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J Thorac Cardiovasc Surg 2000;120:473-477
© 2000 The American Association for Thoracic Surgery
Surgery for Acquired Cardiovascular Disease |
From Loma Linda University Medical Center, Loma Linda, Calif,a and CryoLife, Inc, Marietta, Ga.b
Address for reprints: Steven R. Gundry, MD, Professor and Head, Division of Cardiothoracic Surgery, Loma Linda University, 11175 Campus St, Loma Linda, CA 92354 (E-mail: sgundry{at}som.llu.edu ).
| Abstract |
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| Introduction |
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| Materials and methods |
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To facilitate sutureless coronary artery anastomoses, we procured 12 bovine hearts from the slaughterhouse and rinsed the coronary arteries with a saline-heparin solution. Thawed, previously cryopreserved segments of human saphenous vein (CryoLife) that were unacceptable for human use were used as the conduit material. A total of 42 anastomoses were created with a catheter system that consisted of modified angioplasty balloon catheters (Ideas for Medicine, St Petersburg, Fla) (Fig 1). In brief, the saphenous vein and left coronary artery to be bypassed were brought parallel to each other. Incisions were made on the back of the saphenous vein and the anterior portion of the coronary artery to perform a side-to-side anastomosis. One catheter was introduced into the distal end of the saphenous vein, brought out through the back wall incision of the saphenous vein, and placed into the coronary artery to be bypassed. A second catheter was also introduced into the distal end of the saphenous vein and was placed within the body of the saphenous vein adjacent to the anastomosis to maintain the luminal integrity of the saphenous vein graft. Both balloons were then inflated, so that the two vessels were secured together. The BioGlue adhesive was applied with its standard applicator gun and tip and allowed to set for 2 minutes. After 2 minutes, the balloons were deflated and the catheters removed. The proximal end of the vein graft was fitted with a standard vein graft cannula (Medtronic/DLP, Grand Rapids, Mich) and connected to a pressure-transducing box (Medtronic/DLP). Saline solution was then injected into the proximal vein graft and flow through the distal end of the vein graft assured. Once distal flow through the vein graft was established, the distal end of the graft was clipped with a medium clip (Ligaclip; Ethicon, Inc, Cincinnati, Ohio). The vein graft and coronary arteries were then perfused with a large syringe connected in a Y fashion to the proximal vein graft and the pressure transducer, and saline solution was forcefully injected to achieve a pressure of at least 300 mm Hg. Flow was ascertained through the proximal artery by observing saline solution coming from the coronary ostia and from the distal artery by cutting the heart in a bread loaf slice near the apex of the heart and assessing runoff. Saline solution continued to be infused forcefully to as high a pressure as could be achieved competing with the natural runoff through the coronary arteries.
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| Results |
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In vivo results
All goat hearts were weaned uneventfully from cardiopulmonary bypass. All three hearts had regained normal contractility in the distribution of the distal LAD coronary artery with an open ITA and the crossclamp still in place. In the first goat heart, the proximal LAD was clipped with a Ligaclip. The autopsy of the subsequent two goats found that the Ligaclip had not completely gone over the proximal LAD, resulting in patent LADs in both goats 2 and 3 at 10 months and 1 year after the operation. All goats were fully heparinized before being put to death. After death, the hearts were carefully dissected out, preserving the ITA pedicle. In goat 1, there was a patent ITA graft to the LAD and minimal surrounding tissue reaction. In goat 2, 10 months postoperatively, there were minimal pericardial adhesions, and portions of the BioGlue adhesive surrounding the anastomosis were still present surrounded with a thin capsule. The anastomotic site was completely patent, as was the proximal and distal LAD coronary artery. The mid right ITA was occluded because of a technical error of kinking at the graft coming over the pericardium. Goat 3 was put to death 1 year after the operation. The left ITA was completely patent, as was the anastomotic site. A coronary angiogram was performed through the ITA, and results are shown in Fig 2. These results demonstrated a completely patent anastomosis with no areas of stenosis, distortion, or aneurysm formation. As in goat 2, there were typical pericardial adhesions within the pericardium and there were still areas of BioGlue adhesive that had not been absorbed but were merely surrounded by a capsule-like formation. BioGlue adhesive could easily be peeled off the heart where it had been placed 1 year previously. Histologic sections were made, the results of which are shown in Fig 3. No inflammatory reaction to the BioGlue adhesive was found microscopically. The luminal margins were smooth and also without reaction.
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| Discussion |
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The lack of a significant inflammatory response and the fact that the goats continued to grow for up to 1 year of follow-up suggest that any detrimental reactivity of the glue to the surrounding tissue is minimal. Although it is unknown whether the same amount of minimal reaction might be found in human beings, the current clinical trials of the glue in aortic dissection have shown no untoward reactions to the glue. Therefore, it is likely that these animal results can be extrapolated to human coronary artery anastomoses quite easily. At the very least, the use of this glue as an adjunct to other forms of rapid anastomosis, whether it be with sutures, stapling, or laser, affords new consideration of these techniques in combination with glue as an alternative to standard anastomoses.
1-6
| Conclusion |
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| Appendix: Discussion |
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Dr Gundry. Those histologic specimens are still under review. I waited a full year to do this last animal's autopsy (which I did last week), so I do not have histologic results. Visually and using loupes we could find no intimal irregularities, and there are no intimal irregularities on the angiogram. However, the histologic information is pending.
Dr James W. Frederiksen (Chicago, Ill). Have you considered using BioGlue surgical adhesive to control unsuturable bleeding, for which fibrin sealant is currently recommended?
Dr Gundry. An investigational device exemption (IDE) trial is underway in the United States for the use of BioGlue adhesive in the treatment of acute aortic dissection. In those cases, the investigators, including me, have used BioGlue adhesive for either the prevention of what we believed would be an uncontrollable leak or the subsequent treatment of a leak uncontrollable by suture. Clinically, it works very well.
Dr Verdi J. DiSesa (Chicago, Ill). You say that this adhesive will stick even in the presence of blood?
Dr Gundry. Yes, it will bind to anything. It will bind to the blood actively, as well as to other tissue. And it will set up under water, so the field does not have to be perfectly dry for this substance to work.
Dr Richard P. Cochran (Madison, Wis). Do you think the double-balloon technique will limit the size of vessel that you can use? As the vessels get smaller and smaller, inserting two balloons may be very difficult.
Dr Gundry. These balloons were actually modified 1- to 2-mm angioplasty balloon catheters. We used them initially in yearling goats weighing about 40 kg, so the ITAs were quite small. At autopsy, these animals weighed approximately 65 kg, so they grew with these anastomoses. This glue does not seem to be detrimental to growth. In fact, the glue was flexible at 1 year.
Dr Alain F. Carpentier (Paris, France). It was not clear from your drawing how you positioned the balloon. Could you elaborate on this technical point?
Dr Gundry. The balloons were both placed through the distal ITA. One balloon was placed in the ITA itself, because earlier trials in vitro had shown that the ITA, if totally decompressed or flattened, would stay in that position after the glue was applied. We merely allowed the ITA to be distended by the balloon to keep it from being compressed.
The second balloon went through the anastomosis and was present within the ITA and the LAD across the anastomosis to seal the anastomosis from glue getting inside and to hold the anastomosis steady. The glue was then applied outside, and it was allowed to set up in 2 minutes. The glue gets about 60% of its holding power in 20 seconds and about 95% of its holding power in 2 minutes, so it is a fairly rapid procedure.
Dr Marko I. Turina (Zurich, Switzerland). Other investigators using laser and similar methods found it is simpler to use some stay sutures to support the anastomosis. Did you find this to be the case?
I also have a comment concerning some previous studies that were done, especially in the United Kingdom, with this type of anastomosis, although using laser assistance rather than this method. The fact emerged that early results might be excellent, but there was a very high incidence of late aneurysm at the anastomosis. I would respectfully submit that it is advisable to use a large number of animals and very carefully check for anastomotic aneurysms.
Dr Gundry. I certainly agree with you. We actually used two stay stitches on the outside of the vessels, on the lateral walls, to pull the vessels apart. They were removed after the glue was applied. All the in vitro anastomoses we did totally without sutures. We found it more practical in the living animal to pull the vessel apart with two stay sutures, so those were applied just to hold tissue apart.
Late aneurysm formation is a major problem, particularly with laser-weld anastomoses. That is why I purposely waited so long, 10 months and 1 year, to evaluate these anastomoses for that possibility. Again, the series is extremely small and obviously more experiments in animals have to be done. However, the fact that the glue is still present around the anastomosis at 1 year gives me some encouragement that the late aneurysm formation with other techniques will not be seen in this technique.
Dr DiSesa. Is this is a thin bead of glue or a wad of glue?
Dr Gundry. This is a wad of glue on the outside. It is not purposefully put on the contact area between the two intimal surfaces.
Dr. Mohamed Emara (Cairo, Egypt). How can you exactly fix the size of the ITA and the native coronary artery with your catheter? How can you be sure? And what is the proportion? How much do you open on the ITA and the native artery?
Dr Gundry. We choose a balloon catheter to match the size of the LAD diameter. The balloon catheter actually holds those two vessels apart through that anastomosis and that determines the size of the anastomosis. In other words, if you wanted a 3-mm anastomosis, you would use a 3-mm balloon to spread it that far. If you wanted a 1-mm anastomosis, you would use a 1-mm balloon. It is totally dependent on the balloon size.
| Footnotes |
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| References |
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