Table 2.
Clinically recognizable risk factors (61-65) |
QTc >500 ms (71-74) |
LQT2-type repolarization: notching, long Tpeak–Tend (11,12) |
Use of QT-prolonging drugs (75-77) |
Concurrent use of more than 1 QT-prolonging drug (78-80) |
Rapid infusion by intravenous route (59) |
Heart disease (64,73,75,76) |
Congestive heart failure (39) |
Myocardial infarction (39,73) |
Advanced age (75,77,86) |
Female sex (64,72,73,75-77,79,81-85) |
Hypokalemia (46,74,87-90) |
Hypomagnesemia (89,91-94) |
Hypocalcemia (95,96) |
Treatment with diuretics (72,74,97) |
Impaired hepatic drug metabolism (hepatic dysfunction or drug-drug interactions) (76,79) |
Bradycardia (65,87) |
Sinus bradycardia, heart block, incomplete heart block with pauses (98,99) |
Premature complexes leading to short-long-short cycles (65,72) |
Multiple clinically recognizable risk factors (64,65,76,79,84) |
Clinically silent risk factors |
Occult (latent) congenital LQTS (23,64) |
Genetic polymorphisms (reduced repolarization reserve) (26,27,31,66-69) |