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1 dia, or apparent risk of prolongation of the corrected QT interval.
2 ngation of the action potential duration and corrected QT interval.
3 ormalities, particularly prolongation of the corrected QT interval.
4 T segment shift; and the duration of QRS and corrected QT intervals.
5 TS patients (84% male; age, 26 +/- 15 years; corrected QT interval, 329 +/- 22 ms) were studied, and
9 ts (10 g of ethanol) per day with heart rate-corrected QT interval and heart rate assessed from elect
10 ing therapies may be effective in shortening corrected QT interval and reducing TdP recurrence risk.
12 e variability were assessed every 30 min and corrected QT intervals and T-wave morphology every 60 mi
13 ventricular hypertrophy, prolongation of the corrected QT interval, and repolarization changes (ST/T
14 urther, the majority of LQTS patients have a corrected QT interval below this threshold, and a signif
15 ypes were neither associated with heart rate-corrected QT interval duration (QTc) nor cardiac events
16 were not associated with MeanNN, heart-rate-corrected QT interval duration (QTc), deceleration capac
17 gestive features that, along with heart rate-corrected QT interval duration, may risk stratify perina
19 in serum K(+) resulted in a decrease in the corrected QT interval from 526 +/- 94 to 423 +/- 36 ms (
20 A total of 1,059 LQTS patients with a corrected QT interval > or =450 ms presenting with synco
23 , fatigue in one; hypertension and prolonged corrected QT interval in another) occurred in patients i
24 +/-24.9) was longer than neonatal heart rate-corrected QT interval in both group 2 (491.2+/-27.6; P=0
25 ygotes, revealed an age-dependent heart rate-corrected QT interval increase (1% per additional 10 yea
26 Variants investigated altered heart rate-corrected QT interval irrespective of mutation status, a
28 lf is insufficient for diagnosis, unless the corrected QT interval is repeatedly >/=500 ms without an
30 olic blood pressure, heart rate variability, corrected QT interval, low density lipoprotein (LDL) cho
31 probands displaying ST-segment elevation and corrected QT intervals < or = 360 ms had mutations in ge
32 me is a new clinical entity characterized by corrected QT intervals <300 ms and a high incidence of v
33 cantly (p < 0.05) prolonged, as indexed by a corrected QT interval (mean [+/-SD] 311 +/- 25 to 338 +/
35 n-treatment electrocardiogram occurrences of corrected QT interval more than 500 ms (an indicator of
36 verage age of onset of 10 months, an average corrected QT interval of 676 ms, and a high prevalence o
38 nicity index was increased (P<0.001) and the corrected QT interval on ECG was prolonged (P<0.001) in
40 associated with uncorrected QT interval, HR-corrected QT interval or high-density lipoprotein-choles
41 RE: rs12734991 in meta-analysis: increase in corrected QT interval per C allele: 9.1 +/- 3.2 ms, p =
42 nation was not predicted by the magnitude of corrected QT interval prolongation but was associated wi
43 No significant associations were seen among corrected QT interval prolongation, repolarization chang
44 The proportion of patients who developed corrected QT-interval prolongation (p = 0.16), extrapyra
46 As expected, in TdP patients, many known corrected QT interval-prolonging risk factors were simul
47 a 7.7% +/- 0.9% shortening of the heart rate-corrected QT interval (QTc interval) in Kir2.1-transduce
49 ment depression (STD) >/=50 micro V and rate-corrected QT interval (QTc) >460 ms were examined as mea
50 ic testing correlated significantly with the corrected QT interval (QTc) and clinical diagnostic scor
51 to study the predictive value of heart rate-corrected QT interval (QTc) for incident coronary heart
52 (P<0.05), and an increase in the heart rate-corrected QT interval (QTc) from 379+/-10 to 504+/-11 ms
54 arrhythmia, of which lengthening of the rate-corrected QT interval (QTc) on the electrocardiogram is
55 , 2 of 15 patients experienced dose-limiting corrected QT interval (QTc) prolongation, pneumonitis, o
57 n a recent cohort study, prolongation of the corrected QT interval (QTc) was associated with an indep
58 forms in labeling prolongation of heart rate-corrected QT interval (QTc), an arrhythmia risk marker.
59 ying effects of AKAP9 variants on heart rate-corrected QT interval (QTc), cardiac events, and disease
62 ects differed from control subjects: resting corrected QT interval (QTc, 627 +/- 90 versus 425 +/- 25
63 the risk for TdP included absolute and rate-corrected QT intervals (QTc) on drug therapy, the magnit
65 ized into electrocardiographically affected (corrected QT interval [QTc] > or = 470 ms), borderline (
66 dden cardiac death during childhood included corrected QT interval [QTc] duration > 500 ms (hazard ra
67 males, median age 16 years, average referral corrected QT interval [QTc] of 481 ms) referred with a d
68 G parameters (QRS voltage, QRS duration, and corrected QT interval [QTc]) were evaluated by using mul
70 alyses controlling for risk factors and rate-corrected QT interval, the PCA ratio remained a signific
77 Frontal T axis, heart rate, and heart rate-corrected QT interval were the most significant ECG fact
79 duration of treatment, flecainide levels and corrected QT intervals were recorded; 24 h Holter monito
80 t alcohol units were not associated with the corrected QT interval, with beta = 1.04 (95% confidence
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