Abstract

In the Washington Radiation for In-Stent restenosis Trial (WRIST), patients were first treated with conventional techniques and then randomized to either γ-irradiation ( 192Ir) or placebo (dummy seeds). In the 192Ir group with native coronary in-stent restenosis, we identified 8 patients with edge recurrence and compared them with 21 patients with no recurrence. Serial (postirradiation and follow-up) intravascular ultrasound analysis was performed according to conventional methods. When compared with nonrecurring lesions, lesions with distal edge recurrence had (1) greater decrease in mean distal lumen cross-sectional area (−3.0 ± 1.2 vs −0.7 ± 1.0 mm 2, p = 0.0002), (2) no change in mean distal external elastic membrane cross-sectional area versus an increase in mean distal cross-sectional area of 1.0 ± 0.9 mm 2 in nonrecurring lesions (p = 0.0047), and (3) a greater increase in mean distal plaque + media cross-sectional area (2.9 ± 1.2 mm vs 1.7 ± 0.6 mm 2, p = 0.0103). Within the stented segment, the nonrecurring lesions had no decrease in mean lumen and no increase in mean intimal hyperplasia cross-sectional area. Conversely, lesions with distal edge recurrence had a significant decrease in mean intrastent lumen cross-sectional area (−1.7 ± 1.7 mm 2) and a significant increase in mean intrastent intimal hyperplasia cross-sectional area (1.6 ± 1.6 mm 2). Lesions with distal edge recurrence also had a greater decrease in mean proximal lumen cross-sectional area (−1.7 ± 1.3 vs −0.3 ± 0.8 mm 2, p = 0.0213), with a trend toward a greater increase in mean proximal plaque + media cross-sectional area. Thus, edge recurrence after 192Ir treatment of in-stent restenosis is the result of neointimal hyperplasia (part of generalized treatment failure) and the absence of radiation-induced positive remodeling.

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