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1 ed during sinus rhythm after circumferential pulmonary vein isolation.
2 xation time on CMR and freedom from AF after pulmonary vein isolation.
3 ong association with late recurrent AF after pulmonary vein isolation.
4 All patients underwent successful pulmonary vein isolation.
5 (focal impulse and rotor modulation) before pulmonary vein isolation.
6 AD) therapy in patients with previous failed pulmonary vein isolation.
7 mber of patients with nonparoxysmal AF after pulmonary vein isolation.
8 as terminated in 20 patients (38%) after the pulmonary vein isolation.
9 logic study, symptomatic AFL is common after pulmonary vein isolation.
10 All AF patients received circumferential pulmonary vein isolation.
11 standalone procedure or in combination with pulmonary vein isolation.
12 or producing rapid and effective lesions for pulmonary vein isolation.
13 losure was evaluated through 12 months after pulmonary vein isolation.
14 seconds duration 12 months after undergoing pulmonary vein isolation.
15 hic tracing obtained through 12 months after pulmonary vein isolation.
16 of atrial fibrillation (AF) recurrence after pulmonary vein isolation.
17 tion modality, or ablation strategies beyond pulmonary vein isolation.
18 uate the long-term outcome after cryoballoon pulmonary vein isolation.
19 tic paroxysmal atrial fibrillation underwent pulmonary vein isolation.
20 fibrillation after contact force (CF)-guided pulmonary vein isolation.
21 required spot-ablations to complete electric pulmonary vein isolation.
22 is a novel, nonthermal ablation modality for pulmonary vein isolation.
23 nd may require more extensive treatment than pulmonary vein isolation.
24 Patients with paroxysmal AF underwent pulmonary vein isolation.
25 ed during sinus rhythm in 22 patients before pulmonary vein isolation.
26 before video-assisted thoracoscopic surgical pulmonary vein isolation.
27 paroxysmal AF who were scheduled to undergo pulmonary vein isolation.
28 0 patients; 28%) underwent cryoballoon-based pulmonary vein isolation.
29 Randomized control trials comparing PWI to pulmonary vein isolation (3 studies, 444 patients) yield
31 atients undergoing CF-guided circumferential pulmonary vein isolation, 914 radiofrequency application
36 ation for paroxysmal atrial fibrillation and pulmonary vein isolation+/-additional lesions for persis
41 ved in 84 of 148 (56.5%) of those undergoing pulmonary vein isolation alone and in 111 of 154 (72.1%)
43 trial arrhythmias at 12 months compared with pulmonary vein isolation alone for patients with nonparo
47 of VLR in patients who underwent cryoballoon pulmonary vein isolation alone, had an implantable loop
54 ad undergone cardiac surgery exclusively for pulmonary vein isolation and 17 had no structural heart
55 undergo left atrial appendage ligation plus pulmonary vein isolation and 206 were randomized to unde
56 4.3% with left atrial appendage ligation and pulmonary vein isolation and 59.9% with pulmonary vein i
59 During video-assisted thoracoscopic surgical pulmonary vein isolation and CARTO mapping, BrS patients
60 ry, 14 months; Q1-Q3, 7-36 months) underwent pulmonary vein isolation and completed the entire follow
61 d with a circular mapping catheter to assess pulmonary vein isolation and esophageal temperature moni
62 l or persistent AF who underwent cryoballoon pulmonary vein isolation and had an implantable loop rec
63 regulatory trials, the catheter was used for pulmonary vein isolation and left atrial posterior wall
65 cal practice, physicians have ablated beyond pulmonary vein isolation and left atrial posterior wall
66 randomly assigned to (1) standard ablation (pulmonary vein isolation and nonpulmonary vein trigger a
67 rrhythmia recurrences compared with standard pulmonary vein isolation and nonpulmonary vein trigger a
68 ents with nonparoxysmal AF undergoing antral pulmonary vein isolation and nonpulmonary vein trigger a
71 nt AF and 22 with long-lasting AF, underwent pulmonary vein isolation and substrate modification of c
73 variable, an ablation strategy that involves pulmonary vein isolation and/or a particular set of abla
74 fibrillation between patients who underwent pulmonary-vein isolation and those who underwent the bia
76 and 9 +/- 10 months for the Cox-Maze IV, the pulmonary vein isolation, and the limited Cox-Maze proce
78 ted atrial electrograms (CFAEs) after antral pulmonary vein isolation (APVI) further improves the cli
81 heters have been shown capable of performing pulmonary vein isolation, but not flexible lesion sets s
82 e-shot PFA catheters have been developed for pulmonary vein isolation, but they do not permit flexibl
88 left atrial appendage ligation adjunctive to pulmonary vein isolation did not meet prespecified effic
89 ) and the surgical maze procedure (including pulmonary vein isolation) done during other cardiac surg
92 ablation using a stepwise ablation approach (pulmonary vein isolation, electrogram-guided, and linear
93 en; 61 long-lasting persistent AF) underwent pulmonary vein isolation followed by electrogram-guided
94 th PWI group (n = 170) underwent wide antral pulmonary vein isolation followed by posterior wall isol
95 urrence substantially limits the efficacy of pulmonary vein isolation for AF and is associated with p
97 ial appendage ligation adjunctive to planned pulmonary vein isolation for nonparoxysmal atrial fibril
99 THODS AND Ten consecutive patients underwent pulmonary vein isolation for persistent atrial fibrillat
100 onsecutive patients treated with cryoballoon pulmonary vein isolation for symptomatic AF between 2012
101 Contact force parameters evaluated during pulmonary vein isolation for treating atrial fibrillatio
106 ducibility of atrial fibrillation (AF) after pulmonary vein isolation has been used to guide addition
109 er, no adjunctive lesion set, in addition to pulmonary vein isolation, has been conclusively demonstr
111 uspid isthmus ablation is appropriate during pulmonary vein isolation if AFL has been observed clinic
112 hereas CFAE ablation in addition to standard pulmonary vein isolation improves outcomes in patients w
113 acute), and later than 3 months (late) after pulmonary vein isolation in 25 patients with paroxysmal
114 se, Geneva, Switzerland) was used to perform pulmonary vein isolation in 46 patients with paroxysmal
115 lation strategies in the LAAI group included pulmonary vein isolation in 50 (100%), left atrial isthm
119 e targeted for ablation, in conjunction with pulmonary vein isolation in most patients (n=19; 79%).
120 ce atrial fibrillation (AF) recurrence after pulmonary vein isolation in patients with paroxysmal AF.
121 The use of second-generation cryoballoon for pulmonary vein isolation in patients with paroxysmal atr
122 ) and cryoballoon catheter (CB) ablation for pulmonary vein isolation in patients with paroxysmal atr
123 g CFAEs have been compared with the standard pulmonary vein isolation in persistent as well as paroxy
124 for prevention of early AF recurrences after pulmonary vein isolation in the absence of antiarrhythmi
125 imary outcomes were ability to achieve acute pulmonary vein isolation intraprocedurally and safety at
128 in the first 5 years showed that successful pulmonary vein isolation is achieved in the majority of
134 its high success and low complication rate, pulmonary vein isolation is expected to be increasingly
143 -4.3 months) of which 3 had AF terminated on pulmonary vein isolation, leaving 27 patients that under
144 went epicardial thoracoscopic radiofrequency pulmonary vein isolation, linear ablation, Marshal ligam
145 se remote from the coronary arteries such as pulmonary vein isolation (n=25 patients) and left atrial
147 n, and (3) The efficacy of PWI compared with pulmonary vein isolation on preventing arrhythmia recurr
148 and pulmonary vein isolation and 59.9% with pulmonary vein isolation only (difference, 4.3% [bayesia
149 more frequent (68% versus 59%; P<0.001), and pulmonary vein isolation-only was more frequent (93% ver
151 l fibrillation before electric cardioversion/pulmonary vein isolation or after cardioembolic cerebrov
152 tor for stroke at 126 sites to ablation with pulmonary vein isolation or drug therapy including rate
153 o undergo left atrial appendage ligation and pulmonary vein isolation or pulmonary vein isolation alo
154 ion group underwent further randomization to pulmonary-vein isolation or a biatrial maze procedure.
155 ss II or III heart failure to undergo either pulmonary-vein isolation or atrioventricular-node ablati
156 voltage zones, recovery of posterior wall or pulmonary vein isolation, or other sustaining mechanisms
157 mary effectiveness end point (PEE) was acute pulmonary vein isolation plus freedom from any atrial ar
158 Ablation was performed by circumferential pulmonary vein isolation plus linear ablation of extrapu
159 randomized patients with symptomatic PsAF to pulmonary vein isolation plus posterior wall isolation o
160 nd in 111 of 154 (72.1%) of those undergoing pulmonary vein isolation plus renal denervation (hazard
161 pulmonary vein isolation alone (n = 148) or pulmonary vein isolation plus renal denervation (n = 154
162 reablation after a previously failed initial pulmonary vein isolation procedure were eligible for thi
168 he ablation group were further randomized to pulmonary vein isolation (PVI) (n = 62) or the biatrial
169 ike for paroxysmal atrial fibrillation (AF), pulmonary vein isolation (PVI) alone is considered insuf
172 to compare arrhythmia-free survival between pulmonary vein isolation (PVI) and a stepwise approach (
173 cryoballoon is effective in achieving acute pulmonary vein isolation (PVI) and favorable clinical ou
174 o propensity-score matched cohorts, one with pulmonary vein isolation (PVI) and linear ablation inclu
175 ave been developed to achieve more effective pulmonary vein isolation (PVI) and minimize arrhythmia r
176 ecurrences of atrial fibrillation (AF) after pulmonary vein isolation (PVI) are mainly due to pulmona
178 for atrial fibrillation (AF) has established pulmonary vein isolation (PVI) as a key target for AF ab
179 es recommend a 3-month blanking period after pulmonary vein isolation (PVI) as early recurrence of at
181 Atrial fibrillation (AF) may recur after pulmonary vein isolation (PVI) as the result of either r
182 nd-generation cryoballoon delivers effective pulmonary vein isolation (PVI) associated with superior
183 can be challenging, often involving not only pulmonary vein isolation (PVI) but also additional linea
184 gate whether the combination of conventional pulmonary vein isolation (PVI) by circumferential antral
187 ess and complications in patients undergoing pulmonary vein isolation (PVI) for treatment of atrial f
190 imed to determine the safety and efficacy of pulmonary vein isolation (PVI) in atrial fibrillation (A
191 s the impact of CFAE ablation in addition to pulmonary vein isolation (PVI) in patients undergoing ab
192 nts the gold standard single-shot device for pulmonary vein isolation (PVI) in patients with atrial f
195 ation (PersAF), catheter ablation aiming for pulmonary vein isolation (PVI) is associated with modera
200 tions include not only the durability of the pulmonary vein isolation (PVI) lines, but also the patho
202 with persistent AF were randomly assigned to pulmonary vein isolation (PVI) plus MRI-guided atrial fi
205 eld ablation (PFA) has gained prominence for pulmonary vein isolation (PVI) to treat atrial fibrillat
206 efficacy and safety of combining cryoballoon pulmonary vein isolation (PVI) with SVC ablation compare
207 Background Although proposed to facilitate pulmonary vein isolation (PVI), high-power ablation may
215 transesophageal echocardiogram (TEE) before pulmonary vein isolation (PVI); and 2) the relationship
216 has shown impressive efficacy and safety for pulmonary vein isolation (PVI); however, initial efficac
218 in patients undergoing robotically assisted pulmonary vein isolation (RA-PVI) as compared with manua
221 in isolation, use of a nonstudy catheter for pulmonary vein isolation, repeat procedure (except for o
224 ablation at these sites, in conjunction with pulmonary vein isolation, resulted in AF termination or
225 ion to investigate the hypothesis that acute pulmonary vein isolation results from a combination of i
226 e of second-generation 28-mm cryoballoon for pulmonary vein isolation results in an 80% 1-year succes
228 nt this stalemate, safer, and more effective pulmonary vein isolation seems increasingly realistic.
233 y Holter monitoring at 6 and 12 months after pulmonary vein isolation, symptomatic event monitoring,
234 ciation between LAPEF and recurrent AF after pulmonary vein isolation that persisted after multivaria
237 onitoring in the ADVICE (Adenosine Following Pulmonary Vein Isolation to Target Dormant Conduction El
238 on techniques may facilitate safe and simple pulmonary vein isolation to treat paroxysmal atrial fibr
240 atrial flutter) episodes, failure to achieve pulmonary vein isolation, use of a nonstudy catheter for
241 line pulsed field ablation catheter achieves pulmonary vein isolation using 8 stacked, pose-specific
242 aroxysmal AF, planned for first CLOSE-guided pulmonary vein isolation using a contact force radiofreq
243 se evaluated the feasibility and efficacy of pulmonary vein isolation using a novel PFA system delive
244 ed tomography (CT) before and 3 months after pulmonary vein isolation using duty-cycled phased radio
245 balloon (LB) with wide-area circumferential pulmonary vein isolation using irrigated radiofrequency
246 imilar efficacy as wide-area circumferential pulmonary vein isolation using irrigated RF in patients
249 tiarrhythmic drug(s), who were scheduled for pulmonary vein isolation using second-generation cryobal
251 llows for simple and safe simple single shot pulmonary vein isolation using standard sedation protoco
252 udy confirms the safety and effectiveness of pulmonary vein isolation using the novel 3-dimensional m
253 ulceration and fistula are complications of pulmonary vein isolation using thermal energy sources.
254 risk of pulmonary vein narrowing (PVN) after pulmonary vein isolation, using a novel multi-electrode
255 educing AF recurrence, SOE was high favoring pulmonary vein isolation versus antiarrhythmic medicatio
256 roke to a strategy of catheter ablation with pulmonary vein isolation versus drug therapy with rate/r
260 In this first-in-human clinical study, 100% pulmonary vein isolation was achieved using only PFA wit
269 udy included 140 patients (43 women) in whom pulmonary vein isolation was performed using a second-ge
270 l (35 W), whereas in the experimental group, pulmonary vein isolation was performed using high power
277 th paroxysmal atrial fibrillation undergoing pulmonary vein isolation were followed for 12 months wit
279 nts with atrial fibrillation despite durable pulmonary vein isolation were randomly assigned at 7 cen
280 s circular lesions, deep enough for electric pulmonary vein isolation, were created with a single cir
282 brillation (AF) recurrences than wide antral pulmonary vein isolation (wide antral isolation [WAI]) b
285 rticipants were randomly assigned to receive pulmonary vein isolation with cryoablation (n = 64) or a
286 receive radiofrequency catheter ablation for pulmonary vein isolation with either a standard single W
289 catheter ablation group (n = 1108) underwent pulmonary vein isolation, with additional ablative proce
290 is to identify those who will not respond to pulmonary vein isolation, with novel approaches to pheno
291 y end point favored the group that underwent pulmonary-vein isolation, with an improved questionnaire
292 had similar rates of single-procedure acute pulmonary vein isolation without serious adverse events