Evidence map›Paper›PMID 32848165›Full record

ArticleScientific reports2020

Deep learning and feature based medication classifications from EEG in a large clinical data set.

David O Nahmias, Eugene F Civillico, Kimberly L Kontson

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

David O NahmiasElectrical and Computer Engineering, University of Maryland, College Park, MD, 20740, USA. dnahmias@umd.edu.
Eugene F CivillicoNational Institutes of Health, Bethesda, MD, 20892, USA.
Kimberly L KontsonCenter for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, MD, 20993, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The amount of freely available human phenotypic data is increasing daily, and yet little is known about the types of inferences or identifying characteristics that could reasonably be drawn from that data using new statistical methods. One data type of particular interest is electroencephalographical (EEG) data, collected noninvasively from humans in various behavioral contexts. The Temple University EEG corpus associates thousands of hours of de-identified EEG records with contemporaneous physician reports that include metadata that might be expected to show a measurable correlation with characteristics of the recorded signal. Given that machine learning methods applied to neurological signals are being used in emerging diagnostic applications, we leveraged this data source to test the confidence with which algorithms could predict, using a patient's EEG record(s) as input, which medications were noted on the matching physician report. We comparatively assessed deep learning and feature-based approaches on their ability to distinguish between the assumed presence of Dilantin (phenytoin), Keppra (levetiracetam), or neither. Our methods could successfully distinguish between patients taking either anticonvulsant and those taking no medications; as well as between the two anticonvulsants. Further, we found different approaches to be most effective for different groups of classifications.

Indexed as

Deep LearningElectroencephalographyAnticonvulsantsHumansLevetiracetamPhenytoinAnticonvulsantsLevetiracetamPhenytoin

Identifiers

PMID32848165
PMCPMC7450080

What OpenQuestion holds

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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.