Evidence map›Paper›PMID 42482842›Full record

ArticleTransplantation direct2026

Primary Graft Dysfunction After Lung Transplantation: A Temporal Classification and Machine Learning Clustering.

Balin Özsoy, Bieke Vercauteren, Jan Van Slambrouck, Cedric Vanluyten, Annalisa Barbarossa, Xin Jin, Dirk E Van Raemdonck, Julia Dmitrieva, Anwar Khan, Xander Jacquemyn and 7 more

Abstract read
In one paragraph

Article in Transplantation direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Balin ÖzsoyDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-3976-2286
Bieke VercauterenLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Jan Van SlambrouckDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Cedric VanluytenDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Annalisa BarbarossaDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Xin JinDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Dirk E Van RaemdonckDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Julia DmitrievaLaboratory of Angiogenesis and Vascular Metabolism, Department of Oncology, Center for Cancer Biology, VIB, KU Leuven, Leuven, Belgium.
Anwar KhanLaboratory of Angiogenesis and Vascular Metabolism, Department of Oncology, Center for Cancer Biology, VIB, KU Leuven, Leuven, Belgium.
Xander JacquemynDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Saskia BosLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Robin VosLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Bart N VanaudenaerdeLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Marianne S CarlonLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Jean-Marie AertsDivision Animal and Human Health Engineering, Department of Biosystems, KU Leuven, Leuven, Belgium.
Peter CarmelietLaboratory of Angiogenesis and Vascular Metabolism, Department of Oncology, Center for Cancer Biology, VIB, KU Leuven, Leuven, Belgium.
Laurens J CeulemansDepartment of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-4261-7100

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Primary graft dysfunction (PGD) is a major cause of morbidity and mortality after lung transplantation (LTx). PGD is graded at static time points, limiting insight into its temporal dynamics. Statistical risk-factor analysis may overlook the multifactorial complexity of PGD. Machine learning (ML) may address this but is constrained by small sample sizes. We aim to introduce a temporal PGD classification, perform ML-based clustering and overcome sample-size limitations by generating synthetic patient data. Methods: A prospectively collected database of 794 LTx at University Hospitals Leuven (Belgium) from January 2012 to November 2023 was analyzed. Recipients were classified into 4 temporal PGD phenotypes: no, early, late, and persistent PGD. Unsupervised ensemble Results: Six hundred ninety primary double LTx cases were included. Temporal PGD phenotypes showed significantly different 5-y survival (log-rank test: Conclusions: This study demonstrates the potential of temporal PGD classification to better understand how the dynamic character of PGD affects survival. ML techniques, including unsupervised clustering and synthetic data generation, could be promising strategies to unravel complex interactions between clinical factors and overcome sample-size limitations.

Identifiers

PMID42482842
PMCPMC13387764

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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.