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1Zena and Michael A Wiener Cardiovascular Institute, Marie-Josee and Henry R Kravis Center for Cardiovascular Health, Mount Sinai School of Medicine, Box 1030, New York, NY 10029, USA
Correspondence to: S A Lubitz steven.lubitz@mssm.edu
Cite this as: BMJ 2008;336:819-26
<DOI> 10.1136/bmj.39513.555150.BE http://www.bmj.com/content/336/7648/819
A trial fibrillation is the most common arrhythmia in clinical practice and is associated with significant morbidity and mortality.1 Catheter ablation is increasingly being used to treat atrial fibrillation, although it is not suitable for all patients.2 Referring doctors must confront challenges such as the appropriate selection of patients for ablation and proper management of patients after the procedure, and must be familiar with the expected outcomes. Many unanswered questions exist surrounding the appropriate application of this technique.
This review summarises current ablative techniques and emphasises the appropriate application and limitations of catheter ablation on the basis of recent clinical trials and guidelines.
After the transvenous insertion of catheters into the right atrium, the left atrium is accessed (in the absence of an atrial septal defect or patent foramen ovale) by trans-septal puncture. Catheter positioning, as well as the anatomy of the pulmonary veins and left atrium, are confirmed by fluoroscopy, pulmonary venography, three dimensional electroanatomical mapping, intracardiac echocardiography, computed tomography, remote guidance using magnetic resonance imaging, or combinations of these techniques. Through the application of thermal energy—most commonly by radiofrequency or cryothermy—injury is induced to the myocardium. Ablation can be done in atrial fibrillation or sinus rhythm.
SOURCES AND SELECTION CRITERIA
We searched all entries in PubMed through September 2007 with the medical subject headings “atrial fibrillation”, “catheter ablation”, and “anti-arrhythmia agents”. We reviewed the reference lists of retrieved articles to identify any additional relevant articles for inclusion. Whenever available, we chose randomised controlled trials and meta-analyses over prospective cohort studies. When these were not available, we cited retrospective studies. We included other references if judged relevant for the purposes of discussion. Thus this work is not an exhaustive review but represents an overview of current clinical and technical aspects pertaining to catheter ablation of atrial fibrillation.
SUMMARY POINTS
The underlying factors contributing to atrial fibrillation are complex and multifactorial (fig 1). Current catheter ablation techniques target susceptible atrial substrate, electrical triggers, and autonomic tone, factors that are considered to be important for the initiation and maintenance of atrial fibrillation (box 1). Structural and electrical properties of the atria, such as fibrosis of the atrial myocardium, electromechanical remodelling, and genetic mutations affecting ion channels and gap junction proteins, are critical factors in the genesis of atrial fibrillation. Initial success with attempts to stop atrial fibrillation by creating linear incisions in the atria, as in the surgical Cox-Maze procedure, and replication of these lesions with radiofrequency catheter ablation, supported the concept of susceptible atrial substrate, although the contribution of pulmonary vein isolation was probably overlooked with these early techniques.
Ectopic pulmonary vein foci that communicate with the left atrium through muscular sleeves3 (figs 2 and 3) were later discovered to trigger atrial fibrillation in most patients,4 leading to targeted ablation within the pulmonary veins. As a result of pulmonary vein stenosis often associated with this procedure, techniques emerged that attempted to isolate the left atrium from the pulmonary veins. Predominant approaches included segmental ostial ablation at sites where pulmonary vein signals were detected,5 and anatomically guided circumferential pulmonary vein ablation encircling individual or ipsilateral pairs of pulmonary veins (fig 4).6
Recently, ablation of ganglionated plexi innervating the pulmonary veins and left atrium has emerged with recognition that autonomic tone contributes to the genesis of atrial fibrillation.7, 8 Additionally, targeting complex fractionated electrograms—signals with rapid deflections and short cycle lengths corresponding to areas of wavebreak, vagal innervation, slow conduction, or re-entry—has become increasingly successful.9, 10
The evolution of ablation techniques was illustrated in a survey of centres carrying out atrial fibrillation ablation worldwide between 1995 and 2002.2 In 1995, isolation of pulmonary veins was not reported by any of the centres. Between 1998 and 1999, after elucidation of the role of pulmonary vein triggers in the genesis of atrial fibrillation,4 selective ablation of triggers represented the preferred technique in about 46% of cases. By 2002, pulmonary vein isolation represented 80% of all atrial fibrillation ablation techniques. During the surveyed dates the frequency of the procedure grew from 18 procedures in 1995 to 5450 in 2002.
The multitude of ablation approaches is testimony to the multifactorial causes of atrial fibrillation. Despite the mechanistic rationale that justifies each specific ablative technique, approaches have overlapping effects. For example, during pulmonary vein isolation—the most widely used technique—ablation lines may encompass critical portions of the left atrium. Thus the technique may have substrate modification effects beyond the explicit intention of merely disrupting signal transmission from pulmonary veins to the left atrium.
Fig 1 Factors contributing to development of atrial fibrillation. Clinical factors predisposing patients to atrial fibrillation are complex and may be inter-related. *These conditions may result in structural changes such as left atrial enlargement or stretch, myocardial hypertrophy, or left ventricular systolic dysfunction
The primary end point in most trials of ablation is recurrent atrial fibrillation or atrial arrhythmias in the absence of antiarrhythmic drugs, excluding early and often transient tachyarrhythmias that occur in up to half of patients within the first three months.11, 12, 13 These are thought to result from recovered pulmonary vein conduction or proarrhythmic effects of ablation itself and are often treated with cardioversion, antiarrhythmic drugs, and repeat ablation.
Fig 2 Intracardiac electrogram (recorded at a paper speed of 100 mm/s) from a patient with paroxysmal atrial fibrillation undergoing pulmonary vein isolation. Patient is in sinus rhythm at 50 bpm (cycle length=1200 ms), seen on surface electrograms (I, aVF, V1, V6). An intracardiac atrial electrogram is detected at the same cycle length by a catheter in the coronary sinus, preceding the surface electrogram deflection. A circular lasso catheter in the left upper pulmonary vein (T5) records pulmonary vein potentials occurring at a cycle length of 300 ms and dissociated from sinus activity. Other measurement points from lasso catheter were removed for simplicity
BOX 1: TARGETS OF CURRENT ABLATION TECHNIQUES
*Cellular electrical and structural remodelling occur as a result of previous atrial fibrillation, predisposing to subsequent episodes of atrial fibrillation
Fig 3 Muscular sleeves extending into pulmonary vein. Specimen from pulmonary vein showing muscular sleeves (arrowhead) extending from left atrium into pulmonary vein. Haematoxylin and eosin, ×2 magnification
Initial reports described success rates between 22% and 85%, with better results observed for patients with paroxysmal (self terminating and lasting less than seven days) rather than persistent (not self terminating) or permanent atrial fibrillation (terminating attempts failed or were not attempted). Randomised trials comparing pulmonary vein isolation in symptomatic patients, most with paroxysmal disease, reported success rates ranging from 31% to 88%, with no clearly superior strategy (table 1).14, 15, 16, 17, 18 Long term results are limited by follow-up of generally no more than one year in most trials. Outcomes may have been influenced by the different patient populations studied, ablative techniques and end points utilised, and number of repeat ablations.
Fig 4 Electroanatomical map of left atrium in patient with persistent atrial fibrillation undergoing pulmonary vein isolation. Computed tomogram before ablation procedure is merged with three dimensional electroanatomical map of left atrium created during ablation. Left atrium is viewed from a posterior (panel A) and superior (panel B) orientation, with left atrium appendage on left. Dots represent sites of delivery of radiofrequency energy. Radiofrequency lesions encircle both left and right pulmonary veins, avoiding posterior wall of left atrium, and a line of radiofrequency ablation is seen along the mitral isthmus (region extending from left inferior pulmonary vein to mitral annulus)
Moreover, substantially different methods for surveillance of rhythm were used, such as 12 lead electrocardiography, Holter monitoring, or event monitoring as prompted by symptoms. These methods have varying diagnostic accuracy for detecting occult arrhythmias. As few studies reported the incidence of recurrent asymptomatic atrial fibrillation after ablation, the benefits may have been overestimated. Available data show that asymptomatic recurrences occur in 2% to 16% of patients within the first year of the procedure (table 1),15, 16, 18 although recurrences were prevalent in only 2% of patients with paroxysmal atrial fibrillation two years after ablation in one single centre analysis.19
A consensus statement by the Heart Rhythm Society, European Heart Rhythm Association, and European Cardiac Arrhythmia Society states that patients should be evaluated with electrocardiography within three months of ablation, every six months for the next two years, and assessed with event monitors if they have recurrent palpitations (box 2).20 These are similar to recommendations made by the Venice Chart international consensus group.22 The benefits of more extensive surveillance after ablation are unclear.
Heterogeneity in the methods of published trials limits the ability to compare different techniques (table 1). A recent meta-analysis concluded that substrate ablation without pulmonary vein isolation was associated with no atrial fibrillation in 75% of patients at six months, whereas circumferential pulmonary vein isolation was successful in 67%.23 Substrate ablation seems more important with persistent or permanent atrial fibrillation than with paroxysmal disease, where isolation of triggers may suffice. None the less, a consensus statement by electrophysiological societies in the United States and Europe recognises that electrical pulmonary vein isolation forms the basis of most successful catheter ablations (box 2).20 The ideal approach depends on individual patient characteristics and the chronicity of atrial fibrillation, and may require a combination of strategies (fig 5).
Table 1 Randomised controlled trials comparing efficacy of pulmonary vein isolation techniques (segmental ostial ablation versus circumferential pulmonary vein ablation) for prevention of recurrent atrial fibrillation
CPVA=circumferential pulmonary vein ablation; SOA=segmental ostial ablation; NR=not reported.
*Includes assessment at routine clinic appointments.
†Includes death, cardiac tamponade, transient ischaemic attack or stroke, symptomatic or >50% pulmonary vein stenosis, atrio-oesophageal perforation, vascular complications, or phrenic nerve injury.
Although a strategy for rhythm control with antiarrhythmic drugs or electrical cardioversion offers no survival advantage over a rate control strategy, retrospective analyses of major trials show that maintenance of sinus rhythm may be associated with improved survival24 and quality of life.25 In the atrial fibrillation follow-up investigation of rhythm management (AFFIRM) trial, non-cardiovascular deaths in the rhythm control arm exceeded those in the rate control arm,26 fuelling speculation that adverse effects of antiarrhythmic drugs may obscure the benefits of maintaining sinus rhythm and justifying the comparison of catheter ablation with medical therapy for achievement of sinus rhythm.
Fig 5 Proposed algorithm for management of symptomatic patients with atrial fibrillation referred for rhythm control. Solid lines represent established pathways supported by clinical evidence, guidelines, or expert consensus documents. Dashed lines represent less established pathways. *Appropriate antiarrhythmic drug therapy is outlined in practice guidelines.1 †Underlying stroke risk can be assessed using the CHADS 2 score21; one point each is assigned for a history of heart failure, hypertension, age >75, diabetes mellitus, and two points for previous cerebral ischaemia. Aspirin is generally recommended if the score is 0, aspirin or warfarin if the score is 1, and warfarin if the score is ≥2.1 ‡First line therapy with catheter ablation may be appropriate for patients in whom long term antiarrhythmic drug therapy may be harmful or for those who want to avoid antiarrhythmic drugs. Presence of a left atrial thrombus is an absolute contraindication to catheter ablation. §Summary of surgical techniques for restoration of atrial fibrillation can be found in Heart Rhythm Society consensus document.20 ¶Potential measures include permanent pacing or implantable atrial defibrillators for restoration of sinus rhythm.1 **Repeat catheter ablations should generally be delayed until at least three months after the initial procedure. No consensus exists on what constitutes the maximum number for repeat attempts. ††Substrate ablation in form of linear ablation, or ablation of complex fractionated electrograms or sites of autonomic innervation. Adjunctive ablation may be appropriate in patients with paroxysmal atrial fibrillation in whom an initial attempt has been unsuccessful
In a pilot trial of 70 patients with predominantly paroxysmal atrial fibrillation, pulmonary vein isolation was compared with antiarrhythmic drugs as first line therapy (table 2).27 Freedom from symptomatic atrial fibrillation at one year after a single procedure was 87% compared with 37% for patients treated with antiarrhythmic drugs, most of whom received flecainide. In another study, pulmonary vein isolation in conjunction with antiarrhythmic drugs was compared with antiarrhythmic drugs alone in a group of 137 patients with mostly paroxysmal atrial fibrillation.28 Freedom from atrial arrhythmias at one year was 56% in the ablation and antiarrhythmic drugs group and only 9% in the antiarrhythmic drugs alone group. More recently, pulmonary vein isolation was superior to a pharmacological strategy consisting of flecainide, sotalol, or amiodarone in a group of 198 patients with paroxysmal atrial fibrillation.29 Daily transtelephonic monitoring and periodic Holter monitoring showed that freedom from atrial tachyarrhythmias at one year was 86% in the ablation group and 22% in the antiarrhythmic drug group.
BOX 2: SUMMARY OF A RECENT CONSENSUS STATEMENT ON CATHETER ABLATION OF ATRIAL FIBRILLATION*
Indications
Contraindications
Technique
Thromboembolism prophylaxis after ablation
Minimal surveillance and monitoring after ablation
Repeat procedures
The success of ablation improved to 93% when including second procedures. Two other randomised trials have reported results favouring ablation over medical therapy in patients with predominantly paroxysmal disease during one year of follow-up.30, 31 Catheter ablation specifically in persistent atrial fibrillation was addressed in a trial of 146 patients randomised to treatment with amiodarone and electrical cardioversion alone for up to three months, or in combination with pulmonary vein isolation.32 Freedom from atrial fibrillation or atrial flutter one year after ablation was 74% in the absence of antiarrhythmic drugs, including repeat ablations in 32% of patients. In the intention to treat analysis, 58% of patients in the control arm were free of atrial fibrillation, although 77% crossed over to the ablation arm.
These trials also reported that ablation improves symptoms or quality of life,27, 30, 31, 32 enhances ejection fraction,32 reduces left atrial size,29, 32 and decreases hospital admissions.27, 29 One non-randomised trial reported improved survival with ablation.33
Although traditional strategies for rhythm control do not seem to be cost effective when compared with rate control strategies for the management of atrial fibrillation,34 a recent decision analysis comparing rate control, rhythm control with antiarrhythmic drugs, and catheter ablation in cohorts of patients aged 55 and 65 years, concluded that ablation is cost effective for patients at moderate risk of stroke but not at low risk.35 A cost comparison of ablation and medical therapy using the Canadian Registry of Atrial Fibrillation showed that ablation was initially more expensive than medical therapy, although it was equivalent in cost about four years after ablation, justifying ablation as a “fiscally sensible alternative.”36 Ablation was associated with an initial cost ranging from $C16 278 (£8157; $10 661; €16 441) to $C21 294, with subsequent annual costs of $C1597 to $C2132, whereas costs for medical therapy ranged from $C4176 to $C5060 annually. Caution must be used in interpreting this analysis considering the lack of long-term follow up to support the durable effectiveness of ablation.
BOX 3: POTENTIAL MAJOR COMPLICATIONS OF CATHETER ABLATION OF ATRIAL FIBRILLATION
Table 2 Randomised controlled trials comparing efficacy of catheter ablation versus medical therapy for prevention of recurrent atrial fibrillation
CPVA=circumferential pulmonary vein ablation; SOA=segmental ostial ablation.
*Includes assessment at routine clinic appointments.
†Includes death, cardiac tamponade, transient ischaemic attack or stroke, symptomatic or >50% pulmonary vein stenosis, atrio-oesophageal perforation, vascular complications, or phrenic nerve injury.
‡According to study protocol, patients treated with catheter ablation also received antiarrhythmic drug therapy.
§Various combinations of antiarrhythmic drugs were used.
¶Not specified but 88 class I, 39 class II, 59 class III, and 6 class IV agents were used.
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In summary, evidence from several small trials suggests that isolation of the pulmonary vein is more efficacious than medical rhythm control therapy in select patients with highly symptomatic, drug refractory atrial fibrillation, although long term outcomes remain unclear.
The most undesirable complications of ablation are atriooesophageal fistulae, pulmonary vein stenosis, cardiac tamponade, stroke, and phrenic nerve injury (box 3 and tables 1 and 2). In a randomised trial comparing pulmonary vein isolation techniques, the incidence of pulmonary vein stenosis was 9%, and cerebrovascular events occurred in up to 6% of patients.15 In a worldwide survey of more than 7000 patients, major complications were reported in 6%.2 These included periprocedural death (0.05%), cardiac tamponade (1.2%), stroke or transient ischaemic attack (0.9%), and pulmonary vein stenosis (1.6%). Although lower complication rates reported in many controlled trials are reassuring, procedures done outside of clinical trials and by less experienced operators might result in more adverse effects.
In most trials of ablation, anticoagulation was stopped after three to six months in the absence of recurrent atrial fibrillation without any significant incidence of thromboembolism during follow-up. The baseline risk for stroke as measured by validated tools such as the CHADS 2 index,21 was not, however, reported. In a retrospective analysis of 755 patients, 65% of whom had paroxysmal atrial fibrillation, the incidence of thromboembolism was 0.9% within the two weeks after ablation, and 0.2% between six and 10 months afterwards.37 None of the patients in whom anticoagulation was discontinued had a stroke, including about half of whom had at least one risk factor.
Recent guidelines call for mandatory warfarin therapy for at least two months after ablation (box 2),20 although clinical trials have not specifically assessed the optimal antithrombotic strategy. Until further data confirm the reduced stroke risk and ensure the absence of recurrent atrial fibrillation in a large and heterogeneous population, patients should continue to receive thromboembolism prophylaxis on the basis of their initial stroke risk in accordance with published guidelines.1, 20
The presence of a left atrial thrombus is an absolute contraindication to ablation,20 whereas the inability to anticoagulate represents a relative contraindication. To date, participants enrolled in trials of atrial fibrillation ablation overwhelmingly had highly symptomatic, drug refractory, paroxysmal disease. Most were aged less than 65, had ejection fractions greater than 50%, and did not have markedly enlarged atria. The prevalence of structural heart disease was variable, occasionally constituting more than half of the participants. The duration of atrial fibrillation was generally between three and seven years. Only one randomised controlled trial has compared ablation as first line therapy with medical therapy, although the results were favourable.27 Similarly, one non-randomised prospective controlled trial assessed ablation in patients with congestive heart failure.38 The study showed achievement of sinus rhythm in 78% of patients after about one year, with repeat ablations required in half of the patients, and reported improvements in functional status, symptoms, and ejection fraction with ablation. Recommendations for ablation reflect trial characteristics (box 2).20, 22
Conclusion
Rhythm control of atrial fibrillation is receiving a resurgence of attention with the recognition that catheter ablation may offer benefits not achieved with pharmacological therapy. At present, patients considering ablation must be willing to undergo a prolonged procedure with associated risks, and a significant likelihood of recurrent disease that may necessitate a repeat ablation. As the understanding of mechanisms of atrial fibrillation evolves, catheter ablation techniques will follow suit. Large scale controlled trials assessing ablation in diverse patient populations are necessary for more precise clinical guidelines for its application.
We thank Marc A Miller for his critical review of the manuscript. Figure 3 is courtesy of John Fallon.
Contributors: All authors planned and contributed to the writing of the manuscript. SAL is guarantor.
Competing interests: AF consults for and has received honorariums from Medtronic and receives research support from St Jude Medical.
Provenance and peer review: Not commissioned; externally peer reviewed.
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