Intravascular sonotherapy decreases neointimal hyperplasia after stent implantation in swine

Background-Intimal hyperplasia and subsequent in-stent restenosis remain a major limitation after stent implantation. In vitro cell culture studies sh ow that low-frequency, noncavitational ultrasound energy may impact smooth muscle cell proliferation. Accordingly, we assessed the efficacy of intrava scular sonotherapy treatment on intimal hyperplasia in a swine stent model, Methods and Results-After balloon injury, biliary stents (Johnson & Johnson ) were implanted in the femoral arteries of 14 swine. A total of 48 stented sites were randomized to sonotherapy or sham treatment using a custom-buil t, X-French catheter intravascular sonotherapy system (URX, PharmaSonics In c). After stent deployment, ultrasound energy (700 KHz) was applied to the treatment group for lip to 5 minutes. Smooth muscle cell proliferation was assessed using bromodeoxyuridine histology preparation (BrdU) at 7 days in 28 stented sites. At 28 days, the neointimal thickness and the ratio of neo intimal/stent area (percent stenosis) was calculated by histomorphometric q uantification in 20 stented sites. At 7 days, percent of BrdU staining was significantly reduced in the sonotherapy group compared with the sham group (24.1 +/-7.0% versus 31.2 +/-3.0%, P<0.05). At 28 days, percent stenosis w as significantly less in the sonotherapy group than in the sham group (36<p lus/minus>24% versus 44 +/- 27%, P<0.05), and the mean neointimal thickness in the sonotherapy group was less than in the sham group (417<plus/minus>4 61 mum versus 643 +/- 869 mum, P=0.06). Conclusions-In this swine peripheral model, intravascular sonotherapy seeme d to decelerate cellular proliferation and decrease in-stent hyperplasia. T herefore, intravascular sonotherapy may be an effective form of nonionizing energy to reduce in-stent restenosis.