Key result
Shorter TAVI wait times linked to ~76% lower 1-year mortality compared to longer waiting periods.
Why the study?
Despite advances in TAVI, patient outcomes remain variable and the combined effect of interacting risk factors remains challenging to predict.
Does clinical clustering based on presentation and risk factors predict outcomes in patients undergoing TAVI?
Cohort (n=300)
Does clinical clustering based on presentation and risk factors predict outcomes in patients undergoing TAVI?
TAVI patients with a higher symptomatic burden who undergo earlier intervention (shorter waiting period) have significantly better clinical outcomes than less symptomatic patients who experience longer delays.
Prompt says "challenges_consensus" but also it's observational (Level.
Introduction Despite advances in transcatheter aortic valve implantation (TAVI), patient outcomes remain variable due to the complex interplay of multiple risk factors. Although these factors are well-established predictors, the combined effect of their interactions on clinical outcomes remains challenging to predict. This study aims to stratify TAVI patients according to clinical and risk factor variables, identify distinct risk profile clusters, and examine their association with outcomes. Methods A retrospective analysis of 300 patients who underwent successful TAVI was conducted. A two-step cluster analysis was performed to group patients based on clinical presentation and risk factors. Two clusters were identified: Cluster 1 and Cluster 2. The primary endpoint included death at 30 days, stroke, and hospital readmission within one year. Baseline characteristics, procedural variables, and outcomes were compared between clusters. Results Among 300 TAVI patients, Cluster 1 (n=182) and Cluster 2 (n=32) exhibited similar age and gender distribution, with a mean age of 82±5 and 83±5 years (p=0.6) and females in 54% and 50% (p=0.7), respectively. Comorbidities such as diabetes, chronic kidney disease, and atrial fibrillation were comparable between groups (table 1). Yet, Cluster 1 had a higher prevalence of severe symptoms (NYHA class > 2 in 52% vs. 25%, p=0,005), previous hospitalization for aortic stenosis (28% vs. 3%, p=0.03), and significant mitral regurgitation (30% vs. 12%, p=0,05). Cluster 1 also exhibited a shorter waiting period (48 [24-72] vs. 93 [47-139], p=0,03), potentially reflecting prioritization based on disease presentation severity. Cluster 1 was associated with significantly better outcomes despite a higher symptomatic burden. Outcome analysis revealed that Cluster 2 was associated with worse outcomes, including higher 30-day and 1-year mortalities (12% vs. 2%, p<0.001 and 29% vs. 7%, p<0.001) and stroke (6% vs. 0.5%, p<0.01). Hospital readmission rates were also significantly higher in Cluster 2 (16% vs 0.5%, p<0.001). Symptomatic burden with hospitalization may result in an earlier TAVI, as a shorter waiting time is associated with better outcomes. Conclusion Multivariate clustering of clinical presentation and risk factors successfully identified two distinct clusters of profiles with divergent TAVI outcomes. Notably, despite having more symptomatic disease (as indicated by a higher NYHA class) and a history of hospitalization, patients were associated with better outcomes. The shorter waiting period highlights the potential benefit of earlier intervention for more symptomatic patients. In contrast, Cluster 2 patients experienced higher mortality, stroke, and hospital readmission rates, possibly reflecting the detrimental impact of delays. Earlier prioritization of symptomatic patients for TAVI could significantly improve clinical outcomes.Baseline characteristics Outcomes
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Almeida et al. (2025) conducted a cohort in Aortic stenosis (n=300). Cluster 1 (higher symptomatic burden, shorter waiting period) vs. Cluster 2 (longer waiting period) was evaluated on Death at 30 days, stroke, and hospital readmission within one year. TAVI patients in Cluster 1 (shorter waiting period) had significantly lower 1-year mortality (7% vs 29%, p<0.001) and stroke (0.5% vs 6%, p<0.01) compared to Cluster 2.
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