making a difference in Michigan, providers there say.
Tim Pletcher, DHA
"Just getting people to send ADTs to a statewide service was prioritized by all these different groups as the No. 1 thing that everybody wanted, but then there was just a lot of pushback," says Tim Pletcher, DHA, executive director of Michigan Health Information Network Shared Services (MiHIN), a public and private nonprofit collaboration that has been formally designated as Michigan's statewide HIE by cooperative agreement between the Michigan State Health Information Exchange program and the Office of the National Coordinator for Health Information Technology.
"By packaging things up as a use case," Pletcher explains, "we were able to then ask Blue Cross Blue Shield of Michigan, one of the commercial payers in our state, 'Hey, all that money you give out in incentives—would you tie some piece of it to people doing this use case?' "
Over an 18-month period, aided by MiHIN's existing statewide patient-provider attribution service, the state was able to go from zero to collecting information on 92% of all admissions in the state. "That happened because they connected their incentives and payments to the use case as part of this population health incentive," Pletcher says.
His advice for other interoperability initiatives is to stop trying to solve so much of the interoperability problem at first. "People have been kind of swinging for the fence, and even something as simple as an ADT process has millions and millions of dollars of opportunity for people to sort of get on the same page," Pletcher says. "It is a giant bootstrapping activity to all of the next pieces. Every community has to figure out a strategy that works for them."
Rationale for federal rules
Still, the big problem for the industry is that while individual common interests and use cases may yield pockets of cooperation here and there, that is not sufficient to achieve nationwide interoperability. For years, policymakers have deliberated whether a nationwide set of reciprocal use agreements, also known as rules of the road, are necessary as well.
Such rules would define not just common data standards, but also common protocols for communicating patient consent, as well as identity matching and record location. Even between two systems such as Detroit Medical Center and Henry Ford, the agreements must be in place before any data can flow. "We just need to figure out: How do we do it safely within the construct of what we are regulated to protect? And how do we traffic that information, then store and utilize it?" Henry Ford's Annecharico says. Epic Care Everywhere and CommonWell govern certain reciprocal use within their own networks, but not with health systems in the other network.
Providers still struggle to achieve interoperability even within their own systems if they have multiple vendors' EHR software. Advocate Health Care, with the aid of a systems integrator, built a unified portal for discharged patients that draws from ambulatory settings running the Allscripts TouchWorks EHR for the 1,800-physician Advocate Medical Group, as well as the Cerner Millennium EHR running at nine of Advocate's 12 hospitals, says Mike Delahanty, vice president of information systems application projects at Advocate, which is based in Downers Grove, Illinois, and reported total revenue of $370 million in 2013.
"We wanted this to be a portal for all of Advocate," says Delahanty. "There are other EMRs besides these two in play. We came up with our own patient identifier. We came up with a scheme to get that loaded, how to match it up with our enterprise master patient index, so we knew we were getting the right person, so that we could tie them to all the different EMRs." Like other providers, Advocate has standardized on CCDA documents.
"Composable" standards allow organizations to select and assemble components in various combinations to satisfy unique user requirements. Support for Fast Healthcare Interoperability Resources (FHIR)—a composable set of data standards and APIs defined by HL7 that allows for versatile data exchange uses—is just beginning to become popular in healthcare. One such use is to permit discrete transmission of 16 elements of CCDAs instead of always sending entire documents that then must be interpreted by the receiving EHR or other health information technology.
Jeremy Marut
How interoperability helps patients
Having information returned in FHIR format will simplify continuity of care for populations, according to Jeremy Marut, director of enterprise architecture at Hackensack University Medical Center, part of the 11-hospital, 1,717-licensed-acute-bed Hackensack University Health Network.
Due to its versatility, FHIR will show up in many different use cases throughout healthcare. One of the first on deck is another approach to interoperability sometimes known as the "HIE of one."
Hackensack is an early implementer of FHIR. Motivated by two concussions his daughter received, and the hassles of transporting her medical records from location to location, Hackensack's vice president and chief information officer, Shafiq Rab, MD, MPH, CHICO, recently convened a gathering of five technology vendors to implement a link between Hackensack's Epic EHR via FHIR to Hackensack's new mobile application to assemble data from various providers. When a patient presents to a new provider, as Rab's daughter did during her course of treatment, Hackensack grants that new provider access to the patient's assembled record, including ADT summaries of care and demographics.
Shafiq Rab, MD, MPH, CHICO
"The beauty in the way we are doing it is we are putting the power in the hands of the patient," Rab says. Business reasons for Hackensack were not his primary motivation. "It's because my child had a concussion and we went to different doctors' offices and no information was there," he says. "Secondly, we want to empower our patients."
Rab says the move toward the "HIE of one" is a direct response to ONC's Report on Health Information Blocking, because patients cannot be denied their EHRs under the HIPAA Omnibus law. "That's why we are developing this app," he says. "It takes away the lame excuses of exchanges, the lame excuses of HIEs, the lame excuse of interfaces. All that nonsense goes away. We should fight for a common cause through selfless acts—and urgently, as our patients need us now."
By moving the results of queries away from CCDAs and toward FHIR elements, Hackensack will also enable a more usable longitudinal record query when a patient presents, Marut says. "When we have one patient present, we do a query within a 500-mile radius. So you're getting a lot of CCDs, and each one with a lot of information. And if you ask a doctor, they want to see it, but they don't necessarily want to see all the junk."
Beware unintended consequences
Indeed, one concern about interoperability falls along the lines of the familiar phrase, Be careful what you wish for. Physicians are already bombarded by electronic notifications and alerts from within their own health systems. Is healthcare prepared for even more coming from other care venues?
Detroit Medical Center's Francis acknowledges the importance of the issue. "We don't necessarily alert on every ADT," he says. "The fact that somebody is in the ED because they have a broken foot doesn't mean that I should be alerted because I'm treating them for COPD. You have to have intelligent alerts."
The changing interoperability landscape may also call into question some of the substantial investments made in traditional HIEs. Detroit Medical Center belongs to one of the local Michigan-certified HIEs to pass ADTs, lab results, immunizations, and syndromic surveillance to the state. But another implication of arrangements such as that being finalized between Detroit Medical Center and Henry Ford is the prospect that increasing numbers of interoperability solutions will not involve an HIE but instead data flowing directly between providers, aided and abetted by EHR software vendors working more in cooperation—and less at odds—with each other.
"The major EHR vendors have got the cash," Francis says. "They're willing to pull this stuff together, and it's even better, to a certain extent, than what an HIE can give you."
Providers agree the nation must also find a way to avoid making patients sign multiple consent agreements by arranging an agreement for common data sharing and rules of the road that govern all the disparate networks—whether it's Care Everywhere, CommonWell, or HIEs.
"We should have one standard, but unfortunately, it's not there yet," Rab says.
Yet another interoperability challenge is to slipstream record location and retrieval into clinicians' regular workflows, Allard says. "The trick is working it into regular workflow. If I have to go browse through a library of available information on every patient, it just sort of grinds things to a halt and it's hard to get it done. You can't just dump mail into people's inbox."
A pair of announcements from the Blue Cross Blue Shield Association demonstrates its commitment to arming employers, providers, and members with a great wealth of quality and cost data to inform their healthcare decisions.
The 105 million members of the Blue Cross Blue Shield (BCBS) organizations across the U.S. represent a data set too often unanalyzed and underutilized. But two recent announcements indicate that the 36 independent Blues are bringing their health insurance businesses into closer alignment, powered by a vast increase in useful, shared data.
Maureen Sullivan
The Blue Cross Blue Shield Association (BCBSA), the federation linking all 36 Blues, in late September, announced BCBS Axis, a data service aggregating 2.3 billion procedures conducted annually from more than 20,000 healthcare facilities and 540,000 physicians.
In late October, BCBSA announced Blue Distinction Total Care, a program for employers that emphasizes prevention, wellness, disease management, and coordinated care while reducing costly duplication and waste in care delivery. The 36 independent Blues all committed to offer Total Care as a nationwide network of offerings.
These two announcements have a thread of connection. The Blues will use BCBS Axis as the data mechanism by which medical professionals can be benchmarked and designated for the Total Care network.
To understand Axis better, I recently spoke with Maureen Sullivan, senior vice president of Strategic Services and chief strategy officer for BCBSA. The transcript below has been lightly edited.
HLM:What does BCBS Axis represent in terms of the journey BCBS has been on to bring all its data into more a usable, actionable form?
Sullivan: There's been a commitment from every [BCBS] CEO stepping up and providing data across every zip code. When you look at the spend on the transparency tools, we've quadrupled the number of treatment categories that are available.What that means is, that for our national employers, for our members, and for our provider partners, they'll have a greater wealth of data to draw on, to inform their decisions.
HLM:How will this help providers?
Sullivan: Axis actually powers what happens at the local BCBS plan level. So when a BCBS plan [offers] benchmarking information to the providers, what they want to be able to show is not only how a certain condition is being treated, and what the outcomes are, and what the costs of episodes are within the state, but comparing it more broadly to other like markets. This gives the type of data depth to be able to do that.
HLM: Does this fit into the current trend toward price and quality transparency?
Sullivan: It absolutely does. We believe strongly that being able to provide our members with the right information at the right time will help them make the decisions that are right for themselves and their families.
HLM: Is this effort collectively funded and collectively managed?
Sullivan: Our board is the CEOs of the individual BCBS companies. The board has come together and made a collective investment here. We're going to build on that investment. And we're going to layer on through that a set of decisions to make sure that this is uniform across the country in terms of the amount of data that's available.
HLM: Do you see an analogy between the transparency you're exposing here and what's going on at CMS with the Medicare data that's being published?
Sullivan: Because we're not actually publishing data, it might not be a direct comparison, but it's similar in [that it helps grow our] understanding of how do we do a better job of getting data available so that anyone can make… more informed decisions.
HLM: Do you see this evolving to a point where you're sharing data the same way that Medicare is sharing? Medicare is sharing a whole lot of data these days, allowing a lot of price shopping going on, right on down to the individual physician level. Is that something that's in the Blues' future as well?
Sullivan: It's interesting. One of our plans, BCBS of North Carolina, took the step of taking their transparency tool and making it available to anyone in the state, not just their members. So [anyone] can get on and get all the information. We're actually watching that closely to understand the value.
Individual members may find value if [the tool] can reflect… how their healthcare benefits are structured, and what the copays are, deductibles, coinsurance. We want to understand: Does it have value to put the information out there if it doesn't link to the benefits?
A lot of the innovation that we're working on right now makes it more and more tailored and personalized to individuals, so if you have to go and have procedures done, you really want to know what it's going to cost you, based on your benefits, if you're with BCBS, what you spent already, and what's left. So it's an interesting question, to your point of what's the value, and we're actually looking at that, based on what BCBS of North Carolina is doing.
HLM: The collective commitment of all 36 companies makes me wonder, have they all had this view into each other already, before Axis, or does Axis also represent a new level of transparency among the 36?
Sullivan: It is a new level of transparency with the caveat that if there are two licensees in the market, we keep that separate. Other than that, yes.
HLM: Is what we're seeing today on BCBS Axis complete, or is there is still more to be rolled out?
Sullivan: There will be more data depth in some markets, but you've got most of it right there.
HLM: BCBS Axis includes more than 700,000 reviews of providers by BCBS members. How do we access those reviews?
Sullivan: Members would go on to their local BCBS site.
HLM: Are you publishing APIs so that if a provider wants to do more in-depth analysis of your ratings or your data they could they do that?
Sullivan: What we're doing starting in January, is a much more aggressive effort of reporting out on trends and data, so that it can be used to inform thought leadership and policy makers all the way to a consumer making a choice.
We've looked at knee and hip price variation and cardiac price variation. We're looking at women's heart health patterns versus men. And we are also beginning to look at a research consortium and giving data to certain academics to ask questions.
So we are becoming, in that way, much more public with the insights and the value of the data, because we see that as critical for affecting the kind of change we all need in healthcare.
HLM:How difficult was it to get all 36 organizations on board? Were some more eager than others to do it at this time?
Sullivan: I think the strategic argument was reached easily. There were some operational commitments that needed to be made, and given the weight of the strategic argument, the operational issues were able to be addressed.
Leaders are finding that recruitment from the outside can be useful but difficult, and that internally, talent can be developed to support analytics efforts.
This article appears in the October 2015 issue of HealthLeaders magazine.
Healthcare's many imperatives, including population health, require keen analytical resources coupled with a deep understanding of clinical systems and the obstacles that face healthcare's march to achieve the triple aim.
Finding and training talented staff—from line analysts all the way up to visionary chief medical information officers and chief information officers—remains a tall order. By and large, however, analytics team leaders find it is easier to train clinicians in the art and science of analytics than it is to find, hire, and train data analysts from outside of healthcare.
"It's not a skill that you can learn going through some training program outside of this industry," says Selvan Ekambaram, director of business intelligence and data warehouse at MemorialCare Health System, a six-hospital integrated delivery system in California's Orange and Los Angeles counties, with between 650 and 700 affiliated physicians. "You pretty much need to have healthcare-specific industry experience for you to call yourself a practitioner."
Often, providers such as MemorialCare must contend with job candidates who prefer to remain independent consultants, instead of coming onboard as full-time employees, "because they know the demand for this particular skill set is so high," Ekambaram says. "Recruiting and retaining these specific skill sets that are needed for running a program like a data analytics shop like we're trying to do here is not easy."
MemorialCare has had a couple of full-time positions open for nearly a year. The kind of skills required generally fall into two categories: data integration and content visualization. Data integration involves procuring and consolidating different data sources such as EHR data, claims data, and patient satisfaction data. Then that data must be visualized and deployed, Ekambaram says. All told, the MemorialCare analytics team engages 21 workers. A second branch, which serves the organization's independent physicians associations and medical groups, contains another 25 workers involved in pay-for-performance reporting and quality metrics for ambulatory settings. Six other analysts joined MemorialCare when it acquired Seaside Health Plan.
One successful strategy: Tap into talent at healthcare payers. "We recently rolled in one full-time equivalent who came in from the payer industry, although we would prefer recruits from the provider space," Ekambaram says.
The team uses an iterative process by which it presents data to clinicians and determines if that data is as useful as possible, if there might be ways to better present the data, or if it should enable clinicians to further explore the data presented—an aspect known broadly as self-service business intelligence analytics.
"Some of my colleagues are more toward the self-service side than I am," says Harris Stutman MD, chief medical information officer at MemorialCare. "But we have, within the last couple of months, put together the idea of a physician analytics program, a kind of a mini-fellowship, to take our physician leadership, certainly the folks that are responsible for leading our medical group and leading the best practice initiative within our hospitals—clinical documentation improvement, population health, those sorts of things—and train them in what data sets we have available and what tools we have available, and help them understand that we really need to ask answerable questions," he says.
Harris Stutman, MD
"We invited 13 physicians to be in the initial mini-fellowship class, and all 13 accepted—which really surprised me, because we're not paying them to spend 2 or 3 hours a week in a classroom, learning this material. But they all felt it was sufficiently relevant and important to what they do to make time to attend those programs, and we'll see what positive outcomes develop," says Stutman.
"Vendor partners train us in the tools and the technology," Ekambaram says.
Among the quality improvement programs being driven by the analytics team are quality measures and core measures for sepsis management for MemorialCare's inpatient and pediatric populations. MemorialCare's vice president of population health is also working with the analytics team to gather palliative care metrics.
Vivek Reddy, MD
"It's very important for people to understand what sorts of business problems they're trying to solve, and to make sure that when they start really mining the data, they're doing it with specific goals in mind and not just fooling around to produce some pretty pie charts or bar graphs," Stutman says.
Another provider that has tried dual approaches to recruiting analysts from inside or outside of healthcare is Pittsburgh-based UPMC, which operates more than 20 hospitals and employs more than 3,500 physicians. "We merge the skill sets of both" externally recruited analysts and internal analysts, says Vivek Reddy, MD, chief medical information officer for UPMC's health services division. A major push has been to provide analytics training for UPMC clinicians who "we thought were up-and-comers in our organization that had an aptitude to learn a new skill set," he says. Toward that end, UPMC built a training program in conjunction with nearby Carnegie Mellon University. So far, UPMC has put 75 workers through the program, a mix of clinicians, nurses, and financial employees.
"We put them through a fairly intensive, six-hour-a-week course, with homework, set around analytics and analytics principles," he says. "We've had very strong and powerful results with a lot of our clinical folks that didn't really have a lot of exposure to the idea of using data to drive decision-making really effectively. They were good at receiving reports, but they didn't really understand how you get insight from reports and how you can actually look at data differently, so our clinical folks that go into the program do very well and learn a lot of different skills."
UPMC's next challenge has been to get these newly trained clinicians to spread this data-centric view across the rest of the organization, Reddy says.
"Our firm belief is, this is just a fundamental change in the way people think about their day jobs," he says. Even registration clerks need to understand how what they are doing on a day-to-day basis ties into UPMC's analytics program, he says.
"What we're doing by taking some of our up-and-comers and making them go through this is allowing them to then take that message and help our day-to-day operations start to embrace the idea that if we're going to become a data-driven organization, we really have to look at data integrity and data quality and really be concerned about these things and not just say, 'Oh well, sometimes it's not right' and I just move on to the next problem, or I call someone else to get a new report if I don't like the data that I see," Reddy says.
In the latest cohort of analytics trainees, UPMC is giving its program participants a series of business problems to tackle. "It's a much more practical, hands-on approach," he says. "We'll see how that goes."
Bryan Bliven
At many organizations, analytics resources exist in scattered pockets. This is true for the University of Missouri Health Care, which employs 6,000 physicians, nurses, and healthcare professionals and operates 50 outpatient clinics in central Missouri that receive outpatient visits exceeding 500,000 annually.
Now, UM Health Care is in the process of consolidating such resources under its newly hired chief financial officer. "We're partnering on the academic side with our HIM department and with our master of health administration program to formulate a certificate in healthcare analytics, as well as a degree program," says Bryan Bliven, UM Health Care's chief information officer. To lead this team, UM Health Care wants to hire a registered nurse to act as its director of clinical analytics, he says.
A key objective is for this analytics team at UM Health to "step up our game" to produce more engaged conversations between UM Health leaders during bimonthly enterprisewide operating reviews, when metrics for each department and service line are reviewed and interventions planned as needed, Bliven says.
"We have a population health view, so we'll look at the different contracts we're working on, and look at our performance to that, and it's a similar approach that really helps us kind of see across the organization and catch trends and then get an idea of each organization's ability to engage on the data and where we might need to have some oversight or assistance," he says.
Joe Kimura, MD, MPH
"All of population health management is essentially cohort analytics," says Joe Kimura, MD, MPH, deputy chief medical officer at Atrius Health, an alliance of nonprofit community-based physician groups in eastern Massachusetts and Boston that serves 675,000 patients via 750 physicians, with more than 50% annual revenue coming from risk-based contracts. Atrius is a Pioneer ACO, a pilot CMS program recently found to be saving Medicare $400 million over its first two years.
"If it's a payer-designed cohort like Pioneer, you have a set of patients that is defined by an attribution model or something along those lines, but it could be a disease-based model, just anyone with diabetes, and the question is, how are you defining diabetes in your population?" Kimura says. "Once we actually define that population, we run a whole series of analyses to help
characterize that population, not only in terms of its utilization patterns, disease characteristics, and comorbidities, but also in terms of what we generally understand as care metrics or quality metrics."
Atrius employs four levels of SQL programmers to perform data analytics queries, Kimura says. "Those folks basically take about 16 to 18 months of training to get to a place where they can sit with a business owner and generate a specific ad hoc report," he says.
Such results could also be delivered as discrete information elements in Atrius' EHR, as well as reports in Crystal Reports or Microsoft Excel. More recently, Atrius has turned to SAP Universe and Dashboard technology to provide self-service business intelligence analytics to clinicians.
"We've pivoted there because SAP has single sign-on with Epic, which made it easy to utilize that capability," Kimura says. Although a number of Atrius employees already have statistical training, its academic partnerships in the Boston area allow it to engage with consultants to build BI models in-house and deploy them. If such consultants come from academia, "it's a lot easier for us to recruit them."
Over the course of a year, Atrius currently runs three or four such BI research initiatives, and so continues to engage consultants. "We don't think we're going to invest a lot around bringing in full-time staff to do some of the advanced stuff until we get bigger," Kimura says.
One payoff for Atrius: being named the number two Pioneer ACO in the United States in terms of quality reports in fall 2014, and the top such organization in New England. "We've been able to maintain the highest quality scores in New England and be number two among all Pioneer programs in 2014 and have begun to realize financial savings from CMS," Kimura says.
The prospect of incorporating human genomic data into electronic health records is closer than you think. Extensions to one system promise to improve patient safety, research, and clinical outcomes for 10 neurological disorders, research shows.
The healthcare IT industry has been vigorously touting President Obama's precision medicine initiative all year, ever since he announced it in the State of the Union address.
President Obama delivering the State of the Union address on Jan. 20, 2015. Photo: C-SPAN
No doubt, IT's enthusiasm for precision medicine is fueled by visions of extracting even more IT-oriented revenue from payers and providers. The assumption is that great medical breakthroughs are just around the corner.
Some restraint is in order. With the continuing struggle to simply stand up electronic medical records systems and get them exchanging information, the prospect of incorporating human genomic data into the EHR falls into the category of bright, shiny objects of the moment.
But in September, IL-based NorthShore University HealthSystem published findings about extensions to the Epic EHR which promise to improve patient safety, research and clinical outcomes for 10 neurological disorders, brain health risk assessments, and interventions for Alzheimer's disease. Precision medicine plays a role, and more than 2,000 NorthShore patients have already signed up to participate in a DNA biobank to support the effort.
Most impressively, seven healthcare systems in addition to NorthShore have joined together to form a Neurology Practice-Based Research Network (NPBRN), to share de-identified data and best practices and to help move the state of the art forward that much faster: Dartmouth, University of Pennsylvania, Wake Forest Baptist Health System, Medical University of South Carolina, Ochsner Health System, University of Arkansas, and the University of Nebraska.
Demetrius "Jim" Maraganore, MD
Precision Medicine at the Point of Care Leading all this enthusiastically is Demetrius "Jim" Maraganore, MD, medical director of NorthShore's Neurological Institute and director of the Center for Brain Health. "It's creating precision medicine at the point of care, through the EMR," he says.
Until now, like many other physicians, most neurologists have expressed frustration with EHRs, which seem designed to serve a broad spectrum of healthcare interests, including the meaningful use program, but not to add value for the practice of neurology, Maraganore says.
The problem was such that "on the one hand, the EMR is where medicine now takes place, and on the other hand, it really isn't designed with neurology in mind," he says.
Out of the box, today's EHRs do not allow neurologists to capture neurology-specific standardized information about their patients or to learn about their outcomes, Maraganore says.
Believing that the EHR represents a "Gutenberg moment" for all of healthcare, he decided to create neurology-specific EHR extensions for Epic. "We've been on a quality journey over the last five years that I think has succeeded in accomplishing just that."
The initiative started with Maraganore and his team meeting with neurologists to imagine "the perfect office visit" for a patient with the disorder they specialized in—"Parkinson's, stroke, multiple sclerosis, headache, brain tumors, or epilepsy."
He asked them questions:
If you could spend as much time as you needed, what would you want to learn from that first visit with the patient?
How would you define the patient's disorder? What are the outcomes that matter most to your patients and to you?
What are the best ways of measuring those outcomes in the office, and do you have permission, parenthetically, to use those outcome measures?
And then what factors do you know to independently associate or influence those outcomes, and how would you capture those independent variables also?
Those meetings yielded consensus to focus on conditions which were progressive, variable, and unpredictable. "That's where we have the most opportunity to learn and to improve," Maraganore says.
With the modifications to the Epic system, "neurologists can write very comprehensive, perfectly spelled, perfectly paginated, perfectly structured progress notes. And every click of the mouse would also capture data that could be analyzed to improve quality and to conduct practice-based research and to make discoveries."
Patient-approved and Carefully Vetted Before such discoveries, NorthShore had to convince patients to enroll in the precision medicine portion, to give blood samples for extraction and storage. "As of today, 97% of our patients consent at the point of care," Maraganore says. "Of those, 88% say, 'you can use this not only for your own research, but provided you protect my identity, you can share it with any investigator doing any genomic research at any institution.'"
NorthShore's goal is to enroll 1,000 such patients in each of its 11 cohort studies. It's off to a good start: So far, it has DNA from 700 migraine patients, more than 500 Parkinson's patients, even more than 300 patients with restless leg syndrome, and so on.
It's reassuring to me that these EHR extensions have been carefully vetted with American Academy of Neurology quality guidelines and parameters, as well as common data elements from the National Institute of Neurlogical Disease and Stroke, and guidelines from subspecialty societies.
"We also appreciate the expertise of our NPBRN sites, so when they identify quirkiness in our tools… we invite them and encourage them to give us the feedback," Maraganore says. "If there's consensus across the NPBRN to make the changes, we make the changes, and then we disseminate the upgrades to all the participating sites."
Early learnings from the effort include identifying cognitive impairments in early Parkinson's patients, and alerting clinicians to check in with such patients about any concerns they or those close to them have about their safety while driving a motor vehicle.
"What we basically validated is the need for a history and a physical that both give a valuable perspective on the patient's illness and that are not necessarily measuring the same things. You really need to complement them both to understand what's wrong with your patient."
Can the efforts of neurologists also show the rest of healthcare how to make lemonade out of EHR lemons? It will require leadership such as NorthShore and its network partners are showing. Cooperation will yield faster progress than each academic center of excellence simply competing the old-fashioned way, not sharing information enough to move an entire profession forward.
The effort will also require NPBRN and others to extend beyond the Epic EHR. "Only about 40% of neurology practices are in Epic," Maraganore says. "We know that there is a need to extend our project from the Epic EMR. If we're successful in demonstrating that we can disseminate structured tools within the Epic platform to other sites, we can then go to neurology practices on the Cerner or Allscripts systems, or any of the other popularly-used platforms."
"[Then we can] say 'we will share with you our fields, forms and workflows. If you can build them into our EMR system, we would be happy to share with our content.'" He also points out that for deep analysis, clinical informaticists extract the data from the EHR and present it via a data warehouse, further suggesting EHR-agnostic platforms to come.
Judging by the patient biobanking participation rates in this case, it's also clear that today's slow pace of clinical trials could be supplanted in a few years by patient-driven, data-driven healthcare research, much as we are now seeing in other professions. I find Maraganore's recently published findings a reason for optimism.
Meeting the new federal meaningful use standards will require much heavy lifting. And health IT leaders should already be preparing for what comes next.
What are healthcare CIOs talking about now that ICD-10 is live?
Meaningful use deadlines took center stage at the annual meeting of the College of Healthcare Information Management Executives (CHIME) in Orlando, FL, last week. But attendees also found time to talk about what comes after meaningful use—namely, CCDA and CEHRT.
Liz Johnson
Two meaningful use dates now loom large. The first is December 15, when the 60-day comment period on the stage 3 final rule expires. While some industry observers consider the comment period to pertain just to stage 3, that isn't precisely true. Because ONC and CMS issued a single final rule covering both stage 3 and its amendments to stage 2 in the years 2015, 2016, and 2017, the public has the right to comment on anything in the final rule, says Liz Johnson, CIO of acute care hospitals and applied clinical informatics at Tenet Healthcare, the for-profit hospital operator headquartered in Dallas.
The second big date is February 29, 2016, which is both the starting day of next year's HIMSS conference and the day that all providers receiving Medicare must complete their attestation to their meaningful use of certified EHR software in 2015.
Considering that the final rules amending stage 2 came out nearly a week into the newly shortened 90-day reporting period for 2015, CIOs had to do some fancy footwork to make sure that they were gathering the necessary data starting October 1.
Pam McNutt
Among the lingering questions are challenges in meeting the public health reporting requirements in the newly modified stage 2, which will vary from state to state. Within the CHIME organization, board member Johnson is one of two experts on this devilish detail. The other is Pam McNutt, senior vice president and CIO of Methodist Health System in Dallas.
My October 7 news story on the final rule could only hit some highlights of these voluminous documents. At CHIME, McNutt celebrated the fact that the modified stage 2 rules removed the 50% measure for providing a summary of care record by any means, as well as relaxation of requirements for manual transmission, to better allow providers to tailor the contents of the summary of care document to the transport mechanism, rather than constraining transport to a certified HIE or Direct message.
The final rule "gives you more flexibility on what could be defined as a secure electronic message to your providers, and that is good news," McNutt said. "I know many people were struggling, didn't have an HIE that was functional to get to 10% of your referrals. … So this will give you some latitude to maybe be creative. However, I will tell you we're scrambling with this one ourselves right now, because the reporting period has in fact started, and if you don't have your numbers up to 10%, you've got to scramble."
McNutt and Johnson also cautioned CIOs to be prepared for the final rule's planned jumps in stage 2 patient engagement and e-prescribing metrics in 2017.
Michael McCoy, MD
On the second morning of the CHIME conference, ONC chief health information officer Michael McCoy, MD, told attendees that alignment of financial incentives of healthcare—through value-based purchasing and ACOs—would make health IT interoperability a reality.
"Go to your board and suggest that the data should flow," McCoy said. "We should compete on our service, on our caring, and how well we score, but we shouldn't compete on the data flowing."
One questioner then asked what the most effective path would be to attain useful data exchange between providers.
The answer is Consolidated Clinical Document Architecture (CCDA), McCoy says. "The CCDA is the right path. There are revisions now coming. The challenge we have had with CCDAs is they have been branded as unusable. I have to respectfully push back and disagree. What has been lost in the [EHR] certification rules and the intent over the years is that certification is a floor for the vendors and developers to achieve, not a ceiling. As an example, transmitting information as a CCD [Continuity of Care Document] to whomever … as the sending individual, you probably don't have all the knowledge of what is desired by the receiving individual …. What's missing from the usability side is the receiver should be able to filter what's coming through, and that's more explicit, called out in the 2015 CEHRT rules …. Specialty societies have to be involved in setting some of those defaults."
I got the impression that very few CIOs so far have even begun to read those 2015 CEHRT (Certified EHR Technology) rules, which themselves delineate meaningful use's final stage. With the aforementioned comment period ending December 15, at this point providers could use a good crowdsourcing effort to fully understand and parse those 550 pages, and help an already beleaguered health IT industry catch the next wave of regulation even as the previous wave washes over it.
Wouldn't it be cool if technology could help us with that?
The American Medical Association applauds CMS for allowing a hardship exemption for physicians who are unable to attest in 2015, but calls the final rule, as a whole, "deeply disappointing." The American College of Cardiology says that the program requirements "[remain] difficult to implement."
Despite pleas within the past week from more than 100 members of Congress and various healthcare stakeholders for stage 3 rules to be postponed, the Department of Health and Human Services, with the release Tuesday of twin rules totaling 1302 pages, signaled what it intends to publish in the Federal Register on October 16.
Many healthcare providers have yet to successfully achieve stage 2.
HHS says it is providing a simpler, more flexible set of stage 2 regulations for 2015 through 2017 as the meaningful use regulation era gives way to CMS's transition to value-based compensation.
"We have a shared goal of electronic health records helping physicians, clinicians, and hospitals to deliver better care, smarter spending, and healthier people," said Patrick Conway MD, CMS deputy administrator for innovation and quality and chief medical officer, in a statement.
"We eliminated unnecessary requirements, simplified and increased flexibility for those that remain, and focused on interoperability, information exchange, and patient engagement. By 2018, these rules move us beyond the staged approach of 'meaningful use' and focus on broader delivery system reform."
After CMS's March and April notice of proposed rule-making (NPRM) regarding stage 3 and adjustments to stage 2, Congress passed the Medicare Access and CHIP Reauthorization Act of 2015 (MACRA), which will sunset the meaningful use "payment adjustments," in essence, penalties for noncompliance, at the end of 2018. Instead, Congress has called for the establishment of a Merit-Based Incentive Payment System (MIPS), of which the meaningful use program will form one component.
Due to this interim Congressional action, CMS in its final stage 3 rule said it would allow for an additional 60-day comment period, starting upon enactment of the stage 3 rule, regarding the transition from meaningful use to MIPS. Afterward, CMS may modify its final rules and lay the groundwork for an NPRM in mid-2016 detailing the implementation of MIPS.
Industry Reaction Initial reaction to the final rule was mixed. Providers applauded the relaxation of 2015 requirements, and some applauded the retirement of some process measures that currently must be satisfied in order for providers to successfully attest they have met meaningful use's requirements.
But concerns remain about the complexity of the existing program, issues such as lack of interoperability among EHRs, and what providers still say is too hasty a timetable for adoption of stage 3-certified EHR software.
"Today's release of the meaningful use rules is a mixed bag for hospitals and health systems and the patients they serve," said Rick Pollack, president and CEO of the American Hospital Association, in a statement.
"We are pleased that CMS released the long-awaited modifications rule, which will allow hospitals a 90-day reporting period in 2015 along with other flexibilities in response to AHA concerns. Hospitals will finally have the clarity they need to take steps to ensure they meet the revised requirements.
But Pollack went on to say that the final rule implementing Stage 3, which providers will be required to use beginning January 1, 2018, "is deeply disappointing. Despite the urging of hospitals, physicians, and Congress, the Stage 3 final rule includes many new and more challenging requirements. More than 60% of hospitals and about 90% of physicians have yet to attest to stage 2. The Stage 3 [implementation deadline] is too much too soon."
AHA urged HHS to delay the implementation of Stage 3 and focus instead on ensuring that providers could easily and efficiently share health information to support care delivery and new models of care.
"America's hospitals and health systems remain committed to successfully using electronic health records to improve health care for patients," Pollack said. "We appreciate the changes that CMS has made in response to our concerns and are pleased aspects of the rule are still under debate."
The American Medical Association applauded CMS for allowing a hardship exemption for physicians who are unable to attest in 2015.
"The AMA continues to believe that stage 3 requires significant changes to ensure successful participation, and improve the usability and interoperability of electronic health record systems," said AMA president Steven J. Stack, MD, in a statement.
"We urge CMS to use the additional public comment period provided for Stage 3 to further improve the program and consider changes related to the Medicare Access and CHIP Reauthorization Act, which was signed into law earlier this year. We also want to make sure that EHR vendors have the time they need to further test products for interoperability, usability, safety and security."
A meaningful use modification first introduced in the April NPRM, which had ignited strong opposition from some patients, will, in 2015 and 2016, require hospitals to demonstrate that only a single patient per hospital has viewed, downloaded, or transmitted his medical record, post-discharge. The current meaningful use rule, which required hospitals to demonstrate that 5% of patients used their EHRs in this manner, has been a source of frustration for hospitals.
Still "Difficult to Implement" In the companion EHR certification rule, the Office of the National Coordinator for Health Information Technology finalized some rules which were applauded yesterday by Charles E. Christian, chairman of the board of trustees of the College of Healthcare Information Management Executives (CHIME).
"CHIME supports key provisions in the rule that should lead to greater transparency regarding vendor products; improved testing and surveillance of health IT, and an improved focus on user-centered design," Christian said in a statement released Tuesday.
The final rule's action to reduce what until now had been a multi-stage, multi-year set of implementation stages for providers to a single set of requirements is a concern of the American College of Cardiology.
"The American College of Cardiology has concerns about [Tuesday's] announcement by CMS to align all three stages of meaningful use, as this does not account for the reality of the situation faced by the medical community working every day to implement the meaningful use program and to improve care for their patients," said ACC President Kim Allan Williams Sr., MD, FACC in a statement.
"The ACC is a longtime supporter of electronic health records as a way to improve the quality of patient care," Williams said. "While we applaud CMS for finalizing programmatic changes to the 2015–2017 reporting years, that should ease the difficulties providers face when attempting to meet meaningful use requirements, the decision to combine meaningful use into one single stage and finalize the program requirements at this time remains difficult to implement. Many of the requirements for stage 2 proved unattainable."
According to Williams, large numbers of providers either haven't met the stage 2 requirements, or, after trying and failing, have given up. "That is why it is vital that CMS consider participation data from the current stage to see what is working and what isn't before outlining an upcoming stage," he said.
"We cannot establish a long-term health care program that does not take into account what we can feasibly attain in the short-term, transitional period. The ACC looks forward to continued work with CMS to establish how the meaningful use program will fit into the new Merit-Based Incentives Program (MIPS) slated for 2017."
Both the AMA and CHIME said they would continue to review the regulations and would have more comment in the coming days.
Vendors Respond Some EHR vendors have also become disillusioned about meaningful use as the program has struggled.
"With each new delay, modification, and dilution of the MU program it becomes more and more tangential to the ongoing process of dragging health IT into the 21st century," said Dan Haley, general counsel of athenahealth, in an email to HealthLeaders.
"Happily, that work continues independent of federal efforts. Through private sector initiatives like CommonWell, Sequoia, and others, industry and our provider clients are on track to meet the objectives set forth in the ONC's recently-released 10-year plan well ahead of the government's schedule.
"While we appreciate ONC's and CMS's efforts to address the many concerns that providers have with the direction of the MU program, at this point it would be better for the government to declare victory on EHR adoption and step back."
CMS reviewed and considered more than 2,500 comments on the two proposed rules to create the final policies, the agency said.