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1 fibrillation after contact force (CF)-guided pulmonary vein isolation.
2 as terminated in 20 patients (38%) after the pulmonary vein isolation.
3 required spot-ablations to complete electric pulmonary vein isolation.
4 logic study, symptomatic AFL is common after pulmonary vein isolation.
5 is a novel, nonthermal ablation modality for pulmonary vein isolation.
6 nd may require more extensive treatment than pulmonary vein isolation.
7 Patients with paroxysmal AF underwent pulmonary vein isolation.
8 ed during sinus rhythm in 22 patients before pulmonary vein isolation.
9 before video-assisted thoracoscopic surgical pulmonary vein isolation.
10 paroxysmal AF who were scheduled to undergo pulmonary vein isolation.
11 0 patients; 28%) underwent cryoballoon-based pulmonary vein isolation.
12 ed during sinus rhythm after circumferential pulmonary vein isolation.
13 xation time on CMR and freedom from AF after pulmonary vein isolation.
14 ong association with late recurrent AF after pulmonary vein isolation.
15 All patients underwent successful pulmonary vein isolation.
16 (focal impulse and rotor modulation) before pulmonary vein isolation.
17 AD) therapy in patients with previous failed pulmonary vein isolation.
18 mber of patients with nonparoxysmal AF after pulmonary vein isolation.
20 atients undergoing CF-guided circumferential pulmonary vein isolation, 914 radiofrequency application
27 ad undergone cardiac surgery exclusively for pulmonary vein isolation and 17 had no structural heart
28 During video-assisted thoracoscopic surgical pulmonary vein isolation and CARTO mapping, BrS patients
29 ry, 14 months; Q1-Q3, 7-36 months) underwent pulmonary vein isolation and completed the entire follow
30 ents with nonparoxysmal AF undergoing antral pulmonary vein isolation and nonpulmonary vein trigger a
33 nt AF and 22 with long-lasting AF, underwent pulmonary vein isolation and substrate modification of c
35 variable, an ablation strategy that involves pulmonary vein isolation and/or a particular set of abla
36 fibrillation between patients who underwent pulmonary-vein isolation and those who underwent the bia
37 and 9 +/- 10 months for the Cox-Maze IV, the pulmonary vein isolation, and the limited Cox-Maze proce
39 ted atrial electrograms (CFAEs) after antral pulmonary vein isolation (APVI) further improves the cli
44 ) and the surgical maze procedure (including pulmonary vein isolation) done during other cardiac surg
45 ablation using a stepwise ablation approach (pulmonary vein isolation, electrogram-guided, and linear
46 en; 61 long-lasting persistent AF) underwent pulmonary vein isolation followed by electrogram-guided
47 urrence substantially limits the efficacy of pulmonary vein isolation for AF and is associated with p
48 THODS AND Ten consecutive patients underwent pulmonary vein isolation for persistent atrial fibrillat
49 Contact force parameters evaluated during pulmonary vein isolation for treating atrial fibrillatio
52 ducibility of atrial fibrillation (AF) after pulmonary vein isolation has been used to guide addition
55 uspid isthmus ablation is appropriate during pulmonary vein isolation if AFL has been observed clinic
56 hereas CFAE ablation in addition to standard pulmonary vein isolation improves outcomes in patients w
57 acute), and later than 3 months (late) after pulmonary vein isolation in 25 patients with paroxysmal
58 se, Geneva, Switzerland) was used to perform pulmonary vein isolation in 46 patients with paroxysmal
59 lation strategies in the LAAI group included pulmonary vein isolation in 50 (100%), left atrial isthm
61 e targeted for ablation, in conjunction with pulmonary vein isolation in most patients (n=19; 79%).
62 ce atrial fibrillation (AF) recurrence after pulmonary vein isolation in patients with paroxysmal AF.
63 ) and cryoballoon catheter (CB) ablation for pulmonary vein isolation in patients with paroxysmal atr
64 The use of second-generation cryoballoon for pulmonary vein isolation in patients with paroxysmal atr
65 g CFAEs have been compared with the standard pulmonary vein isolation in persistent as well as paroxy
66 for prevention of early AF recurrences after pulmonary vein isolation in the absence of antiarrhythmi
73 its high success and low complication rate, pulmonary vein isolation is expected to be increasingly
79 went epicardial thoracoscopic radiofrequency pulmonary vein isolation, linear ablation, Marshal ligam
81 l fibrillation before electric cardioversion/pulmonary vein isolation or after cardioembolic cerebrov
82 ion group underwent further randomization to pulmonary-vein isolation or a biatrial maze procedure.
83 ss II or III heart failure to undergo either pulmonary-vein isolation or atrioventricular-node ablati
84 Ablation was performed by circumferential pulmonary vein isolation plus linear ablation of extrapu
85 reablation after a previously failed initial pulmonary vein isolation procedure were eligible for thi
88 to compare arrhythmia-free survival between pulmonary vein isolation (PVI) and a stepwise approach (
89 cryoballoon is effective in achieving acute pulmonary vein isolation (PVI) and favorable clinical ou
90 es recommend a 3-month blanking period after pulmonary vein isolation (PVI) as early recurrence of at
91 Atrial fibrillation (AF) may recur after pulmonary vein isolation (PVI) as the result of either r
92 nd-generation cryoballoon delivers effective pulmonary vein isolation (PVI) associated with superior
93 can be challenging, often involving not only pulmonary vein isolation (PVI) but also additional linea
94 gate whether the combination of conventional pulmonary vein isolation (PVI) by circumferential antral
97 ess and complications in patients undergoing pulmonary vein isolation (PVI) for treatment of atrial f
99 imed to determine the safety and efficacy of pulmonary vein isolation (PVI) in atrial fibrillation (A
100 s the impact of CFAE ablation in addition to pulmonary vein isolation (PVI) in patients undergoing ab
105 tions include not only the durability of the pulmonary vein isolation (PVI) lines, but also the patho
113 transesophageal echocardiogram (TEE) before pulmonary vein isolation (PVI); and 2) the relationship
115 in patients undergoing robotically assisted pulmonary vein isolation (RA-PVI) as compared with manua
118 ablation at these sites, in conjunction with pulmonary vein isolation, resulted in AF termination or
119 ion to investigate the hypothesis that acute pulmonary vein isolation results from a combination of i
120 e of second-generation 28-mm cryoballoon for pulmonary vein isolation results in an 80% 1-year succes
125 ciation between LAPEF and recurrent AF after pulmonary vein isolation that persisted after multivaria
126 onitoring in the ADVICE (Adenosine Following Pulmonary Vein Isolation to Target Dormant Conduction El
127 on techniques may facilitate safe and simple pulmonary vein isolation to treat paroxysmal atrial fibr
128 ed tomography (CT) before and 3 months after pulmonary vein isolation using duty-cycled phased radio
129 balloon (LB) with wide-area circumferential pulmonary vein isolation using irrigated radiofrequency
130 imilar efficacy as wide-area circumferential pulmonary vein isolation using irrigated RF in patients
131 tiarrhythmic drug(s), who were scheduled for pulmonary vein isolation using second-generation cryobal
133 ulceration and fistula are complications of pulmonary vein isolation using thermal energy sources.
134 risk of pulmonary vein narrowing (PVN) after pulmonary vein isolation, using a novel multi-electrode
135 educing AF recurrence, SOE was high favoring pulmonary vein isolation versus antiarrhythmic medicatio
140 udy included 140 patients (43 women) in whom pulmonary vein isolation was performed using a second-ge
143 th paroxysmal atrial fibrillation undergoing pulmonary vein isolation were followed for 12 months wit
145 s circular lesions, deep enough for electric pulmonary vein isolation, were created with a single cir
147 brillation (AF) recurrences than wide antral pulmonary vein isolation (wide antral isolation [WAI]) b
149 y end point favored the group that underwent pulmonary-vein isolation, with an improved questionnaire
150 had similar rates of single-procedure acute pulmonary vein isolation without serious adverse events
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