Abstract
Objective
Atrial fibrillation (AF) is associated with increased early and long-term morbidity/mortality following valve surgery. This study examined long-term influence of concomitant full Cox maze (CM) and mitral valve procedures on freedom from atrial arrhythmia and stroke.
Methods
This sample comprised patients who underwent CM with a mitral valve procedure (N = 473). Data on rhythm, medication status, and clinical events captured according to Heart Rhythm Society guidelines at 6, 9, 12, 18, and 24 months and yearly thereafter up to 7 years.
Results
Mean age was 65 years, mean left atrium size was 5.3 cm, and 15% had paroxysmal AF. Perioperative stroke occurred in 2 patients (0.4%) and operative mortality was 2.7% (n = 13). Return to sinus rhythm regardless of antiarrhythmic drugs at 1, 5, and 7 years was 90%, 80%, and 66%. Sinus rhythm off antiarrhythmic drugs at 1, 5, and 7 years was 83%, 69%, and 55%. Freedom from embolic stroke at 7 years was 96.6% (0.4 strokes per 100 patient-years) with a majority of patients off anticoagulation medication. Greater odds of atrial arrhythmia recurrence during 7 years was associated with longer AF duration (odds ratio [OR], 1.07; P = .001), whereas lower odds were associated with cryothermal energy only (OR, 0.64; P = .045) and greater surgeon experience (OR, 0.98; P = .025).
Conclusions
This study suggests that the addition of CM to mitral valve procedures, even with a high degree of complexity, did not increase operative risk. In long-term follow-up, the CM procedure demonstrated acceptable rhythm success, reduced AF burden, and remarkably low stroke rate. Individual surgeon experience and training may notably influence long-term surgical ablation for AF success.
Keywords: cardiac surgery, atrial fibrillation, mitral valve
Atrial fibrillation (AF) is associated with increased morbidity, decreased survival, and inferior quality of life.1–3 Despite the significant improvement in surgical ablation devices and growing evidence regarding the positive influence of surgical ablation on patient outcomes, surgical ablation for AF is still underperformed and many patients are left untreated.4 Recent guidelines by surgical organizations support the performance of concomitant surgical ablation for AF when indicated. These guidelines clearly state that surgical ablation is effective and safe.5,6 It is especially important to notice that surgical ablation was found to be associated with improved perioperative and late survival and reduced risk of strokes in long-term follow-up.6 It is therefore correct to assume that if AF is left untreated it may be associated with increased long-term mortality and morbidity in patients undergoing valve surgery.7,8 Among the most significant gaps in the current literature is the lack of substantial data regarding the long-term success and potential clinical influence of surgical ablation for AF on outcome. The purpose of this study was to examine the long-term influence of the concomitant full Cox maze (CM) procedure and mitral valve surgery on freedom from atrial arrhythmia and stroke, and to identify the variables associated with long-term success of the CM procedure.
METHODS
Patients who underwent concomitant CM procedures at a single center since September 2005 were part of a prospective follow-up program (N = 714) of which 473patients had a mitral valve procedure. Data on rhythm, medication status, follow-up interventions, and clinical events were captured according to the Heart Rhythm Society (HRS) guidelines at 6, 9, 12, 18, and 24 months and yearly thereafter up to 7 years. Data on survival and clinical events during follow-up were collected throughout the entirety of follow-up. Therefore, data were available for these outcomes even when rhythm status was unavailable. Sinus rhythm status was defined according to HRS guidelines as freedom from atrial arrhythmia > 30 seconds without use of class I/III antiarrhythmic drugs (AADs).9 This study was approved by an institutional review board and written patient consent was waived.
Surgical Procedure
The CM III/IV procedures were performed by multiple surgeons and the lesion set was applied as previously described.10,11 The energy source used for each procedure was based on surgeon discretion. The lesion set for the cryothermal-only procedures was the traditional CM III procedure and for the cryothermal combined with bipolar radiofrequency energy procedures was the CM IV lesion set.10–12 Bipolar radiofrequency was applied 3 to 5 times across the pulmonary veins (Isolator Synergy Clamps; AtriCure Inc, Mason, Ohio). For cryothermal energy only the CryoFlex (10 or 10S; Medtronic, Minneapolis, Minn) or the Cryo 1 Cryo 2 (AtriCure Inc) were used. For cryothermal energy only or in combination with bipolar radiofrequency, the cryolesions were applied for 2 minutes for all lesions crossing the atrioventricular groove both in the right and left atria and the epicardial coronary sinus lesion to complete the left atrial isthmus lesion on the left. The left atrial appendage was managed either by amputation and suture closure or by applying an epicardial clip (AtriCure Inc). In redo cases and minimally invasive right thoracotomy, the left atrial appendage was sutured closed endocardially in 2 layers. Appropriate left atrial appendage closure was confirmed in all cases via transesophageal echocardiography in the operating room.
Patient Management
The management of patients in regard to medications and follow-up interventions after surgery was determined by an institutional protocol.13 Unless contraindicated, all patients received amiodarone at 200 mg twice a day for 5 days after surgery followed by 200 mg daily for 3 months to reduce the risk of early atrial arrhythmia recurrence.14 If patients were in stable sinus rhythm at 3 months after surgery, amiodarone was recommended to be discontinued to allow for at least 6 weeks off the medication by the 6 months follow-up time point. Patients with an amiodarone allergy, history of side effects due to amiodarone, or other clinical contraindications were generally treated with sotalol or flecainide instead, which was prescribed for 3 months after surgery according to the same protocol.
Similarly, unless contraindicated due to high risk for bleeding, all patients were treated with warfarin to maintain international normalized ratio between 2 and 2.5 or higher in applicable cases (eg, mechanical valve implantation). If patients were in stable sinus rhythm off AADs at 6 months after surgery and echocardiography demonstrated a well-excluded or excised left atrial appendage with no signs of blood stagnation in the left heart cavities (ie, smoke), discontinuation of anticoagulation was recommended and patients were maintained on aspirin. Discontinuation of anticoagulation was considered throughout follow-up if patients were qualified, but was under the direction of each individual cardiologist.
Statistical Analysis
All analyses were conducted using IBM SPSS Statistics version 24.0 (IBM Corp, Armonk, NY) and a P value of < .05 two-tailed was considered statistically significant. Continuous data are presented as mean ± standard deviation or median (interquartile range [IQR]) and categorical data are presented as frequency (%). Descriptive statistics were used to illustrate the characteristics and outcomes of the sample (N = 473). Missing values in patient characteristics were present in preoperative left atrium size (n = 22) and duration of AF (n = 33). Multiple imputation was conducted to provide complete data on these 2 variables using left atrium size, duration of AF, and age in the imputation model with 3 iterations. The mean of the 3 iterations was calculated and used to replace the missing values for left atrium size and duration of AF. Patients with mitral valve as the only concomitant procedure and those with mitral and other concomitant procedures were compared on preoperative characteristics and rhythm outcomes using independent-samples t tests or Mann-Whitney U tests for continuous variables and χ2 or Fisher exact test for categorical variables, as appropriate.
Kaplan-Meier survival analysis was conducted to examine freedom from events and mortality during follow-up. A generalized linear mixed model using multivariable binomial logistic regression was conducted to examine the risk factors for recurrence of atrial arrhythmia up to 7 years after surgery. Not all patients in this sample had reached 7 years after surgery, but the mixed model methodology with random intercepts allowed the inclusion of all available follow-up rhythm data and individual-specific random effects. The fixed effects factors included in this model were selected a priori based on clinical and theoretical justification and included age, gender, ejection fraction, left atrium size (cm), duration of AF (years), type of AF as defined by the HRS guidelines (paroxysmal AF vs nonparoxysmal AF), energy source (cryothermia alone vs all others), operative approach (minimally invasive vs median sternotomy), consecutive cases of surgeon experience with surgical ablation at the time of the procedure (continuous variable in 20 case intervals), and mitral valve procedure (repair vs replacement).
RESULTS
The mean age for this sample was 65.3 ± 11.4 years, mean European System for Cardiac Operative Risk Evaluation (EuroSCORE) II was 5% ± 5.4%, and 45% were female patients (Table 1). The mean left atrium size was 5.3 ± 1.0 cm with left atrium size > 5.5 cm in 37% of patients, median preoperative duration of AF was 1.5 years (IQR, 0.2–4.7 years), and 15% of patients with paroxysmal AF type. Preoperative duration of AF was longer than 3 years in 36% and longer than 5 years in 24% of patients. In addition, 9% of patients had left atrium size > 5.5 cm and AF duration > 5 years. Mitral valve was the only concomitant procedure in 46% of patients, 44% had 3 total procedures, and 10% had 4þ procedures. Follow-up rhythm data were available on 92% of eligible patients at 1 year after surgery, 87% of eligible patients at 3 years after surgery, 80% of eligible patients at 5 years after surgery, and 75% of eligible patients at 7 years after surgery. Patients who withdrew or were lost to follow-up did not differ on patient characteristics from the patients with rhythm status available at 7 years after surgery.
TABLE 1.
Characteristic | Total sample (N = 473) | Mitral valve only (n = 217) | Mitral valve + others (n = 256) |
---|---|---|---|
Age (y)* | 65.3 ± 11.4 | 63.9 ± 11.3 | 66.4 ± 11.4 |
| |||
Female | 212 (45) | 102 (47) | 110 (43) |
| |||
Body mass index | 27.1 ± 5.8 | 27.0 ± 5.7 | 27.3 ± 6.0 |
| |||
Ejection fraction (%)* | 54.6 ± 11.0 | 56.2 ± 10.1 | 53.3 ± 11.5 |
| |||
Diabetes | 49 (10) | 16 (7) | 33 (13) |
| |||
Hypertension* | 289 (61) | 122 (56) | 167 (65) |
| |||
Peripheral vascular disease | 27 (6) | 11 (5) | 16 (6) |
| |||
Previous cerebrovascular accident | 26 (6) | 8 (4) | 18 (7) |
| |||
Chronic pulmonary disease | 112 (24) | 46 (21) | 66 (26) |
| |||
Duration of AF (y) | 1.5 (0.2–4.7) | 1.1 (0.2–4.4) | 1.7 (0.3–5.1) |
| |||
Left atrium size (cm) | 5.3 ± 1.0 | 5.3 ± 1.0 | 5.3 ± 1.0 |
| |||
Nonparoxysmal AF type* | 405 (86) | 176 (81) | 229 (90) |
| |||
CHADS2 score ≥2* | 210 (44) | 78 (36) | 132 (52) |
| |||
EuroSCORE II (%)* | 5.0 ± 5.4 | 3.3 ± 3.5 | 6.4 ± 6.3 |
| |||
Elective status* | 400 (85) | 193 (89) | 207 (81) |
| |||
Minimally invasive* | 52 (11) | 48 (22) | 4 (2) |
| |||
Cryothermia only energy source | 258 (55) | 126 (58) | 132 (52) |
| |||
Cases of surgeon experience | 218 (70.5–480.5) | 230 (83–482.5) | 211 (54–476) |
| |||
Concomitant procedures† | |||
CABG surgery | 82 (17) | – | 82 (32) |
Aortic valve surgery | 47 (10) | – | 47 (18) |
Tricuspid valve surgery | 144 (30) | – | 144 (56) |
Values are presented as frequency (%), mean ± standard deviation, or median (interquartile range). AF, Atrial fibrillation; EuroSCORE, European System for Cardiac Operative Risk Evaluation; CABG, coronary artery bypass grafting.
Comparison of mitral valve only and mitral valve + others (P < .05).
Categories are not mutually exclusive.
Rhythm Outcomes
Return to sinus rhythm regardless of AADs at 1, 5, and 7 years was 90%, 80%, and 66%, respectively. Sinus rhythm off AADs at 1, 5, and 7 years was 83%, 69%, and 55%, respectively (Figure 1). At 7 years, monitoring revealed that only 22% of patients with recurrent atrial arrhythmia demonstrated a continuous pattern (Figure 2). The CM procedures in this series were performed by 8 separate surgeons and notable differences in success at 7 years were identified. The more experienced surgeons demonstrated better success than the rest with 50% to 73% at 7 years. Only 1 surgeon had more than 50 patients with at least 7 years of follow-up.
In the group of patients who underwent only mitral valve and CM procedures (n = 217), sinus rhythm regardless of AADs at 1, 5, and 7 years was 92% (153 out of 167), 86% (68 out of 79), and 80% (36 out of 45) and sinus rhythm off AADs at 1, 5, and 7 years was 85% (140 out of 165), 79% (62 out of 79), and 64% (29 out of 45). In contrast, the group of patients who underwent more than mitral valve and CM procedures, had fewer patients in sinus rhythm and sinus rhythm off AADs throughout follow-up. These comparisons reached significance for sinus rhythm regardless of AADs at 3 years (80% vs 90%; P = .035), 6 years (62% vs 86%; P = .004), and 7 years (49% vs 80%; P = .003) and for sinus rhythm off AADs at 3 years (72% vs 85%; P = .008), 5 years (60% vs 79%; P = .010), and 6 years (53% vs 75%; P = .014). In the group of patients with mitral valve repair, return to sinus rhythm regardless of AADs at 1, 5, and 7 years was 92%, 82%, and 73% and sinus rhythm off AADs was 86%, 70%, and 58%, respectively.
Mixed-model logistic regression analysis revealed that greater odds of atrial arrhythmia recurrence during 7 years of follow-up was associated with longer preoperative duration of AF in years (P = .001), whereas lower odds of atrial arrhythmia recurrence was associated with cryothermal energy only (P = .045) and greater cases of surgeon experience (P = .025) (Table 2). For each year increase in duration of AF, there was a 7% greater risk for atrial arrhythmia recurrence during 7 years of follow-up and for each additional 20 cases of surgeon experience, there was a 2% reduction in risk for atrial arrhythmia recurrence. Other factors in the model were not significantly associated with atrial recurrence during 7 years, including age, mitral valve repair, nonparoxysmal AF type, and larger left atrial size (Table 2). The distribution lines presented in Figure 3 highlight the importance of AF duration rather than left atrial size in distinguishing patients in sinus rhythm off AADs at long-term follow-up.
TABLE 2.
Factor | Odds ratio | 95% Confidence interval |
P value |
---|---|---|---|
Age (y) | 1.01 | 0.99–1.03 | .208 |
Female | 1.07 | 0.69–1.66 | .773 |
Ejection fraction (%) | 0.99 | 0.97–1.01 | .430 |
Left atrium size (cm) | 1.06 | 0.85–1.32 | .614 |
Duration of AF (y) | 1.07 | 1.03–1.11 | .001 |
Nonparoxysmal AF type | 1.05 | 0.57–1.94 | .873 |
Surgeon experience | 0.98 | 0.96–0.997 | .025 |
Cryothermia only energy source | 0.64 | 0.41–0.99 | .045 |
Minimally invasive | 0.99 | 0.47–2.06 | .973 |
Mitral valve repair | 0.68 | 0.43–1.06 | .087 |
AF, Atrial fibrillation.
Clinical Outcomes
The incidence of perioperative complications was low for these patients and included the following: pneumonia in 3% (n = 15), perioperative stroke in 0.4% (n = 2), reoperation for bleeding in 2.6% (n = 12), renal failure in 3% (n = 16), renal failure requiring temporary dialysis in 2% (n = 11), and readmissions < 30 days in 11% (n = 52). New pacemakers were implanted in 37 of the 427 patients without a preoperative pacemaker (9%). The indications for pacemaker implantation were sick sinus syndrome in 20 patients (54%), complete atrioventricular block in 10 patients (27%), bradycardia in 4 patients (11%), and sinus node dysfunction in 3 patients (8%). Intraoperative blood products were transfused in 24% of patients (n = 115) and blood products were transfused postoperatively in 32% (n = 149). Specifically, red blood cell units were transfused intraoperatively in 11% of patients (n = 53) and red blood cell units were transfused postoperatively in 25% (n = 120). Median intensive care unit length of stay was 45 hours (IQR, 12–95 hours) and median hospital length of stay was 7 days (IQR, 5–10 days). Operative mortality < 30 days was 2.7% (n = 13) and the observed-to-expected ratio was 0.55 using the EuroSCORE II as the expected value (5%). At discharge, 88% of patients were in sinus rhythm (405 out of 462 patients), 66% were discharged on AADs (314 out of 462 patients), and 92% were discharged on anticoagulation (425 out of 462 patients).
Mean follow-up was 52 ± 37 months (median, 48 months [IQR, 19–77 months]). Preoperative CHADS2 score was ≥2 in 44% of patients and the median CHADS2 score was 1 (IQR, 1–2). Major bleeding events occurred in 44 patients (9%) by 7 years and embolic strokes occurred in 9 patients (2%) by 7 years. For patients with embolic strokes, median CHADS2 score was 2 (IQR, 0.5–2.5), mean left atrium size was 5.2 ± 0.8 cm, median preoperative AF duration was 2.3 years, 4 patients were taking anticoagulation medication at the time of the event for clinical indications, and 5 patients were in sinus rhythm. Of 4 patients not in sinus rhythm at the time of the embolic stroke, 3 were taking anticoagulation medication and 1 had unknown anticoagulation status. Cumulative freedom from embolic stroke at 7 years was 96.6% (95% confidence interval, 0.941–0.992; 0.4 strokes per 100 patient-years of follow-up) (Figure 4). At 7 years, the majority of patients who could clinically discontinue anticoagulation had done so (41 out of 46 patients; 89%) and 87% of patients were off AADs at 7 years. Although only 29% of patients remained on oral anticoagulation medication throughout follow-up, the incidence of embolic stroke was very low. Cumulative survival from the Kaplan-Meier analysis was 77% (95% confidence interval, 0.717–0.823) at 7 years.
DISCUSSION
The results of this study demonstrate that patients undergoing mitral valve surgery and CM III/IV procedures should expect good early and late outcome. The surgical procedures were performed by multiple surgeons achieving acceptable rates of sinus rhythm at 7 years with a notably low stroke rate. The factors associated with atrial arrhythmia recurrence during 7 years were longer preoperative duration of AF, combination ablative energy source (bipolar radiofrequency and cryothermal energy), and lower surgeon experience with surgical ablation.
Since 1987, the CM procedure transitioned from the cut-and-sew technique to a device-based surgical ablation for AF. The only 2 devices that were identified as reliable and consistent for transmural lesions in cases performed with cardiopulmonary support are the bipolar radiofrequency clamp and the cryothermal probes.6 Therefore, this series is unique not only in size and duration of follow-up but also due to the consistent use of these 2 energy sources recognized for consistent transmurality, either as a combination (bipolar radiofrequency and cryothermal) or as a standalone (cryothermal) to perform the CM III/IV procedure.6
The decision making surrounding the inclusion of surgical ablation in the concomitant setting when indicated is still evolving. Currently there is clear variability among surgeons on the degree and type of surgical ablation procedures performed.4,15 The decision is not only dependent on the pathophysiology of AF, but often also related to the unsupported concern of increased risk for morbidity and mortality associated with concomitant surgical ablation. Previous reports by us and by others demonstrated that surgical ablation in the concomitant setting was not associated with increased operative risk.16,17 More importantly recent guidelines clearly documented and recommended addition of surgical ablation to improve perioperative morbidity and mortality.5,6 Another recognized challenge is the inconsistency associated with the type of lesion set and energy sources. The Society of Thoracic Surgeons guidelines clearly state that mitral valve patients with more advanced atrial fibrillation and increased left atrium size should have a biatrial surgical ablation to include the CM procedure because it is associated with a superior outcome.5 The expectations are that these new guidelines and ongoing educational efforts will improve the ability of surgeons to make the right decisions regarding surgical ablation.
In the present study, perioperative mortality and morbidity were acceptable and a low observed-to-expected ratio of 0.55 for mortality was achieved. The safety of the procedure and the potential early influence on outcomes should be considered when operating on patients with coronary artery disease or structural heart disease with AF. The evidence and the recognition of the importance of AF should support the decision-making process to perform surgical ablation for AF when indicated. Long-term follow-up for such patients should be focused on the success in ablating AF, thromboembolic rate, anticoagulation, and survival. The success rate in our series diminished over the 7 years of follow-up and the most important factors associated with recurrence of atrial arrhythmia were longer duration of AF, ablation using a combination of bipolar radiofrequency and cryothermal energy devices rather than cryothermal probes alone, and lower surgeon experience. Our group has observed potential differences in success associated with cryothermal only CM procedures. It is unclear what the mechanism is to explain this difference in outcome, but it is a consistent finding in a few of our recent studies and observations.18 One potential explanation is that the cryothermal devices are not as user-dependent compared with the bipolar radiofrequency devices. There is also a need to improve our understanding of the potential influence of atrial tissue remodeling on the radiofrequency ablation algorithm. It would be very important to design an appropriately powered prospective study to clarify this important result.
In the present study, the distribution of AF duration was shown to be shifted toward higher values in patients with atrial arrhythmia recurrence at 7 years after surgery, whereas the distributions for left atrium size were comparable for patients with and without recurrences at 7 years. This study is not the first to suggest that preoperative AF duration is likely the most important variable directly related to AF that is associated with long-term success of the CM procedure. The group from Washington University reported on their 5-year results with the CM procedure and found that longer duration of AF was significantly associated with failure.19 The duration of AF before surgery may have a direct influence on the degree of atrial tissue remodeling and complexity of the atrial substrate. Therefore, the decision to modify the CM procedure to a simpler left atrial lesion set based on the type of AF may be misleading because patients with long duration of paroxysmal AF may have more advanced disease than realized, especially if there are signs of left atrium enlargement.20,21 Our experience suggests that follow-up should be modified in such patients. Currently, the clinical focus of the referring cardiologist during follow-up is on the non-AF component of cardiovascular disease with no real involvement of the surgeons and electrophysiologists if and when AF recurs. A team approach to these patients could help improve long-term results because AADs and follow-up catheter ablations can improve our understanding of long-term recurrence and patient outcomes.22 Because all patients in this study had mitral valve surgery as well, it would be important to include the status of the mitral valve surgery at the time of failure because it may have a direct influence on left atrial pressure and size. To date there is no information about the potential influence of deteriorated mitral valve surgery and AF recurrence rate, especially when the follow-up period is long enough to detect such changes.
The recently published American Association for Thoracic Surgery guidelines state for the first time the importance of training and guidance to improve surgical treatment of AF.6 In the present study, as in others before, surgeon experience at the time of the procedure was found to be an important factor for long-term success. The CM procedure is composed of multiple steps that each must be performed accurately and precisely. It is also imperative for surgeons to be fully familiar with the nature of different ablation devices as well as all technical aspects related to the application of each lesion to avoid gaps, incomplete ablation lines, and misplaced lesions that may influence patient outcomes. To that end, The American Association for Thoracic Surgery guidelines also highly recommend personal proctorship to surgeons following training when performing their first 3 to 5 surgical ablation cases.
The present study provides unique information on thromboembolic strokes, bleeding complication and anticoagulation. During 7 years of follow-up, freedom from stroke was 96.6% (0.4 strokes per 100 patient-years). Recently, the stroke rate following catheter ablation was demonstrated to be lower than patients in AF, but higher than reported in the present study and with significantly higher rates of treatment with oral anticoagulation medication and bleeding complications.23 The present results are important and demonstrate significant reduction in the risk of thromboembolic and bleeding events. Stroke reduction over time was reported in the past and likely represents a combination of relatively good success rate, lower atrial arrhythmia burden, and management of the left atrial appendage.7,24 When reporting on atrial arrhythmia according to the HRS guidelines, any event longer than 30 seconds is considered a failure to achieve the rhythm goal.9 In our series only 22% had continuous atrial arrhythmia documented at 7 years. Although the long-term monitoring used in the majority of patients in this study was 24-hour Holter, it is reasonable to assume lower atrial arrhythmia burden in the majority of patients. The other important aspect of the procedure is management of the left atrial appendage with the potential influence on the low rate of thromboembolic events even in patients who experienced a recurrence. The relative contribution of each aspect of the procedure on the very low stroke rate and the success in reducing the number of patients on anticoagulation and bleeding complications at follow-up is yet to be determined.25
It is important to recognize that the electrophysiological mechanism of the CM procedure failure was not evaluated in the vast majority of patients in this series and this clinical phenomenon is very common in global practice. Future studies should focus on protocols that will include such an approach as well as a careful assessment of the status of the mitral valve and other valves, if treated in the original surgery, at the time of failure. Such an approach will provide important information regarding the potential association between late hemodynamic changes and recurrence of atrial arrhythmia following surgical ablation.
Limitations
A limitation of this study is that because rhythm status was not continuously monitored, it is possible that patients who are in sinus rhythm at scheduled time points may have experienced atrial arrhythmia recurrences in between, which were not captured. However, an ideal monitoring strategy for patients after surgical ablation for AF has not yet been determined. Implantable devices that continuously monitor have been shown to have high false positives and demonstrated to have no advantage over HRS guidelines for follow-up.26 The Reveal LINQ device (Medtronic) has been shown to have limitations in patients with low AF burden, which is common for patients following the CM procedure, and is also limited by battery life (3 years) and cost.27
It is also possible that the results from this study with highly experienced surgeons may not be generalizable to other centers. Further emphasis on training and increasing mentored surgeon experience can improve the success of CM procedures in combination with mitral valve surgery. Lastly, although descriptive statistics comprised the majority of study analyses, the comparative statistics conducted may have been limited in power by low event rates and further studies are necessary to replicate the results from these analyses.
CONCLUSIONS
In this large cohort study, we reported on 7-year outcomes for patients who underwent concomitant CM III/IV procedures and mitral valve surgery. The safety of this approach is encouraging and replicates findings reported by our group and others. The long-term success rate is acceptable with important influence on outcome associated with the type of energy source, surgeon experience, and training. Avery low stroke rate of 0.4 strokes per 100 patient-years of follow-up was documented with the majority of patients not on oral anticoagulation medication. These findings and the supporting data from recent guidelines should be considered by surgeons when operating on patients with significant history of AF.
Burden of atrial arrhythmias during 7 years of follow-up.
Central Message.
In long-term follow-up, the Cox maze procedure demonstrated acceptable rhythm success, reduced atrial fibrillation burden, and low stroke rate. This evidence should support decision making for surgical ablation for atrial fibrillation.
Perspective.
Surgical ablation for atrial fibrillation remains underperformed despite ablation device improvements and growing evidence on its positive influence. One significant gap in the literature is lack of substantial data regarding long-term success and clinical influence of surgical ablation for atrial fibrillation. This study demonstrated that patients undergoing mitral valve surgery with Cox maze procedures should expect good early and late outcomes.
Abbreviations and Acronyms
- AAD
antiarrhythmic drugs
- AF
atrial fibrillation
- CM
Cox maze procedure
- HSR
Heart Rhythm Society
Footnotes
Read at the 97th Annual Meeting of The American Association for Thoracic Surgery, Boston, Massachusetts, April 29–May 3, 2017.
Webcast
You can watch a Webcast of this AATS meeting presentation by going to: https://aats.blob.core.windows.net/media/17AM/2017-05-02/BallroomABC/05-02-17_BallroomABC_0851_Ad.mp4.
Conflict of Interest Statement
N.A. is a consultant for Medtronic, a member of the speaker’s bureau for AtriCure, proctor and member of the speaker’s bureau for LivaNova, on the advisory board for Nido Surgical, and co-owner of Left Atrial Appendage Occlusion, LLC. All other authors have nothing to disclose with regard to commercial support.
All surgical cases were performed at Inova Fairfax Hospital in Falls Church, Va. Data were collected and maintained by Deborah Lamont, BSN, RN, and Graciela Pritchard, BS, at Inova Fairfax Hospital in Falls Church, Va. The authors thank their colleagues for their contributions.
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