ReviewFrontiers in cardiovascular medicine2026
Therapeutical progress in sepsis-induced cardiomyopathy.
Review in Frontiers in cardiovascular medicine, 2026. 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.
- MicroRNA-223-3p/NLRP3 axis attenuates LPS-induced sepsis-like myocardial dysfunction by suppressing cardiomyocyte pyroptosis.Molecular biology reports · 2026Article
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
Sepsis-induced cardiomyopathy (SCM) is a life-threatening complication of severe sepsis with a high mortality rate. This review comprehensively explores SCM. It details the multifaceted pathogenesis, including inflammatory storm, mitochondrial dysfunction, abnormal calcium handling, complement activation, and emerging mechanisms related to exosomes and non-coding RNAs. We propose an integrated mechanistic model centered on the "energy metabolism-calcium handling" axis to explain the unique reversibility of SCM. Conventional treatments like antibiotic therapy, fluid management, and the use of vasopressors and inotropic agents are discussed, along with their limitations. Promising strategies such as repurposing old drugs, applying traditional Chinese medicine, and new approaches are presented. To bridge the gap between mechanistic understanding and clinical application, we categorize these emerging therapies according to the primary pathological pathway they target: inflammation, mitochondrial dysfunction, or calcium dysregulation. Furthermore, we introduce a framework for phenotype-guided treatment and critically evaluate the level of clinical evidence for each intervention. Small active molecules and nanomedicine also show potential in SCM treatment. Future research should focus on large-scale clinical trials to validate these therapies and integrate precision medicine strategies for better patient outcomes.
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Identifiers
What Socratic holds
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 Socratic graph.