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J Am Coll Cardiol, 2003; 41:1964-1971, doi:10.1016/S0735-1097(03)00397-8
© 2003 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: INTERVENTIONAL CARDIOLOGY

Percutaneous transvenous cellular cardiomyoplasty

A novel nonsurgical approach for myocardial cell transplantation

Craig A. Thompson, MD*{ddagger}||,*, Boris A. Nasseri, MD{dagger}{ddagger}, Joshua Makower, MD, Stuart Houser, MD§, Michael McGarry, MSc§, Theodore Lamson, PhD§, Irina Pomerantseva, MD, PhD*{ddagger}, John Y. Chang, MS ME, Herman K. Gold, MD, FACC*, Joseph P. Vacanti, MD{dagger}{ddagger} and Stephen N. Oesterle, MD, FACC*{ddagger}

* Cardiovascular Division, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA
{dagger} Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA
{ddagger} Tissue Engineering Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA
§ Pathology Department, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA
|| Massachusetts Institute of Technology, Division of Health Sciences and Technology, Cambridge, Massachusetts, USA
TransVascular, Inc., Menlo Park, California, USA

Manuscript received August 15, 2002; revised manuscript received November 2, 2002, accepted December 18, 2002.

* Reprint requests and correspondence: Dr. Craig A. Thompson, Knight Center for Cardiac Catheterization and Intervention, Massachusetts General Hospital, 55 Fruit Street, Blake 950, Boston, Massachusetts 02114, USA.
cathompson{at}partners.org

OBJECTIVES: The study evaluated a nonsurgical means of intramyocardial cell introduction using the coronary venous system for direct myocardial access and cell delivery.

BACKGROUND: Direct myocardial cell repopulation has been proposed as a potential method to treat heart failure.

METHODS: We harvested bone marrow from Yorkshire swine (n = 6; 50 to 60 kg), selected culture-flask adherent cells, labeled them with the gene for green fluorescence protein, expanded them in culture, and resuspended them in a collagen hydrogel. Working through the coronary sinus, a specialized catheter system was easily delivered to the anterior interventricular coronary vein. The composite catheter system (TransAccess) incorporates a phased-array ultrasound tip for guidance and a sheathed, extendable nitinol needle for transvascular myocardial access. A microinfusion (IntraLume) catheter was advanced through the needle, deep into remote myocardium, and the autologous cell–hydrogel suspension was injected into normal heart. Animals were sacrificed at days 0 (n = 2), 14 (n = 1, + 1 control/collagen biogel only), and 28 (n = 2), and the hearts were excised and examined.

RESULTS: We gained widespread intramyocardial access to the anterior, lateral, septal, apical, and inferior walls from the anterior interventicular coronary vein. No death, cardiac tamponade, ventricular arrhythmia, or other procedural complications occurred. Gross inspection demonstrated no evidence of myocardial perforation, and biogel/black tissue dye was well localized to sites corresponding to fluoroscopic landmarks for delivery. Histologic analysis demonstrated needle and microcatheter tracts and accurate cell–biogel delivery.

CONCLUSIONS: Percutaneous intramyocardial access is safe and feasible by a transvenous approach through the coronary venous system. The swine offers an opportunity to refine approaches used for cellular cardiomyoplasty.

Abbreviations and Acronyms
  AIV
  anterior interventricular coronary vein
  CHF
  congestive heart failure
  CS
  coronary sinus
  GCV
  great cardiac vein
  GFP
  green fluorescence protein
  IVUS
  intravascular ultrasound
  MI
  myocardial infarction




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