Artificial intelligence in cardiology in the current era: a narrative review
Review Article

Artificial intelligence in cardiology in the current era: a narrative review

Avilash Mondal1, Harshith Thyagaturu1, Sahas Reddy Jitta2, Binita Bhandari1, Emmett Helsel3, Megha Dogra4, Kesar Prajapati5, Karthik Gonuguntla6

1Department of Cardiology, West Virginia University, Morgantown, WV, USA; 2Department of Internal Medicine, Mercy Hospital St. Louis, St. Louis, MO, USA; 3Department of Internal Medicine, West Virginia University, Morgantown, WV, USA; 4Department of Internal Medicine, Portsmouth Regional Hospital, Portsmouth, NY, USA; 5Department of Internal Medicine, Metropolitan Hospital Center, New York, NY, USA; 6Department of Cardiology, Hartford Hospital, Norwich, CT, USA

Contributions: (I) Conception and design: A Mondal, H Thyagaturu, K Gonuguntla; (II) Administrative support: H Thyagaturu, K Gonuguntla, A Mondal; (III) Provision of study materials or patients: H Thyagaturu, A Mondal, E Helsel, M Dogra, K Prajapati; (IV) Collection and assembly of data: A Mondal, H Thyagaturu, K Gonuguntla, SR Jitta, B Bhandari; (V) Data analysis and interpretation: A Mondal, H Thyagaturu, K Gonuguntla; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Karthik Gonuguntla, MD. Department of Cardiology, Hartford Hospital, 80 Seymour Street, Hartford, CT 06102, USA. Email: karthikg75@gmail.com.

Background and Objective: Artificial intelligence (AI) has transformed cardiovascular healthcare by influencing multimodal imaging, interventional procedures, and remote patient monitoring systems. The rapid growth of available evidence presents challenges for researchers to evaluate the quality of AI systems and their readiness for clinical application. The review examines current AI uses in cardiology by assessing methodological quality to pinpoint key factors for implementing effective AI models.

Methods: We performed extensive search on MEDLINE/PubMed, Web of Science, Scopus, EMBASE for original research, clinical trials, and consensus/guideline statements, published in English from January 2015 through December 2025.

Key Content and Findings: AI applied to electrocardiography (AI-ECG) technology shows practical success in clinical trials for detecting left ventricular systolic dysfunction (LVSD) and predicting atrial fibrillation (AF) from normal heart rhythms. AI in echocardiography performs automated view detection, chamber measurement, and assists novice users. Cardiac magnetic resonance (CMR) uses deep learning (DL) for reconstruction and inline perfusion analysis. Coronary computed tomography angiography (CCTA) employs automated coronary artery calcium (CAC)/plaque analysis and machine learning (ML)-based fractional flow reserve computed tomography (FFRct), while nuclear cardiology uses AI to reduce doses and enhance image quality. The cath lab benefits from AI-assisted intravascular imaging, which helps optimize percutaneous coronary intervention (PCI) planning, robotics systems that lower operator radiation exposure, and angiography-derived physiology [e.g., quantitative flow ratio (QFR)], enabling wire-free ischemia assessment with context-dependent value. Challenges to AI adoption include limited external validation data, unclear calibration methods, and gaps in addressing subgroup fairness, decision impact, and post-deployment performance monitoring.

Conclusions: AI technology has advanced from experimental development to practical solutions for specific cardiology procedures that improve operational efficiency and standardization. Turning accuracy into patient benefits requires researchers to conduct external validation studies, prospective impact assessments, cost-effectiveness evaluations, equity-focused design, workflow integration, and ongoing governance systems. Implementing AI as an assistive tool will enhance healthcare accessibility, reduce unnecessary treatment disparities, and improve outcomes through clinical support, while automation continues to streamline routine tasks.

Keywords: Machine learning (ML); convolutional neural network (CNN); arrhythmia; smartwatch; risk stratification


Submitted Sep 16, 2025. Accepted for publication Feb 28, 2026. Published online Apr 21, 2026.

doi: 10.21037/cdt-2025-510


Introduction

Background

Cardiovascular disease remains a leading cause of morbidity and mortality worldwide, accounting for an estimated 17.9 million deaths annually, or about 31% of all global deaths (1). The increasing volume of cardiovascular encounters generates large repositories of structured and unstructured data within electronic health records (EHRs), imaging archives, and wearable/device streams, enabling data-driven model development and validation. In recent years, artificial intelligence (AI) has emerged as a transformative tool in cardiology, capable of analyzing vast amounts of data with speed and precision, often achieving similar rates of diagnosis as board‐certified cardiologists (2). AI algorithms, especially those based on machine learning (ML), can uncover subtle patterns in echocardiograms, electrocardiograms (ECGs), and radiographic images that might elude human experts.

In our manuscript, AI is an umbrella term describing computational systems that perform tasks typically requiring human intelligence, including perception, pattern recognition, prediction, and language understanding. ML is a subset of AI in which algorithms learn statistical patterns from data to make predictions or classifications without being explicitly rule-programmed. Deep learning (DL) is a subset of ML that uses multi-layer neural networks [e.g., convolutional neural networks (CNNs) and transformer architectures] to learn hierarchical representations directly from raw inputs such as waveforms, images, and text. In cardiovascular medicine, most “traditional” AI applications have been discriminative (e.g., detecting disease or predicting outcomes), whereas the current era increasingly includes generative and foundation-model approaches that can synthesize text or structured outputs, integrate multimodal inputs, and support clinical reasoning tasks, introducing new benefits and new safety risks.

By leveraging AI, cardiology benefits from earlier disease detection, more accurate diagnoses, and personalized treatment strategies that were previously unattainable with conventional methods. It is also important to distinguish between automation and AI. Automation refers to technologies that perform tasks based on explicit, pre-programmed rules, such as robotic systems or scripted workflows. AI, particularly ML and DL, describes systems that learn from data, adapt to new scenarios, and make predictions or decisions beyond fixed rules. Throughout this review, we will clarify which technologies are rule-based automation and which are true Al- driven interventions.

Rationale and knowledge gap

One of the most desirable benefits of using AI is that it decreases workload and increases efficiency in a fast-paced clinical environment. Advanced algorithms allow for automated execution of complex procedures, including magnetic resonance imaging (MRI)-based ejection fraction (EF) and volumetric measurements, as well as real-time hospital telemetry data screening. A recent meta-analysis demonstrated that AI assistance in medical image interpretation reduces reading time by 27%, according to the study (3). Integrating AI predictive models with various data sources, such as physical exam results, auscultation findings, multimodal imaging, lab results, and genomic information, improves patient risk stratification over current risk scores. Essentially, AI offers an efficient solution for cardiology to handle increasing healthcare data while supporting precision medicine initiatives.

Despite the enthusiasm, it is essential to acknowledge that most AI tools in cardiology are still in early stages of clinical adoption (4). The deployment of such methods still faces significant challenges because of inadequate data quality and biased algorithms, as well as the process of getting regulatory approval for use in the real world. Successful translation requires multidisciplinary collaboration among clinical cardiologists, data scientists, and engineers.

Prior reviews have summarized broad applications of AI across cardiology, including electrocardiography, imaging, and EHR-based prediction, and have emphasized recurring limitations such as dataset shift, limited external validation, and uncertain clinical impact (5-8). In contrast, our review centers on practical clinical translation: explicitly distinguishing automation from AI, mapping evidence tiers (internal vs. multisite validation and retrospective performance vs. prospective utility), and highlighting workflow-facing paradigms (generative AI, foundation and multimodal models, privacy-preserving learning, and evolving regulatory expectations) that are likely to determine real-world adoption.

For clarity, this review distinguishes between rule-based automation (deterministic “if-then” logic and traditional decision rules) and data-driven AI, including ML and DL models that learn patterns from data. These categories differ in how they are developed, validated, monitored, and regulated; we use “automation” for rule-based tools and “AI” for data-trained models unless otherwise specified.

Objective

The current literature on AI implementation continues to expand rapidly. The available evidence from real-world applications is limited, and external validation results show considerable variability. Our narrative review examines how AI technology functions in cardiology through its uses in multimodality imaging, ECG/waveforms, EHR risk modeling, and remote monitoring devices. We present this article in accordance with the Narrative Review reporting checklist (available at https://cdt.amegroups.com/article/view/10.21037/cdt-2025-510/rc).


Methods

The authors analyzed AI applications in cardiology through five categories which included multimodality imaging techniques [cardiac computed tomography (CT), cardiac magnetic resonance (CMR), nuclear imaging], ECG/telemetry waveform analysis, and various risk prediction models from EHR data, wearable devices, coronary angiography with percutaneous coronary intervention (PCI) procedures and robotic systems.

The research team conducted database searches through MEDLINE/PubMed, Web of Science, Scopus, EMBASE for studies published between January 1, 2015, and December 21, 2025. The search strategy used both controlled vocabulary terms and free-text words to find studies on AI and ML/DL in cardiology fields [ECG, echocardiography, CMR, coronary computed tomography angiography (CCTA), fractional flow reserve computed tomography (FFRct)/quantitative flow ratio (QFR), and robotics] and their related outcomes (diagnosis, prognosis, and workflow). The researchers performed manual reference list searches for key reviews, major society statements [American College of Cardiology (ACC)/American Heart Association (AHA)/European Society of Cardiology (ESC)/Society for Cardiovascular Magnetic Resonance (SCMR)/Society of Cardiovascular Computed Tomography (SCCT)], and relevant regulatory communications (Table 1). Study selection is summarized in a PRISMA-style flow diagram (Figure 1).

Table 1

Literature search strategy and study selection process

Items Specification
Date of search Last comprehensive search conducted: 21 December 2025
Databases and other sources searched MEDLINE/PubMed, EMBASE, Web of Science, Scopus. Supplemental sources for context and cross-checking: major professional society sites (ACC/AHA/ESC/SCMR/SCCT) and select regulatory communications (e.g., FDA device summaries). Reference lists of included studies and recent high-impact reviews were hand-searched
Search terms used Combined MeSH and free-text terms. Core AI terms: “Artificial Intelligence”[MeSH], “Machine Learning”[MeSH], “Deep Learning”[MeSH], transformer*, “neural network*”, “foundation model*” “large language model”, “LLM”, “generative Al”, “GPT”, “vision-language model”, “self- supervised”, “multimodal”, “federated learning”, “synthetic data”, and “digital twin”. Cardiology terms: “Cardiovascular Diseases”[MeSH], cardiology, cardiovascular, “Electrocardiography”[MeSH] (ECG/EKG), “Echocardiography”[MeSH], “Magnetic Resonance Imaging”[MeSH] (CMR), “Tomography, X-ray Computed”[MeSH] (CCTA), CAD-RADS, FFRct, QFR, OFR, nuclear cardiology, “Tomography, Emission-Computed, Single-Photon”[MeSH] (SPECT), “Positron-Emission Tomography”[MeSH] (PET), wearable*, “Photoplethysmography” (PPG), smartwatch, risk prediction, risk stratification, remote monitoring, interventional cardiology, PCI, angiography, robotics. Filters applied where available: humans, English, publication year 2015–2025
Timeframe Publications from 1 January 2015 to 21 December 2025 (deep-learning era to present). Earlier seminal works were included only if directly foundational to current clinical implementation
Inclusion and exclusion criteria Inclusion: human studies applying AI/ML/DL to cardiology tasks; prospective/retrospective cohorts with temporal or external validation; randomized/non-randomized trials; rigorous reader studies; implementation/decision-impact evaluations; health-technology assessments; consensus/guideline statements with direct relevance to clinical deployment; English language
Exclusion: case reports; n<50 without compelling novelty; simulation-only or purely technical studies lacking clinical application; animal/in-vitro work; non-English articles
Selection process Two reviewers independently screened titles/abstracts and full texts against prespecified criteria; duplicates removed prior to screening. Disagreements were resolved by consensus; a senior author adjudicated unresolved conflicts. Reasons for full-text exclusion were recorded. Study selection is summarized in a PRISMA-style flow diagram (Figure 1)
Additional considerations Appraisal frameworks used: Data extraction captured discrimination (AUC, sensitivity, specificity), calibration (slope/intercept or plots), decision-curve/net benefit, workflow metrics (time, radiation/contrast), patient outcomes (where available), and subgroup/fairness analyses (sex, age, race/ethnicity). No automation tools were used for screening or data extraction. Ethics approval was not required (no individual-level data used)

ACC, American College of Cardiology; AHA, American Heart Association; AI, artificial intelligence; AUC, area under the curve; CAD-RADS, Coronary Artery Disease Reporting and Data System; CCTA, coronary computed tomography angiography; CMR, cardiac magnetic resonance; DL, deep learning; ECG, electrocardiogram; EKG, electrocardiogram; ESC, European Society of Cardiology; FDA, U.S. Food and Drug Administration; FFRct, fractional flow reserve computed tomography; GPT, Generative Pre-trained Transformer; LLM, large language model; ML, machine learning; OFR, optical flow ratio; PCI, percutaneous coronary intervention; PET, positron emission tomography; PPG, photoplethysmography; QFR, quantitative flow ratio; SCCT, Society of Cardiovascular Computed Tomography; SCMR, Society for Cardiovascular Magnetic Resonance; SPECT, single-photon emission computed tomography.

Figure 1 PRISMA flow diagram of the literature search and study selection. Records were identified through database searching and supplemental hand-searching. After deduplication, titles/abstracts were screened and full texts assessed for relevance to cardiology-focused automation and AI applications. Studies were included in the narrative synthesis if they addressed clinically relevant cardiovascular use cases with sufficient methodological detail to support interpretation. AI, artificial intelligence.

The study involved human cardiology research that used AI, ML, and DL methods, including prospective and retrospective cohort designs, randomized and non-randomized trials, reader studies, implementation, decision-impact research, consensus, and guidance documents. It excluded reports with fewer than 50 participants unless they provided significant new information, as well as studies that relied solely on simulations, focused on technical aspects without clinical value, or involved animal or in vitro research. Non-English language content was also excluded.

Two researchers (A.M. and B.B.) independently evaluated titles, abstracts, and full texts before a third reviewer (H.T.) settled any disagreements. The researchers used a standardized form to extract information about study settings and participant demographics, data sources, reference standards, model types, validation approaches, performance metrics, workflow data, clinical results, fairness assessments, and funding sources.

We did not perform a formal risk-of-bias scoring or checklist-based reporting-quality appraisal, consistent with the scope of a structured narrative review. Instead, during extraction we recorded a focused set of methodological characteristics relevant to clinical translation, including study design, data source and reference standard, and whether studies evaluated workflow metrics or patient outcomes. We also noted recurrent limitations that affect real-world reliability, including data leakage, spectrum bias, missing data handling, limited external validation, and absent calibration or subgroup reporting. Ethics approval was not required because no individual-level patient data were used.


Clinical applications of AI in cardiology

In this section, we will explore in detail how AI is transforming various fields within cardiology, examining the diverse ways in which AI and ML are being applied to imaging, diagnostics, risk modeling, and patient monitoring. Table 2 summarizes the difference between rule-based automation and AI/ML approaches across cardiology domains.

Table 2

Critical appraisal of evidence maturity and validation considerations across major AI applications in cardiology

Domain/modality Representative clinical tasks Common model types Evidence maturity/validation highlights Common limitations/implementation gaps
Auscultation/heart sounds Murmur detection; valvular disease screening; triage for LV dysfunction CNN/ML on phonocardiograms (often with feature engineering) Predominantly retrospective development and internal validation; limited prospective workflow evaluation (8-11) Signal noise; device heterogeneity; labeling variability; limited multi-site external validation
ECG Arrhythmia detection; LV dysfunction screening; electrolyte/systemic state prediction; AF risk CNNs; emerging transformer-based ECG models Mostly retrospective; some pragmatic/cluster-randomized evaluation (e.g., EAGLE) (12-16) Dataset shift by vendor/lead set; calibration; alert fatigue; bias and fairness across subgroups
Echocardiography View classification; chamber quantification; EF/strain estimation; valvular assessment CNNs for video; segmentation networks; automated measurement pipelines Large datasets; increasing real-time guidance/automation studies; variable external validation (17-24) Image quality dependence; operator technique; vendor/domain shift; limited prospective outcome evidence
Nuclear cardiology (SPECT/PET) Attenuation correction; perfusion defect detection; risk stratification CNNs/DL reconstruction and classification Primarily retrospective imaging validation; fewer prospective clinical utility studies (25-31) Protocol heterogeneity; ground-truth definition; generalizability across scanners and sites
CMR Segmentation; mapping/QC support; accelerated cine acquisition and reconstruction DL reconstruction; segmentation/quantification networks Growing prospective feasibility reports for DL-accelerated cine; mixed external validation (32-37) Scanner/sequence variability; artifact sensitivity; need for human oversight and QA
CCTA Stenosis/plaque characterization; calcium scoring; physiology surrogates CNN/transformer vision models; segmentation + classification Multi-center datasets exist; validation varies by task; selective prospective evaluation (38-47) Calcium blooming; motion/noise; domain shift; need clinically meaningful endpoints beyond AUC
Wearables & remote monitoring AF detection; rhythm screening; physiologic trend monitoring; decompensation signals ML on PPG/ECG; anomaly detection; time-series models Large-scale consumer/real-world datasets; variable clinical confirmation (48-57) False positives; adherence; equity/representation; unclear downstream workflow and reimbursement
Heart failure Phenotyping; hospitalization risk; decompensation prediction; therapy response support EHR-based ML; multimodal (ECG/imaging + EHR) Mostly observational/retrospective; external validation inconsistent (58-61) Confounding; label leakage; portability; limited prospective impact on outcomes
Arrhythmia subspecialty AF phenotype; QT/drug safety prediction; VT/VF risk Deep nets on ECG; multimodal approaches Large retrospective datasets; limited prospective decision-impact evidence (13,62-66) Generalization across devices/populations; interpretability needs; clinical actionability thresholds
Interventional/angiography/robotics Angiographic assessment; procedural guidance; robotic PCI workflow Computer vision + ML; robotic assistance (often automation-driven) Registries and early trials; evolving evidence base (67-79) Cost and training; integration burden; distinction between automation vs. ML-driven guidance; safety monitoring
Risk prediction & stratification (cross-domain) ACS risk; outcomes prediction; population screening; multimodal risk models Gradient boosting/ML; deep models; multimodal fusion Performance often reported as AUC; need calibration and prospective evaluation (80-88) Overreliance on AUC; limited reporting of absolute risk/CI; drift; governance and monitoring requirements

ACS, acute coronary syndrome; AF, atrial fibrillation; AI, artificial intelligence; AUC, area under the curve; CCTA, coronary computed tomography angiography; CI, confidence interval; CMR, cardiac magnetic resonance; CNN, convolutional neural network; DL, deep learning; EAGLE, ECG AI-guided screening for low ejection fraction; ECG, electrocardiography; EF, ejection fraction; EHR, electronic health record; LV, left ventricle/left ventricular; ML, machine learning; PCI, percutaneous coronary intervention; PET, positron emission tomography; PPG, photoplethysmography; QA, quality assurance; QC, quality control; QT, Q-T interval; SPECT, single-photon emission computed tomography; VF, ventricular fibrillation; VT, ventricular tachycardia.

AI-assisted auscultation

Auscultation is one of the oldest, most commonly used, and highly respected clinical skills in medical diagnosis, especially in cardiovascular medicine. However, despite being a fundamental part of clinical management, it is highly subject to inter-user variability and poor reproducibility (9). A study evaluating 400 residents in training from internal medicine and family practice revealed a disturbingly low identification rate for the most important and commonly encountered cardiac events (9). ML and DL techniques, such as CNN and classifier-trained methods like AdaBoost, are now being used to assist with auscultation, helping to reduce errors and improve accuracy and consistency. First, the stethoscope records the sounds, then undergoes preprocessing and segments sections of the cardiac cycle. It then uses feature extraction and combines classifier training techniques and CNNs to distinguish between normal and abnormal heart sounds (10). Thompson et al. showed that an AI-based murmur detection system achieved a sensitivity of 87% and specificity of 89% detecting heart murmurs almost as accurately as cardiologists, based on results confirmed by the echocardiograms, highlighting its use as a triage tool (11).

However, there are still some challenges. One disadvantage of AI systems stems from their need for a vast amount of audio data that spans multiple patient demographics for proper operation. The current datasets contain insufficient diversity regarding patient demographics and environmental settings, which restricts the models’ ability to generalize their results. The diagnostic performance of AI tools shows significant differences because researchers used different validation approaches and external validation methods according to a systematic review and meta-analysis (89).

Evidence quality and limitations: most AI-auscultation evidence remains derived from retrospective datasets with limited standardization of recording hardware and labeling, which can reduce generalizability across environments and patient groups. Prospective workflow studies and multi-site external validation are still limited; therefore, reported accuracy may not translate directly to bedside performance. Future work should prioritize diverse external validation, calibration, and integration with complementary signals (ECG/echo) to improve clinical actionability (8-10).

AI in ECG

DL has transformed the ECG from a traditional, rule-based diagnostic tool into a comprehensive predictive biosignature. Early landmark studies showed that arrhythmia detection through single-lead ambulatory monitoring met cardiologist standards and revealed underlying signs of left ventricular systolic dysfunction (LVSD) that standard 12-lead ECGs failed to identify (12,90). ECG analysis now extends beyond simple disease detection because advanced models using sinus-rhythm 12-lead ECGs can predict atrial fibrillation (AF) before it occurs, offering better predictive results than existing clinical risk scores, and uncovering hidden electrophysiological patterns in waveforms (13,91).

The EAGLE trial used a cluster-randomized design to show that AI-ECG alerts in primary care settings resulted in higher LVSD detection rates during the first 90 days while reducing the number of echocardiography tests (14). Furthermore, the market expansion of consumer wearable technology has made cardiac monitoring devices accessible to all consumers. A prospective study demonstrated that smartwatch single-lead ECG recordings analyzed through an adjusted algorithm successfully identified EF ≤40% in non-clinical environments, which suggests their potential use for heart failure detection and opening venues for early preventative strategies (92).

Beyond offering insights into cardiac structure and anatomy, ECG can also act as a sensitive marker of metabolic abnormalities, particularly electrolyte imbalances like dyskalemias and systemic conditions such as anemia. This broadens the traditional role of ECGs from detecting cardiac issues to encompassing wider clinical monitoring, utilizing subtle waveform changes that indicate underlying physiological disturbances (93,94).

The methodological approach of CNNs continues to serve as the main framework for complete end-to-end analysis of unprocessed multi-lead EKGs because they show consistent performance in current comparative studies (95). Research has focused on transformer-based and hybrid CNN-transformer models to enhance the detection of extended temporal connections and rhythm changes. Applying unsupervised learning techniques to large unlabeled ECG datasets improves data efficiency and learning, which boosts the performance of subsequent tasks by predicting rhythm and clinical outcomes simultaneously (15).

Community challenges like the PhysioNet/Computing in Cardiology Challenges have been essential for standardizing how we evaluate ECG analysis algorithms. They offer large, multi-institutional datasets and open competitions that encourage reproducibility and model generalizability by requiring public code submissions (e.g., on GitHub) and testing on hidden external data. The field now concentrates on creating models that function across diverse populations and data sources because AUC-ROC results from one study do not guarantee accurate performance on different external datasets (96).

Clinical integration typically follows three models: (I) real-time triage in emergency or prehospital care [e.g., automated ST-elevation myocardial infarction (STEMI)/occlusion myocardial infarction (OMI) alerts from ambulance ECGs]; (II) batch screening of archived ECGs in primary care to identify risk for LVSD or future arrhythmias; (III) remote monitoring through wearables or patches for scalable detection and follow-up. Prehospital studies demonstrate the feasibility and high diagnostic accuracy of automated STEMI detection, with the potential to reduce treatment delays (16). International studies indicate that AIECG can detect occlusion MI across a wide spectrum of acute coronary syndrome (ACS) comprehensively than the STEMI criteria and with performance comparable to expert interpretation (97).

The deployment of this system faces restrictions because its performance becomes less consistent when using different vendors, sampling rates, and patient groups, thus requiring extensive multi-site external validation, continuous drift monitoring, and periodic system recalibration (96). Labeling strategies, such as echo-derived EF within a time window, can introduce noise and bias, affecting achievable performance. Safe and equitable integration requires clinician‑in‑the‑loop review, predefined action pathways, uncertainty‑aware thresholds, secure logging, and privacypreserving governance. Attention to equity is essential, as differential performance by sex, age, or race, and unequal access to connected devices, could exacerbate the digital divide unless explicitly addressed in development and trials (17,95).

Evidence quality and limitations: although many ECG-AI studies report strong discrimination in retrospective cohorts, generalizability depends on device vendor, lead configuration, sampling frequency, and population mix, and performance should be reported with calibration and clinically interpretable measures beyond AUC. The EAGLE trial provides higher-level evidence that ECG-AI can improve screening yield in pragmatic implementation, but broader prospective evaluations and monitoring for bias, alert fatigue, and workflow impact remain needed (12,16,90,91,93,95,96).

AI in cardiac imaging

Echocardiography

The echocardiography workflow has experienced rapid development through AI advancements, which now improve image acquisition, view identification, quality assurance, quantitative analysis, and disease detection processes. Developing video-based DL systems allows for left ventricular (LV) segmentation and EF estimation with each heartbeat. This new technology decreases inconsistencies in clinical readers, which has been possible because of extensive public databases, enhancing reliability (18). These achievements provide a solid foundation for end-to-end interpretation in routine clinical practice, accelerating the integration of automation into everyday echocardiography (19).

Real-time AI guidance enables early clinicians to obtain transthoracic echocardiograms with diagnostic quality. In a multicenter prospective study, nurses without prior ultrasound training successfully performed 10-view limited exams, accurately evaluating left ventricular size and function, right ventricular size, and pericardial effusion in more than 90–98% of patients (20). The first AI-based assessment of EF in a blinded randomized noninferiority trial achieved the same accuracy as experienced sonographers while reducing interpretation time compared to cardiologists. This shows AI can potentially improve cardiac measurement procedures in standard medical practice (21).

Automated view detection and chamber measurement may use rule-based algorithms, while DL models enable adaptive analysis and disease detection. A successful acquisition automation relies on image recognition accuracy, which has been shown to reach a 95% success rate when analyzing standard adult views from large, diverse datasets. Training advanced AI systems with tens of thousands of studies enables them to recognize over 20 different views and detect both off-axis and mislabeled images, while prompting users to reacquire suboptimal scans. These capabilities make the laboratory workflow more efficient by reducing non-diagnostic studies and improving overall exam quality (19,22). The use of DL techniques enables continuous segmentation of the left ventricular cavity and measurement of EF and volumes from apical views, with results that match or surpass human observer accuracy (18).

The AI pipelines developed by commercial organizations now perform left atrial volume measurements, right-sided chamber size assessments, and Doppler envelope analysis for left ventricular outflow tract (LVOT) velocity time integral (VTI) and mitral inflow, along with essential diastolic function parameters. The multicenter validation study of 23 parameters, including volumes, EF, and Doppler metrics, showed that the AI workflow produced results closer to core-laboratory expert readings than human expert discrepancies, supporting AI as a substitute for many quantitative assessments (23). AI models use standard echocardiographic clips to identify complex cardiac conditions, including hypertrophic and infiltrative cardiomyopathies, significant valvular diseases, pericardial effusions, and pulmonary hypertension risk (24).

The AI system analyzed a single apical four-chamber video to distinguish between HFpEF vs. non-HFpEF cases accurately. The research demonstrates that echocardiographic video phenotyping can be a powerful diagnostic tool for complex syndromic conditions requiring multiple parameter assessments (24). The vision language foundation model EchoCLIP achieved zero-shot generalization across various functions, including device identification, by training on more than one million echocardiographic videos and clinical reports (25). This system achieved retrieval and report-aware reasoning abilities, enabling the development of advanced AI assistants that generate structured diagnostic reports and access previous case data examples (25).

Evidence quality and limitations: AI performance can be affected by label noise, often due to inter-reader variability when measuring EF or strain, which highlights the need for quality filters and confidence thresholds. Establishing effective governance requires clinicians to review AI results, implement clear protocols for AI-human assessment and disagreements, conduct bias evaluations for sex, age, BMI, and other clinical parameters, and maintain model version control and secure data management systems. Deploying AI in point-of-care and remote settings demands representative training data and equal device and connectivity access to determine whether AI will improve or hinder healthcare delivery inequalities. Prospective studies demonstrating improved diagnostic accuracy, reduced time-to-diagnosis, or better outcomes remain fewer than retrospective performance reports, highlighting the need for multi-center, outcome-driven evaluations and transparent reporting of failure modes (17-23,97).

AI in nuclear cardiology

Nuclear cardiology is a subspecialty of cardiovascular imaging that uses non-invasive techniques such as SPECT and PET to evaluate the viability of myocardium, assess myocardial perfusion, and determine ventricular function (26). With the growth of DL in nuclear imaging within cardiology, this field will benefit from improvements in image acquisition and timing, attenuation correction, diagnostic advantages in coronary artery disease (CAD) through predictive modeling, and workflow enhancements.

Radiation exposure is a concern for myocardial perfusion imaging (MPI). AI-enhanced imaging using DL methods in MPI-single-photon emission computed tomography (MPI-SPECT) showed that reconstructed AI images were able to reduce dose time and acquire images faster without compromising imaging quality (27). The study was notable for a nearly 25–50% reduction in the time of the MPI-SPECT (27). Similar studies have been completed, such as Ramon et al., using up to one-eighth the dose of radiation (28). This is beneficial for reducing radiation exposure during testing and allows for more testing to be completed.

AI in image attenuation will play a vital role in SPECT imaging. Various facilities lack CT scans, where the approach by Yang et al. used AI to attenuate images using DL methods (29). CT scans are used for attenuation correction for soft tissue artifact in cardiac single-photon emission computed tomography (SPECT). Images obtained using the AI-enhanced features without CT scans will reduce radiation exposure and allow facilities without CT to have attenuation correction. This method’s downside was that female patients with larger body mass index (BMI) created bias; thus, feature AI-enhanced imaging will need more data for their DL network (29). In another study by Sohlberg et al., investigators used DL models to decrease noise artifact with several AI models. Their study summarized that all the DL models outperformed standard technique (30).

AI-generated DL model in nuclear cardiology has also been used to assess CAD and has shown the ability to predict disease better than current models. In Betancur et al., investigators used invasive coronary angiography within 6 months of SPECT to compare standard methods to the DL AI (31). This study found that AI outperformed standard methods on a per-patient and per-coronary vessel basis, and the per-vessel prediction improved sensitivity from 64.4% to 69.8% (31). Another study used a ML AI method to predict early coronary revascularization following MPI (32). This study showed that the AI ML model had the highest area under the curve (AUC) (0.812) versus imaging only (0.786) versus imaging plus clinician variables (0.799); thus, ML had the highest prediction in early coronary revascularization, after incorporation of patient clinical and MPI data (32). This can be helpful for the future by finding early lesions and possibly saving patients from unnecessary procedures.

One of the most significant benefits to AI in nuclear cardiology is workflow optimization. One optimization is screening patients who should undergo studies, saving patients from undergoing invasive angiography (32). Another study, Apostolopoulos et al., shows AI models can use other patient diagnostic data, such as echocardiogram, patient risk factors, along with MPI, to detect disease on the perfusion scan better (33). Like other imaging modalities, AI models in nuclear cardiology have drawbacks. Algorithms may be vendor or site-specific, and some models may not be generalizable to assess all patients. Few tools have been cleared to be used by the FDA thus far; however, it’s reasonable to expect this to start advancing.

Evidence quality and limitations: nuclear cardiology AI evidence is dominated by retrospective imaging studies focused on attenuation correction and perfusion interpretation, with relatively fewer prospective evaluations of clinical utility. Generalizability may be limited by protocol heterogeneity (tracers, cameras, reconstruction settings) and variable ground-truth definitions; therefore, multi-site validation and clinically meaningful endpoints (beyond AUC) are important for translation (24-30).

CMR imaging

AI has also become essential to the CMR pipeline, from planning and acquisition to reconstruction, segmentation, quantification, and end-to-end diagnostic support. Initial advancements showed that using CNN allowed for quick and accurate segmentation of ventricles and atria on a large scale, such as in the UK Biobank study, achieving performance levels comparable to those of clinicians for routine chamber measurements, which are usually very time-consuming (34). Various quality control (QC) frameworks have also identified segmentations, in the process, before clinicians review them (35,36).

Vendor and independent studies have shown that DL-based cine reconstruction can more than halve acquisition time while maintaining image quality and with accurate volumetrics, advancing toward free-breathing, arrhythmia-corrected protocols and higher throughput (37).

In this prospective study, three cine CMR protocols—standard segmented cine, single-breath-hold DL-accelerated cine, and free-breathing motion-corrected DL cine—were implemented in patients undergoing 3T CMR. DL-accelerated protocols reduced total acquisition times by 73% and 62% compared to segmented cine, while preserving image quality and cardiac function assessment (98). In addition to releases of this technology in the market, available resources like CMRxRecon for k-space have played a role in standardizing evaluations and speeding up method development across cine and mapping techniques, resulting in enhanced transparency and comparability within the field (99).

The implementation of AI technology in medical imaging has automated time-consuming post-processing operations, strain analysis, and tissue mapping functions, which decreases inter-observer variability (34,36,100). The DL pipeline integrated into perfusion imaging enables automatic myocardium segmentation and quantitative blood-flow mapping of the myocardium during scanning through a single button operation, which both reduces analysis duration and creates uniform results between different imaging facilities (101). The automated quantitative perfusion results generated by these systems have proven useful as they show excellent predictive value for patient such as death [hazard ratio (HR) 1.93, 95% confidence interval (CI): 1.08–3.48 and HR 2.45, 95% CI: 1.42–4.24] and major adverse cardiovascular events (MACEs) (HR 2.14, 95% CI: 1.58–2.90 and HR 1.74, 95% CI: 1.36–2.22) using stress myocardial blood flow (MBF) and myocardial perfusion reserve (MPR) respectively (102).

The implementation of AI technology has improved the robustness of LGE scar segmentation and radiomics risk marker analysis through automated scar burden detection, which multiple studies have validated for outcome prediction (38,103). The VNE models, which combine cine/T1 maps to generate late gadolinium enhancement (LGE)-like data suggest potential applications for reducing gadolinium usage in particular imaging scenarios but need further prospective studies to confirm clinical equivalence (39).

The diagnostic capabilities of CMR extend beyond its traditional applications. A 2024 multicenter research study published in Nature Medicine (n=9,719) tested a two-stage video-based swin transformer (VS.T) system, which first detects cine abnormalities before using cine and LGE data to identify 11 CVDs with performance levels surpassing human cardiologists in specific tasks (AUC of 0.988±0.3% and 0.991±0.0%, in internal and external cohorts, respectively). The system demonstrates potential for complete CMR decision support integration, but needs further testing before deployment (40).

Future development of these techniques requires extensive testing across multiple sites to validate their performance, along with decision curve reporting and prospective studies that assess diagnostic effects, treatment choices, patient results, and ongoing QC and drift monitoring for safe and fair deployment at large scales (39).

Evidence quality and limitations: CMR AI has advanced rapidly in segmentation and reconstruction, and recent studies suggest that DL-accelerated cine protocols can shorten acquisition time while preserving functional assessment. Nevertheless, performance can vary by scanner vendor, field strength, and sequence parameters, and artifact sensitivity requires robust quality assurance and human oversight. Further multi-center validation and prospective demonstrations of workflow or outcome benefit remain key gaps (31-36).

AI in CCTA

Automated coronary artery calcium (CAC) scoring, detection, and plaque characterization and quantification of stenosis, noninvasive functional assessment like FFRct, and perfusion analysis are a few of the key applications in AI. AI can eliminate tedious manual segmentation of coronary arteries that serve as risk stratification tools for assessing future cardiovascular events. An early study from 2007 on ECG-gated cardiac CT achieved 73.8% sensitivity for detecting coronary calcifications and correctly stratified 93.4% of patients into the proper risk category, demonstrating the feasibility of fully automated CAC scoring (41). Recent DL models report near-perfect alignment with standard CAC scoring. Studies show excellent correlation (Spearman’s ρ ~0.93–0.99) and agreement [intraclass correlation coefficient (ICC) ~0.99] between AI and expert-derived scores, with approximately 89–98% concordance in assigning patients to the same risk categories (42).

AI tools have been developed to assist in quantifying plaque and classifying stenoses, as well as automated Coronary Artery Disease Reporting and Data System (CAD-RADS) scoring, while reducing interobserver variability compared to gold standard invasive measures. With the new dual energy CCTA studies, AI has been able to analyze scans more efficiently. In a sub-group of 232 patients of the CLARIFY trial, expert readers had only moderate agreement in total plaque volume (ρ ~0.7) and poor agreement in plaque composition (ρ ~0.4–0.6) compared to an AI-based quantitative analysis (43). DL models have performed automatic CAD-RADS risk category assessments from CCTA images. In a study by Sandstedt et al., a CNN model achieved a moderate level of diagnostic accuracy with sensitivity ranging from 47% to 82% and specificity ranging from 58% to 91% while providing faster results than clinicians (44). The subsequent models developed through time reached 93% sensitivity and 97% specificity [negative predictive value (NPV) 97%] for detecting significant disease while achieving expert-level performance. The ML model demonstrated 98% accuracy in CAD-RADS category classification, which matched the performance of board-certified imagers according to two separate studies, and has been validated against invasive standards (45,46). For example, an AI-generated contrast density metric demonstrated 75% specificity and 73% NPV when identifying hemodynamically significant lesions when compared to invasive FFR testing (47). The ML model in the CREDENCE trial substudy achieved 84–86% accuracy and showed strong correlation (ICC =0.73) with quantitative coronary angiography while reducing reading time to approximately 10 minutes, compared to hours (48). However, it produced 7.3% of false positive results for severe stenosis detection, which warrants careful evaluation of the results.

Machine-learning approaches have significantly enhanced the diagnostic utility of FFRct and myocardial perfusion analysis on CT. An ML-based FFRct algorithm surpassed CCTA anatomy-only assessment to achieve 78% per-vessel accuracy, higher than the 58% obtained through CCTA alone. The ML-based FFRct system demonstrated high sensitivity between 79–90% and specificity between 94–95% for detecting flow-limiting stenoses while producing results that matched both invasive FFR (r 0.73) and traditional computational FFRct (AUC 0.84) (49,50). In a prospective study, ML-based FFRct reduced the need for angiography as 19.8% of patients with FFRct guidance did not require angiograms compared to 33.3% with standard CCTA, resulting in fewer adverse cardiac events during the first year (51).

Evidence quality and limitations: many CCTA-AI tools are supported by large retrospective datasets and show promise for stenosis and plaque assessment, but performance is vulnerable to motion, noise, and heavy calcification, and may shift across scanners and reconstruction kernels. To support clinical adoption, studies should report calibration and clinically actionable endpoints, and emphasize external validation across diverse practice settings (38-46,103).

AI in wearables & remote monitoring

Wearable technology systems now track patient health data through continuous monitoring of ECG, PPG signals, accelerometry, and sleep metrics, which expands the scope of medical surveillance compared to scheduled outpatient visits (52-57). The application of ML models, particularly CNNs and RNNs has significantly enhanced disease-specific signal detection from real-world datasets. This finds applications in treating multiple medical conditions, which include cardiovascular disease (CVD), sleep apnea, diabetes, mental health disorders, and rehabilitation (52-57). The evidence supporting the broad clinical impact of these technologies in clinical practice is still developing, since researchers need to conduct extended studies and establish systematic integration methods for healthcare systems (52,53,57,58).

The signal processing workflow begins with preprocessing and denoising operations, followed by DL architecture-based feature extraction through CNNs, RNNs, and transformers (59,60). The predictive accuracy of multi-sensor data improves through temporal fusion methods, while researchers now focus on developing methods to quantify uncertainty in their results. The deployment of AI systems follows two main strategies, which include on-device and far-edge inference for fast processing and privacy protection, and cloud-based aggregation for extensive population modelling and model improvement (55,58). The current AI field depends on supervised DL for most applications, but researchers now focus on developing federated learning and explainable AI systems to handle data sharing problems and improve model interpretability and user trust (53,59).

A systematic review of 26 studies demonstrated that AI models used with wearables achieved a combined sensitivity of 94.8% and specificity of 97.0% in their analysis. The performance of deep neural networks surpassed conventional ML models in terms of area under the receiver operating characteristic curve (AUROC) values at 0.981 compared to 0.961. The performance results showed better outcomes when using public and hospital-based datasets instead of proprietary and wearable-based datasets, indicating the need to address dataset shift problems for practical deployment (52). Detecting arrhythmias, sleep apnea, and stress through wearable ECG/PPG data processing now relies on AI systems that use DL models instead of traditional ML approaches. The use of ML for CVD prediction and diagnosis outperforms statistical models, but real-world testing and device precision issues act as limitations for practical applications (60,61). The integration of Edge AI systems allows for real-time analytics that detect decompensation risks and operate independently from constant cloud connections, but requires architectural assessment before deployment to prove additional value and match clinical operational procedures (55).

The verification of accurate data requires sensor error and characterization of motion artifact for device accuracy assessment and model training with diverse calibrated datasets to reduce bias levels (56,59). The implementation of privacy and security frameworks requires organizations to establish data ownership systems and encryption protocols, and obtain consent from users while providing equal access to data resources (54,55). The development of models for better generalization requires researchers to use multicentre, diverse cohorts instead of proprietary datasets for validation and training (52,53,56).

Implementing AI in wearable devices enables healthcare providers to detect diseases earlier and monitor treatment effects objectively while sending specific alerts for preventive care instead of reactive treatment. The successful deployment of wearable-based AI monitoring depends on team-based operational systems, predefined alert limits, medical staff supervision, and EHR system integration for maintaining clinical value and minimizing alert fatigue (54-56,59).

Evidence quality and limitations: wearable AI studies benefit from scale and real-world data streams, but clinical confirmation of detected events and downstream impact are variable across products and populations. False positives can drive unnecessary testing and anxiety, and performance may differ by skin tone, age, comorbidity, and signal quality. Pragmatic evaluations that measure decision impact and equity-focused validation are important for responsible deployment (47-56).

Heart failure

AI can now monitor the entire spectrum of heart failure progression, from detecting LV systolic dysfunction in asymptomatic patients to predicting decompensation and readmissions. One of the most successful uses of AI-ECG technology is its ability to detect LVSD with a 12-lead CNN, which achieved an AUC of 0.93 with 86% sensitivity and 86% specificity for identifying EF ≤35%. It also identified patients who are likely to develop future LV dysfunction at a fourfold higher rate as false positives. Implementing this AI-ECG model improved the detection of new LVSD cases without causing unnecessary tests or follow-ups, demonstrating its practical value in real-world settings (62).

The application of AI technology extends its capabilities to diastolic heart function assessment and systolic function assessment. A ResNet-based AI-ECG system achieved AUC 0.911 (sensitivity 83%, specificity 83%) for predicting elevated LV filling pressure. It demonstrated similar mortality risk stratification performance to echocardiogram in a patient population of approximately 100,000, which makes it possible to use a 10-second ECG as a scalable screening tool for heart failure with preserved ejection fraction (HFpEF) diagnostic pathways (63). Combining structured EHR data with gradient-boosted trees and ensemble algorithms enables risk prediction across entire populations. An extensive study involving multiple hospitals demonstrated that ML models that integrated social determinants of health data achieved C-statistics between 0.79 and 0.80 for in-hospital mortality prediction across different racial groups while outperforming traditional risk scores and providing explainable feature contributions for clinical staff acceptance (64).

Preventing hospital readmissions relies on identifying signs of decompensation early. Supervised time-series ML analysis of wearable multi-sensor data, including ECG, accelerometry, and temperature measurements, enables the prediction of heart failure events before they happen. The LINK-HF study showed that its personalized analytics system could forecast worsening heart failure 7–10 days in advance, with prediction accuracy reaching 0.84–0.89 AUC, sensitivity between 0.76–0.88, and specificity between 0.85–0.86 through continuous signal processing for low-latency alert generation (65).

Evidence quality and limitations: heart-failure AI models often draw on observational EHR data and can be affected by confounding, label leakage, and documentation variability, which can inflate retrospective performance. External validation across institutions and prospective testing of workflow integration and clinical outcomes remain inconsistent, emphasizing the need for transparent reporting and calibration assessment when models are used for risk-guided care (57-60).

Cardiac arrhythmia

Implementing AI in cardiac arrhythmia has led to improved screening methods, predictive tools, monitoring antiarrhythmic drug safety, and analyzing continuous telemetry. The CNN developed by Mayo Clinic used a sinus-rhythm 12-lead ECG to detect latent AF substrate with an AUROC of 0.87 for a single ECG, which reached 0.90 when analyzing multiple ECGs, proving the method can identify cases before they occur (66). A DL model from a single research center demonstrated the ability to identify two-thirds of patients without AF history who developed stroke due to AF before the stroke occurred (13). A 2023 deep-learning classifier achieved 84.1% sensitivity, 89.3% specificity, 55.2% positive predictive value, and 97.3% negative predictive value when detecting AF events from single-lead signals, making it suitable for triage and telemetry applications (67).

The “QTNet” model was trained from more than 7 million ECGs to determine QT intervals and detect QTc prolongation after initiation with dofetilide with 87% sensitivity, 77% specificity, and more than 95% negative predictive value when the pre-test probability is below 25% thus enabling safe outpatient and loading surveillance with wearable devices (68). This will be effective in reducing hospital stays and costs. A multicenter JAMA Cardiology study demonstrated that the ECG-only model achieved 0.93 external AUC with 0.90 sensitivity for detecting (LQTS) cases, which helps with genotype-based treatment decisions and family screening (69). An ECG-based model for sudden cardiac death (SCD) risk assessment achieved 0.889 AUROC in independent testing while providing noninvasive substrate information beyond left ventricular ejection fraction (LVEF) measurements. The “DEEP-RISK” model which combines ECG data with LGE-CMR results and clinical information achieved an AUROC of 0.84 for predicting malignant ventricular tachycardia/ventricular fibrillation (VT/VF) with 0.98 sensitivity and 0.73 specificity while outperforming individual testing methods for implantable cardioverter-defibrillator (ICD) selection (70).

AI can identify AF phenotypes, drug-induced QT risks, and VT/VF occurrences while producing useful results for triage decisions and showing measurable benefits in telemetry systems. Future research needs to focus on conducting prospective trials integrating AI into clinical workflows to determine action thresholds, decision curves, and bias assessments for sex, age groups, and device types, and establish post-deployment monitoring systems to maintain reliable performance.

Evidence quality and limitations: arrhythmia AI has strong retrospective evidence in large ECG datasets, including models for QT risk and AF phenotyping; however, prospective decision-impact evidence is limited, and model performance can vary across device types and recording conditions. Clear action thresholds, interpretability, and monitoring for subgroup performance are needed to reduce unintended harm and improve clinician trust (61-66).

AI in angiography and PCI/interventional procedures, including robotic guided procedures

In the last decade, multiple studies have helped validate the use of AI in coronary angiography. FLASH trial aimed to evaluate the efficacy of AI-QCA (artificial intelligence-based coronary angiography)-assisted PCI compared to optical coherence tomography (OCT)-guided PCI in terms of post-PCI results (71). This was an investigator-initiated, multicenter, randomized, prospective trial conducted at 13 sites in South Korea (n=400), who received either AI or OCT-guided PCI. The primary endpoint was the post-PCI minimal stent area and concluded noninferiority of AI-QCA with a margin of 0.8 mm2. The AI-ENCODE study used a library of more than 20,000 angiograms performed at Mayo Clinic, developed and validated AI algorithms to extract left ventricular EF, diastolic dysfunction, right ventricular dysfunction and cardiac index from 1–2 angiographic views thus validating the ability of AI to broaden diagnostic scope of coronary angiography by automatically extracting physiologic and functional data which can positively impact patient outcomes (72). While robotic PCl systems automate procedural steps through pre- programmed instructions, true Al-driven interventions in interventional cardiology involve ML models that analyze imaging data or predict outcomes to guide clinical decisions.

The combination of robotic systems and AI technologies has transformed the field of interventional cardiology, beginning with guidewire use to improve precision, decrease radiation exposure, and standardize treatment protocols. The coronary robotics market features two leading platforms: Corindus (Siemens Healthineers) CorPath GRX and Robocath R-OneTM. Current research shows that robotic PCI (R-PCI) achieves high success rates in both technical and clinical outcomes, provides significant radiation protection for operators, and maintains procedural speed. However, the superiority of hard clinical endpoints over manual PCI has yet to be proven (73,74).

The R-One (R-EVOLUTION) and GRX registries from multicenter studies demonstrate the feasibility and safety of robotic PCI while showing substantial reductions in operator radiation exposure, which aligns with the expected benefits of cockpit-based control (73). The PARTY trial is a single-center, randomized, prospective clinical trial comparing R-PCI to conventional PCI, which aims to provide answers towards the potential benefits of R-PCI (75). The first human telerobotic PCI procedure from a distant location succeeded in 2019 when an operator located 20 miles from the cath lab controlled coronary devices through GRX. The procedure established a crucial precedent for remote interventions and disaster response, yet exposed operational challenges related to network stability, operator certification, and system delays (76). The deployment of robotic systems on a large scale for patient treatment remains untested and requires validation for widespread use.

Intravascular imaging has experienced rapid AI development, enabling users to pick optimal frames and to help characterize tissue and perform automated measurements of essential structures. The commercial software Abbott’s Ultreon applies ML to OCT imaging for calcium detection, EEL/vessel size estimation, and malapposition/under-expansion identification, which results in more precise, faster, and less variable PCI planning according to comparative studies (77,78).

Angiography-derived physiology, such as QFR, blends a three-dimensional vascular model of the coronary artery from two angiographic views. Then, it uses computational fluid dynamics to simulate blood flow and calculate the pressure gradient to determine the FFR. In FAVOR III China, QFR guidance improved 1-year and sustained 2-year outcomes versus angiography alone (79). But in FAVOR III Europe, QFR was not a match for FFR when a wire-based gold standard was readily available (80). QFR is a credible option where wire physiology is complex or underused, but it does not supplant FFR in settings where FFR is feasible.

OFR technology is a wire-free FFR technology that uses the high resolution and accuracy of OCT images, and reconstructs three-dimensional vascular models through AI technology, simulating the calculation of FFR indicators (81). This provides detailed coronary microstructure imaging through OCT, enhancing diagnostic precision. The system delivers fast and efficient patient care through its non-invasive procedure, which requires only multiple cross-sectional images for hemodynamic assessment. The clinical trials have proven OFR’s reliability through validation, while showing strong agreement with traditional wire-based methods, according to studies (61,82,83).

Evidence quality and limitations: evidence in interventional cardiology spans both ML-driven image analysis and robotics, but it is important to distinguish rule-based automation from adaptive ML guidance. Research studies must evaluate robotic PCI performance against manual PCI results while assessing how AI-based imaging affects stent failure rates. The effectiveness of QFR needs to be assessed in medical facilities that do not implement FFR technology. The safety and reliability of robotic procedures with tele-robotics require additional clinical trials for validation. Current data include registries and early prospective trials; broader evidence on long-term outcomes, operator learning curves, cost-effectiveness, and real-world safety monitoring remains limited. Multi-center trials and transparent reporting of failure modes will be crucial for translation (13,67-78).

Risk prediction & stratification

Risk tools throughout the cardiac continuum now depend on AI technology, which starts in emergency department triage and extends to long-term event prediction. AI models achieve better results than traditional rules-of-thumb, only when implemented correctly, and their performance is validated.

The CoDE-ACS model represents a multicenter machine-learning system that analyzes 10,038 patient data to personalize high-sensitivity troponin results based on clinical factors, including age and sex, comorbidities, and blood sample timing. The CoDE-ACS method demonstrated excellent performance in external testing by correctly eliminating myocardial infarction in 61% of patients with a 99.6% negative predictive value. The model showed a 75.5% positive predictive value and 97.1% specificity when identifying 10% of patients needing immediate myocardial infarction evaluation. The deep-learning ECG models now identify occlusion MI without ST-elevation (OMI), which traditional STEMI criteria fail to detect, while providing immediate reperfusion benefits to these patients, according to observational cohort studies (84).

Wearable devices have demonstrated their ability to perform population-scale AF screening through the Apple Heart Study, which enrolled 419,000 participants to validate an irregular-pulse detection algorithm for AF identification and subsequent monitoring purposes (85). AI technology enables 12-lead EKG analysis to identify future and paroxysmal AF occurrences from sinus-rhythm EKG recordings, which researchers have confirmed through extensive health-system data analysis and clinical trials. A study by Attia et al. demonstrated how their model detects hidden AF risk factors by analyzing EKGs that appear normal (66).

The stroke prediction performance of CHA2DS2-VASc and HAS-BLED risk scores remains limited for death prediction, but advanced ML models, including Multi-Label Gradient Boosting Decision Tree (ML-GBDT) and biomarker-based ABC-AF scores, show better predictive capabilities (86,87). The ML-GBDT model demonstrated better stroke prediction performance than CHA2DS2-VASc in a global registry study, with an AUC of 0.691 compared to 0.613, and it outperformed CHA2DS2-VASc in death and major bleeding risk prediction, with AUC values of 0.785 and 0.698 respectively (86). The ABC-stroke score achieved a c-index of 0.65, which outperformed the CHA2DS2-VASc score with a c-index of 0.60 (87). The AI models provide enhanced risk assessment through their ability to process diverse clinical and biomarker information, which leads to better stroke prevention decisions.

ML models have performed better than conventional stroke risk assessment methods in every analysis. The analysis of 7 million patients through ML models using Extreme Gradient Boosting (XGB) and Random Forest (RF) demonstrated superior performance in stroke prediction and prognosis for AF patients with an average AUROC of 0.75 (88). In contrast, studies on traditional scores like CHA2DS2-VASc often reveal more modest performance, with a c-index as low as 0.55. On the other hand, the ABC-stroke score, which incorporates biomarkers, also showed superior performance with a c-index of 0.64 (104).

AI now predicts lethal arrhythmias and SCD with greater precision than conventional methods. The DL model processed ECG data to achieve a 0.889 (95% CI: 0.861–0.917) AUROC for SCD prediction, which exceeded the conventional model’s 0.712 AUROC (105). The combination of ECG data with LGE MRI, clinical information through a multimodal AI model produced an AUROC of 0.84 (95% CI: 0.71–0.96) and sensitivity of 0.98 (95% CI: 0.75–1.00) and specificity of 0.73 (95% CI: 0.58–0.97) in non-ischemic cardiomyopathy patients (80). The dynamic ML model processed ECG data over time through VAEs to achieve an AUROC of 0.738. The method outperformed the 0.639 result obtained by the static baseline-only model (70). The results demonstrate how AI performs better at risk prediction because it processes intricate and time-dependent data sets.

AI models based on ECG technology have successfully identified asymptomatic LV systolic dysfunction cases. The AI system using ECG data achieved an AUC of 0.839 and 73% sensitivity and 83% specificity for LVSD detection in Chagas disease patients (106). The CNN model processed ECG data to predict EF values below or equal to 35% with a 0.93 AUC and 85.7% total accuracy in general population studies. The model successfully predicted ventricular dysfunction development with a hazard ratio of 4.1 (13). The AI system for LVSD detection in emergency departments achieved a detection accuracy of 0.89, which exceeded the performance of NT-proBNP testing at 0.80 (107). The AI system demonstrated success in detecting diastolic dysfunction and elevated filling pressure by achieving a detection accuracy of 0.911 for increased filling pressure (63). The AI-ECG system demonstrated equivalent prognostic capabilities to echocardiography while providing early detection capabilities.

Evidence quality and limitations: risk prediction studies frequently emphasize AUC while underreporting calibration, absolute risk, confidence intervals, and decision-impact measures, which limits clinical interpretability. Prospective evaluation and monitoring for drift are particularly important when models are deployed across evolving populations and practice patterns. Future work should prioritize calibration, subgroup analyses, and outcome-oriented validation rather than performance metrics alone (79-87).

Emerging paradigms and future directions

Generative AI and large language models (LLMs) in cardiology

Generative AI and LLMs extend cardiovascular AI beyond classification to workflow-facing tasks such as clinical summarization, drafting structured reports (e.g., echocardiography or catheterization narratives from measurements), patient-facing education materials, and guideline-aware decision support. Because these functions address documentation burden and information overload, they may drive adoption faster than incremental gains in retrospective diagnostic performance. However, LLMs pose distinct safety risks, including hallucinations, fabricated citations, and failures under distribution shift when prompts, templates, or workflows differ from training conditions. Deployment therefore requires guardrails, including constrained outputs, retrieval-augmented generation, clinician verification, and monitoring for drift and recurrent error patterns (108).

Foundation models and self-supervised learning in ECG and imaging

Foundation models trained with self-supervised or weakly supervised objectives can be adapted to multiple downstream tasks with limited labeled data, which is attractive in cardiology where labels are costly and heterogeneous. In ECG, learned representations may enable broader diagnostic coverage and improved generalization, though external validation and prospective evaluation remain essential (109). In imaging, transformer-based backbones and multimodal encoders support transfer across tasks such as segmentation, detection, and report generation. These approaches may reduce “data scarcity” but increase requirements for calibration, transparency, and governance across heterogeneous settings (4).

Multimodal models and the end of “Single-Silo” cardiology AI

Multimodal learning integrates waveforms, imaging, structured EHR variables, and clinical text, more closely reflecting clinical reasoning than single-modality models. Potential advantages include robustness to missing inputs, cross-modal retrieval (e.g., linking ECG patterns to imaging phenotypes), and interactive synthesis of longitudinal records. Key risks include label leakage, temporality violations, and evaluation using proxy endpoints; studies should therefore prespecify time ordering and emphasize clinically meaningful outcomes.

Privacy-preserving learning, federated approaches, and synthetic data

Federated learning and privacy-preserving training can enable multi-institutional model development without centralizing raw data, potentially improving generalizability while reducing governance barriers. Synthetic data may support development and testing, but reliability depends on preserving rare, safety-critical edge cases and maintaining performance under real-world artifacts and documentation variability. These methods should be viewed as complementary tools rather than universal solutions, with transparent reporting of data provenance, validation, and failure modes.

Translation, evidence quality, and regulation in the current era

Despite impressive retrospective performance, adoption is constrained by workflow integration, alert fatigue, reimbursement limitations, and calibration drift under dataset shift. Clinical value depends on actionability: outputs must be routed appropriately, paired with thresholds and confirmatory testing, and embedded in follow-up pathways. Evidence should be interpreted by tier, distinguishing internal from multisite external validation and retrospective accuracy from prospective trials demonstrating improved decision-making, time-to-diagnosis, or patient outcomes (110). In addition, the FDA has described mechanisms such as a Predetermined Change Control Plan (PCCP) to support iterative improvement while maintaining safety and effectiveness (111).


Limitations

This narrative review summarizes a rapidly evolving literature with substantial heterogeneity in wearable devices, signals, endpoints, and analytic methods, limiting direct cross-study comparability. Because many studies emphasize feasibility and diagnostic performance rather than clinical outcomes, the strength of evidence supporting downstream outcome improvement remains variable. Publication bias and selective reporting are possible, and the pace of device and software iteration may outdate specific technical implementations over time. Accordingly, the findings should be interpreted as an evidence map of current capabilities and gaps rather than definitive comparative effectiveness conclusions.


Conclusions

Wearable and remote monitoring technologies, increasingly augmented by AI methods, can enable scalable cardiovascular screening and longitudinal risk assessment outside traditional care settings. Current evidence supports feasibility and promising diagnostic performance for select applications, but consistent demonstration of improved hard clinical outcomes remains limited. Future work should prioritize external validation, transparent reporting, bias assessment, and pragmatic trials that measure clinically meaningful endpoints within real-world workflows.


Acknowledgments

None.


Footnote

Reporting Checklist: The authors have completed the Narrative Review reporting checklist. Available at https://cdt.amegroups.com/article/view/10.21037/cdt-2025-510/rc

Peer Review File: Available at https://cdt.amegroups.com/article/view/10.21037/cdt-2025-510/prf

Funding: None.

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://cdt.amegroups.com/article/view/10.21037/cdt-2025-510/coif). K.G. serves as an unpaid editorial board member of Cardiovascular Diagnosis and Therapy from April 2025 to March 2027. The other authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


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Cite this article as: Mondal A, Thyagaturu H, Jitta SR, Bhandari B, Helsel E, Dogra M, Prajapati K, Gonuguntla K. Artificial intelligence in cardiology in the current era: a narrative review. Cardiovasc Diagn Ther 2026;16(2):34. doi: 10.21037/cdt-2025-510

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