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The Official Journal of the International Andreas Gruentzig Society
Friday, May 16, 2008


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Distal Embolic Protection Devices

Plaque embolization occurs during interventional removal of atheroma, often causing a shower of emboli to be released into the circulation and potentially leading to life-threatening intra- or postprocedural complications. Two types of distal embolic protection devices, presently used in carotid stenting and saphenous vein graft interventions, are available for use in the U.S. One is a balloon system that temporarily blocks the vessel distal to the occlusion site during the procedure, catching and aspirating the atheromatous and thrombotic debris that are released before they reach the capillary bed. The second device is a filter system that does not occlude blood flow, but preserves it while capturing thrombi through small pores.

Clinical and Economic Outcomes of Embolic Complications and Strategies for Distal Embolic Protection during Percutaneous Coronary Intervention in Saphenous Vein Grafts
Background. Although distal embolic protection (DEP) is increasingly utilized in saphenous vein graft percutaneous coronary intervention (SVG PCI), the clinical and economic outcomes of different DEP strategies are unknown. Methods. We compared 3 DEP strategies (no DEP, routine DEP, selective DEP in high-risk cases) in 126 consecutive cases of SVG PCI performed without DEP in a single catheterization laboratory over a 4-year period. No SVG PCI was excluded. High risk was defined using 2 multivariate predictors of embolic complication previously validated by NCDR (graft age greater than or equal to 8 years and/or friable appearance with thrombus). Costs were determined by a ratio of cost-to-charges methodology and average cost of the two FDA-approved DEP devices ($1,350) with similar efficacy. Results. Without DEP, the incidence of embolic complications was 17% (22/126), resulting in major adverse coronary events (MACE) in 3.2% (4/126) of all cases: 2 deaths, 1 myocardial infarction, and 1 emergency coronary artery bypass. Embolic complications significantly increased both procedure costs by $2,725 (p < .001) and total hospital costs ~$2,800 (p < 0.05). Risk adjustment for selective DEP use correctly predicted 86% (19/22) of embolic complications, including all MACE, at an incremental cost of $684/patient for selective DEP versus $1,150/patient for routine DEP. Selective DEP would cost $43,127 per death prevented versus $72,461 using routine DEP during the index hospitalization. Conclusions. Embolic complications increase cost in excess of the cost of a DEP device. This risk adjustment model correctly predicted the majority of cases of embolic complication and all MACE, suggesting that selective DEP use may help reduce utilization of DEP by an almost 50% cost reduction compared to routine use.



A Novel Use for a Distal Embolic Protection Device: Stent Retrieval
A Novel Use for a Distal Embolic Protection Device: Stent Retrieval CASE REPORTS: A Novel Use for a Distal Embolic Protection Device: Stent Retrieval - Pavel Guigauri, MD and Harold L. Dauerman, MD Stent embolization is an uncommon but potentially serious complication of percutaneous coronary intervention (PCI). the difficulty in utilizing snares and balloons for stent retrieval, we describe a new method of stent retrieval utilizing a distal embolic ...



Randomized Trial of a Distal Embolic Protection Device During Percutaneous Intervention of Saphenous Vein Aorto-Coronary Bypass Grafts
Randomized Trial of a Distal Embolic Protection Device During Percutaneous Intervention of Saphenous Vein Aorto-Coronary Bypass Grafts Feature: Randomized Trial of a Distal Embolic Protection Device During Percutaneous Intervention of Saphenous Vein Aorto-Coronary Bypass Grafts - Donald S. Baim, MD, Dennis Wahr, MD, Barry George, MD, Martin B. Leon, MD, Joel Greenberg, MD, Donald E. Cutlip, MD, Unsal Kaya, MS, Jeffrey J. Popma, MD, Kalon K.L. Ho, ,MD, MSc, Richard E. Kuntz, MD, MSc; on behalf...



Percusurge Guardwire Balloon-Associated Thrombus ? A Limitation of the Percusurge Distal Protection System
Saphenous vein graft interventions represent a challenge to interventional cardiologists because of the frequent and unpredictable incidence of distal embolization. Distal embolic protection devices have demonstrated a reduction in the incidence of this phenomenon. As the use of these devices becomes more frequent outside research protocols, the limitations of different devices will become apparent. Thrombus at the site of the distal occlusive balloon of the Percusurge distal embolic protection system was noted in the case described and represents a potential drawback of this form of distal protection.



COMMENTARY: Can Distal Embolic Protection Yield Better Results in Acute Myocardial Infarction Treatment?




Distal Embolic Protection ? Don't Cause a Stroke Trying to Prevent One!
Embolic Protection Device (ev3 Inc., Plymouth, Minnesota) provides further evidence of the merit of these newer-generation ? The earlier generation protection devices such as the PercuSurge device (Medtronic, Inc., Minneapolis, Minnesota), the Angiogard device (Cordis Corporation, Miami, Florida), and the Accunet? Soon after the introduction of embolic protection devices in U.S. trials, I found myself excessively manipulating the first-generation devices through many typical high-grade ...



Contemporary Management of Vein Graft Disease
Randomized trial of a distal embolic protection device during percutaneous intervention of saphenous vein aorto-coronary bypass grafts. Randomized evaluation of polytetrafluoroethylene-covered stent in saphenous vein grafts: The Randomized Evaluation of polytetrafluoroethylene COVERed stent in Saphenous vein grafts (RECOVERS) Trial. Clinical outcomes after sirolimus-eluting stent implantation for de novo saphenous vein graft lesions.



Intragraft Nicardipine Prophylaxis to Prevent No-reflow in Triple-vessel Saphenous Vein Graft Intervention
ABSTRACT: Saphenous vein graft angioplasty and stenting has been associated with a relatively high risk of no-reflow and myocardial necrosis. The injectable dihydropyridine calcium channel blocker, nicardipine, is a highly potent arteriolar vasodilator, could be valuable as a prophylactic treatment to prevent no-reflow during SVG interventions. We examined the use of prophylactic, intracoronary (intra-graft) nicardipine, without distal protection, as a means to prevent no-reflow and myocardial necrosis in two consecutive patients undergoing 3-vessel, saphenous vein graft intervention. Following IC nicardipine injection, six stents were placed via direct stenting in the six degenerated SVGs. The average graft age was 13.5 years. Clinical, electrocardiographic, enzymatic (CPK and CPK-MB, troponin) and quantitative coronary angiographic methods were used to assess the safety and efficacy of this treatment in these two high-risk cases. There were no clinical, enzymatic or electrocardiographic signs of ischemia or injury after the use of nicardipine IC injection combined with direct stenting in these cases. Angiograph-ically, TIMI flow was 2.33 ± 0.52 prior to intervention, and improved to 3.0 ± 0.0 after intervention. The mean (TIMI) myocardial blush scores from the 6 SVG distributions improved from 1.82 ± 0.41 prior to intervention, to 2.67 ± 0.52 after intervention. The CPK peaks were 79 IU and 105 IU, respectively, in the two cases (upper limit normal = 190 IU). In summary, the dihydropyridine calcium channel blocker, nicardipine, may provide effective prophylaxis for no-reflow and myocardial necrosis, without the routine use of distal embolic protection devices, in SVG stent interventions. A larger prospective study is warranted to expand upon this preliminary observation.



The Evolving Role of Glycoprotein (GP) IIb/IIIa Receptor Blockade During Percutaneous Coronary Intervention of Saphenous Vein Bypass Grafts
GP receptor blockade trials during SVGB intervention. B. Delayed SVBG intervention after pretreatment with a GP IIb/IIIa receptor blocker. D. Distal protection devices and GP IIb/IIIa receptor blockade.



Massive Air Embolus Treated with Rheolytic Thrombectomy
ABSTRACT: The incidence of air embolism during diagnostic cardiac catheterization and percutaneous coronary intervention is reported at a rate of 0.84% and 0.24%. Although there is no optimal technique to restore blood flow after blockage by air emboli, treatment options include manual aspiration or forcefully injecting saline, with auxiliary supportive measures like 100% oxygen or an intra-aortic balloon pump. The AngioJet (Possis Medical, Inc., Minneapolis, Minnesota) device is a catheter-based device for thrombus removal in which high-velocity saline jets are used to create a localized low-pressure zone at the distal catheter tip (Bernoulli effect), resulting in the maceration and removal of thrombus through an exhaust lumen. The use of rheolytic thrombectomy has been studied in thrombus-containing native coronary arteries as well as saphenous vein graft lesions. We report a case of a massive air embolus that occurred after activation of an AngioJet catheter in a thrombus-laden right coronary artery (RCA). The AngioJet catheter was then utilized to effectively aspirate the air embolus with restoration of coronary blood flow. Use of a guiding catheter that is nonocclusive or with side holes to ensure continuous blood flow from the central aorta may help avoid entrainment of air into the coronary artery during activation of the AngioJet thrombectomy catheter. To our knowledge, this is the first reported case of such a potential complication. In the event of such a complication, the AngioJet catheter can be implemented to aspirate a coronary air embolus. J INVASIVE CARDIOL 2007;19:E182?E184



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