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Eur J Cardiothorac Surg 2006;30:425-430
© 2006 Elsevier Science NL
a Cardiovascular Surgery Department, University of Lausanne, CHUV, Lausanne, Switzerland
b Vascular Medicine Department, University of Lausanne, CHUV, Lausanne, Switzerland
c Intensive Care Unit, University of Lausanne, CHUV, Lausanne, Switzerland
d Idee & Sviluppo, LLC, Bologna, Italy
Received 6 February 2006; received in revised form 29 April 2006; accepted 15 May 2006.
* Corresponding author. Address: Cardiovascular Surgery Department, Centre Hospitalier Universitaire Vaudois (CHUV), Rue du Bugnon 46, 1011 Lausanne, Switzerland. Tel.: +41 21 314 23 08; fax: +41 21 314 22 78. (Email: Piergiorgio.Tozzi{at}hospvd.ch).
| Abstract |
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Key Words: Sutureless vascular anastomosis Vascular connector Suture technique
| 1. Introduction |
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The surgical environment is becoming increasingly challenging for the cardiovascular surgeon ever since minimally invasive approaches and beating heart surgery have been introduced. For example, manual suturing of coronary anastomosis in video-assisted port access surgery on the beating heart, despite the aid of a master-slave robotic surgery system, has proved to be prohibitively difficult [2,3]. Besides, target vessels are increasingly smaller and diseased and surgeons have to deal with vascular reconstructions that are very complex due to the aging of the population and the increasing number of patient's comorbidity.
Surgeons are looking for alternative ways to construct vascular anastomoses in order to reduce the technical demand and improve the quality of the surgical procedure.
The vascular join (VJ) (Idee & Sviluppo Sarl, Bologna, Italy) represents a new anastomotic technology that should reduce the inter-surgeons variability in the anastomosis construction while expediting the anastomosis procedure and seems to fulfill the needs of today's surgeon. In the past 5 years, several sutureless anastomotic devices have been brought to the attention of cardiovascular surgeons [4]. Almost all have excellent early patency rates and are very seductive, however, when we look at long-term results and compare them with historical patency rates as recommended by the FDA in March 2004, the enthusiasm is over. Several connectors have been withdrawn from the market and others never came forth due to poor long-term outcome.
Therefore, based on this detrimental experience, we designed this animal study bearing in mind that the most important aspect is the long-term patency of the sutureless anastomoses with respect to standard running suture technique.
| 2. Methods |
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2.3 Experimental set up
In adult sheep, 4555 kg, under general anaesthesia, ECG, and O2 saturation monitoring, left femoral artery was isolated and a catheter for arterial blood pressure was inserted. Both carotid arteries were isolated and the carotid flow measured using a Doppler probe (Medistim). After administration of Heparin 100 U/kg to keep the activating clotting time above 200 s, one carotid artery was clamped, severed and anastomosed in end-to-end fashion using the connector (Fig. 3
). The same procedure was repeated on the other side with the anastomosis constructed using the running suture technique (6/0 polypropylene) as a control.
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After the procedure, the carotid flow distal to the anastomosis was measured using Doppler probe.
Two animals received carotid angiogram and intra vascular ultra sound (IVUS with Sonicath UltraTM 3.2, 20 MHz-Imaging Catheter, Medi.tech® Boston Scientific Corporation) to acquire images on anastomosis quality. IVUS was also used to measure anastomotic diameters in systole and diastole 1 mm proximal and distal to the suture line. These data were used to calculate the anastomotic cross-sectional compliance. Assuming that the anastomosis has a circular shape, anastomotic area (AA) has been calculated with: AA =
r
2, where r is the anastomotic radius. Cross-sectional anastomotic compliance (CSAC) was calculated as: CSAC =
AA/
P, where
P is the mean pulse pressure and
AA is the mean difference between systolic and diastolic AA.
Animals received Aspirine 100 mg per day. All anastomoses were followed up with Echo-color Doppler control at 3, 6, 9 and 12 months.
After 12 months, animals were sacrificed and both carotid arteries were harvested keeping the inner pressure above 100 mmHg. Histological analysis was carried out to evaluate anastomotic stenosis due to myointimal hyperplasia, thrombosis and vessel inflammatory reaction.
2.4 Specimen preparation
Anastomoses made with the device were fixed in formaldehyde 10%, imbedded in a special acrylic resin, and cut with a diamond-coated wire saw developed for cutting tissue samples with metallic implants in situ. Slices thickness were between 30 and 100 µm. Anastomoses done with the running suture technique were fixed in formaldehyde 10%, included in paraffin and cut with standard microtome. All specimens were stained with hematoxylineeosine and elastine or toluidine blue.
All animals received human care in compliance with the European Convention on Animal Care and our institutional ethics committee has approved the study.
Data are presented as mean and standard deviation and paired student t-test is applied for statistical analysis.
| 3. Results |
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No bleeding was observed in 18 out of 20 sutureless anastomosis. In two cases a trivial leak occurred and it was controlled with sponge compression over 2 min.
Sutureless anastomoses were completed in less than 2 min versus 6 ± 3 min for the running suture.
Two animals received post-operative angiogram that showed patent anastomoses without stenosis.
In two animals IVUS was used to assess anastomoses quality and demonstrated the correct apposition of each vessel wall layer (Fig. 4 ). No intimal flaps or dissections were detected.
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| 4. Discussion |
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In our hands, vascular join has proven to be a reliable surgical instrument providing consistent and reproducible vascular anastomoses. This surgical technique is simple and intuitive. The deployment system is easy to use, the anastomosis construction takes less than 2 min and no major bleeding has been experienced. However, these characteristics are common to all anastomotic devices developed in the last 10 years [46], and in a way, can be considered as a standard requirement for an anastomotic device.
One of the original elements of the VJ is the complete absence of foreign material (metal or polymers) in the vessel lumen, thus in contact with blood stream. IVUS images acquired soon after the anastomoses construction in two animals and histology examination of all anastomoses, including the occluded one, confirm that metallic pins stay in the vessel wall, in the media layer and, in the majority of the specimens, do not even reach the lamina basalis (figure dettaglio isto). Pins have a diameter of 100 µm and their traumatic action on the vessel wall can be compared to that of a 7-0 needle.
Lac of foreign material in the vessel lumen reduces flow disturbances and may reduce the disposition toward the development of intimal hyperplasia or thrombosis [3,8] and data presented seems to support this principle (83% suturless vs 71% sutured anastomoses open, p = 0.001). The 12-month follow-up shows excellent results since the luminal width is comparable to that of the native vessel and the flow is laminar as documented by duplex scan. Moreover, the two connectors having important myointimal hyperplasia, leading in one case to vessel occlusion, were the two investigated with IVUS. We could speculate that IVUS catheter had caused intimal lesions that triggered the myointimal proliferation.
Scheltes and co-workers [7] introduced the concept of the Blood Exposed Non Intimal Surface (BENIS) and compared the BENIS of different connectors with the conventionally sutured anastomoses. The sutured anastomosis BENIS area is about 1.3 mm2 and this was considered as the reference value. Approximate BENIS of several connectors varies from 4.3 to 80 mm2, depending on anastomotic orifice size, wall thickness, and bonding components location and size. They concluded that BENIS = 0 is practically impossible to obtain because it would require the complete eversion of the vessel wall that causes prohibitive high wall shear stress eventually leading to vessel occlusion. The VJ is the only exception to this rule: it has BENIS = 0 and the wall shear stress, even if it has not been measured in this study, is probably very close to that of the natural vessel because there is no wall eversion. From this point of view, the suture technique with its BENIS of 1.3 mm2 has a higher tendency to fail with respect to the sutureless technique examined.
Histology also shows that intima, media and adventitia of the severed vessel, are joined in a physiological way, avoiding the vessel wall eversion. The three layers of the artery wall are faced layer by layer so that intima is in contact with intima, media with media and adventitia with adventitia. This is the first time a surgical technique for vascular anastomosis provides such a natural physiologic vascular reconstruction. The risk of intimal dissection, however, could be a major limiting factor of this physiological reconstruction, even if experimental results do not support it. We can imagine that pins in the vessel wall can play a role in providing some intima layer stabilization.
One potential drawback of this technique is the compliance of the anastomosis because metallic components can alter the elastic properties of the vessel wall. The suture material and the suture technique employed can influence the size and the distensibility of the anastomotic lumen, the wall shear stress and the axial stress eventually affecting the vascular reconstruction outcome [911]. As a general assumption, the more the vascular anastomosis is compliant, the less the probability that it could develop a stenosis due to myointimal hyperplasia is. Direct measurement of CSAC confirms that VJ anastomoses are less compliant than the running suture anastomoses, (3.1 x 103 mm2/mmHg vs 3 x 103 mm2/mmHg) even if the difference is not statistically significant (p = 0.5). Our previous study [12] demonstrates that suture technique has a substantial effect on CSAC of end-to-side anastomoses. Interrupted suture provides a considerably higher CSAC than continuous suture and can be reasonably considered the most physiologic suture because it keeps the biomechanical properties of arterial wall as close as possible to those of the native vessel [10]. This anastomotic behavior appears to result mainly from the elastic recoil of the arterial wall constituents, which is better preserved with interrupted suture [9]. However, there is no clear evidence that interrupted suture technique provides better long-term results than running suture, and data presented in this study support the hypothesis that CSAC probably plays a less important role than believed in determining long-term anastomoses patency. In fact, even if VJ anastomoses are less compliant, long-term results are significantly improved.
The two techniques show similar behavior since the regression coefficient is almost the same (R sutured = 0.64 vs R sutureless = 0.62) meaning that the foreign material present outside the vessel and in the vessel wall does not significantly affect the distensibility of the sutured artery. The CSAA slightly increase during systole causing a reduction in vascular resistance and this can improve the blood flow through the anastomosis as first hypothesised in 1960 by Szilagyi and co-workers [13]. However, when we measured the flow through the anastomosis we did not find any difference in systolic outflow between the two techniques and this is probably due to the sensibility of the flowmeter probe.
None of the existing sutureless anastomotic devices can be used with synthetic grafts because of the stiffness of their wall. Two e-PTFE thick wall grafts were implanted using the VJ without any technical failure and this is another important improvement that VJ brings to anastomotic technology. Moreover, the more the vessel wall is calcified, thus rigid, the easier VJs pins penetrate into it for a safe connection.
4.1 Study limitations
Only the end-to-end device has been studied, and even if the end-to-side device works on the same principles, conclusions cannot be extended to it.
The animal model chosen had normal vessels, and even if the VJ works better with rigid conduits, the assumption that it is the ideal device for calcified vessels has to be confirmed by clinical study.
We have learned from the recent past, that even the most attractive and promising sutureless devices have failed in long-term clinical results stifling our enthusiasm. Therefore, to became widely accepted, a sutureless device must fulfill three essential characteristics: easiness, precision and, above all, evidence of long-term effectiveness. We definitely need prospective clinical studies to prove the long-term effectiveness of this helpful device.
| Acknowledgments |
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