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(Stroke. 2006;37:2378.)
© 2006 American Heart Association, Inc.
Research Reports |
From the Clinic for Internal Medicine II (M.R., I.E., J.B., R.A., E.M., M.S.), Department of Angiology, University of Vienna, Austria; the Clinic for Radiology (M.R., R.A.B.), Department of Interventional Radiology, University of Vienna, Austria; and the Clinic for Neurology (W.L.), University of Vienna, Austria.
Correspondence to Markus Reiter, MD, Clinic for Internal Medicine II, Department of Angiology, University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria. E-mail markus.reiter{at}meduniwien.ac.at
| Abstract |
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Methods We enrolled 698 consecutive patients undergoing elective CAS from a prospective single-center registry database and classified the preinterventional plaque status according to gray-scale median levels and the standardized Beletsky and Gray-Weale plaque scores. Patients were followed for 30-day neurological complications.
Results Neurological complications including transient ischemic attack, minor and major stroke occurred in 5.9% (41/698) of the patients. Median gray-scale median, Beletsky and Gray-Weale scores were 45 (interquartile range [IQR] 25 to 70), 3.0 (IQR 2.0 to 3.0) and 2.0 (IQR 2.0 to 3.0), respectively. None of the scores was significantly associated with adverse outcome adjusting for traditional risk factors, medication, preinterventional symptoms, degree of stenosis, contralateral occlusion and use of cerebral protection, neither with respect to all neurological complications nor with respect to stroke and death (all P>0.05).
Conclusions Plaque echolucency measured by objective and subjective grading did not identify patients with an increased risk of peri-interventional neurological events. Evaluation of plaque echolucency therefore cannot be recommended for risk stratification in CAS patients.
Key Words: carotid artery plaque stents stroke
| Introduction |
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| Materials and Methods |
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Ultrasound Stenosis Grading and Plaque Evaluation
Ultrasound (US) was performed 1 day before treatment by using a XP10 scanner (Acuson) with a 5-MHz-linear probe or an Acuson Sequoia scanner (Siemens) with a 14-MHz-linear probe by 2 medical technical assistants and supervised by 1 of the authors (E.M.). B-mode settings were adjusted and standardized by using a maximum dynamic range (60 dB) and by setting the gain to ensure an almost noiseless vessel lumen (blood) and an echo-dense area of adventitia. Images were stored in tagged-imaged files format and then standardized as described previously on a personal computer by using Adobe Photoshop 7.0 (Adobe Systems) to calculate the GSM score.5,13 Additionally, the standardized images were classified in consensus by 2 observers (M.R., I.E.), not involved in the image acquisition, according to the scores of Beletsky and Gray-Weale.6,7 The score of Beletsky has 3 stages: (1) soft plaque/organized thrombus, (2) intraplaque hemorrhage/fatty deposition, and (3) fibrosis/densely calcified plaques.6 Plaques classified in group 1 exhibited a lower density (&2 times of the blood density) than group 2, which in turn had a lower density than group 3 (as dense as the surrounding connective tissue with/without additional acoustic shadowing).6 The score of Gray-Weale uses the following stages: (1) dominantly echolucent, (2) substantially echolucent with small areas of echogenicity, (3) dominantly echogenic with small areas (<25%) of echolucency, (4) uniformly echogenic, and (5) invisible because of heavy calcification.7
Neurological Evaluation
Neurological history and examination were routinely performed the day before, and the day after CAS by independent neurologists. Baseline cranial CT was mandatory in all patients. If neurological events were suspected, clinical evaluation with cranial CT was performed immediately. A transient ischemic attack (TIA) was defined as a focal ischemic neurological deficit with abrupt onset that resolved completely within 24 hours. A minor stroke was defined as a focal neurological deficit that lasted >24 hours and had a National Institutes of Health Stroke Scale (NIHSS) score
4.14 A major stroke was defined as a focal neurological deficit that lasted >24 hours and had a NIHSS score >4.14
Statistical Methods
Data are given as counts (percentages) or medians (interquartile range [IQR]range from the 25th to the 75th percentile). Univariate analyses were performed applying Yates corrected
2 statistics, exact tests or Mann Whitney U tests, as appropriate. Multivariable logistic regression analysis was applied to assess the association between plaque morphology and neurological complications to adjust for potential confounding factors and to address potential interactions. A probability value <0.05 was considered statistically significant. Analyses were performed using SPSS (Version 12.0) or Stata (release 8.0).
| Results |
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Plaque Characteristics and Complications
In 94 patients (13%) GSM levels and Beletsky score could not be calculated because of poor imaging quality, and the Gray-Weale score could not be calculated in 4 patients (0.6%). Median GSM, Beletsky and Gray-Weale scores were 45 (IQR 25 to 70), 3.0 (IQR 2.0 to 3.0) and 2.0 (IQR 2.0 to 3.0). By univariate analyses none of the indices was significantly different in patients with and without events with respect to all neurological complications or death (P>0.05).
GSM levels were then categorized as low (<25) and high (
25) as reported previously.5 The frequencies of neurological complications and strokes in patients with low versus high GSM levels were 2.7% (4/146) versus 6.6% (30/458; P=0.13) and 2.1% (3/146) versus 3.1% (14/458; P=0.73), respectively.
Being aware of several potential confounders we applied multivariable logistic regression analyses, which demonstrated no significant association of plaque morphology with neurological outcome (Table 2). Furthermore, we tested for interaction by log-likelihood-ratio tests and multiplicative interaction terms between use or nonuse of cerebral protection, neurological outcome and the GSM levels and the 2 predefined scores, without detecting a significant effect modification or change of the model fit. Similarly, no interaction for symptomatic versus asymptomatic patients was observed. Including the 94 patients with inconclusive GSM scores attributable to heavy calcification as a separate category, we observed no significantly increased risk for neurological complications or stroke in the multivariable model (all P>0.05).
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| Discussion |
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Several issues may account for this discrepancy: Biasi et al performed a multicenter trial and included the images of 11 participating centers, which were recorded on video tape (analogue) and then transferred onto a personal computer (digital) for further standardization, thus potentially resulting in a loss of image information.5 The images used in our study were stored immediately as digital images interfaced with the ultrasound machine and therefore could be directly analyzed without further transfer procedures. Besides these potential differences in image quality, a significant influence of investigator and laboratory on the evaluation of carotid stenosis is well known, suggesting a more homogenous dataset obtained by our single-center trial compared with the multicenter (11 different laboratories and US machines) study by Biasi.5,15 Furthermore, a mathematical limitation of the study by Biasi et al is the relatively low number of events (23/418 patients), resulting in high standard deviations of GSM values, which might have caused false-positive resultsin the present study the sample size and number of events was almost double resulting a smaller confidence intervals and higher predictive power.5
A relatively high number of low-quality images (ie, caused by heavily calcified plaques) had to be excluded from further analyses both in our study as well as in the report by Biasi.5 Biasi et al excluded 16% of patients and we also had to exclude 13%. However, even in accurately executed US studies these limitations cannot be completely eliminated based on the examination technique and the advanced atherosclerosis in CAS eligible patients.
Limitations
Some limitations of the present study have to be acknowledged. Although the number of participants and number of events was quite large, false-negative results still cannot be completely ruled out. Furthermore, the time interval for data acquisition was long, and considerable technical developments may have influenced our findings. Nevertheless, we tried to statistically account for presumably important changes, like the introduction of cerebral protection devices, and found a consistent lack of association between GSM levels and the Beletsky and Gray-Weale scores, respectively, and neurological outcome.
Conclusions
Plaque echolucency measured by objective and subjective grading did not identify patients with an increased risk of peri-interventional neurological events. Evaluation of plaque echolucency therefore cannot be recommended for risk stratification in CAS patients.
| Acknowledgments |
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None.
Received February 5, 2006; revision received March 28, 2006; accepted May 3, 2006.
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