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1 l plaque volume was measured by quantitative intravascular ultrasound.
2 maging is hampered by the invasive nature of intravascular ultrasound.
3 served in 16 of 42 patients (38%) undergoing intravascular ultrasound.
4 atheroma progression was evaluated by serial intravascular ultrasound.
5 dent predictors for future cardiac events by intravascular ultrasound.
6 prit lesions identified on virtual-histology intravascular ultrasound.
7 allograft vascular disease (CAV) assessed by intravascular ultrasound.
8 y endovascular treatment using tools such as intravascular ultrasound.
9 red to reduce atheroma volume as measured by intravascular ultrasound.
10 d severe coronary arteriopathy documented by intravascular ultrasound.
11 ared with catheter angiographic findings and intravascular ultrasound.
12 , allograft vasculopathy is best detected by intravascular ultrasound.
13 ive biopsies developed intimal thickening by intravascular ultrasound.
14 ary anatomy was evaluated by angiography and intravascular ultrasound.
15 tients undergoing 3-vessel virtual-histology intravascular ultrasound.
16 CAV was investigated using intravascular ultrasound.
17 by consecutive volumetric three-dimensional intravascular ultrasound.
18 evation myocardial infarction (NSTEMI) using intravascular ultrasound.
19 py with FFR, near-infrared spectroscopy, and intravascular ultrasound.
20 oherence tomography and 0.17+/-0.26 mm(2) on intravascular ultrasound.
21 15 mm vs 1.46 mm, p<0.0001) and quantitative intravascular ultrasound (2.85 mm(2)vs 3.60 mm(2), p<0.0
22 (mean 49 years old) using three-dimensional intravascular ultrasound (3-D IVUS) examination of the l
23 grade IV coronary allograft vasculopathy on intravascular ultrasound, 3 of whom had angiographic dis
24 formation were studied with angiography and intravascular ultrasound 6 months after the index PCI.
25 e in first-year maximal intimal thickness by intravascular ultrasound, a recognized surrogate for lon
28 nsplant recipients had baseline and one-year intravascular ultrasound analysis done to assess the pro
38 in could regress coronary atherosclerosis by intravascular ultrasound and quantitative coronary angio
39 e vessel wall are apparent on angiography or intravascular ultrasound and that it has a prognostic va
40 ated in vivo based on virtual histology (VH) intravascular ultrasound and whether PSS varied accordin
41 ged by means of invasive techniques, such as intravascular ultrasound (and derived techniques), optic
42 intravascular ultrasound (virtual histology intravascular ultrasound) and computational fluid dynami
43 ural infarction using angiographic analysis, intravascular ultrasound, and delayed-enhancement magnet
44 on, including fluoroscopy, echocardiography, intravascular ultrasound, and electron beam computed tom
45 allograft vasculopathy (CAV) assessed by 3D intravascular ultrasound, and incidence of cardiac adver
48 ility have been described by CT angiography, intravascular ultrasound, and optical coherence tomograp
49 eds conventional magnetic resonance imaging, intravascular ultrasound, and optical coherence tomograp
50 rvation systems by quantitative angiography, intravascular ultrasound, and optical coherence tomograp
51 , such as quantitative coronary angiography, intravascular ultrasound, and optical coherence tomograp
52 , such as quantitative coronary angiography, intravascular ultrasound, and optical coherence tomograp
53 erence in luminal dimension was confirmed by intravascular ultrasound assessment of the minimum lumen
57 Follow-up included coronary angiography and intravascular ultrasound at 4 months and clinical assess
58 subgroup of patients (n=56) underwent serial intravascular ultrasound at baseline and 9 months indica
62 laque volume in ACS patients, as assessed by intravascular ultrasound, but no clinical trials assessi
63 cular ultrasound (IB-IVUS), and conventional intravascular ultrasound (C-IVUS) for tissue characteriz
64 agnosis of ISA, initially only possible with intravascular ultrasound, can currently be performed wit
65 ent minus lumen) areas and source-to-target (intravascular ultrasound catheter to external elastic me
66 thod of transthoracic echocardiography (with intravascular ultrasound catheters) at baseline and on d
68 patients who had undergone virtual histology intravascular ultrasound characterization of coronary pl
69 nce assessed by quantitative angiography and intravascular ultrasound; composite clinical endpoints b
70 dicts a suboptimal result based on validated intravascular ultrasound criteria; however, an FFR >/=0.
71 from baseline of percent atheroma volume on intravascular ultrasound, CRP-modulating effects, or MAC
72 ubstudies, 103 patients (54 BMS, 49 PES) had intravascular ultrasound data >/=10 mm distal to the ste
74 raft plaque was divided on virtual histology intravascular ultrasound-derived "inflammatory" (VHD-IP)
75 dy to Evaluate the Effect of Rosuvastatin on Intravascular Ultrasound-Derived Coronary Atheroma Burde
76 dy to Evaluate the Effect of Rosuvastatin on Intravascular Ultrasound-Derived Coronary Atheroma Burde
77 giographic disease (n=23) and NSTEMI (n=24), intravascular ultrasound-derived measures (percent ather
78 ), changes in plaque area, virtual histology intravascular ultrasound-derived plaque composition, and
80 theter thrombolysis regimen, the addition of intravascular ultrasound did not facilitate thrombus res
82 hanges in lipoprotein levels and the primary intravascular ultrasound end point, change in percent at
83 irty-two consecutive HT recipients underwent intravascular ultrasound evaluation at month 1 and year
84 media (EEM-lumen) areas were measured (using intravascular ultrasound) every 1 mm over 5-mm-long refe
85 ith coronary artery disease underwent serial intravascular ultrasound examination in 7 clinical trial
86 cipients between 1993 and 1995 who underwent intravascular ultrasound examination of the coronary art
87 d and received study drug; 502 had evaluable intravascular ultrasound examinations at baseline and af
88 tients with coronary bifurcation lesion, 120 intravascular ultrasound examinations of the MV were per
92 ared serial (postintervention and follow-up) intravascular ultrasound findings in 66 patients with na
93 scribe near-infrared spectroscopy (NIRS) and intravascular ultrasound findings in pre-existing stents
96 nt coronary angiography followed by coronary intravascular ultrasound, fractional flow reserve, and i
98 eration DES (HR=1.75, P=0.02), no procedural intravascular ultrasound guidance (HR=1.75, P=0.04), and
101 ave not systematically evaluated the role of intravascular ultrasound-guided stenting and high platel
103 ified 989 consecutive patients who underwent intravascular ultrasound-guided stenting of 1,015 corona
106 ontemporary imaging technology, particularly intravascular ultrasound, has allowed the study of arter
108 nce tomography (OCT), integrated backscatter intravascular ultrasound (IB-IVUS), and conventional int
110 he left anterior descending coronary artery; intravascular ultrasound images and Doppler velocities w
121 This is the first study of POT guided by intravascular ultrasound in patients with coronary bifur
122 s with symptomatic carotid disease, and with intravascular ultrasound in patients with stable angina.
128 ases (SES: 72; BMS: 50) with complete serial intravascular ultrasound (IVUS) (baseline and 8-month fo
129 re final lumen cross-sectional area (CSA) by intravascular ultrasound (IVUS) (p = 0.001) and restenot
134 general, it has a good correlation with both intravascular ultrasound (IVUS) and histopathology for d
135 tent of coronary atherosclerosis assessed by intravascular ultrasound (IVUS) and its rate of progress
136 hereby assessed whether integrating EIS with intravascular ultrasound (IVUS) and shear stress (ISS) p
138 rwent simultaneous endomyocardial biopsy and intravascular ultrasound (IVUS) at one year of transplan
141 sought to assess the validity of first-year intravascular ultrasound (IVUS) data as a surrogate mark
145 nderwent coronary angiography and volumetric intravascular ultrasound (IVUS) evaluation of the left a
147 s designed to examine the impact of repeated intravascular ultrasound (IVUS) examinations on transpla
150 era of drug-eluting stents, it is unknown if intravascular ultrasound (IVUS) guidance for percutaneou
152 to modest-sized studies suggest a benefit of intravascular ultrasound (IVUS) guidance in noncomplex l
153 l studies have indicated better outcome with intravascular ultrasound (IVUS) guidance when performing
157 neously obtained endomyocardial biopsies and intravascular ultrasound (IVUS) images of coronary arter
160 ultaneous optical coherence tomography (OCT)-intravascular ultrasound (IVUS) imaging at 72 frames per
165 tent malapposition (LSM) is only detected if intravascular ultrasound (IVUS) is performed at implanta
167 uantitative coronary angiographic and planar intravascular ultrasound (IVUS) measurements were perfor
168 T (0.75-mm collimation, 420-ms rotation) and intravascular ultrasound (IVUS) of one coronary artery w
169 who underwent stenting under the guidance of intravascular ultrasound (IVUS) or conventional angiogra
175 mine the optimal minimum lumen area (MLA) by intravascular ultrasound (IVUS) that correlates with fra
179 volumetric (post-irradiation and follow-up) intravascular ultrasound (IVUS) to compare the effective
184 m of this study was to use serial volumetric intravascular ultrasound (IVUS) to evaluate the effects
185 The aim of this study was to use serial intravascular ultrasound (IVUS) to evaluate the long-ter
188 study purposes were to determine 1) whether intravascular ultrasound (IVUS) was more sensitive than
190 tics, quantitative coronary angiography, and intravascular ultrasound (IVUS) were evaluated in subjec
191 s the first intravascular catheter combining intravascular ultrasound (IVUS) with multispectral fluor
192 enal translesional pressure gradients (TPG), intravascular ultrasound (IVUS), and angiographic parame
194 atients (B2) underwent coronary angiography, intravascular ultrasound (IVUS), and optical coherence t
195 to compare color-flow duplex imaging (CFDI), intravascular ultrasound (IVUS), and renal arteriography
199 was to investigate the relationship between intravascular ultrasound (IVUS)-derived measures of athe
200 his study was to evaluate the efficacy of an intravascular ultrasound (IVUS)-guided strategy for pati
216 l (postirradiation and follow-up) volumetric intravascular ultrasound (IVUS): 1) to evaluate the actu
217 s include fractional flow reserve; grayscale intravascular ultrasound (IVUS); IVUS radiofrequency tis
218 dy comparing SES and BMS, serial qualitative intravascular ultrasound (IVUS; at stent implantation an
219 tissue at the site of LRP detected by NIRS, intravascular ultrasound may provide some insight into t
220 ed quantitative angiography and morphometric intravascular ultrasound measurements pre and post proce
221 tin Versus Atorvastatin (SATURN) used serial intravascular ultrasound measures of coronary atheroma v
224 We investigated the role of POT guided by intravascular ultrasound on the main vessel (MV) stent e
225 and a subgroup of patients was scheduled for intravascular ultrasound, optical coherence tomography,
226 hod among quantitative coronary angiography, intravascular ultrasound, optical coherence tomography,
227 ral care were examined, including the use of intravascular ultrasound, optical coherence tomography,
228 re available (eg, fractional flow reserve or intravascular ultrasound) or being validated (eg, instan
229 ive measures of restenosis (angiographic and intravascular ultrasound) or its clinical sequelae.
231 compared with baseline (0.54+/-1.09 mm(2) on intravascular ultrasound, P=0.003 and 0.77+/-1.33 m(2) o
232 imus-eluting stent groups, respectively, and intravascular ultrasound percent neointimal hyperplasia
235 nd points, such as quantitative angiography, intravascular ultrasound, plasma biomarkers, and functio
238 Atheroma volume was determined in serial intravascular ultrasound pullbacks in matched arterial s
239 gnificantly correlated with plaque volume by intravascular ultrasound (r=0.69; P<0.0001) but not with
244 tive randomized trials using serial coronary intravascular ultrasound, serial changes in coronary per
250 these patients subsequently underwent two 3D intravascular ultrasound studies in 2004 to 2006 12 mont
252 one orthotopic heart transplantation, serial intravascular ultrasound studies of the proximal left an
257 n, and time from transplantation to baseline intravascular ultrasound study were not different (P>0.2
258 iren Quantitative Atherosclerosis Regression Intravascular Ultrasound Study) comparing aliskiren with
259 stents (BMS) on distal vessels in the serial intravascular ultrasound substudies of TAXUS IV, V, and
263 e associated with more high-risk features on intravascular ultrasound than those without uptake: posi
264 patients (2433 lesions) were evaluated with intravascular ultrasound to characterize the morphologic
266 m of this study was to use serial volumetric intravascular ultrasound to evaluate the effect of gamma
267 creased the positive predictive value for VH intravascular ultrasound to identify clinical presentati
268 SS improved the ability of virtual-histology intravascular ultrasound to predict MACE in plaques with
270 Recent studies show that virtual histology intravascular ultrasound (VH-IVUS) can identify plaques
271 therosclerotic plaque with virtual histology intravascular ultrasound (VH-IVUS) imaging to assess the
272 vivo CT coregistered with virtual histology intravascular ultrasound (VH-IVUS) in 108 plaques from 5
274 nderwent baseline and 6-month radiofrequency intravascular ultrasound (virtual histology intravascula
277 n lumen size by quantitative angiography and intravascular ultrasound was observed in nonballoon dene
285 AND Combined near-infrared spectroscopy and intravascular ultrasound was performed in 57 vessels in
286 serial (baseline and 1-year post-transplant) intravascular ultrasound was performed in the first 50 m
287 s, 3-vessel gray-scale and virtual histology intravascular ultrasound was performed in the proximal-m
291 by NIRS in a cohort of pre-existing stents, intravascular ultrasound was used to determine the prese
293 ar profiling, using coronary angiography and intravascular ultrasound, was used to reconstruct each a
294 Coronary angiography and three-dimensional intravascular ultrasound were performed at baseline and
295 ne and 6-12 months) coronary angiography and intravascular ultrasound were performed in 2931 lesions
296 uation, serial quantitative angiography, and intravascular ultrasound were performed periprocedurally
298 mography and near-infrared spectroscopy with intravascular ultrasound were used to characterize NA in
299 erity of GVD was determined every 3 weeks by intravascular ultrasound, which quantified intimal area
300 eserve, endothelial function assessment, and intravascular ultrasound with volumetric analysis were p
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