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Sutureless Microvascular Anastomosis: Literature Review

International Microsurgery Journal. 2019;3(2):1
DOI: 10.24983/scitemed.imj.2019.00112
Article Type: Review Article

Abstract

As procedures become increasingly complex, the current surgical techniques become increasingly strained with the demand for a new idea bringing about the birth of some new concept or technique. Traditionally, suturing techniques have been the mainstay for microvascular anastomoses, but owing to its technical difficulty and labour intensity, considerable work has gone into the development of sutureless microvascular anastomoses. In this review, we take a brief look at the developments of this technology through the years, with a focus on the more recent developments of laser-assisted vascular anastomoses, the unilink system, vascular closure staples, tissue adhesives, and magnets. Their working principles, with what has been found concerning their advantages and disadvantages are discussed.

Keywords

  • Anastomosis; microsurgery; microvascular; review; sutureless

Introduction

In order to enable the surgical procedure to move from a macroscopic to a microscopic one, the use of fine instruments is necessary. Traditionally, three main instruments are needed, including a microscope, fine operating instruments, and fine suture material. Although suturing techniques prevail in both experimental and clinical settings, considerable interest exists in the alternative mechanical techniques. Our review focuses on the newly emerging sutureless microvascular anastomosis techniques [1,2].

Several disadvantages to the sutured anastomoses have been identified. Some of these are related to the material itself and others are due to the process. The projection of potentially prothrombotic suture material into the vessel lumen and myointimal hyperplasia secondary to foreign body reaction in the wall of the blood vessel are the disadvantages due to the material itself [3]. The process of pure manual maneuver also has its disadvantages, which include the potential to cause damage to the vessels and a prolonged operating time. Ever since the 1900’s, research had started on other methods of vascular anastomosis and still being continued till this day, concerning the use of lasers, tissue adhesives, extraluminal cuffing rings, and everting pinned-ring devices, metallic stapling devices, and magnets.

A short history of these devices shows the continuous quest for innovative equipment and the increased performance. Lasers have been used for vessel welding since 1979. Jain and Gorisch were the first to report on vascular anastomoses using a neodymium: yttrium- aluminium-garnet laser. Vessel ring anastomosis commenced with Payr’s design (1904) of interlocking magnesium rings, similar to Henroz’s device of bowel anastomosis. Small pins on one side kept the vessel ends everted. The pins passed full-thickness through both vessel walls and the holes in the matching ring before being bent to secure the anastomosis. In 1913, Landon developed a metal ring that was smooth on one end and contained 5 slightly everted teeth on the other. In 1962, Nakayama simplified the initial ring stapler device into two rings that were joined onto each other through 2 flanges, one with 6 pins and the other with 6 holes, to receive the pins of the opposite flange. In 1986, Ostrup and Berggren presented the Unilink System, improving the Nakayama design. It consisted of two polyethylene rings with alternating stainless-steel pins and holes. The most commonly used device was the Coupler from Synovis. In 1992, Kirsch proposed the microvascular anastomosis based on the principle of flanged, extra-vascular, intimal approximation by arcuate-ledges stainless steel clips. Vessel ends underwent 90 degrees eversion and were then held together with extravascular staples. Magnetic energy was introduced in vascular surgery by Obora in 1978 using magnetic rings and hollow cogwheel-shaped metal devices held together by magnetic energy to anastomose vessels up to 2 mm [1,2].

The advantages of these sutureless devices are many, including good contact between the intima, higher patency rates (because there was no exposure of anastomotic material into the lumen), shorter operating times, and less need for microsurgical training, making it increasingly feasible for the less experienced surgeon. Some devices, because they are simple, efficacious, and significantly faster than suturing material, are, in some units, the preferred method of microvascular anastomosis. The best example would be the Coupler for venous anastomosis.

Although the above would be the principles upon which all of the sutureless devices would be based on, they also had some generic disadvantages: sometimes complex and cumbersome instrumentation, reduced vessels distensibility (a rigid foreign body enclosed a dynamic dilating structure), not applicable for significant vessel size discrepancies or end-to-side anastomoses, and increased vessel consumption into the device, which would be contraindicated in growing children because they would not allow for increases in vessel diameter.  All the specific advantages and disadvantages of the techniques are discussed in the review article.

Literature Search

This study followed the methods used in Preferred Reporting Items for Systematic Reviews and Meta-Analyses [4]. Eligibility criteria were specified unambiguously to ensure that studies were selected in a systematic and unbiased manner. Via PubMed, a Medline literature search was performed. Keywords used were sutureless microvascular anastomosis, vascular closure staples, laser, tissue adhesives, and Unilink. This was combined with cross-referencing from the reference lists of all recovered and relevant publications on this subject. In total, 650 publications were discovered, of which, 180 were relevant. The inclusion criteria were sutureless devices or sutureless procedures for microvascular anastomosis, English language, clinical studies, and animal research on technologies already used in clinical practice or on refinements of existing techniques. Out of the 470 articles excluded, 120 were non-animal studies or animal experimental studies with low numbers, and 350 articles were not relevant to our topic (Figure 1).

 

Figure 1. Flow diagram of study retrieval and selection.

 

Laser-Assisted Vascular Anastomosis

In tissue, laser light can be reflected, absorbed, scattered, or transmitted, the absorption being the most important interaction in laser-Assisted Vascular Anastomosis (LAVA). The resultant energy is used to weld the edges of the vessel together. Laser power (watts) and the amount of energy and time required vary for the types of laser and for the size of the vessels. When the carbon-dioxide laser is used, the tissue temperature rises to 80-120 degrees Celsius and adhesion occurs through melting of collagen and coagulation of cells in the media and adventitia. In wound healing, this coagulum is gradually replaced by fibrous and muscular tissue. Argon lasers generate a surface temperature of 43-48 degrees Celsius, which is below the temperature at which collagen degenerates. In this case, the protein bonds are degraded thermally, allowing proteins to rebind to adjacent proteins in a smooth tissue-tissue connection.

The balance between over- and under-exposure of tissue is critical. At a given wavelength, the absorption of laser energy varies within different tissues. Each tissue has its own wavelength-specific absorption coefficient. Tissue absorption, scattering, and the predominant direction of scattering determine the penetration depth of a laser. In the case of moderate to high tissue absorption, it is likely that the penetration should optimally be limited to the adventitia to prevent reactive intimal hyperplasia. In larger vessels, the arterial wall or adventitia layer may be thicker than in microvessels, and thus deeper penetration of laser light and heat is allowed and required. The deposited energy then converts into heat, resulting in a local temperature increase that is responsible for the tissue alterations. The laser parameters important in determining the interaction with tissue are wavelength, power, power density (the intensity of the laser light in terms of power in Watts per unit area) and/or spot size, and time of exposure. The lasers used for LAVA are the carbon-dioxide laser, the Neodymium: Yttrium-Aluminum-Garnet laser, the diode laser, and the argon laser [5].

The lasers have been used in combination with different kinds of protein solutions used as solders and/or dyes in order to create an anastomosis of sufficient strength to withstand physiologic variations in blood pressure. Solders have greatly contributed in optimising LAVA by increasing the leaking point pressure (the pressure at which leakage from the anastomosis is seen). They consist of a protein or protein-like substance applied to the weld to enhance bonding by enlarging the bonding surface. Solder also acts as a heat sink to reduce thermal damage. By adding a wavelength-specific chromophore or dye to the welding site or solder, the laser absorption is greatly enhanced, allowing for more selective heating of tissue with less injury to underlying tissues [6-15].

We identified four clinical series using 1950-nm diode laser [16-19], which were performed after extensive animal experience [20]. This laser seems to have an ideal wavelength for microvascular anastomoses with a 150 mm penetration that matches the thickness of the vascular wall’s adventitia and media [21]. This allows for welding of the vessels without the use of a chromophore or solder preparation, with minimal aneurysm rates and better flow when compared with traditional procedures on MRI [22].

The advantages of LAVA include good patency rates, shorter operating time, reduced needle trauma, and less foreign body reaction. Unlike other sutureless techniques, the diameter mismatch and toxic reactions are no issue in LAVA. Coaptation of vessel walls, however, is important. Ideally, there should be perfect alignment of intima against intima without bulging or wrinkling. This technique can be used in both arterial and venous anastomosis.

As with every other technique, LAVA does also have its disadvantage. Thermal injury can lead to pseudoaneurysm formation. This is one of the reasons for stay stitches still being used. There are several other causes for aneurysms postulated in literature, such as loss of elastic lamina, inappropriate laser parameters, poor apposition of the vessel edges, and inadequate tensile and bursting strength [23-25]. The best way to prevent aneurysm formation is to minimize anastomotic disruption, which is achieved by careful vessel approximation and use of solders [26].

Fibrin Glue

The fibrin glue mimics the final steps of the coagulation cascade to produce a physiologic fibrin clot. It was first used in microvascular anastomosis by Matras et al. and Pearl et al in 1977. Several studies have already reported the utilization of fibrin glue in microvascular anastomoses to complement the LAVA, increasing the bursting strength and decreasing the aneurysm rate [27], or to minimize the number of sutures and to decrease the operative time in conventional suture anastomosis. The technique of clotting fibrinogen solution around the anastomosis does not cause an increase in the rate of thrombosis, but actually strengthens the anastomosis [28]. In one study, the application of fibrin glue decreased the number of sutures required to complete the arterial and venous anastomoses down to 40%, while maintaining adequate patency rates and mechanical strength. Anastomoses were easier and faster to perform [29]. This proved a very useful adjunct in digit replantation, with at least two anastomoses per digit and possibly more than 20 needed in the case of multiple digit replantations requiring vein grafts. The time saved by using fibrin glue can be substantial [30].

Advantages
Overall, fibrin glue was found to decrease the number of sutures and operating time with the same immediate and late patency rates. It is safe and reliable, with no secondary effects, the histological analysis showing no significant differences compared to suturing only [31].

Disadvantages
Sagi et al. used a combination of Vicryl rings and fibrin glue for microvascular anastomosis [32]. They reported an insufficient bonding force for this glue to hold the cut ends of vessels together. Furthermore, some studies suggested that the fibrin glue may increase thrombogenicity when applied onto a vessel. This was refuted by Drake et al. and Frost-Arner et al. who demonstrated that the application of lower concentrations (500 IU/ml) of thrombin in conjunction with fibrinogen did not increase thrombogenicity in epigastric free flap models. The glue takes more time and is more complex to prepare. There is also a theoretical risk of viral disease transmission [32-34].

Unilink System

The venous coupler ring-pin system was first described in the literature by Nakayama in 1962. The Unilink system (3M) based on the same concept, now known as the Microvascular Anastomotic Coupler System (Synovis Micro Companies Alliance, Birmingham, AL), was described by Berggren and Ostrup in 1987.

The Unilink system consists of polyethylene rings with six alternating stainless-steel pins and holes in each ring and an apparatus to approximate the rings and cut vessel ends. Vessel ends are passed through opposing rings and everted on the pins; the coupler device approximates the rings, which stay in place. Studies have evaluated the success of this technique in joining small arteries and veins by using histologic and scanning electron microscopy and also by comparing the patency rate of anastomoses and flap survival with standard suture technique [35,36]. In some units, the coupler device is the preferred method for performing the venous microvascular anastomosis in free tissue transfers [37].

Anastomotic COUPLER System (Synovis) has been specifically designed for use in the anastomosis of veins and arteries having an outside diameter not less than 0.8 mm and not larger than 4.3 mm, and a wall thickness of 0.5 mm or less.

The hemodynamic consequences of anastomosing small arteries and veins with this device are minimal and the hemodynamic characteristics of the repaired vessels recover with the course of the normal healing process. The mean anastomosis time cited in the literature for the artery procedures was 8 minutes and for vein procedures 10 minutes.

Because it is a rigid structure that stretches the friable small vessels between it and the vascular clamps, the main concern would be the histological changes that occur in the vessel wall. The media remains viable outside the device but undergoes patchy necrosis within the device. Intimal hyperplasia occurs adjacent to and within the device. A circumferential triangular zone with loose connective and vascular channels forms at the component junction in 3 weeks. Evidence of injury from both clamp application and the strain of approximation are occasionally present [36-39].

Overall, many of the histopathologic features of the polyethylene ring-pin device are, in general, similar to those observed in suture anastomoses. These features include early sloughing of the endothelium, re-endothelialisation by 3 weeks, early intimal and medial inflammatory processes, resolution of inflammation within 3 weeks, disruption of the internal elastic lamina with a slow process of restoration, medial necrosis near suture or device materials, and local giant cell responses [36,40,41].

Apart from the decreased anastomotic time, which is one of the main advantages of this device, a 20 MHz ultrasonic Doppler has been specifically designed for use in end-to-end anastomosis for the detection of blood flow, in order to confirm vessel patency intra- and postoperatively at the anastomotic site.

In the literature, the incidence of thrombosis in a hand-sewn venous anastomosis is as high as 10%, especially in lower limb trauma reconstruction, and less than 3% in breast reconstruction. The systematic review by Ardehali et al 2014 demonstrates the thrombosis rate with the coupler range from 0 to 3% and less variation compared to the hand-sewn technique. No case-control prospective study or a randomised control trial was identified in the database search [42-47].

With the use of the device over the last twenty years, two main drawbacks have been pointed out. First, a ring-pin device has metallic pins on its ring that penetrate the vessel wall from the outside and permanently remain inside the vessel walls. Although the metallic pins allow very good fixation to the vessel walls, the pins can interfere with the normal restoration and the remodelling process after installation. The vessel walls are atrophied because of the continuous pressure of the blood flow against the rigidly fixed non-absorbable ring-pins complex [36,48,49]. Second, although the procedure for mounting the vessels onto the device is much faster than suturing the vessel walls, surgeons still must manually insert the metallic pins into the vessel walls.

Also, surgeons prefer to use the device for venous anastomosis only. Arterial wall is too thick and stiff most of the times. Although described, the end-to-side anastomosis with the coupler is rarely performed.

Vacuum-Assisted Microvascular Anasto-Coupler

The vacuum-assisted microvascular anasto coupler (VaMAC) presents a dramatic change in the principle and structure of the device that solves these two problems. The VaMAC uses negative pressure as an atraumatic force to fix vessel walls instead of traumatic metallic pins. Negative pressure is also very versatile because surgeons only have to place the vessel walls in the appropriate positions of the device, and the device may semiautomatically attach the vessel walls to the device. The VaMAC was designed to eliminate the need for metallic pins and to shorten the time of the procedure and was tested in rats [49]. This device has not yet been used in clinical practice.

Vascular Closure Staples

The vascular closure staples (VCS) clip clinches to the vessel wall, everting but not penetrating the endothelium, yet grasping the adventitia firmly without crushing. Eversion-stapled anastomoses appear to be more reliable because of the absence of intraluminal foreign bodies, permanent endothelial continuity, avoidance of intimal or mucosal penetration, avoidance of platelet aggregation, and effective re-endothelialization before day 7 [50,51].

VCS clips represent a major advance in the growing-vessel surgery. They allow vessel growth (as do interrupted sutures) and enable enhanced healing owing to the absence of foreign thrombogenic and hyperplasic material on the intimal surface [52].

In 2002, Zeebregts et al. published a comparative study of different techniques used to create microvascular anastomoses in free-flap reconstructions. They performed 474 microvascular anastomoses in 216 consecutive free-tissue transfers. The anastomosis techniques included manual sutures, Unilink rings, and VCS clips. The mean anastomotic time when rings were applied was significantly shorter than when using clips or sutures. Venous anastomoses using clips took less time than those using sutures. Early flap failure was caused by the failure of the arterial anastomosis in eight cases; all of them were sutured. None of the clipped arterial anastomoses failed. Three of the early flap failures due to the failure of venous anastomosis were sutured, seven were anastomosed with rings, and one was clipped. Both the VCS clip-applier system and the Unilink system are easy to handle and allow fast microvascular anastomoses without intraluminal penetration. The patency rate of clipped vessels is at least as good as the patency rates of vessels anastomosed using sutures or rings [53].

The major pitfall of VCS is the deceptively easy application of clips from the anastomotic applier. Although the learning curve for clip application is steep, there is the real and fundamental need for symmetrical vessel wall eversion and approximation with additional corner stitches and the use of everting forceps prior to clip placement. The demand for symmetrical eversion prior to application of a secure clip requires skill and practice, but not to the extent of suture anastomosis [54]. Vascular clips have no significant effect on cellular proliferation, intimal/media changes, or peak systolic velocity at anastomoses [55-57].

Tissue Adhesives

Use of tissue adhesives started from the same search of an easy-to-apply and time-saving technique for microvascular anastomoses. They do, however, necessitate the use of additional sutures in order to prevent aneurysm formation. The prime concern with glues is that they can give rise to allergic reactions and anaphylaxis.

Experimental end-to-end anastomoses have been performed successfully using bucrylate glue (isobutyl-2-cyanocrylate) and histoacryl glue (butyl-2-cyanoacrylate) with two or three stay sutures. The use of Histoacryl glue showed minimal toxicity and was comparable to suture anastomosis. The glued anastomosis was also associated with a shorter completion time, less bleeding, and equivalent patency; the sutureless anastomosis was associated with less intimal thickening compared with the traditional suture group. However, problems were reported with distortion of the vessels by hardened glue and/or thromboses secondary to glue entering the lumen. To overcome these imperfections, a new technique using Histoacryl glue with an intravascular soluble stent to keep the lumen widely patent and prevent intrusion of glue into the lumen was developed [58,59]. The technique was found to be efficient, fast, easy to learn, and readily accessible to the minimally experienced surgeon. No bleeding at the time of clamp removal was observed. However, the pathological study revealed histotoxicity of the glue on the arterial wall without consequence on efficacy [60].

Histological analysis of anastomoses done by suture or by application of bucrylate (isobutyl- 2-cyanoacrylate) following placement of three stay sutures showed degeneration of the media and deposition of calcium in the vessels in the bucrylate group. In addition, a more intense and prolonged foreign-body giant-cell response was noted in comparison to the vessels in the suture group [58].

Following the stent principle, Gurtner used a synthetic polymer - poloxamer assisted anastomoses. When the blood vessels were filled, the liquid polymer was heated. The liquid phased into the solid state at 38 degrees Celsius and was solid at 40 degrees Celsius. The floppy vessels stiffened like straws and could be lined up end-to-end. The vessels were sealed together with Dermabond, and then the clamps were released. The normal body temperature blood rushed into the vessels and hit the thermoreversible polymer. The polymer dissolved within one to two seconds and was excreted by the kidneys. There was no evidence of embolization, toxicity, or end-organ damage. Sutureless anastomoses were completed more efficiently than hand-sewn anastomoses with equivalent patency and burst strengths. Inflammation and scarring were dramatically decreased in the sutureless group. Dermabond, a new class of cyanoacrylate, 2-octyl cyanoacrylate, had a longer chain and was less histotoxic than other tissue adhesives [61].

Magnets

The research done up to now on vascular anastomoses with the use of magnets was mainly on large animal models (foxhound femoral artery) and as side-to-side anastomoses. One longitudinal arteriotomy was performed distal to the proximal clamp and another proximal to the distal clamp. A deployment device firmly held one magnet (with an oval lumen) at the tip of the device and another identical magnet several millimetres above the first with the two magnets aligned. The magnet at the tip was then inserted through the arteriotomy into the proximal artery. When the intravascular magnet was centred in the arteriotomy with slight traction, the deployment device trigger was activated; the magnets attracted and compressed the arterial wall forming a two-magnet vascular port. An identical two-magnet port was created near the distal end of the occluded arterial segment [62-64].

Conclusion

As the current surgical practices are being challenged with increasingly intricate operations, the demand on microsurgery has, and can only be expected, to increase. While the traditional microscope and fine suture have proven to be an invaluable source of healing for many patients, it is still nevertheless labour and time intensive, and not without its complications. From more than a century ago, thought and effort had gone into the development of sutureless microvascular anastomoses, with the aim of increasing the success of the procedure, reducing operation time and reducing the need for subspecialist training, thereby making it increasingly available to the patient population that would otherwise benefit from it. Laser-assisted vascular anastomoses, tissue adhesives, and magnets are all promising ideas, with progress in this field leading to improved anastomotic times and ultimately to better patient outcomes as demonstrated by the coupler system and vascular closure staples.

References

  1. Chang TS (ed). Principles, Techniques and Applications in Microsurgery. Singapore: World Scientific Publishing; 1986. [View Article]
  2. Tozzi P (ed). Sutureless Anastomoses: Secrets for Success. Darmstadt: Springer; 2007. [View Article]
  3. Quigley MR, Bailes JE, Kwaan HC, Cerullo LJ, Block S. Comparison of myointimal hyperplasia in laser-assisted and suture anastomosed arteries. A preliminary report. J Vasc Surg 1986;4(3):217-219. [View Article]
  4. Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: The prisma statement. PLoS Med 2009;6(7):e1000097. [View Article]
  5. Wolf-de Jonge IC, Beek JF, Balm R. 25 years of laser assisted vascular anastomosis (lava): What have we learned? Eur J Vasc Endovasc Surg 2004;27(5):466-476. [View Article]
  6. Fried MP, Moll ER. Microvascular anastomoses. An evaluation of laser-assisted technique. Arch Otolaryngol Head Neck Surg 1987;113(9):968-973. [View Article]
  7. Godlewski G, Rouy S, Dauzat M. Ultrastructural study of arterial wall repair after argon laser micro-anastomosis. Lasers Surg Med 1987;7(3):258-262. [View Article]
  8. Krueger RR, Almquist EE. Argon laser coagulation of blood for the anastomosis of small vessels. Lasers Surg Med 1985;5(1):55-60. [View Article]
  9. Vale BH, Frenkel A, Trenka-Benthin S, Matlaga BF. Microsurgical anastomosis of rat carotid arteries with the co2 laser. Plast Reconstr Surg 1986;77(5):759-766. [View Article]
  10. White RA, Kopchok G, Donayre C, et al. Large vessel sealing with the argon laser. Lasers Surg Med 1987;7(3):229-235. [View Article]
  11. Reali UM, Gelli R, Giannotti V, Gori F, Pratesi R, Pini R. Experimental diode laser-assisted microvascular anastomosis. J Reconstr Microsurg 1993;9(3):203-210; discussion 210-201. [View Article]
  12. Chuck RS, Oz MC, Delohery TM, et al. Dye-enhanced laser tissue welding. Lasers Surg Med 1989;9(5):471-477. [View Article]
  13. Jain KK. Sutureless microvascular anastomosis using a neodymium-yag laser. Microsurgery 1980;1(6):436-439. [View Article]
  14. Bass LS, Treat MR, Dzakonski C, Trokel SL. Sutureless microvascular anastomosis using the thc:Yag laser: A preliminary report. Microsurgery 1989;10(3):189-193. [View Article]
  15. Maitz PK, Trickett RI, Dekker P, et al. Sutureless microvascular anastomoses by a biodegradable laser-activated solid protein solder. Plast Reconstr Surg 1999;104(6):1726-1731. [View Article]
  16. Delacretaz GP, Mordon SR, Schoffs M, et al. 1.9-μm diode-laser-assisted anastomoses in reconstructive microsurgery: Preliminary results in 12 patients. In: Laser-Tissue Interaction, Tissue Optics, and Laser Welding III. SPIE; 1998: 2-8. [View Article]
  17. Leclère FM, Schoofs M, Buys B, Mordon SR. Outcomes after 1.9-microm diode laser-assisted anastomosis in reconstructive microsurgery: Results in 27 patients. Plast Reconstr Surg 2010;125(4):1167-1175. [View Article]
  18. Leclère FM, Schoofs M, Buys B, Mordon SR. 1.9 microm diode laser assisted vascular microanastomoses: Experience in 40 clinical procedures. Lasers Surg Med 2011;43(4):293-297. [View Article]
  19. Leclère FM, Schoofs M, Vogt P, Casoli V, Mordon S. 1950-nm diode laser-assisted microanastomoses (lama): An innovative surgical tool for hand surgery emergencies. Lasers Med Sci 2015;30(4):1269-1273. [View Article]
  20. Kung RTV, Stewart RB, Zelt DT, L'Ltalien GJ, Lamuraglia GM. Absorption characteristics at 1.9 μm: Effect on vascular welding. Lasers in Surgery and Medicine 1993;13(1):12-17. [View Article]
  21. Leclère fm, schoofs m, buys b, germain m, mordon s. Outcomes after 1.9-microm diode laser-assisted anastomosis in reconstructive microsurgery: From animal model to patients. E-mémoires de l'académie nationale de chirurgie 2010;9(2):63-68. [View Article]
  22. Leclère FM, Schoofs M, Auger F, Buys B, Mordon S. [blood flow assessment with magnetic resonance imaging after 1.9 mum diode laser assisted arterial micronastomoses]. Ann Chir Plast Esthet 2011;56(6):540-547. [View Article]
  23. McCarthy WJ, Hartz RS, Yao JS, Sottiurai VS, Kwaan HC, Michaelis LL. Vascular anastomoses with laser energy. J Vasc Surg 1986;3(1):32-41. [View Article]
  24. Neblett CR, Morris JR, Thomsen S. Laser-assisted microsurgical anastomosis. Neurosurgery 1986;19(6):914-934. [View Article]
  25. Quigley MR, Bailes JE, Kwaan HC, Cerullo LJ, Brown JT. Aneurysm formation after low power carbon dioxide laser-assisted vascular anastomosis. Neurosurgery 1986;18(3):292-299. [View Article]
  26. Wang S, Basu S, Thomsen S, et al. Aneurysm formation after laser-assisted microvascular anastomosis: Etiology, growth rate, and prevention. Vascular Surgery 2016;24(8):571-578. [View Article]
  27. Grubbs PE, Jr., Wang S, Marini C, Basu S, Rose DM, Cunningham JN, Jr. Enhancement of co2 laser microvascular anastomoses by fibrin glue. J Surg Res 1988;45(1):112-119. [View Article]
  28. Ashton RC, Jr., Oz MC, Lontz JF, et al. Laser-assisted fibrinogen bonding of vascular tissue. J Surg Res 1991;51(4):324-328. [View Article]
  29. Cho AB, Junior RM. Application of fibrin glue in microvascular anastomoses: Comparative analysis with the conventional suture technique using a free flap model. Microsurgery 2008;28(5):367-374. [View Article]
  30. Isogai N, Cooley BC, Kamiishi H. Clinical outcome of digital replantation using the fibrin glue-assisted microvascular anastomosis technique. Journal of Hand Surgery 2016;21(5):573-575. [View Article]
  31. Cho AB, Junior RM. Effect of fibrin adhesive application in microvascular anastomosis: A comparative experimental study. Plast Reconstr Surg 2007;119(1):95-103. [View Article]
  32. Sagi A, Yu H-L, Ferder M, Gordon MJ, Strauch B. "No suture" microanastomosis using vicryl rings and fibrin adhesive system: An unsuccessful attempt. Plastic and Reconstructive Surgery 1987;79(5):776-777. [View Article]
  33. Ellis DA, Shaikh A. The ideal tissue adhesive in facial plastic and reconstructive surgery. J Otolaryngol 1990;19(1):68-72. [View Article]
  34. Kamer FM, Joseph JH. Histoacryl: Its use in aesthetic facial plastic surgery. Archives of Otolaryngology - Head and Neck Surgery 1989;115(2):193-197. [View Article]
  35. Östrup LT, Berggren A. The unilink instrument system for fast and safe microvascular anastomosis. Annals of Plastic Surgery 1986;17(6):521-525. [View Article]
  36. Berggren A, Ostrup LT, Lidman D. Mechanical anastomosis of small arteries and veins with the unilink apparatus: A histologic and scanning electron microscopic study. Plast Reconstr Surg 1987;80(2):274-283. [View Article]
  37. Chernichenko N, Ross DA, Shin J, Chow JY, Sasaki CT, Ariyan S. Arterial coupling for microvascular free tissue transfer. Otolaryngol Head Neck Surg 2008;138(5):614-618. [View Article]
  38. Blair WF, Steyers CM, Brown TD, Gable RH. A microvascular anastomotic device: Part i. A hemodynamic evaluation in rabbit femoral arteries and veins. Microsurgery 1989;10(1):21-28. [View Article]
  39. Blair WF, Morecraft RJ, Steyers CM, Maynard JA. A microvascular anastomotic device: Part ii. A histologic study in arteries and veins. Microsurgery 1989;10(1):29-39. [View Article]
  40. Östrup LT. Anastomosis of small veins with suture or nakayama's apparatus. A comparative study. Scand J Plast Reconstr Surg 1976;10(1):9-17. [View Article]
  41. Lidman D, Ostrup LT. Blood flow and scanning electron microscope study on venous microvascular anastomoses with nakayamas apparatus and manual suture. Scand J Plast Reconstr Surg 1981;15(2):97-101. [View Article]
  42. Nahabedian MY, Momen B, Manson PN. Factors associated with anastomotic failure after microvascular reconstruction of the breast. Plast Reconstr Surg 2004;114(1):74-82. [View Article]
  43. Kroll SS, Schusterman MA, Reece GP, et al. Timing of pedicle thrombosis and flap loss after free-tissue transfer. Plast Reconstr Surg 1996;98(7):1230-1233. [View Article]
  44. Yu P, Chang DW, Miller MJ, Reece G, Robb GL. Analysis of 49 cases of flap compromise in 1310 free flaps for head and neck reconstruction. Head Neck 2009;31(1):45-51. [View Article]
  45. Fukuiwa T, Nishimoto K, Hayashi T, Kurono Y. Venous thrombosis after microvascular free-tissue transfer in head and neck cancer reconstruction. Auris Nasus Larynx 2008;35(3):390-396. [View Article]
  46. Khouri RK, Cooley BC, Kunselman AR, et al. A prospective study of microvascular free-flap surgery and outcome. Plast Reconstr Surg 1998;102(3):711-721. [View Article]
  47. Ardehali B, Morritt AN, Jain A. Systematic review: Anastomotic microvascular device. J Plast Reconstr Aesthet Surg 2014;67(6):752-755. [View Article]
  48. Ragnarsson R, Berggren A, Ostrup LT. Long term evaluation of the unilink anastomotic system. A study with light and scanning electron microscopy. Scand J Plast Reconstr Surg Hand Surg 1992;26(2):167-171. [View Article]
  49. Tachi K, Furukawa KS, Koshima I, Ushida T. New microvascular anastomotic ring-coupling device using negative pressure. J Plast Reconstr Aesthet Surg 2011;64(9):1187-1193. [View Article]
  50. Gerbault O, Arrouvel C, Servant JM, Revol M, Banzet P. [vcs microclip anastomosis on blood vessels of less than 2 millimeters in diameter. Preliminary experimental study in the rat]. Ann Chir Plast Esthet 1998;43(1):27-39. [View Article]
  51. Lambert F, Couturaud B, Cruel T, Lecoin G, Cariou JL. [vascular microanastomosis by eversion and stapling using vcs forceps. Presentation of the technique and experimental evaluation of its reliability]. Ann Chir Plast Esthet 1998;43(1):14-26. [View Article]
  52. Calles-Vazquez MC, Uson JM, Viguera FJ, Sun F, Paz JI, Uson-Gargallo J. Vascular closure stapler clips versus polypropylene sutures in end-to-end anastomoses of growing arteries and veins. Ann Vasc Surg 2005;19(3):320-327. [View Article]
  53. Zeebregts C, Acosta R, Bolander L, van Schilfgaarde R, Jakobsson O. Clinical experience with non-penetrating vascular clips in free-flap reconstructions. Br J Plast Surg 2002;55(2):105-110. [View Article]
  54. Kirsch WM, Zhu YH, Hardesty RA, Chapolini R. A new method for microvascular anastomosis: Report of experimental and clinical research. Am Surg 1992;58(12):722-727. [View Article]
  55. Boeckx WD, Darius O, van den hof B, van Holder C. Scanning electron microscopic analysis of the stapled microvascular anastomosis in the rabbit. Ann Thorac Surg 1997;63(6 Suppl):S128-134. [View Article]
  56. Caiati JM, Madigan JD, Bhagat G, Benvenisty AI, Nowygrod R, Todd GJ. Vascular clips have no significant effect on the cellular proliferation, intimal changes, or peak systolic velocity at anastomoses in rabbit vein grafts. J Surg Res 2000;92(1):29-35. [View Article]
  57. Lee JW, Choo SJ, Oh JH, et al. Anastomosis of vessels less than 2 mm with the vascular clip system clip applier. J Korean Med Sci 2001;16(3):303-308. [View Article]
  58. Souther SG, Levitsky S, Roberts WC. Bucrylate tissue adhesive for microvascular anastomosis. Technique, results, and histologic evaluation. Arch Surg 1971;103(4):496-499. [View Article]
  59. Middleton WG, Matthews W, Chiasson DA. Histoacryl glue in microvascular surgery. J Otolaryngol 1991;20(5):363-366. [View Article]
  60. Lemaire D, Mongeau J, Dorion D. Microvascular anastomosis using histoacryl glue and an intravascular soluble stent. J Otolaryngol 2000;29(4):199-205. [View Article]
  61. Chang EI, Galvez MG, Hamou CD, Rajadas J, Longaker MT, Gurtner GC. Novel technique for efficient sutureless microvascular anastomosis using thermoreversible poloxamers. Journal of the American College of Surgeons 2008;207(3):S63. [View Article]
  62. Obora Y, Tamaki N, Matsumoto S. Nonsuture microvascular anastomosis using magnet rings: Preliminary report. Surg Neurol 1978;9(2):117-120. [View Article]
  63. Erdmann D, Sweis R, Heitmann C, et al. Side-to-side sutureless vascular anastomosis with magnets. J Vasc Surg 2004;40(3):505-511. [View Article]
  64. Heitmann C, Khan FN, Erdmann D, Olbrich KC, Adam Sharkawy A, Klitzman B. Vein graft anastomoses with magnets. J Plast Reconstr Aesthet Surg 2007;60(12):1296-1301. [View Article]

Editorial Information

Publication History

Received date: July 08, 2018
Accepted date: October 04, 2018
Published date: April 25, 2019

Ethics Approval and Consent to Participate

The study is in accordance with the ethical standards of the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Funding

The study did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Copyright

© 2019 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY).

Department of Plastic, Reconstructive and Hand Surgery, St Vincent's Hospital, Sydney, Australia
Department of Plastic, Reconstructive and Hand Surgery, St Vincent's Hospital, Sydney, Australia
Department of Plastic, Reconstructive and Hand Surgery, St Vincent's Hospital, Sydney, Australia
Department of Plastic, Reconstructive and Hand Surgery, St Vincent's Hospital, Sydney, Australia

Address: 25/13-17 Ithaca Road, Elizabeth Bay, NSW, 2011, Australia
Figure 1.jpg
Figure 1. Flow diagram of study retrieval and selection.

Reviewer 1 Comments

  1. Overall this is an in depth review of various type of sutureless techniques used for microvascular anastomosis. The authors should be commended for their efforts to review the literature and provide readers with useful information and update on the current knowledge. However, there are certain points that I would like the authors to clarify and possibly revise in the manuscript that can improve some of the shortcomings.
    ResponseThank you.
     
  2. The introduction first discusses the disadvantages of the traditional suture method and then jumps straight into the different sutureless methods. I was a bit confused why so much information is written in the introduction, and there seems to be a lack of correlation with the order of the topics presented in the introduction and in the manuscript section. I would recommend shortening the introduction on the various methods used and instead focus more on the advantages and disadvantages of the sutureless methods in general. This would be more in tune with what is written in the first two paragraphs of the introduction.
    ResponseI fully agree with your comments. The introduction was re-written. Please find attached in the article text in red.
     
  3. The way the manuscript is set out, the topic headlines appear to be background, method and, conclusion. The information on the different sutureless methods seem to be under the heading “method” section but I would assume that it should be under a new section called “Results”. It would be less confusing if such a headline was added in, rather than including it all in the “method section”.
    ResponseResults section was added as suggested.
     
  4. Since this is a systematic review, one component to include in a review is the PRISMA flow diagram and the guidelines associated with publishing a systematic review. Please clarify your inclusion and exclusion criteria more clearly in the method section, such as what the authors deem as “unlikely clinical use” for definition.
    ResponseMethods section was re-written as suggested, including the inclusion criteria defined and PRISMA flow chart attached.
     
  5. A critical point that the authors did not discuss in the review is the difference between arterial anastomosis and venous anastomosis. For example, couplers have gained popularity among microsurgeons for its ease to use and protection of the anastomosis site but is still limited to venous vessels, not arterial vessels. In each of the sutureless techniques described, there is a lack of information regarding the indication of use in different situations, especially with regards to arterial versus venous anastomosis. Also, please try to include information on the limitations of the sutureless techniques.
    ResponseAdvantages and disadvantages for each procedure are described with each technique, and both “advantages and disadvantages” words are underlined in the text. Please find in red comments regarding use in venous or arterial anastomosis.
     
  6. Finally, there is a statement in the introduction that I as a traditional microsurgeon disagree with: “There is also the potential for baseline leakage through the needle holes, especially when there is tension at the anastomotic site”. When there is tension at the anastomosis site, none of the sutureless techniques are indicated too, and there is no evidence to suggest that the change in anastomosis technique can overcome this barrier. Please elaborate more clearly the benefits and disadvantages of the traditional vs. sutureless techniques and provide the references to your claims.
    ResponseAgree with your comments. “There is also the potential for baseline leakage through the needle holes, especially when there is tension at the anastomotic site” has been deleted. Introduction section has been re-written with better emphasis on traditional vs sutureless techniques. Please find in the article text in red.
     
  7. Overall, I do think this is an article worth publishing but needs revision to improve the shortcomings described in the review above. I would highly recommend the authors to make these changes in order for the readers to learn more on this interesting topic.
    ResponseThank you. Please find attached.