Department of Cardiovascular Surgery, Bakulev Center, Moscow, Russia.
Xeltis BV, Eindhoven, The Netherlands.
J Thorac Cardiovasc Surg. 2017 Jun;153(6):1542-1550. doi: 10.1016/j.jtcvs.2016.11.071. Epub 2017 Feb 7.
To assess safety and clinical performance of a novel bioabsorbable vascular graft in pediatric patients with univentricular cardiac malformation who received surgical correction via an extracardiac cavopulmonary conduit.
The implanted graft material is designed to attract patient's own cells and proteins, which trigger a cascade of physiological events leading to endogenous tissue restoration. As the graft resorbs progressively after implantation, components of native tissue including collagen, endothelial lining, and capillary blood vessels develop and organize into a natural tissue. Five patients (aged 4-12 years) received this new vascular graft as interposition between the inferior vena cava and the pulmonary artery. They were followed up to 12 months after surgery. The conduit was assessed by echocardiography, computed tomography and magnetic resonance imaging, including 4-dimensional flow.
All patients recovered from the procedure without complications. No device-related adverse events were reported. Two patients required interventional occlusion of aortopulmonary collaterals. At 12 months, there was a significant improvement in the patients' general condition. Imaging studies demonstrated anatomical (conduit diameter, length and wall thickness) and functional (blood flow pattern) stability of the bioabsorbable grafts in all patients with no significant changes at 12 months compared with early postoperative data.
Initial clinical experience with a novel absorbable graft underlines the potential of this new material to improve cardiac and vascular surgical procedures. In addition, better biocompatibility may reduce permanent implant-related complications. A longer follow-up is needed to assess the long-term effectiveness of biodegradable vascular grafts, including their ability to grow.
评估新型可吸收血管移植物在接受心外管道体外腔肺连接术外科矫正的单心室心脏畸形儿科患者中的安全性和临床性能。
植入的移植物材料旨在吸引患者自身的细胞和蛋白质,从而引发一系列生理事件,导致内源性组织修复。随着移植物在植入后逐渐吸收,包括胶原、内皮衬里和毛细血管在内的天然组织成分发育并组织成天然组织。5 名(年龄 4-12 岁)患者在腔静脉和肺动脉之间接受了这种新型血管移植物作为中间移植物。术后随访 12 个月。通过超声心动图、计算机断层扫描和磁共振成像(包括 4 维血流)评估导管。
所有患者均无并发症康复。无器械相关不良事件报告。2 名患者需要对主肺动脉侧支进行介入封堵。12 个月时,患者一般状况明显改善。影像学研究显示,所有患者的生物可吸收移植物在解剖学(导管直径、长度和壁厚)和功能(血流模式)方面均保持稳定,与术后早期数据相比,12 个月时无明显变化。
新型可吸收移植物的初步临床经验强调了这种新材料在改善心脏和血管外科手术方面的潜力。此外,更好的生物相容性可能会减少与永久性植入物相关的并发症。需要更长时间的随访来评估可生物降解血管移植物的长期效果,包括其生长能力。