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1 QTc interval >/=500 ms increased the risk of cardiac eve
2 QTc interval prolongation was defined as QTc interval >5
3 QTc intervals were analyzed according to age (< 16 or >
4 QTc intervals were measured in 241 patients with heart f
5 QTc intervals were prolonged (>440 ms) in 122 (51%) pati
6 C) runs (sertraline: 13.1%; placebo: 12.9%), QTc interval greater than 450 milliseconds at end point
8 nts receiving hydroxychloroquine developed a QTc interval of 500 ms or greater, but the proportion of
9 ed the DSEC were more likely to experience a QTc interval increase of at least 30 milliseconds vs pla
15 pregnant women) with cardiac parameters, all QTc intervals were within normal limits, with no signifi
18 ed abbreviated QRS duration (P = 0.0003) and QTc interval (P = 0.0006) in EV-treated DSG2mt/mt mice.
19 onship between piperaquine concentration and QTc interval throughout pregnancy can inform effective,
20 , PR intervals (P = 0.014), QRS duration and QTc interval (both P = 0.003), but Normal-VLDL did not.
22 ts (PR interval, QRS axis, QRS duration, and QTc interval) were evaluated for single-nucleotide polym
24 Tc) on drug therapy, the magnitude of QT and QTc interval prolongation, and the change in T(peak) to
25 eviation; PR interval, QRS duration, QT, and QTc interval; P, Q, R, S, and T amplitudes in 12 leads;
27 dy and heart weights, prolonged PR, QRS, and QTc intervals, and reduced %EF and %FS at normoxia compa
29 ificantly greater symptoms, increased QT and QTc intervals and QTc dispersion, ventricular tachycardi
32 048 segments showed mean (+/- SD) RR, QT and QTc intervals of 830 +/- 100, 407 +/- 23 and 445 +/- 16
35 QTc interval prolongation was defined as QTc interval >500 ms or increase in QTc of >/=60 ms from
38 luding in patients with normal or borderline QTc intervals (F1 score, 0.70 [95% CI, 0.40-1.00]; sensi
40 red with baseline, the heart rate-corrected (QTc) interval was prolonged by 30 to 60 milliseconds in
42 he findings of this trial suggest that daily QTc interval monitoring during antipsychotic use may hav
45 l hypercholesterolemia, electrocardiographic QTc interval for long QT syndrome, and glycosylated hemo
48 icant shortening of the electrocardiographic QTc interval and reduction of left ventricular systolic
49 athy, including cardiac isoenzyme elevation, QTc interval prolongation, and rapidly reversible cardia
51 iables predicts patients at highest risk for QTc interval prolongation and may be useful in guiding m
52 ed to a patient at moderate or high risk for QTc interval prolongation, a computer alert appeared on
56 binary outcome meta-analyses (human height, QTc interval and gallbladder disease); all previous repo
61 ipants experienced a significant increase in QTc intervals during hypoxia using Bazett's (from 402 +/
63 c repolarization disturbances with increased QTc intervals in both patients and controls, but with a
64 ing of the heart rate-corrected QT interval (QTc interval) in Kir2.1-transduced animals (n = 4) and a
65 ll patients developed corrected QT interval (QTc interval) prolongation (median QTc interval 504 ms,
68 prevalence and factors associated with long QTc interval in a cohort of opioid-dependent HIV-infecte
69 trophy (77% versus 58%; P=0.02) and a longer QTc interval (466+/-36 versus 453+/-41 milliseconds; P=0
70 Compared with men, women exhibit a longer QTc interval and an increased propensity toward torsade
73 ne and lansoprazole had significantly longer QTc intervals (up to 12 ms in white men) and were 1.4 ti
75 consumption of fish is associated with lower QTc interval in free-eating people without any evidence
77 uals receiving the DSEC had a longer maximal QTc interval (mean [SD], 419.4 [11.8] vs 396.1 [15.7] mi
82 riability between hourly minimal and maximal QTc intervals reached their circadian peak shortly after
83 ntipsychotics vs placebo on next-day maximum QTc interval, adjusting for prespecified baseline covari
88 +/- 23 and 445 +/- 16 ms, respectively (mean QTc interval for men 434 +/- 12 ms, 457 +/- 10 ms for wo
89 d relatives, men exhibited the shortest mean QTc interval in chromosome 7q- and 11p-linked blood rela
92 ayo Clinic evaluation, 22 +/- 14 years; mean QTc interval, 427 +/- 25 milliseconds) were dismissed as
96 interval (QTc interval) prolongation (median QTc interval 504 ms, IQR: 477 to 568 ms) within 24 h of
100 n the JLNS family described here have normal QTc intervals (0.43 and 0.44 seconds, respectively).
102 to evaluate the prevalence and predictors of QTc interval prolongation and incidences of LTA during h
103 QT-prolonging drugs and reduces the risk of QTc interval prolongation in hospitalized patients with
105 by examining dose dependency, the percent of QTc intervals higher than 500 msec, and the risk of drug
106 Nevertheless, intra-subject variability of QTc intervals reduces the clinical utility of QTc monito
107 SNPs previously identified as modulators of QTc-interval in genome-wide association studies in the g
113 7%]), Q waves (2 athletes [1.2%]), prolonged QTc interval (2 athletes [1.2%]), and frequent premature
115 isdiagnosis or overdiagnosis was a prolonged QTc interval secondary to vasovagal syncope (n = 87; 30%
119 nt cardiac arrest and dramatically prolonged QTc interval who were both born to healthy parents.
121 95% CI, 1.23 to 4.68), and pre-HCT prolonged QTc interval (HR, 2.55; 95% CI, 1.38 to 4.72) were indep
122 score comprising renal impairment, prolonged QTc interval, and age older than 52 was developed for pr
123 s with shared clinical features of prolonged QTc interval (range 505-725 ms) and documented ventricul
124 wing in recent years, and cases of prolonged QTc interval and torsades de pointes have been described
126 (</= 440 ms [n = 469]), LQTS with prolonged QTc interval (> 440 ms [n = 1,392]), and unaffected fami
129 implantation in 3) and excessively prolonged QTc intervals in 8 (6.7%) (dosage reduced or discontinue
130 ly, both these family members have prolonged QTc intervals and would have been classified as Romano-W
131 ificantly lower than in those with prolonged QTc intervals (15%) (p < 0.001) but higher than in unaff
132 r ACA or SCD only in patients with prolonged QTc intervals (female age > 13 years, hazard ratio: 1.90
133 bradycardia; palpitation; changing PR, QRS, QTc intervals in electrocardiogram; heart failure) for t
134 d >/=120 ms (1.75, 1.17-2.62); corrected QT (QTc) interval >/=450 ms in men or >/=460 ms in women (1.
137 gender differences in the rate-corrected QT (QTc) interval in the presence of a QT-prolonging gene.
138 stigate whether the heart rate-corrected QT (QTc) interval on the electrocardiogram (ECG) is associat
143 and variability of the QT and corrected QT (QTc) intervals over 24 h and to assess their pattern and
146 hisms (SNPs) that modulate the corrected QT (QTc)-interval and the occurrence of cardiac events in 63
148 SCD in patients with LQTS with normal-range QTc intervals (4%) was significantly lower than in those
149 ors ACA or SCD in patients with normal-range QTc intervals included mutation characteristics (transme
150 the baseline, the mean, and the most recent QTc interval recorded before age 10, were less significa
152 the LQT group had a 24% reduction in resting QTc interval (from 617 +/- 92 to 469 +/- 23 ms, P = .004
153 remodeling in response to MI, with shortened QTc intervals, fewer VT episodes, and higher survival ra
155 h the mutation was associated with a shorter QTc interval (P<0.05) and a reduced occurrence of cardia
158 favorable treatment outcome and significant QTc-interval prolongation (QTc >=500 ms or >=60 ms incre
160 1 (95% CI, 0.80-0.85), which was better than QTc interval-based detection (AUC, 0.74; 95% CI, 0.69-0.
163 +/-6 versus 115+/-11 beats/min; P=0.54), the QTc interval had prolonged significantly more in patient
164 To better understand it, we analyzed the QTc interval duration in patients with heart failure wit
168 COMMENDATION 4 (RISK STRATIFICATION): If the QTc interval is greater than 450 ms but less than 500 ms
172 rocardiogram for all patients to measure the QTc interval and a follow-up electrocardiogram within 30
173 4) and a 16.7% +/- 1.8% prolongation of the QTc interval (n = 3) in Kir2.1AAA-transduced animals 72
175 n (n = 44; 15%), or misinterpretation of the QTc interval as a result of inclusion of the U-wave (n =
176 T prolongation, and misinterpretation of the QTc interval) increases awareness and provides critical
177 p < 0.001) as significant predictors of the QTc interval; and heart rate (p < 0.001), genotype (p <
178 gs that cause torsade de pointes prolong the QTc interval and bind to the potassium rectifier channel
179 opic drugs have been reported to prolong the QTc interval and increase the risk of ventricular dysrhy
184 However, recent studies indicate that the QTc interval is nonlinear with respect to heart rate dur
187 pectedly large effects of NOS1AP SNPs on the QTc-interval and a trend for effects on risk of cardiac
188 an analysis for quantitative effects on the QTc-interval, 3 independent SNPs at NOS1AP (rs10494366,
194 up and upward, the risk of AF increased with QTc interval duration in a dose-response manner, reachin