P2217 Serial intravascular ultrasound analysis in TAXUS II: beneficial distal edge effect with paclitaxel-eluting stents

2003 ◽  
Vol 24 (5) ◽  
pp. 421
Author(s):  
M DEGERTEKIN
2002 ◽  
Vol 39 ◽  
pp. 70-71
Author(s):  
Andrea S. Abizaid ◽  
J.Eduardo Sousa ◽  
Pim de Feyter ◽  
Alexandre Abizald ◽  
Egon Wuelfert ◽  
...  

2021 ◽  
Author(s):  
Takuya Tsujimura ◽  
Osamu Iida ◽  
Mitsutoshi Asai ◽  
Masaharu Masuda ◽  
Shin Okamoto ◽  
...  

Abstract Background: Although several clinical reports demonstrated a durable patency rate after a novel fluoropolymer-coated paclitaxel-eluting stent (Eluvia™; Boston Scientific, Marlborough, MA, USA) implantation, aneurysmal degeneration after implanting Eluvia™ has raised clinical concerns. Here, we report a case with exacerbated aneurysmal degeneration on serial angiography and intravascular ultrasound 50 months after Eluvia™ implantation for a superficial femoral artery lesion.Case presentation: A 79-year-old woman with claudication in the right lower extremity decreasing her quality of life was referred to our hospital. Pre-procedural angiography showed severe stenosis from the middle-to-distal part of the right superficial femoral artery, and Eluvia™ was implanted with optimal expansion. However, the patient had a recurrence of intermittent claudication in the right lower extremity 25 months thereafter. Angiography revealed de novo stenosis in the distal part of the popliteal artery and proximal stent edge restenosis at the Eluvia™ implantation site. Subsequently, the patient underwent endovascular therapy for these lesions. In addition, intravascular ultrasound at the time of endovascular therapy revealed vessel enlargement with a mean vessel diameter of 7.2-9.9 mm at the distal edge of the Eluvia™ implantation site. However, intermittent claudication on the right side recurred again 50 months after Eluvia™ implantation. Angiography demonstrated de novo severe stenosis from the distal part of the superficial femoral artery to the middle part of the popliteal artery. Furthermore, peri-stent contrast staining was found at the distal part of the Eluvia™ implantation site. Intravascular ultrasound showed a further enlargement of mean vessel diameter to 11.9 mm at the distal edge of the Eluvia™ stent. Moreover, enlargement of the lumen and stent malapposition were also found, suggesting exacerbated aneurysmal degeneration 50 months after Eluvia™ implantation.Conclusions: We report a case with exacerbated aneurysmal degeneration on serial angiography and intravascular ultrasound 50 months after Eluvia™ implantation for an SFA lesion. Long-term follow-up should be mandatory for patients receiving Eluvia™ implants.


2004 ◽  
Vol 47 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Pavel Červinka ◽  
Josef Šťásek ◽  
Marco Aurelio Costa ◽  
Jan Štursa ◽  
Miloslav Fišer ◽  
...  

The aim of this study was to evaluate the incidence and the cause of “edge restenosis” after implantation of high activity 41.1 μCi±1.2 μCi=1520 kBq±44 kBq, β-emitting (55Co) stents. Proton bombarding in cyclotron has brought the radioactivity. Intravascular ultrasound (IVUS) investigation has been completed in 10 patients. The angiographies performed at 6 month revealed restenosis >50 % in 5 cases (50 %). The analysis of edges (5 mm distally and proximally to the last stent struts) showed no significant changes in TVV (187.3±62.60 mm3 and 176.9±53.5 mm3) but PMV increase significantly (i.e. neointimal proliferation) from 61.9±31.2 mm3 to 82.2±43.4 mm3 (p<0.04) and was the major contributor (from 66 %) to lumen volume loss (125.4±40.7 mm3 and 94.7±22.2 mm3, p<0.02). In conclusion, neither statistically significant positive nor negative remodelling at the “stent edges“, were present. Statistically significant increase in plaque+media volume (i.e. neointimal hyperplasia) and reduction in lumen volume were found. The cause of “edge restenosis” was especially (from 66 %) due to increase in plaque+media volume (i.e. neointimal hyperplasia). Probably, main reason for “edge effect”/neointimal hyperplasia was in this trial sharp fall-off in radiation at the edges of the stents.


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