Pub Date : 2025-08-07eCollection Date: 2025-11-01DOI: 10.1093/ehjdh/ztaf090
Rafael Silva-Teixeira, João Almeida, Francisco A Caramelo, Paulo Fonseca, Marco Oliveira, Helena Gonçalves, João Primo, Ricardo Fontes-Carvalho
Aims: Quality of life (QoL) improvement is a primary driver for atrial fibrillation (AF) catheter ablation (CA), yet its determinants remain unclear. We aimed to identify patient phenotypes with distinct post-ablation QoL trajectories, determine their key predictors, and clarify their association with arrhythmia recurrence and reintervention.
Methods and results: We prospectively followed 213 patients (median age 60 years, 31% female) undergoing AF CA at a tertiary hospital for 2.2 years [interquartile range (IQR): 1.6-2.6]. A digital health application collected real-time electronic patient-reported outcomes (PROs), including the AF Effect on QoL (AFEQT) questionnaire. Reference charts were generated from QoL trajectories of recurrence-free patients. Machine learning (ML) identified subgroups with distinct QoL trajectories, and explainable artificial intelligence (AI) highlighted key predictors. Quality of life improved by +26 AFEQT points [95% confidence interval (CI): 18-33] within 3 months post-ablation and remained stable thereafter, despite significant heterogeneity in individual responses. Patients with AF recurrence showed significantly lower QoL gains (P = 0.010). Machine learning identified three phenotypes: a younger cluster with the largest QoL improvements, an emotive cluster with higher recurrence rates and minimal QoL benefits despite additional antiarrhythmic reinterventions, and an older cluster with established cardiovascular risk factors. Anxiety, age, and AF duration emerged as key discriminators.
Conclusion: ML defined three clinically coherent phenotypes, each exhibiting distinct QoL trajectories and ablation outcomes. Explainable AI clarified how individual psychological and biological traits interact to shape these outcomes, highlighting the potential for tailored multidisciplinary care beyond individualized rhythm control strategies.
{"title":"Predicting patient-related outcomes after atrial fibrillation ablation: insights from explainable artificial intelligence and digital health.","authors":"Rafael Silva-Teixeira, João Almeida, Francisco A Caramelo, Paulo Fonseca, Marco Oliveira, Helena Gonçalves, João Primo, Ricardo Fontes-Carvalho","doi":"10.1093/ehjdh/ztaf090","DOIUrl":"10.1093/ehjdh/ztaf090","url":null,"abstract":"<p><strong>Aims: </strong>Quality of life (QoL) improvement is a primary driver for atrial fibrillation (AF) catheter ablation (CA), yet its determinants remain unclear. We aimed to identify patient phenotypes with distinct post-ablation QoL trajectories, determine their key predictors, and clarify their association with arrhythmia recurrence and reintervention.</p><p><strong>Methods and results: </strong>We prospectively followed 213 patients (median age 60 years, 31% female) undergoing AF CA at a tertiary hospital for 2.2 years [interquartile range (IQR): 1.6-2.6]. A digital health application collected real-time electronic patient-reported outcomes (PROs), including the AF Effect on QoL (AFEQT) questionnaire. Reference charts were generated from QoL trajectories of recurrence-free patients. Machine learning (ML) identified subgroups with distinct QoL trajectories, and explainable artificial intelligence (AI) highlighted key predictors. Quality of life improved by +26 AFEQT points [95% confidence interval (CI): 18-33] within 3 months post-ablation and remained stable thereafter, despite significant heterogeneity in individual responses. Patients with AF recurrence showed significantly lower QoL gains (<i>P</i> = 0.010). Machine learning identified three phenotypes: a younger cluster with the largest QoL improvements, an emotive cluster with higher recurrence rates and minimal QoL benefits despite additional antiarrhythmic reinterventions, and an older cluster with established cardiovascular risk factors. Anxiety, age, and AF duration emerged as key discriminators.</p><p><strong>Conclusion: </strong>ML defined three clinically coherent phenotypes, each exhibiting distinct QoL trajectories and ablation outcomes. Explainable AI clarified how individual psychological and biological traits interact to shape these outcomes, highlighting the potential for tailored multidisciplinary care beyond individualized rhythm control strategies.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 6","pages":"1181-1193"},"PeriodicalIF":4.4,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12629652/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145566338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-05eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf081
Brandon Wadforth, Sobhan Salari Shahrbabaki, Campbell Strong, Jonathan Karnon, Jing Soong Goh, Luke Phillip O'Loughlin, Ivaylo Tonchev, Lewis Mitchell, Taylor Strube, Scott Lorensini, Darius Chapman, Evan Jenkins, Anand N Ganesan
Aims: Spontaneous cardioversion (SCV) is commonly observed in patients presenting to emergency departments (EDs) with primary atrial fibrillation (AF). Predicting SCV could facilitate timely discharge and avoid costly admissions. We sought to evaluate whether SCV could be predicted using artificial intelligence-enabled electrocardiograms (AI-ECGs) and whether this could produce cost savings.
Methods and results: We recruited patients presenting to EDs with primary AF throughout 2022-23. Patients were excluded if the outcome of their AF episode was unclear, or the ECG was not accessible. Spontaneous cardioversion prediction was attempted using ResNet50, EfficientNet, and DenseNet convolutional neural network (CNN) architectures and subsequently an ensemble learning model. We then performed a cost-minimization analysis to estimate the cost effect of a prediction-guided 'wait-and-see' protocol. There were 1159 presentations to the ED, of which 502 had sufficient data for inclusion. The median age was 74.0 years and 54.0% were women. Spontaneous cardioversion occurred in 227 (45.2%) patients and was more frequent in younger patients (P < 0.001). The ensemble learning model outperformed individual CNNs, achieving an accuracy of 69.7% (SD 5.91) and a receiver operating characteristic area under the curve (ROC AUC) of 0.742 (SD 0.037) with a sensitivity and specificity of 0.736 (SD 0.068) and 0.657 (SD 0.150), respectively. The per patient cost was $4681 if all patients were admitted, which reduced to $3398 with a prediction-guided 'wait-and-see' protocol with a 33.3% reduction in overall hospitalization.
Conclusion: Artificial intelligence-enabled electrocardiogram can predict SCV in patients presenting to EDs with primary AF, and a prediction-guided 'wait-and-see' protocol utilizing AI-ECG could lead to substantial cost savings and reduced hospitalization.
{"title":"Predicting the spontaneous cardioversion of atrial fibrillation using artificial intelligence-enabled electrocardiography.","authors":"Brandon Wadforth, Sobhan Salari Shahrbabaki, Campbell Strong, Jonathan Karnon, Jing Soong Goh, Luke Phillip O'Loughlin, Ivaylo Tonchev, Lewis Mitchell, Taylor Strube, Scott Lorensini, Darius Chapman, Evan Jenkins, Anand N Ganesan","doi":"10.1093/ehjdh/ztaf081","DOIUrl":"10.1093/ehjdh/ztaf081","url":null,"abstract":"<p><strong>Aims: </strong>Spontaneous cardioversion (SCV) is commonly observed in patients presenting to emergency departments (EDs) with primary atrial fibrillation (AF). Predicting SCV could facilitate timely discharge and avoid costly admissions. We sought to evaluate whether SCV could be predicted using artificial intelligence-enabled electrocardiograms (AI-ECGs) and whether this could produce cost savings.</p><p><strong>Methods and results: </strong>We recruited patients presenting to EDs with primary AF throughout 2022-23. Patients were excluded if the outcome of their AF episode was unclear, or the ECG was not accessible. Spontaneous cardioversion prediction was attempted using ResNet50, EfficientNet, and DenseNet convolutional neural network (CNN) architectures and subsequently an ensemble learning model. We then performed a cost-minimization analysis to estimate the cost effect of a prediction-guided 'wait-and-see' protocol. There were 1159 presentations to the ED, of which 502 had sufficient data for inclusion. The median age was 74.0 years and 54.0% were women. Spontaneous cardioversion occurred in 227 (45.2%) patients and was more frequent in younger patients (<i>P</i> < 0.001). The ensemble learning model outperformed individual CNNs, achieving an accuracy of 69.7% (SD 5.91) and a receiver operating characteristic area under the curve (ROC AUC) of 0.742 (SD 0.037) with a sensitivity and specificity of 0.736 (SD 0.068) and 0.657 (SD 0.150), respectively. The per patient cost was $4681 if all patients were admitted, which reduced to $3398 with a prediction-guided 'wait-and-see' protocol with a 33.3% reduction in overall hospitalization.</p><p><strong>Conclusion: </strong>Artificial intelligence-enabled electrocardiogram can predict SCV in patients presenting to EDs with primary AF, and a prediction-guided 'wait-and-see' protocol utilizing AI-ECG could lead to substantial cost savings and reduced hospitalization.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"969-978"},"PeriodicalIF":4.4,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450503/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-05eCollection Date: 2025-11-01DOI: 10.1093/ehjdh/ztaf088
Ying Wang, Shan-Shan Zhou, Yu-Qi Liu, Dan-Dan Li, Shun-Ying Hu, Xi Wang, Li Yi, Ya-Ni Yu, Yun-Dai Chen
Aims: This study aims to investigate the ownership of wearable health devices across different demographic groups and usage patterns among Chinese adults.
Methods and results: This was a cross-sectional study, with all data originating from the Huawei Blood Pressure Health Study, a real-world study aimed at exploring blood pressure management through wearable devices in China. Data were remotely collected using mobile phones and Huawei Watch D from 23 February 2022 to 31 March 2024. The system utilized artificial intelligence algorithms to assess participants' risk of hypertension and provided risk alarm feedback via mobile phones and watches. A total of 75 918 participants from 31 provinces were included, with an average age of 47 years. Most of the participants were concentrated in the economically developed South China and East China regions. Among the participants, 73.8% used the Watch D for blood pressure monitoring, and 10.5% received risk alerts. The rate of blood pressure monitoring on the day they received the alert was 78%. However, the rate significantly decreased between 6 months and 1 year (Mann-Kendall test, Z = -2.85, P < 0.05). For hypertensive patients, the blood pressure monitoring rate was 84% on the day they joined the study and decreased over time (Mann-Kendall test, Z = -3.09, P < 0.05). However, it remained above 50% within 6 months.
Conclusion: This study provides evidence of the digital health divide in the utilization of wearable devices among the Chinese population. Additionally, it proposes a potentially follow-up interval for employing wearable devices for maintaining compliance with blood pressure monitoring.
Study registration: URL: https://www.chictr.org.cn/.
Unique identifier for huawei-bphs: ChiCTR2200057354.
目的:本研究旨在调查中国不同人口群体中可穿戴健康设备的拥有率和使用模式。方法和结果:这是一项横断面研究,所有数据来自华为血压健康研究,这是一项旨在探索中国可穿戴设备血压管理的现实研究。从2022年2月23日至2024年3月31日,通过手机和华为Watch D远程收集数据。该系统利用人工智能算法评估参与者患高血压的风险,并通过手机和手表提供风险警报反馈。共有来自31个省份的75918名参与者,平均年龄为47岁。大多数参与者集中在经济发达的华南和华东地区。在参与者中,73.8%的人使用Watch D进行血压监测,10.5%的人收到了风险警报。收到警报当天的血压监测率为78%。但6个月至1年期间发病率显著下降(Mann-Kendall检验,Z = -2.85, P < 0.05)。高血压患者入组当天血压监测率为84%,随时间推移血压监测率逐渐降低(Mann-Kendall检验,Z = -3.09, P < 0.05)。然而,在6个月内,它仍保持在50%以上。结论:本研究为可穿戴设备在中国人群中的使用提供了数字健康鸿沟的证据。此外,它提出了使用可穿戴设备来维持血压监测依从性的潜在随访间隔。研究注册:URL: https://www.chictr.org.cn/.Unique华为-bphs的标识符:ChiCTR2200057354。
{"title":"Accessibility and usage patterns of wearable devices among Chinese adults: the Huawei Blood Pressure Health Study.","authors":"Ying Wang, Shan-Shan Zhou, Yu-Qi Liu, Dan-Dan Li, Shun-Ying Hu, Xi Wang, Li Yi, Ya-Ni Yu, Yun-Dai Chen","doi":"10.1093/ehjdh/ztaf088","DOIUrl":"10.1093/ehjdh/ztaf088","url":null,"abstract":"<p><strong>Aims: </strong>This study aims to investigate the ownership of wearable health devices across different demographic groups and usage patterns among Chinese adults.</p><p><strong>Methods and results: </strong>This was a cross-sectional study, with all data originating from the Huawei Blood Pressure Health Study, a real-world study aimed at exploring blood pressure management through wearable devices in China. Data were remotely collected using mobile phones and Huawei Watch D from 23 February 2022 to 31 March 2024. The system utilized artificial intelligence algorithms to assess participants' risk of hypertension and provided risk alarm feedback via mobile phones and watches. A total of 75 918 participants from 31 provinces were included, with an average age of 47 years. Most of the participants were concentrated in the economically developed South China and East China regions. Among the participants, 73.8% used the Watch D for blood pressure monitoring, and 10.5% received risk alerts. The rate of blood pressure monitoring on the day they received the alert was 78%. However, the rate significantly decreased between 6 months and 1 year (Mann-Kendall test, <i>Z</i> = -2.85, <i>P</i> < 0.05). For hypertensive patients, the blood pressure monitoring rate was 84% on the day they joined the study and decreased over time (Mann-Kendall test, <i>Z</i> = -3.09, <i>P</i> < 0.05). However, it remained above 50% within 6 months.</p><p><strong>Conclusion: </strong>This study provides evidence of the digital health divide in the utilization of wearable devices among the Chinese population. Additionally, it proposes a potentially follow-up interval for employing wearable devices for maintaining compliance with blood pressure monitoring.</p><p><strong>Study registration: </strong>URL: https://www.chictr.org.cn/.</p><p><strong>Unique identifier for huawei-bphs: </strong>ChiCTR2200057354.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 6","pages":"1264-1272"},"PeriodicalIF":4.4,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12629657/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145566360","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-04eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf004
Bojan Hartmann, Niels-Ulrik Hartmann, Julia Brandts, Marlo Verket, Nikolaus Marx, Niveditha Dinesh, Lisa Schuetze, Anna Emilia Pape, Dirk Müller-Wieland, Markus Kollmann, Katharina Marx-Schütt, Martin Berger, Andreas Puetz, Felix Michels, Luca Leon Happel, Lars Müller, Guido Kobbe, Malte Jacobsen
Aims: Recurrent congestive episodes are a primary cause of hospitalizations in patients with heart failure. Hitherto, outpatient management adopts a reactive approach, assessing patients clinically through frequent follow-up visits to detect congestion early. This study aims to assess the capabilities of a self-supervised contrastive learning-derived risk index to detect episodes of acute decompensated heart failure (ADHF) in patients using continuously recorded wearable time-series data.
Methods and results: This is the protocol for a single-arm, prospective cohort pilot study that will include 290 patients with ADHF. Acute decompensated heart failure is diagnosed by clinical signs and symptoms, as well as additional diagnostics (e.g. NT-proBNP). Patients will receive standard-of-care treatment, supplemented by continuous wearable-based monitoring of vital signs and physical activity, and are followed for 90 days. During follow-up, study visits will be conducted and presentations without clinical ADHF will be referred to as 'regular' and data from these episodes will be presented to a deep neural network that is trained by a self-supervised contrastive learning objective to extract features from the time-series that are typical in regular periods. The model is used to calculate a risk index measuring the dissimilarity of observed features from those of regular periods. The primary outcome of this study will be the risk index's accuracy in detecting episodes with ADHF. As secondary outcome data integrity and the score in the validated questionnaire System Usability Scale will be evaluated.
Conclusion: Demonstrating reliable congestion detection through continuous monitoring with a wearable and self-supervised contrastive learning could assist in pre-emptive heart failure management in clinical care.
Clinical trial registration: The study was registered in the German clinical trials register (DRKS00034502).
{"title":"Congestion assessment using a self-supervised contrastive learning-derived risk index in patients with congestive heart failure (CONAN): protocol and design of a prospective cohort study.","authors":"Bojan Hartmann, Niels-Ulrik Hartmann, Julia Brandts, Marlo Verket, Nikolaus Marx, Niveditha Dinesh, Lisa Schuetze, Anna Emilia Pape, Dirk Müller-Wieland, Markus Kollmann, Katharina Marx-Schütt, Martin Berger, Andreas Puetz, Felix Michels, Luca Leon Happel, Lars Müller, Guido Kobbe, Malte Jacobsen","doi":"10.1093/ehjdh/ztaf004","DOIUrl":"10.1093/ehjdh/ztaf004","url":null,"abstract":"<p><strong>Aims: </strong>Recurrent congestive episodes are a primary cause of hospitalizations in patients with heart failure. Hitherto, outpatient management adopts a reactive approach, assessing patients clinically through frequent follow-up visits to detect congestion early. This study aims to assess the capabilities of a self-supervised contrastive learning-derived risk index to detect episodes of acute decompensated heart failure (ADHF) in patients using continuously recorded wearable time-series data.</p><p><strong>Methods and results: </strong>This is the protocol for a single-arm, prospective cohort pilot study that will include 290 patients with ADHF. Acute decompensated heart failure is diagnosed by clinical signs and symptoms, as well as additional diagnostics (e.g. NT-proBNP). Patients will receive standard-of-care treatment, supplemented by continuous wearable-based monitoring of vital signs and physical activity, and are followed for 90 days. During follow-up, study visits will be conducted and presentations without clinical ADHF will be referred to as 'regular' and data from these episodes will be presented to a deep neural network that is trained by a self-supervised contrastive learning objective to extract features from the time-series that are typical in regular periods. The model is used to calculate a risk index measuring the dissimilarity of observed features from those of regular periods. The primary outcome of this study will be the risk index's accuracy in detecting episodes with ADHF. As secondary outcome data integrity and the score in the validated questionnaire System Usability Scale will be evaluated.</p><p><strong>Conclusion: </strong>Demonstrating reliable congestion detection through continuous monitoring with a wearable and self-supervised contrastive learning could assist in pre-emptive heart failure management in clinical care.</p><p><strong>Clinical trial registration: </strong>The study was registered in the German clinical trials register (DRKS00034502).</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"1076-1083"},"PeriodicalIF":4.4,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450524/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf087
Olof Persson Lindell, Martin Henriksson, Lars O Karlsson, Staffan Nilsson, Emmanouil Charitakis, Magnus Janzon
Aims: Atrial fibrillation (AF) is a common arrythmia that increases the risk of thromboembolism. Despite the effectiveness of anticoagulation in AF, underuse remains a substantial problem. Clinical decision support (CDS) systems may increase adherence to guideline recommended anticoagulation in AF. However, evidence regarding the cost-effectiveness of these interventions is lacking. The aim of this study was therefore to evaluate the cost-effectiveness of a CDS for AF.
Methods and results: We developed a disease progression model with a Markov structure and simulated a cohort of hypothetical individuals with AF through a standard of care and a CDS strategy. The adherence to anticoagulation in the model was based on the treatment effect reported in the CDS-AF trial, which evaluated the effect of a CDS in patients with AF in the primary care in Östergötland, Sweden. The cost-effectiveness of the CDS-AF intervention compared with standard of care was determined by estimating costs and quality-adjusted life years (QALYs) gained over a lifetime time horizon and was reported as an incremental cost-effectiveness ratio (ICER) assessed against a decision-threshold of €50 000. Uncertainty was evaluated using both one-way and probabilistic sensitivity analysis (PSA). The CDS-intervention resulted in fewer ischaemic strokes but more bleedings. The mean per patient gain in QALYs was 0.012 and the ICER was €963 per QALY gained. The result of the PSA indicated a high probability that the ICER was below €50 000.
Conclusion: The CDS intervention used in the CDS-AF trial appears to yield health gains at a lower cost than typically considered cost-effective.
{"title":"Cost-effectiveness of a clinical decision support system for atrial fibrillation: an RCT-based modelling study.","authors":"Olof Persson Lindell, Martin Henriksson, Lars O Karlsson, Staffan Nilsson, Emmanouil Charitakis, Magnus Janzon","doi":"10.1093/ehjdh/ztaf087","DOIUrl":"10.1093/ehjdh/ztaf087","url":null,"abstract":"<p><strong>Aims: </strong>Atrial fibrillation (AF) is a common arrythmia that increases the risk of thromboembolism. Despite the effectiveness of anticoagulation in AF, underuse remains a substantial problem. Clinical decision support (CDS) systems may increase adherence to guideline recommended anticoagulation in AF. However, evidence regarding the cost-effectiveness of these interventions is lacking. The aim of this study was therefore to evaluate the cost-effectiveness of a CDS for AF.</p><p><strong>Methods and results: </strong>We developed a disease progression model with a Markov structure and simulated a cohort of hypothetical individuals with AF through a standard of care and a CDS strategy. The adherence to anticoagulation in the model was based on the treatment effect reported in the CDS-AF trial, which evaluated the effect of a CDS in patients with AF in the primary care in Östergötland, Sweden. The cost-effectiveness of the CDS-AF intervention compared with standard of care was determined by estimating costs and quality-adjusted life years (QALYs) gained over a lifetime time horizon and was reported as an incremental cost-effectiveness ratio (ICER) assessed against a decision-threshold of €50 000. Uncertainty was evaluated using both one-way and probabilistic sensitivity analysis (PSA). The CDS-intervention resulted in fewer ischaemic strokes but more bleedings. The mean per patient gain in QALYs was 0.012 and the ICER was €963 per QALY gained. The result of the PSA indicated a high probability that the ICER was below €50 000.</p><p><strong>Conclusion: </strong>The CDS intervention used in the CDS-AF trial appears to yield health gains at a lower cost than typically considered cost-effective.</p><p><strong>Trial registration: </strong>NCT02635685.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"997-1005"},"PeriodicalIF":4.4,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450513/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-25eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf086
Giorgia Panichella, Manuel Garofalo, Laura Sasso, Alessandra Milazzo, Alessandra Fornaro, Josè Manuel Pioner, Alfonso Bueno-Orovio, Mark van Gils, Annariina Koivu, Luca Mainardi, Virginie Le Rolle, Felix Agakov, Maurizio Pieroni, Katriina Aalto-Setälä, Jari Hyttinen, Iacopo Olivotto, Annamaria Del Franco
Hypertrophic cardiomyopathy (HCM) is a heterogeneous disease where, despite recent advances, accurate diagnosis, risk stratification, and personalized treatment remain challenging. Artificial intelligence (AI) offers a transformative approach to HCM by enabling rapid, precise analysis of complex data. This article reviews the current and potential applications of AI in HCM. AI enhances diagnostic accuracy by analysing electrocardiograms, echocardiography, and cardiac magnetic resonance images, differentiating HCM from other forms of left ventricular hypertrophy, identifying subtle phenotypic variations, and standardizing myocardial fibrosis assessment. Multimodal AI-driven approaches improve risk stratification, therapeutic decision-making, and monitoring of both established and novel therapies, such as cardiac myosin inhibitors. Emerging AI-driven in silico trials and digital twin platforms highlight the potential of combining data-driven and knowledge-based AI with biophysical models to simulate patient-specific disease trajectories, supporting preclinical evaluation and personalized care. As a multidisciplinary case study, the SMASH-HCM consortium is presented to illustrate how digital twin technologies and hybrid modelling can bring AI into clinical practice. Integration of genetic data further enhances AI's ability to identify at-risk individuals and predict disease progression. However, widespread AI applications raise concerns regarding data privacy, ethical considerations, and the risk of biases. Guidelines for researchers and developers-e.g. on trustworthy AI, regulatory frameworks, and transparent policies-are essential to address these possible pitfalls. As AI rapidly evolves, it has the potential to revolutionize drug discovery, disease management, and the patient journey in HCM, making interventions more precise, timely, and patient-centred.
{"title":"Artificial intelligence applications in hypertrophic cardiomyopathy: turns and loopholes.","authors":"Giorgia Panichella, Manuel Garofalo, Laura Sasso, Alessandra Milazzo, Alessandra Fornaro, Josè Manuel Pioner, Alfonso Bueno-Orovio, Mark van Gils, Annariina Koivu, Luca Mainardi, Virginie Le Rolle, Felix Agakov, Maurizio Pieroni, Katriina Aalto-Setälä, Jari Hyttinen, Iacopo Olivotto, Annamaria Del Franco","doi":"10.1093/ehjdh/ztaf086","DOIUrl":"10.1093/ehjdh/ztaf086","url":null,"abstract":"<p><p>Hypertrophic cardiomyopathy (HCM) is a heterogeneous disease where, despite recent advances, accurate diagnosis, risk stratification, and personalized treatment remain challenging. Artificial intelligence (AI) offers a transformative approach to HCM by enabling rapid, precise analysis of complex data. This article reviews the current and potential applications of AI in HCM. AI enhances diagnostic accuracy by analysing electrocardiograms, echocardiography, and cardiac magnetic resonance images, differentiating HCM from other forms of left ventricular hypertrophy, identifying subtle phenotypic variations, and standardizing myocardial fibrosis assessment. Multimodal AI-driven approaches improve risk stratification, therapeutic decision-making, and monitoring of both established and novel therapies, such as cardiac myosin inhibitors. Emerging AI-driven <i>in silico</i> trials and digital twin platforms highlight the potential of combining data-driven and knowledge-based AI with biophysical models to simulate patient-specific disease trajectories, supporting preclinical evaluation and personalized care. As a multidisciplinary case study, the SMASH-HCM consortium is presented to illustrate how digital twin technologies and hybrid modelling can bring AI into clinical practice. Integration of genetic data further enhances AI's ability to identify at-risk individuals and predict disease progression. However, widespread AI applications raise concerns regarding data privacy, ethical considerations, and the risk of biases. Guidelines for researchers and developers-e.g. on trustworthy AI, regulatory frameworks, and transparent policies-are essential to address these possible pitfalls. As AI rapidly evolves, it has the potential to revolutionize drug discovery, disease management, and the patient journey in HCM, making interventions more precise, timely, and patient-centred.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"853-867"},"PeriodicalIF":4.4,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450525/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-23eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf083
Tanmay A Gokhale, Nathan T Riek, Brent Medoff, Rui Qi Ji, Belinda Rivera-Lebron, Ervin Sejdic, Murat Akcakaya, Samir F Saba, Salah Al-Zaiti, Catalin Toma
Aims: Among patients with acute pulmonary embolism (PE), rapid identification of those with highest clinical risk can help guide life-saving treatment. However, current risk stratification algorithms involve a multistep process requiring physical exam, imaging, and laboratory results. We investigated the utility of electrocardiogram (ECG) alone to rapidly identify patients at elevated clinical risk by developing and validating a feature-based artificial intelligence (AI) model to predict clinical risk.
Methods and results: Patients who were diagnosed with PE over a 9-year period, had an ECG within 1 day of presentation, and were evaluated by our PE response team (PERT) were included. A feature-based random forest model was trained to predict the PERT team's risk stratification from the ECG alone. The ability of the model to predict the clinical risk categorization and the accuracy of both risk stratification approaches in predicting mortality were examined on a holdout test set. Of the overall cohort of 1376 patients, 55% had a submassive (intermediate risk) or massive (high risk) PE, which were grouped together as 'severe PE'. The AI-ECG model was able to predict the clinical classification (low-risk vs. severe PE) with an AUC of 0.83 and F1 score of 0.78 in a holdout test set. A 30-day mortality and in-hospital mortality were significantly different between patients classified by the model as low vs. elevated risk.
Conclusion: AI-based analysis of 12-lead ECGs may provide a useful tool in the risk stratification of PE, allowing for rapid identification and treatment of those at highest risk of adverse outcomes.
{"title":"Artificial intelligence-driven electrocardiogram analysis for risk stratification in pulmonary embolism.","authors":"Tanmay A Gokhale, Nathan T Riek, Brent Medoff, Rui Qi Ji, Belinda Rivera-Lebron, Ervin Sejdic, Murat Akcakaya, Samir F Saba, Salah Al-Zaiti, Catalin Toma","doi":"10.1093/ehjdh/ztaf083","DOIUrl":"10.1093/ehjdh/ztaf083","url":null,"abstract":"<p><strong>Aims: </strong>Among patients with acute pulmonary embolism (PE), rapid identification of those with highest clinical risk can help guide life-saving treatment. However, current risk stratification algorithms involve a multistep process requiring physical exam, imaging, and laboratory results. We investigated the utility of electrocardiogram (ECG) alone to rapidly identify patients at elevated clinical risk by developing and validating a feature-based artificial intelligence (AI) model to predict clinical risk.</p><p><strong>Methods and results: </strong>Patients who were diagnosed with PE over a 9-year period, had an ECG within 1 day of presentation, and were evaluated by our PE response team (PERT) were included. A feature-based random forest model was trained to predict the PERT team's risk stratification from the ECG alone. The ability of the model to predict the clinical risk categorization and the accuracy of both risk stratification approaches in predicting mortality were examined on a holdout test set. Of the overall cohort of 1376 patients, 55% had a submassive (intermediate risk) or massive (high risk) PE, which were grouped together as 'severe PE'. The AI-ECG model was able to predict the clinical classification (low-risk vs. severe PE) with an AUC of 0.83 and F1 score of 0.78 in a holdout test set. A 30-day mortality and in-hospital mortality were significantly different between patients classified by the model as low vs. elevated risk.</p><p><strong>Conclusion: </strong>AI-based analysis of 12-lead ECGs may provide a useful tool in the risk stratification of PE, allowing for rapid identification and treatment of those at highest risk of adverse outcomes.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"989-996"},"PeriodicalIF":4.4,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450519/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-23eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf084
Paulien Vermunicht, Christophe Buyck, Sebastiaan Naessens, Wendy Hens, Caro Verberckt, Emeline Van Craenenbroeck, Kris Laukens, Lien Desteghe, Hein Heidbuchel
Introduction: Sensor placement, activity type influencing wrist movements, and individual characteristics impact accuracy of wrist-worn photoplethysmography (PPG)-based heart rate (HR) monitors. This study investigated technical interventions to optimize PPG accuracy in patients with cardiac disease.
Methods and results: The Fitbit Inspire 2 PPG monitor was evaluated across three cohorts, using a Polar H10 chest strap as reference: (ⅰ) 10 healthy volunteers performed wrist movements with the monitor placed one or three fingers above the wrist to identify optimal placement; (ⅱ) 10 volunteers engaged in sport activities (walking, running, cycling, rowing); (ⅲ) 30 cardiac rehabilitation patients were monitored during exercise to assess baseline accuracy. Patients with low accuracy [mean absolute percentage error (MAPE) < 10% for <70% of training time] underwent technical interventions (sensor cleaning, forearm shaving, position fixation, and/or relocation to the volar wrist). Placement three vs. one fingers above the wrist was significantly more accurate (mean difference in MAPE: -11.4%, P < 0.001). Walking showed the highest accuracy (MAPE = 3.8%), followed by cycling (MAPE = 6.9%) and running (MAPE = 8.5%), while rowing had the lowest accuracy (MAPE = 13.4%, P < 0.001). Among CR patients, 66.7% achieved high baseline accuracy. Technical interventions improved accuracy in 50.0% of those with low baseline accuracy, but no significant predictors of optimization success were identified.
Conclusion: Accurate PPG-based monitoring requires a sensor placed higher on the wrist. Nevertheless, only two-thirds of patients are suitable for such monitoring, with improvement by technical adaptations possible (but impractical) in the others. Therefore, assessing baseline accuracy is a prerequisite before relying on these devices for activity guidance.
{"title":"Optimization and pre-use suitability selection for wrist photoplethysmography-based heart rate monitoring in patients with cardiac disease.","authors":"Paulien Vermunicht, Christophe Buyck, Sebastiaan Naessens, Wendy Hens, Caro Verberckt, Emeline Van Craenenbroeck, Kris Laukens, Lien Desteghe, Hein Heidbuchel","doi":"10.1093/ehjdh/ztaf084","DOIUrl":"10.1093/ehjdh/ztaf084","url":null,"abstract":"<p><strong>Introduction: </strong>Sensor placement, activity type influencing wrist movements, and individual characteristics impact accuracy of wrist-worn photoplethysmography (PPG)-based heart rate (HR) monitors. This study investigated technical interventions to optimize PPG accuracy in patients with cardiac disease.</p><p><strong>Methods and results: </strong>The Fitbit Inspire 2 PPG monitor was evaluated across three cohorts, using a Polar H10 chest strap as reference: (ⅰ) 10 healthy volunteers performed wrist movements with the monitor placed one or three fingers above the wrist to identify optimal placement; (ⅱ) 10 volunteers engaged in sport activities (walking, running, cycling, rowing); (ⅲ) 30 cardiac rehabilitation patients were monitored during exercise to assess baseline accuracy. Patients with low accuracy [mean absolute percentage error (MAPE) < 10% for <70% of training time] underwent technical interventions (sensor cleaning, forearm shaving, position fixation, and/or relocation to the volar wrist). Placement three vs. one fingers above the wrist was significantly more accurate (mean difference in MAPE: -11.4%, <i>P</i> < 0.001). Walking showed the highest accuracy (MAPE = 3.8%), followed by cycling (MAPE = 6.9%) and running (MAPE = 8.5%), while rowing had the lowest accuracy (MAPE = 13.4%, <i>P</i> < 0.001). Among CR patients, 66.7% achieved high baseline accuracy. Technical interventions improved accuracy in 50.0% of those with low baseline accuracy, but no significant predictors of optimization success were identified.</p><p><strong>Conclusion: </strong>Accurate PPG-based monitoring requires a sensor placed higher on the wrist. Nevertheless, only two-thirds of patients are suitable for such monitoring, with improvement by technical adaptations possible (but impractical) in the others. Therefore, assessing baseline accuracy is a prerequisite before relying on these devices for activity guidance.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"1024-1035"},"PeriodicalIF":4.4,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450509/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126682","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-18eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf082
Julian Kreutz, Jonathan Bamberger, Lukas Harbaum, Klevis Mihali, Georgios Chatzis, Nikolaos Patsalis, Mohamed Ben Amar, Styliani Syntila, Martin C Hirsch, Fabian Lechner, Bernhard Schieffer, Birgit Markus
Aims: The role of temporary mechanical circulatory support (tMCS) after out-of-hospital cardiac arrest (OHCA) remains controversial. This study evaluates machine learning (ML) models for predicting mortality and neurological outcomes, highlighting their potential as a tool to guide early tMCS decision-making.
Methods and results: This retrospective study analysed five years of data from 564 adult non-traumatic OHCA patients treated at Marburg University Hospital. Four ML models (ANN, SVM, RF, XGBoost) were trained to predict in-hospital mortality and neurological outcome based on demographic, clinical, and treatment-related variables. Feature selection and SHAP analysis were used to optimize performance and identify patients potentially benefiting from tMCS. Overall, 144 patients (31.2%) out of 461 patients who fulfilled the inclusion criteria received tMCS: 39 left-ventricular microaxial flow pump, 76 venoarterial extracorporeal membrane oxygenation (VA-ECMO), and 29 biventricular support (ECMELLA). In 69 patients (14.9%) VA-ECMO implantation was performed as part of extracorporeal cardiopulmonary resuscitation. The survival rate of the tMCS group was 34.7% (50/144) compared to 52.7% (167/317) in the non-tMCS group. The highest predictive power for survival probability (with/without tMCS) could be achieved by XGBoost and RF when applied to the non-tMCS group. Machine learning identified 2.5% of non-tMCS patients likely to survive if treated with tMCS. In 23 (RF model) and 31 (XGBoost model) patients, the probability of survival increased by at least 5% with tMCS compared to their predicted outcome without tMCS. RF slightly outperformed XGBoost [area under the receiver operating characteristic curve (AUC) 0.85 vs. AUC 0.82].
Conclusion: XGBoost and RF models accurately predict mortality and tMCS benefit in OHCA patients, supporting ML-based personalized therapy.
目的:院外心脏骤停(OHCA)后临时机械循环支持(tMCS)的作用仍然存在争议。本研究评估了预测死亡率和神经预后的机器学习(ML)模型,强调了它们作为指导早期tMCS决策工具的潜力。方法和结果:本回顾性研究分析了在马尔堡大学医院治疗的564名成年非创伤性OHCA患者的5年数据。训练四种ML模型(ANN、SVM、RF、XGBoost),根据人口统计学、临床和治疗相关变量预测住院死亡率和神经预后。使用特征选择和SHAP分析来优化性能并确定可能受益于tMCS的患者。总体而言,461例符合纳入标准的患者中有144例(31.2%)接受了tMCS: 39例左心室微轴流泵,76例静脉体外膜氧合(VA-ECMO), 29例双心室支持(ECMELLA)。在69例(14.9%)患者中,VA-ECMO植入作为体外心肺复苏的一部分。tMCS组生存率为34.7%(50/144),非tMCS组为52.7%(167/317)。当应用于非tMCS组时,XGBoost和RF对生存概率(有/没有tMCS)的预测能力最高。机器学习识别出2.5%的非tMCS患者在接受tMCS治疗后可能存活。在23例(RF模型)和31例(XGBoost模型)患者中,与没有tMCS的预测结果相比,tMCS的生存概率至少增加了5%。RF略优于XGBoost[接收器工作特性曲线下面积(AUC) 0.85 vs AUC 0.82]。结论:XGBoost和RF模型可准确预测OHCA患者的死亡率和tMCS获益,支持基于ml的个性化治疗。
{"title":"Evaluation of machine learning models for personalized prediction of benefit from temporary mechanical circulatory support after out-of-hospital cardiac arrest.","authors":"Julian Kreutz, Jonathan Bamberger, Lukas Harbaum, Klevis Mihali, Georgios Chatzis, Nikolaos Patsalis, Mohamed Ben Amar, Styliani Syntila, Martin C Hirsch, Fabian Lechner, Bernhard Schieffer, Birgit Markus","doi":"10.1093/ehjdh/ztaf082","DOIUrl":"10.1093/ehjdh/ztaf082","url":null,"abstract":"<p><strong>Aims: </strong>The role of temporary mechanical circulatory support (tMCS) after out-of-hospital cardiac arrest (OHCA) remains controversial. This study evaluates machine learning (ML) models for predicting mortality and neurological outcomes, highlighting their potential as a tool to guide early tMCS decision-making.</p><p><strong>Methods and results: </strong>This retrospective study analysed five years of data from 564 adult non-traumatic OHCA patients treated at Marburg University Hospital. Four ML models (ANN, SVM, RF, XGBoost) were trained to predict in-hospital mortality and neurological outcome based on demographic, clinical, and treatment-related variables. Feature selection and SHAP analysis were used to optimize performance and identify patients potentially benefiting from tMCS. Overall, 144 patients (31.2%) out of 461 patients who fulfilled the inclusion criteria received tMCS: 39 left-ventricular microaxial flow pump, 76 venoarterial extracorporeal membrane oxygenation (VA-ECMO), and 29 biventricular support (ECMELLA). In 69 patients (14.9%) VA-ECMO implantation was performed as part of extracorporeal cardiopulmonary resuscitation. The survival rate of the tMCS group was 34.7% (50/144) compared to 52.7% (167/317) in the non-tMCS group. The highest predictive power for survival probability (with/without tMCS) could be achieved by XGBoost and RF when applied to the non-tMCS group. Machine learning identified 2.5% of non-tMCS patients likely to survive if treated with tMCS. In 23 (RF model) and 31 (XGBoost model) patients, the probability of survival increased by at least 5% with tMCS compared to their predicted outcome without tMCS. RF slightly outperformed XGBoost [area under the receiver operating characteristic curve (AUC) 0.85 vs. AUC 0.82].</p><p><strong>Conclusion: </strong>XGBoost and RF models accurately predict mortality and tMCS benefit in OHCA patients, supporting ML-based personalized therapy.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"979-988"},"PeriodicalIF":4.4,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450520/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126704","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-17eCollection Date: 2025-09-01DOI: 10.1093/ehjdh/ztaf080
David Hong, Sung-Hee Song, Heayoung Shin, Minjung Bak, Juwon Kim, Darae Kim, Ju Youn Kim, Jeong Hoon Yang, Seung-Jung Park, Jin-Oh Choi, Young Keun On, Kyoung-Min Park
Aims: Heart failure with preserved ejection fraction (HFpEF) is difficult to diagnose due to the lack of a definitive diagnostic marker; multiple tests are required, including advanced evaluations. This study aimed to develop an artificial intelligence (AI)-enabled electrocardiogram (ECG) model for predicting HFpEF.
Methods and results: This retrospective cohort study included patients from a single tertiary centre who underwent echocardiography, N-terminal prohormone of B-type natriuretic peptide measurement, and ECG within a defined timeframe. Patients were classified as HFpEF (HFA-PEFF score ≥5) or control (HFA-PEFF score <5). Patients were divided into training, validation, and test subsets at a 7:1:2 ratio for model development and validation. Using the collected ECGs, a convolutional neural network was trained to predict HFpEF; its performance was assessed using the area under the receiver operating characteristic curve (AUROC). Among the 13 081 patients included, 5795 (44.3%) were classified as HFpEF and 7286 (55.7%) were classified as control. The AI-enabled ECG model demonstrated good discriminative performance [AUROC 0.81; 95% confidence interval (CI) 0.79-0.82]. Subgroup analyses stratified by HFpEF risk factors confirmed consistent model performance. Prognostic evaluation revealed that patients with a positive AI-ECG classification experienced significantly worse outcomes relative to those with a negative classification, including higher risks of cardiac death (1.1% vs. 0.1%; hazard ratio 9.56; 95% CI 1.24-73.53; P = 0.030) and heart failure hospitalization (2.8% vs. 0.6%; hazard ratio 5.91; 95% CI 2.08-16.81; P = 0.001) at 5 year.
Conclusion: The AI-ECG model is a reliable tool for predicting HFpEF, as defined by the HFA-PEFF score, and effectively stratifies patients according to prognosis. Integration of this model into clinical practice may simplify and enhance the diagnostic process for HFpEF.
目的:由于缺乏明确的诊断指标,保留射血分数的心力衰竭(HFpEF)难以诊断;需要进行多次测试,包括高级评估。本研究旨在开发一种人工智能(AI)支持的心电图(ECG)模型来预测HFpEF。方法和结果:这项回顾性队列研究包括来自单一三级中心的患者,他们在规定的时间内接受了超声心动图、b型利钠肽n端激素原测量和心电图检查。患者在5年时被分为HFpEF (HFA-PEFF评分≥5)或对照组(HFA-PEFF评分P = 0.030)和心力衰竭住院(2.8% vs. 0.6%;风险比5.91;95% CI 2.08-16.81; P = 0.001)。结论:AI-ECG模型是预测HFA-PEFF评分定义的HFpEF的可靠工具,可根据预后对患者进行有效分层。将该模型整合到临床实践中可以简化和提高HFpEF的诊断过程。
{"title":"Artificial intelligence-enabled electrocardiogram model for predicting heart failure with preserved ejection fraction: a single-center study.","authors":"David Hong, Sung-Hee Song, Heayoung Shin, Minjung Bak, Juwon Kim, Darae Kim, Ju Youn Kim, Jeong Hoon Yang, Seung-Jung Park, Jin-Oh Choi, Young Keun On, Kyoung-Min Park","doi":"10.1093/ehjdh/ztaf080","DOIUrl":"10.1093/ehjdh/ztaf080","url":null,"abstract":"<p><strong>Aims: </strong>Heart failure with preserved ejection fraction (HFpEF) is difficult to diagnose due to the lack of a definitive diagnostic marker; multiple tests are required, including advanced evaluations. This study aimed to develop an artificial intelligence (AI)-enabled electrocardiogram (ECG) model for predicting HFpEF.</p><p><strong>Methods and results: </strong>This retrospective cohort study included patients from a single tertiary centre who underwent echocardiography, N-terminal prohormone of B-type natriuretic peptide measurement, and ECG within a defined timeframe. Patients were classified as HFpEF (HFA-PEFF score ≥5) or control (HFA-PEFF score <5). Patients were divided into training, validation, and test subsets at a 7:1:2 ratio for model development and validation. Using the collected ECGs, a convolutional neural network was trained to predict HFpEF; its performance was assessed using the area under the receiver operating characteristic curve (AUROC). Among the 13 081 patients included, 5795 (44.3%) were classified as HFpEF and 7286 (55.7%) were classified as control. The AI-enabled ECG model demonstrated good discriminative performance [AUROC 0.81; 95% confidence interval (CI) 0.79-0.82]. Subgroup analyses stratified by HFpEF risk factors confirmed consistent model performance. Prognostic evaluation revealed that patients with a positive AI-ECG classification experienced significantly worse outcomes relative to those with a negative classification, including higher risks of cardiac death (1.1% vs. 0.1%; hazard ratio 9.56; 95% CI 1.24-73.53; <i>P</i> = 0.030) and heart failure hospitalization (2.8% vs. 0.6%; hazard ratio 5.91; 95% CI 2.08-16.81; <i>P</i> = 0.001) at 5 year.</p><p><strong>Conclusion: </strong>The AI-ECG model is a reliable tool for predicting HFpEF, as defined by the HFA-PEFF score, and effectively stratifies patients according to prognosis. Integration of this model into clinical practice may simplify and enhance the diagnostic process for HFpEF.</p>","PeriodicalId":72965,"journal":{"name":"European heart journal. Digital health","volume":"6 5","pages":"959-968"},"PeriodicalIF":4.4,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12450526/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}