Evidence map›Paper›PMID 41694544›Full record

ArticleAmerican heart journal plus : cardiology research and practice2026

Identification of patients at risk for adverse events and poor symptom improvement after transcatheter aortic valve implantation.

Kees van Bergeijk, Constantijn Stijn Venema, Bob Ophuis, Luca Plekkenpol, Mara Tomei, Hayman Al-Barwary, Jasper Tromp, Yoran Hummel, Wouter Ouwerkerk, Ad van den Heuvel and 7 more

Abstract read
In one paragraph

Article in American heart journal plus : cardiology research and practice, 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

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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.

No citing paper in PubMed yet.

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

17 authors.

Kees van BergeijkDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Constantijn Stijn VenemaDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Bob OphuisDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Luca PlekkenpolDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Mara TomeiDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Hayman Al-BarwaryDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Jasper TrompDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Yoran HummelUs2.ai, Singapore, Singapore.
Wouter OuwerkerkDepartment of Dermatology, University of Amsterdam Medical Centre, Amsterdam, Netherlands.
Ad van den HeuvelDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Hindrik van der WerfDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Yvonne DouglasDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Dajiro TomiiDepartment of Cardiology, Inselspital, University of Bern, Bern, Switzerland.
Thomas PilgrimDepartment of Cardiology, Inselspital, University of Bern, Bern, Switzerland.
Stephan WindeckerDepartment of Cardiology, Inselspital, University of Bern, Bern, Switzerland.
Adriaan VoorsDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Joanna WykrzykowskaDepartment of Cardiology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Transcatheter aortic valve implantation (TAVI) aims to improve symptoms and prognosis, while minimising adverse outcomes. Available prediction models focus on individual outcomes, but those combining adverse events and symptom improvement in a single prediction model are scarce, and include only few variables and lack external validation. Using machine learning, we developed a clinically relevant model to identify patients at high risk of both adverse events and poor symptom improvement after TAVI. Methods: In total, 72 candidate variables including clinical, medication use, biomarkers and (AI-derived) echocardiographic parameters were collected in patients with severe symptomatic AS undergoing TAVI. The primary outcome was a combination of poor symptom improvement (NYHA compared with baseline) and a composite of cardiovascular mortality, stroke or heart failure hospitalisation) at one year follow-up. LASSO Logistic regression was used for variable selection. External validation was performed in the Bern TAVI-registry. Results: From a total of 827 patients (age 79.2 (± 7.29), 53% female), 101 patients (12%) had both adverse events and poor symptom improvement during one-year follow-up after TAVI, while 529 (64%) improved without any adverse events. Predictors for the combined primary outcome were history of COPD, use of vitamin-K antagonist, concomitant heart failure, reflected by mineralocorticoid receptor antagonists use, lower sodium and higher urea and (log-)NT-proBNP levels, lower AV mean gradient and larger LVOT diameter (area under the curve (AUC): 0.74 (internal validation: 0.72 and external validation: 0.66)). Conclusion: Our externally validated model can reasonably identify patients with both poor symptom improvement and adverse events after TAVI.

Indexed as

Adverse outcomesAI derived parametersEchocardiographySymptomsTAVI

Identifiers

PMID41694544
PMCPMC12906061

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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.