Sang-Eun Lee1, Hyuk-Jae Chang2, Asim Rizvi3, Martin Hadamitzky4, Yong-Jin Kim5, Edoardo Conte6, Daniele Andreini6, Gianluca Pontone6, Valentina Volpato6, Matthew J Budoff7, Ilan Gottlieb8, Byoung Kwon Lee9, Eun Ju Chun10, Filippo Cademartiri11, Erica Maffei11, Hugo Marques12, Jonathon A Leipsic13, Sanghoon Shin14, Jung Hyun Choi15, Namsik Chung1, James K Min16. 1. Division of Cardiology, Severance Cardiovascular Hospital, Integrative Cardiovascular Imaging Center, Yonsei University Health System, Seoul, South Korea. 2. Division of Cardiology, Severance Cardiovascular Hospital, Integrative Cardiovascular Imaging Center, Yonsei University Health System, Seoul, South Korea. Electronic address: hjchang@yuhs.ac. 3. Dalio Institute of Cardiovascular Imaging, New York-Presbyterian Hospital and Weill Cornell Medical College, New York, NY, USA. 4. Division of Cardiology, University of Munich, Munich, Germany. 5. Seoul National University Hospital, South Korea. 6. Centro Cardiologico Monzino, IRCCS, Milan, Italy. 7. Department of Medicine, Harbor UCLA Medical Center, Los Angeles, CA, USA. 8. Department of Radiology, Casa de Saude São Jose, Rio de Janeiro, Brazil. 9. Gangnam Severance Hospital, South Korea. 10. Seoul National University Bundang Hospital, South Korea. 11. Department of Radiology, Montréal Heart Institute/Université de Montréal, Montréal, Quebec, Canada. 12. Hospital da Luz, Lisbon, Portugal. 13. Department of Radiology, St Paul's Hospital, University of British Columbia, Vancouver, Canada. 14. National Health Insurance Service Ilsan Hospital, South Korea. 15. Busan University Hospital, South Korea. 16. Dalio Institute of Cardiovascular Imaging, New York-Presbyterian Hospital and Weill Cornell Medical College, New York, NY, USA. Electronic address: jkm2001@med.cornell.edu.
Abstract
BACKGROUND: The natural history of coronary artery disease (CAD) in patients with low-to-intermediate risk is not well characterized. Although earlier invasive serial studies have documented the progression of atherosclerotic burden, most were focused on high-risk patients only. The PARADIGM registry is a large, prospective, multinational dynamic observational registry of patients undergoing serial coronary computed tomographic angiography (CCTA). The primary aim of PARADIGM is to characterize the natural history of CAD in relation to clinical and laboratory data. DESIGN: The PARADIGM registry (ClinicalTrials.govNCT02803411) comprises ≥2,000 consecutive patients across 9 cluster sites in 7 countries. PARADIGM sites were chosen on the basis of adequate CCTA volume, site CCTA proficiency, local demographic characteristics, and medical facilities to ensure a broad-based sample of patients. Patients referred for clinically indicated CCTA will be followed up and enrolled if they had a second CCTA scan. Patients will also be followed up beyond serial CCTA performance to identify adverse CAD events that include cardiac and noncardiac death, myocardial infarction, unstable angina, target vessel revascularization, and CAD-related hospitalization. SUMMARY: The results derived from the PARADIGM registry are anticipated to add incremental insight into the changes in CCTA findings in accordance with the progression or regression of CAD that confer prognostic value beyond demographic and clinical characteristics. Copyright Â
BACKGROUND: The natural history of coronary artery disease (CAD) in patients with low-to-intermediate risk is not well characterized. Although earlier invasive serial studies have documented the progression of atherosclerotic burden, most were focused on high-risk patients only. The PARADIGM registry is a large, prospective, multinational dynamic observational registry of patients undergoing serial coronary computed tomographic angiography (CCTA). The primary aim of PARADIGM is to characterize the natural history of CAD in relation to clinical and laboratory data. DESIGN: The PARADIGM registry (ClinicalTrials.govNCT02803411) comprises ≥2,000 consecutive patients across 9 cluster sites in 7 countries. PARADIGM sites were chosen on the basis of adequate CCTA volume, site CCTA proficiency, local demographic characteristics, and medical facilities to ensure a broad-based sample of patients. Patients referred for clinically indicated CCTA will be followed up and enrolled if they had a second CCTA scan. Patients will also be followed up beyond serial CCTA performance to identify adverse CAD events that include cardiac and noncardiac death, myocardial infarction, unstable angina, target vessel revascularization, and CAD-related hospitalization. SUMMARY: The results derived from the PARADIGM registry are anticipated to add incremental insight into the changes in CCTA findings in accordance with the progression or regression of CAD that confer prognostic value beyond demographic and clinical characteristics. Copyright Â
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