Circulation, Vol 66, 917-922, Copyright © 1982 by American Heart Association
TA Sanborn, DP Faxon, D Waugh, DM Small, C Haudenschild, SB Gottsman and TJ Ryan
We used polarized light microscopy and thin-layer chromatography to
determine whether embolization of atherosclerotic material occurs after
transluminal angioplasty. The experimental model consisted of an in vivo
perfusion system of the atherosclerotic rabbit left iliac artery. Of eight
rabbits that underwent successful angioplasty, four had angiographic
evidence of dissection and three showed aneurysm formation. Histologic
studies demonstrated fracture of the intimal plaque, dissection, and
stretching of the noninvolved portion of the vessel. Perfusate analysis
revealed no detectable cholesterol by thin- layer chromatography in six of
eight rabbits. In two rabbits, a very small amount of cholesterol was
measured, which was totally accounted for by hemorrhage into the perfusate
rather than from cholesterol in the plaque. No evidence of arterial wall
embolic debris could be detected by polarized light microscopy in seven
rabbits, but lipid debris from the plaque was found in the perfusate of one
rabbit that had excessive arterial trauma. We conclude that the major
mechanism of successful transluminal angioplasty in this experimental model
is intimal fracture combined with stretching of a noninvolved portion of
the vessel. Furthermore, embolization of atheromatous lipid debris was an
uncommon event related to arterial trauma during catheter placement rather
than transluminal angioplasty itself.
ARTICLES
Transluminal angioplasty in experimental atherosclerosis. Analysis for embolization using an in vivo perfusion system
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