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The Outrageous, the Outraged and the Courageous: Another Attempt to Halt the Healthcare IT Evolution
The Outrageous
On February 2nd 2011 the American Medical Association wrote to the Secretary of the U.S. Department of Health and Human Services, Kathleen Sebelius, to urge her to immediately halt the Health Insurance Portability and Accountability Act (HIPAA) mandate to implement ICD-10.
The AMA wasn’t only asking to immediately halt an endeavor that had officially started on January 16, 2009, over three years ago, when HHS published one of several final rules but they are also asking to re-evaluate the penalty program timelines related to Meaningful Use (MU) of Electronic Health Records, e-Prescribing and Physician Quality Reporting System (PQRS).
I would have been more amenable to read something like “reassess the timeline or extend the timeline due to significant concerns of our constituent members” but to immediately halt the program? Could someone please explain to me why we should halt any national Healthcare IT project?
They should have asked to immediately halt incentive payments as well! Why? Because we, the U.S. taxpayers, are actually paying physicians across the entire United States to implement and meaningfully use an Electronic Health Record system to keep our health data in a digital format that can be easily and safely transmitted between myriad providers and so that we, as patients, can have access to it as well. It’s not financial aid from the government that is paying for the Meaningful Use of Electronic Health Records but it’s us the People of the United States that are paying for it.
From what I also understood by reading between lines they want to be paid to implement ICD-10. Sorry docs, us rabbits are running out of carrots! Under the same reasons why shouldn’t we go ahead and pay for their mobile tablets as well because in my opinion it would abide to the same logic?
The AMA claims the difficulty of transitioning from the ICD-9 13,000 diagnosis codes to the ICD-10 68,000 diagnosis codes. Maybe the five-fold arithmetic expression raises eyebrows to some but the truth is that the scarce 13,000 codes used by ICD-9 have created an undecipherable conundrum of clinical data throughout several decades. Most clinicians and clerical staff would choose a diagnosis code based on the expected reimbursement amount and not on the actual clinical diagnosis and how could this be considered sane in a scientific realm? A lot of healthcare data used in claims processing is absolutely unauditable. It’s actually a toss and start over rather than a transition. We don’t want to deal with the cluster of conundrums created by all the garbage that has gone into the databases since garbage in=garbage out (GIGO).
AMA is clear to state that it’s not just a technology project and that’s because they are well aware that the Health IT technologists can solve the problem and I know this because I am a Health IT technologist and I know there is no technical impediment to solving the ICD-9 to ICD-10 transition. There may be semantic interoperability issues in the conversion but that can happen with any transition from any coding system to another.
Another outrageous event was the unclear response by the acting CMS Administrator, Marilyn Tavenner, who on Tuesday, February 14th indicated to the reporters that the CMS will re-examine the time-frame. Further exacerbation came along when the Secretary of HHS announced the intent to delay the ICD-10 compliance date on February 16th. Responding so quickly to pressure from one letter seems like a sign of weakness from a leader.
The Outraged
Many of us are outraged. Many of us stood mostly silently and briefly tweeting 140 characters at a time what we were thinking in protest to the unfolding of the ICD-10 debacle. Most of us were expecting the HHS Secretary to adopt a strong position defending the interests of her Constituents, We the Patients of the United States of America. What was perceived was that there is some extra-caution due to the re-election climate in the air, there is fear to uphold the interests of the Constituents.
Many of us are outraged as citizens, tax-payers, patients or relatives of seriously-ill patients. We should be since it’s our hard-earned money going to waste. We have never had an opportunity to transform our wasteful healthcare system as the one we are living today. We don’t want to miss this opportunity since it may take decades before it could happen again.
We are outraged because it’s always the same story. Powerful groups of healthcare in the US will claim many reasons they have to not implement technology. They’ll claim too much work, workflow disruption, physician <-> patient intrusion, not enough reimbursement, no incentives, etc …
But the truth is that many have made great strides in ICD-10 conversions so who is the AMA actually advocating for?
Continuing the use of ICD-9 is continuing to put the lives of many at risk. Who is responsible for the deaths or injuries caused by improper coding?
I wanted to write this blog before but I was also waiting for some other organizations with muscle to cry-out loud and they finally did. I call these groups “The Courageous”.
The Courageous
When I first read The American Health Information Management Association’s (AHIMA) request to urge HHS to move forward with ICD-10 plans and to not delay the compliance date I finally felt relief from my outrage.
HIMSS also raised their voice and recommends not delaying the ICD-10 implementation.
There is too much to lose here. Meaningful Use stages 2 and 3 depend on quality data and ICD-9 does not fulfill this requirement.
Many will start speaking up in defense of the ICD-10 transition and hopefully HHS will listen to our shouts.
Readers, we are paying for the transformation of the U.S. healthcare system out of our pockets. Don’t let special interest groups steal this opportunity from us.
Courageous, raise your voices!
I always tend to “cringe” when I read about comparisons between Health IT, medical devices and other healthcare related software with respect to other verticals (e.g., finance, insurance, retail).
Why compare?
Saying that the financial industry is many “light years” ahead is extremely inaccurate. Comparing the processing of debits, credits, interests, etc. with medical information and imagery is like comparing apples to guanabanas (a tropical fruit found worldwide near the Equator).
Healthcare is definitely more complex than other verticals therefore it has complex interoperability issues.
The reason healthcare has interoperability challenges is because it has to deal with extremely complex workflows, scenarios and data. It also faces other regulatory constraints that hinder sharing of data between diverse organizations that interact with the same patients. State local laws also hinder as well.
Healthcare is the number 1 trail-blazer for technology.
Many technologies currently used by other verticals had their birth in trying to solve medical problems; companies in order to survive the regulatory red-tape (read FDA) diverted their attention to applying their inventions to other areas. For example, the CAD (Computer Aided Detection) for health anomalies would modify their products to serve other areas such as security and defense.
Healthcare has provided quite good interoperability solutions to the world. DICOM is ubiquitous in the radiology sub-domain of healthcare. HL7 has been quite successful for exchanging patient data between various source systems. X12 is also a standard for exchanging information between providers and payors.
SQL and MUMPS are of the same technological era.
Great minds from the Massachusetts General Hospital contributed to the creation of MUMPS. MUMPS was created near 1967 and SQL in 1970, so if we want to compare them based on age they are both post-baby-boomers.
SQL may have conquered more market but that does not necessarily mean that it’s better. In technology like any other space the consumer trend has nothing to do with quality. If the opposite were the case then there would be more Apples than PCs. Intersystems Cache is an example of vanguard technology.
Excerpt from Wikipedia: “The European Space Agency announced on May 13, 2010 that it will use MUMPS (InterSystems Caché) to support the Gaia mission. This mission aims to map the Milky Way with unprecedented precision.’
Why didn’t the agency choose SQL? Obviously there is a big reason. Maybe it’s because SQL has no way of meeting the high-bar of unprecedented precision.
We should try to stop blaming technology for the US healthcare problems. Most of these problems root-causes stem from poor policies, savage competition between providers, imprisonment of the patient data, organizational silos, etc.
Dear Mr. Planchart:
Thank you for sharing your thoughts about legislation to combat online infringement and digital theft.
Last Congress, the Senate considered, but did not pass, legislation entitled the Combating Online Infringement and Counterfeits Act (COICA). The aim of this legislation was to assist the Department of Justice in tracking and shutting down “rogue websites.” These sites provide unauthorized downloads, streaming, or direct sale of copyrighted material. Similar legislation, entitled the Preventing Real Online Threats to Economic Creativity and Theft of Intellectual Property (PROTECT IP) Act, has been introduced in the Senate. The PROTECT IP Act narrows the definition of “rogue website” in an effort to target only the most egregious purveyors of digital theft and counterfeit crime.
In an age of advancing technology, it is critical we have laws that protect internet users from unfair, deceptive, or fraudulent marketplace practices. Too many consumers today purchase goods over the internet that may pose a significant threat to their health and wellbeing. For example, a consumer may unknowingly purchase counterfeit prescription drugs online that contain incorrect amounts of active ingredients, and thus pose a serious risk to ill individuals.
Additionally, illegal file sharing and unauthorized copying of digital material prevents musicians, producers, filmmakers, software designers, and many others from reaping the fruits of their labor. Such activity has the potential to stifle artistic creativity and compromise electronic innovation. Ultimately, intellectual property theft costs our economy billions of dollars and can result in hundreds of thousands of lost jobs.
However, I have also heard from individuals with concerns about the scope of this legislation, as well as its First Amendment implications. I take these concerns seriously. Should this legislation come before the full Senate for a vote, I will keep your views in mind. Thank you again for getting in touch with me.
Sincerely,
Sherrod Brown
United States Senator
I have nothing against open source software, as a matter of a fact I am a fan of it, and I use many applications developed under this paradigm for my daily activities, I even enjoy them as weekend projects (e.g. ClearCanvas, PatientOS, Mirth Project, OpenDICOM, etcetera), but I just don’t see them fit for the demanding and critical healthcare IT domain.
VistA is not an example of the typical open source application so let’s not bring it to the table for this discussion.
CCHIT‘s step to support the FOSS realm is indeed laudable, Mark Leavitt has proven to be a nice guy, this is a genuine gesture which gives you (the open source guys) the opportunity to certify your Electronic Health Record (EHR) products. But this isn’t the gateway to success since you may still have a long stretch to go.
Let me explain why:
Healthcare IT is extremely demanding and it requires discipline a discipline which can only be delivered by highly organized and structured entities.
Companies such as: GE Healthcare, HP, McKesson, MEDITECH, Philips, SIEMENS, and similar others have for many years devoted themselves to the development of highly reliable clinical applications and medical devices. Most of these aforementioned companies have strict product development methodologies and strategies that they have had to implement in order to meet with the ever increasing and strict requirements of the FDA for the verification and validation (V and V) of medical devices and related software.
Many may argue that for the software product development process they don’t use the same guidelines as they do for the manufacturing of their medical devices, but knowing how these companies operate, and I have worked closely for and with them for many years, I am absolutely sure that they do.
Maybe the adventurism into the healthcare IT domain taking place by Google, Novell, and Sun Microsystems (soon to be part of Oracle), among many, and albeit this latter one at one point in time built very sophisticated medical image viewing workstations based on their SPARC technology, are probably giving you an over optimistic perception.
In my opinion these companies currently just don’t have the culture to fit into this rigorous process. Undoubtedly, they are extremely successful organizations in their activities but just not in this one. You see, this is a different beast.
And maybe you do a great job at creating software, perfect software. But this is not the only piece of the puzzle since there is the rigid documentation process required for clinical product development. Only the documentation process will overwhelm your budget if not drain it completely.
The very laid back and lax nature of open source development is the antithesis of what is required to develop critical clinical applications.
The FDA has formed a working group to determine whether or not Electronic Health Records should be regulated and to what extent if such is the case. Let’s say that they do decide to regulate them, and then this would be your demise in healthcare IT. The costs involved in meeting FDA requirements go beyond those that the most daring venture capitalists are willing to risk. Only companies with an infrastructure and logistics similar to those of GE Healthcare and SIEMENS can actually survive and strive in a scenario described here.
My recommendation to you, open source developers, is that along with the FOSS community members, you continue pouring your energies into your projects but don’t expect to take the industry by storm. It just won’t happen, sorry.
Stick with trying to overcome Microsoft Office some day in the remote future, maybe by 2021, or by creating a user friendly operating system that is not tailored “only for geeks”, like Linux is. Did you know that almost 90% of the workstations currently used by clinicians are Microsoft technologies based? You see, open source is “only for geeks” and not for the real world, the real users.
And I am not referring to geeks in a derogatory way since I consider myself one as well. But I do have a professional maturity level to understand that I have to create solutions for real world users and not savvy information technology experts.
Once you break out of your silicon shell then let’s sit down and talk seriously.
Thanks for reading!
During HIMSS 2009, and lately as well, I have been asked by several people what qualities or attributes would help a healthcare solutions architect be successful, so I decided to initially list at least five key attributes that I consider extremely valuable:
1. Be technology agnostic:
The Healthcare IT scenario is plagued with a myriad of solutions of disparate technologies and they will continue in the landscape for many years to come. Healthcare interoperability is a huge concern and anything you design has to be able to integrate with whatever is out there. You can’t be picky by going down the path you feel comfortable with.
In a hospital facility you may find current and legacy applications such as: MEDITECH, Emageon, Lawson, etc., and all of these are based on different technologies (e.g. Magic or MUMPS, Java, RPG 4).
If you are in an Integrated Delivery Network (IDN) scenario you may find that many facilities have differing technologies. One might be a MEDITECH shop while another one may be a SIEMENS one. The reason for this is that many IDNs merge new hospitals into their network and they can’t swap their Health Information Systems (HIS) applications overnight. Some migrations can take several years from start to finish. Some never take place because the clinicians of the newly incorporated facility actually like, or are accustomed to, their applications or they fear the unknowns of a new information system. Most likely implementing their HIS was a painful and long process and they may not want to go through that again.
What you design will have to live inside this Tower of Babel so you may find yourself creating pieces consisting of various technologies (e.g. Java, .NET, native C++, etc.). Your products will most likely have to exchange information with legacy applications and silos are no longer welcome in the healthcare domain so be ready to create loosely coupled interfaces to the outside world.
2. Know the standards:
HL7 and DICOM have been around for over 20 years and don’t think they will go away anytime soon to give room to the new industry wide standards. In many of your creations you will encounter these standards in one way or another. Don’t start complaining just because you don’t understand them or they seem different than more generalized standards out there. HL7 has been out in the playing field longer than XML and DICOM has been kicking the ball around before the Object Management Group (OMG) came into being. Both HL7 and DICOM have been adopted by major players in the healthcare IT domain worldwide.
HL7 goes beyond messaging. HL7 has defined other useful standards such as CCOW (Context Management) and the CDA (Clinical Document Architecture). All of these standards will gain momentum during this healthcare modernization era.
3. Know the harmonization initiatives:
IHE and HITSP are organizations that have been formed to be able to sort out the mess mainly created by the excessive flexibility of HL7. DICOM is a more rigid standard although it is also afflicted by the different interpretations given to it by the various vendors that implement it albeit in the last several years this has been largely normalized.
IHE and HITSP are all about interoperability. Both create profiles for implementation that are based on real world use cases.
Personally I recommend that if you are new to healthcare IT and software development you should start learning the standards through these harmonization processes. Learning HL7 from ground zero can be tortuous and understanding DICOM is a career all by itself.
ELINCS is another harmonization process, albeit of smaller scope, that was created by the California Healthcare Foundation to unravel the complexities of the exchange of information between Electronic Health Records (EHR) and Laboratories. If you are going to deal with EHRs and laboratory interoperability then here you will find peace of mind. ELINCS has been adopted by HL7, IHE, and HITSP so it is not a standalone effort as many believe.
4. Understand the CCHIT process:
Certification has become a big deal. You will not survive if you don’t deliver products that meet the “Meaningful Use” criteria or that when they play in a healthcare setting they at least contribute to this criteria. CCHIT is defining 3 different certification processes and your product will most likely fall into one of those. Modules have been accounted for for the certification and even in-house developments have been considered. This change in CCHIT’s processes is indeed welcome by many of us.
CCHIT has held its position of owning the EHR certification process. There are no indications that other organizations will perform this role. Anyways, if new organizations participate they will most likely follow the same approach CCHIT has created.
5. Get the hang on clinical workflow:
If you want the product you are creating to survive the battle of implementing it in a given clinical setting then you must understand clinical workflow in the various use cases that exist out there. Most applications fail during implementation because they are obtrusive, invasive, and detrimental to the workflow.
This is one of the main reasons that EHRs get launched and then after a short period of time they get tossed out the door, and by the way, not through the front one it came in.
Lack of understanding of the clinician’s workflow by many software developing companies has been a major factor of having generated the apathy that exists in clinicians towards information technology.
Almost all softwarel UI paradigms have been designed to be used by people who sit in front of a computer all day long with a keyboard and a mouse pretending to be working at all moments. These input devices are unsuitable for someone who is treating patients in real time. Get the difference? Would you like the doctor or nurse to be sitting in front of a computer while they have an encounter with you? I know I wouldn’t!
Biometrics has come a long way and so has artificial intelligence. Investigate how these can aid in creating solutions that augment the workflow. You must start thinking out of the box. Don’t think in technology terms but think in solutions to real problems. You would be surprised of how many complex problems have been solved by thinking simpler.
If you want your product to reach the whopping 80% of the unattended healthcare delivery market that’s out there waiting for you with their arms closed, and the remaining 20% of the highly unsatisfied current user base then you have to cause a paradigm switch: Think workflow and make the shift!
Coming soon: 5 More Attributes of a Successful Healthcare Solutions Architect
Thanks for reading!
