Journal List > Korean Circ J > v.40(9) > 1016598

TOOLS
Lee, Oh, Shin, Kim, Choi, Jang, Park, Youn, Lee, Chung, Seung, Rho, Kim, and Choi: A Transthoracic Echocardiographic Follow-Up Study After Catheter Ablation of Atrial Fibrillation: Can We Detect Pulmonary Vein Stenosis by Transthoracic Echocardiography?
Original Article
Korean Circulation Journal

Korean Circulation Journal 2010; 40(9): 442-447.

Published online: 30 September 2010

DOI: https://doi.org/10.4070/kcj.2010.40.9.442

A Transthoracic Echocardiographic Follow-Up Study After Catheter Ablation of Atrial Fibrillation: Can We Detect Pulmonary Vein Stenosis by Transthoracic Echocardiography?

Dong-Hyeon Lee, MD, Yong-Seog Oh, MD, Woo-Seung Shin, MD, Ji-Hoon Kim, MD, Yun-Seok Choi, MD, Sung-Won Jang, MD, Chul-Soo Park, MD, Ho-Joong Youn, MD, Man-Young Lee, MD, Wook-Sung Chung, MD, Ki-Bae Seung, MD, Tai-Ho Rho, MD, Jae-Hyung Kim, MD, Kyu-Bo Choi, MD

Division of Cardiology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Correspondence: Yong-Seog Oh, MD, Division of Cardiology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul 137-701, Korea. Tel: 82-2-2258-6029, Fax: 82-2-591-1506, oys@catholic.ac.kr

Received 24 November 2009       Revised 15 March 2010       Accepted 30 March 2010

Copyright © 2010 The Korean Society of Cardiology

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background and Objectives

While pulmonary vein isolation (PVI) is an effective curative procedure for patients with atrial fibrillation (AF), pulmonary vein (PV) stenosis is a potential complication which may lead to symptoms that are often unrecognized. The aim of this study was to compare differences between ablation sites in pulmonary venous flow (PVF) measured by transthoracic Doppler echocardiography (TTE) before and after PVI.

Subjects and Methods

One hundred five patients (M : F=64 : 41; mean age 56±10 years) with paroxysmal AF (n=78) or chronic, persistent AF (n=27) were enrolled. PVI strategies consisted of ostial ablation (n=75; OA group) and antral ablation using an electroanatomic mapping system (n=30; AA group). The ostial diameter was estimated by magnetic resonance imaging (MRI) in patients with PVF ≥110 cm/sec by TTE after PVI.

Results

No patient complained of PV stenosis-related symptoms. Changes in mean peak right PV systolic (-6.7±28.1 vs. 10.9±25.9 cm/sec, p=0.038) and diastolic (-4.1±17.0 vs. 9.9±25.9 cm/sec, p=0.021) flow velocities were lower in the AA group than in the OA group. Although the change in mean peak systolic flow velocity of the left PV before and after PVI in the AA group was significantly lower than the change in the OA group (-13.4±25.1 vs. 9.2±22.3 cm/sec, p=0.016), there was no difference in peak diastolic flow velocity. Two patients in the OA group had high PVF velocities (118 cm/sec and 133 cm/sec) on TTE, and their maximum PV stenoses measured by MRI were 62.5% and 50.0%, respectively.

Conclusion

PV stenosis after PVI could be detected by TTE, and PVI by antral ablation using an electroanatomic mapping system might be safer and more useful for the prevention of PV stenosis.

Keywords: Atrial fibrillation, Catheter ablation, Pulmonary veins, Echocardiography

Introduction

Because the pulmonary vein (PV) plays an important role in atrial fibrillation (AF), pulmonary vein isolation (PVI) using high frequency energy is definitely an effective curative procedure for patients with AF.1-5) PV stenosis is a rare but critical complication associated with this procedure, and related symptoms can vary.6-9) The incidence of significant PV stenosis or total PV obstruction is 1 to 10% during a period of 1.3 to 15 months after PVI.10-12) Pappone et al.13-15) has reported that antral ablation is associated with high success and low complication rates, especially in paroxysmal AF, although it is only partly successful in chronic, persistent AF. Although computed tomography (CT) or magnetic resonance imaging (MRI) are currently the standard methods for predicting PV stenosis after PVI, radiation exposure and their costs remain drawbacks.
The aim of this study was to predict PV stenosis after PVI, and compare efficacy results and pulmonary venous flows (PVFs) using classical transthoracic Doppler echocardiography (TTE) in patients undergoing antral ablation (AA group) guided by an electroanatomic mapping system and patients undergoing ostial ablation (OA group).

Subjects and Methods

Subjects

The study population consisted of 105 individuals {M : F=64 : 41 (61% : 39%), mean age: 56±10 years} who underwent high-frequency catheter ablation for AF at St. Mary's Hospital, The Catholic University of Korea, between June 2005 and June 2006. All subjects complained of chest discomfort, and their AF had been refractory to medical treatment.
A total of 78 (74%) out of 105 enrolled patients had paroxysmal AF; whereas 27 (26%) had chronic, persistent AF. Out of 105 individuals, 30 (29%) underwent antral ablation assisted by an electroanatomic mapping system, while the remaining 75 (71%) patients underwent ostial ablation. The mean symptomatic period was 11±7 years, and the mean period of resistance to antiarrythmic agents, including (Category I or III, such as flecainide, propafenone, amiodarone), β-blockers, calcium channel blockers, or digoxin, was 2.8±4 years.
This study was approved by our Institutional Review Committee. The participants were informed of the investigative nature of the study, and written informed consent was obtained before enrollment.

Mapping and catheter ablation

Medical history before the procedure, physical examination, electrocardiography, and TTE, including PVF velocity were obtained for all patients. PV anatomy was assessed by integrating multidetector computed tomography (MDCT) images with an electroanatomic mapping system (CARTO; Biosense Webster Inc., Diamond Bar, CA, USA). Oral anticoagulants such as coumadin were taken 1 month before the procedure and stopped 5 days prior to it. All patients also underwent transesophageal echocardiography (TEE) to rule out left atrial thrombosis. The procedure was performed as follows. Four catheter insertion sites were obtained through the right jugular vein and bilateral femoral veins. A 10-electrode catheter was maneuvered into the coronary sinus through the right jugular vein, after which another 10-electrode catheter and a 6-electrode catheter were placed at the top of the right atrium and the bundle of His, respectively, through the right femoral vein. Finally, a pigtail catheter was placed at the right pulmonary artery through the left femoral vein, passing through the inferior vena cava, right atrium, and right ventricle. At this stage in the procedure, the outline of the PV was identified in a few seconds using selective biplane pulmonary angiography {right anterior oblique (RAO) 45°, left anterior oblique (LAO) 45°} from both the right and left sides. This anatomical image became the basis for the procedure. To isolate the PV through the left atrium, a Brockenbrough needle (Medtronic, USA) and two 8F SL1 long transseptal sheaths (St. Jude Medical, Daig Division, USA and Multipurpose, Medtronic, USA) were used to make two artificial atrial septal defects, and 5,000 IU of heparin was infused intravenously. The heparin dosage was chosen to maintain an activated clotting time of 300 seconds, measured every hour. The ablation technique for each patient was chosen as follows: ostial ablation using a Lasso catheter was performed in the first 75 patients (OA group) and then the antral ablation using the CARTOMERGE system was performed in the subsequent 30 patients (AA group).

Ostial ablation group (Fig. 1)

A LASSO variable catheter (25 mm) (Biosense-Webster, Inc.) was placed at the ostium of the PV through a long branch of the left femoral vein. Then, under LASSO guidance, an 8 mm-tip ablation catheter (Biosense-Webster, Inc.) was placed 1-2 cm away from the ostium for ablation. In patients with atrial flutter, ablation was performed at the right atrial cavotricuspid isthmus.

Antral ablation group (Fig. 2)

Mapping catheters (Navistar; Bioscience Webster, Inc., Belgium) were placed into each PV and pulled toward the left atrium. Then, the CARTOMERGE system was implemented, using the 3-dimensional real-time nonradioactive electroanatomic mapping CARTO system to obtain the structures of the left atrium and of the 2 PVs, which were integrated with MRI or CT images obtained before the procedure. When mapping was completed, a 30-mm or 35-mm LASSO catheter was positioned at the antrum of the left atrium, and ablation was completed by an 4 mm-tip ablation catheter (Navistar; Biosense-Webster, Inc.) under LASSO and CARTOMERGE guidance. Patients with atrial flutter underwent ablation at the cavotricuspid isthmus.
A Stockert 70 RF Generator (500 kHz; Stockert GMBH, Freiburg, Germany) was used to generate high-frequency energy, and the target temperature was set at 35℃ for each movement, every 10-20 seconds. The maximum energy was set at 60 W. Patients with AF during the procedure received intracardiac cardioversion using 5-10 J.

Echocardiographic indices

All TTE and TEE assessments were carried out using the Philips Sonos 5500 (Philips Healthcare, Andover, MA, USA) and General Electric System FiVe ultrasound imaging systems.

Transesophageal echocardiography

All patients were placed in the lateral supine position under mild sedation using intravenous (IV) midazolam 2-5 mg, and oximeter surveillance. TEE was performed using a multiplane transducer the day before PVI. The left atrial appendage was carefully examined for thrombosis, and a blood flow of 0.4 m/sec was considered safe for procedure.

Transthoracic Doppler echocardiography (Fig. 3A)

All patients underwent TTE before and after PVI. The PVF velocities of the right and left PVs were calculated by pulse-wave Doppler in the apical 4-chamber view to compare incidence rates of PV stenosis and PVF changes between the AA group and the OA group. PV stenosis was defined as a postprocedural maximum PVF >110 cm/sec, corresponding to data published by Yu et al.16) After PVI, a decrease in PV diameter by ≥50% measured by CT or MRI was considered significant, and we compared pre- with postprocedure PV diameters (Fig. 3B and C). The rates of ablation success, symptom recurrence, complications such as pericardial effusion or cardiac tamponade, stroke, esophageal injury, and phrenic nerve injury were also recorded.

Statistical analysis

Statistical analysis was conducted using SAS statistical software, version 9.1 (SAS Institute, Cary, NC, USA), and the results were expressed as mean±standard deviation. Comparisons of PVF before and after the two different procedures, namely AA group with CARTOMERGE and the OA group without CARTOMERGE, were done using the paired Wilcoxon signed ranks test and the Mann-Whitney U-test. A p less than 0.05 was considered statistically significant.

Results

Clinical features (Table 1)

No patient complained of PV stenosis-associated symptoms. The success rates for the OA group and AA group were both 80.0% (n=60 and n=40, respectively), and the recurrence rates of the OA group and AA group were both 20.0% (n=15 and n=6, respectively). PV stenosis was only observed in the OA group (2.7%, n= 2), and pericardial effusion or cardiac tamponade was observed in 2.7% of patients from the OA group (n=2), and 3.3% from the AA group (n=1).

Echocardiographic results before and after the procedure (Table 1 and 2)

Left ventricular ejection fractions (LVEF, %) of the OA and AA groups were 62±6% and 63±7% (p=0.136), respectively, and left atrial appendage (LAA) velocities were 67±21 cm/sec and 59±17 cm/sec, respectively (p=0.936) (Table 1).
Left atrial dimension changes before and after the procedure were 42±8 mm and 42±9 mm (p=0.832), respectively. Left atrial end-diastolic volume (LAEDV) changes were 61±25 mL and 59±24 mL (p=0.706), respectively; left atrial end-systolic volume (LAESV) changes were 45±21 mL and 44±21 mL (p=0.340), respectively (Table 2).
Right systolic PVF velocity changes before and after the procedure were 57±19 cm/sec and 63±26 cm/sec (p=0.098), respectively, whereas the right diastolic PVF velocity changes were 53±17 cm/sec and 59±23 cm/sec (p=0.067), respectively. Left systolic PVF velocity changes before and after the procedure were 53±20 cm/sec and 55±22 cm/sec (p=0.440), respectively; left diastolic PV velocity changes were 51±17 cm/sec and 53±19 cm/sec (p=0.370), respectively (Table 2).
Peak systolic flow velocity changes of the right PV were significantly lower in the AA group (-6.7±28.1 cm/sec) using CARTOMERGE, compared to the OA group (10.9±25.9 cm/sec) without CARTOMERGE (p=0.038) (Fig. 4A). Similarly, peak diastolic flow velocity changes of the right PV were also significantly lower in the AA group (-4.1±17.0 cm/sec) than in the OA group (9.9±25.9 cm/sec) (p=0.021) (Fig. 4B). Peak systolic flow velocity changes of the left PV were -13.4±25.1 cm/sec and 9.2±22.3 cm/sec, for the AA and OA groups, respectively. The AA group had significantly lower values compared to the OA group (p=0.016) (Fig. 4C). The peak diastolic flow velocity changes of the left PV were also lower in the AA group (-4.4±25.2 cm/sec) than in the OA group (5.8±22.4 cm/sec), but the difference did not achieve statistical significance (p=0.447) (Fig. 4D).
Two patients in the OA group had PVF velocities of 118 cm/sec and 133 cm/sec detected by TTE. By MRI assessments, the maximum stenosis of their PVs were 62.5% and 50.0%, respectively (Fig. 3B and C).

Discussion

Although high-frequency PVI is an effective procedure for treating patients with AF, complications associated with this procedure include PV stenosis, atrio-esophageal fistula, peri-esophageal vagal nerve damage, postablation atrial tachycardia, thromboembolism, air embolism, and cardiac tamponade. In our study, there were no cases of atrio-esophageal fistula, peri-esophageal vagal nerve damage, postablation atrial tachycardia, or thromboembolism; however, there were cases of PV stenosis (n=2, 1.9%) and cardiac tamponade (n=3, 2.7%).
To diagnose these complications, various methods, including CT, MRI, TEE, lung ventilation perfusion scanning, eso-phagography, and esophageal manometry can be used.6-9) Our study, however, documents the effectiveness of TTE in diagnosing PV stenosis before and after ablation, by comparing TTE measurements with MRI measurements. Recently, Packer et al.17) reported that intracardiac echocardiography can be useful for assessing endocardiac structures during PVI and preventing PV stenosis after the procedure. Also, Saad et al.18) stated that progression of PV stenosis is rare three months after the procedure, and if it occurs, is usually stable or improves gradually. Various approaches using high-frequency catheter ablation, including PVI, PV denervation, elimination of anchor points, vein of Marshall exclusion, elimination of AF arising from the posterior LA, and reduction of antral volume, have been introduced to treat patients with AF according to its diverse etiology.19-24)
Left atrial circumferential ablation, also known as "circumferential PVI," was first attempted by Pappone et al.13)14) and refers to "figure-of-eight" ablation around the two left and two right PVs. The use of antral ablation to treat AF has been the subject of controversy. Stabile et al.25) reported a success rate of only 37% in 51 patients; whereas Oral et al.26) reported a high success rate of 88%. However, in our study, the AA group and the OA group showed equivalent success rates of 80%, and although the difference did not achieve statistical significance, only the OA group developed PV stenosis (n=2, 2%).
There are several possible reasons for the high success, low recurrence, and low complication rates in the AA group of this study. First, center experience should be considered. There are reports that even highly successful centers initially have a low success rate. Second, the type of high-frequency energy source needs to be considered. Although our study used an energy source of 60 W and 55℃, other studies have reported using energy sources of 60-100 W and 50-60℃ for similar research.19)20) Therefore, the difference in success rates could be a result of using different types of energy sources. Third, subject selection might play a role. In our study, patients with paroxysmal AF and chronic, persistent AF accounted for 74% (n=78) and 26% (n=27) of the studied population, respectively. Different numbers in the types of AF making up the selected patients may explain the differences in success rates.
Finally, the technical aspect may be a factor, as the results can vary depending on the training level of the procedure administrator.

Limitations

The limitations of this study are as follows; first, although PV stenosis can be detected easily by TTE, CT or MRI are the standard methods for predicting PV stenosis after PVI. Moreover, we did not perform postprocedure CT or MRI in all patients after PVI; thus we cannot determine the time course of PV stenosis development. Second, the endpoint of the study was unclear. The mean period for follow-up duration was 4.3±9.9 months in our study. A longer prognostic evaluation is necessary to prove not only the actual rate of PV stenosis, but also the safety and efficacy of antral ablation. Finally, the accuracy of the CARTOMERGE method needs to be considered. CARTOMERGE is a nonradioactive and global positioning system (GPS)-like method, and is superior in that it uses a mapping technology. But as the timing of MDCT imaging and the actual procedure differ, discrepancies in the length and volume of the left atrium may occur while integrating the images of the CARTO apparatus and MDCT.

Conclusion

Although PVI using high-frequency energy is definitely an effective curative procedure for patients with AF, it is associated with PV stenosis, a critical but rare complication. Our study indicates that PV stenosis can be detected easily by TTE, and that antral ablation can be safely performed with the electroanatomic CARTOMERGE mapping system to minimize the incidence of this complication. In all patients after PVI, long-term follow-up examination of PV patency by MRI or TTE is necessary.

Figures and Tables

Fig. 1
Fluoroscopic image demonstrating segmental ostial ablation of PV using Lasso guidance. LAO: left anterior oblique view, PV: pulmonary vein; HRA: high right atrium, CS: coronary sinus, ABL: ablation catheter.
kcj-40-442-g001
Fig. 2
CARTOMERGE images of LA and PV that have registered a 3-D CT image with the GPS-like CARTO system (endoscopic view). LA: left atrium, PV: pulmonary vein, 3-D CT: 3-dimensional computed tomography, GPS: global positioning system.
kcj-40-442-g002
Fig. 3
Doppler (A) and MR imaging (B: pre ablation, C: post ablation) of PV in patients with pulmonary vein stenosis that developed after PVI. The white arrow showed significant right superim vein stenosis. MR: magnetic resonance, PV: pulmonary vein, PVI: pulmonary vein isolation.
kcj-40-442-g003
Fig. 4
Changes in peak flow velocity according to ablation sites and use of an electroanatomic (CARTOMERGE) mapping system. This figure shows changes in peak systolic and diastolic flow velocities of RPV (A and B) and LPV (C and D) before and after PVI. RPV: right pulmonary vein, LPV: left pulmonary vein, PVI: pulmonary vein isolation, OA: ostial ablation, AA: antral ablation.
kcj-40-442-g004
Table 1
Clinical characteristics
kcj-40-442-i001

OA: osteal ablation, AA: antral ablation, HDL-C: high density lipoprotein-cholesterol, LDL-C: low density lipoprotein-cholesterol, hs-CRP: highly sensitivity C-reactive protein, Pro-BNP: pro-brain natriuretic peptide

Table 2
Echocardiographic findings
kcj-40-442-i002

PVI: pulmonary vein isolation

References

1. Jais P, Haissaguerre M, Shah DC, et al. A focal source of atrial fibrillation treated by discrete radiofrequency ablation. Circulation. 1997. 95:572–576.
2. Haissaguerre M, Jais P, Shah DC, et al. Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. N Engl J Med. 1998. 339:659–666.
3. Kim YH. Rhythm control versus rate control of atrial fibrillation: pharmacologic and non-pharmacologic therapy. Korean Circ J. 2003. 33:553–558.
4. Hong GR, Shin DG, Park JS, et al. Effects of pulmonary vein isolation using intraoperative radiofrequency catheter ablation for the treatment of atrial fibrillation associated with mitral valvular heart diseases. Korean Circ J. 2002. 32:596–603.
5. Rha SW, Kim YH, Park HN, et al. Initiation and maintenance mechanism of atrial fibrillation assessed by 3-dimensional non-contact mapping system. Korean Circ J. 2004. 34:195–203.
6. Robbins IM, Colvin EV, Doyle TP, et al. Pulmonary vein stenosis after catheter ablation of atrial fibrillation. Circulation. 1998. 98:1769–1775.
7. Scanavacca MI, Kajita LJ, Vieira M, Sosa EA. Pulmonary vein stenosis complicating catheter ablation of focal atrial fibrillation. J Cardiovasc Electrophysiol. 2000. 11:677–681.
8. Yu WC, Hsu TL, Tai CT, et al. Acquired pulmonary vein stenosis after radiofrequency catheter ablation of paroxysmal atrial fibrillation. J Cardiovasc Electrophysiol. 2001. 12:887–892.
9. Ernst S, Ouyang F, Goya M, et al. Total pulmonary vein occlusion as a consequence of catheter ablation for atrial fibrillation mimicking primary lung disease. J Cardiovasc Electrophysiol. 2003. 14:366–370.
10. Saad EB, Rossillo A, Saad CP, et al. Pulmonary vein stenosis after radiofrequency ablation of atrial fibrillation: functional characterization, evolution and influence of the ablation strategy. Circulation. 2003. 108:3102–3107.
11. Haissaguerre M, Jais P, Shah DC, et al. Electrophysiological end point for catheter ablation of atrial fibrillation initiated from multiple pulmonary venous foci. Circulation. 2000. 101:1409–1417.
12. Arentz T, Jander N, von Rosenthal J, et al. Incidence of pulmonary vein stenosis 2 years after radiofrequency catheter ablation of refractory at-rial fibrillation. Eur Heart J. 2003. 24:963–969.
13. Pappone C, Rosanio S, Oreto G, et al. Circumferential radiofrequency ablation of pulmonary vein ostia: a new anatomic approach for curing atrial fibrillation. Circulation. 2000. 102:2619–2628.
14. Pappone C, Oreto G, Rosanio S, et al. Atrial electroanatomic remodeling after circumferential radiofrequency pulmonary vein ablation: efficacy of an anatomic approach in a large cohort of patients with atrial fibrillation. Circulation. 2001. 104:2539–2544.
15. Pappone C, Rosanio S, Augello G, et al. Mortality, morbidity, and quality of life after circumferential pulmonary vein ablation for atrial fibrillation: outcomes from a controlled nonrandomized long-term study. J Am Coll Cardiol. 2003. 42:185–197.
16. Yu WC, Hsu TL, Tai CT, et al. Acquired pulmonary vein stenosis after radiofrequency catheter ablation of paroxysmal atrial fibrillation. J Cardiovasc Electrophysiol. 2001. 12:887–892.
17. Packer DL, Stevens CL, Curley MG, et al. Intracardiac phased-array imaging: methods and initial clinical experience with high resolution, under blood visualization: initial experience with intracardiac phased-array ultrasound. J Am Coll Cardiol. 2002. 39:509–516.
18. Saad EB, Rossillo A, Saad CP, et al. Pulmonary vein stenosis after radiofrequency ablation of atrial fibrillation: functional characterization, evolution, and influence of the ablation strategy. Circulation. 2003. 108:3102–3107.
19. Jalife J, Berenfeld O, Mansour M. Mother rotors and fibrillatory conduction: a mechanism of atrial fibrillation. Cardiovasc Res. 2002. 54:204–216.
20. Jalife J. Rotors and spiral waves in atrial fibrillation. J Cardiovasc Electrophysiol. 2003. 14:776–780.
21. Hwang C, Wu TJ, Doshi RN, Peter CT, Chen PS. Vein of marshall cannulation for the analysis of electric activity in patients with focal atrial fibrillation. Circulation. 2000. 101:1503–1505.
22. Haissaguerre M, Jais P, Shah DC, et al. Electrophysiological end point for catheter ablation of atrial fibrillation initiated from multiple pulmonary venous foci. Circulation. 2000. 101:1409–1417.
23. Lin WS, Tai CT, Hsieh MH, et al. Catheter ablation of paroxysmal atrial fibrillation initiated by non-pulmonary vein ectopy. Circulation. 2003. 107:3176–3183.
24. Moe GK. A conceptual model of atrial fibrillation. J Electrocardiol. 1968. 1:145–146.
25. Stabile G, Turco P, La Rocca V, Nocerino P, Stabile E, De Simone A. Is pulmonary vein isolation necessary for curing atrial fibrillation? Circulation. 2003. 108:657–660.
26. Oral H, Scharf C, Chugh A, et al. Catheter ablation for paroxysmal atrial fibrillation: segmental pulmonary vein ostial ablation versus left atrial ablation. Circulation. 2003. 108:2355–2360.
TOOLS
Similar articles