Vijayan Vikram, Shukla Nilima, Johnson Jason L, Gadsdon Patricia, Angelini Gianni D, Smith Frank C T, Baird Roger, Jeremy Jamie Y
Vascular Unit, The Bristol Royal Infirmary, Bristol BS2 8HW, UK.
J Vasc Surg. 2004 Nov;40(5):1011-9. doi: 10.1016/j.jvs.2004.08.047.
The development of neointimal hyperplasia with subsequent atherosclerotic deposition has been proposed to cause most late vein graft failures. Our unit has previously demonstrated that placement of a macroporous, loose-fitting polyester external stent prevents neointimal thickening in porcine vein grafts, and has been proposed as a therapeutic strategy to prevent late vein graft failure. To reduce any potential long-term complications of the permanent polyester stent, a study was undertaken to investigate the effect of a biodegradable external stent on porcine vein graft thickening at 1 month and to identify its longer term effects at 6 months.
Bilateral saphenous vein to common carotid artery interposition grafting was performed in Large White pigs (25-32 kg; n = 6 per time course group) according to UK Home Office guidelines. A commercially constructed loose-fitting 8-mm-diameter polyglactin stent was placed externally around the vein graft on one side, and the contralateral side remained unstented to serve as control. The external stent was designed to biodegrade and hence disappear within 90 days. Grafts were left in situ for 1 month in 1 group of animals, and for up to 6 months in the other group, before explantation. Graft morphometric features were assessed with computer-aided planimetry.
At 1 month the vein grafts fitted with the polyglactin stent demonstrated a statistically significant decrease in neointimal thickening (0.038 mm; interquartile range [IQR], 0.035-0.039 mm) compared with the unstented control grafts (0.13 mm; IQR; 0.11-0.19; P = .0012), and also in medial thickening (0.09 mm; IQR, 0.086-0.093) compared with unsheathed control grafts (0.302 mm; IQR, 0.272-0.414; P = .0012). The 6-month polyglactin stented grafts also demonstrated a statistically significant reduction in neointimal thickening (0.049 mm; IQR, 0.047-0.07; P = .0012) compared with control grafts (0.178 mm; IQR, 0.164-0.19), and also in medial thickening (0.105 mm; IQR, 0.095-0.143) compared with unstented grafts (0.421 mm; IQR, 0.35-0.44; P = .0012, Mann-Whitney U test).
The loose-fitting biodegradable polyglactin external stent reduces porcine vein graft thickening at 1 month, which persists in the long term, even after degradation of the stent itself. This effective removal of the stent may therefore reduce the long-term risks for infection and mechanical complications associated with implanted prosthetic material while still eliciting the primary objective of preventing graft thickening over the long term. Biodegradable external stents therefore have potential advantages over permanent stent material in clinical application.
Arteriovenous bypass graft failure has a huge economic effect on health care resources, and a devastating effect o the patient. The attenuation of vein wall thickening, with subsequent luminal narrowing and occlusion, is a major goal in improving the longevity of the venous graft, to reduce secondary percutaneous and surgical interventions. The biodegradable external stent demonstrated in this study has possible clinical applications in bypass procedures with autogenous venous tissue, and represents a novel approach to ameliorating the problem of intimal hyperplasia that plagues these grafts.
新内膜增生伴随后续动脉粥样硬化沉积的发展被认为是导致大多数晚期静脉移植物失败的原因。我们单位先前已证明,放置大孔、宽松贴合的聚酯外支架可防止猪静脉移植物的新内膜增厚,并已被提议作为预防晚期静脉移植物失败的治疗策略。为了减少永久性聚酯支架的任何潜在长期并发症,开展了一项研究,以调查可生物降解外支架对猪静脉移植物1个月时增厚的影响,并确定其在6个月时的长期效果。
根据英国内政部指南,在大白猪(25 - 32千克;每个时间进程组n = 6)中进行双侧大隐静脉至颈总动脉的搭桥术。将一个商业制造的直径8毫米的宽松贴合的聚乙交酯支架外部放置在一侧的静脉移植物周围,对侧不放置支架作为对照。外部支架设计为可生物降解,因此在90天内消失。一组动物的移植物原位保留1个月,另一组保留长达6个月,然后进行取出。使用计算机辅助平面测量法评估移植物的形态计量学特征。
在1个月时,与未放置支架的对照移植物(0.13毫米;四分位间距[IQR],0.11 - 0.19;P = .0012)相比,装有聚乙交酯支架的静脉移植物新内膜增厚有统计学显著降低(0.038毫米;IQR,0.035 - 0.039毫米),与未包裹的对照移植物(0.302毫米;IQR,0.272 - 0.414;P = .0012)相比,中膜增厚也有降低(0.09毫米;IQR,0.086 - 0.093)。与对照移植物(0.178毫米;IQR,0.164 - 0.19)相比,6个月时装有聚乙交酯支架的移植物新内膜增厚也有统计学显著降低(0.049毫米;IQR,0.047 - 0.07;P = .0012),与未放置支架的移植物(0.421毫米;IQR,0.35 - 0.44;P = .0012,曼 - 惠特尼U检验)相比,中膜增厚也有降低(0.105毫米;IQR,0.095 - 至0.143)。
宽松贴合的可生物降解聚乙交酯外支架可减少猪静脉移植物1个月时的增厚,这种效果长期持续,即使在支架本身降解后也是如此。因此,这种有效的支架移除可能会降低与植入假体材料相关的长期感染和机械并发症风险,同时仍能实现长期预防移植物增厚的主要目标。因此,可生物降解外支架在临床应用中比永久性支架材料具有潜在优势。
动静脉搭桥术失败对医疗资源有巨大的经济影响,对患者有毁灭性影响。减轻静脉壁增厚以及随之而来的管腔狭窄和闭塞,是提高静脉移植物使用寿命、减少二次经皮和外科干预的主要目标。本研究中展示的可生物降解外支架在自体静脉组织搭桥手术中可能有临床应用,代表了一种改善困扰这些移植物的内膜增生问题的新方法。