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J Thorac Cardiovasc Surg 2006;131:146-153
© 2006 The American Association for Thoracic Surgery
Evolving Technology |
a Department of Cardiac Surgery, Innsbruck Medical University, Innsbruck, Austria.
b Department of Cardiac Anesthesia, Innsbruck Medical University, Innsbruck, Austria.
c Department of Cardiology, Innsbruck Medical University, Innsbruck, Austria.
Received for publication February 13, 2005; revisions received July 3, 2005; accepted for publication July 19, 2005. * Address for reprints: Johannes Bonatti, MD, Associate Professor of Surgery, Innsbruck Medical University, Department of Cardiac Surgery, Anichstrasse 35, A-6020 Innsbruck, Austria (Email: johannes.o.bonatti{at}uibk.ac.at).
| Abstract |
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METHODS: From October 2001 through October 2004, 40 patients received robotically assisted totally endoscopic left internal thoracic artery grafts to the left anterior descending coronary artery system with the da Vinci telemanipulation device. All patients underwent remote access cardiopulmonary bypass perfusion through groin access, and all anastomoses were performed on the arrested heart.
RESULTS: Undesirable technical events of various grades occurred in 20 (50%) of 40 patients: bleeding from a port hole in 3 (8%), left internal thoracic artery damage in 3 (8%), epicardial lesion in 3 (8%), remote access perfusion problems in 9 (23%), bleeding from the anastomosis in 4 (10%), and anastomotic stenosis in 2 (5%). There was no hospital mortality. The following differences were noted between patients without technical difficulties (group 1) and those in whom problems occurred (group 2): total operative time of 314 minutes (260-540 minutes) versus 418 minutes (270-690 minutes; P = .007), ventilation time of 6 hours (0-26 hours) versus 14 hours (0-278 hours; P = .004), intensive care unit stay of 20 hours (11-70 hours) versus 44 hours (16-336 hours; P = .183), hospital stay of 7 days (4-13 days) versus 8 days (5-21 days; P = .038), and cumulative freedom from angina at 36 months of 93% versus 100% (P = .317).
CONCLUSION: We conclude that technical difficulties during totally endoscopic coronary artery bypass grafting translate into markedly increased operative time, moderately prolonged postoperative ventilation time, and slightly increased hospital stay. Short-term survival and freedom from angina, however, do not seem to be compromised.
| Introduction |
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In the mid-1990s, several initial attempts to perform endoscopic coronary artery bypass grafting (CABG) with conventional thoracoscopic instrumentation failed. The following introduction of surgical telemanipulation systems enabled more complex intrathoracic maneuvers, and Loulmet and colleagues
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carried out the first totally endoscopic coronary artery bypass (TECAB) procedure in 1998. Despite this successful step, only a limited number of TECAB operations have thus far been carried out worldwide. The high cost of the equipment and procedure time issues are the main arguments against robotic endoscopic CABG. Another reason for poor acceptance might also be the fact that this operation remains a technically difficult surgical challenge.
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Thus far, little has been reported about specific technical obstacles that might be encountered during the TECAB procedure. Given the fact that several surgical teams are planning or currently installing a robotic cardiac surgery program, communication of our experience regarding technical difficulties, their management, and the development of preemptive strategies might be useful for the implementation of robotic endoscopic cardiac procedures. It was the aim of this study to describe surgeon-related technical difficulties in arrested heart totally endoscopic coronary artery bypass (AHTECAB) during an implementation phase, to evaluate risk factors, and to determine the clinical consequences associated with undesirable surgical events.
| Patients and Methods |
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Operative Technique
Anesthesia
After induction of anesthesia, a left-sided, double-lumen endobronchial tube was placed. Anesthesia was maintained with remifentanil (0.2-0.5 µg · kg1 · min1) and propofol or sevoflurane. A central venous line, a Swan-Ganz catheter, and percutaneous defibrillator patches were placed. Bilateral radial arterial pressure lines and transesophageal echocardiography completed monitoring.
Surgical procedure
The patient was positioned in a 30° right lateral decubitus position. After setup of the da Vinci system (Intuitive Surgical, Sunnyvale, Calif) a camera port was introduced into the left fifth intercostal space on the anterior axillary line under left lung collapse. CO2 was insufflated at target pressures of 10 mm Hg. Instrument ports were then inserted through the third and seventh intercostal spaces on the mamillary line under thoracoscopic vision. The internal thoracic artery (ITA) was localized, and the endothoracic fascia and transverse thoracic muscle were removed from the ITA pedicle to adequately visualize the vessel. By using electrocautery at 20 W and endoscopic clips for division of pedicle side branches, the ITA was harvested from the first onto the fifth intercostal space. Heparin (300 IE/kg) was administered, and after endoscopic placement of a temporarily occluding bulldog clamp, preparation of the distal graft portion, as well as free flow check, were carried out.
The pericardial fat pad was removed from the pericardium by using electrocautery. After incision of the pericardium, the left anterior descending coronary artery was identified and marked with a clip onto the adjacent epicardial fat. Care was taken to see the left anterior descending coronary artery running around the apex of the heart to avoid confusion with diagonal branches.
In parallel to these steps, the femoral artery and femoral vein were exposed in the left groin. The right atrium was cannulated for cardiopulmonary bypass with a 25F or 27F Medtronic venous return cannula (96370; Medtronic, Minneapolis, Minn). A 21F Remote Access Perfusion cardiopulmonary bypass system (ESTECH, Danville, Calif) or a 21F Endoreturn (Heartport, Redwood City, Calif) arterial cannula was inserted, cardiopulmonary bypass was started, and the ascending aortic occlusion balloon was inflated for induction of cardioplegia.
Thereafter, the target vessel was exposed and incised with a lancet endoscopic knife. The left ITA (LITA) was then sutured robotically to the target vessel with a 7-0 Pronova (PN 8713; Johnson and Johnson, Somerville, NJ) running suture. The sternal and heel parts of the anastomosis were sutured first and carried out in an outside-in manner, and thereafter, the toe of the anastomosis and the lateral portion were carried out in an inside-out manner.
After deflating the endoaortic occlusion balloon, the heart was reperfused and defibrillated percutaneously if necessary. After rewarming and reperfusion, the patient was weaned from cardiopulmonary bypass and decannulated. Intraoperative graft angiography was a routine measure of quality control in all cases.
Undesirable surgical events occurred in 20 (50%) of our patients. Patients without technical problems were assigned to group 1, and patients with technical problems were assigned to group 2.
Definition and Grading of Technical Difficulties
Technical difficulties were graded as shown in Table 1.
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Statistics
The statistical computer package SPSS 11.0.0 for Windows (SPSS, Chicago, Ill) was used for statistical analysis. Categoric variables are presented as percentages and absolute values, and continuous variables are presented as medians and ranges. Intergroup comparisons were performed by using the
2 test for categoric variables and the Mann-Whitney U test for continuous variables. Life-table analysis was taken for calculation of freedom from angina. In the figures mean severity level of technical difficulties is presented as the mean ± standard deviation.
| Results |
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| Discussion |
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Detailed reports on the frequency of technical difficulties in cardiac surgery procedures and their severity levels and management strategies are rare in the literature. Technical difficulties are also rarely included in risk factor analyses of different procedures in cardiac surgery. A potential reason for this fact might be that except for notes in the operative report, technical errors are not recorded in standard cardiac surgery databases. For a new and complex totally endoscopic operation, such as AHTECAB, a detailed analysis of undesirable surgical events should help to improve the quality of the procedure and should be a useful tool for teaching this operation. When looking at the results of our analysis, it should be clearly remembered that an implementation phase with a variety of learning curves is described.
5,6
A technical difficulty in our series was very broadly defined, and the event rate in half of our patients might seem high. It can be stated, however, that all difficulties were under control of the surgical team and that all problems could be corrected at least during the first postoperative hours. In addition, the overall severity level was low, and trends toward improvement were noted for some types of difficulties with increasing experience. Our conversion rate of 15% was comparable with that of others in the field of robotic totally endoscopic CABG.
3,4
It was our group's strategy to generously perform sternotomies in view of technical difficulties because we think that this approach offers the best overview and enables a broad surgical reaction spectrum. Including postoperative revisions, 33% of our patients ended up with a larger incision, either minithoracotomy or sternotomy. This makes AHTECAB probably a difficult offer for the patient, and intense technological, as well as procedure-related, development will be necessary to increase the rate of procedures that can be achieved in a completely endoscopic fashion. Despite the high rate of revisions, which was already obvious at the beginning of our program, no patient refused the AHTECAB procedure because of this fact, and we are continuing to perform this operation. Ideally, prospective randomized trials will show whether robotic totally endoscopic procedures can compete with the straightforward off-pump coronary artery bypass sternotomy approach, which is today favored by many surgeons.
Risk Factors for Technical Problems
No single demographic risk factor was associated with the occurrence of technical difficulties, which was most likely influenced by the preselection of coronary patients with only a few comorbidities.
Port-hole Problems
There were no immediate problems with port positioning, but port bleeding after a smooth intraoperative course occurred in 3 patients of our series. One technical modification that we introduced after these events was to rigorously inspect the port holes with the camera from inside after port removal and to pack the port holes with collagen sponges before closure.
LITA Damage
LITA damage necessitating conversion or revision was observed in 3 cases of our series. Rigorous intraoperative quality control by means of on-table angiography helped to detect one significant intramural hematoma. LITA damage has been described in other TECAB series but also in series in which conventional thoracoscopic instrumentation was used to endoscopically harvest the vessel.
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Epimyocardial Lesions
In 3 cases of our series, a laceration of the right ventricular outflow tract had to be repaired with endoscopic sutures. These lesions all occurred when an instrument was inserted without direct videoscopic view. Special attention therefore needs to be paid that instruments are brought into the thoracic cavity by the patient-side surgeon only under clear direct vision. Dogan and coworkers
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have previously underlined the critical role of the patient-side surgeon for various aspects of the procedure. As a preemptive strategy, we try to avoid personnel changes in the TECAB team. In the case that required conversion, forced inflation of the right lung after separation from cardiopulmonary bypass under single-lung ventilation probably played a role in the occurrence of a laceration.
Anastomotic Bleeding
One special feature of telemanipulation-enhanced endoscopic CABG is that the anastomosis is sutured by the console surgeon in a running fashion without countertraction by an assistant. We regard this fact as the main reason why 4 cases of bleeding occurred in our learning series. Similar bleeding problems have been described by Dogan and coworkers.
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The console surgeon during the learning phase has to adapt to the degree of suture tension that is necessary for an avoidance of loose slings, which might cause anastomotic leakage. Two cases of anastomotic bleeding were diagnosed by means of intraoperative angiography and visualized by means of extravasation of contrast medium. Two further cases were diagnosed by means of direct inspection during a revision procedure for bleeding. In all these cases, final inspections with videoendoscopy had shown a blood-tight anastomosis. There might be factors that could lead to loosening of the single surgeonperformed suture during the immediate postoperative period. We changed our protocol in such a way that preventive repair stitches are placed in any case of doubtful oozing after release of the LITA bulldog and that fibrin glue is generously applied onto the anastomosis after heparin reversal. No case of bleeding has occurred after introduction of these measures.
Target Vessel Occlusion
We experienced 2 cases of target vessel occlusion close to the heel of the anastomosis. Both cases occurred in patients with significant local vessel wall pathology, and both were detected on intraoperative angiography. One possible explanation could be the current suture technique, in which the heel stitches are placed on the target vessel in an outside-in fashion. Local plaque mobilization might have been a consequence of this technique, leading to local vessel obstruction by the plaque. A consequence of the target vessel occlusions was increased concentration at placement of the heel stitches under inspection of the whole surgical team and endoscopic probing of all anastomoses. Narrowing of the anastomosis at the heel has not occurred throughout the second half of the series.
Remote Access Perfusion Problems
In our series one single severity level 5 technical difficulty (external iliac artery injury caused by an additional perfusion cannula in the groin contralateral to the RAP cannula) was encountered with remote access perfusion. This event was unrelated to the specific remote access perfusion cannula, which was used in all our cases.
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Aortic dissection, which was described in early arrested heart TECAB series by other groups, did not occur.
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We attribute this in part to the fact that preoperative computed tomographic scans were performed in every patient for detection of significant aortic or iliacal atherosclerotic lesions and for determination of an adequate ascending aortic diameter for balloon placement. Nevertheless, failure of correct positioning of the occlusion balloon necessitated conversion to sternotomy in 2 cases. It might be of note that the majority of remote access perfusion problems in our series were level 1 in severity, leading only to a delay in operative time.
Overall Outcome
According to our experience, technical problems in AHTECAB increased the postoperative ventilation time. Single-lung ventilation and prolonged cardiopulmonary bypass time in combination with a surgically complicating event are probable explanations for this fact. Hospital stay was also increased by only 1 day if technical difficulties occurred. It is satisfying that despite significant challenges, no mortality occurred. Our 0% mortality is also in line with low mortality rates reported by other TECAB groups during their learning curve.
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The overall freedom from angina and graft potency at 3 years were not affected by surgeon-related technical difficulties. There was no target vessel reintervention on the robotically sutured LITA grafts in the whole study group.
Limitations of the Study
Our study is limited by the fact that a small and selected group of patients has been chosen for performance of TECAB. Results will have to be confirmed with much larger patient numbers in multicenter registries and expansion of AHTECAB into multivessel disease. Larger patient series will also show whether the too-high rate of larger incisions in about one third of the patients can be reduced.
Limitations of the AHTECAB Procedure
The current rate of LITA injuries in 1 of 10 patients, anastomotic problems in 1 of 5 patients, and remote access perfusion difficulties in 1 of 4 patients also requires significant improvement. It is clear that with off-pump coronary artery bypass sternotomy or minimally invasive direct coronary artery bypass grafting (MIDCAB) techniques, cardiopulmonary bypass could be avoided completely and that compared with a sternotomy, on-pump procedure cardiopulmonary bypass time and aortic cross-clamp time, with their known side effects, are significantly increased.
| Conclusion |
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| Addendum |
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| References |
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