Evidence map›Paper›PMID 34457160›Full record

ArticleAMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science

Empirical Findings on the Role of Structured Data, Unstructured Data, and their Combination for Automatic Clinical Phenotyping.

Asher Moldwin, Dina Demner-Fushman, Travis R Goodwin

Abstract read
In one paragraph

Article in AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Using Multimodal Data to Improve Precision of Inpatient Event Timelines.Advances in knowledge discovery and data mining : ... Pacific-Asia Conference, PAKDD ..., proceedings. Pacific-Asia Conference on Knowledge Discovery and Data Mining · 2024
    Article
  6. Article
  7. Review
  8. Developing an LSTM Model to Identify Surgical Site Infections using Electronic Healthcare Records.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science · 2023
    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.

Asher MoldwinU.S. National Library of Medicine, Bethesda, MD, USA.
Dina Demner-FushmanU.S. National Library of Medicine, Bethesda, MD, USA.
Travis R GoodwinU.S. National Library of Medicine, Bethesda, MD, USA.

Funding

Providing timely and effortless access to reliable health-related information for decision support and educationZIALM010019 · NLM · NATIONAL LIBRARY OF MEDICINE · PI DEMNER-FUSHMAN, DINA · 2021 to 2025
$12.0M
6 · The paper itself

Abstract

The objective of this study is to explore the role of structured and unstructured data for clinical phenotyping by determining which types of clinical phenotypes are best identified using unstructured data (e.g., clinical notes), structured data (e.g., laboratory values, vital signs), or their combination across 172 clinical phenotypes. Specifically, we used laboratory and chart measurements as well as clinical notes from the MIMIC-III critical care database and trained an LSTM using features extracted from each type of data to determine which categories of phenotypes were best identified by structured data, unstructured data, or both. We observed that textual features on their own outperformed structured features for 145 (84%) of phenotypes, and that Doc2Vec was the most effective representation of unstructured data for all phenotypes. When evaluating the impact of adding textual features to systems previously relying only on structured features, we found a statistically significant (p < 0.05) increase in phenotyping performance for 51 phenotypes (primarily involving the circulatory system, injury, and poisoning), one phenotype for which textual features degraded performance (diabetes without complications), and no statistically significant change in performance with the remaining 120 phenotypes. We provide analysis on which phenotypes are best identified by each type of data and guidance on which data sources to consider for future research on phenotype identification.

Indexed as

Critical CareElectronic Health RecordsDatabases, FactualHumansPhenotype

Identifiers

PMID34457160
PMCPMC8378600

What OpenQuestion holds

Textmetadata
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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.