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1 orphic ventricular tachycardia ('torsades de pointes').
2 ythmias (eg, long QT syndrome and torsade de pointes).
3 T interval and/or development of torsades de pointes).
4 methadone may be associated with torsade de pointes.
5 e thought to trigger episodes of torsades de pointes.
6 arket after being associated with torsade de pointes.
7 tion are not capable of inducing torsades de pointes.
8 ia displaying characteristics of torsades de pointes.
9 ial arrhythmias, but it can cause torsade de pointes.
10 the QT interval but rarely causes torsade de pointes.
11 the potentially fatal arrhythmia torsades de pointes.
12 the potential for development of torsade de pointes.
13 ricular arrhythmias, specifically torsade de pointes.
14 ymorphic ventricular tachycardia torsades de pointes.
15 nd an increased propensity toward torsade de pointes.
16 the link between hypokalemia and torsade de pointes.
17 T interval syndrome (diLQTS) and torsades de pointes.
18 rrhythmic agents known to promote torsade de pointes.
19 ificant predictor of drug-induced torsade de pointes.
20 abnormal heart rhythms, including torsade de pointes.
21 erventions to reduce the risk of torsades de pointes.
22 h the rare adverse drug reaction torsades de pointes.
23 ts including QT prolongation and torsades de pointes.
24 mine the risk of rare events like torsade de pointes.
25 tion of L-type channels, such as Torsades de Pointes.
26 rug-induced long QT syndrome and torsades de pointes.
27 afterdepolarizations (EADs), and torsade de pointes.
28 and the lethal cardiac arrhythmia torsade de pointes.
29 n are more vulnerable than men to torsade de pointes.
30 ation with the associated risk of torsade de pointes.
31 ndividuals to QT prolongation and torsade de pointes.
32 associated with case reports of torsades de pointes.
33 polarizations thought to trigger torsades de pointes.
37 olong the QT interval and lead to torsade de pointes, a life-threatening ventricular arrhythmia, this
38 t in cases of QTc prolongation or torsade de pointes after dofetilide (a known proarrhythmic drug) an
39 acebo group (0.3% versus 0.1% for torsade de pointes and 0.9% versus 0.2% for severe neutropenia).
41 Macrolides are known to cause torsade des pointes and other ventricular arrhythmias, and a recent
45 dol have been documented to cause torsade de pointes and sudden death, the most marked risk is with t
47 On the other hand, drug-induced torsades de pointes and symptomatic long QT syndrome have a female p
54 amilial and drug-induced cases of torsade de pointes, and the recognition of the role of noncardiac d
56 ective against dofetilide-induced torsade de pointes arrhythmias (TdP), while maintaining calcium hom
59 n the electrocardiogram and cause torsade de pointes arrhythmias not by direct block of the cardiac p
60 associated with life-threatening torsade de pointes arrhythmias that develop as a consequence of the
62 nd fibrillations reminiscent of Torsades des Pointes arrhythmias, and they exhibit severely increased
66 ct which patients are at risk for torsade de pointes, careful assessment of the risk to benefit ratio
67 ing a persistent increase in TDR; Torsade de Pointes developed or could be induced only in the presen
70 ing QT interval prolongation and torsades de pointes, errors in the use of medications that may prolo
71 bservation of QT prolongation and torsade de pointes found with astemizole intake may principally be
74 es of prolonged QTc interval and torsades de pointes have been described in HIV-infected patients on
75 s developed in 7 patients (5.8%) (torsade de pointes in 2), significant bradycardia in 20 (16.7%) (ra
76 bservation of QT prolongation and torsade de pointes in a patient with undetectable serum concentrati
77 ftercontractions occurred before torsades de pointes in an in vivo dog model of drug-induced long-QT1
78 ificant predictor of drug-induced torsade de pointes in an independent sample of 216 cases compared w
79 amine susceptibility to acquired torsades de pointes in chronic atrioventricular block and for compar
80 duced BVR (P<0.01), and abolished torsade de pointes in hearts treated with either 20 nmol/L E-4031 o
83 been recognized as a hallmark of torsade de pointes in the acquired LQTS, plays a major role in the
85 o electrophysiologic mechanism of torsade de pointes in the long QT syndrome is described, using as a
86 higher incidences of drug-induced torsade de pointes in women than in men are incompletely defined, a
87 ictors of risk for progression to torsade de pointes, in addition to the degree of QT prolongation, w
88 rdiac medications known to cause torsades de pointes, including fluoroquinolones and intravenous halo
89 ly reports of QTc prolongation or torsade de pointes increased from a mean of 0.3 (95% CI, 0.1 to 0.5
90 on effect of many drugs producing torsade de pointes is block of the rapidly activating component of
91 T interval and the occurrence of torsades de pointes is similar to more expensive alternative medicat
93 darone, and drugs associated with torsade de pointes may have contributed to poor outcomes early in t
94 differences in propensity toward torsade de pointes may reflect the relatively greater presence in m
95 ata suggest that cisapride caused torsade de pointes not only by blocking IKr but also by rescuing ce
97 rsus WT (8/26; 31%; P<0.05), and Torsades de Pointes occurred more frequently (73% Cav3.1(-/-) versus
101 tricular block animals exhibited torsades de pointes on dofetilide, the arrhythmia was induced in onl
104 patients with QT prolongation or torsade de pointes, or both, associated with protease inhibitors, u
106 drug-induced long QT syndrome and torsade de pointes pose unique challenges for clinicians, researche
109 rugs, patients with low risk for torsades de pointes receiving selected class III agents, in whom dat
110 atient suffered recurrent runs of torsade de pointes, refractory to aggressive medical management and
111 Drug-induced QT prolongation and torsades de pointes remain significant and often unpredictable clini
112 ongation to be common (24%), with Torsade de Pointes representing 6% of in-hospital cardiac arrests.
115 set of drugs with known clinical torsade de pointes risk was selected to develop and calibrate the i
119 /L totally suppressed spontaneous torsade de pointes (TdP) and reduced the vulnerable window during w
120 long QT syndrome (LQTS) include torsades de pointes (TdP) and/or 2 degrees atrioventricular block, b
121 jects and may be associated with torsades de pointes (TdP) arrhythmia, we tested the hypothesis that
122 d and acquired long-QT associated torsade de pointes (TdP) arrhythmias, and sympathetic discharge is
124 Dose-dependent susceptibility to Torsade de Pointes (TdP) by class III drug dofetilide, 3, 10, and 3
125 chycardia with characteristics of torsade de pointes (TdP) developed in the presence of dl-sotalol.
126 re more prone than men to develop torsade de pointes (TdP) in a defined cohort of patients exposed to
127 it hearts are more susceptible to torsade de pointes (TdP) in acquired long QT type 2 than males, in-
129 tion (TDR) and the development of Torsade de Pointes (TdP) in models of LQT1, LQT2 and LQT3 forms of
130 re associated with initiation of torsades de pointes (TdP) in patients with acquired (a-) and congeni
131 study was to identify markers of torsades de pointes (TdP) in patients with drug-associated long QT s
132 may be related to the genesis of torsade de pointes (TdP) in patients with the long-QT (LQT) syndrom
133 sion of repolarization (TDR), and torsade de pointes (TdP) induced by beta-adrenergic agonists under
136 F, excessive QT prolongation and torsades de pointes (TdP) often occur shortly after sinus rhythm is
138 larization (TDR) and induction of torsade de pointes (TdP) under conditions mimicking the LQT1, LQT2,
141 ADs and the mechanisms underlying Torsade de Pointes (TdP) were investigated in a model of long QT sy
142 systolic activity and spontaneous torsade de pointes (TdP) were never observed, and stimulation-induc
143 n producing a trigger to initiate torsade de pointes (TdP) with QT prolongation induced by dl-sotalol
144 lmodulin inhibitor W-7 suppresses torsade de pointes (TdP) without shortening the QT interval, which
146 with documented prolonged QTc and Torsade de Pointes (TdP), and in an adult woman with QTc >500 ms, a
154 luding the risk of drug-induced 'torsades de pointes' (TdP) arrhythmia, is a major concern in the dev
155 Women have a higher incidence of torsades de pointes than men, but it is not known if the risk of dru
156 ng medications can predispose to torsades de pointes, there is a relative paucity of information that
157 correlate with a higher risk of torsades de pointes, there is no established threshold below which p
164 ventricular tachycardia (VT), and torsade de pointes VT) in the antiarrhythmic drug arm of the AFFIRM
172 lapsed APL developed asymptomatic torsade de pointes, which resolved spontaneously and did not recur
173 The characteristic association of torsade de pointes with T-wave alternans and short-long cardiac seq
174 lymorphic ventricular tachycardia torsade de pointes, with drugs or other environmental stressors suc
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