Evidence map›Paper›PMID 32012059›Full record

ArticleJMIR medical informatics2020

Clinical Annotation Research Kit (CLARK): Computable Phenotyping Using Machine Learning.

Emily R Pfaff, Miles Crosskey, Kenneth Morton, Ashok Krishnamurthy

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Emily R PfaffNorth Carolina Translational and Clinical Sciences Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID https://orcid.org/0000-0002-6840-9756
Miles CrosskeyCoVar Applied Technologies, Durham, NC, United States.ORCID https://orcid.org/0000-0002-0625-7718
Kenneth MortonCoVar Applied Technologies, Durham, NC, United States.ORCID https://orcid.org/0000-0002-9352-8669
Ashok KrishnamurthyRenaissance Computing Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID https://orcid.org/0000-0002-3215-7622
Applied Technologies (United States) · USUniversity of North Carolina at Chapel Hill · US

Funding

Re-Entry Supplement: Investigation of Oral Microbial Enzymes for the Detection and Treatment of Periodontal DiseaseUL1TR002489 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, SHAHEEN, NICHOLAS J · 2018 to 2022
$48.6M
NCATS NIH HHS UL1 TR002489
6 · The paper itself

Abstract

Computable phenotypes are algorithms that translate clinical features into code that can be run against electronic health record (EHR) data to define patient cohorts. However, computable phenotypes that only make use of structured EHR data do not capture the full richness of a patient's medical record. While natural language processing (NLP) methods have shown success in extracting clinical features from text, the use of such tools has generally been limited to research groups with substantial NLP expertise. Our goal was to develop an open-source phenotyping software, Clinical Annotation Research Kit (CLARK), that would enable clinical and translational researchers to use machine learning-based NLP for computable phenotyping without requiring deep informatics expertise. CLARK enables nonexpert users to mine text using machine learning classifiers by specifying features for the software to match in clinical notes. Once the features are defined, the user-friendly CLARK interface allows the user to choose from a variety of standard machine learning algorithms (linear support vector machine, Gaussian Naïve Bayes, decision tree, and random forest), cross-validation methods, and the number of folds (cross-validation splits) to be used in evaluation of the classifier. Example phenotypes where CLARK has been applied include pediatric diabetes (sensitivity=0.91; specificity=0.98), symptomatic uterine fibroids (positive predictive value=0.81; negative predictive value=0.54), nonalcoholic fatty liver disease (sensitivity=0.90; specificity=0.94), and primary ciliary dyskinesia (sensitivity=0.88; specificity=1.0). In each of these use cases, CLARK allowed investigators to incorporate variables into their phenotype algorithm that would not be available as structured data. Moreover, the fact that nonexpert users can get started with machine learning-based NLP with limited informatics involvement is a significant improvement over the status quo. We hope to disseminate CLARK to other organizations that may not have NLP or machine learning specialists available, enabling wider use of these methods.

Indexed as

electronic health recordsmachine learningnatural language processing

Identifiers

PMID32012059
PMCPMC7007592
OpenAlexW2996406085

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.