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J Thorac Cardiovasc Surg 1998;116:220-224
© 1998 Mosby, Inc.
Surgery for Adult Cardiovascular Disease |
From the Department of Cardiovascular Surgery, National Cardiovascular Center, Osaka, Japan.
Received for publication June 27, 1997. Revisions requested Oct. 20, 1997; revisions received March 4, 1998. Accepted for publication March 5, 1998. Address for reprints: Fumitaka Isobe, MD, Department of Cardiovascular Surgery, Osaka National Hospital, 2-1-14 Hoenzaka, Chuo-ku, Osaka, 540-0006, Japan.
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| Introduction |
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| Patients and methods |
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Surgical procedures
The operative procedure was mitral valve surgery alone in 12 patients. As the concomitant procedure, aortic valve surgery was done in six patients, combined aortic and tricuspid valve surgery in one patient, tricuspid valve surgery in nine patients, and coronary bypass surgery in two patients. Two patients underwent reoperation. Mitral valve surgery involved valve repair in eight patients and valve replacement in 22 patients (all with mechanical valves). Preoperative thromboembolic episodes occurred in six patients: five to the brain and one in the coronary artery.
The maze procedure we used was the same as the Cox maze III, except that, if the sinus node artery was a left posterior type arising from the left circumflex artery and running between the left atrial appendage and left superior pulmonary vein, the incision between the isolation incision for the pulmonary veins and the stump of the left atrial appendage was abandoned so as not to injure the sinus node artery and was moved to the area between the stump of the left atrial appendage and the posterior mitral anulus with a small cryolesion at the anulus like another mitral incision (Fig. 1).
8 We routinely used coronary angiography to define the type of sinus node artery before the operation. If it was a left posterior type or if coronary angiography was not done because of an emergency operation, we used this modification. All patients in this series were operated on by the same surgeon.
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Statistical analysis
Continuous variables were compared with the Mann-Whitney U test. The statistical analysis was performed with a software package (StatView J-4.5; Abacus Concepts, Inc., Berkeley, Calif.).
| Results |
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No patient died. We followed up all of the patients at the outpatient clinic. The follow-up period ranged from 0.8 to 3.4 years (2.12 ± 0.85 years), a total of 63.7 patient-years. One patient in the SR group had a small lacunar infarction at 2.8 months after mitral valve replacement with a mechanical prosthesis.
Postoperative rhythm
Among 30 patients undergoing the complete operation, SR was restored in 27 patients (90%), and AF persisted in three patients (10%). AF did not recur after the operation in any patient. We evaluated the cardiac rhythm at more than 6 months after the operation. Even in the SR group, two patients showed a tendency toward the development of the sick sinus syndrome with occasional junctional bradycardia, and one other patient had sick sinus syndrome with atrioventricular reentrant tachycardia.
Because an antiarrhythmic drug was necessary to control atrioventricular reentrant tachycardia, it worsened sinus node function, and pacemaker implantation was required. This was the only patient who needed a pacemaker in the group (3.3%).
Preoperative clinical parameters in relation to postoperative status
There were statistically significant differences of some parameters between the groups, as shown in Fig. 2. A low f-wave voltage, a large CTR, a large left atrium, and a long duration of AF were predisposing factors for the postoperative persistence of AF (Fig. 2).
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| Discussion |
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With the maze I procedure, Cox encountered much sinus node dysfunction necessitating the implantation of a pacemaker. Therefore he modified his procedure to maze III to prevent postoperative sinus node dysfunction.
There are three patterns of sinus node artery anatomy: the right, left, and posterior types.
10 The right sinus node artery originates from the proximal right coronary artery, passes across the anteromedial wall of the right atrium, and usually passes in a counterclockwise manner in relation to the superior vena cava and then penetrates the atrial septum below the interatrial bundle. The left sinus node artery arises from the proximal portion of the left coronary artery and courses through the left anterior ramus of the interatrial bundle. The site of the origin of the left posterior sinus node artery varies, but its initial course over the lateral wall of the left atrium between the atrial appendage and the left superior pulmonary vein is very characteristic.
The maze I procedure had the potential to damage all three types of sinus node artery. Cox moved the transverse atriotomy across the dome of the left atrium posteriorly and finally placed the septal incision posterior to the superior vena cava in the maze III procedure. The incision between the isolation incision for the pulmonary veins and the stump of the left atrial appendage was not changed in all types of maze procedure. Therefore injury to the left posterior sinus node artery could not be avoided even with the maze III procedure, and the occurrence of sick sinus syndrome, which necessitated the implantation of a pacemaker after maze III, was reported to be as high as 25%.
3 We therefore moved this incision to the area between the stump of the left atrial appendage and the posterior mitral anulus and applied a small cryolesion at the anulus like another mitral incision (Fig. 1). Apart from this modification, the procedure was the same as the original maze III involving a "cut and suture" technique. Even though this modification was used, it was still possible for the peripheral portion of the sinus node artery just before entry into the sinus node to be cut when making the incision on the lateral wall of the right atrium. In our series, just one patient needed a pacemaker (3.3%) because of bradycardia after medication for atrioventricular reentrant tachycardia. Two other patients had occasional junctional bradycardia, suggesting a tendency for sick sinus syndrome, but it was not severe enough to need a pacemaker. Accordingly, our modification seems to be effective to preserve all types of blood supply to the sinus node, and damage to the peripheral portion of the sinus node artery by the incision of the right lateral atrial wall might not impair its function severely.
In this study, we applied a combination of the maze procedure and mitral valve surgery to consecutive patients who had chronic AF with mitral valve disease irrespective of the duration of AF, the severity of symptoms, and the size of the heart.
Chua and associates
11 reported that mitral valve repair should be done before or soon after the onset of AF to maximize the chance of postoperative SR and all of the patients in their study with a recent onset AF (within 3 months) resumed SR. In our series, the shortest duration of AF was 1.5 months, and this patient recovered SR after operation. However, it was usually difficult to define the exact onset of AF, so we calculated the duration from the earliest date when AF was reliably documented in the medical records. Thus there is a strong possibility that the calculated duration of AF was shorter than the true duration. Therefore if the exact onset of AF was clear and the duration was under 3 months, there might be no indication for the maze procedure in such a patient. On the other hand, the postoperative AF group had a significantly longer duration of AF before operation, and they showed no recovery of left atrial function even after the restoration of SR.
The patients who did not experience the resumption of SR all had severe dilation of the left atrial cavity, with a CTR of more than 70% and a left atrial systolic dimension of more than 80 mm. They also had a lower f-wave voltage and a longer duration of AF than the other patients.
Three reoperation cases excluded from present study showed AF after operation after the modified maze procedure with cryolesion as a substitute for real incision because it was thought to be dangerous to use the cut and suture technique because of the severe calcification and adhesions in the area between the left atrial appendage and the mitral anulus.
Among the patients in whom SR was restored after operation, 66.7% of the left atria and 100% of the right atria were functioning. The duration of AF was significantly longer in the patients with no left atrial function detected after operation. However, atrial function was still not normal in those with recovery, because the A/E ratio was one half to one third of the normal value as in other reports.
6,12,13 The reason for the low rate of left atrial functional recovery might be severe injury of the left atrial myocardium by myocarditis and/or mechanical stress as the result of the mitral valve lesion, because the right atrium showed a contrasting excellent result.
The other important advantage of the maze procedure is the prevention of thromboembolic events. In our series, no patient had an apparent thromboembolic event after the operation, but one patient with SR had a small lacunar infarct with complete recovery at 2.8 months after mitral valve replacement with a mechanical valve. Therefore it seems possible that the maze procedure diminishes the occurrence of thromboembolic events after mitral valve replacement. However, it is too early to decide whether the maze procedure has any efficacy for preventing thromboembolism. We need more patients and a longer follow-up period.
With respect to the need for anticoagulation therapy, mitral valve repair is better than replacement as the type of mitral valve surgery to perform with the maze procedure. A tissue valve is also more suitable than a mechanical valve for replacement. However, a tissue valve is not recommended for younger patients (under the age of 70 years) because of its limited durability in the mitral position.
14-16 There are arguments that the maze procedure may not be beneficial because anticoagulant therapy is mandatory for patients with a mechanical valve.
17 Two thirds of our patients had restored left atrial function, and a regular cardiac rhythm might contribute to reducing the risk of thromboembolism even in patients whose atrial function is impaired. Therefore the maze procedure might still benefit patients undergoing mitral valve replacement with a mechanical valve as well as those undergoing valve repair and valve replacement with a tissue valve.
Various methods of modifications of the maze procedure have been developed, including cryolesion as a substitute for actual incision
6 or a limited procedure at the left atrium (partial maze procedure).
5,7 Myocardial cryolesions are usually created by a 1- to 2-minute application of a 6 to 10 mm cylindrical probe cooled to 60° to 70° C with nitrous oxide or carbon dioxide. With a carbon dioxide cryoprobe (6 mm diameter) with a head temperature of 70° C applied for 1 to 2 minutes to a normothermic canine heart during cardiopulmonary bypass, an iceball 19 ± 1 mm in diameter was created.
18 A lower cryoprobe temperature resulted in a larger cryolesion, and the volume of the cryolesions created during profound myocardial hypothermia in the absence of coronary artery perfusion was 6 to 10 times greater than the volume of cryolesions created in normothemic, perfused myocardium.
19 To achieve interruption of electrical conduction by the creation of cryolesions, profound hypothermia might be necessary, and cryosurgery would usually be done with cardiac arrest induced by the cool cardioplegia. Therefore use of cryolesions as a substitute for actual incision might produce a wide band of frozen atrium that would become noncontractile myocardium and would oppose the purpose of the maze procedure. In the case of limited maze procedures, these methods have no theoretic support from experiments. Therefore we will continue to use "cut and suture" techniques as in the original maze III procedure.
In conclusion, the indications for the maze procedure combined with mitral valve surgery appear to be as follows: the maze III procedure should be done for patients with AF lasting more than 3 months before operation, a CTR of less than 70%, and a left atrial systolic dimension of less than 80 mm. Patients should be excluded if they have a CTR of 70% or more and a left atrial systolic dimension of 80 mm or more, although potential exclusions would be those who have a low f-wave voltage or those in whom the complete procedure cannot be performed because of extensive calcification and severe atrial adhesions.
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