Sousa J Eduardo, Costa Marco A, Abizaid Alexandre, Feres Fausto, Seixas Ana C, Tanajura Luiz F, Mattos Luiz A, Falotico Robert, Jaeger Judith, Popma Jeffrey J, Serruys Patrick W, Sousa Amanda G M R
Institute Dante Pazzanese of Cardiology, São Paulo, Brazil.
Circulation. 2005 May 10;111(18):2326-9. doi: 10.1161/01.CIR.0000164271.01172.1A. Epub 2005 Apr 25.
Despite the proven superiority of sirolimus-eluting stents (SESs) compared with bare stents in the first year after implantation, long-term outcomes of patients treated with these novel devices remain unknown. Our goal was to evaluate the clinical, angiographic, and intravascular ultrasound (IVUS) outcomes of patients treated with SESs 4 years after implantation.
The study included 30 patients treated with sirolimus-eluting Bx Velocity stenting (slow release [SR; n=15] and fast release [FR; n=15]). Twenty-six patients underwent 4-year angiographic and IVUS follow-up and had matched assessments at all time points (index and 4-, 12-, 24-, and 48-month follow-up). One death occurred during the study period in a patient with a patent SES. There were no target-vessel revascularizations or thromboses between 2- and 4-year follow-up examinations. There was no stent thrombosis, target-lesion revascularization, death, or myocardial infarction in the SR group up to 4 years. Cumulative event-free survival rate was 87% for the total population (80% in the FR group and 93% in the SR group). In-stent late loss was slightly greater in the FR group (0.41+/-0.49 mm) than the SR group (0.09+/-0.23) after 4 years. One patient in the FR group had a 52% in-stent restenosis lesion. Percent neointimal hyperplasia volume, as detected by IVUS, remained minimal after 4 years (FR=9.1% and SR=5.7%).
This study confirms the longevity of the optimal outcomes observed in patients treated with sirolimus-eluting Bx Velocity stents 4 years after implantation. In-stent lumen dimensions remained essentially unchanged at 4-year follow-up, particularly in the population treated with the currently available SES (SR formulation).
尽管在植入后的第一年,与裸支架相比,西罗莫司洗脱支架(SES)已被证明具有优越性,但使用这些新型器械治疗的患者的长期预后仍不明确。我们的目标是评估植入SES 4年后患者的临床、血管造影和血管内超声(IVUS)预后。
该研究纳入了30例接受西罗莫司洗脱Bx Velocity支架置入术的患者(缓释[SR;n = 15]和速释[FR;n = 15])。26例患者接受了4年的血管造影和IVUS随访,并在所有时间点(索引及4、12、24和48个月随访)进行了匹配评估。研究期间,1例植入SES的患者死亡。在2至4年的随访检查期间,未发生靶血管血运重建或血栓形成。SR组在4年内未发生支架血栓形成、靶病变血运重建、死亡或心肌梗死。总人群的累积无事件生存率为87%(FR组为80%,SR组为93%)。4年后,FR组的支架内晚期管腔丢失(0.41±0.49 mm)略大于SR组(0.09±0.23)。FR组1例患者出现52%的支架内再狭窄病变。通过IVUS检测,4年后新生内膜增生体积百分比仍保持在最低水平(FR = 9.1%,SR = 5.7%)。
本研究证实了植入西罗莫司洗脱Bx Velocity支架4年后患者所观察到的最佳预后的持久性。在4年随访时,支架内腔尺寸基本保持不变,特别是在接受目前可用的SES(SR制剂)治疗的人群中。