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Volume 135, Issue 2, Pages 243-245 (26 June 2009)


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Distribution pattern of neointimal hyperplasia following sirolimus-eluting stent implantation assessed by 3-dimensional intravascular ultrasound

Hideaki Kaneda, Junya Ako, Mitsuyasu Terashima, Katsuhisa Waseda, Paul G. Yock, Peter J. FitzgeraldCorresponding Author Informationemail address

Received 24 November 2007; accepted 20 January 2008. published online 20 June 2008.

Abstract 

Sirolimus-eluting stents (SES) have been shown to reduce intimal hyperplasia (IH) within the stent. Although angiographic studies have suggested focal distribution of IH, these data are limited by its spatial resolution and the minimal amount of IH. Therefore, the exact distribution pattern of SES IH remains unclear. Ninety-six SIRIUS trial patients who underwent SES (51) or bare metal stent (45) implantation and three-dimensional IVUS at 8 months follow-up were enrolled. Neointimal area (stent—lumen area) was obtained at every 0.5-mm interval throughout the stented segment. The length of each stent with IVUS-detectable neointima was determined and divided by the stented length in each case to normalize the data. Even with IVUS, IH was detectable in very limited SES stented segments (median 8% of total stented length) compared to the diffuse nature of IH within BMS with only 5 stented lesions having segments free from IH. In 25% (13 of 51) of patients, no IH was detectable within whole SES stented segments. In conclusion, SES has reduced not only the total amount of IH, but also limited the distribution. These data suggest that local conditions (heterogeneity of biological responses of particular plaques, pharmacokinetics, or their combination) may play a role in IH following SES implantation.

Center for Research in Cardiovascular Interventions, Stanford University, Stanford, CA, United States

Corresponding Author InformationCorresponding author. Center for Research in Cardiovascular Interventions, Stanford University Medical Center, 300 Pasteur Drive, Room H3554, Stanford, CA 94305, United States. Tel.: +1 650 498 6034; fax: +1 650 498 6027.

PII: S0167-5273(08)00430-0

doi:10.1016/j.ijcard.2008.01.054


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