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1 boembolic events-European Registry in Atrial Fibrillation).
2 or subclinical and clinical new-onset atrial fibrillation).
3 s with both paroxysmal and persistent atrial fibrillation.
4 than 2% of admissions were always in atrial fibrillation.
5 vely inhibits both Abeta oligomerization and fibrillation.
6 ndex were among the top predictors of atrial fibrillation.
7 et if there was no prior diagnosis of atrial fibrillation.
8 d specific stroke mechanisms, such as atrial fibrillation.
9 s and NOACs (n=71 681) in nonvalvular atrial fibrillation.
10 hromboembolic events in patients with atrial fibrillation.
11 one of the most potent antagonists of Abeta fibrillation.
12 that pH serves as an on/off switch for betaS fibrillation.
13 associated with an increased risk of atrial fibrillation.
14 duced ventricular tachycardia or ventricular fibrillation.
15 hromboembolism even in the absence of atrial fibrillation.
16 ronic treatments to all patients with atrial fibrillation.
17 rdiac atrial disorders independent of atrial fibrillation.
18 on around the world for patients with atrial fibrillation.
19 s into the trigger and maintenance of atrial fibrillation.
20 ke/systemic embolism in patients with atrial fibrillation.
21 or harmful in patients with ESRD and atrial fibrillation.
22 ulation is underused in patients with atrial fibrillation.
23 nagement of patients with nonvalvular atrial fibrillation.
24 tal findings on inhibiting full-length Abeta fibrillation.
25 ial infarction, non-fatal stroke, and atrial fibrillation.
26 g cardiac dysrhythmias, most commonly atrial fibrillation.
27 t disease, heart failure, stroke, and atrial fibrillation.
28 one of the most potent antagonists of Abeta fibrillation.
29 bleeding in patients with nonvalvular atrial fibrillation.
30 uch as the long-QT syndrome (LQT) and atrial fibrillation.
31 cardiomyopathy given its parallels to atrial fibrillation.
32 arfarin for patients with nonvalvular atrial fibrillation.
33 r disease, stroke, heart failure, and atrial fibrillation.
34 tachycardias converted to VT or ventricular fibrillation.
35 ions, stroke severity, and history of atrial fibrillation.
36 history of ischemic heart disease or atrial fibrillation.
37 her rates of device complications and atrial fibrillation.
38 rence of ventricular tachycardia/ventricular fibrillation.
39 indicated after the first episode of atrial fibrillation.
40 dial infarction, non-fatal stroke, or atrial fibrillation.
41 8.9% had ventricular tachycardia/ventricular fibrillation.
42 een associated with increased risk of atrial fibrillation.
43 thromboembolism, QT prolongation, and atrial fibrillation.
44 chycardia (IART) (61.6%), followed by atrial fibrillation (28.8%), and focal atrial tachycardia (9.5%
45 evalence of hypotension (57% vs 48%), atrial fibrillation (50% vs 40%), and other adverse events did
46 ) with heart failure, 109 (9.2%) with atrial fibrillation, 89 (8%) with myocardial infarction, 11 (0.
47 METHODS AND Patients undergoing first atrial fibrillation ablation and postinterventional esophageal
48 been reported with all modalities of atrial fibrillation ablation despite esophageal temperature mon
52 We prospectively studied 33 AT (post- atrial fibrillation ablation or surgical mitral valve repair).
53 total, 1802 patients underwent first atrial fibrillation ablation procedure between January 2013 and
55 foration is a dreaded complication of atrial fibrillation ablation that occurs in 0.1% to 0.25% of at
56 Since the original description of atrial fibrillation ablation, numerous studies have demonstrate
59 of intracardiac electrograms to guide atrial fibrillation (AF) ablation has yielded conflicting resul
60 LA) fibrosis is a strong predictor of atrial fibrillation (AF) ablation success and has been associat
61 sure (BP) lowering prevents recurrent atrial fibrillation (AF) after catheter ablation in patients wi
62 K antagonists (VKAs) in patients with atrial fibrillation (AF) and coexisting valvular heart disease
67 (CHD) are assumed to be vulnerable to atrial fibrillation (AF) as a result of residual shunts, anomal
68 n to prevent stroke for patients with atrial fibrillation (AF) but are often underused in community p
69 schemic stroke rates in patients with atrial fibrillation (AF) but increase the risk of bleeding.
70 ry artery evaluation in patients with atrial fibrillation (AF) by using invasive coronary angiography
71 ly published analysis of contemporary atrial fibrillation (AF) cohorts showed an association between
72 e long-term probability of developing atrial fibrillation (AF) considering genetic predisposition and
73 challenging in patients with extended atrial fibrillation (AF) duration and persistent/long-standing
78 Patients with heart failure (HF) and atrial fibrillation (AF) have higher circulating levels of NT-p
79 se-dependent termination of simulated atrial fibrillation (AF) in the absence of AF-induced electrica
92 s role on prognosis in anticoagulated atrial fibrillation (AF) patients and determined whether its ad
93 to the quality of anticoagulation in atrial fibrillation (AF) patients, reflected by time in therape
95 y has been associated with drivers of atrial fibrillation (AF) risk, including left ventricular and p
100 is associated with atrial remodeling, atrial fibrillation (AF), and increased incidence of arrhythmia
101 Atrial tachy-arrhytmias, such as atrial fibrillation (AF), are characterised by irregular electr
102 for thromboembolism in patients with atrial fibrillation (AF), but less is known about how diabetes
103 iants at >30 loci that associate with atrial fibrillation (AF), including rare coding mutations in th
104 l treatment, and clinical outcomes of atrial fibrillation (AF), sustained ventricular arrhythmias, an
106 ipose tissue (EAT) is associated with atrial fibrillation (AF), the most frequent cardiac arrhythmia.
107 ted conflicting mechanisms underlying atrial fibrillation (AF), with the spatial resolution of data o
120 (PVR) still determines recurrences of atrial fibrillation after contact force (CF)-guided pulmonary v
121 n predicts incident heart failure and atrial fibrillation; among patients with heart failure, it stro
122 WAS) included 17,931 individuals with atrial fibrillation and 115,142 referents; the exome-wide assoc
123 Danish cohort study of patients with atrial fibrillation and a single stroke risk factor, there was
125 to the risk of stroke associated with atrial fibrillation and as a determinant of arrhythmia progress
133 resent in the EGM recordings only for atrial fibrillation and some atrial flutter propagations patter
135 lation Versus Medical Rate Control in Atrial Fibrillation and Systolic Dysfunction [CAMERA-MRI]; ACTR
136 important role in the development of atrial fibrillation and that CLICs and structural type IV colla
138 ted cardiac arrest or documented ventricular fibrillation and ventricular tachycardia (lasting >/=30
139 identified determinants of new-onset atrial fibrillation and, using propensity matching, characteriz
140 arization, incident heart failure, or atrial fibrillation) and ASCVD (fatal or nonfatal myocardial in
142 ndent risk factor for both stroke and atrial fibrillation, and in the setting of AF, type 2 diabetes
143 use of medications for heart failure, atrial fibrillation, and left ventricular systolic dysfunction.
144 athy, cardiac conduction disturbance, atrial fibrillation, and malignant ventricular arrhythmias.
145 insights into the molecular basis of atrial fibrillation, and may facilitate the identification of n
146 ause of age but also stroke severity, atrial fibrillation, and prestroke functional limitations.
147 higher rates of acute kidney injury, atrial fibrillation, and transfusion requirements, whereas TAVR
149 rdial breakthrough waves (EBW) during atrial fibrillation are important elements of the arrhythmogeni
150 rt disease, atrial septal defect, and atrial fibrillation are made, and the arrhythmia (atrial fibril
151 fibrosis in patients with persistent atrial fibrillation are mandatory and may inform strategies to
152 ke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) trial reported that apixaban th
153 were obtained from 17 simulations of atrial fibrillation, atrial flutter, and focal atrial tachycard
154 oubles the likelihood of freedom from atrial fibrillation, atrial flutter, or atrial tachycardia whil
155 locus led to ventricular arrhythmias, atrial fibrillation, atrioventricular conduction defects, and d
156 therapy in patients with nonvalvular atrial fibrillation because these drugs have several benefits o
157 short-term mortality, renal failure, atrial fibrillation, bleeding, and length of intensive care uni
158 ent clinics if they had no history of atrial fibrillation but had any of the following: CHA2DS2-VASc
159 of stroke than warfarin in trials of atrial fibrillation, but large-scale evaluations in clinical pr
160 ght is an independent risk factor for atrial fibrillation, but the underlying mechanisms are unknown.
161 ons of this simulation, patients with atrial fibrillation can be triaged to an optimal warfarin thera
162 tion study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in
163 prevention, suffered more often from atrial fibrillation, chronic kidney disease, diabetes mellitus,
164 ides stroke prevention in nonvalvular atrial fibrillation comparable to warfarin, with additional red
165 patients taking NOACs for nonvalvular atrial fibrillation, concurrent use of amiodarone, fluconazole,
166 bocytopenia, acute coronary syndrome, atrial fibrillation, congestive heart failure, DM 2, and smokin
168 ogy consultation, anticoagulation for atrial fibrillation, discharge on statin, lipid management, neu
169 atients with long-standing persistent atrial fibrillation (duration, 12-72 months) underwent phase/fr
170 tients with diabetes also had a lower Atrial Fibrillation Effects on Quality of Life score of 80 (int
172 petitive ventricular tachycardia/ventricular fibrillation episodes alternating with periods of sinus
173 d those with an antecedent history of atrial fibrillation experienced the highest risk of HF associat
174 issue provides a clinical overview of atrial fibrillation, focusing on diagnosis, treatment, and prac
175 to October 2013 with newly diagnosed atrial fibrillation formed the study cohort (65 734 [44.8%] men
176 ith warfarin therapy in patients with atrial fibrillation from the perspective of the US health care
177 Radiofrequency catheter ablation for atrial fibrillation has become an important therapy for AF; how
178 ded warfarin dosing for patients with atrial fibrillation have demonstrated conflicting results.
179 tation had higher adjusted hazards of atrial fibrillation (hazard ratio [HR], 3.12; 95% confidence in
182 ug refractory, symptomatic paroxysmal atrial fibrillation in 172 participants recruited from 21 sites
183 idence, risk factors, and outcomes of atrial fibrillation in a cohort of critically ill patients with
184 enetic loci have been associated with atrial fibrillation in European and Asian ancestry groups.
187 h the general population, the risk of atrial fibrillation in men with type 1 diabetes was slightly ra
188 icular pacing (RVP) increases risk of atrial fibrillation in patients with implantable cardioverter-d
191 oci were specifically associated with atrial fibrillation in the Japanese population after comparing
192 estigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a
194 detection from 60% to 70% of time in atrial fibrillation in unipolar recordings and from 0% to 62% i
195 reafter to cardiac arrest due to ventricular fibrillation, including rhythms shockable by an automati
200 nd frequently unrecognized, new-onset atrial fibrillation is associated with poor hospital outcomes.
202 reatment options to all patients with atrial fibrillation is difficult, despite recent improvements i
208 llation are made, and the arrhythmia (atrial fibrillation) is indicative diagnosed from health, by ch
209 c disease was defined as a history of atrial fibrillation, ischemic heart diseases, or congestive hea
210 tion (PeAF), long-standing persistent atrial fibrillation (LPeAF), or paroxysmal atrial fibrillation
211 rillation, rotors potentially explain atrial fibrillation maintenance, but their ablation remains con
212 Among 91330 patients with nonvalvular atrial fibrillation (mean age, 74.7 years [SD, 10.8]; men, 55.8
213 Stented subjects with nonvalvular atrial fibrillation (n=2124) were randomized 1:1:1 to administr
214 r of ventricular tachycardias or ventricular fibrillation, negatively affects short- and long-term su
215 tory of sudden death (FHSD), syncope, atrial fibrillation, non-sustained ventricular tachycardia (nsV
216 antially outside the South, including atrial fibrillation (Northwest), aortic aneurysm (Midwest), and
217 d electrocardiogram without pacing or atrial fibrillation noted on their baseline Jackson Heart Study
219 (1.4%) in the PFO closure group, and atrial fibrillation occurred in 29 patients (6.6%) after PFO cl
221 One serious adverse event (transient atrial fibrillation) occurred in 205 subjects who underwent PFO
222 ide polymorphisms was associated with atrial fibrillation (odds ratio=0.89 per SD change; 95% confide
227 bserved six cases of self-terminating atrial fibrillation or flutter and six cases of partial electri
229 IF) are used in the treatment of ventricular fibrillation or tachycardia; however, only few studies h
230 inical trials, enrolled patients with atrial fibrillation or venous thromboembolism, compared a novel
231 diac defibrillator discharge for ventricular fibrillation or ventricular tachycardia >240 bpm) and 36
233 l fibrillation (LPeAF), or paroxysmal atrial fibrillation (PAF); if right atrial sites are important;
235 patients if sources drive persistent atrial fibrillation (PeAF), long-standing persistent atrial fib
238 the number of known genetic loci for atrial fibrillation, provide insights into the molecular basis
239 for ARISTOTLE-eligible patients with atrial fibrillation provides clinical benefits at an incrementa
242 term survival in shock-resistant ventricular fibrillation/pulseless ventricular tachycardia; however,
243 Robust evidence from patients with atrial fibrillation randomized to NOACs or warfarin demonstrate
244 s >/=18 years of age with nonvalvular atrial fibrillation, randomized to either VKAs or NOACs, or rec
245 presence of surfactant/LPS, accelerates the fibrillation rate of CsgA by circumventing the lag phase
246 a significantly higher prevalence of atrial fibrillation (rate ratio [RR], 1.62; 95% CI, 1.20-21.8),
247 presented reentrant activity just in atrial fibrillation recordings accounting for approximately 80%
249 ference was observed in terms of free atrial fibrillation-recurrence rates: 79.4% in control versus 7
250 stry for Better Informed Treatment of Atrial Fibrillation) registry, a prospective, nationwide, outpa
254 In human long-standing persistent atrial fibrillation, rotors potentially explain atrial fibrilla
255 utations that cause a genetic form of atrial fibrillation, S140G and V141M, drastically slow IKs deac
256 evalence of asymptomatic, subclinical atrial fibrillation (SCAF) in patients with pacemakers and pati
257 rior stroke, diabetes, pacemaker use, atrial fibrillation, slow gait speed, and nonfemoral access wer
258 tion, new or worsening heart failure, atrial fibrillation, stroke, deep venous thrombosis, cardiovasc
259 ate-quality evidence that concomitant atrial fibrillation surgery approximately doubles the likelihoo
263 ersistent or long-standing persistent atrial fibrillation, the outcomes of initial ablative strategie
264 ed by ventricular tachycardia or ventricular fibrillation, the rate of 1-year survival was higher in
265 enhance the occurrence of EBW during atrial fibrillation, thereby promoting atrial fibrillation pers
266 ion with Factor Xa Next Generation in Atrial Fibrillation-Thrombolysis in Myocardial Infarction 48),
269 dian age, 63.5 years) with persistent atrial fibrillation underwent epicardial thoracoscopic radiofre
270 paroxysmal (n=345; 42%) or persistent atrial fibrillation underwent postprocedural esophageal endosco
272 ted ventricular tachycardia (VT)/ventricular fibrillation (VF) and Brugada syndrome-related symptoms,
273 After defibrillation of initial ventricular fibrillation (VF), it is crucial to prevent refibrillati
276 refractory out-of-hospital (OH) ventricular fibrillation (VF)/ventricular tachycardia (VT) cardiac a
277 prediction of very late recurrence of atrial fibrillation (VLRAF) occuring >12 months after catheter
279 ed by ventricular tachycardia or ventricular fibrillation was associated with higher rates of long-te
280 gression analyses, clinical new-onset atrial fibrillation was associated with increased hospital mort
283 h normoalbuminuria, no excess risk of atrial fibrillation was noted in men with type 1 diabetes who h
286 Hospital for Long-Standing Persistent Atrial Fibrillation), we sought to assess, in patients with sym
287 for warfarin therapy in patients with atrial fibrillation, we performed a cost-effectiveness analysis
288 o further define the genetic basis of atrial fibrillation, we performed large-scale, trans-ancestry m
289 acteristics from 14 206 patients with atrial fibrillation were integrated into a validated warfarin c
290 eless ventricular tachycardia or ventricular fibrillation were stratified by prompt (</=2 minutes) ve
291 ry failure, and new-onset subclinical atrial fibrillation, which occurred in 8% of admissions, were a
292 included 140 patients with paroxysmal atrial fibrillation, which was refractory to antiarrhythmic dru
293 on: Should patients with preoperative atrial fibrillation who are undergoing cardiac surgery undergo
294 uding 91330 patients with nonvalvular atrial fibrillation who received at least 1 NOAC prescription o
295 cohorts of patients with non-valvular atrial fibrillation with incident exposure to dabigatran, rivar
296 on recruiting high-risk patients with atrial fibrillation with more than 2 stroke risk factors, with
297 etermine the association of new-onset atrial fibrillation with outcomes, including ICU length of stay
298 probability of a first occurrence of atrial fibrillation within the following 24 hours, we performed
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