Abellas-Sequeiros Rosa Alba, Ocaranza-Sanchez Raymundo, Trillo-Nouche Ramiro, Gonzalez-Juanatey Carlos, Gonzalez-Juanatey Jose Ramon
Interventional Cardiology Unit, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Interventional Cardiology Unit, Lucus Augusti Universitary Hospital, Lugo, Spain.
Heart Vessels. 2017 Sep;32(9):1077-1084. doi: 10.1007/s00380-017-0980-9. Epub 2017 Apr 21.
Beneficial properties of bioresorbable vascular scaffolds (BVS) regarding to vasomotility restoration and no caging of the vessel make them attractive devices in chronic total occlusions (CTO) revascularization. However, more evidence is needed attending to their use in this specific setting. We aim to determine feasibility and safety of BVS use in CTO revascularization attending to struts coverage and apposition, as well as re-stenosis and stent thrombosis (ST) rates. 29 BVS were deployed in 9 CTO lesions revascularization (mean J-CTO score ≥3) with an acute procedural success rate of 100%. Clinical and angiographic follow-up was performed 6 months later, including intracoronary analyses from optical coherence tomography (OCT) images. 44,723 struts were analyzed within the total 636 mm of scaffolded vessel. Mean length scaffolded per lesion was 70.66 ± 31.01 mm with a mean number of 3.22 BVS. 2051 struts (4.59%) were identified as uncovered, being most of them (98.4%) neither malapposed nor disrupted. Mean thickness of struts' coverage was 0.13 ± 0.05 mm. Incomplete strut apposition (ISA) percentage was 0% as no malapposed struts were detected and 134 struts were identified as disrupted, which represents a 0.29% from the total. Mean vessel, scaffold, and lumen diameters were 3.87 ± 0.51, 2.97 ± 0.49, and 2.68 ± 0.50 mm, respectively. Neither in-stent re-stenosis nor ST was detected. During follow-up, none of our patients died, suffered from stroke or needed target lesion revascularization. Clinical and angiographic 6-month follow-up (including OCT analyses) of BVS in CTO revascularization suggests their effectiveness and safety, even in very complex chronic occluded lesions. Nevertheless, more evidence is needed.
生物可吸收血管支架(BVS)在恢复血管舒缩功能以及不对血管造成束缚方面的有益特性,使其成为慢性完全闭塞(CTO)病变血管重建中具有吸引力的器械。然而,在这种特定情况下使用它们还需要更多证据。我们旨在确定在CTO血管重建中使用BVS的可行性和安全性,关注支架小梁的覆盖和贴靠情况,以及再狭窄和支架血栓形成(ST)率。在9例CTO病变血管重建(平均J-CTO评分≥3)中植入了29个BVS,急性手术成功率为100%。6个月后进行了临床和血管造影随访,包括对光学相干断层扫描(OCT)图像进行冠状动脉内分析。在总共636毫米的支架血管中分析了44,723个支架小梁。每个病变的平均支架长度为70.66±31.01毫米,平均植入3.22个BVS。2051个支架小梁(4.59%)被确定为未覆盖,其中大多数(98.4%)既未贴靠不良也未破坏。支架小梁覆盖的平均厚度为0.13±0.05毫米。由于未检测到贴靠不良的支架小梁,不完全支架小梁贴靠(ISA)百分比为0%,134个支架小梁被确定为破坏,占总数的0.29%。平均血管、支架和管腔直径分别为3.87±0.51、2.97±0.49和2.68±0.50毫米。未检测到支架内再狭窄和ST。随访期间,我们的患者均未死亡、发生中风或需要进行靶病变血管重建。CTO血管重建中BVS的6个月临床和血管造影随访(包括OCT分析)表明了其有效性和安全性,即使在非常复杂的慢性闭塞病变中也是如此。然而,还需要更多证据。