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Circulation: Cardiovascular Interventions
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on February 20, 2009

Circulation: Cardiovascular Interventions. 2009
Published online before print February 20, 2009, doi: 10.1161/CIRCINTERVENTIONS.108.778647
A more recent version of this article appeared on April 1, 2009
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Original Article

A Randomized Controlled Trial of Angiography Versus Intravascular Ultrasound-Directed Bare-Metal Coronary Stent Placement (The AVID Trial)

Robert J. Russo1,13; Patricia D. Silva1; Paul S. Teirstein1; Michael J. Attubato2; Charles J. Davidson3; Anthony C. DeFranco4; Peter J. Fitzgerald5; Steven L. Goldberg6; James B. Hermiller7; Martin B. Leon8; Frederick S. Ling9; Jennifer E. Lucisano1; Richard A. Schatz1; S. Chiu Wong10; Neil J. Weissman11 and David M. Zientek12

1 Scripps Clinic;
2 New York University Medical Center;
3 Northwestern University Feinberg School of Medicine;
4 Comprehensive Cardiovascular Care Group, WI;
5 Stanford University;
6 University of Washington Medical Center;
7 St. Vincent Hospital, IN;
8 Columbia University;
9 Strong Memorial Hospital of the University of Rochester;
10 Cornell University;
11 MedStar Research Institute, MD;
12 Austin Heart Hospital

13 E-mail: russo.robert{at}scrippshealth.org

Background—AVID (Angiography Vs. Intravascular ultrasound-Directed stent placement) is a multicenter, randomized controlled trial designed to assess the effect of intravascular ultrasound (IVUS)-directed stent placement on the 12-month rate of target lesion revascularization (TLR).

Methods and Results—After elective coronary stent placement and an optimal angiographic result (<10% stenosis), 800 patients were randomized to Angiography- or IVUS-directed therapy. Blinded IVUS was performed in the Angiography group without further therapy. In the IVUS group, IVUS criteria for optimal stent placement (<10% area stenosis, apposition, and absence of dissection) were applied. Final minimum stent area was 6.90±2.43 mm2 in the Angiography group and 7.55±2.82 mm2 in the IVUS group (P=0.001). In the IVUS group, only 37% with inadequate expansion (<90%) received further therapy. The 12-month TLR rate was 12.0% in the Angiography group and 8.1% in the IVUS group (P=0.08, 95% CI [-8.3%, 0.5%]). When vessels with a distal reference diameter <2.5 mm by core laboratory angiography measurement were excluded from analysis, the 12-month TLR rate was 10.1% in the Angiography group and 4.3% in the IVUS group (P=0.01, 95% CI [-10.6%, -1.2%]). With a prestent angiographic stenosis of ≥70%, the TLR rate was lower in the IVUS group compared to the Angiography group (3.1% vs. 14.2%; P=0.002; 95% CI [-18.4%, -4.2%]).

Conclusions—IVUS-directed bare-metal stent placement results in larger acute stent dimensions without an increase in complications and a significantly lower 12-month TLR rate for vessels ≥2.5 mm by angiography and for vessels with high-grade prestent stenosis. However, for the entire sample analyzed on an intention-to-treat basis, IVUS-directed bare-metal stent placement does not significantly reduce the 12-month TLR rate when compared to stent placement guided by angiography alone. In addition, IVUS evaluation of adequate stent expansion is underutilized by experienced operators.

Key Words: angiography • imaging • restenosis • stents • intravascular ultrasound


Related Article

A Randomized Controlled Trial of Angiography Versus Intravascular Ultrasound-Directed Bare-Metal Coronary Stent Placement (The AVID Trial)
Robert J. Russo, Patricia D. Silva, Paul S. Teirstein, Michael J. Attubato, Charles J. Davidson, Anthony C. DeFranco, Peter J. Fitzgerald, Steven L. Goldberg, James B. Hermiller, Martin B. Leon, Frederick S. Ling, Jennifer E. Lucisano, Richard A. Schatz, S. Chiu Wong, Neil J. Weissman, David M. Zientek for the AVID Investigators
Circ Cardiovasc Interv 2009 2: 113-123. [Abstract] [Full Text] [PDF]



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