HOME SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES CARDIOSOURCE SEARCH HELP FEEDBACK		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Figures Only Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Takano, Y. Articles by Tobis, J. M. Search for Related Content PubMed PubMed Citation Articles by Takano, Y. Articles by Tobis, J. M.

CLINICAL STUDY

Optimizing stent expansion with new stent delivery systems

^a University of California, Los Angeles Center for Health Sciences, Los Angeles, California, USA

Manuscript received April 10, 2001; revised manuscript received July 20, 2001, accepted August 15, 2001.

^* Reprint requests and correspondence: Dr. Jonathan M. Tobis, 10833 Le Conte Avenue, Room BL-394 CHS, Los Angeles, California 90095-1717 USA
jtobis{at}mednet.ucla.edu

OBJECTIVES

The purpose of this study was to assess whether the newer stent delivery systems provide a stented lumen cross-sectional area (CSA) that is equal to the delivery balloon nominal dimensions.

BACKGROUND

First generation stents were often not adequately expanded with their delivery system and frequently required higher pressure or a larger balloon after deployment. Newer stents were designed to optimize expansion with noncompliant, high-pressure balloons provided as the delivery systems.

METHODS

Intravascular ultrasound (IVUS) was used to evaluate 38 stents in 32 patients after deployment at 14 to 16 atm with their delivery balloon system. Minimum stent lumen CSA and stent minimum lumen diameter (MLD) were measured by IVUS imaging. The manufacturer’s expected stent diameter was defined as the balloon diameter measured by the company at the maximum pressure used. The manufacturer’s expected stent area was calculated based on the manufacturer’s expected stent diameter.

RESULTS

The MLD (2.5 ± 0.5 mm) and minimum stent CSA (6.0 ± 1.7 mm²) by IVUS were significantly smaller than the manufacturer’s expected stent diameter (3.5 ± 0.4 mm) and area (9.5 ± 1.9 mm²) (p < 0.0001, respectively). The mean MLD by IVUS was 72 ± 8% of the expected stent diameter, and the mean minimum stent CSA by IVUS was 62 ± 10% of the expected stent area.

CONCLUSIONS

Despite moderately high-pressure inflations, the mean minimum stent CSA actually achieved was, on average, only 62% of the manufacturer’s expected stent area. To optimize stent deployment, these IVUS observations should be considered during coronary artery stenting.

Abbreviations and Acronyms   CSA = cross-sectional area   IVUS = intravascular ultrasound   MLD = minimum lumen diameter   QCA = quantitative coronary angiography

This article has been cited by other articles:

				E. Romagnoli, G. M. Sangiorgi, J. Cosgrave, E. Guillet, and A. Colombo Drug-Eluting Stenting: The Case for Post-Dilation J. Am. Coll. Cardiol. Intv., February 1, 2008; 1(1): 22 - 31. [Abstract] [Full Text] [PDF]

				S. Aziz, J. L Morris, R. A Perry, and R. H Stables Stent expansion: a combination of delivery balloon underexpansion and acute stent recoil reduces predicted stent diameter irrespective of reference vessel size Heart, December 1, 2007; 93(12): 1562 - 1566. [Abstract] [Full Text] [PDF]

				V. Spanos, G. Stankovic, J. Tobis, and A. Colombo The challenge of in-stent restenosis: insights from intravascular ultrasound Eur. Heart J., January 2, 2003; 24(2): 138 - 150. [Full Text] [PDF]