Evidence map›Paper›PMID 33539357›Full record

ArticlePLoS neglected tropical diseases2021

Latent Class Analysis: Insights about design and analysis of schistosomiasis diagnostic studies.

Artemis Koukounari, Haziq Jamil, Elena Erosheva, Clive Shiff, Irini Moustaki

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Reproducibility matters: intra- and inter-sample variation of the point-of-care circulating cathodic antigen test in twoPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Article
  4. Modelling diagnostics forOne health (Amsterdam, Netherlands) · 2022
    Article
  5. 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

5 authors.

Artemis KoukounariProduct Development Personalized Health Care, F. Hoffmann-La Roche Ltd., Welwyn Garden, United Kingdom.ORCID 0000-0001-5574-3934
Haziq JamilMathematical Sciences, Faculty of Science, Universiti Brunei Darussalam, Bandar Seri Begawan, Brunei.ORCID 0000-0003-3298-1010
Elena EroshevaDepartment of Statistics, School of Social Work, Center for Statistics and the Social Sciences, University of Washington, Seattle, Washington, United States of America.
Clive ShiffMolecular Microbiology and Immunology Department, John Hopkins Bloomberg School of Public Health.
Irini MoustakiDepartment of Statistics, London School of Economics and Political Science, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various global health initiatives are currently advocating the elimination of schistosomiasis within the next decade. Schistosomiasis is a highly debilitating tropical infectious disease with severe burden of morbidity and thus operational research accurately evaluating diagnostics that quantify the epidemic status for guiding effective strategies is essential. Latent class models (LCMs) have been generally considered in epidemiology and in particular in recent schistosomiasis diagnostic studies as a flexible tool for evaluating diagnostics because assessing the true infection status (via a gold standard) is not possible. However, within the biostatistics literature, classical LCM have already been criticised for real-life problems under violation of the conditional independence (CI) assumption and when applied to a small number of diagnostics (i.e. most often 3-5 diagnostic tests). Solutions of relaxing the CI assumption and accounting for zero-inflation, as well as collecting partial gold standard information, have been proposed, offering the potential for more robust model estimates. In the current article, we examined such approaches in the context of schistosomiasis via analysis of two real datasets and extensive simulation studies. Our main conclusions highlighted poor model fit in low prevalence settings and the necessity of collecting partial gold standard information in such settings in order to improve the accuracy and reduce bias of sensitivity and specificity estimates.

Indexed as

Models, StatisticalDiagnostic ErrorsDiagnostic Tests, RoutineHumansLatent Class AnalysisReference StandardsSchistosomiasisSensitivity and Specificity

Identifiers

PMID33539357
PMCPMC7888681

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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.