ReviewFrontiers in cardiovascular medicine2026
Federated learning for cardiovascular disease prediction: a systematic review of clinical applications, validation, and translation readiness.
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 2 papers.
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
2 citing papers in PubMed.
- Artificial Intelligence for Precision Antiarrhythmic Drug Therapy in Atrial Fibrillation: From Recurrence Prediction to Comparative Treatment Selection.Medicina (Kaunas, Lithuania) · 2026Review
- AI-Driven Atrial Fibrillation Management: From Signal to Strategy.Balkan medical journal · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Data silos and privacy constraints limit the centralized development of machine learning models for cardiovascular disease. Federated learning enables multi-institutional training without sharing raw patient records, but the evidence base in cardiology and deployment-grade evaluation remains uneven. Objective: To synthesize how federated learning has been implemented for cardiovascular disease prediction and to identify factors that determine clinical translation readiness, including heterogeneity handling, validation quality, privacy and security safeguards, and operational feasibility. Methods: A systematic literature review was conducted in PubMed, Web of Science, and IEEE Xplore, with supplementary searches in arXiv and Google Scholar, covering studies published from January 2022 through December 2025. Studies applying federated learning to clinically meaningful cardiovascular disease prediction tasks were included. We extracted data on clinical tasks, modalities, federation types, training strategies, evaluation designs, and deployment considerations, and synthesized the findings qualitatively. Results: Twenty-two studies were included, spanning early screening, clinical diagnosis, prognostic evaluation, and emerging treatment-related decision-support applications. Modalities included electronic health records, electrocardiograms, phonocardiograms, echocardiography, cardiac imaging, and wearable data. Most studies used horizontal federated learning with FedAvg baselines, with variants targeting non-IID heterogeneity, personalization, and efficiency. Some studies reported that FL performance approached centralized training or exceeded local baselines. However, the evidence base was predominantly retrospective and frequently relied on public datasets or simulated client splits, while reporting of held-out-site validation, calibration, subgroup performance, privacy safeguards, robustness, and system costs was inconsistent. Conclusion: Federated learning is a promising paradigm for privacy-preserving, multi-institutional cardiovascular disease prediction, yet the evidence remains mainly retrospective, with heterogeneous validation and limited deployment-grade reporting. This review synthesizes task, modality, federation design, and operational constraints, and highlights adoption priorities: held-out-site and external validation with calibration and subgroup fairness monitoring, communication-efficient personalization under drift, auditable privacy and security safeguards, and clinical-grade MLOps for monitoring, rollback, and continual updating.
Indexed as
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.