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Ann Thorac Surg 2005;79:485-490
© 2005 The Society of Thoracic Surgeons
a Department of Cardiovascular Surgery, University Hospital Hamburg-Eppendorf, Hamburg
b Department of Cardiac Surgery, University Hospital Munich-Grosshadern, Munich, Germany
Accepted for publication June 11, 2004.
* Address reprint requests to Dr Detter, Department of Cardiovascular Surgery, University Hospital Hamburg-Eppendorf, Martinistr 52, D-20246 Hamburg, Germany (E-mail: detter{at}uke.uni-hamburg.de).
| Abstract |
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METHODS: In 120 patients mitral valve surgery was performed through a small right minithoracotomy using either the Port-Access endovascular cardiopulmonary bypass system (Port-Access, n = 60) or the transthoracic clamp technique (MICRO, n = 60). Mean patient age was 61.5 ± 10.5 years (81 patients with isolated mitral valve insufficiency, 39 patients with combined mitral valve disease).
RESULTS: Eighty-one (67.5%) patients underwent mitral valve repair and 39 (32.5%) patients had valve replacement. Mean time of surgery was 4.5 ± 3.5 and 4.1 ± 3.2 hours (p = 0.07), aortic cross-clamp time 89 ± 69 and 78 ± 65 minutes (p = 0.08), mean intensive care unit stay 1.5 ± 2.1 and 1.6 ± 2.5 days (p = ns), and hospital stay 9.0 ± 10.5 and 9.2 ± 9.7 days (p = ns) in the Port-Access and MICRO groups, respectively. In the Port-Access group, there were 6 reexplorations for bleeding, one perforation of the right ventricle with the endopulmonary vent, and 2 reconstructions of the femoral artery necessary after femoral cannulation, compared to one reexploration for bleeding in the MICRO group. There was only one minor paravalvular leak after replacement and 2 cases of residual greater than or equal to grade II mitral valve regurgitation after mitral valve repair in the Port-Access group, necessitating reoperation. In both groups, there was no mortality, no cerebrovascular accident, no aortic dissection, and no conversion to sternotomy.
CONCLUSIONS: Minimally invasive mitral valve surgery has become a standard approach for isolated mitral valve operations at our institution. The MICRO technique tends to shorten the time of surgery and aortic cross-clamping and reduces perioperative costs by simplifying the operative procedure.
| Introduction |
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| Patients and Methods |
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The left ventricular ejection fraction ranged from 35% to 84% with a mean of 55.8% (Table 1). Thirty-nine patients (32.5%) showed severely destroyed postrheumatic mitral valve pathologies and underwent mitral valve replacement. Seventy-one patients (59.2%) suffered from a prolapse of the posterior mitral valve leaflet with or without annular dilatation, ten patients (8.3%) from an additional prolapse of the anterior mitral leaflet, and all of them underwent mitral valve repair. In the beginning, no complex mitral valve diseases and only isolated posterior valve leaflet pathologies were selected for minimally invasive techniques. With growing experience, anterior leaflet pathology and more complex mitral valve disease, including both leaflets, were also included.
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Minimally Invasive Mitral Valve Surgery
Patients were intubated with a double-lumen endotracheal tube or a regular endotracheal tube. Both radial arteries were used in the PAMVR group for invasive blood pressure monitoring to detect partial or total occlusion of the brachiocephalic trunk by the endoaortic balloon. Patients were placed in a supine position with slight elevation of the right hemithorax to about 30 degrees. Initially, an 8 to 10 cm skin incision was made; with growing experience, a 4.5 to 8 cm incision was performed in the right inframammary groove and the fourth intercostal space was entered. A soft tissue retractor (Cardiovations, Ethicon Inc) was used to open the intercostal space and retract the subcutaneous tissue and underlying muscle.
A thoracic port was inserted cranially of the thoracic incision to allow thoracoscopic axial vision of the mitral valve apparatus. The 5 mm 2D endoscope (Karl Storz GmbH, Tuttlingen, Germany) or 3D endoscope (Vista Cardiothoracic Systems Inc, Westborough, MA) was attached to the voice controlled robotic arm (AESOP) for camera guidance (Fig 1). The robotic arm was mounted onto the operating table adjacent to the left shoulder of the patient and reached over the patients chest.
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In the PAMVR group, aortic occlusion was achieved by inflation of the endoaortic balloon about 2 cm above the aortic valve. Ventricular fibrillation was induced electrically to allow correct balloon placement monitored by TEE. Antegrade cold crystalloid cardioplegia was delivered at the tip of the balloon.
For the MICRO technique, a transthoracic aortic clamp (Fig 2) was used, introduced by a separate 5 mm incision in the midaxillary line. Antegrade cardioplegia was applied directly into the ascending aorta by a needle-vent catheter (Fig 3).
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In case of mitral valve replacement, the posterior and, in most cases, also the anterior leaflets were preserved. The valve was then measured and replaced by a mechanical (n = 11) or biological (n = 28) valve prosthesis using interrupted annular valve sutures (Table 2).
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All surgeons had prior experience with mitral valve repair as well as with Port-Access technology for coronary artery bypass graft (CABG) and atrial septal defect closure. Additional operative costs per patient were around $3,000 (Endo-CPB system) in the PAMVR group versus $200 (venous cannula) in the MICRO group apart for videoscopic and special instrument equipment, which were used in both groups.
Statistical Analysis
Continuous data were analyzed using the unpaired Students t test, categorical data using the
2 test. Values were expressed as mean ± standard deviation. Probability values (p) of less than 0.05 were considered significant. Statistical analysis was performed using the SPSS statistical software package 10.0 for Windows (SPSS Inc, Chicago, IL).
| Results |
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The complications are listed in Table 4. There were less reexplorations for bleeding (6 vs 1, p = 0.11) and a lower incidence of delayed wound healing (4 vs 0, p = 0.12) and lymphatic fistula development (2 vs 0, p = 0.50) in the groin using the MICRO technique; however, these were not significantly different. In addition, there was one perforation of the right ventricle with the endopulmonary vent, which was solved through the minithoracotomy and two reconstructions of the femoral artery necessary after femoral cannulation in the PAMVR group. One injury of the trachea occurred during placement of the double lumen endotracheal tube in the MICRO group. However, no major complications occurred, particularly no cerebrovascular accident, and no aortic dissection in both groups. No differences were found for the length of postoperative ventilation (15.2 ± 23.4 vs 14.8 ± 19.6 hours, p = ns), total intensive care unit (ICU) stay (1.5 ± 2.1 vs 1.6 ± 2.5 days, p = ns), and hospital stay (9.0 ± 10.5 vs 9.2 ± 9.7 days, p = ns) between the PAMVR and the MICRO groups (Table 3).
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At three month follow-up, mortality was 0%. Eighty-five percent and 86.7% of patients were in New York Heart Association (NYHA) class I, and there were no patients in NYHA classes equal to or greater than III (p = ns). No new onset mitral valve grade II insufficiencies were observed by transthoracic echocardiography. Two patients with residual grade III mitral valve regurgitation after mitral valve repair in the PAMVR group underwent subsequent reoperation and conventional mitral valve replacement 6 weeks and 3 months postoperatively. Both patients had an uneventful postoperative recovery.
| Comment |
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The mortality in our series was 0%. No cerebrovascular accidents and no aortic dissections were observed in either group. To achieve good results with video-assisted minimally invasive mitral valve surgery (MIC-MVS), careful patient selection is crucial. Furthermore, the vast majority (>95%) of MIC-MVSs in this study were performed only by two experienced surgeons.
We found trends towards shorter surgery times and aortic cross-clamp times in the MICRO cases compared to the PAMVR technique. In addition, postoperative complication rates were slightly less with the transthoracic clamp procedure. Although none of the complication rates reached statistical significance comparing both groups, in total significantly less complications were found in the MICRO group. However, most complications in the PAMVR group were most likely not system related but rather due to the learning curve combined with the minimally invasive approach. Other groups also demonstrated major differences between the first patients during the learning curve and those who followed [10]. Mohr and colleagues [11] reported on a high mortality rate in their early Port-Access cases; partially procedure related. Two out of 62 patients suffered an aortic dissection; hospital mortality was 11%. After simplification of the surgical procedure and establishment of the solo surgical technique by using the AESOP robotic arm, their early mortality decreased to 3%. With the introduction of the MICRO technique, neurologic complications were significantly reduced [12].
However, the Port-Access system is a highly sophisticated technique originally developed for endoscopic cardiac surgery. It implicates retrograde balloon positioning with the potential risk of aortic dissection or balloon migration. It still is applied in redo-operations and totally endosurgical procedures. The transthoracic clamp technique is a useful simplification of the operative procedure during minimally invasive mitral valve surgery, reducing the risk of system-related complications, and is thus favored in our institution.
Echocardiography at discharge demonstrated excellent results after mitral valve repair with 75.0% and 76.7% of patients showing no mitral valve regurgitation in the PAMVR and MICRO group, respectively, and two patients in the PAMVR group retaining greater than or equal to grade II regurgitation. These two patients had to be reoperated 6 weeks and 3 months following mitral valve repair. Both patients had a conventional mitral valve replacement with an uneventful postoperative recovery. These results are similar to those of other experienced groups [13]. Three months after surgery, mortality remained at 0% and there were no new onset mitral valve regurgitations greater than or equal to grade II. The majority of patients in both groups regained physical function according to NYHA class I.
We did not observe differences in postoperative recovery as documented by ventilation time, length of ICU stay, and hospital stay between the groups. However, mean extra costs were found to differ markedly between both minimally invasive procedures in favor of the MICRO technique. When compared to conventional mitral valve operations through median sternotomy, the PAMVR technique results in about $3,000 in extra costs per patient. The generated MICRO technique comprised only extra costs of $200 per patient. In addition, time of surgery was lower with the MICRO technique, resulting in lower operating room costs. No differences in the costs of the postoperative course were found between the groups since patients in both groups had a comparable fast postoperative recovery and hospitalization.
In conclusion, minimally invasive mitral valve surgery with a right anterolateral minithoracotomy can be performed successfully with excellent results without increasing morbidity or mortality, including sophisticated valve reconstructions using either of the described techniques. Thus, MIC-MVS has become a standard approach for isolated mitral valve operations at our institution. The transthoracic clamp technique tends to shorten the time of surgery and aortic cross-clamping, to reduce perioperative complication rates by simplifying the operative procedure, and significantly saves operative costs. Thus, our group recommends the use of the transthoracic clamp over the balloon occluder. However, the Port Access technique is still indicated in redo-minimally invasive mitral valve surgery. A careful patient selection for minimally invasive procedures remains crucial in order to obtain excellent results.
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