Methods: Between March 2010 and February 2018, a total of 34 patients (8 males, 26 females; mean age 58.3 years; range, 34 to 78 years) who underwent robotic-assisted concomitant procedures during mitral valve surgery were retrospectively analyzed. Demographic characteristics of the patients, comorbidities, medical, and surgical histories, operative and laboratory results, electrocardiographic findings, postoperative intensive care unit and ward outcomes, and cardiac follow-up data were recorded. Atrial fibrillation-related medication use, stroke, or other thromboembolic events, and electrocardiographic reports in patients who underwent cryoablation were reviewed at three and 12 months after the operation.
Results: A total of 76 robotic-assisted concomitant procedures were performed during mitral valve repair (n=11) or replacement (n=23) in 34 patients. These procedures were cryoablation (n=29), tricuspid valve repair (n=6), tricuspid valve replacement (n=2), left atrial appendage ligation (n=32), atrial septal defect and patent foramen ovale closure (n=5), and left atrial thrombectomy (n=2). The mean preoperative EuroSCORE values were 5.1±2.5. The mean duration of cardiopulmonary bypass and cross-clamp was 156±69.4 min and 101±42 min, respectively. Normal sinus rhythm was restored in 85% of the patients (24/28) after cryoablation and two patients (5.8%) had permanent pacemaker within a year during follow-up. There was one (2.9%) mortality in the early postoperative period due to hemorrhage related to the posterior left ventricular wall rupture. No blood product was used in 82.4% of the patients. One patient had a transient cerebral event and symptoms regressed completely within two months.
Conclusion: Technological improvements and growing experience can decrease the suspects related to prolonged operational duration during robotic-assisted cardiac surgery. Concomitant procedures in addition to mitral valve operations can be performed with low complication rates in centers with experience of robotic surgery.
In the present study, we present our clinical experience and mid-term results with robotic-assisted concomitant procedures during mitral valve operations.
The severity of the mitral or tricuspid valve pathology and existence of other abnormalities were evaluated using transthoracic echocardiography. Coronary arteries were evaluated with conventional coronary angiography or computed tomography angiography. On the operating table, transesophageal echocardiography (TEE) was performed to evaluate the structure of valvular and subvalvular mitral apparatus and the options for valve repair. It also showed mitral and tricuspid valve annular size, evaluate the interatrial septum, the existence of calcification at ascending aorta and the other pathologies. In addition, TEE guided us not only prior the operation, but also during all part of the operation such as arterial cannulation and placing the venous cannulas to the jugular vein and vena cava inferior. The cannulation sides were examined via Doppler ultrasonography (USG), the existence of calcification at the femoral artery and the size of cannulas were determined. All interventions were evaluated via TEE following the removal of CC and reintervention was performed, if necessary.
Surgical technique
Our technique for robotic surgery has been already
described in detail elsewhere.[5,6] Briefly, following
TEE examination, double-lumen endotracheal tube was
inserted. Venous cannulation was achieved by internal
jugular and femoral veins (Medtronic Bio-Medicus,
Eden Prairie, MN, USA) and arterial cannulation
(Medtronic Bio-Medicus, Eden Prairie, MN, USA)
was performed via the femoral artery under the TEE
guidance. A 3-cm incision was made between the
anterior axillary and midclavicular line at the fourth
intercostal space and a small soft tissue retractor
(Applied Medical, Rancho Santa Margarita, CA, USA)
was placed. The right arm port was placed through the
first or second intercostal spaces inferior to the soft
tissue retractor, and the left arm port was placed one
intercostal space superiorly (Figure 1). The robotic
arms were docked. Following CPB institution, the heart
was arrested with the Chitwood aortic clamp which
was inserted through the chest wall in the direction
of the transverse sinus and using of cold crystalloid
cardioplegia (Custodiol, Essential Pharmaceuticals
LLC, NC, USA) delivered into the aortic root via a
temporary transthoracic cannula through the working
port. The inferior and superior vena cavas were
occluded with bulldog clamps.[6] The inter-atrial groove
was dissected, left atriotomy was performed and the
atrial retractor was placed into the left atrium (LA).
Figure 1: An intraoperative view of set-up for robotic-assisted mitral valve procedure.
The LA appendage was ligated in all patients with AF using a double-layered running Prolene 3.0 suture from the inside of the LA. In patients with AF, the cryoablation probe was delivered through the working port (Cardioblate, CryoFlex Medtronic Inc., MN, USA) which can be fit to the shape of the atrial wall, creating cryolesions of 1 to 10 cm in length. Principally, atrial cryolesions in this series were performed for 90 sec reaching local temperatures of -130°C and started with an ablation line extending from the atriotomy to the mitral valve annulus in the region P2/P3. The left and right pulmonary veins were isolated, an inferior and superior ablation line was placed to complete the box lesion for isolation of the posterior atrial wall, and an additional lesion was placed to connect the box to the closure line of the LA appendage. The LA was closed following the completion of mitral valve repair or replacement. In case of right atrial (RA) pathology, right atriotomy was created and the atrial retractor was placed into the RA. Additional cryoablation was performed in patients with atrial flutter or atrial fibrillation with an enlarged right RA. The RA lesion set consisted of an intercaval lesion extending from the superior vena cava to the inferior vena cava; from this lesion to tricuspid valve annulus, and finally from the first lesion to RA appendage. In patients with tricuspid valve insufficiency, valve was examined, annulus was sized for prosthesis, and pledgeted sutures were implanted. Once all the sutures were completed, they were passed through the annulus of the valve or ring prosthesis outside the thoracic cavity. The valve or ring was removed from its holder and deployed through the soft tissue retractor. The pledgeted sutures of the valve or ring were secured with an automatic mechanical knot fastening system (Cor-Knot, LSI Solution, Victor, NY, USA). The atriotomy was closed using a premade loop suture. Both bulldog clamps were released. After deairing, the aortic CC was released. Subsequently, TEE examination was performed to check any abnormal situation or air trap. The patient was, then, weaned from CPB, cannulas were removed, and protamine was administered.
Clinical, procedural, and postoperative data were prospectively recorded into the institutional database and retrieved for this retrospective review. Mortality was defined as death occurring at any time during the hospital stay and anywhere during a year after the operation.
Statistical analysis
Statistical analysis was performed using the
Predictive Analytics SoftWare (PASW) version 18.0
statistical package (SPSS Inc., Chicago, IL, USA).
Descriptive data were expressed in mean±standard
deviation (SD), median (min-max), or number and
frequency. A p value of <0.05 was considered
statistically significant.
Table 1: Baseline demographic characteristics and postoperative outcomes (n=34)
Table 2: Types of concomitant procedures during robotic-assisted surgery (n=34)
The mean preoperative EuroSCORE values were 5.1±2.5. The mean duration of CPB and CC was 156±69.4 min and 101±42 min, respectively. Normal sinus rhythm was restored in 85% of the patients (24/28) after cryoablation and two patients (5.8%) had permanent pacemaker within a year during follow-up.
There was one (2.9%) mortality in the early postoperative period due to hemorrhage related to the posterior left ventricular wall rupture. No blood product was used in 82.4% of the patients. None of the patients developed renal failure requiring dialysis or permanent stroke. One patient had a transient cerebral event and symptoms totally resolved within two months following the procedure.
Robotic technology demonstrates obvious advantages over traditional video-assisted thoracoscopic surgery. Its three-dimensional (3D) high definition capabilities and articulating wrists allow a greater freedom of movement in an enclosed space compared with traditional long-shafted instruments.[7] Beside the other advantages of robotic-assisted surgery, the da Vinci® robotic technology provides long and thinner shafted instruments with articulating instruments to move with six degrees of freedom, rather than four degrees and eliminates the surgeon's tremor, if present. Moreover, magnified 3D images and dynamic atrial retractor provide excellent exposure to the mitral valve and subannular anatomy allows one to address the entire spectrum of pathological complexity and intervention at more proximity to the surgical field. All these advantages of robotic assistance compared to the conventional or thoracoscopic approach may enhance the probability of valvular repair. The other fact is that it is more difficult to perform the correction of the pathology with straight-shafted and long instruments during direct vision or endoscopic technique versus dexterous robotic arms. In a recent study, Loulmet et al.[2] showed e xcellent results in 500 patients undergoing mitral valve procedure with robotic assistance. The results reflect an overall repair rate of 99.4% (100% in degenerative disease without mitral annular calcification) with 0.6% early mortality and a 1.2% stroke rate. With both conventional median sternotomy or endoscopic technique, this success rate is likely not as applicable as robotics for many patients with complex mitral valve disease.
In the literature, there is a very limited number of studies showing the results of cryoablation procedure with robotic assistance.[8] During one-year follow up, 85% of our patients with preoperative AF had sinus rhythm following cryoablation. The cryoprobe can be molded to conform geometrically to an individual atrial anatomy with the use of robotic forceps. The combination of dynamic LA retraction, improved dexterity using EndowristTM technology (Intuitive Surgical Inc., Sunnyvale, CA, USA), and 3D vision allows surgeon for precise placement of the cryoprobe and avoidance of skips caused by folds in the floor of the LA (Figure 2).
All patients with moderate-to-severe tricuspid valve insufficiency during concomitant robotic mitral valve surgery underwent tricuspid valve repair or replacement in our study. The need for bicaval occlusion necessitates some changes regarding the strategy for cannulation; as such, unlike robotic mitral operations, the venous cannulas at the superior and inferior vena cavas should not reach the RA, but be away, leaving at least 1 to 2 cm of open space for endoscopic bulldog clamps.
Furthermore, robotic ASD closure is technically feasible and safe with a high success and a low complication rate.[9-12] In our study, ASD or PFO was observed in addition to mitral valve pathology in four patients and the defects were closed with primary suture or pericardial patch. All intraoperative measurements including the size of the pericardial patch should be done with a ruler. The magnified robotic images may mislead one to improper sizing. Also, the anatomical position of the interatrial septum may necessitate the use of a 0° endocamera, unlike robotic mitral operations.
However, there are some disadvantages of this technology such as limited availability of robotic systems and high costs. There is also a necessity of a learning curve and the lack of tactile feedback. With the growing experience, robotic surgeons have become familiar with relying on visualization to judge the amount of force being applied to tissues. Future robotic systems would likely incorporate some special sensors to the robotic arms allowing for haptic feedback and precise control of force.[12]
In our program, we do not have any systematic exclusion criteria for robotic mitral valve procedures, although intensive pleural adhesions may complicate the procedure during pleural dissection. Symptomatic coronary artery disease, aortic valve insufficiency, and pectus excavatum may be also other contraindications for this procedure.
The present study report only one-year follow-up period which is one of the main limitations of our study; however, previous studies of long-term results of robotic-assisted mitral valve surgery have demonstrated that survival and durability are similar to those obtained with non-robotic approaches.[2-4] These excellent results in a large series, similar to those of others, emphasize that the results are reproducible.[7] In addition, retrospective nature of our study and the small patient population were some of the other limitations of our report.
In conclusion, robotic-assisted concomitant procedures during mitral valve surgery can be performed with low complication rates in centers with the experience of robotic cardiac surgery. We believe that technological improvements and growing experience would further decrease the suspects related to prolonged operational duration during roboticassisted cardiac surgery.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
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