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J Am Coll Cardiol Intv, 2008; 1:192-201, doi:10.1016/j.jcin.2008.02.003
© 2008 by the American College of Cardiology Foundation
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Stent Malapposition After Sirolimus-Eluting and Bare-Metal Stent Implantation in Patients with ST-Segment Elevation Myocardial Infarction

Acute and 9-Month Intravascular Ultrasound Results of the MISSION! Intervention Study

Bas L. van der Hoeven, MD*, Su-San Liem, MD*, Jouke Dijkstra, MSc{dagger}, Sandrin C. Bergheanu, MD*, Hein Putter, MSc{ddagger}, M. Louisa Antoni, MD*, Douwe E. Atsma, MD*, Marianne Bootsma, MD*, Katja Zeppenfeld, MD*, J. Wouter Jukema, MD*, Martin J. Schalij, MD*,*

* Department of Cardiology, Leiden University Medical Center, Leiden, the Netherlands
{dagger} Department of Medical Statistics and Bio-Informatics, Leiden University Medical Center, Leiden, the Netherlands
{ddagger} Department of Radiology, Division of Image Processing, Leiden University Medical Center, Leiden, the Netherlands.


Figure 1
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Figure 1 IVUS Contours and Measurements

Schematic diagram illustrating intravascular ultrasound (IVUS) contours and measurements.

 

Figure 2
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Figure 2 Change of EEM and P&M CSA During the Follow-Up Period for All Individual SM Sites

(A) Bare-metal stent (BMS); (B) sirolimus-eluting stent (SES). The stent malapposition (SM) sites are categorized as resolved, persistent, or acquired SM. Delta ({Delta}) denotes change (follow-up minus post-procedure). (A) BMS: Most of the acute SM sites (resolved and persistent) are located above the x axis, indicating an increase in the plaque and media (P&M) cross-sectional area (CSA) during the follow-up period. Acquired SM sites are very rare after BMS implantation. (B) SES: The external elastic membrane (EEM) and P&M CSA are virtually unchanged in most persistent SM sites. Acquired SM sites are mostly located around the positive x axis, indicating that positive remodeling (enlargement of the EEM CSA, while the P&M CSA remains virtually unchanged) is the mechanism of development of SM in these sites. In a minority of sites, plaque reduction (decrease of the P&M CSA, while the EEM CSA remains virtually unchanged) plays a role.

 

Figure 3
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Figure 3 Mechanism of Change in Lumen CSA During the Follow-Up Period

(A) BMS; (B) SES. Delta ({Delta}) denotes change (follow-up minus post-procedure). (A) BMS: Changes of the lumen CSA are predominantly determined by changes in P&M CSA, which is positive in the majority of sites. Most likely this is due to neointimal growth. Clearly, remodeling (mostly negative) plays a small role in change of the lumen CSA. (B) SES: Change of the lumen CSA is mainly caused by remodeling after SES implantation, either negative (below x axis) or positive (above x axis). The P&M CSA remains virtually unchanged in most SM sites. Some SM sites demonstrate a clear reduction in P&M CSA, which may be due at least in part to resolution of thrombus behind the stent. Abbreviations as in Figure 2.

 

Figure 4
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Figure 4 Examples of the Mechanism of Resolved and Acquired SM

The green circle indicates the EEM and the red circle the lumen contour. Delta ({Delta}) denotes change (follow-up minus post-procedure). (A) Resolved proximal edge SM due to increase of plaque burden and some negative remodeling. (Stent CSA: 10.7 mm2, lumen behind stent [LBS] CSA: 5.7 mm2, {Delta}EEM CSA: –2.1 mm2, {Delta}P&M CSA: 4.9 mm2, {Delta}lumen CSA: –7.0 mm2). (B) Acquired body SM because of positive remodeling. (Stent CSA: 6.1 mm2, LBS CSA: 7.0 mm2, {Delta}EEM CSA: 7.1 mm2, {Delta}P&M CSA: 0.1 mm2, {Delta}lumen CSA: 7.0 mm2). (C) Acquired body SM because of plaque reduction. (Stent CSA: 8.6 mm2, LBS CSA: 3.3 mm2, {Delta}EEM CSA: 0.2 mm2, {Delta}P&M CSA: 3.2 mm2, {Delta}lumen CSA: 3.3 mm2). Abbreviations as in Figure 2.

 




 
   
 
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