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1 raits (RR, P-wave, PR, and QRS intervals and corrected QT interval).
2 apeutics that can induce prolongation of the corrected QT interval.
3 dia, or apparent risk of prolongation of the corrected QT interval.
4 ngation of the action potential duration and corrected QT interval.
5 ormalities, particularly prolongation of the corrected QT interval.
6 T segment shift; and the duration of QRS and corrected QT intervals.
7 TS patients (84% male; age, 26 +/- 15 years; corrected QT interval, 329 +/- 22 ms) were studied, and
13 ts (10 g of ethanol) per day with heart rate-corrected QT interval and heart rate assessed from elect
14 f this diagnosis even with a normal maternal corrected QT interval and lead to the initiation of spec
15 ing therapies may be effective in shortening corrected QT interval and reducing TdP recurrence risk.
17 e variability were assessed every 30 min and corrected QT intervals and T-wave morphology every 60 mi
18 ventricular hypertrophy, prolongation of the corrected QT interval, and repolarization changes (ST/T
20 urther, the majority of LQTS patients have a corrected QT interval below this threshold, and a signif
21 rolongation of either the QT interval or the corrected QT interval (calculated with Fridericia's form
22 ypes were neither associated with heart rate-corrected QT interval duration (QTc) nor cardiac events
23 were not associated with MeanNN, heart-rate-corrected QT interval duration (QTc), deceleration capac
24 gestive features that, along with heart rate-corrected QT interval duration, may risk stratify perina
27 in serum K(+) resulted in a decrease in the corrected QT interval from 526 +/- 94 to 423 +/- 36 ms (
28 A total of 1,059 LQTS patients with a corrected QT interval > or =450 ms presenting with synco
32 , fatigue in one; hypertension and prolonged corrected QT interval in another) occurred in patients i
33 +/-24.9) was longer than neonatal heart rate-corrected QT interval in both group 2 (491.2+/-27.6; P=0
34 ygotes, revealed an age-dependent heart rate-corrected QT interval increase (1% per additional 10 yea
36 Variants investigated altered heart rate-corrected QT interval irrespective of mutation status, a
38 lf is insufficient for diagnosis, unless the corrected QT interval is repeatedly >/=500 ms without an
40 olic blood pressure, heart rate variability, corrected QT interval, low density lipoprotein (LDL) cho
41 probands displaying ST-segment elevation and corrected QT intervals < or = 360 ms had mutations in ge
42 me is a new clinical entity characterized by corrected QT intervals <300 ms and a high incidence of v
43 cantly (p < 0.05) prolonged, as indexed by a corrected QT interval (mean [+/-SD] 311 +/- 25 to 338 +/
44 -lumefantrine extended the electrocardiogram corrected QT interval (mean increase at 52 h compared wi
46 n-treatment electrocardiogram occurrences of corrected QT interval more than 500 ms (an indicator of
47 verage age of onset of 10 months, an average corrected QT interval of 676 ms, and a high prevalence o
49 nicity index was increased (P<0.001) and the corrected QT interval on ECG was prolonged (P<0.001) in
52 associated with uncorrected QT interval, HR-corrected QT interval or high-density lipoprotein-choles
53 RE: rs12734991 in meta-analysis: increase in corrected QT interval per C allele: 9.1 +/- 3.2 ms, p =
54 l fibrillation (9.4%), heart failure (8.6%), corrected QT interval prolongation (8.0%), and cardiac i
55 ated with a 23-fold increased odds of marked corrected QT interval prolongation (P=4x10(-25)), a mark
57 nation was not predicted by the magnitude of corrected QT interval prolongation but was associated wi
58 No significant associations were seen among corrected QT interval prolongation, repolarization chang
59 ed cardiac arrest, acute kidney failure, and corrected QT interval prolongation, were not significant
60 e groups, with the exception of asymptomatic corrected QT interval prolongation, which was significan
62 The proportion of patients who developed corrected QT-interval prolongation (p = 0.16), extrapyra
64 As expected, in TdP patients, many known corrected QT interval-prolonging risk factors were simul
65 a 7.7% +/- 0.9% shortening of the heart rate-corrected QT interval (QTc interval) in Kir2.1-transduce
67 ment depression (STD) >/=50 micro V and rate-corrected QT interval (QTc) >460 ms were examined as mea
68 ic testing correlated significantly with the corrected QT interval (QTc) and clinical diagnostic scor
69 to study the predictive value of heart rate-corrected QT interval (QTc) for incident coronary heart
71 (P<0.05), and an increase in the heart rate-corrected QT interval (QTc) from 379+/-10 to 504+/-11 ms
74 arrhythmia, of which lengthening of the rate-corrected QT interval (QTc) on the electrocardiogram is
75 instigates an exploration into the causes of corrected QT interval (QTc) prolongation in these cases,
76 , 2 of 15 patients experienced dose-limiting corrected QT interval (QTc) prolongation, pneumonitis, o
79 n a recent cohort study, prolongation of the corrected QT interval (QTc) was associated with an indep
80 ded, manual measurements of QT intervals and corrected QT interval (QTc) were performed independently
81 forms in labeling prolongation of heart rate-corrected QT interval (QTc), an arrhythmia risk marker.
83 ying effects of AKAP9 variants on heart rate-corrected QT interval (QTc), cardiac events, and disease
84 gistic regression identified EMW, heart rate-corrected QT interval (QTc), female sex, and LQTS genoty
90 rate; systolic and diastolic blood pressure; corrected QT interval (QTc); sodium; potassium; aspartat
91 ects differed from control subjects: resting corrected QT interval (QTc, 627 +/- 90 versus 425 +/- 25
92 the risk for TdP included absolute and rate-corrected QT intervals (QTc) on drug therapy, the magnit
94 ized into electrocardiographically affected (corrected QT interval [QTc] > or = 470 ms), borderline (
95 IQR], 7.7-23; range, 0-59, median heart rate-corrected QT interval [QTc] at diagnosis 557 ms (IQR, 52
96 dden cardiac death during childhood included corrected QT interval [QTc] duration > 500 ms (hazard ra
97 males, median age 16 years, average referral corrected QT interval [QTc] of 481 ms) referred with a d
98 G parameters (QRS voltage, QRS duration, and corrected QT interval [QTc]) were evaluated by using mul
100 ar-old female with an exaggerated heart rate-corrected QT interval response to metoclopramide ( QTc o
102 alyses controlling for risk factors and rate-corrected QT interval, the PCA ratio remained a signific
111 Frontal T axis, heart rate, and heart rate-corrected QT interval were the most significant ECG fact
113 duration of treatment, flecainide levels and corrected QT intervals were recorded; 24 h Holter monito
114 t alcohol units were not associated with the corrected QT interval, with beta = 1.04 (95% confidence