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J Am Coll Cardiol Intv, 2009; 2:373-383, doi:10.1016/j.jcin.2009.03.004
© 2009 by the American College of Cardiology Foundation
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State-of-the-Art Paper

The Pre-Clinical Animal Model in the Translational Research of Interventional Cardiology

Yoriyasu Suzuki, MD*,{dagger}, Alan C. Yeung, MD*, Fumiaki Ikeno, MD*,*

* Division of Cardiovascular Medicine, School of Medicine, Stanford University, Stanford, California
{dagger} Department of Cardiovascular Medicine, Nagoya Heart Center, Aichi, Japan

* Reprint requests and correspondence: Dr. Fumiaki Ikeno, Stanford University, Division of Cardiovascular Medicine, 300 Pasteur Drive, Falk CVRB007, Stanford, California 94305 (Email: fikeno{at}cvmed.stanford.edu).

Scientific discoveries for improvement of human health must be translated into practical applications. Such discoveries typically begin at "the bench" with basic research, then progress to the clinical level. In particular, in the field of interventional cardiology, percutaneous cardiovascular intervention has rapidly evolved from an experimental procedure to a therapeutic clinical setting. Pre-clinical studies using animal models play a very important role in the evaluation of efficacy and safety of new medical devices before their use in human clinical studies. This review provides an overview of the emerging role, results of pre-clinical studies and development, and evaluation of animal models for percutaneous cardiovascular intervention technologies for patients with symptomatic cardiovascular disease.

Key Words: pre-clinical study • animal model • cardiovascular intervention

Abbreviations and Acronyms
  AS = aortic stenosis
  CTO = chronic total occlusion
  DES = drug-eluting stent(s)
  LAA = left arterial appendage
  MI = myocardial infarction
  MR = mitral regurgitation
  PES = paclitaxel-eluting stent(s)
  PFO = patent foramen ovale
  SES = sirolimus-eluting stent(s)
  VHD = valvular heart disease




This article has been cited by other articles:


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Vascular Responses to Percutaneous Coronary Intervention With Bare-Metal Stents and Drug-Eluting Stents: A Perspective Based on Insights From Pathological and Clinical Studies
J. Am. Coll. Cardiol., March 15, 2011; 57(11): 1323 - 1326.
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