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From Vulnerable Plaque to Vulnerable Patient: A Call for New Definitions and Risk Assessment Strategies: Part II

  • Morteza Naghavi
  • , Peter Libby
  • , Erling Falk
  • , S. Ward Casscells
  • , Silvio Litovsky
  • , John Rumberger
  • , Juan Jose Badimon
  • , Christodoulos Stefanadis
  • , Pedro Moreno
  • , Gerard Pasterkamp
  • , Zahi Fayad
  • , Peter H. Stone
  • , Sergio Waxman
  • , Paolo Raggi
  • , Mohammad Madjid
  • , Alireza Zarrabi
  • , Allen Burke
  • , Chun Yuan
  • , Peter J. Fitzgerald
  • , David S. Siscovick
  • Chris L. De Korte, Masanori Aikawa, K. E.Juhani Airaksinen, Gerd Assmann, Christoph R. Becker, James H. Chesebro, Andrew Farb, Zorina S. Galis, Chris Jackson, Ik Kyung Jang, Wolfgang Koenig, Robert A. Lodder, Keith March, Jasenka Demirovic, Mohamad Navab, Silvia G. Priori, Mark D. Rekhter, Raymond Bahr, Scott M. Grundy, Roxana Mehran, Antonio Colombo, Eric Boerwinkle, Christie Ballantyne, William Insull, Robert S. Schwartz, Robert Vogel, Patrick W. Serruys, Goran K. Hansson, David P. Faxon, Sanjay Kaul, Helmut Drexler, Philip Greenland, James E. Muller, Renu Virmani, Paul M. Ridker, Douglas P. Zipes, Prediman K. Shah, James T. Willerson
  • The University of Texas Health Science Center at Houston
  • Texas Heart Institute
  • Assoc. Eradication of Heart Attack
  • Brigham and Women's Hospital
  • Aarhus University Hospital
  • University of Athens
  • University of Kentucky
  • University Medical Centre Utrecht
  • Mount Sinai Medical Centre
  • Tufts Medical Center
  • Tulane University School of Medicine
  • Armed Forces Institute of Pathology
  • University of Washington School of Medicine
  • Stanford University Medical Center
  • Erasmus MC
  • University Hospital Muenster Albert-Schweitzer-Campus
  • University of Münster
  • Mayo Clinic School of Medicine
  • Emory University School of Medicine
  • University of Bristol
  • Massachusetts General Hospital
  • Ulm University
  • James J. Peters VA Medical Center
  • University of Texas
  • University of California, Los Angeles
  • University of Pavia
  • Pfizer Inc.
  • St. Agnes HealthCare
  • University of Texas Southwestern Medical Center
  • Lenox Hill Hospital
  • Centro Cuore Columbus
  • University of Texas
  • Baylor College of Medicine
  • Minneapolis Heart Institute
  • University of Maryland School of Medicine
  • Karolinska University Hospital
  • Cedars-Sinai Medical Center
  • Leibniz University Hannover
  • Northwestern University Feinberg School of Medicine
  • Dept. Med., Indiana Univ. Sch. Med.
  • McGill University

Research output: Contribution to a Journal (Peer & Non Peer)Review articlepeer-review

1397 Citations (Scopus)

Abstract

Atherosclerotic cardiovascular disease results in > 19 million deaths annually, and coronary heart disease accounts for the majority of this toll. Despite major advances in treatment of coronary heart disease patients, a large number of victims of the disease who are apparently healthy die suddenly without prior symptoms. Available screening and diagnostic methods are insufficient to identify the victims before the event occurs. The recognition of the role of the vulnerable plaque has opened new avenues of opportunity in the field of cardiovascular medicine. This consensus document concludes the following. (1) Rupture-prone plaques are not the only vulnerable plaques. All types of atherosclerotic plaques with high likelihood of thrombotic complications and rapid progression should be considered as vulnerable plaques. We propose a classification for clinical as well as pathological evaluation of vulnerable plaques. (2) Vulnerable plaques are not the only culprit factors for the development of acute coronary syndromes, myocardial infarction, and sudden cardiac death. Vulnerable blood (prone to thrombosis) and vulnerable myocardium (prone to fatal arrhythmia) play an important role in the outcome. Therefore, the term "vulnerable patient" may be more appropriate and is proposed now for the identification of subjects with high likelihood of developing cardiac events in the near future. (3) A quantitative method for cumulative risk assessment of vulnerable patients needs to be developed that may include variables based on plaque, blood, and myocardial vulnerability. In Part I of this consensus document, we cover the new definition of vulnerable plaque and its relationship with vulnerable patients. Part II of this consensus document will focus on vulnerable blood and vulnerable myocardium and provide an outline of overall risk assessment of vulnerable patients. Parts I and II are meant to provide a general consensus and overviews the new field of vulnerable patient. Recently developed assays (eg, C-reactive protein), imaging techniques (eg, CT and MRI), noninvasive electrophysiological tests (for vulnerable myocardium), and emerging catheters (to localize and characterize vulnerable plaque) in combination with future genomic and proteomic techniques will guide us in the search for vulnerable patients. It will also lead to the development and deployment of new therapies and ultimately to reduce the incidence of acute coronary syndromes and sudden cardiac death. We encourage healthcare policy makers to promote translational research for screening and treatment of vulnerable patients.

Original languageEnglish
Pages (from-to)1772-1778
Number of pages7
JournalCirculation
Volume108
Issue number15
DOIs
Publication statusPublished - 14 Oct 2003

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Atherosclerosis
  • Coronary disease
  • Death
  • Myocardial infarction
  • Plaque
  • Sudden

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