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

**Authors:** 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, Hindrik van der Werf, Yvonne Douglas, Dajiro Tomii, Thomas Pilgrim, Stephan Windecker, Adriaan Voors, Joanna Wykrzykowska

PMC · DOI: 10.1016/j.ahjo.2026.100735 · 2026-02-02

## TL;DR

This study uses machine learning to identify patients at high risk of both poor symptom improvement and adverse events after a heart valve procedure called TAVI.

## Contribution

The study introduces a new, externally validated machine learning model combining adverse events and symptom improvement after TAVI.

## Key findings

- 101 out of 827 patients experienced both adverse events and poor symptom improvement after TAVI.
- Predictors included COPD history, vitamin-K antagonist use, heart failure, and specific biomarker levels.
- The model showed reasonable accuracy with an AUC of 0.74 in internal validation and 0.66 in external validation.

## Abstract

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.

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.

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)).

Our externally validated model can reasonably identify patients with both poor symptom improvement and adverse events after TAVI.

Predictors for poor symptom improvement and adverse events one year post-TAVI. Main findings of this retrospective observational cohort study, showing predictors for no symptom improvement and adverse events one-year post-TAVI. AV P Mean: Aortic Valve Mean Gradient, COPD: Chronic Obstructive Pulmonary Disease, MRA: Mineralocorticoid Receptor Antagonist, LVOT: Left ventricular outflow tract, NT-proBNP: N-terminal pro-B-type natriuretic peptide, OR: Odds Ratio, Vit. K ant: vitamin K antagonist.Unlabelled Image

## Linked entities

- **Chemicals:** urea (PubChem CID 1176), sodium (PubChem CID 5360545)
- **Diseases:** aortic stenosis (MONDO:0042981), COPD (MONDO:0005002), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** heart failure (MESH:D006333), stroke (MESH:D020521), COPD (MESH:D029424)
- **Chemicals:** sodium (MESH:D012964), vitamin-K antagonist (-), urea (MESH:D014508)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12906061/full.md

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Source: https://tomesphere.com/paper/PMC12906061