TY - JOUR
T1 - Serial intravascular ultrasound analysis of edge recurrence after intracoronary gamma radiation treatment of native artery in-stent restenosis lesions
AU - Ahmed, Javed M.
AU - Mintz, Gary S.
AU - Waksman, Ron
AU - Lansky, Alexandra J.
AU - Mehran, Roxana
AU - Wu, Hongsheng
AU - Weissman, Neil J.
AU - Pichard, Augusto D.
AU - Satler, Lowell F.
AU - Kent, Kenneth M.
AU - Leon, Martin B.
PY - 2001/5/15
Y1 - 2001/5/15
N2 - 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 mm2, 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 mm2 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 mm2, 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 mm2) and a significant increase in mean intrastent intimal hyperplasia cross-sectional area (1.6 ± 1.6 mm2). 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 mm2, 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.
AB - 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 mm2, 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 mm2 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 mm2, 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 mm2) and a significant increase in mean intrastent intimal hyperplasia cross-sectional area (1.6 ± 1.6 mm2). 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 mm2, 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.
UR - http://www.scopus.com/inward/record.url?scp=0035873449&partnerID=8YFLogxK
U2 - 10.1016/S0002-9149(01)01483-7
DO - 10.1016/S0002-9149(01)01483-7
M3 - Article
C2 - 11356387
AN - SCOPUS:0035873449
SN - 0002-9149
VL - 87
SP - 1145
EP - 1149
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 10
ER -