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a Department of Cardiology, Karolinska Institute at Södersjukhuset, Karolinska Institute at Karolinska University Hospital, Stockholm, Sweden
b Department of Cardiothoracic Surgery and Anesthesiology, Karolinska Institute at Karolinska University Hospital, Stockholm, Sweden
c Department of Cardiology, Karolinska Institute at Karolinska University Hospital, Stockholm, Sweden
Accepted for publication July 22, 2008.
* Address correspondence to Dr Lundberg, Department of Cardiology, Södersjukhuset, Stockholm, SE-118 83, Sweden (Email: lundbergcatharina{at}gmail.com).
| Abstract |
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Methods: Thirty-four patients underwent the maze III procedure for paroxysmal (n = 9), persistent (n = 15) or permanent (n = 10) AF. Quality of life was assessed with the Swedish Short Form-36 survey. Mean follow-up time was 35 ± 6 months.
Results: Sinus rhythm was maintained in 32 patients (94%). For all domains except bodily pain, all patients reported substantial worse QoL at baseline as compared with healthy controls. Postoperatively all scores improved significantly to the level of the general population, and for the majority of the scoring items this was observed after 12 months. Improvement was maintained during the remaining observation period.
Conclusions: The maze III procedure significantly improves QoL in patients with AF. The results are consistent during an observation time of 35 months. Based on QoL effects in a long-term perspective, maze surgery should be considered in symptomatic patients with AF refractory to pharmacologic treatment or catheter ablation.
| Introduction |
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In the last two decades, several invasive strategies with intention to cure AF have evolved, among these the maze III procedure. The success rate of this operation has been evaluated in clinical, objective aspects, but there is a lack of data regarding the effects on QoL more than 12 months postoperatively. The aim of this study was to assess QoL after the maze III procedure in a long-term perspective.
| Patients and Methods |
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The mean age of the study group was 57 ± 10 years (range, 33 to 75) and the majority of the patients were male (74%). Nine patients (26%) had paroxysmal, 15 patients (44%) persistent, and 10 patients (29%) permanent AF. The atrial fibrillation was severely symptomatic in all patients and they suffered from dyspnea, dizziness, palpitations, or fatigue. In all patients, several antiarrhythmic drugs had failed or had been withdrawn due to intolerable side effects. The patients had been treated with a mean of 3.7 ± 2 antiarrhythmic drugs (Vaughan Williams class I–IV). Seventeen patients (50%) had tried both classes I and III antiarrhythmic therapy, and 12 patients (35%) had been treated with amiodarone. Twenty-five patients (73%) were on warfarin treatment prior to surgery. Preoperative treatment with anticoagulants was based on the referring cardiologists' preference. Patient characteristics and predisposing factors for AF are depicted in Table 1.
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Quality-of-Life Questionnaires
The QoL was assessed with the Swedish Short Form 36 (SF-36) survey elaborated within the framework of International Quality of Life Assessment (IQOLA) in order to match the original US SF-36 Health Survey Manual and Interpretation guide [8]. The SF-36 is an internationally validated generic health scale frequently used in arrhythmia studies. Our patient material has been compared with an age- and sex-matched population norm. Normative data have been collected from a control group consisting of 8,930 Swedish subjects [8]. The scale evaluates eight health domains: physical functioning, role-physical, bodily pain, general health, vitality, social functioning, role-emotional, and mental health. The scores range from 0 to 100, higher scores reflecting better functional status and well-being. Treatment of missing items and scoring was performed according to the SF-36 manual and a scale score was calculated if a respondent answered at least 50% of the items on that particular scale. The QoL was evaluated before surgery and 6, 12, 24, and 36 months postoperatively. The questionnaire was handed out during visits at the hospital or delivered by mail. Patients who did not return the questionnaire were contacted by phone or by mail. A clinical evaluation including 12-lead electrocardiogram and 24-hour Holter recording was performed annually.
Statistical Analysis and Definitions
All values are expressed as mean ± SD. All patients were compared with the control group using the Student unpaired t test. The differences between baseline and the following 36-months postoperative values were tested using analysis of variance for repeated measures. Statistical significance was selected at p < 0.05. During the study, the definitions of AF elaborated by the International consensus on nomenclature and classification of atrial fibrillation were used [9].
| Results |
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Apart from reduced arrhythmia-related symptoms, there was no change in cardiovascular symptoms during the observation time, with the exception for 2 patients. One patient who had mitral stenosis as primary indication for surgery improved substantially regarding exertion dyspnea. Aggravated symptoms were observed in one patient who, for unknown reasons, postoperatively developed pulmonary hypertension and congestive heart failure (NYHA class II).
Perioperative complications in general were minor and transient. Three patients developed symptoms of sinus node disease requiring pacemaker implantation postoperatively. One patient developed a third degree atrioventricular block due to the surgical procedure itself and received a pacemaker, remaining in sinus rhythm.
Five patients (15%) were on warfarin treatment at the end of follow-up. They had a history of thromboembolism preoperatively or had other factors predisposing for thromboembolic events.
SF-36
Mean clinical follow-up time was 35 ± 6 months. Before surgery, patients reported significantly lower QoL scores in all domains except for bodily pain, as compared with the age- and sex-matched control group of the general Swedish population. The lowest preoperative scores were obtained for role-physical and vitality (Table 1; Fig 1). The preoperative scores were compared with the scores obtained at 6, 12, 24, and 36 months follow-up. Missing data were 2%, 15%, 6.9%, 12%, and 5.9%, respectively. All subscales of the SF-36 significantly improved after the maze III procedure except for bodily pain that remained unaltered (p = not significant). Physical functioning, vitality, social functioning, role-emotional, and mental health reached the level of the Swedish population 12 months postoperatively. General health improved earlier, while role-physical significantly differed from the control group until 24 months follow-up. The greatest change in scoring was seen for the items role-physical, vitality, and role-emotional (Table 2;
Fig 1). The improvement of QoL was consistent during the rest of the observation time.
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| Comment |
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The classic maze III procedure has a high success rate in restoring and maintaining sinus rhythm. Freedom from AF has been reported in 64% to 97% of patients in long-term studies with a mean follow-up period of at least 4 years [16–19]. A statistical significant improvement in QoL after the maze III procedure has previously been shown at one-year follow-up in two studies, with 25 and 18 patients, respectively [20, 21], but there is limited documentation on the long-term effects on QoL.
The aim of this study was to evaluate health-related QoL after maze surgery in a long-term perspective of 35 months. The QoL, assessed with SF-36, was markedly impaired preoperatively compared with age- and sex-matched Swedish controls [8]. We found that QoL significantly improved and reached the level of the Swedish control population after the maze III operation in all items except for bodily pain, which was normal already before intervention [8]. The improvement in QoL was maintained during a follow-up of 35 months.
Hemels and colleagues [17] recently presented a study of 29 patients, in which there was no statistically significant difference in reported QoL between the maze patients and healthy control subjects at the end of an observation period of a mean of 4.8 years. In this report, mean age was 48 ± 6 years, and all patients underwent a stand-alone maze III procedure due to lone AF [17]. In our study, mean age was 57 ± 10 years, and 17 patients had structural heart disease with concomitant surgery performed in 8 patients. Despite these differences in patient selection, the results in both studies are very similar regarding both objective measures as restored sinus rhythm and in improvement of QoL during prolonged follow-up. Noteworthy is that in both studies the patients were predominantly male (74% to 93%), why the results should be applied on a female population with caution [17].
The maze III procedure is an open heart procedure that has been perceived as complex and highly invasive, and therefore it has not been widely adopted. Instead, in recent years, surgical ablation procedures have evolved mostly for patients with AF undergoing concomitant surgery. In this study, as well as in other reports [16–18], use of the classic maze III procedure was followed by a high success rate in restoring sinus rhythm and a considerable and consistent improvement in QoL. Thus, despite its invasiveness, maze surgery should be considered in selected severely symptomatic patients with AF refractory to pharmacologic treatment or catheter ablation.
In most patients in this study, AF was the primary indication for surgery, but a few had concomitant mitral valve surgery or coronary bypass grafting. However, results were similar in the study of Hemels and colleagues [17], in which no concomitant procedures were performed. The improvement in one to several domains of QoL after surgery can be secondary to pharmacologic treatment, and a reduction of side effects. The main limitation of this study is the small sample size and that the majority of the patients were men.
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