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Mapping ICD-10 and ICD-10-CM Codes to Phecodes: Workflow Development and Initial Evaluation.

作者信息

Wu Patrick, Gifford Aliya, Meng Xiangrui, Li Xue, Campbell Harry, Varley Tim, Zhao Juan, Carroll Robert, Bastarache Lisa, Denny Joshua C, Theodoratou Evropi, Wei Wei-Qi

机构信息

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, United States.

Medical Scientist Training Program, Vanderbilt University School of Medicine, Nashville, TN, United States.

出版信息

JMIR Med Inform. 2019 Nov 29;7(4):e14325. doi: 10.2196/14325.


DOI:10.2196/14325
PMID:31553307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6911227/
Abstract

BACKGROUND: The phecode system was built upon the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) for phenome-wide association studies (PheWAS) using the electronic health record (EHR). OBJECTIVE: The goal of this paper was to develop and perform an initial evaluation of maps from the International Classification of Diseases, 10th Revision (ICD-10) and the International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) codes to phecodes. METHODS: We mapped ICD-10 and ICD-10-CM codes to phecodes using a number of methods and resources, such as concept relationships and explicit mappings from the Centers for Medicare & Medicaid Services, the Unified Medical Language System, Observational Health Data Sciences and Informatics, Systematized Nomenclature of Medicine-Clinical Terms, and the National Library of Medicine. We assessed the coverage of the maps in two databases: Vanderbilt University Medical Center (VUMC) using ICD-10-CM and the UK Biobank (UKBB) using ICD-10. We assessed the fidelity of the ICD-10-CM map in comparison to the gold-standard ICD-9-CM phecode map by investigating phenotype reproducibility and conducting a PheWAS. RESULTS: We mapped >75% of ICD-10 and ICD-10-CM codes to phecodes. Of the unique codes observed in the UKBB (ICD-10) and VUMC (ICD-10-CM) cohorts, >90% were mapped to phecodes. We observed 70-75% reproducibility for chronic diseases and <10% for an acute disease for phenotypes sourced from the ICD-10-CM phecode map. Using the ICD-9-CM and ICD-10-CM maps, we conducted a PheWAS with a Lipoprotein(a) genetic variant, rs10455872, which replicated two known genotype-phenotype associations with similar effect sizes: coronary atherosclerosis (ICD-9-CM: P<.001; odds ratio (OR) 1.60 [95% CI 1.43-1.80] vs ICD-10-CM: P<.001; OR 1.60 [95% CI 1.43-1.80]) and chronic ischemic heart disease (ICD-9-CM: P<.001; OR 1.56 [95% CI 1.35-1.79] vs ICD-10-CM: P<.001; OR 1.47 [95% CI 1.22-1.77]). CONCLUSIONS: This study introduces the beta versions of ICD-10 and ICD-10-CM to phecode maps that enable researchers to leverage accumulated ICD-10 and ICD-10-CM data for PheWAS in the EHR.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/ed67c1d77888/medinform_v7i4e14325_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/9ee240a6e902/medinform_v7i4e14325_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/d88be9f65528/medinform_v7i4e14325_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/8693b9b399bc/medinform_v7i4e14325_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/ed67c1d77888/medinform_v7i4e14325_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/9ee240a6e902/medinform_v7i4e14325_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/d88be9f65528/medinform_v7i4e14325_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/8693b9b399bc/medinform_v7i4e14325_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/6911227/ed67c1d77888/medinform_v7i4e14325_fig4.jpg

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Mapping ICD-10 and ICD-10-CM Codes to Phecodes: Workflow Development and Initial Evaluation.

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本文引用的文献

[1]
Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA).

PLoS One. 2019-2-13

[2]
Learning from Longitudinal Data in Electronic Health Record and Genetic Data to Improve Cardiovascular Event Prediction.

Sci Rep. 2019-1-24

[3]
Electronic Medical Record Context Signatures Improve Diagnostic Classification Using Medical Image Computing.

IEEE J Biomed Health Inform. 2018-12-28

[4]
Effect of vocabulary mapping for conditions on phenotype cohorts.

J Am Med Inform Assoc. 2018-12-1

[5]
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.

Nat Genet. 2018-8-13

[6]
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.

Nat Genet. 2018-7-30

[7]
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.

Nat Genet. 2018-6-28

[8]
Public Opinions Toward Diseases: Infodemiological Study on News Media Data.

J Med Internet Res. 2018-5-8

[9]
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.

Circulation. 2018-10-23

[10]
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.

Science. 2018-3-16

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