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1 NSVT (HR, 4.47 [95% CI, 1.87-10.72]; P=0.001) and VT ind
2 NSVT and ventricular ectopy were common early after TPVR
3 NSVT episodes were characterized by QRS morphology, dura
4 NSVT occurred frequently during the acute and convalesce
5 NSVT was not associated with LGE on CMR or VT inducibili
6 NSVT was significantly associated with ICD-treated VT/VF
7 NSVTs may serve as an initiator, and sustained VT induci
8 to 5,435) and increased with age (p < 0.01); NSVT was associated with greater left ventricular hypert
10 atients without (group 1) and with (group 2) NSVT were balanced for variables: age, etiology of heart
14 OR, 6.20 [95 CI, 2.74-13.99]; P < .001), and NSVT (OR, 2.29 [95% CI, 1.10-4.51]; P = .03) at each fol
15 5), couplets (1.9 +/- 5 vs. 1.2 +/- 10), and NSVT runs (0.4 +/- 0.8 vs. 0.06 +/- 0.4) than non-DE pat
16 ure patients with ventricular arrhythmia and NSVT have a significantly increased risk of premature ca
17 e risk of paroxysmal atrial fibrillation and NSVT during sleep is markedly increased shortly after a
20 d quality of life in patients with NIDCM and NSVT treated with amiodarone or an ICD are not statistic
21 3 beats; rate, >=120 bpm; lasting <30 s) and NSVT characteristics (coupling interval, duration, cycle
22 ection fraction < or =0.35, and asymptomatic NSVT were randomized to receive either amiodarone or an
23 h CAD and impaired LV function, asymptomatic NSVT identified in-hospital, compared with that identifi
25 ologic testing in patients with asymptomatic NSVT, CAD and LV dysfunction, eligible patients were enr
27 for NSVT episodes, with associations between NSVT- and ICD-treated ventricular arrhythmias examined.
28 There was a time-varying interaction between NSVT and cardiovascular death such that NSVT was signifi
29 treated with reperfusion and beta-blockers, NSVT is not an independent predictor of long-term mortal
31 , and most probably genetic channelopathies, NSVT carries prognostic significance, whereas its indepe
37 djusting other variables, especially for EF, NSVT was not an independent predictor of all-cause morta
38 d syncope (1.9 to 14.9) (p = 0.002); 1.9 for NSVT (0.7 to 5.0) (p = 0.18) and 2.9 for LVWT (1.1 to 7.
39 terrogated and ambulatory ECGs monitored for NSVT episodes, with associations between NSVT- and ICD-t
41 postimplant telemetry, 27 patients (50%) had NSVT, including 1 who had torsade de pointes, but most h
42 ; interquartile range, 8-23 g), 62 (54%) had NSVT on Holter, and sustained monomorphic VT was inducib
44 In acute myocardial infarction, in-hospital NSVT has an adverse prognostic significance when detecte
45 treated patients with in-hospital-identified NSVT and 11% and 21% for the out-of-hospital group (adju
47 d in 35% and 28% of the patients whose index NSVT occurred in-hospital and out-of-hospital, respectiv
48 ent for clinical variables, exercise-induced NSVT did not independently increase the risk of total mo
50 and coronary risk factors, exercise-induced NSVT was not significantly associated with total mortali
56 ss(i) (p < 0.001), and a higher frequency of NSVT (odds ratio 1.2; 95% confidence interval: 1.1 to 1.
57 variable demonstrated that the frequency of NSVT did not add significant information beyond the clin
58 ar arrhythmias, supporting the importance of NSVT in hypertrophic cardiomyopathy risk stratification.
60 fied time from presentation to occurrence of NSVT as the strongest predictor of mortality (P<0.0001).
61 the time from presentation to occurrence of NSVT increased, plateauing at approximately 24 hours wit
63 0.0001); DE was an independent predictor of NSVT (relative risk 7.3, 95% confidence interval 2.6 to
64 Holters were assessed for the presence of NSVT (>=3 beats; rate, >=120 bpm; lasting <30 s) and NSV
68 minute), shorter (</=7), or a single run of NSVT were not associated with ICD-treated ventricular ar
70 ), longer (>7 beats), and repetitive runs of NSVT were more highly predictive of ICD-treated VT/VF.
73 etermined the prevalence and significance of NSVT in patients with PVCs and heart failure and on vaso
76 Contrary to prevailing clinical opinion, NSVT that occurs in the setting of acute MI does have im
80 es not have an associated adverse prognosis, NSVT that occurs beyond the first several hours after pr
81 during exercise, and especially at recovery, NSVT indicates increased cardiovascular mortality within
85 nown predictors of mortality in SCD-HeFT, RR-NSVT was independently associated with appropriate ICD s
91 ate nonsustained ventricular tachycardia (RR-NSVT) during routine implantable cardioverter-defibrilla
92 The clinical evaluation of patients with RR-NSVT should include intensification of medical therapy,
93 with patients without RR-NSVT, those with RR-NSVT were less likely to be taking beta-blockers, statin
96 on, coronary artery disease, and symptomatic NSVT are at highest risk of receiving appropriate ICD sh
98 T-segment elevation acute coronary syndrome, NSVT occurring beyond 48 h after admission indicates an
100 on and nonsustained ventricular tachycardia (NSVT) as well as a predilection for sudden cardiac death
103 tes of nonsustained ventricular tachycardia (NSVT) have been reported early after transcatheter pulmo
104 nduced nonsustained ventricular tachycardia (NSVT) in a large population of asymptomatic volunteers.
105 nce of nonsustained ventricular tachycardia (NSVT) in patients with hypertrophic cardiomyopathy is in
106 nce of nonsustained ventricular tachycardia (NSVT) in patients with premature ventricular contraction
108 which nonsustained ventricular tachycardia (NSVT) is discovered on the rate of inducibility of susta
109 aneous nonsustained ventricular tachycardia (NSVT) on Holter, VT inducibility during electrophysiolog
110 ncy of nonsustained ventricular tachycardia (NSVT) was the most powerful predictor and remained a sig
111 s, and nonsustained ventricular tachycardia (NSVT) were more common in patients with DE than those wi
112 (VT), nonsustained ventricular tachycardia (NSVT), and Lown's grade >=2 premature ventricular comple
113 titive nonsustained ventricular tachycardia (NSVT), or 3) premature ventricular contractions (PVCs).
114 ables: nonsustained ventricular tachycardia (NSVT), syncope, exercise blood pressure response (BPR),
118 omatic nonsustained ventricular tachycardia (NSVT; HR, 9.1; 95% CI, 2.8-29.2; P=0.001) were associate
120 ifically, the currently accepted notion that NSVT that occurs within 48 hours of acute MI has no prog
121 ween NSVT and cardiovascular death such that NSVT was significantly associated with increased risk wi
123 fibrillation occurred more frequently in the NSVT group (9% versus 0% in the control group; P<0.001),
124 the clinical variables with and without the NSVT variable demonstrated that the frequency of NSVT di
126 (61% vs. 11%; p < 0.001) and polymorphic VA (NSVT and VT: 19% vs. 2%; p = 0.002; premature ventricula
127 ilar patients, the clinical setting in which NSVT is discovered should be taken into account when for
133 risk of cardiovascular death associated with NSVT was the greatest during the first 30 days after pre
134 tion that approximately 50% of patients with NSVT and approximately 5% of patients with PVCs have ind
135 s after presentation; however, patients with NSVT detected during the convalescent phase were also at
140 with NSVT and 6 of 74 patients (8%) without NSVT experienced ICD-treated ventricular tachycardia (VT