Nakatani Shimpei, Onuma Yoshinobu, Ishibashi Yuki, Muramatsu Takashi, Iqbal Javaid, Zhang Yao-Jun, van Geuns Robert-Jan, Ormiston John A, Serruys Patrick W
Thoraxcenter, Erasmus Medical Center, Rotterdam, The Netherlands.
EuroIntervention. 2015 Mar;10(11):1288-98. doi: 10.4244/EIJV10I11A218.
The long-term follow-up of the first-in-man ABSORB Cohort B trial showed that angiographic binary restenosis can occur early, late or very late after implantation of the Absorb everolimus-eluting bioresorbable vascular scaffold (Absorb BVS). Since the mechanical support of the scaffold decreases during bioresorption, the mechanism of in-segment restenosis (ISR) of the Absorb BVS might be different from that of metallic stents. The objective of the current analysis was to review the multimodality imaging of cases with binary restenosis to elucidate the mechanism of ISR after Absorb BVS implantation.
The ABSORB Cohort B trial enrolled 101 patients with a maximum of two de novo coronary lesions. At the three-year imaging and clinical follow-up, there were six cases of in-segment binary restenosis: two early ISR (<6 months), one late ISR (6-12 months) and three very late ISR (>12 months). Three of these ISR cases seemed to be induced by anatomical or procedural factors. In the other three cases, intravascular imaging (IVUS/OCT) demonstrated that the main mechanism of restenosis was significant intra-scaffold tissue growth, while the structural circularity and diameter of the scaffold were not affected.
Early and late restenosis after implantation of the Absorb bioresorbable scaffold could be related to anatomical or procedural factors. In this small cohort of patients late or very late restenosis seems to be attributed to pure intra-scaffold tissue growth without extrinsic encroachment of the scaffold.
首例人体ABSORB队列B试验的长期随访表明,在植入依维莫司洗脱生物可吸收血管支架(Absorb BVS)后,血管造影二元再狭窄可在早期、晚期或极晚期出现。由于支架的机械支撑在生物吸收过程中会降低,Absorb BVS节段内再狭窄(ISR)的机制可能与金属支架不同。本分析的目的是回顾二元再狭窄病例的多模态成像,以阐明Absorb BVS植入后ISR的机制。
ABSORB队列B试验纳入了101例最多有两处初发冠状动脉病变的患者。在三年的影像学和临床随访中,有6例节段内二元再狭窄:2例早期ISR(<6个月),1例晚期ISR(6 - 12个月),3例极晚期ISR(>12个月)。其中3例ISR病例似乎是由解剖或手术因素引起的。在另外3例病例中,血管内成像(IVUS/OCT)显示再狭窄的主要机制是支架内组织显著生长,而支架的结构圆度和直径未受影响。
Absorb生物可吸收支架植入后的早期和晚期再狭窄可能与解剖或手术因素有关。在这一小群患者中,晚期或极晚期再狭窄似乎归因于单纯的支架内组织生长,而没有支架的外在挤压。