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May 7, 2007Circulation841 citations

Incomplete Stent Apposition and Very Late Stent Thrombosis After Drug-Eluting Stent Implantation

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SCStéphane CookPWPeter WenaweserMTMario Togni

Key Result

Incomplete stent apposition was found in 77% of patients with very late stent thrombosis, compared to 12% in controls (P < 0.001).

Key Points

  • The study aims to investigate differences in stented segments between patients with and without very late stent thrombosis after drug-eluting stent implantation.
  • Patients with very late stent thrombosis underwent intravascular ultrasound since January 2004.
  • Findings were compared with a control group of 144 patients who did not experience stent thrombosis for ≥2 years.
  • Measurements included lesion length, stent length, stent overlap, and incomplete stent apposition.
  • Very late stent thrombosis occurred in 13 patients at a mean of 630±166 days post-implantation.
  • Patients with thrombosis had significantly longer lesions (23.9 mm vs 13.3 mm; P <0.001) and stents (34.6 mm vs 18.6 mm; P <0.001).
  • Incomplete stent apposition was more frequent in patients with thrombosis (77% vs 12%; P <0.001).

Structured PICO

Are there differences in intravascular ultrasound findings, specifically incomplete stent apposition, between patients with and without very late stent thrombosis after drug-eluting stent implantation?

P
Population
Patients who underwent drug-eluting stent (DES) implantation
I
Intervention
Patients presenting with very late stent thrombosis (>1 year) after DES implantation
C
Comparator
Control patients who did not experience stent thrombosis for ≥2 years after DES implantation
O
Outcome
Intravascular ultrasound (IVUS) findings of the stented segment (including incomplete stent apposition, lesion length, stent length, and cross-sectional area)surrogate

Incomplete stent apposition is highly prevalent in patients experiencing very late stent thrombosis after drug-eluting stent implantation, suggesting it plays a mechanistic role in this adverse event.

Abstract

Background— Stent thrombosis may occur late after drug-eluting stent (DES) implantation, and its cause remains unknown. The present study investigated differences of the stented segment between patients with and without very late stent thrombosis with the use of intravascular ultrasound. Methods and Results— Since January 2004, patients presenting with very late stent thrombosis (>1 year) after DES implantation underwent intravascular ultrasound. Findings in patients with very late stent thrombosis were compared with intravascular ultrasound routinely obtained 8 months after DES implantation in 144 control patients, who did not experience stent thrombosis for ≥2 years. Very late stent thrombosis was encountered in 13 patients at a mean of 630±166 days after DES implantation. Compared with DES controls, patients with very late stent thrombosis had longer lesions (23.9±16.0 versus 13.3±7.9 mm; P <0.001) and stents (34.6±22.4 versus 18.6±9.5 mm; P <0.001), more stents per lesion (1.6±0.9 versus 1.1±0.4; P <0.001), and stent overlap (39% versus 8%; P <0.001). Vessel cross-sectional area was similar for the reference segment (cross-sectional area of the external elastic membrane: 18.9±6.9 versus 20.4±7.2 mm 2 ; P =0.46) but significantly larger for the in-stent segment (28.6±11.9 versus 20.1±6.7 mm 2 ; P =0.03) in very late stent thrombosis patients compared with DES controls. Incomplete stent apposition was more frequent (77% versus 12%; P <0.001) and maximal incomplete stent apposition area was larger (8.3±7.5 versus 4.0±3.8 mm 2 ; P =0.03) in patients with very late stent thrombosis compared with controls. Conclusions— Incomplete stent apposition is highly prevalent in patients with very late stent thrombosis after DES implantation, suggesting a role in the pathogenesis of this adverse event.

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Cite This Study

Cook et al. (2007) studied this question. Incomplete stent apposition was found in 77% of patients with very late stent thrombosis, compared to 12% in controls (P < 0.001).

synapsesocial.com/papers/697e17e8c6bddb15e361a2a4https://doi.org/10.1161/circulationaha.106.658237
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