Evidence map›Paper›PMID 25601137›Full record

ArticleJMIR medical informatics2014

Next generation phenotyping using the unified medical language system.

Tomasz Adamusiak, Naoki Shimoyama, Mary Shimoyama

Abstract read
In one paragraph

Article in JMIR medical informatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. PheNormGPT: a framework for extraction and normalization of key medical findings.Database : the journal of biological databases and curation · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Using UMLS for electronic health data standardization and database design.Journal of the American Medical Informatics Association : JAMIA · 2020
    Article
  7. Article
  8. Article
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  11. Article
  12. Article
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  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Tomasz AdamusiakHuman and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI, United States. tomasz@mcw.edu.
Naoki Shimoyama
Mary Shimoyama

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR031973 · NCRR · MEDICAL COLLEGE OF WISCONSIN · PI SHAKER, REZA NONE · 2010 to 2011
$7.9M
NCRR NIH HHS UL1 RR031973
6 · The paper itself

Abstract

backgroundStructured information within patient medical records represents a largely untapped treasure trove of research data. In the United States, privacy issues notwithstanding, this has recently become more accessible thanks to the increasing adoption of electronic health records (EHR) and health care data standards fueled by the Meaningful Use legislation. The other side of the coin is that it is now becoming increasingly more difficult to navigate the profusion of many disparate clinical terminology standards, which often span millions of concepts.

objectiveThe objective of our study was to develop a methodology for integrating large amounts of structured clinical information that is both terminology agnostic and able to capture heterogeneous clinical phenotypes including problems, procedures, medications, and clinical results (such as laboratory tests and clinical observations). In this context, we define phenotyping as the extraction of all clinically relevant features contained in the EHR.

methodsThe scope of the project was framed by the Common Meaningful Use (MU) Dataset terminology standards; the Systematized Nomenclature of Medicine Clinical Terms (SNOMED CT), RxNorm, the Logical Observation Identifiers Names and Codes (LOINC), the Current Procedural Terminology (CPT), the Health care Common Procedure Coding System (HCPCS), the International Classification of Diseases Ninth Revision Clinical Modification (ICD-9-CM), and the International Classification of Diseases Tenth Revision Clinical Modification (ICD-10-CM). The Unified Medical Language System (UMLS) was used as a mapping layer among the MU ontologies. An extract, load, and transform approach separated original annotations in the EHR from the mapping process and allowed for continuous updates as the terminologies were updated. Additionally, we integrated all terminologies into a single UMLS derived ontology and further optimized it to make the relatively large concept graph manageable.

resultsThe initial evaluation was performed with simulated data from the Clinical Avatars project using 100,000 virtual patients undergoing a 90 day, genotype guided, warfarin dosing protocol. This dataset was annotated with standard MU terminologies, loaded, and transformed using the UMLS. We have deployed this methodology to scale in our in-house analytics platform using structured EHR data for 7931 patients (12 million clinical observations) treated at the Froedtert Hospital. A demonstration limited to Clinical Avatars data is available on the Internet using the credentials user "jmirdemo" and password "jmirdemo".

conclusionsDespite its inherent complexity, the UMLS can serve as an effective interface terminology for many of the clinical data standards currently used in the health care domain.

Indexed as

CPTHCPCSICD-10ICD-9LOINCmeaningful useRxNormsemantic interoperabilitySNOMED CTUMLS

Identifiers

PMID25601137
PMCPMC4288084

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.