Evidence map›Paper›PMID 34568771›Full record

ArticleJAMIA open2021

Quantifying representativeness in randomized clinical trials using machine learning fairness metrics.

Miao Qi, Owen Cahan, Morgan A Foreman, Daniel M Gruen, Amar K Das, Kristin P Bennett

Open access · goldAbstract read
In one paragraph

Article in JAMIA open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Fair Canonical Correlation Analysis.Advances in neural information processing systems · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Framework for Research in Equitable Synthetic Control Arms.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2023
    Article
  16. Recommendations on compiling test datasets for evaluating artificial intelligence solutions in pathology.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Review
  17. Article
  18. The Problem of Fairness in Synthetic Healthcare Data.Entropy (Basel, Switzerland) · 2021
    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

6 authors at 2 institutions in 1 country.

Miao QiDepartment of Computer Science, Rensselaer Polytechnic Institute, Troy, New York, USA.
Owen CahanDepartment of Mathematical Sciences, Rensselaer Polytechnic Institute, Troy, New York, USA.
Morgan A ForemanCenter for Computational Health, IBM Research, Cambridge, Massachusetts, USA.
Daniel M GruenDepartment of Mathematical Sciences, Rensselaer Polytechnic Institute, Troy, New York, USA.
Amar K DasCenter for Computational Health, IBM Research, Cambridge, Massachusetts, USA.
Kristin P BennettDepartment of Computer Science, Rensselaer Polytechnic Institute, Troy, New York, USA.
Rensselaer Polytechnic Institute · USComputational Physics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe help identify subpopulations underrepresented in randomized clinical trials (RCTs) cohorts with respect to national, community-based or health system target populations by formulating population representativeness of RCTs as a machine learning (ML) fairness problem, deriving new representation metrics, and deploying them in easy-to-understand interactive visualization tools. MATERIALS AND

methodsWe represent RCT cohort enrollment as random binary classification fairness problems, and then show how ML fairness metrics based on enrollment fraction can be efficiently calculated using easily computed rates of subpopulations in RCT cohorts and target populations. We propose standardized versions of these metrics and deploy them in an interactive tool to analyze 3 RCTs with respect to type 2 diabetes and hypertension target populations in the National Health and Nutrition Examination Survey.

resultsWe demonstrate how the proposed metrics and associated statistics enable users to rapidly examine representativeness of all subpopulations in the RCT defined by a set of categorical traits (eg, gender, race, ethnicity, smoking status, and blood pressure) with respect to target populations. DISCUSSION: The normalized metrics provide an intuitive standardized scale for evaluating representation across subgroups, which may have vastly different enrollment fractions and rates in RCT study cohorts. The metrics are beneficial complements to other approaches (eg, enrollment fractions) used to identify generalizability and health equity of RCTs.

conclusionBy quantifying the gaps between RCT and target populations, the proposed methods can support generalizability evaluation of existing RCT cohorts. The interactive visualization tool can be readily applied to identified underrepresented subgroups with respect to any desired source or target populations.

Indexed as

health equitymachine learningpopulation representativenessrandomized clinical trialssubgroup

Identifiers

PMID34568771
PMCPMC8460438
OpenAlexW3202137438

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.