Evidence map›Paper›PMID 33156808›Full record

ArticleJMIR medical informatics2020

Development of Phenotyping Algorithms for the Identification of Organ Transplant Recipients: Cohort Study.

Lee Wheless, Laura Baker, LaVar Edwards, Nimay Anand, Kelly Birdwell, Allison Hanlon, Mary-Margaret Chren

Open access · goldAbstract read
In one paragraph

Article in JMIR medical informatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. The Association of Solid Organ and Hematopoietic Stem Cell Transplant Indication With Skin Cancer Risk.Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.] · 2025
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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

7 authors at 2 institutions in 1 country.

Lee Wheless *Department of Dermatology, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-8162-5971
Laura BakerDepartment of Dermatology, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-0655-0164
LaVar EdwardsDepartment of Dermatology, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-6288-3932
Nimay AnandMeharry Medical College, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-9968-4478
Kelly BirdwellDivision of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-7996-3947
Allison HanlonDepartment of Dermatology, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID https://orcid.org/0000-0002-3937-7038
Mary-Margaret ChrenDepartment of Dermatology, Vanderbilt University Medical Center, Nashville, TN, United States.ORCID https://orcid.org/0000-0001-8009-7014
Vanderbilt University Medical Center · USMeharry Medical College · US

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
NCATS NIH HHS UL1 TR000445NCRR NIH HHS UL1 RR024975
6 · The paper itself

Abstract

backgroundStudies involving organ transplant recipients (OTRs) are often limited to the variables collected in the national Scientific Registry of Transplant Recipients database. Electronic health records contain additional variables that can augment this data source if OTRs can be identified accurately.

objectiveThe aim of this study was to develop phenotyping algorithms to identify OTRs from electronic health records.

methodsWe used Vanderbilt's deidentified version of its electronic health record database, which contains nearly 3 million subjects, to develop algorithms to identify OTRs. We identified all 19,817 individuals with at least one International Classification of Diseases (ICD) or Current Procedural Terminology (CPT) code for organ transplantation. We performed a chart review on 1350 randomly selected individuals to determine the transplant status. We constructed machine learning models to calculate positive predictive values and sensitivity for combinations of codes by using classification and regression trees, random forest, and extreme gradient boosting algorithms.

resultsOf the 1350 reviewed patient charts, 827 were organ transplant recipients while 511 had no record of a transplant, and 12 were equivocal. Most patients with only 1 or 2 transplant codes did not have a transplant. The most common reasons for being labeled a nontransplant patient were the lack of data (229/511, 44.8%) or the patient being evaluated for an organ transplant (174/511, 34.1%). All 3 machine learning algorithms identified OTRs with overall >90% positive predictive value and >88% sensitivity.

conclusionsElectronic health records linked to biobanks are increasingly used to conduct large-scale studies but have not been well-utilized in organ transplantation research. We present rigorously evaluated methods for phenotyping OTRs from electronic health records that will enable the use of the full spectrum of clinical data in transplant research. Using several different machine learning algorithms, we were able to identify transplant cases with high accuracy by using only ICD and CPT codes.

Indexed as

electronic health recordorgan transplant recipientsphenotyping

Identifiers

PMID33156808
PMCPMC7759442
OpenAlexW3096684096

What OpenQuestion holds

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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.