Circulation, Vol 90, 2348-2355, Copyright © 1994 by American Heart Association
FJ Pinto, A Chenzbraun, J Botas, HA Valantine, FG St Goar, EL Alderman, SN Oesterle, JS Schroeder and RL Popp
BACKGROUND--Serial quantitative coronary angiography is used to assess
progression of coronary disease; however, pathology studies have
demonstrated angiographic insensitivity for determining atheroma.
Intracoronary ultrasound (ICUS) can define and measure the components of
the arterial wall and offers the potential for precise quantitative
assessment of disease progression on serial examinations. The present study
was done to test the feasibility of serially assessing intimal
proliferation at the same coronary site with ICUS imaging in cardiac
transplant recipients. METHODS AND RESULTS--ICUS imaging was done with a
30-MHz, 5F or 4.3F ultrasound imaging catheter at the time of angiography
in 70 cardiac allografts (3.8 sites per patient) initially and 1 year
later. Mean intimal thickness (IT), luminal area (LA), and total area (TA)
of lumen plus intima and an index of intimal thickness (II = TA - LA/TA)
were measured at each site. Additionally, vessels were graded using a scale
incorporating criteria of intimal thickness and circumferential
involvement. Side-by-side comparisons of paired angiograms were performed
both to verify the similarity of ICUS imaging site and to detect new
angiographic abnormalities. At least one site could be assessed serially by
ICUS in 100% of patients, but only 189 of the original 263 coronary sites
(72%) (2.7 sites per patient) could be matched satisfactorily on the second
study. Thirty-nine patients (56%) had mild IT and 31 patients (44%) had
moderate or severe IT on the initial study. Both groups showed the same IT
progression the following year (delta = 0.05 +/- 0.13 versus 0.07 +/- 0.15
mm; P = NS). Twenty- seven of the 70 patients (39%) showed progression by
ICUS. The 23 patients with ICUS progression and angiographically normal
vessels had the same progression in intimal thickening as the 4 patients
with ICUS progression but showing angiographic disease (delta = 0.17 +/-
0.13 versus 0.22 +/- 0.10 mm; P = NS). CONCLUSIONS--Replication of the
intracoronary imaging site by judgment of two observers at an initial study
and at a second study 1 year later was possible in at least one vessel site
in 100% of the 70 patients and in 72% (189 of 263) of the original imaging
sites (2.7 sites per patient). Serial ICUS demonstrates progression of
intimal thickening at specific sites in only some cardiac transplant
patients. Progression of intimal proliferation can occur in individuals in
the presence or absence of initially increased intimal thickening or of
angiographic disease at the time of the initial studies. Angiography is
insensitive for recognizing early intimal thickening of the coronary
vessels.
ARTICLES
Feasibility of serial intracoronary ultrasound imaging for assessment of progression of intimal proliferation in cardiac transplant recipients
Division of Cardiovascular Medicine, Stanford University School of Medicine, CA 94305.
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