=Paper= {{Paper |id=None |storemode=property |title=Ontologies Put More Meaning into Meaningful Use |pdfUrl=https://ceur-ws.org/Vol-952/paper_25.pdf |volume=Vol-952 |dblpUrl=https://dblp.org/rec/conf/swat4ls/AdamusiakSFS12 }} ==Ontologies Put More Meaning into Meaningful Use== https://ceur-ws.org/Vol-952/paper_25.pdf
      Ontologies put more meaning into Meaningful Use

             Tomasz Adamusiak1 , Naoki Shimoyama1 , Alexandra Fuiks1 , and
                                 Mary Shimoyama1,2
  1
        Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI,
                                         United States
      2
         Department of Surgery, Medical College of Wisconsin, Milwaukee, WI, United States
                              {tadamusiak,shimoyama}@mcw.edu



         Abstract The Health Information Technology for Economic and Clinical Health
         (HITECH) Act, enacted as part of the American Recovery and Reinvestment Act
         of 2009, positioned the Meaningful Use of interoperable Electronic Health Re-
         cords as a critical goal and encouraged nationwide EHR adoption. The Consol-
         idated Health Informatics (CHI) initiative recommended the following three ter-
         minologies for EHRs: SNOMED CT, LOINC, and RxNorm to meet the Meaning-
         ful Use objectives. All three are integrated within the Unified Medical Language
         System (UMLS), designed and maintained by the US National Library of Medi-
         cine.
         The Clinical Informatics team at the Medical College Wisconsin is developing
         ClinMynEHR, a clinical data portal created to annotate EHRs for selected pedi-
         atric patients treated at the Children’s Hospital of Wisconsin. Data for the system
         consists of many clinical and referral documents the patients have accumulated
         along their clinical odysseys. ClinMynEHR consists of a comprehensive clinical
         database, query and reporting tools, and incorporates phenotypes, clinical meas-
         urements, lab test results, medications and other clinical information standardized
         through Meaningful Use ontologies integrated within the UMLS.


Introduction
Informatics have a long history in medicine [10], but with some notable exceptions
[14] their impact on medical practice was relatively low and predominantly motivated
by advances in medical imaging. The U.S. health care system is now in the process of
nationwide transformation through the adoption of Electronic Health Records (EHRs).
The federal EHR Incentive Programs only this year provided payments to more than
100,000 health care providers for their implementation and Meaningful Use certified
EHR technology [2].
    The 2009 HITECH Act introduced the concept of Meaningful Use of information
technology in health care. The definition of Meaningful Use in this context is complex
and consists of several objectives and measures the providers have to demonstrate in
three stages and within strict timelines in order to be eligible for early adopter incent-
ives and later on to avoid penalties for non-compliance. From the standpoint of semantic
interoperability perhaps the most interesting are the recently released Meaningful Use
Stage 2 Rules as they define the mandatory vocabularies to be used in EHR data ex-
change [1].
    SNOMED CT (Systematized Nomenclature of Medicine, Clinical Terms) is the
most comprehensive, multilingual biomedical terminology in the world. It provides
terms, synonyms and relations covering a number of clinical domains including dis-
eases, findings, and procedures [17]. LOINC (Logical Observation Identifiers Names
and Codes) is a universal standard for identifying laboratory observations. It can be con-
sidered the lingua franca of clinical observation exchange as it has more than 15,000
users in 145 countries [13]. RxNorm is a standardized nomenclature for generic and
branded drugs, as well as drug delivery devices [16]. All three terminologies are integ-
rated within the UMLS (Unified Medical Language System) maintained by the National
Library of Medicine (NLM) [11].
    ClinMynEHR is our clinical research portal for information on selected pediatric pa-
tients with suspected genetic disorders treated at the Children’s Hospital of Wisconsin.
This group of patients is unique as making a definitive diagnosis often requires extens-
ive workup and involves disparate health care providers. Clinical documents within the
system are manually annotated with ontology terms from SNOMED CT, LOINC and
RxNorm. In our experience, these ontologies provide sufficient coverage for disease
phenotypes, lab results, procedures, and medications for our research related use cases.
Manual curation, while time consuming, is more flexible and provides higher precision
and recall than currently available text-mining algorithms. We envision that in the fu-
ture it would be possible to import annotated data directly from the hospital’s EHR. In
that sense, using Meaningful Use ontologies is a means of future proofing our system.


Next-generation phenotyping

Hripcsak et al. postulated that with the unprecedented amount of clinical data becoming
available we will also need a paradigm shift in how we approach the valuable inform-
ation locked in current generation EHRs and novel phenotyping methods that take into
account often incomplete or inaccurate, complex data [7].
    Clinical narrative in its raw form is generally not amenable to computational ana-
lysis. On the other hand, structured data entry has its own disadvantages as it is more
time-consuming [12,4] and offers less flexibility and expressiveness in data capture
[15,9]. Unfortunately, the use of narrative encourages redundancy through copy-and-
paste [5,21,6], and some parts of the records exist solely for medicolegal, reimburse-
ment, and regulatory requirements [3].
    As much as 16% of clinical notes may never be read by anyone [8]. Clinically
important documents related to continuity of care (signouts) are often not recorded
electronically, as they are traditionally not included as part of an official medical record
[20,18]. Finally, some relevant information is invariably lost when laboratory tests are
sent to external reference laboratories or when patients fill their prescriptions outside
provider’s network [12].
    Not all information in electronic health records is likely to be relevant. It is reason-
able to expect that some of the information can be ignored depending on the application
context. Quality assessment can be to some extent standardized using dedicated instru-
ments, such as the one developed by Stetson et al. [19].
Conclusion

There are some unique challenges in applying ontologies to clinical data as well as how
we traditionally perceive health records as simple collections of documents. Enabling
interoperability on unprecedented scale, widespread use of standard and universal on-
tologies will be the driving force behind the transformation of health care and the more
meaningful use of health information technology.


References
 1. Health Information Technology: Standards, Implementation Specifications, and Certification
    Criteria for Electronic Health Record Technology, 2014 Edition; Revisions to the Permanent
    Certification Program for Health Information Technology (2012)
 2. U.S. Department of Health & Human Services. News release. More than 100 000 health care
    providers paid for using electronic health records. June 19, 2012 (2012)
 3. Cusack, C.M., Hripcsak, G., Bloomrosen, M., Rosenbloom, S.T., Weaver, C.A., Wright, A.,
    Vawdrey, D.K., Walker, J., Mamykina, L.: The future state of clinical data capture and doc-
    umentation: a report from AMIA’s 2011 Policy Meeting. Journal of the American Medical
    Informatics Association : JAMIA (Sep 2012)
 4. Gilbert, J.A.: Physician data entry: providing options is essential. Health data management
    6(9), 84–6, 88, 90–2 (Sep 1998)
 5. Hirschtick, R.E.: A piece of my mind. Copy-and-paste. JAMA : the journal of the American
    Medical Association 295(20), 2335–6 (May 2006)
 6. Hirschtick, R.E.: John Lennon’s Elbow. JAMA: The Journal of the American Medical Asso-
    ciation 308(5), 463 (Aug 2012)
 7. Hripcsak, G., Albers, D.J.: Next-generation phenotyping of electronic health records. Journal
    of the American Medical Informatics Association : JAMIA (Sep 2012)
 8. Hripcsak, G., Vawdrey, D.K., Fred, M.R., Bostwick, S.B.: Use of electronic clinical docu-
    mentation: time spent and team interactions. Journal of the American Medical Informatics
    Association : JAMIA 18(2), 112–7 (2011)
 9. Johnson, S.B., Bakken, S., Dine, D., Hyun, S., Mendonça, E., Morrison, F., Bright, T., Van
    Vleck, T., Wrenn, J., Stetson, P.: An electronic health record based on structured narrative.
    Journal of the American Medical Informatics Association : JAMIA 15(1), 54–64 (2008)
10. Ledley, R.S., Lusted, L.B.: Reasoning foundations of medical diagnosis; symbolic logic,
    probability, and value theory aid our understanding of how physicians reason. Science (New
    York, N.Y.) 130(3366), 9–21 (Jul 1959)
11. Lindberg, D.A., Humphreys, B.L., McCray, A.T.: The Unified Medical Language System.
    Methods of information in medicine 32(4), 281–91 (Aug 1993)
12. McDonald, C.J.: The barriers to electronic medical record systems and how to overcome
    them. Journal of the American Medical Informatics Association : JAMIA 4(3), 213–21
    (1997)
13. McDonald, C.J.: LOINC, a Universal Standard for Identifying Laboratory Observations: A
    5-Year Update. Clinical Chemistry 49(4), 624–633 (Apr 2003)
14. McDonald, C.J., Tierney, W.M., Overhage, J.M., Martin, D.K., Wilson, G.A.: The Regen-
    strief Medical Record System: 20 years of experience in hospitals, clinics, and neighborhood
    health centers. M.D. computing : computers in medical practice 9(4), 206–17 (1992)
15. van Mulligen, E.M., Stam, H., van Ginneken, A.M.: Clinical data entry. Proceedings / AMIA
    ... Annual Symposium. AMIA Symposium pp. 81–5 (Jan 1998)
16. Parrish, F., Do, N., Bouhaddou, O., Warnekar, P.: Implementation of RxNorm as a termin-
    ology mediation standard for exchanging pharmacy medication between federal agencies.
    AMIA ... Annual Symposium proceedings / AMIA Symposium. AMIA Symposium p. 1057
    (Jan 2006)
17. Stearns, M.Q., Price, C., Spackman, K.A., Wang, A.Y.: SNOMED clinical terms: overview
    of the development process and project status. Proceedings / AMIA ... Annual Symposium.
    AMIA Symposium pp. 662–6 (Jan 2001)
18. Stein, D.M., Wrenn, J.O., Johnson, S.B., Stetson, P.D.: Signout: a collaborative document
    with implications for the future of clinical information systems. AMIA ... Annual Sym-
    posium proceedings / AMIA Symposium. AMIA Symposium pp. 696–700 (Jan 2007)
19. Stetson, P.D., Bakken, S., Wrenn, J.O., Siegler, E.L.: Assessing Electronic Note Quality Us-
    ing the Physician Documentation Quality Instrument (PDQI-9). Applied clinical informatics
    3(2), 164–174 (Jan 2012)
20. Vidyarthi, A.R., Arora, V., Schnipper, J.L., Wall, S.D., Wachter, R.M.: Managing discontinu-
    ity in academic medical centers: strategies for a safe and effective resident sign-out. Journal
    of hospital medicine : an official publication of the Society of Hospital Medicine 1(4), 257–
    66 (Jul 2006)
21. Wrenn, J.O., Stein, D.M., Bakken, S., Stetson, P.D.: Quantifying clinical narrative redund-
    ancy in an electronic health record. Journal of the American Medical Informatics Association
    : JAMIA 17(1), 49–53 (2010)