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Circulation, Vol 82, 560-569, Copyright © 1990 by American Heart Association
GP Rodgers, ST Minor, K Robinson, D Cromeens, SC Woolbert, LC Stephens, JR Guyton, K Wright, GS Roubin and AE Raizner
Early thrombosis has complicated human stent implantation in several
trials. To determine the best anticoagulation/antiplatelet therapy to
maintain stent patency after percutaneous transluminal coronary
angioplasty, we implanted the flexible balloon-expandable coil stent into
the left anterior descending coronary artery of 28 atherosclerotic
8-month-old Hanford miniature swine. Animals were randomly assigned to one
of three treatment groups: group A, aspirin (1 mg/kg/day) and dipyridamole
(1 mg/kg three times a day); group B, aspirin and dipyridamole (same doses)
plus Coumadin (dose required to prolong prothrombin time 1.3-1.5-fold that
of normal); and group C, control. Adjuvant therapy was begun 3 days before
stenting. Two pigs (one from group A and one from group B) died during
implantation, both without thrombosis. Twenty-six animals survived until
follow-up angiography and sacrifice at 1 month. No occlusive thrombosis of
the stent occurred in survivors. Reduction of the stent lumen diameter was
observed in every case at follow-up. Percent lumen reduction was 19% in
group A, 26% in group B, and 24% in group C. Marked smooth muscle cell
hyperplasia was seen by light and transmission electron microscopy at stent
struts. Scanning electron microscopy of the luminal surface showed a
variable morphology consisting of normal endothelium, adherent leukocytes,
stellate periluminal cells, and occasional fibrin strands and red blood
cells. Luminal narrowing was not affected by anticoagulation therapy,
antiplatelet drugs, cholesterol level, or stent sizing. We conclude that
occlusive thrombosis does not complicate stent implantation in this model
but that substantial luminal narrowing due in part to smooth muscle
hyperplasia does occur. The significance of luminal narrowing at the stent
site requires further study.
ARTICLES
Adjuvant therapy for intracoronary stents. Investigations in atherosclerotic swine
Baylor College of Medicine, Houston, Tex.
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