ArticleJournal of cardiovascular translational research2025
Bayesian Reanalysis of Mortality Outcomes in Cardiovascular Trials: Addressing Limitations of Traditional Significance Testing.
Article in Journal of cardiovascular translational research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The American Statistical Association (ASA) has cautioned against overreliance on p-values, noting that rigid thresholds (e.g., p < 0.05) can obscure statistical uncertainty and clinical meaning. This study illustrates how Bayesian methods can enrich trial interpretation by estimating the probability of treatment benefit. We reanalyzed all-cause mortality outcomes from two randomized trials-EMPULSE (empagliflozin in acute heart failure) and DanGer Shock (microaxial flow pump in cardiogenic shock)-using Bayesian hierarchical random-effects models with reference and data-derived priors. For EMPULSE, posterior probabilities of mortality benefit were high (RR < 1: 90%-99%; RR < 0.85: 72%-86%). In DanGer Shock, they were lower and more uncertain (RR < 1: 76%-98%; RR < 0.85: 15%-72%). Although both trials had similar frequentist p-values (0.04 and 0.05), Bayesian analysis revealed differing levels of certainty. These results highlight the value of Bayesian approaches in providing more nuanced, decision-relevant insights, particularly when trial results lie near conventional significance thresholds.
Indexed as
Identifiers
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Registered trials
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.