Evidence map›Paper›PMID 38777085›Full record

ArticleJournal of biomedical informatics2024

Converting OMOP CDM to phenopackets: A model alignment and patient data representation evaluation.

Kayla Schiffer-Kane, Cong Liu, Tiffany J Callahan, Casey Ta, Jordan G Nestor, Chunhua Weng

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

6 authors.

Kayla Schiffer-KaneDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
Cong LiuDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
Tiffany J CallahanDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
Casey TaDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
Jordan G NestorDepartment of Medicine, Division of Nephrology, Columbia University Irving Medical Center, New York, NY, USA.
Chunhua WengDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: cw2384@cumc.columbia.edu.

Funding

Training in Biomedical Informatics at Columbia UniversityT15LM007079 · NLM · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI NOEMIE ELHADAD, GEORGE M HRIPCSAK · 1992 to 2026
$28.9M
OMOP information model for eMERGE phenotypingU01HG008680 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wendy K Chung, GEORGE M HRIPCSAK · 2015 to 2026
$13.3M
Computational Bioscience Program Training GrantT15LM009451 · NLM · UNIVERSITY OF COLORADO DENVER · PI Katherina Kechris-Mays, Arjun Krishnan · 2007 to 2026
$11.7M
RESCUE: Rare Disease Detection and Escalation Support via a Learning Health SystemR01HG012655 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Cong Liu · 2022 to 2026
$4.1M
Fair Phenotype Annotation and Genomic ReinterpretationR01HG013031 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wendy K Chung, CHUNHUA WENG · 2023 to 2026
$3.5M
Deep phenotyping in Electronic Health Records for Genomic MedicineR01LM012895 · NLM · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WANG, KAI, WENG, CHUNHUA · 2018 to 2021
$3.3M
Translator Red Knowledge (TReK)OT2TR003434 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DUMONTIER, MICHEL, TA, CASEY NGHIA · 2020 to 2024
$2.3M
NCATS NIH HHS OT2 TR003434NHGRI NIH HHS R01 HG012655NHGRI NIH HHS R01 HG013031NHGRI NIH HHS U01 HG008680NLM NIH HHS R01 LM012895NLM NIH HHS T15 LM007079NLM NIH HHS T15 LM009451
6 · The paper itself

Abstract

objectiveThis study aims to promote interoperability in precision medicine and translational research by aligning the Observational Medical Outcomes Partnership (OMOP) and Phenopackets data models. Phenopackets is an expert knowledge-driven schema designed to facilitate the storage and exchange of multimodal patient data, and support downstream analysis. The first goal of this paper is to explore model alignment by characterizing the common data models using a newly developed data transformation process and evaluation method. Second, using OMOP normalized clinical data, we evaluate the mapping of real-world patient data to Phenopackets. We evaluate the suitability of Phenopackets as a patient data representation for real-world clinical cases.

methodsWe identified mappings between OMOP and Phenopackets and applied them to a real patient dataset to assess the transformation's success. We analyzed gaps between the models and identified key considerations for transforming data between them. Further, to improve ambiguous alignment, we incorporated Unified Medical Language System (UMLS) semantic type-based filtering to direct individual concepts to their most appropriate domain and conducted a domain-expert evaluation of the mapping's clinical utility.

resultsThe OMOP to Phenopacket transformation pipeline was executed for 1,000 Alzheimer's disease patients and successfully mapped all required entities. However, due to missing values in OMOP for required Phenopacket attributes, 10.2 % of records were lost. The use of UMLS-semantic type filtering for ambiguous alignment of individual concepts resulted in 96 % agreement with clinical thinking, increased from 68 % when mapping exclusively by domain correspondence.

conclusionThis study presents a pipeline to transform data from OMOP to Phenopackets. We identified considerations for the transformation to ensure data quality, handling restrictions for successful Phenopacket validation and discrepant data formats. We identified unmappable Phenopacket attributes that focus on specialty use cases, such as genomics or oncology, which OMOP does not currently support. We introduce UMLS semantic type filtering to resolve ambiguous alignment to Phenopacket entities to be most appropriate for real-world interpretation. We provide a systematic approach to align OMOP and Phenopackets schemas. Our work facilitates future use of Phenopackets in clinical applications by addressing key barriers to interoperability when deriving a Phenopacket from real-world patient data.

Indexed as

Unified Medical Language SystemAlzheimer DiseaseElectronic Health RecordsHumansMedical InformaticsNatural Language ProcessingPrecision MedicineSemanticsTranslational Research, BiomedicalData modelHealth data standardsInteroperabilityOMOP-CDMPhenopackets schemaPhenotyping

Identifiers

PMID38777085
PMCPMC11181468

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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.