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1 inued treatment because of an adverse event (syncope).
2 on [AF], and 4% with a history of arrhythmic syncope).
3 haemorrhage, severe anaemia, and cardiogenic syncope).
4 or cardiac failure, atrial fibrillation, and syncope).
5 ina, non-ST-elevation myocardial infarction, syncope).
6 rliest BP decrease occurred 9 minutes before syncope.
7 ity, and the remaining 6 addressed vasovagal syncope.
8 es among adult patients with reflex-mediated syncope.
9 ruction and symptoms of dyspnea, angina, and syncope.
10 lude dyspnoea, chest pain, palpitations, and syncope.
11 in patients with cardioinhibitory vasovagal syncope.
12 A 45-year-old woman presented with syncope.
13 patients hospitalized for a first episode of syncope.
14 outcome measure was the first recurrence of syncope.
15 but without postural lightheadedness or near syncope.
16 being on fludrocortisone prevents vasovagal syncope.
17 class, Canadian Cardiology Society class, or syncope.
18 there were alternative explanations for the syncope.
19 se neurological symptoms such as vertigo and syncope.
20 ystole>6 s is strongly associated with ictal syncope.
21 ed palpitations, 47% fatigue, and 30% (near-)syncope.
22 ic information for emergency department (ED) syncope.
23 rare, serious, and often treatable cause of syncope.
24 ictal asystole episodes, 15 of which led to syncope.
25 ricular failure with shortness of breath and syncope.
26 eactions (6 were hypotensive) and 6 reported syncope.
27 ode of aborted sudden death, and 8 (20%) had syncope.
28 table cardioverter defibrillator shocks, and syncope.
29 unaltered (placebo) followed by LBNP to pre-syncope.
30 a future role in the management of falls and syncope.
31 abdominal pains, breathing difficulties, and syncope.
32 ty, with no apparent increase in the risk of syncope.
33 d ventricular tachycardia, or arrhythmogenic syncope.
34 tween 2006 and 2012 for diagnostic workup of syncope.
35 apy, and the use of pacemakers for vasovagal syncope.
36 tients at a median time of 58 seconds before syncope.
37 ts without previous comorbidity admitted for syncope.
38 tifies AS patients with an increased risk of syncope.
39 lization, device implantation, and recurrent syncope.
40 ed from subclinical to occasional exertional syncope.
41 lack race, intramural course, and exertional syncope.
42 associated with lower likelihood of cardiac syncope.
43 y identify patients with and without cardiac syncope.
44 in hypothesis of the physiology of vasovagal syncope.
45 d prognostic information in ED patients with syncope.
46 nd GG males had 9% versus 77% likelihoods of syncope.
47 sible gene variants associate with vasovagal syncope.
48 e broad spectrum of patients presenting with syncope.
49 ermine the prevalence of PE in patients with syncope.
50 ssociated with greater likelihood of cardiac syncope.
51 chycardia [6], near-drowning [2], exertional syncope [1], symptoms on therapy [2], LQT3 [1], QTc>520
52 luding non-specific chest pain, dyspnoea and syncope (1368 [6%] deaths), and respiratory disorders (2
55 ed ventricular tachycardia; or aborted SCD), syncope, 24-hour premature ventricular complexes count,
56 al fibrillation 58 (70%) or neurocardiogenic syncope 25 (30%), New York Heart Association class<II an
57 and 28.9% for controls; P=0.045), presyncope/syncope (27.8% for cases and 21.3% for controls; P<0.001
58 ly different between groups in time to first syncope: 29.2 months (95% CI: 15.3 to 29.2 months) versu
59 sudden cardiac death were presyncope (61%), syncope (31%), previous cardiac arrest (14%), ventricula
60 % versus 5.5%, P=0.0006), greater history of syncope (32% versus 17%, P=0.020), and higher rate of su
61 y incontinence (18.5% vs 3.9%; P = .04), and syncope (37% vs 9.6%; P = .01) did not hold up after cor
62 ccessfully clamped at baseline levels at pre-syncope (38.3 +/- 2.7 vs. 38.5 +/- 2.5 mmHg respectively
65 , 34 400 (95% CI, 31 200-37 600) episodes of syncope, 43 400 (95% CI, 39 400-47 500) serious electrol
67 ing tachycardia, and these patients had more syncope (5/11 [45%] versus 0/15 [0%]; P<0.01), slower or
68 ntrols, patients with DAPs had more frequent syncope (5/26 [19%] versus 3/73 [4%]; P=0.02) and ventri
69 Patients with MPE more often presented with syncope (59.1% [26 of 44] vs. 25.0% [23 of 92]; p = 0.00
72 53%), 25 were preoperatively symptomatic (15 syncope, 7 near-drowning, and 3 resuscitated sudden deat
75 ) increased hazard of a composite of cardiac syncope, aborted cardiac arrest, and sudden cardiac deat
76 ith a 1% to 5% annual risk of LQTS-triggered syncope, aborted cardiac arrest, or sudden cardiac death
77 etine prevents arrhythmic events (arrhythmic syncope, aborted cardiac arrest, or sudden cardiac death
78 tive in reducing the risk of cardiac events (syncope, aborted cardiac arrest, sudden cardiac death).
79 ge: 34.0+/-13.8 years) with cardioinhibitory syncope, advanced atrioventricular block or sinus arrest
80 severity AEs were reported in two subjects; syncope after a single 250 mg dose (one subject) and abd
83 ,017 patients with a first-time diagnosis of syncope and 185,085 control subjects; their median age w
85 ope beyond patients with recurrent vasovagal syncope and asystole documented by implantable loop reco
86 efit of pacing among patients with recurrent syncope and asystole documented by implantable loop reco
87 collected baseline characteristics, time of syncope and ED arrival, and the Canadian Syncope Risk Sc
90 2.7%) who had an alternative explanation for syncope and in 52 of the 205 patients (25.4%) who did no
91 2 class IIa recommendations, LVEF >35% with syncope and LVEF >35% with inducible ventricular arrhyth
92 inostat 160 mg twice daily: one (2%) grade 3 syncope and one (2%) grade 3 myalgia event in different
93 re, whether pacing reduces risk of recurrent syncope and relevant clinical outcomes among adult patie
94 dered during the evaluation of syncope, near-syncope and seizures, especially in the setting of exerc
97 2%) and 14,251 (7.1%) deaths occurred in the syncope and the control population, respectively, yieldi
98 n as the start of an HR decrease (HR) before syncope and used logarithms of SV, HR, and TPR ratios to
106 d observational studies examining pacing and syncope, and the bibliographies of known systematic revi
110 lass, family history of sudden death (FHSD), syncope, atrial fibrillation, non-sustained ventricular
111 leads to paroxysmal dizziness, fatigue, and syncope because of a temporarily or permanently reduced
112 upport the use of pacing for reflex-mediated syncope beyond patients with recurrent vasovagal syncope
115 ow promising diagnostic accuracy for cardiac syncope, but diagnostic thresholds require validation.
116 portion of patients with recurrent vasovagal syncope by at least 40%, representing a pre-specified mi
120 ding heart failure, infarction, arrhythmias, syncope, cardiomyopathy, angina, heart transplantation a
123 ne plasmatic level define a distinct form of syncope, distinguish it from VVS, and suggest a causal r
124 in 163 patients with tilt-induced vasovagal syncope documented by continuous ECG and video EEG monit
125 AF to the risk of cardiac events defined as syncope, documented torsades de pointes, and aborted car
126 ther at rest or induced by hypocapnia at pre-syncope does not impact OT, probably due to a compensato
128 the PENFS group, two in the sham group), and syncope due to needle phobia (n=1; in the sham group).
130 es of serious adverse events of hypotension, syncope, electrolyte abnormalities, and acute kidney inj
131 nd (ii) serious adverse events (hypotension, syncope, electrolyte abnormalities, bradycardia, or acut
132 ower-body negative pressure (LBNP) until pre-syncope; end-tidal carbon dioxide (P ET , CO 2) was clam
134 (HR: 1.74; 95% CI: 1.68 to 1.80), recurrent syncope event rate of 45.1 per 1,000, stroke event rate
139 h patients age >/=40 years, with high burden syncope (>/=5 episodes, >/=2 episodes in the past year),
142 o third quartiles, 2.0-4.5), 622 people with syncope had an occupational accident requiring hospitali
144 syndrome and aborted sudden cardiac death or syncope have higher risks for ventricular arrhythmias (V
145 risk of LAE was associated with a history of syncope (hazard ratio [HR]: 4.54; p = 0.02), with the do
146 able analysis, type 1 electrocardiogram with syncope (hazard ratio: 4.96; 95% confidence interval: 1.
147 outcome included previous cardiac arrest or syncope (hazard ratio=3.4; 95% confidence interval, 1.4-
148 0.97-3.09]), 3.0% vs 2.4%, respectively, for syncope (HR, 1.23 [95% CI, 0.76-2.00]), 4.0% vs 2.7% for
149 sone significantly reduced the likelihood of syncope (HR: 0.63; 95% CI: 0.42 to 0.94; p = 0.024).
150 lation (hazard ratio [HR]: 4.38; p = 0.002), syncope (HR: 3.36; p < 0.001), participation in strenuou
151 rs of severe anaphylaxis were defined as (1) syncope, hypotension, or hypoxia; (2) signs and symptoms
152 nts, cognitive impairment, fractures, falls, syncope, hypotension, withdrawals due to adverse events,
153 302 patients with anaphylaxis, 55 (18%) had syncope, hypoxia, or hypotension, 57 (19%) required hosp
154 should be considered in patients with ictal syncope if they are not considered good candidates for e
156 ts without previous comorbidity admitted for syncope in Denmark from 2001 to 2009 were identified in
157 MT c.472 A alleles associated with decreased syncope in males but increased in females ( P=0.017).
158 promoter L alleles associated with decreased syncope in males but increased in females ( P=0.059).
160 he yield of stress MPI for the evaluation of syncope in patients at risk but without known coronary a
162 is, only Zva was an independent predictor of syncope in patients with AS (odds ratio, 2.02; 95% confi
165 cing was effective in reducing recurrence of syncope in patients with presumed neurally mediated sync
167 was a marginally nonsignificant reduction in syncope in the fludrocortisone group (hazard ratio [HR]:
168 ailure (in 3% of patients in each group) and syncope (in 2% of the riociguat group and in 3% of the p
174 ary embolism among patients hospitalized for syncope is not well documented, and current guidelines p
176 drocortisone for the prevention of vasovagal syncope; ISRCTN51802652; Prevention of Syncope Trial 2 [
181 tatus; extent of structural disease; cardiac syncope; male sex; the presence of multiple mutations or
182 ears) and had a history of fewer episodes of syncope (median of 2 [interquartile range [IQR]: 1 to 2.
183 rawn postapproval after visual disturbances, syncope, myasthenia gravis, and hepatotoxicity were note
185 and inability to remember behavior prior to syncope (n = 323; sensitivity, 5% [95% CI, 0%-9%]; speci
186 associated with higher likelihood of cardiac syncope (n = 323; sensitivity, 8% [95% CI, 2%-14%]; spec
187 ssociated with greater likelihood of cardiac syncope (n = 323; sensitivity, 91% [95% CI, 85%-97%]; sp
189 associated with lower likelihood of cardiac syncope (n = 456; range of sensitivity, 89%-91%, range o
190 epsis (n=2 [4%]), abdominal pain (n=1 [2%]), syncope (n=1 [2%]), cellulitis (n=1 [2%]), pneumonitis (
193 hould be considered during the evaluation of syncope, near-syncope and seizures, especially in the se
194 in patients with presumed neurally mediated syncope (NMS) and documented asystole but syncope still
197 atients in the placebo group (P = 0.12), and syncope occurred in 4.0% of the patients in the vericigu
201 18 patients (22%) and anemia, headache, and syncope of grade 3 or higher each occurred in 2 patients
203 linded ISSUE-3 (Third International Study on Syncope of Uncertain Etiology) trial, which demonstrated
204 ents in patients with bifascicular block and syncope of undetermined origin implanted with permanent
205 In patients with bifascicular block and syncope of undetermined origin, the use of a dual chambe
206 ad an aborted cardiac arrest, 2 patients had syncope only, 10 patients had >/=1 appropriate ICD disch
214 nts (BCEs) were defined as LQTS-attributable syncope or seizures, aborted cardiac arrest, appropriate
215 d to DDD60 led to a significant reduction of syncope or symptomatic events associated with a cardioin
216 with sustained ventricular tachycardia with syncope or systolic heart failure as a result of ischemi
218 ythmias or structural heart disease (cardiac syncope), or other causes, such as vasovagal syncope or
226 recorded cardiopulmonary dynamics in supine syncope patients and healthy volunteers (aged 15-27 year
227 ac pacing was effective in neurally mediated syncope patients with documented asystolic episodes in w
228 of the following: chest/abdominal/back pain, syncope, perfusion deficit, and if AAS was in the differ
229 rade 3 increased aspartate aminotransferase, syncope, pericardial effusion, and hyperkalaemia, and gr
230 is, the incidence rate ratio in the employed syncope population was higher than in the employed gener
234 artment visits, atrial fibrillation/flutter, syncope/presyncope, end-stage liver disease, malignancy,
237 symptoms (palpitations, fatigue, and [near-]syncope), PVC burden on 24-hour Holter, NT-proBNP levels
238 tors of RV pathology included the following: syncope; Q waves or precordial QRS amplitudes <1.8 mV; 3
239 ent-years; HR, 0.87; P = .50) and arrhythmic syncope rates (3.1 [95% CI, 2.6-4.6] vs 1.9 [95% CI, 1.1
242 currence by 7-fold, prolonging time to first syncope recurrence in patients age >/=40 years with head
243 At 21 months, the estimated product-limit syncope recurrence rates were 55% and 5%, respectively (
246 11 hospitals in Italy for a first episode of syncope, regardless of whether there were alternative ex
247 associated with a 70% reduction in recurrent syncope (relative risk [RR]: 0.30; 95% confidence interv
248 cm s(-1) (31%; P </= 0.001), but time to pre-syncope remained similar between trials (placebo: 1123 +
250 n-flight medical emergencies were related to syncope, respiratory symptoms, or gastrointestinal sympt
252 n Fransisco Syncope Rule (SFSR) and Canadian Syncope Risk Score (CSRS) served as the prognostic compa
255 er defibrillator shock or (2) arrhythmogenic syncope, seizures, or aborted cardiac arrest after LCSD.
257 stained ventricular tachycardia, unexplained syncope, septal diameter z-score, left ventricular poste
258 ggest that the term vasodepression in reflex syncope should not be limited to reduced arterial vasoco
259 who experienced episodes of exertion-induced syncope since age 10, had normal QT interval, and displa
263 he multivariable Evaluation of Guidelines in Syncope Study (EGSYS) score, which is based on 6 clinica
264 alleles of serotonin signaling and vasovagal syncope, supporting the serotonin hypothesis of the phys
267 ain, nonspecific pain, headache, hypotension/syncope, tachycardia (including postural orthostatic tac
269 ), pulmonary toxic effects (six [24%] vs 0), syncope (three [12%] vs two [8%]), dyspnoea (three [12%]
274 sments, in patients >45years presenting with syncope to the emergency department (ED) in a prospectiv
275 ry embolism (PE) in patients presenting with syncope to the emergency department (ED) is largely unkn
284 the uncontrolled trial, yet the time to pre-syncope was comparable between trials (544 +/- 130 vs. 5
285 ly diagnosed heart failure, arrhythmias, and syncope was generally found to be Appropriate or May Be
287 No significant difference in the risk of syncope was observed with conventional versus therapy re
288 n the uncontrolled trial, P ET , CO 2 at pre-syncope was reduced by 10.9 +/- 3.9 mmHg (P </= 0.001).
289 eligible for diagnostic assessment, cardiac syncope was the adjudicated diagnosis in 234 patients (1
292 duals, 21 729 with a first-time diagnosis of syncope were identified, with a median age 48.4 years (f
293 associated with lower likelihood of cardiac syncope were mood change or prodromal preoccupation with
296 seizure with asystole duration</=6 s led to syncope, whereas 94% (15/16) of seizures with asystole d
297 generally much higher among ED patients with syncope who had a 30-day SAE, this blood test added litt
299 ry findings of 15 patients with sudden-onset syncope without prodromes who had a normal heart and nor
300 indings of patients affected by sudden-onset syncope without prodromes who had a normal heart and nor