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. 2018 Apr 20;9:363. doi: 10.3389/fphar.2018.00363

Table 1.

Demographic, clinical and laboratory characteristics of patients with Torsades de pointes.

Patients, n 48
Age, median years (interquartile range) 81(73–85)
Females, n 31/48(65%)
Mean QTc, ms(range) 596.0 ± 80.7(490–910)
Electrolyte imbalances, n 37/47(79%)
Hypokaliemia 28/45(62%)
Hypocalcemia 22/37(59%)
Hypomagnesemia 7/27(26%)
Concomitant diseases*, n 45/48(94%)
Cardiac diseases 40/48(83%)
Left ventricular hypertrophy 19/48(40%)
Dilated cardiomyopathy/heart failure 13/48(27%)
II-III degree atrioventricular block 10/48(21%)
Acute coronary syndrome 9/48(19%)
Chronic coronary artery disease 7/48(15%)
Sinus bradycardia 6/48(13%)
Extra-cardiac diseases 20/48(42%)
Diabetes mellitus type II 13/48(27%)
Chronic kidney disease 8/48(17%)
Hypothyroidism 2/48(4%)
Subarachnoid hemorrhage 1/48(2%)
Cirrhosis 1/48(2%)
Anorexia nervosa 1/48(2%)
HIV infection 1/48(2%)
QTc prolonging-medications, n 34/48(71%)
Amiodarone 14/48(29%)
Citalopram 5/48(10%)
Sertraline 4/48(8%)
Fluconazole 3/48(6%)
Trazodone 3/48(6%)
Levofloxacin 2/48(4%)
Clarithromycin 2/48(4%)
Promazine 2/48(4%)
Quetiapine 2/48(4%)
Mean medication number per patient 1.1 ± 1.0
Anti-Ro/SSA positivity, n 18/32(56%)
Systemic inflammation, n 38/48(79%)
C-reactive protein, mg/dl(range) 2.66(0.1–29.65)
Definite inflammatory diseases 22/48(46%)
Acute infections 15/48(31%)
Immuno-mediated diseases 5/48(10%)
Others 2/48(4%)
Mean QTc-prolonging risk factor number per patient§ 5.3 ± 1.5

Except where indicated otherwise, data are expressed as mean ± standard deviation or median (range).

Appropriate serum potassium, calcium or magnesium measurements available in 45, 37, and 27 out of 48 patients, respectively; anti-Ro/SSA antibodies tested in 32 out of 48 patients.

*

Diseases recognized to be a risk factor for QTc prolongation (Viskin, 1999; El-Sherif and Turitto, 2003; Drew et al., 2010).

Increased C-reactive protein level (>0.5 mg/dl) with or without a definite inflammatory disease.

§

Including electrolyte imbalances, diseases, QTc-prolonging medications, anti-Ro/SSA positivity, and systemic inflammation (Viskin, 1999; El-Sherif and Turitto, 2003; Drew et al., 2010; Yue et al., 2015; Lazzerini et al., 2016, 2017b).