Sirolimus-eluting stent implants effectively inhibit neointimal hyperplasia in diabetes

Key points
- Sirolimus-eluting stent implants effectively inhibit neointimal hyperplasia in diabetic patients.
- According to a study from Spain, "A predefined intravascular ultrasound (IVUS) substudy was performed to evaluate the vascular effects of sirolimus -eluting stent (SES) versus bare-metal stent (BMS).
- "Serial intravascular ultrasound analyses were performed in 140 lesions (SES=75; BMS 65) immediately after stent implantation and at 9-month follow-up.
- Qualitative assessment of residual dissections and stent apposition were also performed," presented P.
Sirolimus-eluting stent implants effectively inhibit neointimal hyperplasia in diabetic patients.
According to a study from Spain, "A predefined intravascular ultrasound (IVUS) substudy was performed to evaluate the vascular effects of sirolimus -eluting stent (SES) versus bare-metal stent (BMS). The Diabetes and Sirolimus-Eluting Stent (DIABETES) trial is a prospective, multicenter, randomized, controlled trial aimed at demonstrating the efficacy of the SES compared with BMS in diabetic patients."
"Serial intravascular ultrasound analyses were performed in 140 lesions (SES=75; BMS 65) immediately after stent implantation and at 9-month follow-up. Vessel, luminal, and stent mean areas and volumes were evaluated at both edges and within the stented segment.
Qualitative assessment of residual dissections and stent apposition were also performed," presented P. Jimenez-Quevedo and colleagues, San Carlos University Hospital.
The results revealed, "Baseline clinical and angiographic characteristics were similar between groups. At 9 months, in-stent neointimal hyperplasia (NIH) mean area and volume were significantly reduced in the SES group (median NIH area 0.01 mm(2) [0.0 to 0.1] vs. 2.0 mm(2) [1.0 to 2.9] and median NIH volume 0.11 mm(3) [0 to 2.1] vs. 35.3 mm(3) [16.6 to 62.6]; both p<0.0001).
"In the SES group, stent edges evidenced significant increase in lumen dimensions mainly due to significant increase in vessel volume, whereas those of the BMS group presented vessel shrinkage leading to significant lumen reduction. Late acquired incomplete stent apposition was observed in 11 lesions (14.7%) in the SES group and 0 in the BMS group (p= 0.001). At 1 year, no stent thromboses occurred in malapposed stents."
The researchers concluded, "The SES implantation effectively inhibits NIH in diabetic patients. The antirestenotic effect of SES is also appreciated at the stent edges. Late acquired stent malapposition is a frequent phenomenon in diabetic patients treated with SES."
Jimenez-Quevedo and colleagues published their study in the Journal of the American College of Cardiology (Vascular effects of sirolimus-eluting versus bare-metal stents in diabetic patients - Three-dimensional ultrasound results of the diabetes and sirolimus-eluting stent (DIABETES) trial. J Am Coll Cardiol, 2006;47(11):2172-2179).
Written and revised by
Gerald Hurowitz, M.D.
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