Clinical Presentation, Investigation, and Management of Pulmonary Vein Stenosis Complicating Ablation for Atrial Fibrillation
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循环学杂志 2005年第2期
the Division of Cardiac Electrophysiology/Cardiology, Department of Internal Medicine, Mayo Clinic and Foundation, Rochester, Minn.
Abstract
Background— Although segmental or circumferential ablation is effective in eliminating pulmonary vein (PV)–mediated atrial fibrillation (AF), this procedure may be complicated by the occurrence of PV stenosis.
Methods and Results— To establish the clinical presentation, diagnostic manifestations, and interventional management of PV stenosis, 23 patients with stenosis of 34 veins complicating ablation of AF were evaluated. Each patient became symptomatic 103±100 days after undergoing ablation. In 8 veins, the ablation producing the PV stenosis was a repeated procedure for continued AF. Nineteen patients presented with dyspnea on exertion, 7 with dyspnea at rest, 9 with cough, and 6 with chest pain. On multirow spiral computed tomography examination, the narrowest lumen of the affected PVs measured 3±2 mm compared with 13±3 mm at baseline (P0.001). The relative perfusion of affected lung segments on isotope scans was reduced to 4±3% of total perfusion compared with 22±10% in unaffected segments. At percutaneous intervention, these veins showed 80±13% stenosis, with a mean gradient of 12±5 mm Hg. This was significantly reduced to a residual stenosis of 9±8% (P0.001) and a residual gradient of 3±4 mm Hg (P0.001). Twenty veins were treated with balloon dilatation alone, whereas 14 veins were stented with standard 10-mm-diameter bare-metal stents. Although the symptomatic response was nearly immediate and impressive, 14 patients developed in-stent or in-segment restenosis, requiring repeated interventions in 13.
Conclusions— Percutaneous intervention produces rapid and dramatic symptom relief in patients with highly symptomatic PV stenosis after radiofrequency ablation for AF. Nevertheless, alternative treatment methods will be required to decrease recurrent in-stent or in-segment restenosis.
Key Words: fibrillation, atrial ; ablation, catheter ; pulmonary heart disease ; stenosis ; stents
Introduction
The presence of focal arrhythmogenic triggers arising within pulmonary veins (PVs) in patients with atrial fibrillation (AF)1–6 is well documented. Furthermore, the elimination of AF through (1) targeted energy delivery to focal "sites" within the vein4; (2) PV isolation through circumferential or segmental ablation at the venoatrial junction2,3,5,6; or (3) electrical isolation of the PVs from the left atrium (LA) by radiofrequency energy delivery outside the PV ostia7–9 confirms this mechanism.
Nevertheless, as the clinical experience with ablation has grown, the risk of PV stenosis has become more apparent. Reports suggest that 1% to 10% of patients undergoing ablation develop PV stenosis.3,4,10–15 Although several case reports have chronicled isolated experiences,16–21 the accompanying clinical manifestations and diagnostic and therapeutic interventions have been incompletely examined. This report, therefore, presents a series of 23 patients along with their presentations and long-term outcomes after intervention.
Methods
Patient Population
Radiofrequency Ablation Procedure
During the reference ablation, up to 30 W of radiofrequency energy (temperature 50°C) was typically directed in 20- to 30-second deliveries from an 8F steerable catheter with a 4- to 5-mm tip, either at the focal origin of the tachycardia, in a wedged-shape segment extending out toward the vein orifice, or subsequently at the orifice of the targeted vein. The end point of the ablation was the elimination of spontaneously occurring AF, AF after direct-current cardioversion, other ectopic activity, and/or all PV potentials. Each patient was followed up through telephone contact, clinic follow-up visits, and/or communication with the patient’s primary referring physician.
Preinterventional Evaluation
Before each ablation, patients underwent multirow spiral computed tomography (SCT) and transesophageal echocardiographic (TEE) examinations to assess the number and characteristics of the PVs.21 On return for assessment of symptomatic PV stenosis, patients underwent a repeated chest x-ray, CT scanning, TEE, and radioisotopic ventilation/perfusion (V/Q) scanning.
CT Scanning
Patients underwent evaluation according to a 2-phase protocol with a multirow SCT system (GE Medical Systems).22 In the first phase, a range-finding scan was undertaken at 10-mm intervals to determine the superior and inferior borders of the heart. A complete image set was then obtained after injection of 125 mL of contrast medium, yielding images at 1.25 mm. These allowed a 0.6-mm axial image interval when reconstructed. For analysis, 150 to 450 SCT image slices were analyzed with Analyze, Vitria II, or GE Advantage software. The acquired set of axial images was reformatted for assessment of each PV from axial, coronal, sagittal, and most important, oblique images. The location of a PV stenotic lesion on follow-up studies and its quantitative characteristics were established by comparison with baseline images at that specific site. The characteristics of the stenotic lesion were determined and referenced to the vessel orifice, which in turn was taken as the point of departure of the vein tangent from the curvature of the LA.
Transesophageal Echocardiography
TEE was performed with a biplane, phased-array probe positioned at an appropriate level within the esophagus. The scope was oriented to provide optimal imaging of each of the 4 PVs. In addition to 2D imaging at 3.5 to 7.5 MHz for measuring PV dimensions at the orifice and at the stenotic site, blood flow was assessed via color flow and pulsed-wave Doppler techniques.
V/Q Scanning Techniques
Radionuclide lung scans were performed with dual-headed, large-field cameras (Helix or VG system, GE Medical) with a low-energy, all-purpose collimator interfaced with an Xpert computer (GE Medical).23 For ventilation studies, 15 to 25 mCi (555 to 925 MBq) xenon-133 images were obtained with a 20% window around the 80-keV photopeak. Anterior and posterior first-breath images were obtained for 200K counts or as long as the patient held his or her breath. Immediately after the first-breath anterior, posterior, and anterior and posterior oblique views were acquired for 100K to 200K counts, late 1-minute equilibrium and 4 subsequent 1-minute interval washout images were obtained.
For perfusion studies, 4 to 6 mCi (150 to 220 MBq) technetium-99m macro aggregated human albumin was given intravenously. Eight 1000K-count images, including those in the anterior, posterior, lateral, and anterior and posterior oblique views, were obtained with a 20% window around a 140-keV photopeak in a 256x256 word matrix. For quantification of perfusion, rectangular regions of interest, drawn over anterior and posterior images, were divided into apical, middle, and basal regions. The geometric means of counts from the anterior and posterior images for each lung field and for each of these specific regions were derived and expressed as a percent of total right and left lung ventilation or perfusion counts. These formed the bases for comparison of perfusion in normal and stenotic segments.23
PV Angiography, Dilatation, and Stenting
In the catheterization laboratory, intracardiac echocardiographic (ICE) imaging was performed with a 10F multidirectional, 64-element, phased-array catheter (Acuson Corp) advanced into the right atrium.24 A Swan-Ganz catheter was advanced through the right heart to facilitate right heart hemodynamic monitoring and selective pulmonary arteriography. A second venous access site was used for transseptal catheterization, performed under fluoroscopic and ICE guidance.
PVs were imaged by ICE to corroborate the preprocedural CT and TEE findings. The pattern of blood flow and presence of any disturbance of laminar blood flow were assessed with color flow imaging. Color flow jets were also used as "contrast imaging" to locate the orifice of the PV in the case of tightly stenotic lesions. Pulsed-wave Doppler interrogation of the vein was undertaken to establish blood flow velocity and apparent gradient.
A multipurpose catheter was positioned via the transseptal sheath into the LA and advanced across the lesion of interest to measure the transstenotic gradient and to perform venography. On the basis of this imaging and ICE sizing, a balloon with an appropriate diameter and length was selected to engage each stenotic lesion. In general, a balloon-to-vein ratio of 1.0 to 1.2 was chosen, and repeated inflations of 6 to 12 atm were undertaken, as guided fluoroscopically and by ICE. In the first 3 patients, a bare-metal stent of appropriate dimensions was positioned across the residual PV stenosis, with the end of the stent positioned at the venoatrial junction, under fluoroscopic and ICE guidance. In all subsequent patients, a stent was placed only if rebound stenosis was seen after balloon dilatation.
Follow-Up
Eighteen to 24 hours after the interventional procedure, the CT and V/Q scans and the TEE examination were repeated. Patients were subsequently discharged on warfarin to a target international normalized ratio (INR) of 2 to 3, along with 75 mg clopidogrel per day thereafter. Low-molecular-weight heparin was given subcutaneously twice daily until the INR was 2.0. Patients were followed up by telephone contact and repeated clinic evaluation, as well as repeated studies at 3 months.
Statistical Analysis
All data are presented as mean±SD. Comparisons between preintervention and postintervention vessel size and lesion characteristics were made with nonparametric methods. In all patients except 7, the stenosis data could be compared with baseline information from that particular patient. Correlation between 2 variables was established by least-squares methods. A probability value 0.05 was taken as significant.
Results
Ablative Intervention
Symptom Development
These patients developed symptoms over the course of 103±100 days of follow-up. Nineteen had increasing dyspnea on exertion, 7 had dyspnea at rest, and a recurrent cough was present in 9. Six had aching or burning chest pain, which was pleuritic in 5. Flulike symptoms, including fatigue, myalgia, and low-grade fever, were noted by 3 patients. Three had received a course of antibiotics for the presumptive diagnosis of bronchitis, without benefit. Three patients developed hemoptysis.
Initial Physical/Laboratory Examination
In 22 patients, the physical examination was normal, whereas one had inspiratory crackles over the affected lung region. None had evidence of pulmonary hypertension. One patient had interstitial changes on the chest x-ray film in the absence of cardiomegaly, but no radiographic abnormalities were seen in the remaining 22 patients. The average PaO2 in the 8 patients tested was 86±16 mm Hg (saturation, 94±3%), with no change during exercise.
CT Imaging
Transesophageal Echocardiography
The affected PVs were well visualized in 16 of 34 Mayo cases. Lesion narrowing (mean, 5±3 mm; range, 2 to 12) was seen in 11. A pulmonary artery systolic pressure >40 mm Hg was seen in only 1 case. Flow velocities (mean, 1.7±0.6 m/s), measured from the PVs, were 2.5 m/s in 3, 2.0 to 2.5 m/s in 1, 1.5 to 2.0 m/s in 6, and between 1.0 and 1.5 m/s in 6. In each case, there was turbulent blood flow with increased aliasing on color flow examination.
V/Q Imaging
Ventilation scanning was completely normal in 17 of 22 patients, with a defect in only 10 of 38 regions corresponding to affected veins (Figure 2). A perfusion defect that could be correlated with the stenotic lesion was seen in the distribution of all 34 affected veins (Figure 2; 40 of 132 segments).
The relative perfusion from an affected segment contributed between 0% and 9% (4±3%) of total perfusion. This compared with a value of 22±10% seen in other segments without any corresponding PV abnormality (P0.001). In 14 patients, quantitative analysis of perfusion indicated highly asymmetric tracer uptake within the lungs, suggesting a major impediment to PV drainage. There was a matching reduction in ventilation in only 3 patients.
Interventional Procedure
Postinterventional Imaging
Follow-Up
All 23 patients had a substantial reduction in symptoms within minutes to 1 hour after vessel treatment. Nevertheless, 14 patients (57%) developed recurrent symptoms at 3.2±2.8 months after the initial intervention, with dyspnea on exertion in 13 and cough or chest pain in 5. Two of the 14 experienced hemoptysis, whereas one reported cough and pleuritic chest pain. Thirteen patients required repeated interventions on 14 of the originally treated veins. Six of these veins had been previously dilated, whereas 8 veins were stented at the time of the original procedure. Four of these latter veins showed in-stent restenosis, whereas 4 showed in-segment PV stenosis at sites proximal or distal to the stent. Six patients also developed significant stenosis in 6 previously undilated veins. One lesion had progressed to total occlusion and could not be redilated.
Three patients again developed dyspnea on exertion, associated with cough or fatigue, requiring another intervention on 3 veins. One vessel was redilated and 2 were stented. One patient required a fourth intervention. On long-term follow-up at 18±12 months (range, 3 to 34), 15 patients remain completely asymptomatic from PV stenosis, and 4 have mild and 3 have moderate symptoms.
Discussion
These data provide substantial insight into the clinical syndrome of acquired PV stenosis occurring after radiofrequency ablation for AF. Patients with this malady can be extremely symptomatic but respond almost immediately to percutaneous intervention. Although initial results are encouraging, the occurrence of restenosis, including in- and out-of-stent abnormalities, remains a concern.
PV stenosis is an established complication occurring with radiofrequency energy delivery for focal AF ablation. Robbins et al25 reported multivessel PV stenosis after linear ablation for AF in 2 patients. The prevalence of this problem in the setting of linear ablation likely ranges between 2% and 7%.26 The exact prevalence of PV stenosis in patients undergoing focal or segmental AF ablation is becoming more clear.3,4,10–15 In one of the larger series, Chen et al4 initially described apparent PV stenosis in 42% of their 79 patients. This represents an overestimation of this problem, however, because an increased TEE flow velocity was used to establish the diagnosis. A later study from the same group noted a 33% incidence of PV narrowing, again established by TEE methods.13 Gerstenfeld and coworkers10 have reported an 8.3% occurrence of clinically relevant PV stenosis in an early series of 40 patients undergoing focal AF ablation. Similarly, Saad and coworkers27 reported a 5% incidence of severe PV stenosis (>75%) in patients undergoing electrical isolation of their PVs. In their initial series, Haissaguerre et al3 reported a 5% occurrence rate but have recently suggested a decrease to <1% overall with additional experience in ablation. Pappone et al7,8 also reported a <1% PV stenosis rate with ablation limited to atrial tissue outside the PV orifice. Other groups have reported cases of patients with PV stenosis requiring venoplasty or stenting.16–21 In the absence of a clear-cut "denominator," however, it is not possible to decipher the incidence of this complication in those studies.
The prevalence of this problem has decreased because of a variety of factors, including (1) abandonment of in-vein ablation at the site of the AF focus; (2) limiting ablation at or outside the orifice of the vessel; (3) the use of ICE to guide catheter placement and monitor energy delivery; (4) a reduction in target ablation temperature and the amounts of energy deliveries; and (5) increased operator experience.12 This report represents 6.0% of the initial 203 patients who underwent PV ablation at this institution.12 In the first 100 patients undergoing ablation, 11 developed a stenotic lesion, whereas only 1 has developed a stenotic lesion requiring intervention in the last 100 patients. This "learning curve" has also been documented by Saad et al,15 who underscored the importance of experience, ablation outside the PV, and intracardiac ultrasound use for decreasing moderate and severe PV stenosis occurrence from 7.9% to 1.4%. Recent review of the European experience with AF ablation documented PV stenosis rates approaching 20% in the centers performing <50 PV isolation procedures.29
The exact pathology of PV stenosis has not been elucidated. In the present series, patients undergoing a first dilatation procedure had both soft and more fibrotic components of PV pathology. In most cases, a clear-cut waist in the venoplasty balloon was seen with balloon inflation. In some cases, 10 to 12 atm of pressure were required for elimination of that apparent scarring. In 3 cases, the stenosis was partially reopened simply by passing a guidewire through it. This, and subsequent in-stent restenosis, suggests a component of neointimal hyperplasia and/or thrombus as well. No pathological specimens were obtained for histology, however. Taylor and coworkers30 found both extensive architectural remodeling and fibrosis, as well as neointimal hyperplasia. In parallel studies, we have also found neointimal hyperplasia in a canine model of PV stenosis occurring with both radiofrequency and ultrasound energy delivery31 and a marked inflammatory process.32 Additional studies will be required to elucidate further the molecular and histological pathways of this problem.
Regardless of pathology, these patients were highly symptomatic. Most presented with dyspnea on exertion as the initial manifestation of this process, which typically evolved over the course of 1 to 3 months. Although pleuritic chest pain is a late manifestation of the process, hemoptysis was uncommon during follow-up in this series. Both processes are likely related to complete vessel or branch occlusion in these individuals. Blood gas assessment and pulmonary function testing were not useful as screening measures for early stenosis. These symptoms and chest x-ray changes may lead to an erroneous diagnosis of bronchitis or other pulmonary parenchymal process, delaying establishment of PV stenosis. In a recent series of PV stenosis, patients were often misdiagnosed by their primary care givers as having bronchitis.27 This occurrence of "garden-variety" respiratory symptoms could also contribute to an underestimation of the prevalence of this process.
CT Scanning
CT evaluation was the most helpful in identifying the location and extent of the stenoses. Establishment of the true endocardial PV orifice was a straightforward and reproducible process. Postprocessing of the very thin axial slices allowed near-isotropic voxel coronal, oblique, sagittal, and 3D renderings for review and measurement. There was a limited yet significant correlation between the extent of stenosis seen on the CT scan images and that at the time of angiography. This is likely due to the difference in imaging plane for each technique. The angiographic views were right and left anterior oblique to the patient, whereas the CT views were orthogonal to the vessel. Vessels may still be patent on venography, even if they appear occluded on CT imaging. Comparable experience with magnetic resonance imaging is limited.33
V/Q Scanning
V/Q scanning was helpful for establishing the pathophysiology of the stenosis and its progression. Ventilation abnormalities occurred only in extreme cases. In contrast, perfusion abnormalities were marked. These abnormalities appeared similar to the changes seen in pulmonary embolism. Although in most cases the perfusion deficit was limited to the distribution of the involved vein, several patients showed a reduction in perfusion in the ipsilateral lung. The exact cause of this is unclear but suggests the presence of a compensatory mechanism affecting multiple vascular beds. Furthermore, the perfusion abnormalities in some patients did not normalize over the course of their follow-up, indicating persistent physiological abnormalities in the setting of normalized anatomy.
Echocardiographic Evaluation
Although TEE imaging was useful in providing a good view of the superior PVs, imaging of the right and left inferior PVs was inconsistent. In contrast, ICE allowed straightforward, real-time imaging of all PVs. The right superior PV at its orifice was typically viewed en face,24 with additional rotation required to view the vessel along its long axis. Imaging into each of the vessels provided a good view into the first 1 to 3 cm of the vein. Color flow contrast imaging was also useful in identifying the location of the orifice of the most tightly stenotic vessels. The flow velocities seen in these vessels were elevated, but not to the extent expected, because of the impact of a tight stenosis and longer lesions with accompanying reductions in blood flow.
ICE facilitated accurate stent placement by reliably identifying the orifice of the tightly stenotic vessels. This imaging modality disclosed an additional problem of stent placement in left PVs. Because these orthogonal superior and inferior vessels can form an antrum before entrance into the LA, great care is required to ensure that the positioning of a stent in one PV does not obstruct the orifice of the paired vessel.
Intervention
Although in some cases the initial lesion accepted balloons of only 4 to 6 mm in diameter, dilatation with 10-mm balloons was possible in the majority of cases. This experience suggests that inflation to 10 to 12 atm may be required. In the majority of these patients, achieving this outcome required breaking through an apparently fibrous waist. At this point in our experience, larger stents were not deployed because of concerns about vessel dissection. The patient who sustained a PV dissection was dilated with a 12-mm balloon.
Restenosis
Unfortunately, both in-stent and in-segment restenoses have recurred during 17 months of follow-up. This confirms the findings of Qureshi and colleagues,34 who observe a 47% restenosis rate 11 months after the intervention. Those within the body of the stent are likely caused by neointimal hyperplasia and fibrosis.35 Out-of-stent restenoses were observed at bifurcation points beyond the stent into the vessel, also suggesting the progression of PV pathology, despite stent placement. There is no experience to date with the use of sirolimus or paclitaxel drug-eluting stents in this situation, but such a high restenosis rate makes a strong case for the investigation of such devices and larger-diameter stents. Furthermore, the utility of brachytherapy and surgical intervention are also unclear, and the latter has been disappointing when used as treatment for congenital stenosis.36,37
Limitations
First, although this is the largest interventional series with the longest duration of follow-up published to date, the numbers remain small and may or may not apply to all patients with ablation-induced PV stenosis. Assessment of the relative merits of simple balloon dilatation versus stenting is also hampered by the limited number of patients with stenosis. Given this, a PV stenosis registry will be required to further assess the impact of this process and treatment in resolution of symptoms. Furthermore, these data reflect the learning curve present in this new venue of occlusive disease. The study also fails to indicate precisely which of the multiple energy deliveries in a single vein created the stenosis. On the basis of our prior review, this occurrence is most likely due to multiple deliveries.
Clinical Implications
It has been established that changes in ablation approaches and traversing the ablation learning curve have reduced the rate of this complication at individual, high-volume centers. Nevertheless, with the currently widespread application of ablation for AF, this problem will undoubtedly continue to affect many patients in the "real world." Recently reported cases of late progressive PV stenosis in patients with minor abnormalities on initial postablation venography or follow-up CT scanning further predict a higher prevalence over time.11,38 Furthermore, the presence of PV stenosis is commonly misdiagnosed and underestimated in the absence of surveillance of all patients undergoing PV ablation. As such, preventive approaches and effective therapy for this process will continue to be critical. The diagnostic and interventional strategies outlined in this report represent an important and early step along that pathway.
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Abstract
Background— Although segmental or circumferential ablation is effective in eliminating pulmonary vein (PV)–mediated atrial fibrillation (AF), this procedure may be complicated by the occurrence of PV stenosis.
Methods and Results— To establish the clinical presentation, diagnostic manifestations, and interventional management of PV stenosis, 23 patients with stenosis of 34 veins complicating ablation of AF were evaluated. Each patient became symptomatic 103±100 days after undergoing ablation. In 8 veins, the ablation producing the PV stenosis was a repeated procedure for continued AF. Nineteen patients presented with dyspnea on exertion, 7 with dyspnea at rest, 9 with cough, and 6 with chest pain. On multirow spiral computed tomography examination, the narrowest lumen of the affected PVs measured 3±2 mm compared with 13±3 mm at baseline (P0.001). The relative perfusion of affected lung segments on isotope scans was reduced to 4±3% of total perfusion compared with 22±10% in unaffected segments. At percutaneous intervention, these veins showed 80±13% stenosis, with a mean gradient of 12±5 mm Hg. This was significantly reduced to a residual stenosis of 9±8% (P0.001) and a residual gradient of 3±4 mm Hg (P0.001). Twenty veins were treated with balloon dilatation alone, whereas 14 veins were stented with standard 10-mm-diameter bare-metal stents. Although the symptomatic response was nearly immediate and impressive, 14 patients developed in-stent or in-segment restenosis, requiring repeated interventions in 13.
Conclusions— Percutaneous intervention produces rapid and dramatic symptom relief in patients with highly symptomatic PV stenosis after radiofrequency ablation for AF. Nevertheless, alternative treatment methods will be required to decrease recurrent in-stent or in-segment restenosis.
Key Words: fibrillation, atrial ; ablation, catheter ; pulmonary heart disease ; stenosis ; stents
Introduction
The presence of focal arrhythmogenic triggers arising within pulmonary veins (PVs) in patients with atrial fibrillation (AF)1–6 is well documented. Furthermore, the elimination of AF through (1) targeted energy delivery to focal "sites" within the vein4; (2) PV isolation through circumferential or segmental ablation at the venoatrial junction2,3,5,6; or (3) electrical isolation of the PVs from the left atrium (LA) by radiofrequency energy delivery outside the PV ostia7–9 confirms this mechanism.
Nevertheless, as the clinical experience with ablation has grown, the risk of PV stenosis has become more apparent. Reports suggest that 1% to 10% of patients undergoing ablation develop PV stenosis.3,4,10–15 Although several case reports have chronicled isolated experiences,16–21 the accompanying clinical manifestations and diagnostic and therapeutic interventions have been incompletely examined. This report, therefore, presents a series of 23 patients along with their presentations and long-term outcomes after intervention.
Methods
Patient Population
Radiofrequency Ablation Procedure
During the reference ablation, up to 30 W of radiofrequency energy (temperature 50°C) was typically directed in 20- to 30-second deliveries from an 8F steerable catheter with a 4- to 5-mm tip, either at the focal origin of the tachycardia, in a wedged-shape segment extending out toward the vein orifice, or subsequently at the orifice of the targeted vein. The end point of the ablation was the elimination of spontaneously occurring AF, AF after direct-current cardioversion, other ectopic activity, and/or all PV potentials. Each patient was followed up through telephone contact, clinic follow-up visits, and/or communication with the patient’s primary referring physician.
Preinterventional Evaluation
Before each ablation, patients underwent multirow spiral computed tomography (SCT) and transesophageal echocardiographic (TEE) examinations to assess the number and characteristics of the PVs.21 On return for assessment of symptomatic PV stenosis, patients underwent a repeated chest x-ray, CT scanning, TEE, and radioisotopic ventilation/perfusion (V/Q) scanning.
CT Scanning
Patients underwent evaluation according to a 2-phase protocol with a multirow SCT system (GE Medical Systems).22 In the first phase, a range-finding scan was undertaken at 10-mm intervals to determine the superior and inferior borders of the heart. A complete image set was then obtained after injection of 125 mL of contrast medium, yielding images at 1.25 mm. These allowed a 0.6-mm axial image interval when reconstructed. For analysis, 150 to 450 SCT image slices were analyzed with Analyze, Vitria II, or GE Advantage software. The acquired set of axial images was reformatted for assessment of each PV from axial, coronal, sagittal, and most important, oblique images. The location of a PV stenotic lesion on follow-up studies and its quantitative characteristics were established by comparison with baseline images at that specific site. The characteristics of the stenotic lesion were determined and referenced to the vessel orifice, which in turn was taken as the point of departure of the vein tangent from the curvature of the LA.
Transesophageal Echocardiography
TEE was performed with a biplane, phased-array probe positioned at an appropriate level within the esophagus. The scope was oriented to provide optimal imaging of each of the 4 PVs. In addition to 2D imaging at 3.5 to 7.5 MHz for measuring PV dimensions at the orifice and at the stenotic site, blood flow was assessed via color flow and pulsed-wave Doppler techniques.
V/Q Scanning Techniques
Radionuclide lung scans were performed with dual-headed, large-field cameras (Helix or VG system, GE Medical) with a low-energy, all-purpose collimator interfaced with an Xpert computer (GE Medical).23 For ventilation studies, 15 to 25 mCi (555 to 925 MBq) xenon-133 images were obtained with a 20% window around the 80-keV photopeak. Anterior and posterior first-breath images were obtained for 200K counts or as long as the patient held his or her breath. Immediately after the first-breath anterior, posterior, and anterior and posterior oblique views were acquired for 100K to 200K counts, late 1-minute equilibrium and 4 subsequent 1-minute interval washout images were obtained.
For perfusion studies, 4 to 6 mCi (150 to 220 MBq) technetium-99m macro aggregated human albumin was given intravenously. Eight 1000K-count images, including those in the anterior, posterior, lateral, and anterior and posterior oblique views, were obtained with a 20% window around a 140-keV photopeak in a 256x256 word matrix. For quantification of perfusion, rectangular regions of interest, drawn over anterior and posterior images, were divided into apical, middle, and basal regions. The geometric means of counts from the anterior and posterior images for each lung field and for each of these specific regions were derived and expressed as a percent of total right and left lung ventilation or perfusion counts. These formed the bases for comparison of perfusion in normal and stenotic segments.23
PV Angiography, Dilatation, and Stenting
In the catheterization laboratory, intracardiac echocardiographic (ICE) imaging was performed with a 10F multidirectional, 64-element, phased-array catheter (Acuson Corp) advanced into the right atrium.24 A Swan-Ganz catheter was advanced through the right heart to facilitate right heart hemodynamic monitoring and selective pulmonary arteriography. A second venous access site was used for transseptal catheterization, performed under fluoroscopic and ICE guidance.
PVs were imaged by ICE to corroborate the preprocedural CT and TEE findings. The pattern of blood flow and presence of any disturbance of laminar blood flow were assessed with color flow imaging. Color flow jets were also used as "contrast imaging" to locate the orifice of the PV in the case of tightly stenotic lesions. Pulsed-wave Doppler interrogation of the vein was undertaken to establish blood flow velocity and apparent gradient.
A multipurpose catheter was positioned via the transseptal sheath into the LA and advanced across the lesion of interest to measure the transstenotic gradient and to perform venography. On the basis of this imaging and ICE sizing, a balloon with an appropriate diameter and length was selected to engage each stenotic lesion. In general, a balloon-to-vein ratio of 1.0 to 1.2 was chosen, and repeated inflations of 6 to 12 atm were undertaken, as guided fluoroscopically and by ICE. In the first 3 patients, a bare-metal stent of appropriate dimensions was positioned across the residual PV stenosis, with the end of the stent positioned at the venoatrial junction, under fluoroscopic and ICE guidance. In all subsequent patients, a stent was placed only if rebound stenosis was seen after balloon dilatation.
Follow-Up
Eighteen to 24 hours after the interventional procedure, the CT and V/Q scans and the TEE examination were repeated. Patients were subsequently discharged on warfarin to a target international normalized ratio (INR) of 2 to 3, along with 75 mg clopidogrel per day thereafter. Low-molecular-weight heparin was given subcutaneously twice daily until the INR was 2.0. Patients were followed up by telephone contact and repeated clinic evaluation, as well as repeated studies at 3 months.
Statistical Analysis
All data are presented as mean±SD. Comparisons between preintervention and postintervention vessel size and lesion characteristics were made with nonparametric methods. In all patients except 7, the stenosis data could be compared with baseline information from that particular patient. Correlation between 2 variables was established by least-squares methods. A probability value 0.05 was taken as significant.
Results
Ablative Intervention
Symptom Development
These patients developed symptoms over the course of 103±100 days of follow-up. Nineteen had increasing dyspnea on exertion, 7 had dyspnea at rest, and a recurrent cough was present in 9. Six had aching or burning chest pain, which was pleuritic in 5. Flulike symptoms, including fatigue, myalgia, and low-grade fever, were noted by 3 patients. Three had received a course of antibiotics for the presumptive diagnosis of bronchitis, without benefit. Three patients developed hemoptysis.
Initial Physical/Laboratory Examination
In 22 patients, the physical examination was normal, whereas one had inspiratory crackles over the affected lung region. None had evidence of pulmonary hypertension. One patient had interstitial changes on the chest x-ray film in the absence of cardiomegaly, but no radiographic abnormalities were seen in the remaining 22 patients. The average PaO2 in the 8 patients tested was 86±16 mm Hg (saturation, 94±3%), with no change during exercise.
CT Imaging
Transesophageal Echocardiography
The affected PVs were well visualized in 16 of 34 Mayo cases. Lesion narrowing (mean, 5±3 mm; range, 2 to 12) was seen in 11. A pulmonary artery systolic pressure >40 mm Hg was seen in only 1 case. Flow velocities (mean, 1.7±0.6 m/s), measured from the PVs, were 2.5 m/s in 3, 2.0 to 2.5 m/s in 1, 1.5 to 2.0 m/s in 6, and between 1.0 and 1.5 m/s in 6. In each case, there was turbulent blood flow with increased aliasing on color flow examination.
V/Q Imaging
Ventilation scanning was completely normal in 17 of 22 patients, with a defect in only 10 of 38 regions corresponding to affected veins (Figure 2). A perfusion defect that could be correlated with the stenotic lesion was seen in the distribution of all 34 affected veins (Figure 2; 40 of 132 segments).
The relative perfusion from an affected segment contributed between 0% and 9% (4±3%) of total perfusion. This compared with a value of 22±10% seen in other segments without any corresponding PV abnormality (P0.001). In 14 patients, quantitative analysis of perfusion indicated highly asymmetric tracer uptake within the lungs, suggesting a major impediment to PV drainage. There was a matching reduction in ventilation in only 3 patients.
Interventional Procedure
Postinterventional Imaging
Follow-Up
All 23 patients had a substantial reduction in symptoms within minutes to 1 hour after vessel treatment. Nevertheless, 14 patients (57%) developed recurrent symptoms at 3.2±2.8 months after the initial intervention, with dyspnea on exertion in 13 and cough or chest pain in 5. Two of the 14 experienced hemoptysis, whereas one reported cough and pleuritic chest pain. Thirteen patients required repeated interventions on 14 of the originally treated veins. Six of these veins had been previously dilated, whereas 8 veins were stented at the time of the original procedure. Four of these latter veins showed in-stent restenosis, whereas 4 showed in-segment PV stenosis at sites proximal or distal to the stent. Six patients also developed significant stenosis in 6 previously undilated veins. One lesion had progressed to total occlusion and could not be redilated.
Three patients again developed dyspnea on exertion, associated with cough or fatigue, requiring another intervention on 3 veins. One vessel was redilated and 2 were stented. One patient required a fourth intervention. On long-term follow-up at 18±12 months (range, 3 to 34), 15 patients remain completely asymptomatic from PV stenosis, and 4 have mild and 3 have moderate symptoms.
Discussion
These data provide substantial insight into the clinical syndrome of acquired PV stenosis occurring after radiofrequency ablation for AF. Patients with this malady can be extremely symptomatic but respond almost immediately to percutaneous intervention. Although initial results are encouraging, the occurrence of restenosis, including in- and out-of-stent abnormalities, remains a concern.
PV stenosis is an established complication occurring with radiofrequency energy delivery for focal AF ablation. Robbins et al25 reported multivessel PV stenosis after linear ablation for AF in 2 patients. The prevalence of this problem in the setting of linear ablation likely ranges between 2% and 7%.26 The exact prevalence of PV stenosis in patients undergoing focal or segmental AF ablation is becoming more clear.3,4,10–15 In one of the larger series, Chen et al4 initially described apparent PV stenosis in 42% of their 79 patients. This represents an overestimation of this problem, however, because an increased TEE flow velocity was used to establish the diagnosis. A later study from the same group noted a 33% incidence of PV narrowing, again established by TEE methods.13 Gerstenfeld and coworkers10 have reported an 8.3% occurrence of clinically relevant PV stenosis in an early series of 40 patients undergoing focal AF ablation. Similarly, Saad and coworkers27 reported a 5% incidence of severe PV stenosis (>75%) in patients undergoing electrical isolation of their PVs. In their initial series, Haissaguerre et al3 reported a 5% occurrence rate but have recently suggested a decrease to <1% overall with additional experience in ablation. Pappone et al7,8 also reported a <1% PV stenosis rate with ablation limited to atrial tissue outside the PV orifice. Other groups have reported cases of patients with PV stenosis requiring venoplasty or stenting.16–21 In the absence of a clear-cut "denominator," however, it is not possible to decipher the incidence of this complication in those studies.
The prevalence of this problem has decreased because of a variety of factors, including (1) abandonment of in-vein ablation at the site of the AF focus; (2) limiting ablation at or outside the orifice of the vessel; (3) the use of ICE to guide catheter placement and monitor energy delivery; (4) a reduction in target ablation temperature and the amounts of energy deliveries; and (5) increased operator experience.12 This report represents 6.0% of the initial 203 patients who underwent PV ablation at this institution.12 In the first 100 patients undergoing ablation, 11 developed a stenotic lesion, whereas only 1 has developed a stenotic lesion requiring intervention in the last 100 patients. This "learning curve" has also been documented by Saad et al,15 who underscored the importance of experience, ablation outside the PV, and intracardiac ultrasound use for decreasing moderate and severe PV stenosis occurrence from 7.9% to 1.4%. Recent review of the European experience with AF ablation documented PV stenosis rates approaching 20% in the centers performing <50 PV isolation procedures.29
The exact pathology of PV stenosis has not been elucidated. In the present series, patients undergoing a first dilatation procedure had both soft and more fibrotic components of PV pathology. In most cases, a clear-cut waist in the venoplasty balloon was seen with balloon inflation. In some cases, 10 to 12 atm of pressure were required for elimination of that apparent scarring. In 3 cases, the stenosis was partially reopened simply by passing a guidewire through it. This, and subsequent in-stent restenosis, suggests a component of neointimal hyperplasia and/or thrombus as well. No pathological specimens were obtained for histology, however. Taylor and coworkers30 found both extensive architectural remodeling and fibrosis, as well as neointimal hyperplasia. In parallel studies, we have also found neointimal hyperplasia in a canine model of PV stenosis occurring with both radiofrequency and ultrasound energy delivery31 and a marked inflammatory process.32 Additional studies will be required to elucidate further the molecular and histological pathways of this problem.
Regardless of pathology, these patients were highly symptomatic. Most presented with dyspnea on exertion as the initial manifestation of this process, which typically evolved over the course of 1 to 3 months. Although pleuritic chest pain is a late manifestation of the process, hemoptysis was uncommon during follow-up in this series. Both processes are likely related to complete vessel or branch occlusion in these individuals. Blood gas assessment and pulmonary function testing were not useful as screening measures for early stenosis. These symptoms and chest x-ray changes may lead to an erroneous diagnosis of bronchitis or other pulmonary parenchymal process, delaying establishment of PV stenosis. In a recent series of PV stenosis, patients were often misdiagnosed by their primary care givers as having bronchitis.27 This occurrence of "garden-variety" respiratory symptoms could also contribute to an underestimation of the prevalence of this process.
CT Scanning
CT evaluation was the most helpful in identifying the location and extent of the stenoses. Establishment of the true endocardial PV orifice was a straightforward and reproducible process. Postprocessing of the very thin axial slices allowed near-isotropic voxel coronal, oblique, sagittal, and 3D renderings for review and measurement. There was a limited yet significant correlation between the extent of stenosis seen on the CT scan images and that at the time of angiography. This is likely due to the difference in imaging plane for each technique. The angiographic views were right and left anterior oblique to the patient, whereas the CT views were orthogonal to the vessel. Vessels may still be patent on venography, even if they appear occluded on CT imaging. Comparable experience with magnetic resonance imaging is limited.33
V/Q Scanning
V/Q scanning was helpful for establishing the pathophysiology of the stenosis and its progression. Ventilation abnormalities occurred only in extreme cases. In contrast, perfusion abnormalities were marked. These abnormalities appeared similar to the changes seen in pulmonary embolism. Although in most cases the perfusion deficit was limited to the distribution of the involved vein, several patients showed a reduction in perfusion in the ipsilateral lung. The exact cause of this is unclear but suggests the presence of a compensatory mechanism affecting multiple vascular beds. Furthermore, the perfusion abnormalities in some patients did not normalize over the course of their follow-up, indicating persistent physiological abnormalities in the setting of normalized anatomy.
Echocardiographic Evaluation
Although TEE imaging was useful in providing a good view of the superior PVs, imaging of the right and left inferior PVs was inconsistent. In contrast, ICE allowed straightforward, real-time imaging of all PVs. The right superior PV at its orifice was typically viewed en face,24 with additional rotation required to view the vessel along its long axis. Imaging into each of the vessels provided a good view into the first 1 to 3 cm of the vein. Color flow contrast imaging was also useful in identifying the location of the orifice of the most tightly stenotic vessels. The flow velocities seen in these vessels were elevated, but not to the extent expected, because of the impact of a tight stenosis and longer lesions with accompanying reductions in blood flow.
ICE facilitated accurate stent placement by reliably identifying the orifice of the tightly stenotic vessels. This imaging modality disclosed an additional problem of stent placement in left PVs. Because these orthogonal superior and inferior vessels can form an antrum before entrance into the LA, great care is required to ensure that the positioning of a stent in one PV does not obstruct the orifice of the paired vessel.
Intervention
Although in some cases the initial lesion accepted balloons of only 4 to 6 mm in diameter, dilatation with 10-mm balloons was possible in the majority of cases. This experience suggests that inflation to 10 to 12 atm may be required. In the majority of these patients, achieving this outcome required breaking through an apparently fibrous waist. At this point in our experience, larger stents were not deployed because of concerns about vessel dissection. The patient who sustained a PV dissection was dilated with a 12-mm balloon.
Restenosis
Unfortunately, both in-stent and in-segment restenoses have recurred during 17 months of follow-up. This confirms the findings of Qureshi and colleagues,34 who observe a 47% restenosis rate 11 months after the intervention. Those within the body of the stent are likely caused by neointimal hyperplasia and fibrosis.35 Out-of-stent restenoses were observed at bifurcation points beyond the stent into the vessel, also suggesting the progression of PV pathology, despite stent placement. There is no experience to date with the use of sirolimus or paclitaxel drug-eluting stents in this situation, but such a high restenosis rate makes a strong case for the investigation of such devices and larger-diameter stents. Furthermore, the utility of brachytherapy and surgical intervention are also unclear, and the latter has been disappointing when used as treatment for congenital stenosis.36,37
Limitations
First, although this is the largest interventional series with the longest duration of follow-up published to date, the numbers remain small and may or may not apply to all patients with ablation-induced PV stenosis. Assessment of the relative merits of simple balloon dilatation versus stenting is also hampered by the limited number of patients with stenosis. Given this, a PV stenosis registry will be required to further assess the impact of this process and treatment in resolution of symptoms. Furthermore, these data reflect the learning curve present in this new venue of occlusive disease. The study also fails to indicate precisely which of the multiple energy deliveries in a single vein created the stenosis. On the basis of our prior review, this occurrence is most likely due to multiple deliveries.
Clinical Implications
It has been established that changes in ablation approaches and traversing the ablation learning curve have reduced the rate of this complication at individual, high-volume centers. Nevertheless, with the currently widespread application of ablation for AF, this problem will undoubtedly continue to affect many patients in the "real world." Recently reported cases of late progressive PV stenosis in patients with minor abnormalities on initial postablation venography or follow-up CT scanning further predict a higher prevalence over time.11,38 Furthermore, the presence of PV stenosis is commonly misdiagnosed and underestimated in the absence of surveillance of all patients undergoing PV ablation. As such, preventive approaches and effective therapy for this process will continue to be critical. The diagnostic and interventional strategies outlined in this report represent an important and early step along that pathway.
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