Evidence map›Paper›PMID 33711541›Full record

ArticleJournal of biomedical informatics2021

Generalized and transferable patient language representation for phenotyping with limited data.

Yuqi Si, Elmer V Bernstam, Kirk Roberts

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Automated Shared Phenotype Discovery in Undiagnosed Cohorts for Rare Disease Research.Proceedings of the ... International Conference on Machine Learning and Applications. International Conference on Machine Learning and Applications · 2024
    Article
  4. 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.

Yuqi SiSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, TX, USA.
Elmer V BernstamSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, TX, USA; Division of General Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX, USA.
Kirk RobertsSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, TX, USA. Electronic address: kirk.roberts@uth.tmc.edu.

Funding

Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
Harnessing the power of CTSA-CDRN data networks: Using social determinants of health, frailty and functional status to identify at-risk patients and improve risk adjustmentU01TR002393 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHIREMAN, PAULA K · 2018 to 2021
$3.1M
Patient Medical History Representation, Extraction, and Inference from EHR DataR01LM011829 · NLM · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TAO, CUI · 2014 to 2018
$1.7M
Natural Language Question Understanding for Electronic Health RecordsR00LM012104 · NLM · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ROBERTS, KIRK EDWARD · 2016 to 2018
$747k
NCATS NIH HHS U01 TR002393NCATS NIH HHS UL1 TR000371NLM NIH HHS R00 LM012104NLM NIH HHS R01 LM011829
6 · The paper itself

Abstract

The paradigm of representation learning through transfer learning has the potential to greatly enhance clinical natural language processing. In this work, we propose a multi-task pre-training and fine-tuning approach for learning generalized and transferable patient representations from medical language. The model is first pre-trained with different but related high-prevalence phenotypes and further fine-tuned on downstream target tasks. Our main contribution focuses on the impact this technique can have on low-prevalence phenotypes, a challenging task due to the dearth of data. We validate the representation from pre-training, and fine-tune the multi-task pre-trained models on low-prevalence phenotypes including 38 circulatory diseases, 23 respiratory diseases, and 17 genitourinary diseases. We find multi-task pre-training increases learning efficiency and achieves consistently high performance across the majority of phenotypes. Most important, the multi-task pre-training is almost always either the best-performing model or performs tolerably close to the best-performing model, a property we refer to as robust. All these results lead us to conclude that this multi-task transfer learning architecture is a robust approach for developing generalized and transferable patient language representations for numerous phenotypes.

Indexed as

LanguageNatural Language ProcessingHumansDeep learningLanguage representationPatient representationPhenotype prediction

Identifiers

PMID33711541
PMCPMC11577729

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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.