Evidence map›Paper›PMID 38168296›Full record

ArticleResearch square2023

Machine learning algorithms using national registry data to predict loss to follow- up during tuberculosis treatment.

Moreno M S Rodrigues, Beatriz Barreto-Duarte, Caian L Vinhaes, Mariana Araújo-Pereira, Eduardo R Fukutani, Keityane Bone Bergamaschi, Afrânio Kristki, Marcelo Cordeiro-Santos, Valeria C Rolla, Timothy R Sterling and 2 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Moreno M S RodriguesFundação Oswaldo Cruz.
Beatriz Barreto-DuarteUniversidade Salvador.
Caian L VinhaesEscola Bahiana de Medicina e Saúde Pública.
Mariana Araújo-PereiraCentro Universitário Faculdade de Tecnologia e Ciências.
Eduardo R FukutaniInstituto Gonçalo Moniz, Fundação Oswaldo Cruz.
Keityane Bone BergamaschiFundação Oswaldo Cruz.
Afrânio KristkiUniversidade Federal do Rio de Janeiro.
Marcelo Cordeiro-SantosFundação Medicina Tropical Doutor Heitor Vieira Dourado.
Valeria C RollaInstituto Nacional de Infectologia Evandro Chagas.
Timothy R SterlingVanderbilt University School of Medicine.
Artur T L QueirozFundação Oswaldo Cruz.
Bruno B AndradeInstituto Gonçalo Moniz, Fundação Oswaldo Cruz.
Vanderbilt University · USFundação Oswaldo Cruz · BREscola Bahiana de Medicina e Saúde Pública · BRUniversidade Federal do Rio de Janeiro · BR

Funding

CCASAnet: Caribbean, Central and South America NetworkU01AI069923 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Pedro Enrique Cahn, Jessica L Castilho · 2006 to 2026
$41.6M
NIAID NIH HHS U01 AI069923
6 · The paper itself

Abstract

Background: Identifying patients at increased risk of loss to follow-up (LTFU) is key to developing strategies to optimize the clinical management of tuberculosis (TB). The use of national registry data in prediction models may be a useful tool to inform healthcare workers about risk of LTFU. Here we developed a score to predict the risk of LTFU during anti-TB treatment (ATT) in a nationwide cohort of cases using clinical data reported to the Brazilian Notifiable Disease Information System (SINAN). Methods: We performed a retrospective study of all TB cases reported to SINAN between 2015-2022; excluding children (<18 years-old), vulnerable groups or drug-resistant TB. For the score, data before treatment initiation were used. We trained and internally validated three different prediction scoring systems, based on Logistic Regression, Random Forest, and Light Gradient Boosting. Before applying our models we split our data into train (~80% data) and test (~20%), and then we compare model metrics using a test data set. Results: Of the 243,726 cases included, 41,373 experienced LTFU whereas 202,353 were successfully treated and cured. The groups were different with regards to several clinical and sociodemographic characteristics. The directly observed treatment (DOT) was unbalanced between the groups with lower prevalence in those who were LTFU. Three models were developed to predict LTFU using 8 features (prior TB, drug use, age, sex, HIV infection and schooling level) with different score composition approaches. Those prediction scoring system exhibited an area under the curve (AUC) ranging between 0.71 and 0.72. The Light Gradient Boosting technique resulted in the best prediction performance, weighting specificity, and sensibility. A user-friendly web calculator app was created (https://tbprediction.herokuapp.com/) to facilitate implementation. Conclusions: Our nationwide risk score predicts the risk of LTFU during ATT in Brazilian adults prior to treatment commencement. This is a potential tool to assist in decision-making strategies to guide resource allocation, DOT indications, and improve TB treatment adherence.

Indexed as

loss to follow-upmachine learningscore predictiontuberculosis

Identifiers

PMID38168296
PMCPMC10760311
OpenAlexW4389540855

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.