ArticleNature communications2026
Compliance modulation of a soft robotic atrioventricular model of heart failure with preserved ejection fraction.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Heart failure with preserved ejection fraction (HFpEF) is a common yet highly complex form of heart failure (HF). A major challenge in obtaining market approval for medical devices targeting HFpEF treatment is the absence of highly controllable testing models. This work introduces an in-vitro, biomimetic, left-heart, atrioventricular simulator, with a closed-loop control system designed to model HFpEF disease progression. While at proof-of-concept stage, its unique capabilities show promise for higher-dimensional modeling than existing models. The simulator employs artificial muscle fibers which are highly controllable on their relaxation stroke. Its goal-oriented control system enables compliance modulation of the artificial myocardium during diastole. By setting hemodynamic targets, the myocardium dynamically responds, replicating the biomechanics of HFpEF progression. The model effectively recreates key hallmarks of HFpEF phenotypes, including impaired relaxation, pericardial restraint, and increased ventricular stiffness, capturing both hemodynamic and biomechanic aspects of the disease. Its capability is further validated, simulating mechanical circulatory support for HFpEF treatment. While more work is needed to demonstrate clinical application through control system development, actuation speed improvements, and further clinical validation, this work shows promise as a powerful tool for device development and pathophysiological studies, advancing our understanding and treatment of heart diseases.
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.