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Thrombus capture by withdrawal of an open filter device: a useful treatment for large non-occlusive coronary thrombus
Samer Arnous1, Maria Agelaki, Nizar Shakhshir
1Manchester Heart Centre, Manchester Royal Infirmary, Biomedical Research Centre, Manchester, United Kingdom.
Insights
This study shows that the ev3 Spider™ filter device safely and effectively removes large coronary thrombi resistant to standard treatments. This novel technique achieved successful thrombus removal and TIMI 3 flow in all patients, reducing no-reflow risk.
Area of Science:
- Interventional Cardiology
- Vascular Surgery
Background:
- Large "cannon-ball" non-occlusive intracoronary thrombi pose treatment challenges.
- Standard thrombectomy aspiration catheters are often ineffective for these large thrombi.
Purpose of the Study:
- To evaluate the safety and feasibility of using the ev3 Spider™ filter device for manual removal of non-occlusive coronary thrombus.
- To assess the efficacy of this novel technique in achieving substantial thrombus removal and restoring coronary blood flow.
Main Methods:
- A case series of nine patients with large, non-occlusive intracoronary thrombi refractory to standard aspiration thrombectomy.
- Utilized the ev3 Spider™ filter device for manual thrombus retrieval.
- Assessed procedural success, prevention of no-reflow/slow flow, and achievement of TIMI 3 flow post-intervention.
Main Results:
- The ev3 Spider™ filter device successfully achieved substantial or complete thrombus removal in all nine patients.
- Prevention of no-reflow/slow flow phenomenon and TIMI 3 flow post-stenting were achieved in all cases.
- One instance of coronary dissection occurred in a heavily calcified lesion; no other device-related complications were reported.
Conclusions:
- Manual removal of large intracoronary thrombi using the ev3 Spider™ filter device is a safe and feasible option.
- This technique demonstrates a high procedural success rate and may reduce the risk of no-reflow in complex thrombus cases.
- This is the first case series to describe the use of the ev3 Spider™ filter device for refractory intracoronary thrombus removal.
Aims:
The aim of this study was to assess the safety and feasibility of manual removal of a non-occlusive coronary thrombus using an open filter device. Between April 2006 and December 2011, 1,102 patients were treated percutaneously for acute coronary syndrome at our institution. Of these, nine (1%) had a large "cannon-ball" non-occlusive intracoronary thrombus, which did not improve with standard thrombectomy aspiration catheters. In these patients, we describe a novel technique of thrombus removal using the ev3 Spider™ filter device. Four patients had LAD thrombus, three had RCA thrombus, one LCX thrombus and one SVG thrombus. The primary endpoint of substantial or complete thrombus removal, prevention of no-reflow/slow flow phenomenon and achievement of TIMI 3 flow post stenting was achieved in all cases. Coronary dissection occurred in one case where the lesion was heavily calcified. There were no other complications related to the device. This is the first case series describing the use of the ev3 Spider™ filter device for the removal of a large intracoronary thrombus refractory to conventional treatment. This was associated with a high procedural success rate and may reduce the risk of no-reflow in these cases.
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