Copyright © 1996 by the European Society of Cardiology.
© The European Society of Cardiology
Interventional cardiology
Differences in the morphology of unstable and stable coronary lesions and their impact on the mechanisms of angioplasty. An in vivo study with intravascular ultrasound
II. Medizinische Klinik und Poliklinik, Johannes Gutenberg University Langenbeckstrasse 1, 55101 Mainz, Germany
Abteilung Kardiologie, Universitätsklinikum Essen Hufelandsirasse 55, 45122 Essen, Germany
Received 25 September 1995; accepted 25 October 1995.
Correspondence: P. Kearney, Department of Cardiology, Western General Hospital, Crewe Road South, Edinburgh EH4 2XU, Scotland
Abstract
The aim of this study was to compare the morphology of stable and unstable coronary lesions using intravascular ultrasound in patients undergoing coronary balloon angioplasty and to determine whether lesion morphology had any influence on the mechanism of balloon angioplasty.
Thirty three (15 stable and 18 unstable) patients undergoing single lesion percutaneous transluminal coronary angio plasty were studied with intravascular ultrasound before and after intervention. All examinations, recorded on S-VHS video tape, were studied off-line and matched sites from the point of minimum lumen area after the procedure and the corresponding site prior to intervention were com pared. The morphology of lesions before intervention was noted and the mechanisms of angioplasty (vessel stretch, lesion remodelling and lesion tears) were determined by comparing pre- and post-interventional morphology and dimensions.
The only significant morphological difference between stable and unstable lesions was the presence of a demarcated inner layer in unstable lesions, delimited by a fine circumferential line. This pattern was noted in 77% (14/18) of unstable lesions and in 7% (1/15) of stable lesions (P<0·0l). Unstable lesions tended to have more echolucent zones than stable lesions (72% (13/18) vs 46% (7/15), P=0·13) The mechanisms of angioplasty were also found to differ. Whereas lesion remodelling (or ‘compression’) was seen in 77% (14/18) of unstable lesions, it occurred in only 13% (2/15) of stable lesions and mean lesion cross- sectional area reduction was greater in unstable lesions, –14·8±8·3% (2·1+1·3 mm2) compared to stable lesions, –4sup1+8·4% (0·42+0·9 mm P<0·0l. In contrast, vessel stretch was seen more frequently in stable lesions (73%, 11/15) compared to unstable lesions (22%, 4/18) P<0·0l and the mean increase in vessel cross-sectional area was +13·5±6·8 (1·6±0·9 mm2 in stable lesions compared to +5·5±5·6% (0·8+0·9 mm2 in unstable lesions, P<0·01. Lesion tear was present to a similar degree in both groups of patients.
In this observational study we found a set of echographic markers that distinguished unstable lesions. The mechanisms of angioplasty differed between stable and unstable angina, with greater lesion remodelling seen in unstable lesions and vessel stretch in stable lesions. Taken together, these findings suggest that the markers we describe may be echographic indicators of mural thrombus.
Key Words: Unstable angina • intravascular ultrasound • PTCA • thrombus
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