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(Circulation. 2004;110:515-521.)
© 2004 American Heart Association, Inc.
Original Articles |
From the Department of Pathology, University of Padua Medical School, Padua (A.A., F.M., M.D.B., G.T.), and the Cardiology Division, San Martino Hospital, Genoa (P.R., F.A., M.V., S.C.), Italy.
Correspondence to Gaetano Thiene, MD, Department of Pathology, University of Padua Medical School, Via A. Gabelli, 61, 35121 Padua, Italy. E-mail cardpath{at}unipd.it
Received October 29, 2003; de novo received February 13, 2004; revision received April 29, 2004; accepted April 30, 2004.
| Abstract |
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Methods and Results Elective coronary stenting with the use of a protective filter was attempted in 39 consecutive coronary artery lesions with >60% stenosis (mean, 67.6±8.79%). Debris was present in 75.6% of the filters. Particle size ranged from 47.16 to 2503.48 µm (mean, 518.83±319.61 µm) in the major axis. Particles >300 µm were found in 24 of 28 filters with debris (85.7%), and particles >1000 µm were present in 10 of 28 filters (35.7%). Patients with unstable angina had greater particles (mean maximum longitudinal diameter, 1098.33±714.3 µm) than those with stable angina (412.91±453 µm; P<0.001). The presence of unstable angina (OR, 65; CI, 1.2 to 3420; P=0.03) and age >67 years (OR, 42; CI, 1 to 1698; P=0.04) were found to be the only independent predictors of embolic particle size.
Conclusions By limiting embolization, protective devices may prevent a number of potentially unfavorable events, thereby improving outcome. Our data support the use of these devices, especially in lesions with higher embolic potential, such as those occurring in older patients and in those with unstable angina.
Key Words: angioplasty stents embolism pathology coronary disease
| Introduction |
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Recently, a few protective devices able to prevent particulate debris from embolizing distally after PCI have been developed.811 Among others, the Angioguard device (Cordis Corp) is a guidewire equipped with a filter basket at the distal end designed to trap emboli during intravascular interventions.
The aim of this study was threefold: (1) to evaluate the microembolization phenomenon during procedures of stent implantation in native coronary arteries of patients with stable and unstable angina, (2) to assess the amount and characteristics of the debris captured by the Angioguard, and (3) to investigate the relation between clinical and angiographic variables and pathological data.
| Methods |
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Patients undergoing stent implantation for a de novo lesion of a native coronary artery were considered for the study. Clinical exclusion criteria were acute myocardial infarction within 7 days or chest pain at rest within 48 hours (unstable angina class III according to the Braunwald classification12). Angiographic exclusion criteria included distal lesion location, vessel diameter <3.0 mm by online quantitative coronary angiography, tortuosity, diffuse disease or angiographic evidence of thrombus in the target vessel, presence of a side branch
2.0 mm in diameter at the site of the lesion, tapering or branching of the vessel distal to the target lesion preventing the correct placement of the filter, and total vessel occlusion with Thrombolysis in Myocardial Infarction (TIMI) flow grade 0 or 1.13
The Angioguard device is a single-use, steerable 0.014-in guidewire equipped with a filter basket at the distal end. During the procedure, plaque debris is collected by the filter, whereas the blood can flow freely through the porous membrane. At the end of the procedure, the filter basket retaining the embolic material is collapsed again by use of another sheath and removed through the guiding catheter.
Procedure
All patients received aspirin 100 mg/d and ticlopidine 500 mg before the procedure. The use of glycoprotein IIb/IIIa inhibitors was left to the operators judgment. Unfractionated heparin was administered to maintain an activated clotting time between 250 and 300 seconds. The procedure was performed by the femoral approach using a 7F guiding catheter. Serum creatine kinase MB fraction (CK-MB) was assessed 8 and 24 hours after the procedure.
Qualitative and quantitative angiographic parameters of the treated vessel were evaluated before and after the procedure.14,15
Moreover, plaque area recognized as an index of plaque burden was calculated by the quantitative coronary angiography software.
Pathological Evaluation
The tip of the Angioguard device was cut and processed for macroscopic morphometric analysis (Image-Pro plus computer software by Media Cybernetics) and light microscopy.16
The following quantitative parameters were assessed: (1) the percentage of the area of the filter membrane occupied by debris, (2) the number of the captured particles, (3) the 2 longest perpendicular diameters of the largest particles (particle size), and (4) the embolic burden obtained by summarizing the surface area of each particle for every patients. These parameters were assumed to represent quantitative indexes of embolization. Finally, the material was gently removed from the filter and processed for histology. Paraffin-embedded serial sections 5 µm thick were stained with hematoxylin and eosin, azan Mallory modified by Heidenhaim trichrome, and Massons trichrome. The specimens were analyzed by 2 expert pathologists who were blinded to the patients clinical diagnosis. The specimens were analyzed for the presence of thrombus material (fibrin, platelets, and red and white cells) and for the presence of atherosclerotic plaque tissue (extracellular matrix, necrotic gruel, fibrous fragments, foam cells, cholesterol clefts, and calcium deposits).
Definitions and Statistical Analysis
Device success was defined as successful deployment and retrieval of the Angioguard device without angiographic complications, such as dissection, spasm, or thrombosis. Myocardial infarction was defined as an increase in CK-MB exceeding 3 times the upper normal value.
Continuous variables are presented as mean±SD, and discrete variables are reported as counts and percentages. The differences between groups were assessed with a Fishers exact test for categorical variables. A Mann-Whitney U test was performed to compare independent variables of 2 nonhomogeneous groups. The relation between quantitative angiographic parameters and quantitative indexes of embolization was assessed by use of linear regression analysis.
A multiple logistic regression analysis was used to investigate the predictive value of baseline and procedural variables on the quantitative indexes of embolization. The variables included in the model were age, sex, cardiovascular risk factors, previous myocardial infarction, previous surgical or percutaneous coronary revascularization, unstable angina, target vessel, direct stenting, quantitative angiographic parameters, stent implantation pressure, and postprocedural CK-MB elevation. Continuous variables were dichotomized at their median value. Results were expressed with ORs and their associated 95% CIs.
All statistical analyses were performed with the SPSS statistical software package (SPSS Inc). A probability value of P<0.05 was considered statistically significant.
| Results |
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Histopathological Results
The results of histopathological analysis are shown in Table 3. Particles could be detected in 28 of 37 filters (75.6%), with a mean particle number of 10.8±6.03 (Figures 1 and 2
). The average covered area of the plastic filter was 26.3±20.17%. Particle size ranged from 47.16 to 2503.48 µm (mean, 518.83±319.61 µm) in the major axis and from 27.95 to 1214.61 µm (mean, 242.5±122.46 µm) in the minor axis. The distribution of particle size is shown in Figure 3, which shows that 50% of the retrieved particles had a diameter >600 µm. The mean embolic burden per patient, assessed as mean surface area of all the particles for each patient, was 2. 41±1.8 mm2, with a range of 0.25 to 6.78 mm2.
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Risk Factors for Embolization on Univariate Analysis
No significant correlation between quantitative angiographic parameters and quantitative indexes of embolization was identified. In particular, this was true for plaque area, which can be considered an angiographic index of plaque burden (Figure 4).
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The captured particles were statistically significantly larger in patients with unstable angina than in those with stable angina (1098.33±714.30 versus 412.91±453 µm, P=0.001) and were larger in eccentric plaques than in concentric ones (1096.59±610.23 versus 605.18±659.79 µm, P=0.03) (Table 4). No other significant association between baseline and procedural variables, the pressure of stent implantation, postprocedural CK-MB elevation, and particle size was identified. Moreover, no univariate predictor of the other quantitative indexes of embolization (percentage of filter area occupied by debris, number of particles, and embolic burden) was found.
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Risk Factors for Embolization on Multivariate Analysis
The presence of unstable angina (OR, 65; CI, 1.2 to 3420; P=0.03) and age >67 years (OR, 42; CI, 1 to 1698; P=0.04) were the only independent predictors of embolization of particles larger than 600 µm. Furthermore, no variable was found to be independently associated with the percentage filter area occupied by debris, with the number of particles, or with the embolic burden.
Qualitative Evaluation
Qualitative analysis, performed with light microscopy, confirmed that the particles were characterized by fibrin strandentrapped platelets, leukocytes, and red cells suggestive of thrombus material, fibrous tissue, calcium spots, soft acellular and amorphous material, macrophages, foam cells, and more rarely cholesterol clefts, typically identifiable in atheromatous plaques (Figure 5). The assessment made on the retrieved material revealed that thrombotic components accounted for 74.3±13.1% of the debris, whereas plaque fragments accounted for 25.7±13.1%. The retrieved material was not qualitatively different in patients with stable and unstable angina. In patients with stable angina, the thrombotic component was 69.6±7.2%, whereas in those with unstable angina, it was 78.9±16% (P=NS) (Table 5). No association between baseline or procedural variables and qualitative data of the retrieved material was found.
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| Discussion |
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Factors Associated With Embolization
The lack of association between pathological morphometric evaluation and angiographic indexes of plaque burden suggests that plaque composition can be more important in determining embolization than the plaque size.
The association between plaque composition and embolization was also suggested by the results of multivariate analysis, which showed that unstable lesions and lesions of older patients released embolic material with larger particles. This finding is consistent with the observation that coronary stenting in unstable angina is associated with a greater incidence and magnitude of myocardial injury.5
The univariate finding that eccentric lesions produced larger emboli also suggests that plaque composition may determine the size of embolizing fragments.
Previous studies consistently demonstrated that eccentric and angiographically complex stenoses are markers of histologically "complicated" and more unstable plaque substrates.1721 In atherectomy specimens of patients with stable and unstable angina, thrombus and plaque disruption were present in 57% and 81% of angiographically complex lesions, respectively.22 In patients with unstable angina, complex angiographic lesion morphology was associated with a higher Braunwald class and worse prognosis.23,24
The number of embolizing particles and the percent filter area occupied by debris were not predicted by any of the variables tested. However, the size of the embolic fragments may be considered the most relevant of the quantitative indexes of embolization evaluated in the study, because larger emboli can cause greater damage by obstructing larger arteries.
The lack of association between baseline or angiographic or procedural variables and quality of the retrieved material is in keeping with the evidence that histopathological features of atherosclerotic plaques are not pathognomonic of any clinical acute coronary syndromes. Although the thrombotic component was slightly higher in the unstable angina patients, the difference between stable and unstable angina patients was not statistically significant. This could be because of the exclusion criteria of angiographic evidence of thrombus in the target vessel.
Relevance of the Study
Distal protection using either occlusion balloons or filtering devices has been shown to be effective in preventing embolization of atheromatous material dislodged during vascular interventions in carotid arteries8,16,25 and in saphenous vein grafts.9,10,26 However, very few data are available on the use of protective devices in native coronary arteries.10,27,28 In fact, our study, apart from being the result of the first systematic application of such an approach in native coronary arteries, is the first that addresses the relation between qualitative and quantitative characteristics of the material captured by the filter and the baseline clinical, angiographic, and procedural variables.
Clinical Implications
Distal microembolization of the coronary circulation has been considered the most frequent cause of periprocedural increases of biochemical markers of myocardial necrosis.11 This event, even when occurring in otherwise successful procedures, is associated with an unfavorable long-term outcome.11 The role of embolizing debris in causing microvascular obstruction during coronary interventions is clearly shown by our study as well as by a previous investigation.10 Indeed, the size of most of the emboli trapped by the filter is far too large to cross the microvascular bed.
Another in vivo demonstration of the role of microembolization of plaque fragments was provided by the study by Kotani et al,7 who showed that in patients with acute coronary syndromes undergoing percutaneous interventions, a larger amount of plaque debris could be aspirated from the target vessel when no-reflow occurred. Although glycoprotein IIb/IIIa inhibitors have been shown to reduce the incidence of periprocedural myocardial infarction, pharmacological therapy cannot be expected to play a decisive role when large amounts of plaque material are embolized distally.
Practical Considerations
Because distal protection increases the cost and complexity of the procedure, it would be important to identify the patients and the lesions with the greater embolic potential that could benefit most from the use of those devices. According to our results, distal protection appears to be particularly useful in patients with unstable angina and in those of older age.
In our experience, the use of the Angioguard device in highly selected lesions was technically feasible and safe.
Study Limitations
The embolic fragments captured by the filter may underestimate the actual amount of embolizing material. Embolization may occur while the Angioguard device crosses the stenosis before the deployment of the filter. Moreover, some debris may pass through the pores of the filter or sneak through the filter and the vessel wall if the contact between the two is defective. In addition, embolizing material can enter side branches proximal to the filter.
The possibility cannot be excluded that some of the retrieved thrombotic material could have been produced inside the bag while the filter remains in the cardiovascular system. However, it is well known that the material dislodged during PCI is highly thrombogenic. This suggests a sudden activation of the coagulative cascade within the PCI procedure at the plaque site rather than a later activation inside the filter.
The study was performed in a relatively small group of selected patients, and no control group was provided. Therefore, the clinical role of distal protection with filter devices has to be confirmed by further controlled studies enrolling larger patient cohorts.
Conclusions
Distal protection during percutaneous coronary artery intervention may limit embolization of atherosclerotic debris potentially able to wedge into small vessels and to cause myocardial injury. Our data support the use of distal protection devices especially in lesions with greater embolic potential, such as unstable plaques, and lesions in older patients.
| Acknowledgments |
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| References |
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