Abstract

This study aimed to evaluate the biocompatibility and patency of our newly developed titanium vascular anastomotic device (TVAD) in a pig jugular vein. TVAD was made of commercially pure grade 2 titanium. The patency and anastomotic time were simultaneously confirmed in an ex-vivo system developed by the authors and in vivo using pig jugular veins. Five 8-month-old pigs, with body weights of 50–60 kg, underwent anastomosis of both jugular veins using the device. Graft patency was evaluated for 12 weeks by biplane angiography and sonography. All tissue biopsy samples were analysed by histology. In all 10 cases, the anastomosis was completed in < 5 min. The vessel lumen was not damaged, and the inner vessel wall was completely endothelialised at the anastomotic site. No foreign body reactions were observed at the vessel lumen, vessels, and outer vessel walls by histopathologic analysis. Patency and absence of leakage at the anastomotic site of the follow-up period were confirmed clearly by angiography and sonography. This preliminary animal study proved that our newly developed device is a very promising tool for intima-to-intima contact anastomosis. TVAD can be used as a feasible and safe medical tool for vessel anastomosis.

Highlights

  • This study aimed to evaluate the biocompatibility and patency of our newly developed titanium vascular anastomotic device (TVAD) in a pig jugular vein

  • The reported anastomosis failure rate of 2–6% due to suturing errors may cause the failure of the whole reconstructive surgery and increase healthcare ­costs[2,3]

  • There could be anastomotic failures such as tearing, leaking, and narrowing of the lumen, through-stitching, and inclusion of the adventitia, they decrease with improvement in the surgeon’s skill due to the learning curve associated with ­anastomosis[4,5]

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Summary

Introduction

This study aimed to evaluate the biocompatibility and patency of our newly developed titanium vascular anastomotic device (TVAD) in a pig jugular vein. Patency and absence of leakage at the anastomotic site of the follow-up period were confirmed clearly by angiography and sonography. This preliminary animal study proved that our newly developed device is a very promising tool for intima-to-intima contact anastomosis. Various types of vascular couplers for anastomosis without the use of sutures to reduce tissue ischaemic-reperfusion injury and organ warm ischaemic time as well as improve vascular patency and prevent life-threatening complications have been devised to overcome this f­ailure[6,7,8,9]. These devices are mostly made of biocompatible absorbent plastic ­materials[12,13,14], triggering concerns about the strength of the anastomosis in organ t­ ransplants[15,16,17]

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