The advent of minimally invasive mitral valve surgery has conferred numerous benefits to patients. The demand for such less invasive procedures is steadily increasing, driven by the imperative to reduce patient morbidity and enhance recovery. This trend is facilitated by continuous advancements in technology and surgical instruments, all aimed at improving the safety and efficacy of surgery. In this study, we focus on the application of totally 3D endoscopic surgery in mitral valve repair, assessing early and long-term outcomes. Furthermore, we evaluate the feasibility and effectiveness of our novel valve exposure technique—an innovation that represents a significant advancement in our surgical approach.
In our study, the mitral valve repair rate was 96%, with 5 cases (4%) necessitating conversion to prosthetic mitral valve replacement. We classified the complexity of mitral valve lesions to evaluate and predict the likelihood of successful mitral valve repair as follows: simple (annuloplasty alone; single leaflet segment lesion), complex (multiple segment lesions on a single leaflet), and highly complex (bileaflet repair or involving multiple complex techniques, e.g., leaflet patch augmentation, chordal transfer, neochordae replacement). The repair rate for simple lesions was 100%. There were 34 cases categorized as complex and highly complex, representing 28% of the cohort, with a successful repair rate of 85% (29 out of 34 patients) in this group. All instances of repair failure were in the complex anterior leaflet group (4 out of 5 patients) and the highly complex bileaflet group (1 out of 5 patients), with etiologies including infective endocarditis (3 out of 5 patients) and degenerative disease (2 out of 5 patients). Generally, the repair rates in various studies differ significantly, depending on patient selection criteria, lesion morphology, techniques, equipment, and the surgeon's experience. Based on our experience with 122 patients, we propose that certain lesions may not be suitable for the initial implementation of endoscopic mitral valve repair techniques. These include extensive anterior leaflet prolapse involving multiple segments, bileaflet prolapse without commissural involvement, and infective endocarditis.
One of the key factors in determining the success of mitral repair is the adequate exposure of the valve. Numerous instruments have been developed to achieve optimal exposure of the mitral valve in minimally invasive surgery. During the course of our surgical experience, we evaluated various methods and ultimately selected the most suitable approach based on our specific conditions and accumulated expertise. We employed a technique that exclusively utilizes retraction sutures to achieve mitral valve exposure. The materials used for this technique include 3/0 or 4/0 monofilament polypropylene sutures, which are widely accessible. This approach obviates the need for an additional thoracic wall incision, unlike conventional trans-thoracic retractors, thereby mitigating the risks of chest wall bleeding, internal thoracic artery injury, and iatrogenic damage to the leaflet hinge and the bundle of His. Furthermore, employing these sutures ensures that the surgical field remains unobstructed by retractor systems, thus reducing conflicts with surgical instruments. This exposure method is particularly well-suited for a totally endoscopic field, involving a minimal thoracic incision of 3–4 cm, as per our surgical protocol. In instances where the left atrium is small and deviates leftward, the thoracic cavity is deep, or the chest anatomy is unfavorable (e.g., pectus carinatum or pectus excavatum), obtaining satisfactory exposure with a conventional retractor can be challenging. Our technique enables surgeons to place more sutures and select their positions with greater flexibility in blind spots, thereby enhancing visualization. This method was employed in all patients within our study. Mitral valve exposure was successfully achieved in all repair cases and in the five patients who required valve replacement due to complex lesions, which were not related to inadequate exposure. Notably, there were no complications such as tissue tearing requiring additional sutures, ischemic damage, or conversion to sternotomy due to poor visualization.
Several intraoperative complications were observed. Associated with peripheral CPB, a significant complication occurred when the right internal jugular vein and right subclavian artery were perforated during percutaneous cannulation, resulting in substantial bleeding into the pleural cavity. This rare but severe complication necessitated immediate and meticulous intervention. Simple perforations of the internal jugular vein into the pleural cavity can often be managed with endoscopic assistance. However, the concomitant injury to the right subclavian artery presents a risk of acute exsanguination and inadequate CPB flow, potentially requiring conversion to sternotomy and dissection of the sternoclavicular joint to access and control the subclavian artery injury. Our intraoperative management involved maintaining the cannula within the vessel, temporarily controlling the bleeding by suturing the external surrounding tissue, and introducing a new superior vena cava cannula directly through the main working port. Subsequently, the patient underwent endoscopic mitral valve repair as per standard protocol. Immediately following the completion of the surgery, the patient was transferred to the catheterization laboratory. The internal jugular vein cannula was then removed concurrently with angiographic evaluation, during which an arteriovenous fistula involving the right subclavian artery and internal jugular vein was identified. A covered stent was promptly deployed in the subclavian artery, thereby restoring vascular integrity and achieving hemostasis. This endovascular approach facilitated the successful management of this complex complication without necessitating sternotomy or dissection of the sternoclavicular joint.
In our research, 3 patients (2.5%) required conversion to sternotomy: 2 cases due to severe right pleural adhesions and 1 case due to left atrial appendage injury. In global studies, several causes necessitate conversion to sternotomy, including bleeding, pleural adhesions, and aortic dissection. Bleeding can originate from multiple sources such as the pulmonary artery (due to thoracic aortic cross-clamping),5 the left atrial appendage (due to Chitwood clamp),6 the left ventricular apex (during valve testing), and the ascending aorta (direct cannulation).7 Additionally, pleural adhesions frequently necessitate conversion to sternotomy. While pleural adhesions can sometimes be predicted based on a patient’s history of tuberculosis, radiation therapy, or prior surgeries, routine preoperative chest X-rays and CT scans may not always accurately identify these risks. Aortic dissection has also been reported in several studies, predominantly associated with balloon occlusion of the aorta or in patients with underlying atherosclerosis or aortic calcification. Other intraoperative challenges include insufficient peripheral CPB flow,8 inadequate valve exposure, and circumflex artery injury,7 all of which have been documented and serve as valuable lessons for surgical practice. The two cases requiring conversion to traditional surgery due to pleural adhesions in our study involved challenging adhesiolysis, which resulted in significant pulmonary and pleural injury during the process. The patient with left atrial appendage injury necessitated conversion to sternotomy for control bleeding. However, with the accumulation of surgical experience over time, we have successfully managed this complication via endoscopy in subsequent mitral valve replacement patients.
The early mortality rate in our study was 1.6%, with all affected patients requiring early reoperation. One patient underwent reoperation on postoperative day 3 due to a rupture of the ascending aorta at the site of the cardioplegia needle insertion. This patient experienced hemorrhagic shock and cardiac arrest, necessitating an emergency sternotomy and replacement of the ascending aorta; however, the patient succumbed 24 hours later. The second patient required reoperation on postoperative day 6 due to hemolysis following mitral valve repair (neochordae replacement and annuloplasty). Hemolysis following mitral valve repair is a known complication of prosthetic valve replacement, but its occurrence post-repair is relatively rare and hazardous, with a mortality rate of up to 31%, as reported by Buu Khanh Lam. The mechanisms of hemolysis after mitral valve repair are not fully understood, but several patterns have been proposed, such as fragmentation, collision, rapid acceleration, free jet, and slow deceleration. 9, 10 Despite understanding these mechanisms, predicting and early detection of this complication remain challenging. In our study, the patient underwent reoperation and mechanical mitral valve replacement; however, the patient's condition deteriorated due to coagulopathy, hemorrhage, multi-organ failure, septic shock, and ultimately died on postoperative day 22.
In our study, two patients (1.6%) experienced complications of unilateral pulmonary edema (UPE). UPE is an infrequent yet life-threatening condition. Renner et al. reported five instances of UPE following minimally invasive mitral valve surgery over an eight-year period, all necessitating immediate ECMO support. 11 The etiology and pathogenesis of UPE remain ambiguous. Some hypotheses suggest that UPE is a manifestation of permeable pulmonary edema, with prolonged CPB times exacerbating ischemia-reperfusion lung injury.11–13 Tutschka's research identified prolonged CPB duration, COPD, preoperative pulmonary hypertension, and severe right ventricular dysfunction as significant risk factors for UPE. 12 Additionally, Keyl emphasized surgical factors, such as the potential for obstruction or stenosis of the right pulmonary vein (caused by excessive traction on the pericardium and sutures used for left atrial exposure) leading to secondary increases in hydrostatic pressure and subsequent right-sided pulmonary edema.13 In our cohort, one patient required ECMO support due to UPE. Both patients received intensive care management, including the administration of corticosteroids to mitigate the severity of pulmonary edema. The patient on ECMO was successfully weaned off, and both patients achieved full recovery without any residual sequelae.
In terms of early results, echocardiography at discharge revealed no cases of severe MR. Moderate MR was observed in 9 patients (7.7%), mild MR in 37.1%, and no MR in the majority of patients (55.2%). These findings indicate that TEMVR achieves favorable short-term outcomes with a variety of techniques comparable to the conventional sternotomy approach.
For long-term outcomes, there was one case of mortality at 6 months postoperatively due to infective endocarditis on a bioprosthetic mitral valve. The late survival probability over the 5-year follow-up period was 96.7 ± 1.6%. Two patients experienced severe recurrent MR at 6 and 24 months, necessitating reoperation: one underwent repeat mitral valve repair, and the other required valve replacement. Freedom from reoperation after 5 years was 98.4 ± 1.2%. The probability of freedom from moderate or severe MR at 72 months was 86.1 ± 3.1%.