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Valvular heart disease (VHD) is becoming more prevalent in an ageing population, leading to challenges in diagnosis and management. This two-part Series offers a comprehensive review of changing concepts in VHD, covering diagnosis, intervention timing, novel management strategies, and the current state of research. The first paper highlights the remarkable progress made in imaging and transcatheter techniques, effectively addressing the treatment paradox wherein populations at the highest risk of VHD often receive the least treatment. These advances have attracted the attention of clinicians, researchers, engineers, device manufacturers, and investors, leading to the exploration and proposal of treatment approaches grounded in pathophysiology and multidisciplinary strategies for VHD management. This Series paper focuses on innovations involving computational, pharmacological, and bioengineering approaches that are transforming the diagnosis and management of patients with VHD. Artificial intelligence and digital methods are enhancing screening, diagnosis, and planning procedures, and the integration of imaging and clinical data is improving the classification of VHD severity. The emergence of artificial intelligence techniques, including so-called digital twins-eg, computer-generated replicas of the heart-is aiding the development of new strategies for enhanced risk stratification, prognostication, and individualised therapeutic targeting. Various new molecular targets and novel pharmacological strategies are being developed, including multiomics-ie, analytical methods used to integrate complex biological big data to find novel pathways to halt the progression of VHD. In addition, efforts have been undertaken to engineer heart valve tissue and provide a living valve conduit capable of growth and biological integration. Overall, these advances emphasise the importance of early detection, personalised management, and cutting-edge interventions to optimise outcomes amid the evolving landscape of VHD. Although several challenges must be overcome, these breakthroughs represent opportunities to advance patient-centred investigations.
Assuntos
Inteligência Artificial , Doenças das Valvas Cardíacas , Humanos , Doenças das Valvas Cardíacas/diagnóstico , Doenças das Valvas Cardíacas/terapiaRESUMO
Large language models (LLMs) are a unique form of machine learning that facilitates inputs of unstructured text/numerical information for meaningful interpretation and prediction. Recently, LLMs have become commercialized, allowing the average person to access these incredibly powerful tools. Early adopters focused on LLM use in performing logical tasks, including-but not limited to-generating titles, identifying key words, summarizing text, initial editing of scientific work, improving statistical protocols, and performing statistical analysis. More recently, LLMs have been expanded to clinical practice and academia to perform higher cognitive and creative tasks. LLMs provide personalized assistance in learning, facilitate the management of electronic medical records, and offer valuable insights into clinical decision making in cardiology. They enhance patient education by explaining intricate medical conditions in lay terms, have a vast library of knowledge to help clinicians expedite administrative tasks, provide useful feedback regarding content of scientific writing, and assist in the peer-review process. Despite their impressive capabilities, LLMs are not without limitations. They are susceptible to generating incorrect or plagiarized content, face challenges in handling tasks without detailed prompts, and lack originality. These limitations underscore the importance of human oversight in using LLMs in medical science and clinical practice. As LLMs continue to evolve, addressing these challenges will be crucial in maximizing their potential benefits while mitigating risks. This review explores the functions, opportunities, and constraints of LLMs, with a focus on their impact on cardiology, illustrating both the transformative power and the boundaries of current technology in medicine.
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Single coronary artery, giant coronary artery aneurysm, and coronary cameral fistula are rare congenital anomalies, and can cause a range of presentations. To our knowledge, this is the first reported case of all 3 entities occurring simultaneously in 1 patient, with largely unknown implications. Multimodal imaging was essential in prompt diagnosis and management.
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To provide accurate predictions, current machine learning-based solutions require large, manually labeled training datasets. We implement persistent homology (PH), a topological tool for studying the pattern of data, to analyze echocardiography-based strain data and differentiate between rare diseases like constrictive pericarditis (CP) and restrictive cardiomyopathy (RCM). Patient population (retrospectively registered) included those presenting with heart failure due to CP (n = 51), RCM (n = 47), and patients without heart failure symptoms (n = 53). Longitudinal, radial, and circumferential strains/strain rates for left ventricular segments were processed into topological feature vectors using Machine learning PH workflow. In differentiating CP and RCM, the PH workflow model had a ROC AUC of 0.94 (Sensitivity = 92%, Specificity = 81%), compared with the GLS model AUC of 0.69 (Sensitivity = 65%, Specificity = 66%). In differentiating between all three conditions, the PH workflow model had an AUC of 0.83 (Sensitivity = 68%, Specificity = 84%), compared with the GLS model AUC of 0.68 (Sensitivity = 52% and Specificity = 76%). By employing persistent homology to differentiate the "pattern" of cardiac deformations, our machine-learning approach provides reasonable accuracy when evaluating small datasets and aids in understanding and visualizing patterns of cardiac imaging data in clinically challenging disease states.
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Ecocardiografia , Aprendizado de Máquina , Humanos , Masculino , Ecocardiografia/métodos , Feminino , Pessoa de Meia-Idade , Doenças Raras/diagnóstico por imagem , Pericardite Constritiva/diagnóstico por imagem , Pericardite Constritiva/diagnóstico , Cardiomiopatia Restritiva/diagnóstico por imagem , Estudos Retrospectivos , Idoso , Ventrículos do Coração/diagnóstico por imagem , Ventrículos do Coração/fisiopatologia , Insuficiência Cardíaca/diagnóstico por imagem , AdultoRESUMO
AIMS: Age-related changes in cardiac structure and function are well recognized and make the clinical determination of abnormal left ventricular (LV) diastolic dysfunction (LVDD) particularly challenging in the elderly. We investigated whether a deep neural network (DeepNN) model of LVDD, previously validated in a younger cohort, can be implemented in an older population to predict incident heart failure (HF). METHODS AND RESULTS: A previously developed DeepNN was tested on 5596 older participants (66-90 years; 57% female; 20% Black) from the Atherosclerosis Risk in Communities Study. The association of DeepNN predictions with HF or all-cause death for the American College of Cardiology Foundation/American Heart Association Stage A/B (n = 4054) and Stage C/D (n = 1542) subgroups was assessed. The DeepNN-predicted high-risk compared with the low-risk phenogroup demonstrated an increased incidence of HF and death for both Stage A/B and Stage C/D (log-rank P < 0.0001 for all). In multi-variable analyses, the high-risk phenogroup remained an independent predictor of HF and death in both Stages A/B {adjusted hazard ratio [95% confidence interval (CI)] 6.52 [4.20-10.13] and 2.21 [1.68-2.91], both P < 0.0001} and Stage C/D [6.51 (4.06-10.44) and 1.03 (1.00-1.06), both P < 0.0001], respectively. In addition, DeepNN showed incremental value over the 2016 American Society of Echocardiography/European Association of Cardiovascular Imaging (ASE/EACVI) guidelines [net re-classification index, 0.5 (CI 0.4-0.6), P < 0.001; C-statistic improvement, DeepNN (0.76) vs. ASE/EACVI (0.70), P < 0.001] overall and maintained across stage groups. CONCLUSION: Despite training with a younger cohort, a deep patient-similarity-based learning framework for assessing LVDD provides a robust prediction of all-cause death and incident HF for older patients.
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Disfunção Ventricular Esquerda , Humanos , Feminino , Idoso , Masculino , Idoso de 80 Anos ou mais , Disfunção Ventricular Esquerda/diagnóstico por imagem , Disfunção Ventricular Esquerda/fisiopatologia , Aprendizado Profundo , Medição de Risco , Insuficiência Cardíaca/diagnóstico por imagem , Ecocardiografia/métodos , Estados Unidos , Estudos de Coortes , Redes Neurais de Computação , Diástole , Fatores EtáriosRESUMO
El reemplazo de válvulas aórticas transcatéter es una opción de tratamiento excelente para pacientes con estenosis aórtica severa sintomática y riesgo alto o intermedio para cirugía. Con base en evidencia científica sólida en reemplazo de válvulas aórticas transcatéter, obtenida de estudios clínicos aleatorios y con ya cerca de ocho años de experiencia comercial, ¿por qué importaría pensar en la durabilidad de estas válvulas y por qué esta duda acaba de salir a la luz pública? La durabilidad a largo plazo de las válvulas utilizadas en reemplazo de válvulas aórticas transcatéter, ha sido motivo de interés como respuesta a diferentes factores: El desarrollo continuo de la tecnología reduce los riesgos del procedimiento y mejora la expectativa de vida. Cada vez el reemplazo de válvulas aórticas transcatéter se utiliza con más frecuencia en pacientes jóvenes, aun con patología congénita como la válvula aórtica bivalva, y en aquellas más complejas incluidas las bioprótesis disfuncionales, con estenosis regurgitación severa, procedimiento que se conoce como válvula en válvula1), (2. Sin embargo, pese a la penetración cada vez mayor de la técnica, una gran población con estenosis aórtica severa sintomática, que podría ser potencial candidata a reemplazo de válvulas aórticas transcatéter en un futuro, permanece sin diagnóstico y sin tratamiento.