Waseda Katsuhisa, Ako Junya, Kume Teruyoshi, Fitzgerald Peter J, Honda Yasuhiro
Stanford University, Division of Cardiovascular Medicine, 300 Pasteur Drive, Room H3554, Stanford, CA 94305-5637 USA.
J Invasive Cardiol. 2016 Aug;28(8):323-9. Epub 2015 Dec 15.
This study aim was to investigate the morphometric parameters of late-acquired incomplete stent apposition (ISA) following use of Cypher sirolimus-eluting stent (SES; Cordis), Taxus paclitaxel-eluting stent (PES; Boston Scientific), and Resolute zotarolimus-eluting stent (ZES; Medtronic).
Characteristics of late-acquired ISA between first-generation and second-generation drug-eluting stents (DESs) have not been systematically examined.
Late-acquired ISA was defined as separation of at least 1 stent strut from the vessel wall with evidence of blood speckle behind the strut, where poststent implantation intravascular ultrasound (IVUS) revealed complete apposition. A total of 30 late-acquired ISA cases (12 SES, 10 PES, 8 ZES) were included in this IVUS analysis. Corresponding cross-sections at post procedure were selected for comparison. Vessel, lumen, peristent tissue, and stent area were measured in the late-acquired ISA arc as referenced to stent center.
Late-acquired ISA area was 2.4 ± 1.5 mm² in SES, 2.2 ± 2.7 mm² in PES, and 0.9 ± 0.6 mm² in ZES (P=.02 for SES vs ZES). Vessel area increased from post procedure to follow-up in SES (4.6 ± 1.7 mm² to 7.0 ± 2.5 mm²; P<.01) and PES (3.6 ± 1.7 mm² to 5.7 ± 3.8 mm²; P=.06), but not in ZES. Vessel expansion was the main mechanism in SES and PES groups; however, tissue regression and stent recoil, as well as vessel expansion, also contributed to late-acquired ISA in ZES. Per-patient analyses demonstrated that vessel expansion was the predominant mechanism of late-acquired ISA in 83% of SES, 60% in PES, and 50% of ZES cases.
The magnitude and mechanism of late-acquired ISA appear to be different between first-generation and second-generation DESs, possibly due to varying vessel response to different stent component types.
本研究旨在调查使用西罗莫司洗脱支架(Cypher SES;科迪斯公司)、紫杉醇洗脱支架(Taxus PES;波士顿科学公司)和佐他莫司洗脱支架(Resolute ZES;美敦力公司)后迟发性不完全支架贴壁(ISA)的形态学参数。
第一代和第二代药物洗脱支架(DES)之间迟发性ISA的特征尚未得到系统研究。
迟发性ISA定义为至少1个支架小梁与血管壁分离,且小梁后方有血液斑迹,而支架植入后血管内超声(IVUS)显示为完全贴壁。本IVUS分析共纳入30例迟发性ISA病例(12例SES、10例PES、8例ZES)。选取术后相应横截面作比较。以支架中心为参照,在迟发性ISA弧段测量血管、管腔、残留组织和支架面积。
SES组迟发性ISA面积为2.4±1.5mm²,PES组为2.2±2.7mm²,ZES组为0.9±0.6mm²(SES与ZES比较,P = 0.02)。SES组(4.6±1.7mm²至7.0±2.5mm²;P<0.01)和PES组(3.6±1.7mm²至5.7±3.8mm²;P = 0.06)血管面积从术后至随访时增加,而ZES组未增加。血管扩张是SES组和PES组的主要机制;然而,组织退缩和支架回缩以及血管扩张也导致了ZES组的迟发性ISA。患者个体分析表明,83%的SES病例、60%的PES病例和50%的ZES病例中,血管扩张是迟发性ISA的主要机制。
第一代和第二代DES之间迟发性ISA的程度和机制似乎不同,这可能是由于血管对不同类型支架组件反应不同所致。