ArticleERJ open research2026
Self-organising map clustering identifies high-risk clusters of post-acute mortality in a prospective multicentre study of community-acquired pneumonia.
Article in ERJ open research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02139163 (Epidemiological Study on Community Acquired Pneumonia), which is not on this map. Not yet cited in PubMed.
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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.
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.
Epidemiological Study on Community Acquired Pneumonia
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Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Community-acquired pneumonia (CAP) is a leading cause of morbidity and mortality. While tools predicting short-term prognosis exist, there is urgent need for the early identification of patients requiring close follow-up monitoring for post-acute mortality. We therefore conducted cluster analysis of baseline clinical data to investigate predictors of post-acute mortality in CAP. Methods: We analysed 7840 participants from the German CAPNETZ cohort, using self-organising map (SOM)-clustering and survival analyses. Random survival forest (RSF) models were used to identify key predictors of mortality, which were then analysed using time-dependent area under the curve and Cox proportional hazard regression models. Results: SOM-clustering based on 10 predictors identified 879 (12%, in four clusters) patients with high risk for post-acute (30-180 days) mortality. Across the cohort, age and urea were the most important predictors of post-acute mortality, while in the high-risk cohort, body mass index emerged as the strongest predictor, as identified by RSF modelling. In one high-risk cluster, there was an association with elevated platelet counts (HR: 1.13, 95% CI 1.03-1.21, p=0.01; increments of 40 platelets·nL Conclusion: Using 10 clinical predictors for post-acute mortality in CAP, predictive SOM-clustering revealed several high-risk subgroups, with heterogeneous biomarkers, suggestive of differences in the underlying pathophysiology (thrombocytes, urea, CRP). Adapting medical therapy to these high-risk subgroups may reduce post-acute mortality following CAP.
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Registered trials
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