Evidence map›Paper›PMID 38774373›Full record

ArticleEuropean heart journal. Digital health2024

Predicting multifaceted risks using machine learning in atrial fibrillation: insights from GLORIA-AF study.

Juan Lu, Arnaud Bisson, Mohammed Bennamoun, Yalin Zheng, Frank M Sanfilippo, Joseph Hung, Tom Briffa, Brendan McQuillan, Jonathon Stewart, Gemma Figtree and 3 more

Abstract read
In one paragraph

Article in European heart journal. Digital health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Artificial intelligence in clinical thrombosis and hemostasis: A review.Research and practice in thrombosis and haemostasis · 2025
    Review
  7. Review
  8. Article
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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

13 authors.

Juan LuLiverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Thomas Drive, Liverpool L14 3PE, UK.ORCID https://orcid.org/0000-0002-7508-0565
Arnaud BissonLiverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Thomas Drive, Liverpool L14 3PE, UK.
Mohammed BennamounHarry Perkins Institute of Medical Research, 5 Robin Warren Dr, Murdoch WA 6150, Australia.
Yalin ZhengLiverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Thomas Drive, Liverpool L14 3PE, UK.
Frank M SanfilippoSchool of Population and Global Health, The University of Western Australia, Perth, Australia.ORCID https://orcid.org/0000-0003-3639-0787
Joseph HungMedical School, The University of Western Australia, 35 Stirling Hwy, Crawley WA 6009, Australia.ORCID https://orcid.org/0000-0002-4468-6097
Tom BriffaSchool of Population and Global Health, The University of Western Australia, Perth, Australia.
Brendan McQuillanMedical School, The University of Western Australia, 35 Stirling Hwy, Crawley WA 6009, Australia.
Jonathon StewartMedical School, The University of Western Australia, 35 Stirling Hwy, Crawley WA 6009, Australia.
Gemma FigtreeKolling Institute and Charles Perkins Centre, University of Sydney, Sydney, Australia.
Menno V HuismanDepartment of Thrombosis and Hemostasis Leiden University Medical Center, Leiden, The Netherlands.
Girish DwivediMedical School, The University of Western Australia, 35 Stirling Hwy, Crawley WA 6009, Australia.ORCID https://orcid.org/0000-0003-0717-740X
Gregory Y H LipLiverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Thomas Drive, Liverpool L14 3PE, UK.ORCID https://orcid.org/0000-0002-7566-1626

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims: Patients with atrial fibrillation (AF) have a higher risk of ischaemic stroke and death. While anticoagulants are effective at reducing these risks, they increase the risk of bleeding. Current clinical risk scores only perform modestly in predicting adverse outcomes, especially for the outcome of death. We aimed to test the multi-label gradient boosting decision tree (ML-GBDT) model in predicting risks for adverse outcomes in a prospective global AF registry. Methods and results: We studied patients from phase II/III of the Global Registry on Long-Term Oral Anti-Thrombotic Treatment in Patients with Atrial Fibrillation registry between 2011 and 2020. The outcomes were all-cause death, ischaemic stroke, and major bleeding within 1 year following the AF. We trained the ML-GBDT model and compared its discrimination with the clinical scores in predicting patient outcomes. A total of 25 656 patients were included [mean age 70.3 years (SD 10.3); 44.8% female]. Within 1 year after AF, ischaemic stroke occurred in 215 (0.8%), major bleeding in 405 (1.6%), and death in 897 (3.5%) patients. Our model achieved an optimized area under the curve in predicting death (0.785, 95% CI: 0.757-0.813) compared with the Charlson Comorbidity Index (0.747, Conclusion: The ML-GBDT model outperformed clinical risk scores in predicting the risks in patients with AF. This approach could be used as a single multifaceted holistic tool to optimize patient risk assessment and mitigate adverse outcomes when managing AF.

Indexed as

Atrial fibrillationDeathIschaemic strokeMachine learningMajor bleedingRisk

Identifiers

PMID38774373
PMCPMC11104470

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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.