Evidence map›Paper›PMID 30646959›Full record

ArticleSystematic reviews2019

Machine learning algorithms for systematic review: reducing workload in a preclinical review of animal studies and reducing human screening error.

Alexandra Bannach-Brown, Piotr Przybyła, James Thomas, Andrew S C Rice, Sophia Ananiadou, Jing Liao, Malcolm Robert Macleod

Abstract read
In one paragraph

Article in Systematic reviews, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 15 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

76 citing papers in PubMed, 15 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. Pooled it
  9. Pooled it
  10. Pooled it
  11. Pooled it
  12. Pooled it
  13. Pooled it
  14. Pooled it
  15. Pooled it
  16. Trial
  17. Article
  18. Review
  19. Review
  20. Article

16 more citing papers are in PubMed but not listed here.

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.

Alexandra Bannach-BrownCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland. a.bannach-brown@ed.ac.uk.ORCID 0000-0002-3161-1395
Piotr PrzybyłaNational Centre for Text Mining, School of Computer Science, University of Manchester, Manchester, England.
James ThomasEPPI-Centre, Department of Social Science, University College London, London, England.ORCID 0000-0003-4805-4190
Andrew S C RicePain Research, Department of Surgery and Cancer, Imperial College, London, England.ORCID 0000-0002-1237-4769
Sophia AnaniadouNational Centre for Text Mining, School of Computer Science, University of Manchester, Manchester, England.
Jing LiaoCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland.
Malcolm Robert MacleodCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland.ORCID 0000-0001-9187-9839

Funding

Medical Research Council MR/J005037/1Medical Research Council MR/N015665/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/L000970/1Wellcome TrustWellcome Trust MR/N015665/1
6 · The paper itself

Abstract

backgroundHere, we outline a method of applying existing machine learning (ML) approaches to aid citation screening in an on-going broad and shallow systematic review of preclinical animal studies. The aim is to achieve a high-performing algorithm comparable to human screening that can reduce human resources required for carrying out this step of a systematic review.

methodsWe applied ML approaches to a broad systematic review of animal models of depression at the citation screening stage. We tested two independently developed ML approaches which used different classification models and feature sets. We recorded the performance of the ML approaches on an unseen validation set of papers using sensitivity, specificity and accuracy. We aimed to achieve 95% sensitivity and to maximise specificity. The classification model providing the most accurate predictions was applied to the remaining unseen records in the dataset and will be used in the next stage of the preclinical biomedical sciences systematic review. We used a cross-validation technique to assign ML inclusion likelihood scores to the human screened records, to identify potential errors made during the human screening process (error analysis).

resultsML approaches reached 98.7% sensitivity based on learning from a training set of 5749 records, with an inclusion prevalence of 13.2%. The highest level of specificity reached was 86%. Performance was assessed on an independent validation dataset. Human errors in the training and validation sets were successfully identified using the assigned inclusion likelihood from the ML model to highlight discrepancies. Training the ML algorithm on the corrected dataset improved the specificity of the algorithm without compromising sensitivity. Error analysis correction leads to a 3% improvement in sensitivity and specificity, which increases precision and accuracy of the ML algorithm.

conclusionsThis work has confirmed the performance and application of ML algorithms for screening in systematic reviews of preclinical animal studies. It has highlighted the novel use of ML algorithms to identify human error. This needs to be confirmed in other reviews with different inclusion prevalence levels, but represents a promising approach to integrating human decisions and automation in systematic review methodology.

Indexed as

AlgorithmsMachine LearningSystematic Reviews as TopicAnimalsBibliometricsDepressive DisorderHumansModels, AnimalSensitivity and SpecificityWorkloadAnalysis of human errorAutomation toolsCitation screeningMachine learningSystematic review

Identifiers

PMID30646959
PMCPMC6334440

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.