Evidence map›Paper›PMID 33045017›Full record

ArticlePloS one2020

A predictive Bayesian network that risk stratifies patients undergoing Barrett's surveillance for personalized risk of developing malignancy.

Alison Bradley, Sharukh Sami, Hwei N G, Anne Macleod, Manju Prasanth, Muneeb Zafar, Niroshini Hemadasa, Gregg Neagle, Isobelle Rosindell, Jeyakumar Apollos

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Review
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

10 authors at 1 institution in 1 country.

Alison BradleyDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.ORCID 0000-0002-3899-8457
Sharukh SamiDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Hwei N GDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.ORCID 0000-0002-9077-2367
Anne MacleodDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Manju PrasanthDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Muneeb ZafarDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Niroshini HemadasaDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Gregg NeagleDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Isobelle RosindellDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Jeyakumar ApollosDepartment of General Surgery, Dumfries and Galloway Royal Infirmary, NHS Dumfries and Galloway, Dumfries, Scotland, United Kingdom.
Dumfries and Galloway Royal Infirmary · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBarrett's esophagus is strongly associated with esophageal adenocarcinoma. Considering costs and risks associated with invasive surveillance endoscopies better methods of risk stratification are required to assist decision-making and move toward more personalised tailoring of Barrett's surveillance.

methodsA Bayesian network was created by synthesizing data from published studies analysing risk factors for developing adenocarcinoma in Barrett's oesophagus through a two-stage weighting process.

resultsData was synthesized from 114 studies (n = 394,827) to create the Bayesian network, which was validated against a prospectively maintained institutional database (n = 571). Version 1 contained 10 variables (dysplasia, gender, age, Barrett's segment length, statin use, proton pump inhibitor use, BMI, smoking, aspirin and NSAID use) and achieved AUC of 0.61. Version 2 contained 4 variables with the strongest evidence of association with the development of adenocarcinoma in Barrett's (dysplasia, gender, age, Barrett's segment length) and achieved an AUC 0.90.

conclusionThis Bayesian network is unique in the way it utilizes published data to translate the existing empirical evidence surrounding the risk of developing adenocarcinoma in Barrett's esophagus to make personalized risk predictions. Further work is required but this tool marks a vital step towards delivering a more personalized approach to Barrett's surveillance.

Indexed as

PrognosisAdenocarcinomaAdultAgedBarrett EsophagusBayes TheoremDisease ProgressionEndoscopyEsophageal NeoplasmsFemaleHumansMaleMiddle AgedRisk Factors

Identifiers

PMID33045017
PMCPMC7549831
OpenAlexW3092198255

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.